Somatic Cell and Molecular Genetics (scientific journal)

published in (P1433)

Q56866528	Q56866528
Q54423843	5-Azacytidine-induced conversion to cadmium resistance correlates with early S phase replication of inactive metallothionein genes in synchronized CHO cells.
Q52235845	?1?4-galactosyltransferase gene expression is regulated during entry into the cell cycle and during the cell cycle
Q41121668	A cell line selected for resistance to ionizing radiation exhibits cross resistance to other genotoxic agents and a mutator phenotype for loss of heterozygosity events
Q30893748	A combination of genetic suppressor elements produces resistance to drugs inhibiting DNA replication
Q36800493	A cyclophilin gene-like sequence maps to human X-chromosome
Q41274816	A densely methylated DNA island is associated with a chromosomal replication origin in the human RPS14 locus
Q41742783	A dominant negative mutation in two proteins created by ectopic expression of an AU-rich 3' untranslated region
Q28261743	A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids
Q43889819	A gene that partially complements xeroderma pigmentosum group A cells maps to human chromosome 8
Q45289744	A genetic linkage map of the chromosome 4 short arm.
Q64389855	A hamster-human subchromosomal hybrid cell panel for chromosome 2
Q33900270	A human ADP/ATP translocase gene has seven pseudogenes and localizes to chromosome X.
Q30857612	A human HP1 pseudogene maps to chromosome 11p14.
Q38547769	A matrix associated region localizes the human SOCS-1 gene to chromosome 16p13.13.
Q54271591	A mutation in codon 717 of the CHO-K1 elongation factor 2 gene prevents the first step in the biosynthesis of diphthamide.
Q69844272	A new approach to gene mapping by in situ hybridization on isolated chromosomes
Q78014001	A new efficient method for transfection of neonatal cardiomyocytes using histone H1 in combination with DOSPER liposomal transfection reagent
Q41002270	A panel of partial chromosome paints and YAC probes specific for human chromosome 2.
Q41138953	A respiration-deficient Chinese hamster cell line with a defect in mitochondrial protein synthesis: Rapid turnover of some mitochondrial transcripts
Q28340195	A reversible selection system for UMP synthase gene amplification and deamplification
Q78013994	A role for RNA processing in regulating expression from transfected genes
Q28512293	A role for certain mouseAprt sequences in resistance to toxic adenine analogs
Q67514613	A single base change at a splice acceptor site leads to a truncated CAD protein in Urd-A mutant Chinese hamster ovary cells
Q68569153	A transcriptional terminator between enhancer and promoter does not affect remote transcriptional control
Q41701606	A very large spontaneous deletion at aprt locus in CHO cells: sequence similarities with small aprt deletions
Q69047424	A-11: cell type-specific and single-active-X transcription controls of newly found gene in cultured human cells
Q68166216	A-raf oncogene localizes on mouse X chromosome to region some 10-17 centimorgans proximal to hypoxanthine phosphoribosyltransferase gene
Q68732899	Abilities of wild-type and thymidine kinase-deficient Friend mouse erythroleukemia cells to undergo unscheduled DNA synthesis following mutagen treatment
Q54275182	Ablation of stimulation of a cAMP-responsive promoter in CHO cell lines defective in their cAMP-dependent protein kinase system
Q41741271	Absence of uvomorulin in a slowly compacting variant of H6 embryonal carcinoma cells
Q41987539	Accelerated age-related decline in replicative life-span of Duchenne muscular dystrophy myoblasts: implications for cell and gene therapy
Q38289693	Acquisition of multiple copies of a mutant topoisomerase IIalpha allele by chromosome 17 aneuploidy is associated with etoposide resistance in human melanoma cell lines
Q58020726	Activation of human? 1,-antitrypsin genes in rat hepatoma � human fibroblast hybrid cell lines is correlated with demethylation
Q45873743	Adenovirus-mediated correction of the genetic defect in hepatocytes from patients with familial hypercholesterolemia
Q41445848	Adenylosuccinate synthetase: a dominant amplifiable genetic marker in mammalian cells
Q45888840	Adult mammalian hepatocyte as target cell for retroviral gene transfer: a model for gene therapy
Q72010002	Alignment of physical and genetic maps of human 8q23-qter using somatic cell hybrid mapping panel
Q69971461	Allelic variation linked to adenine phosphoribosyltransferase locus in mouse teratocarcinoma cell line and feral-derived mouse strains
Q38492772	Allocyclic X chromosome visualized by drug-induced premature chromosome condensation
Q54410759	Altered expression of ribonucleotide reductase and role of M2 gene amplification in hydroxyurea-resistant hamster, mouse, rat, and human cell lines.
Q54404686	Altered form of subunit 6 of mitochondrial ATP synthase complex in oligomycin-resistant mutants of Chinese hamster ovary cells.
Q44130350	Amphotericin B enhances efficiency of DNA-mediated gene transfer in mammalian cells
Q70087992	Amplification and expression of phenylalanine hydroxylase in mouse erythroleukemia cells
Q70932015	Amplification versus mutation as a mechanism for reversion of an HGPRT mutation
Q45298596	Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins
Q54373861	An eighth complementation group of rodent cells hypersensitive to ultraviolet radiation.
Q41778111	An established avian fibroblast cell line without mitochondrial DNA.
Q46124476	An evaluation of the inactive mouse X chromosome in somatic cell hybrids
Q41432205	An extended panel of hamster-human hybrids for chromosome 2q.
Q41566795	An insertion-deletion event in murine immunoglobulin kappa gene resembles mutations at heavy-chain disease loci
Q38504043	An intron 1 regulatory region from the murine adenosine deaminase gene can activate heterologous promoters for ubiquitous expression in transgenic mice
Q43984916	Analysis of Ah gene locus by somatic cell hybridization: expression of Ah regulatory gene product for 2,3,7,8,-tetrachlorodibenzo-p-dioxin in mouse L-cell x mouse hepatoma cell hybrids
Q41741879	Analysis of GPT activity in mammalian cells with a chromosomally integrated shuttle vector containing altered gpt genes
Q42817342	Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids
Q24312170	Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis
Q64390459	Analysis of homologous recombination in cultured mammalian cells in transient expression and stable transformation assays
Q41432758	Analysis of human chromosome 11 by somatic cell genetics: reexamination of derivatives of human-hamster cell line J1.
Q70149347	Analysis of hybridoma mutants defective in synthesis of immunoglobulin M
Q41580170	Analysis of large deletions in the HPRT gene of primary human fibroblasts using the polymerase chain reaction
Q40887284	Analysis of mechanisms and frequency of CDKN2A/B gene loss during progression of RAS-transformed rat embryo fibroblast clones
Q48076624	Analysis of mutations in alleles of the fur gene from an endoprotease-deficient Chinese hamster ovary cell strain
Q72536343	Analysis of mutations introduced into the chromosomal immunoglobulin mu gene
Q36712751	Analysis of region-specific library constructed by sequence-independent amplification of microdissected fragments surrounding weaver (wv) gene on mouse chromosome 16.
Q41134361	Analysis of second-step mutations of class II and class III CHO aprt heterozygotes: chromosomal differences in deletion frequencies
Q41638461	Analysis of sequence specificity of 5-bromodeoxyuridine-induced reversion in cells containing multiple copies of a mutantgpt gene
Q45035258	Analysis of spontaneous mutations in a chromosomally located HSV-1 thymidine kinase (TK) gene in a human cell line
Q42824636	Analysis of the heavy metal-responsive transcription factor MTF-1 from human and mouse
Q41445843	Analysis of tumor suppressor gene on human chromosome 9 in mouse x human somatic cell hybrids
Q70950290	Analysis of variability in albumin content of sister hepatoma cells and a model for geometric phenotypic variability (quantitative shift model)
Q40794154	Antigen S1, encoded by the MIC1 gene, is characterized as an epitope of human CD59, enabling measurement of mutagen-induced intragenic deletions in the AL cell system
Q41728946	Antisense RNA inhibition of HPRT synthesis
Q48942371	Antisense RNA production in transgenic mice
Q46391275	Aphidicolin hypersensitive mutant of Chinese hamster V79 fibroblasts that underproduces DNA polymerase-alpha antigen
Q41050616	Applications of green fluorescent protein as a marker of retroviral vectors
Q45237722	Assignment of Amog (adhesion molecule on glia) gene to mouse chromosome 11 near Zfp-3 and Asgr-1,2 and to human chromosome 17.
Q69842045	Assignment of dioxin-inducible cytochrome P-450 gene family to Chinese hamster chromosome 4
Q34195340	Assignment of gene coding human T-cell differentiation antigen, Tp120, to chromosome 11.
Q67942908	Assignment of gene for coagulation factor V to chromosome 1 in man and to chromosome 13 in rat
Q58199272	Assignment of gene for human cell-surface membrane antigen Trop-4 to chromosome 11
Q70018763	Assignment of genes encoding dihydrofolate reductase and hexosaminidase B to Mus musculus chromosome 13
Q68719513	Assignment of human 3-hydroxy-3-methylglutaryl coenzyme A reductase gene to q13----q23 region of chromosome 5
Q43881222	Assignment of human dihydrofolate reductase gene to band q23 of chromosome 5 and of related pseudogene psi HD1 to chromosome 3.
Q70098891	Assignment of human gamma crystallin multigene family to chromosome 2
Q67942911	Assignment of human gene encoding testis-specific lactate dehydrogenase C to chromosome 11, region p14.3-p15.5.
Q52083129	Assignment of human gene encoding thymidylate synthase to chromosome 18 using interspecific cell hybrids between thymidylate synthase-negative mouse mutant cells and human diploid fibroblasts.
Q70149342	Assignment of human nerve growth factor receptor gene to chromosome 17 and regulation of receptor expression in somatic cell hybrids
Q53878770	Assignment of human preprothyrotropin-releasing hormone (TRH) gene to chromosome 3.
Q28250593	Assignment of human thyrotropin-releasing hormone (TRH) receptor gene to chromosome 8
Q34559787	Assignment of human tryptophan hydroxylase locus to chromosome 11: gene duplication and translocation in evolution of aromatic amino acid hydroxylases
Q47239813	Assignment of low-molecular-weight human (2', 5')A synthetase to chromosome 11.
Q70163631	Assignment of mouse beta-spectrin gene to chromosome 12
Q69731659	Assignment of retinoblastoma susceptibility gene to mouse chromosome 14
Q69849875	Assignment of the gene encoding cytosolic phosphoenolpyruvate carboxykinase (GTP) to Mus musculus chromosome 2
Q34263952	Assignment of the human MARS gene, encoding methioninyl-tRNA synthetase, to chromosome 12 using human X Chinese hamster cell hybrids
Q34442260	Assignment of the human gene encoding eukaryotic initiation factor 4E (EIF4E) to the region q21-25 on chromosome 4.
Q28254499	Assignment of the human lens fiber cell MP19 gene (LIM2) to chromosome 19q13.4, and adjacent to ETFB
Q52254757	Assignment of the lactotransferrin gene to human chromosome 3 and to mouse chromosome 9.
Q41111261	Assignment of the possible HTLV receptor gene to chromosome 17q21-q23.
Q32067626	Assignment of three human markers in chromosome 21q11 to mouse chromosome 16.
Q69834134	Assignment of three rat cellular RAS oncogenes to chromosomes 1, 4, and X
Q44774656	Association of foreign DNA sequence with male sterility and translocation in a line of transgenic mice
Q45992528	Association of high rate of recombination with amplification of dominant selectable gene in human cells.
Q41626400	At least two distinct epigenetic mechanisms are correlated with high-frequency "switching" for APRT phenotypic expression in mouse embryonal carcinoma stem cells
Q55242092	Autonomous growth of lymphoid cells following IL-2 expression from retrovirus vectors containing HIV-1 trans-acting elements.
Q42216113	Biochemical analysis of toxic effects of 5-hydroxymethyl-2'-deoxyuridine in mammalian cells
Q54350579	Biochemical and genetic analysis of toxic effect of HOE 15030 in mammalian cells.
Q41693012	Biosynthesis of lysosomal enzymes in cells of the End3 complementation group conditionally defective in endosomal acidification
Q50756443	Br-cAMP induction of apoptosis in synchronized CHO cells.
Q38291803	Breakpoints and junctional regions of intragenic deletions in the HPRT gene in human T-Cells
Q45351669	Bromodeoxyuridine- and cyclic AMP-mediated regulation of tyrosinase in Syrian hamster melanoma cells
Q41685539	CAIII a marker for early myogenesis: analysis of expression in cultured myogenic cells.
Q41530617	Caffeine enhanced measurement of mutagenesis by low levels of gamma-irradiation in human lymphocytes
Q52255992	Candidate for inherited neurobiological dysfunction in schizophrenia.
Q54141877	Cell cycle control is aberrant in Chinese hamster ovary cell mutants exhibiting apoptosis after serum deprivation.
Q28305888	Cell cycle-dependent repair of double-strand DNA breaks in a gamma-ray-sensitive Chinese hamster cell
Q69838900	Cell fusion and cell agglutination: enhancing effect by a combined use of lectin and polycation
Q70379926	Cell fusion-mediated improvement in transfection competence for repair-deficient mutant of mouse T cell line
Q42797824	Cell genetic evidence of correlation of intracellular translocation of protein kinase C (PKC) and PKC-mediated phosphorylation of 80-kDa protein with mitogenic action of tumor promoters
Q68719510	Cell-surface antigens determined by human chromosomes 1 and 12: comparative serological and somatic cell genetic analysis of eight antigenic systems
Q41597575	Characterisation and correction of a mammalian cell mutant defective in late step of base excision repair
Q28609350	Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin gene
Q36458252	Characterization and mapping of DNA sequence homologous to mouse U1a1 snRNA: localization on chromosome 11 near the Dlb-1 and Re loci
Q40941333	Characterization of a human genomic DNA fragment which rescues defective lipid-linked oligosaccharide synthesis in a mutant G258 cell line isolated from the FM3A mouse mammary carcinoma cell line
Q45168946	Characterization of a mouse cell line selected for hydroxyurea resistance by a stepwise procedure: drug-dependent overproduction of ribonucleotide reductase activity
Q28270690	Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain
Q41400918	Characterization of cDNAs coding for glucose phosphate isomerase and phosphoglycerate kinase in chinese hamster ovary cell line CHO-K1 and identification of defects in R1.1.7, a glycolysis-deficient variant of CHO-K1
Q38510383	Characterization of chimpanzee-hamster hybrids by chromosome painting.
Q41483566	Characterization of diphtheria-toxin-resistant mutants lacking receptor function or containing nonribosylatable elongation factor 2.
Q54342281	Characterization of human IFN-gamma response using somatic cell hybrids of hematopoietic and nonhematopoietic origin.
Q45288394	Characterization of human folylpolyglutamate synthetase expressed in Chinese hamster ovary cells
Q69808198	Characterization of mouse nuclear and mitochondrial mutants with increased resistance to cytochrome b inhibitors
Q41200328	Characterization of mutants involving partial exon duplications in the hprt gene of Chinese hamster V79 cells
Q54447977	Characterization of pyrazofurin-resistant HeLa cells with amplification of UMP synthase gene.
Q57278716	Characterization of reiterated human DNA with respect to mammalian X chromosome homology
Q46634302	Characterization of single-copy probe from vicinity of centromere of human chromosome 1.
Q33527718	Characterization of somatic cell hybrids by bivariate flow karyotyping and fluorescence in situ hybridization
Q71472151	Characterization of somatic cell hybrids exhibiting extinction of AFP, albumin and an AFP-HPRT transgene
Q41434114	Characterization of spontaneous and induced mutations in SV40-transformed normal and ataxia telangiectasia cell lines
Q42477709	Characterization of stem cells in human airway capable of reconstituting a fully differentiated bronchial epithelium
Q42459701	Characterization of the defect in a variant of HL-60 promyelocytic leukemia cells with reduced transferrin receptor expression
Q42522422	Characterization of the promoter region of human steroid sulfatase: a gene which escapes X inactivation
Q69921836	Characterization, evolutionary relationships, and chromosome location of processed mouse HPRT pseudogene
Q80491290	Chemically induced premature chromosome condensation in human fibroblast cell lines: fundamental study for applications to the biodosimetry of local exposure
Q42828362	Chimeric envelope glycoproteins constructed between amphotropic and xenotropic murine leukemia retroviruses
Q42815424	Chinese hamster cells deficient in ornithine decarboxylase activity: reversion by gene amplification and by azacytidine treatment
Q36425732	Chinese hamster cells with a minichromosome containing the centromere region of human chromosome 1.
Q54437452	Chromatin structure of active and inactive human X-linked phosphoglycerate kinase gene.
Q28314823	Chromosomal Sublocalization of the Transcribed Human Telomere Repeat Binding Factor 2 Gene and Comparative Mapping in the Mouse
Q64389236	Chromosomal aberrations induced by defined DNA double-strand breaks: the origin of achromatic lesions
Q68744905	Chromosomal assignment of c-MEL, a human transforming oncogene, to chromosome 19 (p13.2-q13.2)
Q70149350	Chromosomal assignment of gene encoding the largest subunit of RNA polymerase II in the mouse
Q70082015	Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor
Q70033287	Chromosomal assignments of genes coding for human leukocyte common antigen, T-200, and lymphocyte function-associated antigen 1, LFA-1 beta subunit
Q46575595	Chromosomal assignments of genes for tissue plasminogen activator and urokinase in mouse
Q70950296	Chromosomal assignments of genes for trypsin, chymotrypsin B, and elastase in mouse
Q69336527	Chromosomal assignments of human 27-kDa heat shock protein gene family
Q34264023	Chromosomal assignments of human genes for serine proteases trypsin, chymotrypsin B, and elastase
Q44001446	Chromosomal assignments of mouse connexin genes, coding for gap junctional proteins, by somatic cell hybridization
Q72752924	Chromosomal assignments of mouse genes for connexin 50 and connexin 33 by somatic cell hybridization
Q69849868	Chromosomal distribution of genes coding for fast twitch skeletal muscle myosin light chains
Q44436612	Chromosomal evolution in secretory and nonsecretory subline of MOPC 21.
Q34348484	Chromosomal localization and cDNA sequence of human BTEB, a GC box binding protein
Q24323874	Chromosomal localization and cDNA sequence of human ralB, a GTP binding protein
Q28145664	Chromosomal localization and genomic structure of the human arsenite-stimulated ATPase (hASNA-I)
Q41471240	Chromosomal localization and sequence analysis of a human episomal sequence with in vitro differentiating activity
Q48060306	Chromosomal localization of 15 ion channel genes
Q67683035	Chromosomal localization of Cd1d genes in the mouse
Q28285893	Chromosomal localization of a human cDNA containing a DIDS binding domain and demonstrating high homology to yeast omnipotent suppressor 45
Q70629166	Chromosomal localization of a sequence with in vivo activity for initiation of DNA replication
Q24336604	Chromosomal localization of gene for human glutamate receptor subunit-7
Q28298683	Chromosomal localization of human gene for histidyl-tRNA synthetase: clustering of genes encoding aminoacyl-tRNA synthetases on human chromosome 5
Q67978465	Chromosomal localization of the IL-6 receptor signal transducing subunit, gp130 (IL6ST)
Q34279624	Chromosomal localization of the gene for a human cytosolic thyroid hormone binding protein homologous to the subunit of pyruvate kinase, subtype M2.
Q72087736	Chromosomal localization of the gene for human B-cell antigen CD40
Q28305784	Chromosomal localization of three human ras genes by in situ molecular hybridization
Q73672889	Chromosomal localization of two human genes involved in phosphate homeostasis: the type IIb sodium-phosphate cotransporter and stanniocalcin-2
Q34442267	Chromosomal localization to 19q13.3, partial genomic structure and 5' cDNA sequence of the human symplekin gene
Q41580182	Chromosomal location and structure of amplicons in two human cell lines with coamplification of c-myc and Ki-ras oncogenes
Q28298757	Chromosomal location of human genes encoding major heat-shock protein HSP70
Q33860552	Chromosomal mapping of a skeletal muscle specific LIM-only protein FHL3 to the distal end of the short arm of human chromosome 1.
Q70938805	Chromosomal rearrangements and gene expression in CHO cells: mapping of alleles for eight enzyme loci on CHO chromosomes Z3, Z4, Z5, and Z7
Q68716948	Chromosomally integrated shuttle vectors and molecular analysis of mutagenesis in mammalian cells
Q41736505	Chromosome aberration induction in Chinese hamster ovary cells by restriction enzymes with different methylation sensitivity
Q46035370	Chromosome localization and cDNA sequence of murine and human genes for ras p21 GTPase activating protein (GAP).
Q28243745	Chromosome localizations of genes for five cAMP-specific phosphodiesterases in man and mouse
Q43703963	Chromosome mapping of biological pathways by fluorescence-activated cell sorting and cell fusion: human interferon gamma receptor as a model system
Q39702016	Chromosome microdissection and microcloning in human molecular genetics
Q41626395	Circulating human or canine factor IX from retrovirally transduced primary myoblasts and established myoblast cell lines grafted into murine skeletal muscle
Q46190099	Cloned mouse lymphocytes permit analysis of somatic mutations that occur in vivo
Q43802756	Cloning and characterization of Chinese hamster CDC7 (ChCDC7).
Q36289282	Cloning and characterization of DNA sequences amplified in multidrug-resistant Djungarian hamster and mouse cells.
Q28285686	Cloning and characterization of the promoter of baboon XRCC1, a gene involved in DNA strand-break repair
Q28292118	Cloning and chromosomal location of human genes inducible by type I interferon
Q61147286	Cloning and comparative mapping of recently evolved human chromosome 22-specific alpha satellite DNA
Q30983023	Cloning muscle isoforms of neural cell adhesion molecule using an episomal shuttle vector
Q36418987	Cloning of DNA libraries from mouse Y chromosomes purified by flow cytometry
Q36418168	Cloning of TPA-inducible early (TIE) genes by differential hybridization using TPA-nonresponsive variant of mouse 3T3-L1 cells
Q42805194	Cloning of a cDNA encoding a putative human very low density lipoprotein/apolipoprotein E receptor and assignment of the gene to chromosome 9pter-p23.
Q36586672	Cloning of a functional human adenine phosphoribosyltransferase (APRT) gene: Identification of a restriction fragment length polymorphism and preliminary analysis of DNAs from APRT-deficient families and cell mutants
Q36458383	Cloning of rat liver arginase cDNA and elucidation of regulation of arginase gene expression in H4 rat hepatoma cells
Q67978460	Cockayne's syndrome fibroblasts are characterized by hypersensitivity to deoxyguanosine and abnormal DNA precursor pool metabolism in response to deoxyguanosine or ultraviolet light
Q40941094	Cointegration of DNA molecules introduced into mammalian cells by electroporation
Q28267538	Colocalization of P2Y2 and P2Y6 receptor genes at human chromosome 11q13.3-14.1
Q70194197	Colony hybridization to identify mammalian cells containing amplified, transfected, or expressed sequences
Q72751923	Comparative analysis of mouse-human hybrids with rearranged chromosomes 1 by in situ hybridization and southern blotting: High-resolution mapping of NRAS, NGFB, and AMY on human chromosome 1
Q69826756	Comparative study of DNase I sensitivity at the X-linked human HPRT locus
Q43940223	Comparison of methods for introducing vectors based on bovine papillomavirus-1 DNA into mammalian cells
Q70508601	Comparison of mitochondrially synthesized polypeptides of human, mouse, and monkey cell lines by a two-dimensional protease gel system
Q59565703	Complementation analysis of Chediak-Higashi Syndrome: The same gene may be responsible for the defect in all patients and species
Q69835172	Complementation analysis of locus for hypoxanthine guanine phosphoribosyltransferase in Chinese hamster cells
Q54415541	Complementation between glucocorticoid receptor and lymphocytolysis in somatic cell hybrids of two glucocorticoid-resistant human leukemic clonal cell lines.
Q52197290	Complementation group assignments in fanconi anemia fibroblast cell lines from North America
Q41580176	Complementation of DNA repair defect in xeroderma pigmentosum cells of group C by the transfer of human chromosome 5.
Q69826759	Complementation of metabolic defect in phosphoglycerate kinase (PGK)-deficient line of Chinese hamster ovary cells by introduction of human PGK cDNA
Q41715560	Complementing mutant alleles define three loci involved in mannosylation of Man5-GlcNAc2-P-P-dolichol in Chinese hamster ovary cells
Q41616902	Complete hamster CAD protein and the carbamylphosphate synthetase domain of CAD complement mammalian cell mutants defective in de novo pyrimidine biosynthesis
Q36800489	Complete set of eleven region-specific microdissection libraries for human chromosome 2.
Q68716944	Computational tools for using and analyzing DNA sequences
Q68716937	Conference proceedings: The next 25 years in human genetics. November 1986, Denver
Q54289870	Confocal microscopy of genome exposure in normal, cancer, and reverse-transformed cells
Q31047780	Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome
Q36728217	Construction and characterization of region-specific microdissection libraries and single-copy microclones for short arm of human chromosome 2.
Q42825486	Construction and characterization of single-transcript tricistronic retroviral vectors using two internal ribosome entry sites
Q36832016	Construction and characterization of three region-specific microdissection libraries for human chromosome 18.
Q41152226	Construction of a functional cDNA clone of the hamster ERCC2 DNA repair and transcription gene
Q44533217	Construction of microcell hybrid panel containing different neo gene insertions in mouse chromosome 17 used for chromosome-mediated gene transfer
Q71110177	Coordinate extinction of melanocyte-specific gene expression in hybrid cells
Q71110169	Coordinate suppression of myeloma-specific genes and expression of fibroblast-specific genes in myeloma X fibroblast somatic cell hybrids
Q54458509	Correction of a nucleotide-excision-repair mutation by human chromosome 19 in hamster-human hybrid cells.
Q68166203	Correction of deletions in mammalian cells by gene conversion
Q46076278	Correction of excision repair in xeroderma pigmentosum by hamster chromosome fragments involves both classes of pyrimidine dimers
Q41596418	Correction of methylmalonyl-CoA mutase deficiency in Mut0 fibroblasts and constitution of gene expression in primary human hepatocytes by retroviral-mediated gene transfer
Q41050622	Correction of the Bloom syndrome cellular phenotypes.
Q40776758	Creation of a stable human reporter cell line suitable for FACS-based, transdominant genetic selection
Q36795736	Cross contamination of the genomes in human/hamster cell hybrids by multiple short recombination events.
Q42817722	Cross-resistance of novobiocin-resistant BHK cell line to topoisomerase II inhibitors
Q33364855	Cyclic AMP-resistant mutants of S49 mouse lymphoma cells hemizygous for expression of regulatory subunit of type I cyclic AMP-dependent protein kinase
Q71472156	Cyclin D1 induced apoptosis maintains the integrity of the G1/S checkpoint following ionizing radiation irradiation
Q41604682	Cyclin-dependent kinase 2 (cdk2) in the murine Cdc2 kinase TS mutant
Q42815663	Cytogenetic analysis of amplification and deamplification of UMP synthase genes in Chinese hamster cells
Q68519857	Cytogenetic evidence of gene amplification as a mechanism for tumor cell invasion
Q69092032	Cytokeratin gene expression in hepatoma hybrid cells: evidence for regulation in cis
Q45127513	Cytological localization of adenosine kinase, nucleoside phosphorylase-1, and esterase-10 genes on mouse chromosome 14.
Q42214727	Cytoplasmic suppression of tumor progression in reconstituted cells
Q70955405	Cytotoxicity of plant lectins for mouse embryonal carcinoma cells
Q44654729	DNA base sequence changes induced by ethyl methanesulfonate in a chromosomally integrated shuttle vector gene in mouse cells
Q38346604	DNA binding factors for the CpG-rich island containing the promoter of the human X-linked PGK gene
Q57390879	DNA methylation and genetic inactivation at thymidine kinase locus: Two different mechanisms for silencing autosomal genes
Q52035178	DNA methylation of the fragile X locus in somatic and germ cells during fetal development: relevance to the fragile X syndrome and X inactivation.
Q41701610	DNA methylation of two X chromosome genes in female somatic and embryonal carcinoma cells
Q41186580	DNA topoisomerase II inhibitors enhance random integration of transfected vectors into human chromosomes
Q54482200	DNA-mediated restoration of phenylalanine hydroxylase gene expression in enzyme-deficient derivatives of enzyme-constitutive mouse cell hybrids.
Q52466362	DNA-mediated transfer of complex I genes into three different respiration-deficient Chinese hamster mutant cell lines with defects in complex I of electron transport chain.
Q80491286	Damage-repair kinetics and early adaptive response induced by gamma rays in murine leukocytes in vivo
Q44849554	Death of solid tumor cells induced by Fas ligand expressing primary myoblasts
Q42814057	Defective DNA topoisomerase I activity in a DNAts mutant of Balb/3T3 cells
Q80491282	Defective NF-kappaB signaling in dedifferentiated hepatoma cells
Q41169381	Defective myogenesis in NFB-s mutant associated with a saturable suppression of MYF5 activity
Q41676726	Deficient synthesis of MTHFD, a trifunctional folate-dependent enzyme, in the CHO Ade E mutant
Q67920644	Definition of selectable cell surface markers for human chromosomes and chromosome segments in rodent-human hybrids
Q54415538	Delayed mutation in Chinese hamster cells.
Q36428567	Deletion and hypermethylation of thymidine kinase gene in V79 Chinese hamster cells resistant to bromodeoxyuridine
Q44784340	Deletion mapping of highly conserved transcribed sequence downstream from APRT locus
Q41152214	Delivery of cytosolic liver arginase into the mitochondrial matrix space: a possible novel site for gene replacement therapy
Q41025994	Demethylation of the human MDR1 5' region accompanies activation of P-glycoprotein expression in a HL60 multidrug resistant subline
Q46914470	Demethylation of two specific DNA sequences in expressed human immunoglobulin light kappa constant genes
Q48122678	Deoxycytidine methylation and the origin of spontaneous transition mutations in mammalian cells
Q41100322	Depletion of mitochondrial DNA by ddC in untransformed human cell lines.
Q40776745	Deregulated expression of the keratin 18 gene in human colon carcinoma cells
Q30824850	Deregulation of DNA polymerase ? by sense and antisense RNA expression in mouse 3T3 cells alters cell growth
Q54420356	Derepression of HPRT locus on inactive X chromosome of human lymphoblastoid cell line.
Q68072679	Description of a selection method highly cytotoxic for cystinotic fibroblasts but not normal human fibroblasts
Q32064506	Detailed analysis of a 17q21 microdissection library by sequence bioinformatics and isolation of region-specific clones
Q68716950	Detecting sequence changes in a gene
Q54420594	Detection of amplified sequences in mammalian DNA by in-gel renaturation and SINE hybridization.
Q41498202	Detection of deletion mutations extending beyond the HPRT gene by multiplex PCR analysis
Q41635326	Detection of multiple tumor suppressor genes for Syrian hamster fibrosarcomas by somatic cell hybridization
Q69849872	Detection of species specific chromosomes in somatic cell hybrids
Q42813215	Detection, frequency, and stability of cotransformants expressing nonselectable human enzymes
Q35016627	Determinants for lentiviral infection of non-dividing cells
Q38309846	Determination of the genotype of a panel of human tumor cell lines for the human homologues of yeast cell cycle checkpoint control genes: identification of cell lines carrying homoallelic missense base substitutions
Q46821017	Development and characterization of mutant chicken cell lines for somatic cell genetics studies
Q41321410	Developmental genetics: new approaches and opportunities
Q44477288	Different genetic alterations underlie dual hypersensitivity of CHO mutant UV-1 to DNA methylating and cross-linking agents
Q67984110	Differential mRNA stabilities affect mRNA levels in mutant mouse myeloma cells
Q72293326	Dimethylsulfate methylation of guanine residues in mammalian DNA: inverse correlation between methylation susceptibility and mutagenesis by bromodeoxyuridine and thymidine
Q46785300	Direct DNA injection into mouse tongue muscle for analysis of promoter function in vivo
Q43626992	Direct formation of microcells from mitotic cells for use in chromosome transfer
Q44792961	Direct selection of Chinese hamster ovary strains deficient in CTP synthetase activity
Q67506714	Direct selection of hepatoma cell variants deficient in alpha 1-antitrypsin gene expression
Q31047770	Directed isolation of human genes that escape X inactivation
Q28280782	Distribution of genes for gap junction membrane channel proteins on human and mouse chromosomes
Q41200333	Dominant genetic instability and sensitivity to DNA damaging agents in a mammalian cell line
Q35066733	Dominant mutation in mouse cells associated with resistance to Hoechst 33258 dye, but sensitivity to ultraviolet light and DNA base-damaging compounds
Q54200422	Drug-specific rearrangements of chromosome 12 in hydroxyurea-resistant mouse SEWA cells: support for chromosomal breakage model of gene amplification.
Q35016646	EIAV, CAEV and other lentivirus vector systems
Q46547294	Effect of an adjacent base on detection of a point mutation by restriction enzyme digestion
Q44787261	Effect of cell cycle position on transformation by microinjection
Q52489839	Effect of gamma rays at the dihydrofolate reductase locus: deletions and inversions.
Q67974439	Effect of gamma rays on efficiency of gene transfer in DNA repair-proficient and -deficient cell lines
Q72835395	Effect of vector topology on homologous recombination at the CHO aprt locus
Q40522447	Effects of Ape1 overexpression on cellular resistance to DNA-damaging and anticancer agents
Q45835055	Effects of Bloom's syndrome fibroblasts on genetic recombination and mutagenesis of herpes simplex virus type 1.
Q41676721	Effects of flanking base sequences on 5-bromodeoxyuridine mutagenesis in mammalian cells
Q44786181	Effects of homology length and donor vector arrangement on the efficiency of double-strand break-mediated recombination in human cells
Q41186576	Effects of infection rate and selection pressure on gene expression from an internal promoter of a double gene retroviral vector
Q43657654	Effects of nicks on repair of single-stranded loops in heteroduplex DNA in mammalian cells
Q64388232	Effects of sequence divergence on the efficiency of extrachromosomal recombination in mismatch repair proficient and deficient mammalian cell lines
Q54286319	Effects of vector cutting on its recombination with the chromosomal immunoglobulin gene in hybridoma cells.
Q67532848	Efficiency and limitations of the hn-cDNA library approach for the isolation of human transcribed genes from hybrid cells
Q52827178	Efficient DNA-mediated transfer of selectable genes and unselected sequences into differentiated and undifferentiated mouse melanoma clones
Q41298824	Efficient modification of the APRT gene by FLP/FRT site-specific targeting
Q41597560	Efficient selection of mu m-mutants from mu m-expressing myeloma cells by treatment with ricin A-conjugated anti-mu antibody
Q35140234	Electro-gene-transfer: a new approach for muscle gene delivery
Q72752916	Electron microscopic analysis of in vitro replication products of ors 8, a mammalian origin enriched sequence
Q42518209	Elevated levels of homologous DNA recombination activity in the regenerating rat liver
Q53543391	Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines.
Q41403556	Endogenous and transfected mouse alpha-fetoprotein genes in undifferentiated F9 cells are activated in transient heterokaryons.
Q41728959	Energy dependence of DNA-mediated gene transfer and expression
Q35140219	Engineering the surface properties of synthetic gene delivery vectors
Q41557085	Enhanced expression of alpha-type DNA polymerase genes reduces AZT cytotoxicity in hamster tr5 cells
Q70397835	Enhancement of DNA repair capacity of mammalian cells by carcinogen treatment
Q43525912	Establishment and characterization of continuous cell lines derived from temperature-sensitive mutants of Drosophila melanogaster
Q44757207	Establishment of mouse cell lines homozygous for temperature-sensitive mutation in catalase gene
Q35016661	Ethical considerations in the use of lentiviral vectors for genetic transfer
Q54351034	Ethyl methane sulfonate- and bleomycin-generated deletion mutations at HPRT locus in xeroderma pigmentosum complementation group D fibroblasts.
Q41678119	Evaluation of the mutagenic effects of SV40 in mouse, hamster, and mouse-human hybrid cells
Q57675198	Evidence for erosion of mouse CpG islands during mammalian evolution
Q71542660	Evidence for gene silencing by DNA methylation in normal human diploid fibroblasts
Q43862263	Evidence for indirect involvement of thymidine kinase in excision repair processes in mouse cell lines
Q54475267	Evidence for mutagenic repair in V79 cell mutant with aphidicolin-resistant DNA polymerase-alpha.
Q41169359	Evidence that heteronuclear proteins interact with XIST RNA in vitro.
Q46237098	Evidence that resistance to osmotic stress is mediated by gene amplification
Q57877954	Exon trapping and sequence-based methods of gene finding in transcript mapping of human 4p 16.3
Q42075770	Expression of Drosophila hsp 70-CAT hybrid gene in Aedes cells induced by heat shock
Q41121659	Expression of Rap 1 suppresses genomic instability of H-ras transformed mouse fibroblasts
Q41676716	Expression of a human cDNA encoding a protein containing GAR synthetase, AIR synthetase, and GAR transformylase corrects the defects in mutant Chinese hamster ovary cells lacking these activities
Q54660767	Expression of catalytic domains of human UMP synthase in uridine auxotrophic bacteria.
Q54474907	Expression of class I histocompatibility antigens on human T-B lymphoblast hybrids.
Q52091783	Expression of fragile X chromosome in human-rodent somatic cell hybrids.
Q73499709	Expression of human O6-methyl guanine methyl transferase (MGMT) in post replication repair (PRR) deficient CHO-UV-1 cells: Compensation for hypersensitivity to methylating and ethylating agents but not to mitomycin C
Q42810847	Expression of human argininosuccinate synthetase after retroviral-mediated gene transfer
Q41858311	Expression of human argininosuccinate synthetase in murine hematopoietic cells in vivo
Q68969909	Expression of human chromosome 11-encoded cell-surface antigens by DNA-mediated transfectants
Q54415535	Expression of mouse dihydrofolate reductase gene confers methotrexate resistance in transgenic petunia plants.
Q44569694	Expression of the receptor for epidermal growth factor correlates with increased dosage of chromosome 7 in malignant melanoma
Q67978462	Extinction of liver/bone/kidney alkaline phosphatase in osteosarcoma hybrid cells
Q35016640	FIV vector systems
Q42804652	Factors influencing efficiency and reproducibility of polybrene-assisted gene transfer
Q41684774	Factors influencing transient expression in cytotoxic T cells following DEAE dextran-mediated gene transfer
Q45831591	Factors involved in production of helper virus-free retrovirus vectors.
Q74773103	Fanconi anemia group A and D cell lines respond normally to inhibitors of cell cycle regulation
Q28281289	Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12
Q42650914	Fingerprinting cell lines: use of human hypervariable DNA probes to characterize mammalian cell cultures
Q70136184	Fractionation of large mammalian DNA restriction fragments using vertical pulsed-field gradient gel electrophoresis
Q41742056	Frequency and mechanisms of factor independence in IL-3-dependent cell lines
Q41458425	Functional and molecular analysis of liver arginase promoter sequences from man and Macaca fascicularis
Q54431972	Functional hemizygosity for the MDH2 locus in Chinese hamster ovary cells.
Q69927326	Further characterization of a somatic cell mutant defective in regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase
Q41741275	GC-rich murine adenosine deaminase gene promoter supports diverse tissue-specific gene expression
Q56866497	GM1-gangliosidosis: Chromosome 3 assignment of the?-galactosidase-A gene (? GAL A )
Q41728943	Gene complementing xeroderma pigmentosum group A cells maps to distal human chromosome 9q.
Q28279341	Gene dosage and Down's syndrome: metabolic and enzymatic changes in PC12 cells overexpressing transfected human liver-type phosphofructokinase
Q54374345	Gene dosage mutants at adenine phosphoribosyltransferase locus induced by colcemid in Chinese hamster V79-AP4 cells.
Q68093527	Gene encoding human p250 T-cell activation antigen maps to human chromosome 11
Q41676731	Gene expression and metastasis of somatic cell hybrids between murine fibroblast cell lines of different malignant potential
Q45175532	Gene expression in ataxia telangiectasia cells as perturbed by bleomycin treatment
Q54354665	Gene expression in implanted rat hepatocytes following retroviral-mediated gene transfer.
Q41298790	Gene expression in response to retinoic acid in novel human chromosome 21 monochromosomal cell hybrids
Q68166210	Gene for M1 subunit of ribonucleotide reductase is amplified in hydroxyurea-resistant hamster cells
Q69731665	Gene for alpha 2(I) collagen is on mouse chromosome 6 not 16
Q70965038	Gene for apolipoprotein CII is on human chromosome 19
Q68459268	Gene for lipoamide dehydrogenase maps to human chromosome 7
Q43728659	Gene for murine alpha 1----3-galactosyltransferase is located in the centromeric region of chromosome 2.
Q53536175	Gene mapping and physical arrangements of human chromatin in transformed, hybrid cells: fluorescent and autoradiographic in situ hybridization compared.
Q68643859	Gene mapping of mouse laminin A and B2 subunits using mouse-Chinese hamster somatic cell hybrids
Q54357757	Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation.
Q41753132	Gene regulation in reverse transformation: cyclic AMP-induced actin homolog in CHO cells
Q44115749	Gene replacement by homologous recombination in mammalian cells
Q41658673	Gene silencing in mammalian cells by direct incorporation of electroporated 5-methyl-2?-deoxycytidine 5?-triphosphate
Q44773300	Gene silencing in mammalian cells by uptake of 5-methyl deoxycytidine-5?-triphosphate
Q41328290	Gene targeting in mouse embryonic stem cells with an adenoviral vector
Q41616098	Gene targeting using a mouse HPRT minigene/HPRT-deficient embryonic stem cell system: inactivation of the mouse ERCC-1 gene
Q44441663	Gene transfer into rat airway epithelial cells using retroviral vectors
Q68166221	General protocol for microcell-mediated chromosome transfer
Q31047775	Generation and characterization of a human chromosome 9 cosmid library.
Q41667000	Generation and characterization of irradiation hybrids of human chromosome 4.
Q48052802	Generation of a contig comprising YACs and BACs within chromosome region 1p13.1.
Q45873126	Generation of a mouse model for citrullinemia by targeted disruption of the argininosuccinate synthetase gene
Q73296874	Generation of a panel of radiation-reduced hybrids containing human 11q22-23 fragments bearing a HPRT selective marker: identification of hybrids carrying various subregions around the ataxia-telangiectasia locus
Q41743009	Generation of a panel of somatic cell hybrids containing unselected fragments of human chromosome 10 by X-ray irradiation and cell fusion: application to isolating the MEN2A region in hybrid cells
Q74149043	Generation of p53 suppressor peptide from the fragment of p53 protein
Q68598692	Genes for C4b-binding protein alpha- and beta-chains (C4BPA and C4BPB) are located on chromosome 1, band 1q32, in humans and on chromosome 13 in rats
Q69731662	Genes for HMG-CoA reductase and serotonin 1a receptor are on mouse chromosome 13
Q69372862	Genes for beta 2-adrenergic receptor and platelet-derived growth factor receptor map to mouse chromosome 18
Q34553279	Genes for human vitamin K-dependent plasma proteins C and S are located on chromosomes 2 and 3, respectively
Q73087994	Genes transfected into embryonal carcinoma stem cells are both lost and inactivated at high frequency
Q42489527	Genetic analysis of L-ethionine-mediated induction of alpha-fetoprotein in mice
Q28284372	Genetic analysis of XR-1 mutation in hamster and human hybrids
Q41715572	Genetic analysis of a vital mammalian housekeeping locus using CHO cells that express a transfected mutant allele
Q42823274	Genetic analysis of control of proliferation in fibroblastic cells in culture. I. Isolation and characterization of mutants temperature-sensitive for proliferation or survival of untransformed diploid rat cell line 3Y1.
Q45796923	Genetic analysis of control of proliferation in fibroblastic cells in culture. II. Alteration in proliferative and survival phenotypes in a set of temperature-sensitive mutants of rat 3Y1 cells after infection or transformation with simian virus 40
Q70194215	Genetic analysis of hyperproduction of epidermal growth factor receptors in human epidermoid carcinoma A431 cells
Q41658346	Genetic analysis of resistance to total bromodeoxyuridine substitution in mammalian cell hybrids
Q53550541	Genetic analysis of tumerigenesis: XVI. Chromosome changes in azacytidine- and insulin-induced tumorigenesis
Q53524441	Genetic analysis of tumorigenesis. XXXI: Retention of short arm of chromosome 3 in suppressed CHEF cell hybrids containing c-Ha-ras (EJ) gene.
Q69834130	Genetic analysis of tumorigenesis: XXI. Suppressor genes in CHEF cells
Q44187090	Genetic analysis of tumorigenesis: XXXII. Localization of constitutionally amplified KRAS sequences to Chinese hamster chromosomes X and Y by in situ hybridization
Q43782915	Genetic assignment of GP90, leukocyte adhesion glycoprotein to human chromosome 21.
Q36458143	Genetic counterselective procedure to isolate interspecific cell hybrids containing single human chromosomes: construction of cell hybrids and recombinant DNA libraries specific for human chromosomes 3 and 4.
Q72730500	Genetic diversity of mitomycin C-hypersensitive Chinese hamster cell mutants: a new complementation group with chromosomal instability
Q41518706	Genetic instability on chromosome 16 in a human B lymphoblastoid cell line
Q39487483	Genetic mapping in chromosome 21 and its implications for Down's syndrome and other diseases
Q67966706	Genetic mapping in the mouse of four loci related to the jun family of transcriptional activators
Q70124787	Genetic mapping of Pim-1 putative oncogene to mouse chromosome 17
Q68716940	Genetic mapping of human chromosome 11: use of human cell surface antigens
Q69836319	Genetic regulation of growth control: role of cyclic AMP and cell cytoskeleton
Q36816746	Genetic transformation of Drosophila cells in culture by P element-mediated transposition
Q77907218	Genetic variation in the 3' untranslated region of the neurofibromatosis 1 gene: application to unequal allelic expression
Q39702046	Genetics and the future of medicine
Q40897082	Genome exposure and regulation in mammalian cells
Q37936036	Genome regulation in mammalian cells
Q54465349	Genomic DNA-mediated gene transfer for argininosuccinate synthetase.
Q28205155	Genomics of the human genes encoding four TAFII subunits of TFIID, the three subunits of TFIIA, as well as CDK8 and SURB7
Q57162584	Germ-Line chromosomal localization of genes in chromosome 11p linkage: Parathyroid hormone, ?-globin, c-Ha-ras-1, and insulin
Q43753304	Germ-line chromosomal localization of human C-Erb-A oncogene
Q71472160	Germinal HPRT splice donor site mutation results in multiple RNA splicing products in T-lymphocyte cultures
Q69876155	Glucocorticoid resistance is a dominant trait in hybrids between cytolytic T-lymphocyte lines and AKR thymomas
Q70172633	Glucocorticoid-dependent maturation of viral proteins in mouse lymphoma cells: isolation of defective and hormone-independent cell variants
Q70938812	Glutathione-S-transferase gene mapped to chromosome 11 is GST3 not GST1
Q44551025	Growth suppression of hybrids between transformed cells and normal fibroblasts in serum-free medium: correlation with retention of human chromosomes
Q35016623	HIV-1 replication
Q35016631	HIV-1 vector systems
Q35016635	HIV-2 and SIV vector systems
Q41659042	HPRT gene expression differs in mutants derived from normal and Fanconi anemia cells: analysis of spontaneous and psoralen-photoinduced mutants
Q41557956	Hemidemethylation is sufficient for chromatin relaxation and transcriptional activation of methylatedaprt gene in mouse P19 embryonal carcinoma cell line
Q68716933	Hemopexin is localized to human chromosome 11
Q45871366	Hepatic gene therapy: efficient retroviral-mediated gene transfer into rat hepatocytes in vivo
Q43782718	Herpes simplex virus thymidine kinase gene is stably maintained and expressed in cells transformed by protoplast fusion
Q47937097	Heteroplasmic segregation associated with trisomy-9 in cultured human cells.
Q36615293	High frequency "switching" at the adenine phosphoribosyltransferase locus in multipotent mouse teratocarcinoma stem cells
Q41274806	High frequency recombination between loxP sites in human chromosomes mediated by an adenovirus vector expressing Cre recombinase
Q68365084	High level of aphidicolin resistance with multiple mutations in mouse FM3A cell mutants
Q53542607	High spontaneous mutation frequency of BPV shuttle vector.
Q53550741	High-efficiency polyethylene glycol-mediated transformation of mammalian cells
Q46295799	High-efficiency retroviral infection of primary myoblasts
Q41941708	High-efficiency stable gene transfection using chloroquine-treated Chinese hamster ovary cells
Q54362280	High-frequency deletion event at aprt locus of CHO cells: detection and characterization of endpoints.
Q72751927	High-frequency induction by 5-azacytidine of proline independence in CHO-K1 cells
Q72009993	High-frequency loss of specific immunoglobulin production in hybridoma cell lines bearing a chromosomal immunoglobulin kappa gene modified by homologous recombination
Q68997841	High-frequency reactivation of X-linked genes in Chinese hamster X human hybrid cells
Q36458257	High-frequency transfection of CHO cells using polybrene
Q35140224	Histidine containing peptides and polypeptides as nucleic acid vectors.
Q68997846	Histochemical staining of clonal mammalian cell lines expressing E. coli beta galactosidase indicates heterogeneous expression of the bacterial gene
Q64389295	Homologous junctions formed between a vector and human genomic repetitive line-1 elements as a result of one-sided invasion
Q70116705	Hotspots for spontaneous and mutagen-induced lesions in regulatory subunit of cyclic AMP-dependent protein kinase in S49 mouse lymphoma cells
Q68932905	Human alpha 2-macroglobulin gene is located on chromosome 12
Q70141388	Human apolipoprotein B: chromosomal mapping and DNA polymorphisms of hepatic and intestinal species
Q41489356	Human beta:alpha but not gamma interferon binding site is a product of the chromosome 21 interferon action gene
Q36682811	Human cDNA clones that modify radiomimetic sensitivity of ataxia-telangiectasia (group A) cells
Q44070305	Human cell variants resistant to rhodamine 6G.
Q28115726	Human chromosome 19 contains the neurotrophin-5 gene locus and three related genes that may encode novel acidic neurotrophins
Q44049766	Human cyclin B1 gene (CCNB1) assigned to chromosome 5 (q13-qter)
Q34162905	Human gastrin-releasing peptide gene is located on chromosome 18.
Q24295485	Human gastrin-releasing peptide gene maps to chromosome band 18q21
Q34181128	Human gene coding for granulocyte-colony stimulating factor is assigned to the q21-q22 region of chromosome 17.
Q28257409	Human gene for proliferating cell nuclear antigen has pseudogenes and localizes to chromosome 20
Q34180221	Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively
Q43489457	Human globin gene expression in hybrid 2S MEL X human fibroblast cells
Q41368871	Human insulin-related DNA sequences map to chromosomes 2 and 11.
Q34179602	Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localization
Q70141393	Human liver fatty acid binding protein gene is located on chromosome 2
Q34181453	Human luteinizing hormone-releasing hormone gene (LHRH) is located on short arm of chromosome 8 (region 8p11.2----p21).
Q61763460	Human muscle cell surface antigen 16.3A5 is encoded by a gene on chromosome 11
Q48652625	Human renin gene is on chromosome 1.
Q41677044	Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase gene.
Q69945380	Hyal-1, a locus determining serum hyaluronidase polymorphism, on chromosome 9 in mice
Q69053497	Hypomethylation and ADA gene expression in mouse CAK cells
Q70094454	Identification and localization of DNA alteration in Chinese hamster ovary cell mutants (Urd-) defective in the first three enzymes of de novo pyrimidine synthesis
Q41444550	Identification of 200,000-dalton human cell surface protein encoded by gene mapped to long arm of chromosome 11.
Q36832032	Identification of a locus of zinc finger genes in human chromosome 19q13.1-q13.3 region by fluorescence in situ hybridization
Q36731921	Identification of human chromosome region 3p14.2-21.3-specific YAC clones using Alu-PCR products from a radiation hybrid
Q45010084	Identification of human gene complementing ts AlS9 mouse L-cell defect in DNA replication following DNA-mediated gene transfer
Q72417764	Identification of multiple B-cell transcriptional repressor elements in S mu-C mu intron of mouse IgH chain locus
Q39536397	Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids
Q34296450	Identification of the human neuronal nicotinic cholinergic alpha 2 receptor locus, (CHRNA2), within an 8p21 mapped locus, by sequence homology with rat DNA.
Q41488793	Identification of two complementation groups in Fanconi anemia
Q69336509	Imbalance of purine nucleotides in alanosine-resistant baby hamster kidney cells
Q41221040	Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure
Q42819269	Immortalization of xeroderma pigmentosum cells by simian virus 40 DNA having a defective origin of DNA replication
Q54429230	Immunological studies with different classes of mutants affected at the adenosine kinase locus in CHO cells.
Q41428204	In situ localization of murine c-Ki-ras-2 oncogene: preliminary evidence for conservation of telomeric territory of oncogenes?
Q46072579	In vivo aging of human fibroblasts does not alter nuclear plasticity in heterokaryons
Q41935055	Inactivation and reactivation of sex-linked steroid sulfatase gene in murine cell culture
Q72481763	Inclusion of synthetic DNA templates of similar length and base composition to PCR-amplified products in restriction enzyme digestions: an efficient aid in characterization of point mutations
Q69941592	Increase in clonal variation in Chinese hamster ovary cells after treatment with mutagens
Q28340652	Increase of extrachromosomal circular DNA in mouse 3T6 cells on perturbation of DNA synthesis: implications for gene amplification
Q45303756	Induction and reversion of asparagine auxotrophs in CHO-K1 and V79 cells
Q47855542	Induction of fragility at the human RNU2 locus by cytosine arabinoside is dependent upon a transcriptionally competent U2 small nuclear RNA gene and the expression of p53.
Q41283077	Induction of sister chromatid exchanges by the thymidine analog 5-hydroxymethyl-2'-deoxyuridine
Q54357759	Infection of bovine cells of embryonic origin by amphotropic retroviral vectors.
Q40864270	Influence of DNA delivery method on gene targeting frequencies in human cells
Q41174441	Influence of cellular sequences on instability of plasmid integration sites in human cells
Q40897086	Inhibition of solid tumor growth by Fas ligand-expressing myoblasts
Q39702035	Insertion of dominant selectable markers into the human genome
Q41685534	Instability of immunoglobulin genes in S107 cell line.
Q69354349	Insulin-like growth factor I receptor gene is concordant with c-Fes protooncogene and mouse chromosome 7 in somatic cell hybrids
Q70508597	Integration of Drosophila heat-shock genes transfected into cultured Drosophila melanogaster cells
Q69887667	Integration of a dominant selectable marker into human chromosomes and transfer of marked chromosomes to mouse cells by microcell fusion
Q69842047	Interferon-beta-related DNA on human chromosome 4
Q34387266	Interferon-regulated human 2-5A synthetase gene maps to chromosome 12.
Q71007195	Interleukin 2 (IL2) is assigned to human chromosome 4
Q43639625	Interspecific genetic complementation analysis of human and sheep fibroblasts with beta-galactosidase deficiency
Q35140227	Intracellular targets for DNA delivery: nuclei and mitochondria
Q41742050	Intragenic interspecific complementation of glucose 6-phosphate dehydrogenase in human-hamster cell hybrids
Q72636010	Intragenic regions of the murine Pgk-1 locus enhance integration of transfected DNAs into genomes of embryonal carcinoma cells
Q36785074	Introduction of YACs containing a putative mammalian replication origin into mammalian cells can generate structures that replicate autonomously
Q45741212	Introduction of plasmid DNA and oligonucleotides into lung epithelial cells by the hemagglutinating virus of Japan (HVJ)-liposome method
Q35016620	Introduction to retroviruses and retroviral vectors
Q30590512	Inversion and transposition of Tc1 transposon of C. elegans in mammalian cells
Q42795879	Involvement of unstable chromosomal regions containing C-heterochromatin and fragile sites in the integration of amplified dhfr domains
Q67920646	Irradiation-reduced human chromosome 21 hybrids
Q68203829	Is DNA methylation of X chromosome genes stable during aging?
Q42820209	Isolation and characterization of Chinese hamster cell line resistant to monofunctional alkylating agents
Q41186562	Isolation and characterization of HPRT-deficient human hepatoma cells
Q69744549	Isolation and characterization of S49 mouse lymphoma cell mutants deficient in adenosine deaminase
Q54478245	Isolation and characterization of a CHO amino acid transport mutant resistant to melphalan (L-phenylalanine mustard).
Q70935965	Isolation and characterization of a Chinese hamster lung cell tryptophanyl-tRNA synthetase mutant
Q69006402	Isolation and characterization of a glycine transport mutant in an established mammalian cell line, CHO(PEOT/1)
Q41483063	Isolation and characterization of a mutant Chinese hamster cell line resistant to the glutamine analog 6-diazo-5-oxo-L-norleucine
Q36586777	Isolation and characterization of human factor IX cDNA: identification of Taq I polymorphism and regional assignment
Q72988641	Isolation and characterization of human hepatoma cells with targeted insertions of a gpt selectable marker in the alpha 1-antitrypsin locus
Q36586676	Isolation and characterization of human random cDNA clones homologous to DNA from the X chromosome
Q41692064	Isolation and characterization of irradiation fusion hybrids from mouse chromosome 1 for mapping Rmc-1, a gene encoding a cellular receptor for MCF class murine retroviruses
Q42812923	Isolation and characterization of novobiocin-resistant BHK cells
Q68007110	Isolation and characterization of radiation-reduced hybrids containing portions of the proximal long arm of the human X chromosome: identification of hybrids containing the Menkes' disease locus
Q44844584	Isolation and genetic characterization of human KB cell lines resistant to multiple drugs
Q70955409	Isolation and partial characterization of lectin-resistant F9 cells
Q36423843	Isolation and regional mapping of random X sequences from distal human X chromosome
Q73499719	Isolation of DNA markers for the ratSai 1 gene for suppression of anchorage independence by using representational difference analysis
Q36696139	Isolation of a clone partially encoding hill kangaroo X-linked hypoxanthine phosphoribosyltransferase: Sex differences in methylation in the body of the gene
Q48052805	Isolation of a hamster cDNA homologous to the mouse and human cyclin kinase inhibitory protein p27Kip1.
Q70183606	Isolation of a human cDNA encoding amidophosphoribosyltransferase and functional complementation of a CHO Ade-A mutant deficient in this activity
Q52829714	Isolation of a mutant cell line derived from ICR 2A frog cells hypersensitive to the induction of non-dimer DNA damage by solar ultraviolet radiation.
Q41701615	Isolation of a mutant of Chinese hamster ovary cells with defective secretion of a subset of secretory proteins
Q28280682	Isolation of an abundantly expressed sequence from the human X chromosome by differential screening
Q36615872	Isolation of genomic clones homologous to transcribed sequences from human X chromosome
Q72574627	Isolation of highly malignant Thy-1-positive revertants from cultured cloned Thy-1-negative lymphoma cells of low tumorigenicity
Q36885978	Isolation of human ear specific cDNAs and construction of cDNA libraries from surgically removed small amounts of inner ear tissues
Q72536344	Isolation of new nonsense and frameshift mutants in the immunoglobulin mu heavy-chain gene of hybridoma cells
Q41722604	Isolation of temperature-sensitive CHO-K1 cell mutants exhibiting chromosomal instability and reduced DNA synthesis at nonpermissive temperature
Q44234292	Isolation of temperature-sensitive mouse FM3A cell mutants exhibiting conditional chromosomal instability
Q36728210	Isolation of two contigs of overlapping cosmids derived from human chromosomal band 3p21.1 and identification of 5 new 3p21.1 genes
Q24312059	Isolation, characterization, and mapping of gene encoding dihydrolipoyl succinyltransferase (E2k) of human alpha-ketoglutarate dehydrogenase complex
Q53532150	Karyotype instability of Chinese hamster cells during in vivo tumor progression.
Q41667440	Kinds and locations of mutations arising spontaneously in the coding region of theHPRT gene of finite-life-span diploid human fibroblasts
Q28270113	Lamin A/C gene and a related sequence map to human chromosomes 1q12.1-q23 and 10
Q52832701	Lectin-resistant CHO cells: selection of four new pea lectin-resistant phenotypes.
Q41734836	Lectin-resistant CHO cells: selection of seven new mutants resistant to ricin
Q74593193	Ligand-histone H1 conjugates: increased solubility of DNA complexes, but no enhanced transfection activity
Q48064270	Linkage mapping of microdissected clones from distal mouse chromosome 16.
Q68744909	Localization of Chinese hamster dihydrofolate reductase gene to band p23 of chromosome 2
Q28285697	Localization of PiUS, a stimulator of cellular phosphate uptake to human chromosome 3p21.3
Q70334092	Localization of UDP glucuronosyltransferase gene(s) on mouse chromosome 5
Q36832020	Localization of a novel zinc finger gene to human chromosome 7q22 region by fluorescence in situ hybridization
Q34407131	Localization of a novel zinc finger gene to the human chromosome 7p11.2-p12 by fluorescence in situ hybridization
Q28254509	Localization of acyl coenzyme A:cholesterol acyltransferase gene to human chromosome 1q25
Q36615411	Localization of cloned mouse chromosome 7-specific DNA to lethal albino deletions
Q69377183	Localization of fructose 6-P,2-kinase: fructose 2,6-bisphosphatase to human chromosome X
Q28242492	Localization of gene for human syndecan, an integral membrane proteoglycan and a matrix receptor, to chromosome 2
Q72731701	Localization of human U1 small nuclear RNA genes to band p36.3 of chromosome 1 by in situ hybridization
Q44217305	Localization of human phosphoribosylpyrophosphate synthetase subunit I and II genes (PRPS1 and PRPS2) to different regions of the X chromosome and assignment of two PRPS1-related genes to autosomes
Q70965042	Localization of human type II procollagen gene (COL2A1) to chromosome 12
Q54426183	Localization of multidrug resistance-associated DNA sequences to human chromosome 7.
Q28251253	Localization of the candidate tumor suppressor gene ING1 to human chromosome 13q34
Q28118419	Localization of the gene encoding the alpha 2 subunit of the human VLA-2 receptor to chromosome 5q23-31
Q28277339	Localization of the human homolog of the yeast cell division control 27 gene (CDC27) proximal to ITGB3 on human chromosome 17q21.3
Q52013674	Localization of the mouse lissencephaly-1 gene to mouse chromosome 11B3, in close proximity to D11Mit65.
Q36832027	Localization of three novel zinc finger genes to the centromeric region of human chromosome 10 by fluorescence in situ hybridization
Q46005174	Long-range activation of transcription by SV40 enhancer is affected by "inhibitory" or "permissive" DNA sequences between enhancer and promoter.
Q69361141	Long-range restriction map around 11p13 aniridia locus
Q41789676	Long-range structure of H-ras 1-selected transgenomes.
Q43511209	Long-term expression of a retrovirally introduced beta-galactosidase gene in rodent cells implanted in vivo using biodegradable polymer meshes
Q41736359	Loss of alleles in aprt mutants of CHO cells demonstrated by BclI restriction-fragment-length variation
Q67817977	Loss of expression of the uvomorulin gene in compaction-defective embryonal carcinoma cells
Q41587979	Maintenance of X inactivation of theRps4, Zfx, andUbe1 genes in a mouse in vitro system
Q41100328	Maintenance of hypomethylation status and preferential expression of exogenous human MDR1/PGY1 gene in mouse L cells by YAC mediated transfer
Q67683031	Major chromatin changes accompany extinction of alpha-fetoprotein gene in hepatoma x fibroblast hybrids
Q41444741	Mammalian X chromosome inactivation: testing the hypothesis of transcriptional control.
Q67808051	Mammalian sex chromosomes. III. Activity of pseudoautosomal steroid sulfatase enzyme during spermatogenesis in Mus musculus
Q35140231	Mannose receptor-mediated gene delivery into antigen presenting dendritic cells.
Q28251264	Map location, genomic organization and expression patterns of the human RED1 RNA editase
Q31039831	Mapping and characterization of 129 cosmids on human chromosome 11p
Q42200317	Mapping and characterization of mutations induced by benzo[a]pyrene diol epoxide at dihydrofolate reductase locus in CHO cells
Q33898002	Mapping and characterization of the eukaryotic early pregnancy factor/chaperonin 10 gene family.
Q46388929	Mapping and gene order of U1 small nuclear RNA, endogenous viral env sequence, amylase, and alcohol dehydrogenase-3 on mouse chromosome 3.
Q54196003	Mapping human chromosomes in somatic cell hybrids using a low-copy-number repetitive sequence.
Q68716930	Mapping of Lmyc and Nmyc to rat chromosomes 5 and 6
Q33244304	Mapping of cosmid clones in Huntington's disease region of chromosome 4.
Q67918995	Mapping of gene encoding mouse placental alkaline phosphatase to chromosome 4
Q70136187	Mapping of haploid expressed genes: genes for both mouse protamines are located on chromosome 16
Q70145225	Mapping of human autosomal phosphoglycerate kinase sequence to chromosome 19
Q70045944	Mapping of human fibronectin receptor beta subunit gene to chromosome 10
Q34462166	Mapping of prolactin and tumor necrosis factor-beta genes on human chromosome 6p using lymphoblastoid cell deletion mutants
Q34381648	Mapping of the P2U purinergic receptor gene to human chromosome 11q 13.5-14.1.
Q60021890	Mapping of the genes for human endoplasmic reticular heat shock protein gp96/grp94
Q28238014	Mapping of the human GSPT1 gene, a human homolog of the yeast GST1 gene, to chromosomal band 16p13.1
Q48047466	Mapping of the human P84 gene to the subtelomeric region of chromosome 20p.
Q68726877	Mapping thyrotropin beta subunit gene in man and mouse
Q46173626	Membrane-bound neomycin phosphotransferase confers drug-resistance in mammalian cells: a marker for high-efficiency targeting of genes encoding secreted and cell-surface proteins
Q42823325	Metastatic properties of distinct phenotypic classes of lectin-resistant mutants isolated from murine MDAY-D2 cell line
Q46578083	Methylation analysis by genomic sequencing of 5' region of mouse Pgk-1 gene and a cautionary note concerning the method
Q41729916	Methylation of mouse adenine phosphoribosyltransferase gene is altered upon cellular differentiation and loss of phenotypic expression
Q48058036	Methylation sensitive protein binding to an intragenic active X-specific methylated region in the M. robustus Hprt gene
Q71542656	Mevalonate regulates polysome distribution and blocks translation-dependent suppression of 3-hydroxy-3-methylglutaryl coenzyme A reductase mRNA: relationship to translational control
Q33495526	Microdissection and microcloning of human chromosome 7q22-32 region
Q41432213	Minimum essential region of CCG1/TAFII250 required for complementing the temperature-sensitive cell cycle mutants, tsBN462 and ts13 cells, of hamster BHK21 cells.
Q67918994	Mitochondrial chloramphenicol-resistant mutants can have deficiencies in energy metabolism
Q54423401	Mitochondrial protein synthesis in interspecific somatic cell hybrids.
Q42826203	Mitotic and post mitotic consequences of genomic instability induced by oncogenic Ha-ras
Q54438476	Mitotic segregation of mitochondrial DNAs in human cell hybrids and expression of chloramphenicol resistance.
Q77395193	Modified giemsa-11 staining protocol for chromosomes of human and hybrid cells
Q71700403	Modulation of APRT transcription by altering spacing between cis-regulatory elements
Q70998898	Molecular analysis and breakpoint definition of a set of human chromosome 21 somatic cell hybrids
Q28298821	Molecular analysis and chromosomal mapping of amplified genes isolated from a transformed mouse 3T3 cell line
Q41692079	Molecular analysis of APRT deficiency in mouse P19 teratocarcinoma stem cell line
Q70406939	Molecular analysis of expression of parental cell properties in hybrids between monocytes and a myeloma cell line
Q69836316	Molecular analysis of human repetitive sequence family and its use as genetic marker
Q70346646	Molecular analysis of immunoglobulin expression in variants of murine B lymphoma, 70Z/3
Q41756370	Molecular and genetic characterization of human cell lines resistant to L-asparaginase and albizziin
Q36423426	Molecular approach to analyzing the human 5p deletion syndrome, cri du chat
Q44806005	Molecular characterization of PKU allele prevalent in southern Europe and Ireland
Q52018361	Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivation.
Q46062192	Molecular characterization of human minichromosomes with centromere from chromosome 1 in human-hamster hybrid cells
Q48081369	Molecular characterization of multilocus deletions at a diploid locus in CHO cells: association with an intracisternal-A particle gene
Q35335273	Molecular cloning and localization to chromosome 6 of mouse INT1L1 gene
Q42816749	Molecular cloning and nucleotide sequence of cDNA encoding a functional murine low-density-lipoprotein receptor
Q36285055	Molecular cloning of MER-2, a human chromosome-11-encoded red blood cell antigen, using linkage of cotransfected markers
Q41616092	Molecular cloning of a gene involved in methotrexate uptake by DNA-mediated gene transfer
Q41715577	Molecular cloning of a mammalian gene involved in the fixation of UV-induced mutations
Q22008711	Molecular cloning of a zinc finger gene eZNF from a human inner ear cDNA library, and in situ expression pattern of its mouse homologue in mouse inner ear
Q35625002	Molecular cloning of human A1S9 locus: an X-linked gene essential for progression through S phase of the cell cycle
Q36786711	Molecular cloning of the human gene SUVCC3 associated with the formation of DNA-protein crosslinks following exposure to solar UV radiation
Q41186569	Molecular comparison of cultured hybridoma cells that switch isotypes at high and low rates.
Q24319811	Molecular genetic characterization and comparative mapping of the human PCP4 gene
Q68719924	Molecular genetics of PKU in eastern Europe: a nonsense mutation associated with haplotype 4 of the phenylalanine hydroxylase gene
Q44112914	Molecular mechanisms of extinction of liver-specific functions in mouse hepatoma rat fibroblast hybrids: extinction of alpha-fetoprotein gene
Q41646538	Molecular mechanisms of spontaneous and induced loss of heterozygosity in human cells in vitro
Q41722615	Monochromosomal mouse microcell hybrids containing inserted selectable neo genes
Q34662498	Mouse Huntington's disease gene homolog (Hdh).
Q70495786	Mouse immune interferon (IFN-gamma) gene is on chromosome 10
Q72404100	Mouse kidney renin gene is on chromosome one
Q40956803	Mouse-human somatic cell hybrids: loss of mouse and human chromosomes
Q59287981	Multiple DNA-protein interactions at the CpG island of the human pseudoautosomal geneMIC2
Q67509804	Multiple elements regulate phosphoenolpyruvate carboxykinase gene expression in hepatoma hybrid cells
Q33952029	Multiple pathways of DNA double-strand break processing in a mutant Indian muntjac cell line
Q39702022	Multiple recurrent genomic rearrangements and fragile sites in human cancer
Q72536350	Multiple regulatory elements ensure accurate transcription of a human ribosomal protein gene
Q69838896	Multipotent mutator strain of mouse teratocarcinoma cells
Q69735636	Mutant Chinese hamster ovary cells with defective methotrexate uptake are distinguishable by reversion analysis
Q41703349	Mutants from V79 fibroblasts exhibiting hypersensitivity to aphidicolin and 3'-azido-3'-deoxythymidine
Q36728213	Mutation and expression of the XPA gene in revertants and hybrids of a xeroderma pigmentosum cell line.
Q52593659	Mutation in mammalian cells: theory and implications.
Q73555274	Mutation inhibition by beta-estradiol after low doses of gamma-irradiation of mammalian cells
Q77427054	Mutation measurement in mammalian cells. IV: Comparison of gamma-ray and chemical mutagenesis
Q41580188	Mutational analysis in a patient with a variant form of Gaucher disease caused by SAP-2 deficiency
Q41186587	Mutations induced by DNA double-strand breaks: the influence of genomic site
Q41169375	Myoblast-mediated expression of colony stimulating factor-1 (CSF-1) in the cytokine-deficient op/op mouse
Q52458633	Natural and synthetic heat shock protein gene promoters assayed in Drosophila cells.
Q28260637	Neurofibromatosis type 1 gene product (neurofibromin) associates with microtubules
Q41667937	New DNA markers in the Huntington's disease gene candidate region
Q48363652	New RNA species is produced by alternate polyadenylation following rearrangement associated with CAD gene amplification
Q28202963	New chromosomal mapping assignments for argininosuccinate synthetase pseudogene 1, interferon-beta 3 gene, and the diazepam binding inhibitor gene
Q49083415	New mutations and phenotypes associated with glutamate and aspartate transport in Chinese hamster ovary (CHO-K1) cells
Q72835391	New patterns of bulk DNA repair in ultraviolet irradiated mouse embryo carcinoma cells following differentiation
Q36785069	New vector for transfer of yeast artificial chromosomes to mammalian cells
Q41659048	Newly formed chromosome-like structures in independent mouse P388 sublines with developed in vivo mdr1 gene amplification
Q54196458	Non-P-glycoprotein-mediated multidrug-resistant human KB cells selected in medium containing adriamycin, cepharanthine, and mezerein.
Q41146343	Nonrandom chromosome losses in tumorigenic revertants of hybrids between isogeneic immortal and neoplastic human uroepithelial cells
Q44328934	Novel approach for restriction mapping repetitive DNA elements using DNA transformation
Q93520515	Novel genetic instability associated with a developmentally regulated glycosyltransferase locus in Chinese hamster ovary cells
Q41597568	Novel method for isolating mammalian cells defective in fluid-phase endocytosis
Q54438480	Novel mutants of CHO cells resistant to adenosine analogs and containing biochemically altered form of adenosine kinase in cell extracts.
Q41152235	Nuclear inheritance of a gene affecting mitochondrial gene expression
Q41152243	Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus
Q73496391	Nucleolin promotes homologous DNA pairing in vitro
Q48648721	Observations on the Menkes' and brindled mouse phenotypes in cell hybrids
Q41755045	On the DNA polymerase-a mutant: immunofluorescence assay of UV-induced thymidine dimers in Aphr-4-2 cells
Q72417772	On the role of lipids in cell regulatory economy
Q74149051	On the spontaneous mutability of CpG sites in cultured S49 mouse lymphoma cells
Q68716954	Ordered disposition of parental genomes and individual chromosomes in reconstructed plant nuclei, and their implications
Q38344392	Organization and expression of human telomere repeat binding factor genes
Q36586781	Organization of the HPRT gene and related sequences in the human genome
Q70938802	Origin, transmission, and segregation of mitochondrial DNA dimers in mouse hybrid and cybrid cell lines
Q41532797	Osmotic stress variants in Chinese hamster cells
Q54426187	Ouabain-resistant mutants of Chinese hamster ovary cells are not directly affected in Na+, K+-ATPase.
Q41545887	Overexpression of asparagine synthetase in albizziin-resistant murine diploid embryonic stem cells
Q48336119	Overlapping transcription units in the transient receptor potential locus of Drosophila melanogaster
Q39702028	Overview of human cells in genetic research: altered phenotypes in human cells caused by transferred genes
Q54196461	Oxygen-resistant multipotent embryonic carcinoma cell lines exhibit antimutator phenotypes.
Q30736832	PAC and cosmid contig spanning the HOXA cluster on human chromosome 7p15.
Q44254417	Paradoxical regulation of human argininosuccinate synthetase cDNA minigene in opposition to endogenous gene: evidence for intragenic control sequences
Q70172637	Parasexual analysis of human pepsinogen molecular heterogeneity
Q41566806	Paroxysmal nocturnal hemoglobinuria: correction of abnormal phenotype by somatic cell hybridization
Q40776751	Partial activation of gene activity and chromatin remodeling of the human 14q32.1 serpin gene cluster by HNF-1 alpha and HNF-4 in fibroblast microcell hybrids
Q52830579	Partial physical map of human chromosome 21.
Q52536875	Periodicity of eight nucleotides in purine distribution around human genomic CpG dinucleotides.
Q71700406	Peripherin gene is linked to keratin 18 gene on human chromosome 12
Q71855544	Persistence during G1 of gamma ray- or mitomycin C-induced lesions eliciting SCE in murine salivary gland cells in vivo
Q45000610	Persistent expression of genes transferred in the fetal rat liver via retroviruses
Q69731655	Perspectives on UV light mutagenesis: investigation of the CHO aprt gene carried on a retroviral shuttle vector
Q38338475	Phenotypic correction of ataxia-telangiectasia cellular defect by exogenously introduced human or mouse subchromosomal fragments
Q34404457	Phleomycin resistance as a dominant selectable marker in CHO cells.
Q74110050	Phosphatase inhibitors and premature chromosome condensation in human peripheral lymphocytes at different cell-cycle phases
Q35140242	Photochemical transfection: a technology for efficient light-directed gene delivery
Q45296863	Physical and genetic localization of quinonoid dihydropteridine reductase gene (QDPR) on short arm of chromosome 4.
Q72009996	Physical map of small cell lung cancer deletion region on short arm of human chromosome 3 (3p13-22) based on radiation fusion hybrid analysis
Q33499792	Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids.
Q67487992	Physical mapping of loci in the distal half of the short arm of the human X chromosome: Implications for the spreading of X-chromosome inactivation
Q41729597	Pigmented cell lines of mouse albino melanocytes containing a tyrosinase cDNA with an inducible promoter
Q41728950	Polyacrylamide gel analysis of polypeptides in gene transfer cell lines
Q48338886	Polyadenylation of Chinese hamster dihydrofolate reductase genomic genes and minigenes after gene transfer
Q40522434	Polycation-mediated transfection: how to overcome undesirable side effects of sticky DNA complexes
Q39702011	Polymorphic DNA markers on the human genomic map: signposts for localization of unknown genes
Q69686575	Preferential loss or inactivation of chromosome Z4 APRT allele in CHO cells
Q40925102	Prevention of DNA 5-methylcytosine reutilization in human cells
Q41152221	Production and characterization of human 293 cell lines expressing the site-specific recombinase Cre.
Q41253074	Production of transmitochondrial mouse cell lines by cybrid rescue of rhodamine-6G pre-treated L-cells
Q52237599	Programmed demethylation in CpG islands during human fetal development.
Q39702041	Progress in understanding mechanisms of the serum cholesterol risk factor in atherosclerosis
Q45879211	Propionate metabolism in cultured human cells after overexpression of recombinant methylmalonyl CoA mutase: implications for somatic gene therapy
Q35016656	Prospects for gene therapy using HIV-based vectors
Q70932009	Provisional assignment of MPI, PKM2, PGM3, and ME1 to Chinese hamster chromosome 4
Q45221691	Proximity of thyroglobulin and c-myc genes on human chromosome 8.
Q72840408	Pseudogene of dihydrolipoyl succinyltransferase (E2k) found by PCR amplification and direct sequencing of rodent-human cell hybrid DNAs
Q34158526	Pyruvate dehydrogenase E1 alpha subunit genes in the mouse: mapping and comparison with human homologs
Q70950287	Quantitative phenotypic variation in single normal and malignant cells from liver and breast occurs along a geometric series
Q58492821	Radiation Hybrid Mapping of Human Cytosolic Malate Dehydrogenase (hcMDH) to the Short Arm of Chromosome 2
Q43676867	Radiation fusion hybrids for human chromosomes 3 and X generated at various irradiation doses
Q44766631	Radiation hybrids for mapping and cloning DNA sequences of distal 16p
Q36751739	Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1.
Q69844270	Rapid and quantitative detection of unique sequence donor DNA in extracts of cultured mammalian cells: an aid to chromosome mapping
Q38505097	Rapid characterization of human chromosomes in hybrid cell lines by primed in situ (PRINS) labeling
Q28267529	Rare microsatellite polymorphisms in the DNA repair genes XRCC1, XRCC3 and XRCC5 associated with cancer in patients of varying radiosensitivity
Q68459259	Rat c-raf oncogene is located on chromosome 4 and may be activated by sequences from chromosome 13
Q62498308	Rates of generation of methotrexate-resistant variants in cells temperature-sensitive for malignant transformation
Q53533924	Reactivation of X-linked genes in human fibroblasts transformed by origin-defective SV40.
Q69101665	Reactivation of hprt on the inactive X chromosome with DNA demethylating agents
Q41684778	Reactivation of psoralen-reacted plasmid DNA in Fanconi anemia, xeroderma pigmentosum, and normal human fibroblast cells
Q70472937	Recessive 2-(methylamino)-isobutyrate (MeAIB)-resistant mutant of Chinese hamster ovary cells (CHO-K1) with increased transport through ASC system
Q35152352	Recombination hotspot activity of hypervariable minisatellite DNA requires minisatellite DNA binding proteins
Q45878913	Reconstitution of enzymatic activity in hepatocytes of phenylalanine hydroxylase-deficient mice
Q41636556	Recovery of the missing tumorigenicity in mitochondrial DNA-less HeLa cells by introduction of mitochondrial DNA from normal human cells
Q41692070	Region- and cell type-specific de novo DNA methylation in cultured mammalian cells
Q36731915	Region-specific microdissection library and single-copy microclones for human chromosome 2p11-p13.
Q28270806	Regional assignment of human amylase (AMY) to p22----p21 of chromosome 1
Q53556188	Regional assignment of human protooncogenec-myb to 6q21?qter
Q68459264	Regional assignment of human tissue factor gene (F3) to chromosome 1p21-p22
Q43699266	Regional localization of CCG1 gene which complements hamster cell cycle mutation BN462 to Xq11-Xq13.
Q41458411	Regional localization of DPP4 (alias CD26 and ADCP2) to chromosome 2q24.
Q70334087	Regional localization of carbonic anhydrase genes CA1 and CA3 on human chromosome 8
Q68776891	Regional localization of the gene coding for sphingolipid activator protein SAP-1 on human chromosome 10
Q28593513	Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome
Q68796018	Regional location of alpha 1-antichymotrypsin and alpha 1-antitrypsin genes on human chromosome 14
Q28284830	Regional mapping of RBP4 to 10q23----q24 and RBP1 to 3q21----q22 in man
Q72536351	Regional mapping of the gene encoding dihydroorotate dehydrogenase, an enzyme involved in UMP synthesis, electron transport, and superoxide generation, to human chromosome region 16q22
Q74593196	Regional mapping panels for human chromosomes 1, 2, and 7
Q41646548	Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase synthesis in Syrian hamster C100 cells by mevinolin, 25-hydroxycholesterol, and mevalonate: the role of posttranscriptional control
Q42815331	Regulation of G418 selection efficiency by cell-cell interaction in transfection
Q52256076	Regulation of cell proliferation by oncogene products and growth factors.
Q44262607	Regulation of cytochrome P-450c in differentiated and dedifferentiated rat hepatoma cells: role of the Ah receptor
Q69336517	Regulation of human argininosuccinate synthetase gene: induction by positive-acting nuclear mechanism in canavanine-resistant cell variants
Q35457263	Regulation of tyrosinase mRNA levels in mouse melanoma cell clones by melanocyte-stimulating hormone and cyclic AMP.
Q43467254	Regulatory sequences clustered at the 5' end of the first intron of the human thymidylate synthase gene function in cooperation with the promoter region
Q56911589	Relationship between production of epidermal growth factor receptors, gene amplification, and chromosome 7 translocation in variant A431 cells
Q61763464	Relationships between genes on human chromosome 11 encoding cell-surface antigens
Q41728954	Relative frequencies of homologous recombination between plasmids introduced into DNA repair-deficient and other mammalian somatic cell lines
Q40522440	Removal of UV photoproducts from an adenovirus-encoded reporter gene following infection of unirradiated and UV-irradiated human fibroblasts
Q41471217	Removal of cyclobutane pyrimidine dimers from a UV-irradiated shuttle vector introduced into human cells
Q70935967	Repair of DNA adducts in asynchronous CHO cells and the role of repair in cell killing and mutation induction in synchronous cells treated with 7-bromomethylbenz[a]anthracene
Q70082013	Replication of pSV2-gpt in COS-1 cells: stability of plasmid DNA in the presence and absence of biochemical selection
Q41121674	Replication timing properties of the human HPRT locus on active, inactive and reactivated X chromosomes.
Q41722602	Replication-dependent mutagenesis by 5-bromodeoxyuridine: identification of base change and sequence effects on mutability
Q70508593	Rescue of a Drosophila temperature-sensitive mutant cell line by DNA transfection
Q54431969	Resistance to paraquat in a mammalian cell line.
Q43546373	Resistance to toxic effects of 5-hydroxymethyl-2'-deoxyuridine in mammalian cells
Q54482196	Retention of both parental mitochondrial DNA species in mouse-Chinese hamster somatic cell hybrids.
Q68303284	Retroviral vector-mediated in vivo expression of low-density-lipoprotein receptors in the Watanabe heritable hyperlipidemic rabbit
Q34179756	Ribosomal protein gene sequences map to human chromosomes 5, 8, and 17.
Q41169368	Roberts syndrome fibroblasts showing cisplatin hypersensitivity have normal host cell reactivation of cisplatin-treated adenovirus and normal capacity of cisplatin-treated cells for adenovirus DNA synthesis
Q44187683	Role of nuclear background and in vivo environment in variable segregation behavior of the aging-dependent T414G mutation at critical control site for human fibroblast mtDNA replication
Q41753139	SV40-mediated tumor selection and chromosome transfer to enrich for cystic fibrosis region
Q35016651	Safety considerations in vector development
Q54398407	Selection and characterization of mycophenolic acid-resistant leukemia cells.
Q45888762	Selection for phenylalanine hydroxylase activity in cells transformed with recombinant retroviruses
Q72226030	Selection of Chinese hamster ovary cells (CHO-K1) with reduced glutamate and aspartate uptake
Q72536347	Selection of a lysine-resistant CHO-K1 mutant with reduced amino acid transport through multiple systems
Q52833961	Selection of highly transfectable variant from mouse mastocytoma P815.
Q52831920	Selection of variant neuroblastoma cell line which has lost cell surface expression of antigen detected by monoclonal antibody PI153/3.
Q54320543	Selective enrichment for temperature-sensitive secretion mutants of mammalian cells using plant lectin, concanavalin A.
Q41111265	Selective loss of the hepatic phenotype due to the absence of a transcriptional activation pathway
Q41545803	Sensitivity of Roberts syndrome cells to gamma radiation, mitomycin C, and protein synthesis inhibitors
Q54355312	Sequence analysis of mouse mitochondrial chloramphenicol-resistant mutants.
Q47869479	Sequence analysis of the 5'-flanking region of the gene encoding human HOXA-7.
Q71771074	Sequence requirements for Afr-2 regulation of alpha-fetoprotein gene expression during liver regeneration
Q42206790	Sequence specificity of mutations induced by benzo[a]pyrene-7,8-diol-9,10-epoxide at endogenous aprt gene in CHO cells
Q69836313	Sequential expression in the nervous system of c-myb and VIP genes, located in human chromosomal region 6q24
Q71542651	Severe phenotype in mice with termination mutation in exon 2 of cystic fibrosis gene
Q52241634	Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations
Q54798432	Shuttling of integrated vectors from mammalian cells to E. coli is mediated by head-to-tail multimeric inserts.
Q41247843	Simultaneous induction of epigenetic variants
Q69945383	Single-step selection of mammalian cell mutants deficient in CTP synthetase
Q40823461	Sister chromatid exchange formation in mammalian cells is modulated by deoxyribonucleotide pool imbalance
Q70145223	Site specificity of DNA methylation and expression of herpes simplex thymidine kinase gene
Q73499715	Site-directed substitution of Ser1406 of hamster CAD with glutamic acid alters allosteric regulation of carbamyl phosphate synthetase II
Q41677816	Sodium butyrate causes reexpression of three membrane proteins on glycolipid-anchoring mutants
Q61898998	Somatic cell genetic analysis of two classes of CHO cell mutants expressing opposite phenotypes in sterol-depedent regulation of cholesterol metabolism
Q41471223	Somatic cell genetic and biochemical characterization of cell lines resulting from human genomic DNA transfections of Chinese hamster ovary cell mutants defective in sterol-dependent activation of sterol synthesis and LDL receptor expression
Q54479013	Somatic cell hybrid selection with a transfectable dominant marker
Q54407547	Somatic cell hybridization of Roberts syndrome and normal human fibroblasts transfected with plasmids carrying dominant selection markers.
Q45011104	Somatic cell hybridization of human tumor samples
Q41145920	Somatic cell hybridization of roberts syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes
Q70141390	Somatic mutations at a heterozygous autosomal locus in human cells occur more frequently by allele loss than by intragenic structural alterations
Q41242385	Some ras-transformed cells have increased radiosensitivity and decreased repair of sublethal radiation damage
Q35140246	Sonoporation: mechanical DNA delivery by ultrasonic cavitation
Q54200417	Spectrum of spontaneous missense mutations causing cyclic AMP-resistance phenotypes in cultured S49 mouse lymphoma cells differs markedly from those of mutations induced by alkylating mutagens.
Q44468796	Spontaneous CHO APRT heterozygotes reflect high-frequency, allele-specific deletion of the chromosome Z4 APRT gene
Q41498219	Spontaneous and induced homologous recombination between lacZ chromosomal direct repeats in CV-1 cells
Q41445831	Spontaneous mutations at aprt locus in a mammalian cell line defective in mismatch recognition
Q34048064	Spontaneous reversion of novel Lesch-Nyhan mutation by HPRT gene rearrangement
Q67654782	Stability of DNA methylation of X-chromosome genes during aging
Q70136182	Stability of DNA methylation of the human hypoxanthine phosphoribosyltransferase gene
Q43842361	Stability of retrovirally transduced markers in a rat cell line
Q44100462	Steady-state and nuclear run-on analyses of transcription in a temperature-sensitive Chinese hamster cell mutant with a defect in RNA metabolism
Q28270961	Stem cell factor (SCF), a novel hematopoietic growth factor and ligand for c-kit tyrosine kinase receptor, maps on human chromosome 12 between 12q14.3 and 12qter
Q68791467	Steps toward experimental measurement of total mutations relevant to human disease
Q48710025	Structural and developmental analysis of the mouse peripherin/rds gene
Q77907211	Structural and functional analysis of the protein products derived from mutant fur alleles in an endoprotease-deficient Chinese hamster ovary cell strain
Q52230253	Structural and functional mitochondrial abnormalities associated with high levels of partially deleted mitochondrial DNAs in somatic cell hybrids.
Q34416997	Structural characterization and fine chromosomal mapping of the human P2Y1 purinergic receptor gene (P2RY1).
Q34168294	Structural gene encoding human factor XII is located at 5q33-qter.
Q40956808	Structural organization of the human reduced folate carrier gene: evidence for 5' heterogeneity in lymphoblast mRNA.
Q34662620	Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat
Q54350445	Structure of four amplified DNA novel joints.
Q53541845	Studies on gene transfer and reversion to UV resistance in xeroderma pigmentosum cells.
Q41530622	Subchromosomal localization of a gene (XRCC5) involved in double strand break repair to the region 2q34-36.
Q41432222	Subclonal heterogeneity of the multidrug resistance phenotype in a cell line expressing antisense MDR1 RNA.
Q41736033	Sublocalization on chromosome 21 of human interferon-alpha receptor gene and the gene for an interferon-gamma response protein
Q38497644	Suppression of chimpanzee NORS in hamster/chimpanzee hybrid: report on cell line R48-26.
Q40897091	Suppression of neoplastic transformation and regulation of cytoskeleton by tropomyosins
Q72835401	Suppression of tyrosinase gene expression by bromodeoxyuridine in Syrian hamster melanoma cells is not due to its incorporation into upstream or coding sequences of the tyrosinase gene
Q35140215	Supramolecular assemblies of DNA delivery systems
Q41748545	Susceptibility for N-ras-mediated transformation requires loss of tumor suppressor activity
Q42665202	Synergistic enzyme induction by glucocorticoids and cyclic AMP observed in glioma x hepatoma cell hybrids but not in their parents
Q54442100	Synthesis and incorporation of human ribosomal protein S14 into functional ribosomes in human-Chinese hamster cell hybrids containing human chromosome 5: human RPS14 gene is the structural gene for ribosomal protein S14.
Q38325015	Targeted delivery of antisense oligonucleotides by molecular conjugates
Q41722609	Targeted gene replacement at the endogenous APRT locus in CHO cells
Q64388978	Targeted recombination at the Chinese hamster APRT locus using insertion versus replacement vectors
Q54597590	Targeted retroviral gene transfer into the rat biliary tract.
Q41545880	Targeting vector configuration and method of gene transfer influence targeted correction of the APRT gene in Chinese hamster ovary cells
Q43698711	Temperature-sensitive non-fusing myoblast variant and spontaneous revertant: isolation and characterization
Q41013512	Testis and somatic Xrcc-1 DNA repair gene expression
Q45875418	Tetracycline-regulated gene expression following direct gene transfer into mouse skeletal muscle
Q41715554	The Chinese hamster V79 cell mutant V-H4 is phenotypically like Fanconi anemia cells
Q68643856	The IL-1 alpha and beta genes are closely linked (less than 70 kb) on mouse chromosome 2
Q28279524	The IL-4 and IL-5 genes are closely linked and are part of a cytokine gene cluster on mouse chromosome 11
Q54055616	The Na+-dependent glutamate and aspartate transporter supports glutathione maintenance and survival of CHO-K1 cells.
Q34337251	The UDP-galactose translocator gene is mapped to band Xp11.23-p11.22 containing the Wiskott-Aldrich syndrome locus
Q71052579	The XIST locus replicates late on the active X, and earlier on the inactive X based on FISH DNA replication analysis of somatic cell hybrids
Q69913009	The coding sequence for the human 18,000-dalton hydrophobic pulmonary surfactant protein is located on chromosome 2 and identifies a restriction fragment length polymorphism
Q72730508	The effectiveness of restriction endonucleases in cell killing and mutation
Q69872631	The effects of exogenous thymidine on endogenous deoxynucleotides and mutagenesis in mammalian cells
Q69914737	The embryonic and adult mouse U1 snRNA genes map to different chromosomal loci
Q69817875	The family of mouse phosphoglycerate kinase genes and pseudogenes
Q64389079	The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome
Q68420708	The gene encoding CD23 leukocyte antigen (FCE2) is located on human chromosome 19
Q28276223	The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7
Q41530613	The gene for the iron sulfur protein of succinate dehydrogenase (SDH-IP) maps to human chromosome 1p35-36.1.
Q34659059	The gonadotropin-releasing hormone (Gnrh) gene maps to mouse chromosome 14 and identifies a homologous region on human chromosome 8
Q28142641	The human RNA helicase A (DDX9) gene maps to the prostate cancer susceptibility locus at chromosome band 1q25 and its pseudogene (DDX9P) to 13q22, respectively
Q70314289	The human galactosyltransferase gene is on chromosome 9 at band p13
Q57337299	The independent expression of HLA and? 2-microglobulin on human-mouse hybrids
Q48069408	The mammalian RPS6 gene, homolog of the Drosophila air8 tumor suppressor gene: is it an oncosuppressor gene?
Q30982307	The mouse alanine:glyoxylate aminotransferase gene (Agxt1): cloning, expression, and mapping to chromosome 1.
Q68830359	The mouse smooth muscle gamma actin gene is on chromosome 6
Q72481752	The receptor-recycling and lysosome biogenesis mutant TfT1.11 belongs to a new complementation group, End6
Q38518901	The role of acentric chromosome fragments in gene amplification
Q44489639	The serotonin receptor subtype 2 locus HTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14.
Q41604676	The use of human repetitive DNA to target selectable markers into only the human chromosome of a human-hamster hybrid cell line (AL)
Q41667445	The use of irradiation and fusion gene transfer (IFGT) hybrids to isolate DNA clones from human chromosome region 9q33-q34
Q41532789	The use of methylthioadenosine phosphorylase activity to select for human chromosome 9 in interspecies and intraspecies hybrid cells
Q34296444	Three distinct loci on human chromosome 21 contribute to interferon-alpha/beta responsiveness.
Q57001008	Three functional ribosomal protein genes are unlinked in mouse genome
Q43863255	Three human cell surface antigen systems determined by genes on chromosome 12
Q45034939	Three new complementation groups of temperature-sensitive Chinese hamster ovary cell mutants defective in the endocytic pathway
Q36797742	Three region-specific microdissection libraries for the long arm of human chromosome 2, regions q33-q35, q31-q32, and q23-q24.
Q34179910	Threonyl-tRNA synthetase gene maps close to leucyl-tRNA synthetase gene on human chromosome 5.
Q42527440	Thymidylate metabolism in fragile X syndrome cells
Q70950306	Timing of mutation-fixation events in ethyl methane sulfonate-treated Chinese hamster cells
Q72752921	Tissue-specific extinguisher loci in the human genome: a screening study based on random marking and transfer of human chromosomes
Q36724716	Tissue-specific extinguisher loci in the murine genome: a screening study based on a rat/mouse microcell hybrid panel
Q31919804	Toward expression mapping of albinism-deafness syndrome (ADFN) locus on chromosome Xq26.
Q45880951	Towards liver-directed gene therapy: retrovirus-mediated gene transfer into human hepatocytes
Q73296878	Transcribed sequences encoded in the region involved in contiguous deletion syndrome that comprises X-linked stapes fixation and deafness
Q41676738	Transduction of the CHO aprt gene into mouse L cells using an adeno-5/APRT recombinant virus
Q45836318	Transfection of lymphoblastoid cells using DNA-loaded reconstituted Sendai virus envelopes: expression of transfected DNA and selection of transfected cells
Q72831821	Transfer of Chinese hamster chromosome 1 to mouse cells and regional assignment of 7 genes: a combination of gene transfer and microcell fusion
Q54432153	Transfer of antibiotic resistance genes between yeast and mammalian cells under conditions favoring cell fusion.
Q67817974	Transfer of the human HPRT and GART genes from yeast to mammalian cells by microinjection of YAC DNA
Q41992151	Transformation associated p53 protein is encoded by a gene on human chromosome 17.
Q68726872	Transforming growth factor beta gene maps to human chromosome 19 long arm and to mouse chromosome 7
Q70098884	Translocation chromosome 7 of A431 cells contains amplification and rearrangement of EGF receptor gene responsible for production of variant mRNA
Q46014133	Tumor necrosis factor receptor genes, TNFR1 and TNFR2, on human chromosomes 12 and 1.
Q35140237	Tumor-targeted gene transfer with DNA polyplexes
Q36587135	Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter
Q70938809	Two cell-surface markers for human chromosome 1 in interspecies hybrids
Q54460965	Two cytoplasmically inherited oligomycin-resistant Chinese hamster cell lines exhibit an altered mitochondrial translation product.
Q41442008	Two membrane-bound proteins associated with alanine resistance and increased A-system amino acid transport in mutants of CHO-K1.
Q54377553	Two pathways of transferrin recycling evident in a variant of mouse LMTK- cells.
Q69945377	Two types of mouse FM3A cell mutants deficient in 5-aminoimidazole-4-carboxamide ribonucleotide transformylase and their transformants isolated by human chromosome-mediated gene transfer
Q34288994	UMP synthase activity expressed in deficient hamster cells by separate transferase and decarboxylase proteins or by linker-deleted bifunctional protein
Q44087960	Ultraviolet-induced reactivation, amplification, and hypomethylation of a herpes simplex virus thymidine kinase gene
Q69971468	Unique chromosomal location of amplified EGF receptor genes in EGF receptor-hyperproducing tumor cell line NA
Q72636014	Unstable integration of transfected DNAs into embryonal carcinoma cells
Q69834132	Use of fluorescence-activated cell sorter to isolate mutant mammalian cells deficient in an internal protein, dihydrofolate reductase
Q70116700	Variant of A431 cells isolated by ricin A-conjugated monoclonal antibody directed to EGF receptor: phosphorylation of EGF receptor and phosphatidylinositol
Q43704521	Variants inducible for glutamine synthetase in V79-56 cells
Q72391461	Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene
Q69971456	X-chromosome inactivation in cultured cells from human chorionic villi
Q68365078	X-ray induction of methotrexate resistance due to dhfr gene amplification
Q49074365	XIST expression is repressed when X inactivation is reversed in human placental cells: A model for study ofXIST regulation
Q41471231	Xist is expressed in female embryonal carcinoma cells with two active X chromosomes
Q36795741	YAC analysis and minimal tiling path construction for chromosome 21q.
Q71768719	YAC contig mapping of six expressed sequences encoded by human chromosome 21
Q41715566	Zinc treatment, metallothionein expression, and resistance to cisplatin in mouse melanoma cells
Q34168287	cDNA cloning and assignment to chromosome 21 of IFI-78K gene, the human equivalent of murine Mx gene
Q48354895	cDNA sequence and mapping of the mouse Copb gene encoding the beta subunit of the COPI coatomer complex

P6981	ACNP journal ID	14894
		2113067
P1159	CODEN	SCMGDN
P8375	Crossref journal ID	13457
P1058	ERA Journal ID	2294
P646	Freebase ID	/m/0glnv46
P1160	ISO 4 abbreviation	Somat. Cell Mol. Genet.
P236	ISSN	0740-7750
		1572-9931
P7363	ISSN-L	0740-7750
P1055	NLM Unique ID	8403568
P243	OCLC control number	10009256
P856	official website	http://firstsearch.oclc.org/journal=0740-7750;screen=info;ECOIP
		http://www.kluweronline.com/issn/0740-7750/contents
		http://www.springer.com/biomed/human+genetics/journal/11188
P10283	OpenAlex ID	S198917220
P3181	OpenCitations bibliographic resource ID	98550
P7662	Scilit journal ID	2186200
P1156	Scopus source ID	19024
P5983	Springer journal ID	11188
P4616	UniProt journal ID	1740

P495	country of origin	United States of America	Q30
P571	inception	1975-01-01
P8875	indexed in bibliographic review	Scopus	Q371467
P407	language of work or name	English	Q1860
P921	main subject	cell biology	Q7141
P123	publisher	Springer Science+Business Media	Q176916
P1476	title	Somatic Cell and Molecular Genetics

Somatic Cell and Molecular Genetics

scientific journal

Reverse relations