An STS-based radiation hybrid map of the human genome

scientific article published on May 1997

An STS-based radiation hybrid map of the human genome is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1101/GR.7.5.422
P698PubMed publication ID9149939

P50authorJohn QuackenbushQ6253638
P2093author name stringQin F
Hadley D
Brady S
Myers RM
Harris M
Fan JB
O'Connor K
Sanders C
Lee R
Aggarwal A
Stewart EA
Chu A
Hussain S
Cox DR
Fang N
Perkins S
Sun WL
Mader C
Bajorek E
Piercy M
Tabar P
Cowles S
Maratukulam A
McKusick KB
Reif T
She X
Voyticky S
P2860cites workA Gene Map of the Human GenomeQ22065571
A comprehensive genetic map of the human genome based on 5,264 microsatellitesQ27860812
Complementary DNA sequencing: expressed sequence tags and human genome projectQ29618255
Continuum of overlapping clones spanning the entire human chromosome 21q.Q33191456
A radiation hybrid map of 506 STS markers spanning human chromosome 11.Q34327393
The development of sequence-tagged sites for human chromosome 4.Q34357358
An STS-based map of the human genomeQ36787753
Multipoint radiation hybrid mapping: comparison of methods, sample size requirements, and optimal study characteristicsQ41034311
A radiation hybrid map with 60 loci covering the entire short arm of chromosome 12.Q41300503
A method for constructing radiation hybrid maps of whole genomesQ41470289
Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomesQ42125680
NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2.Q42809129
A common language for physical mapping of the human genomeQ46940837
Statistical methods for polyploid radiation hybrid mapping.Q51650449
Experimental design and error detection for polyploid radiation hybrid mapping.Q52330147
The CEPH Consortium Linkage Map of Human Chromosome 11Q58673448
The volumes and morphology of human chromosomes in mitotic reconstructionsQ58884757
Hyping up the letdown geneQ59039413
New method for mapping genes in human chromosomesQ59082669
P433issue5
P304page(s)422-433
P577publication date1997-05-01
P1433published inGenome ResearchQ5533485
P1476titleAn STS-based radiation hybrid map of the human genome
P478volume7

Reverse relations

cites work (P2860)
Q31917676"KARIBIN," an information resource for obtaining genomic information in a cytogenetic band
Q779826774th Workshop of the European CMT-Consortium--62nd ENMC International Workshop: rare forms of Charcot-Marie-Tooth disease and related disorders 16-18 October 1998, Soestduinen, The Netherlands
Q44915047A 12,000-rad porcine radiation hybrid (IMNpRH2) panel refines the conserved synteny between SSC12 and HSA17.
Q35024138A 3-Mb high-resolution BAC/PAC contig of 12q22 encompassing the 830-kb consensus minimal deletion in male germ cell tumors
Q44064895A candidate gene study in low HDL-cholesterol families provides evidence for the involvement of the APOA2 gene and the APOA1C3A4 gene cluster
Q33884988A comparative gene map of the horse (Equus caballus)
Q34012360A comparative radiation hybrid map of bovine chromosome 18 and homologous chromosomes in human and mice
Q35024913A comprehensive view of human chromosome 1.
Q28776426A fast and scalable radiation hybrid map construction and integration strategy
Q30828600A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome
Q38554333A first-generation whole genome-radiation hybrid map spanning the mouse genome
Q24534339A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23
Q34018339A genome-wide map of human genetic interactions inferred from radiation hybrid genotypes
Q28203342A high-resolution map of human chromosome 12
Q24796752A high-resolution radiation hybrid map of chicken chromosome 5 and comparison with human chromosomes
Q37019175A high-resolution radiation hybrid map of rhesus macaque chromosome 5 identifies rearrangements in the genome assembly
Q30725861A maize map standard with sequenced core markers, grass genome reference points and 932 expressed sequence tagged sites (ESTs) in a 1736-locus map.
Q24291103A new spectrin, beta IV, has a major truncated isoform that associates with promyelocytic leukemia protein nuclear bodies and the nuclear matrix
Q22011049A novel human opsin in the inner retina
Q57272455A physical map of the human Y chromosome
Q34146234A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23
Q35026456A radiation hybrid map of the cat genome: implications for comparative mapping
Q40814016A radiation hybrid map of the rat genome containing 5,255 markers
Q40931514A radiation hybrid map of the zebrafish genome.
Q34607431A scan for linkage disequilibrium across the human genome.
Q34387777A second locus for familial high myopia maps to chromosome 12q
Q34606230A second-generation genetic linkage map of the domestic dog, Canis familiaris.
Q33204169A web server for performing electronic PCR.
Q22008043A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles
Q22254763ADAMTS9, a novel member of the ADAM-TS/ metallospondin gene family
Q73747003ARHI is the center of allelic deletion on chromosome 1p31 in ovarian and breast cancers
Q57304630ATB(0)/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis
Q51972185Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndrome.
Q34076660An update of the goat genome assembly using dense radiation hybrid maps allows detailed analysis of evolutionary rearrangements in Bovidae
Q24539202Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24
Q24296479Characterization and localization of a human serine racemase
Q28214444Characterization of XAGE-1b, a short major transcript of cancer/testis-associated gene XAGE-1, induced in melanoma metastasis
Q30784770Characterization of physical gap sizes at human telomeres
Q77845947Chromosomal deletions occur in restricted regions of 5q in testicular germ cell cancer
Q40415431Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes
Q28208057Cloning and characterization of IL-1HY2, a novel interleukin-1 family member
Q24623075Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells
Q22253909Cloning and functional expression of two families of beta-subunits of the large conductance calcium-activated K+ channel
Q28511634Cloning and genetic characterization of an evolutionarily conserved human olfactory receptor that is differentially expressed across species
Q22003986Cloning of a novel C-terminal kinesin (KIFC3) that maps to human chromosome 16q13-q21 and thus is a candidate gene for Bardet-Biedl syndrome
Q30392113Construction of a radiation hybrid panel and the first yellowtail (Seriola quinqueradiata) radiation hybrid map using a nanofluidic dynamic array
Q57239987Coordination of human genome sequencing via a consensus framework map
Q54622491Development of a deer mouse whole-genome radiation hybrid panel and comparative mapping of Mus chromosome 11 loci.
Q34032960Developmental expression of functional cyclooxygenases in zebrafish.
Q59167176Dissecting Plant Chromosomes by the Use of Ionizing Radiation
Q34075037Effects of genome-wide copy number variation on expression in mammalian cells
Q31965814Electronic PCR: bridging the gap between genome mapping and genome sequencing
Q36380621Endosperm tolerance of paternal aneuploidy allows radiation hybrid mapping of the wheat D-genome and a measure of γ ray-induced chromosome breaks
Q74450790Evaluation of mouse Sfrp3/Frzb1 as a candidate for the lst, Ul, and Far mutants on chromosome 2
Q35893955Evolutionary relationships among Rel domains indicate functional diversification by recombination
Q35028744Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project
Q35031123Extensive conservation of sex chromosome organization between cat and human revealed by parallel radiation hybrid mapping
Q34386217Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype
Q34130421Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene
Q35435104Gene amplification in PNETs/medulloblastomas: mapping of a novel amplified gene within the MYCN amplicon
Q34390210Genetic linkage of hyper-IgE syndrome to chromosome 4.
Q36441268Genetic screening reveals a link between Wnt signaling and antitubulin drugs
Q28204842Genomic sequence and expression analyses of human chromatin assembly factor 1 p150 gene
Q35024299High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1.
Q28365983High-resolution physical and transcript map of human chromosome 2p21 containing the sitosterolaemia locus.
Q35025252High-resolution physical map and transcript identification of a prostate cancer deletion interval on 8p22.
Q34895503High-resolution radiation hybrid map of wheat chromosome 1D.
Q24290123Human and mouse homologues of the Drosophila melanogaster tweety (tty) gene: a novel gene family encoding predicted transmembrane proteins
Q22010886Human peroxisome proliferator activated receptor gamma coactivator 1 (PPARGC1) gene: cDNA sequence, genomic organization, chromosomal localization, and tissue expression
Q58054034INCONSISTENCIES BETWEEN MAPS OF HUMAN CHROMOSOME 22 CORRELATE WITH INCREASED FREQUENCY OF DISEASE-RELATED LOCI
Q24290830Identification and characterization of BTBD1, a novel BTB domain containing gene on human chromosome 15q24
Q33935707Identification and characterization of a novel human cDNA encoding a 21 kDa pRb-associated protein
Q24316109Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects
Q30328184Identification of a novel gene on chromosome 13 between BRCA-2 and RB-1.
Q22009450Identification of a novel human adenylate kinase. cDNA cloning, expression analysis, chromosome localization and characterization of the recombinant protein
Q34085454Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.
Q39764047Identification of the myelin protein plasmolipin as the cell entry receptor for Mus caroli endogenous retrovirus.
Q24290845Identification of the platelet ADP receptor targeted by antithrombotic drugs
Q36777792Improved assay-dependent searching of nucleic acid sequence databases
Q21045365Initial sequencing and analysis of the human genome
Q24628031Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb
Q73852560Mapping the chromosome 16 cadherin gene cluster to a minimal deleted region in ductal breast cancer
Q38527588Maternal and embryonic expression of zebrafish lef1.
Q34970591Mechanism of cell entry and transformation by enzootic nasal tumor virus.
Q34610942Microsatellite variation and recombination rate in the human genome.
Q47867520Molecular characterization and population study of an X chromosome homolog of the Y-linked microsatellite DYS391.
Q28201723Molecular characterization of hiwi, a human member of the piwi gene family whose overexpression is correlated to seminomas
Q22008554Molecular cloning and characterization of a novel retinoic acid-inducible gene that encodes a putative G protein-coupled receptor
Q22009031Molecular cloning and characterization of prostase, an androgen-regulated serine protease with prostate-restricted expression
Q22004179Molecular cloning and functional expression of a novel human gene encoding two 41-43 kDa skeletal muscle internal membrane proteins
Q24290384Molecular cloning of a human, hemicholinium-3-sensitive choline transporter
Q30731578Mouse BAC ends quality assessment and sequence analyses
Q57555808Notes from the SNP vs. haplotype front
Q30168459PACSIN 3 is a novel SH3 domain cytoplasmic adapter protein of the pacsin-syndapin-FAP52 gene family.
Q28511923PALML, a novel paralemmin-related gene mapping on human chromosome 1p21
Q24654907Panhandle PCR strategy to amplify MLL genomic breakpoints in treatment-related leukemias
Q32048269Parallel radiation hybrid mapping: a powerful tool for high-resolution genomic comparison.
Q22010485Phosphorylation of deoxycytidine analog monophosphates by UMP-CMP kinase: molecular characterization of the human enzyme
Q34467519Physical mapping resources for large plant genomes: radiation hybrids for wheat D-genome progenitor Aegilops tauschii.
Q35159291Precise gene localization by phenotypic assay of radiation hybrid cells
Q34610419Production and characterization of maize chromosome 9 radiation hybrids derived from an oat-maize addition line
Q31958280Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.
Q40416838RHO--radiation hybrid ordering
Q60307926Radiation Hybrid Mapping
Q80081443Radiation hybrid map of the porcine genome comprising 2035 EST loci
Q34567076Radiation hybrid mapping of the species cytoplasm-specific (scsae) gene in wheat
Q36431265Radiation hybrid mapping of the zebrafish genome
Q40115465Radiation hybrid maps of Medaka chromosomes LG 12, 17, and 22.
Q41588799Rapid construction of genome maps
Q93161967Reduced Folate Carrier: an Entry Receptor for a Novel Feline Leukemia Virus Variant
Q33804653Retrovirus vectors bearing jaagsiekte sheep retrovirus Env transduce human cells by using a new receptor localized to chromosome 3p21.3.
Q34064640Sequence mapping by electronic PCR
Q36430977Sequence-tagged connectors: a sequence approach to mapping and scanning the human genome
Q24536337Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.
Q37216995Systematic evaluation of map quality: human chromosome 22.
Q28145358The DNA sequence of human chromosome 21
Q22254615The GIT family of ADP-ribosylation factor GTPase-activating proteins. Functional diversity of GIT2 through alternative splicing
Q24627734The Genexpress IMAGE knowledge base of the human brain transcriptome: a prototype integrated resource for functional and computational genomics
Q22008840The RD114/simian type D retrovirus receptor is a neutral amino acid transporter
Q35023322The comprehensive mouse radiation hybrid map densely cross-referenced to the recombination map: a tool to support the sequence assemblies
Q81128220The feline major histocompatibility complex is rearranged by an inversion with a breakpoint in the distal class I region
Q34994110The first-generation whole-genome radiation hybrid map in the horse identifies conserved segments in human and mouse genomes
Q35030708The genexpress IMAGE knowledge base of the human muscle transcriptome: a resource of structural, functional, and positional candidate genes for muscle physiology and pathologies
Q24310204The human glutamate receptor delta 2 gene (GRID2) maps to chromosome 4q22
Q24291646The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders
Q28594377The mahogany protein is a receptor involved in suppression of obesity
Q24290809The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism
Q28585714The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice
Q42638206Zebrafish ae2.2 encodes a second slc4a2 anion exchanger.
Q33279472Zebrafish orthologs of human muscular dystrophy genes
Q40417631Zebrafish slc4a2/ae2 anion exchanger: cDNA cloning, mapping, functional characterization, and localization
Q22008042beta2-Adrenergic receptor regulation by GIT1, a G protein-coupled receptor kinase-associated ADP ribosylation factor GTPase-activating protein
Q30852257bloodthirsty, an RBCC/TRIM gene required for erythropoiesis in zebrafish
Q22007991cDNA cloning and characterization of sciellin, a LIM domain protein of the keratinocyte cornified envelope
Q24310670hEST2, the putative human telomerase catalytic subunit gene, is up-regulated in tumor cells and during immortalization
Q33923367p190-A, a human tumor suppressor gene, maps to the chromosomal region 19q13.3 that is reportedly deleted in some gliomas

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