scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF01534853 |
P698 | PubMed publication ID | 6089358 |
P2093 | author name string | Caskey CT | |
Ledbetter DH | |||
Patel PI | |||
Nussbaum RL | |||
Chinault AC | |||
gramson PE | |||
P2860 | cites work | Deletion and amplification of the HGPRT locus in Chinese hamster cells | Q36939839 |
P433 | issue | 5 | |
P304 | page(s) | 483-493 | |
P577 | publication date | 1984-09-01 | |
P1433 | published in | Somatic Cell and Molecular Genetics | Q7559232 |
P1476 | title | Organization of the HPRT gene and related sequences in the human genome | |
P478 | volume | 10 |
Q35643742 | A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies |
Q40565199 | A HindIII RFLP for the HPRT pseudogene on chromosome 3 (HPRTP1). |
Q34519085 | A molecular survey of hypoxanthine-guanine phosphoribosyltransferase deficiency in man. |
Q33975820 | A review of the molecular basis of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency |
Q43454315 | Acetaldehyde-induced mutation at the hprt locus in human lymphocytes in vitro |
Q54447037 | Alterations of the hprt gene in human in vivo-derived 6-thioguanine-resistant T lymphocytes. |
Q43988977 | C4A gene deletion and HLA associations in black Americans with systemic lupus erythematosus |
Q68347436 | Characterization of three new deletions at the 5' end of the HPRT structural gene |
Q35200319 | Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21. |
Q24337628 | Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa |
Q48024808 | Clinical correlates, serum autoantibodies and the role of the major histocompatibility complex in French Canadian and non-French Canadian Caucasians with SLE. |
Q36458511 | Cloning and sequence analysis of cDNA for human argininosuccinate lyase |
Q36356099 | Cloning of phenotypically different human lymphocytes originating from a single stem cell |
Q35196862 | DNA typing and genetic mapping with trimeric and tetrameric tandem repeats |
Q28646733 | Data supporting the design and evaluation of a universal primer pair for pseudogene-free amplification of HPRT1 in real-time PCR |
Q46555780 | Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation |
Q35889247 | Evaluation of 13 short tandem repeat loci for use in personal identification applications |
Q34322626 | Fidelity of DNA polymerases in DNA amplification |
Q34684524 | Fine structure of the human hypoxanthine phosphoribosyltransferase gene |
Q34614818 | Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups |
Q37723405 | Genotype-phenotype correlations in neurogenetics: Lesch-Nyhan disease as a model disorder |
Q34303544 | Heavy ion mutagenesis: Linear energy transfer effects and genetic linkage |
Q36918883 | Herpes simplex virus type 2 mutagenesis: characterization of mutants induced at the hprt locus of nonpermissive XC cells |
Q35595365 | Hypoxanthine-guanine phosphoribosyltransferase. Genetic evidence for identical mutations in two partially deficient subjects |
Q24679024 | Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency |
Q48053736 | Identification of a novel tissue-specific processed HPRT gene and comparison with X-linked gene transcription in the Australian marsupial Macropus robustus |
Q35194960 | Identification of repeat sequence heterogeneity at the polymorphic short tandem repeat locus HUMTH01[AATG]n and reassignment of alleles in population analysis by using a locus-specific allelic ladder |
Q44841620 | In vivo somatic mutations in human lymphocytes frequently result from major gene alterations |
Q45249700 | Lack of dose-rate effect for mutation induction by gamma-rays in human TK6 cells |
Q69927661 | Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe |
Q54352758 | Locus specificity for mutation induction in human cells exposed to accelerated heavy ions. |
Q69735089 | Molecular analyses of in vivo hprt mutant T cells from atomic bomb survivors |
Q42147020 | Molecular analyses of in vivo hprt mutations in human T-lymphocytes: IV. Studies in newborns |
Q35198822 | Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype |
Q69922871 | Molecular analysis of formaldehyde-induced mutations in human lymphoblasts and E. coli |
Q57748331 | Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in Italian Lesch-Nyhan patients: Identification of nine novel mutations |
Q36835999 | Molecular characterization of 15 rearrangements among 90 human in vivo somatic mutants shows that deletions predominate |
Q28116025 | Molecular cloning and chromosomal localization of human 4-beta-galactosyltransferase |
Q24609670 | Mutator phenotype of Werner syndrome is characterized by extensive deletions |
Q36114648 | Plasmid mediated mutagenesis of a cellular gene in transfected eukaryotic cells |
Q46851751 | Pseudogenes of the human HPRT1 gene |
Q73355646 | Research dealing with mutations in the X-chromosomal housekeeping hypoxanthine-guanine phosphoribosyltransferase (HPRT) |
Q35245512 | Resolution of a missense mutant in human genomic DNA by denaturing gradient gel electrophoresis and direct sequencing using in vitro DNA amplification: HPRT Munich |
Q63429287 | Screening for molecular pathologies in Lesch-Nyhan syndrome |
Q34856809 | Somatic cell gene mutations in humans: biomarkers for genotoxicity |
Q71808572 | Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch‐Nyhan syndrome |
Q35200834 | The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1. |
Q33982784 | The point mutation of hypoxanthine-guanine phosphoribosyltransferase (HPRTEdinburgh) and detection by allele-specific polymerase chain reaction |
Q35200643 | Thymidylate synthase-deficient Chinese hamster cells: a selection system for human chromosome 18 and experimental system for the study of thymidylate synthase regulation and fragile X expression |
Search more.