Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
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Hypoxanthine-guanine phosphoribosyltransferase deficiency: activity in normal, mutant, and heterozygote-cultured human skin fibroblastsEvidence for transfer of enzyme product as the basis of metabolic cooperation between tissue culture fibroblasts of Lesch-Nyhan disease and normal cells.Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome.X-chromosome inactivation and developmental patterns in mammals.The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease.Activation of variants of hypoxanthine-guanine phosphoribosyl transferase by the normal enzyme.Purine metabolism in normal and thioguanine-resistant neuroblastoma.Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect.Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation.Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type).Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation.Linkage relationships of X-linked enzymes glucose-6-phosphate dehydrogenase and hypoxanthine guanine phosphoribosyltransferase: recombination in female offspring of compound heterozygotesHalf chromatid mutations: transmission in humans?B lymphocytes from X-linked agammaglobulinemia. Delayed expression of light chain and demonstration of Lyonization in carriers.Hypoxanthine-guanine phosphoribosyltransferase variant associated with accelerated purine synthesis.Gene loss in human teratomas.A temperature-sensitive glucose-6-phosphate dehydrogenase in mutant cultured human cells.Transfer of cloned human class I major histocompatibility complex genes into HLA mutant human lymphoblastoid cells.Purine requirement of cells cultured from humans affected with Lesch-Nyhan syndrome (hypoxanthine-guanine phosphoribosyltransferase deficiency).Hypoxanthine-guanine phosphoribosyltransferase deficiency: chemical agents selective for mutant or normal cultured fibroblasts in mixed and heterozygote cultures.Mutagenicity to mammalian cells of epoxides and other derivatives of polycyclic hydrocarbons.
P2860
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P2860
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
description
1968 nî lūn-bûn
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1968年の論文
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1968年学术文章
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1968年学术文章
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1968年学术文章
@zh-hans
1968年学术文章
@zh-my
1968年学术文章
@zh-sg
1968年學術文章
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1968年學術文章
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1968年學術文章
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name
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
@ast
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
@en
type
label
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
@ast
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
@en
prefLabel
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
@ast
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
@en
P2093
P2860
P356
P1476
Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
@en
P2093
P2860
P304
P356
10.1073/PNAS.60.2.545
P407
P577
1968-06-01T00:00:00Z