Hypoxanthine-guanine phosphoribosyltransferase deficiency: chemical agents selective for mutant or normal cultured fibroblasts in mixed and heterozygote cultures (Q37480785)

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scientific article published on July 1971

Language	Label	Description	Also known as
English	Hypoxanthine-guanine phosphoribosyltransferase deficiency: chemical agents selective for mutant or normal cultured fibroblasts in mixed and heterozygote cultures	scientific article published on July 1971

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Hypoxanthine-guanine phosphoribosyltransferase deficiency: chemical agents selective for mutant or normal cultured fibroblasts in mixed and heterozygote cultures (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

0 references

author name string

Fujimoto WY

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Subak-Sharpe JH

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Seegmiller JE

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

1 July 1971

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Proceedings of the National Academy of Sciences of the United States of America

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Europe PubMed Central

PMC publication ID

20 August 2017

68

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Europe PubMed Central

PMC publication ID

20 August 2017

7

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1516-1519

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION

1 reference

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THE INOSINIC ACID PYROPHOSPHORYLASE ACTIVITY OF MOUSE FIBROBLASTS PARTIALLY RESISTANT TO 8-AZAGUANINE

1 reference

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Gene action in the X-chromosome of the mouse (Mus musculus L.)

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Biosynthesis of the purines. XV. The effect of aza-L-serine and 6-diazo-5-oxo-L-norleucine on inosinic acid biosynthesis de novo

1 reference

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Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

1 reference

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Inheritance of purine phosphoribosyltransferases in man

1 reference

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Evidence for transfer of enzyme product as the basis of metabolic cooperation between tissue culture fibroblasts of Lesch-Nyhan disease and normal cells

1 reference

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Hypoxanthine-guanine phosphoribosyltransferase deficiency: activity in normal, mutant, and heterozygote-cultured human skin fibroblasts

1 reference

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1 reference

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A biochemical basis for resistance of L1210 mouse leukemia to 6-thioguanine.

1 reference

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X-Linked Recessive Inheritance of a Syndrome of Mental Retardation With Hyperuricemia

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X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations

1 reference

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Detection of females heterozygous for the Lesch-Nyhan mutation by 8-azaguanine-resistant growth of cultured fibroblasts

1 reference

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Biochemical diagnosis of an X-linked disease in utero.

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A comparison of the metabolism of purines and purine analogs by susceptible and drug-resistant bacterial and neoplastic cells.

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BIOCHEMICALLY MARKED VARIANTS OF THE SYRIAN HAMSTER FIBROBLAST CELL LINE BHK21 AND ITS DERIVATIVES

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HEREDITARY CHOREOATHETOSIS, SELF-MUTILATION AND HYPERURICEMIA IN YOUNG MALES

1 reference

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Metabolic co-operation between biochemically marked mammalian cells in tissue culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/5283941

12 December 2020

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inferred from PubMed ID database lookup

The metabolism of 6-thioguanine in normal and neoplastic tissues

1 reference

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inferred from PubMed ID database lookup

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: Detection of heterozygotes by selective medium

1 reference

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Studies on the mode of action of azaserine

1 reference

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Identifiers

10.1073/PNAS.68.7.1516

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1971PNAS...68.1516F

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

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