(Q33709252)

English

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

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

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

1 reference

Europe PubMed Central

28 July 2017

Lesch-Nyhan syndrome

0 references

1 reference

based on heuristic

inferred from title

author name string

Cox RP

1

1 reference

Europe PubMed Central

28 July 2017

Krauss MR

2

1 reference

Europe PubMed Central

28 July 2017

Balis ME

3

1 reference

Europe PubMed Central

28 July 2017

Dancis J

4

1 reference

Europe PubMed Central

28 July 2017

language of work or name

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publication date

1 November 1970

1 reference

Europe PubMed Central

28 July 2017

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

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Europe PubMed Central

28 July 2017

67

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Europe PubMed Central

28 July 2017

1573-1579

1 reference

Europe PubMed Central

28 July 2017

3

1 reference

Europe PubMed Central

28 July 2017

Protein measurement with the Folin phenol reagent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=283392

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=283392

21 June 2018

Cell population density and phenotypic expression of tissue culture fibroblasts from heterozygotes of Lesch-Nyhan's disease (inosinate pyrophosphorylase deficiency)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=283392

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=283392

21 June 2018

Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=283392

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=283392

21 June 2018

Alkaline phosphatase content and the effects of prednisolone on mammalian cells in culture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=283392

30 October 2018

The metabolism of P32-labeled ribonucleotides in tissue slices and cell suspensions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=283392

30 October 2018

Diagnosis of Lesch-Nyhan syndrome by direct study of skin specimens

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated AMP pyrophosphorylase activity in congenital IMP pyrophosphorylase deficiencey (Lesch-Nyhan disease)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exchange between hamster cells in culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A method for the prenatal diagnosis of congenital hyperuricemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hurler and Hunter syndromes: mutual correction of the defect in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Turnover of rat liver tyrosine transaminase: stabilization after inhibition of protein synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of mosaicism in the lymphocyte in X-linked congenital hyperuricosuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic test for congenital hyperuricemia with central nervous system dysfunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inborn errors of mucopolysaccharide metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/5274481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.67.3.1573

1 reference

Europe PubMed Central

28 July 2017

1970PNAS...67.1573C

0 references

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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