(Q53789245)

English

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

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scholarly article

1 reference

Europe PubMed Central

19 May 2018

http://europepmc.org/abstract/MED/5369312

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

1 reference

10.1007/BF00485483

https://api.crossref.org/works/10.1007/BF00485483

9 May 2023

Lesch-Nyhan syndrome

0 references

culture technique

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5369312

9 May 2023

1 reference

10.1007/BF00485483

https://api.crossref.org/works/10.1007/BF00485483

9 May 2023

1 reference

10.1007/BF00485483

https://api.crossref.org/works/10.1007/BF00485483

9 May 2023

author name string

J. Dancis

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5369312

9 May 2023

R. P. Cox

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5369312

9 May 2023

P. H. Berman

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5369312

9 May 2023

V. Jansen

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5369312

9 May 2023

M. E. Balis

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5369312

9 May 2023

language of work or name

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5369312

9 May 2023

publication date

1 December 1969

1 reference

Europe PubMed Central

19 May 2018

http://europepmc.org/abstract/MED/5369312

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00485483.pdf

Portable Document Format

1 reference

10.1007/BF00485483

https://api.crossref.org/works/10.1007/BF00485483

9 May 2023

http://link.springer.com/article/10.1007/BF00485483/fulltext.html

1 reference

10.1007/BF00485483

https://api.crossref.org/works/10.1007/BF00485483

9 May 2023

http://link.springer.com/content/pdf/10.1007/BF00485483

1 reference

10.1007/BF00485483

https://api.crossref.org/works/10.1007/BF00485483

9 May 2023

Biochemical Genetics

1 reference

Europe PubMed Central

19 May 2018

http://europepmc.org/abstract/MED/5369312

3

1 reference

Europe PubMed Central

19 May 2018

http://europepmc.org/abstract/MED/5369312

609-615

1 reference

Europe PubMed Central

19 May 2018

http://europepmc.org/abstract/MED/5369312

6

1 reference

Europe PubMed Central

19 May 2018

http://europepmc.org/abstract/MED/5369312

https://scigraph.springernature.com/pub.10.1007/bf00485483

0 references

Clonal growth in vitro of epithelial cells from normal human tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid proliferation of sublines of NCTC clone 929 (strain L) mouse cells in a simple chemically defined medium (MB 752/1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

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/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lesch-Nyhan Mutation: Prenatal Detection with Amniotic Fluid Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

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/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Repression of alkaline phosphatase in human cell cultures by cystine and cysteine

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radioautography, principles and procedures

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

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/5369312

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/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purine requirement of cells cultured from humans affected with Lesch-Nyhan syndrome (hypoxanthine-guanine phosphoribosyltransferase deficiency).

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

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/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoxanthine-guanine phosphoribosyltransferase deficiency in the Lesch-Nyhan syndrome and gout

1 reference

https://pubmed.ncbi.nlm.nih.gov/5369312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00485483

1 reference

Europe PubMed Central

19 May 2018

http://europepmc.org/abstract/MED/5369312

release_jprr52zdb5anbg6boh6bgqk5we

1 reference

https://api.fatcat.wiki/v0/release/jprr52zdb5anbg6boh6bgqk5we

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

19 May 2018

http://europepmc.org/abstract/MED/5369312

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