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Mutations causing deficiency of APRT in fibroblasts cultured from human heterozygous for mutant APRT alleles.

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Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/7101101

title

Mutations causing deficiency of APRT in fibroblasts cultured from human heterozygous for mutant APRT alleles. (English)

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Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/7101101

author name string

Steglich C

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1

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Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/7101101

DeMars R

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2

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30 May 2018

http://europepmc.org/abstract/MED/7101101

publication date

1 January 1982

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30 May 2018

http://europepmc.org/abstract/MED/7101101

published in

Somatic Cell Genetics

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30 May 2018

http://europepmc.org/abstract/MED/7101101

volume

8

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30 May 2018

http://europepmc.org/abstract/MED/7101101

page(s)

115-141

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30 May 2018

http://europepmc.org/abstract/MED/7101101

issue

1

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Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/7101101

cites work

Validation of conditions for efficient detection of HPRT and APRT mutations in suspension-cultured Chinese hamster ovary cells

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https://api.crossref.org/works/10.1007%2FBF01538655

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21 January 2018

Quantification of chemical mutagenesis in diploid human fibroblasts: Induction of azaguanine-resistant mutants by N-methyl-N′-nitro-N-nitrosoguanidine

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https://api.crossref.org/works/10.1007%2FBF01538655

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21 January 2018

Comparative effects of adenine analogs upon metabolic cooperation between Chinese hamster cells with different levels of adenine phosphoribosyltransferase activity

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https://api.crossref.org/works/10.1007%2FBF01538655

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21 January 2018

Studies of the mutagenic activity of nucleic acid base-analogues in Drosophila

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21 January 2018

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10.1007/BF01538655

1 reference

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Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/7101101

PubMed ID

7101101

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Europe PubMed Central

30 May 2018

http://europepmc.org/abstract/MED/7101101

(Q54523543)

Mutations causing deficiency of APRT in fibroblasts cultured from human heterozygous for mutant APRT alleles.

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