An enumerative assay of purine analogue resistant lymphocytes in women heterozygous for the Lesch-Nyhan Mutation. (Q54551391)

31 May 2018

title

An enumerative assay of purine analogue resistant lymphocytes in women heterozygous for the Lesch-Nyhan Mutation. (English)

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31 May 2018

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G H Strauss

1

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31 May 2018

E F Allen

series ordinal

2

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31 May 2018

R J Albertini

series ordinal

3

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31 May 2018

publication date

1 June 1980

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31 May 2018

published in

Biochemical Genetics

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31 May 2018

volume

18

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31 May 2018

issue

5-6

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31 May 2018

page(s)

529-547

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31 May 2018

Enumeration of 6-thioguanine-resistant peripheral blood lymphocytes in man as a potential test for somatic cell mutations arising in vivo

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00484400

Somatic cell mutation detection and quantification of X-ray-induced mutation in cultured, diploid human fibroblasts

21 January 2018

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Variability of the time at which PHA-stimulated lymphocytes initiate DNA synthesis

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6-Thioguanine Resistant Peripheral Blood Lymphocytes in Humans Following Psoralen, Long-Wave Ultraviolet Light (PUVA) Therapy

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Lymphocyte transformation in vitro. I. Tissue culture conditions and quantitative measurements

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Isoenzymes of hypoxanthine-guanine-phosphoribosyl transferase in a family with partial deficiency of the enzyme

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Lesch-Nyhan syndrome: absence of the mutant enzyme in erythrocytes of a heterozygote for both normal and mutant hypoxanthine-guanine phosphoribosyl transferase.

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12 December 2020

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

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DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS

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Purine base incorporation into erythrocyte nucleotides in hypoxanthine-guanine phosphoribosyltransferase deficiency

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An hypothesis on the mechanism of action of 6-thioguanine

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12 December 2020

Studies on hair roots for carrier detection in hypoxanthine-quanine phosphoribosyl transferase deficiency

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12 December 2020

Lesch-Nyhan Mutation: Prenatal Detection with Amniotic Fluid Cells

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12 December 2020

Symposium on immunosuppressive drugs. Biochemistry and pharmacology of purine analogues

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12 December 2020

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

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12 December 2020

Genetic studies of HG- PRT deficiency and the Lesch-Nyhan syndrome with cultured human cells

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12 December 2020

Identification of the enzymatic pathways of nucleotide metabolism in human lymphocytes and leukemia cells

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Mechanisms of action of 6-thioguanine, 6-mercaptopurine, and 8-azaguanine

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12 December 2020

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

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12 December 2020

Detection of heterozygous carriers of the Lesch-Nyhan syndrome by electrophoresis of hair root lysates

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12 December 2020

Diploid Azaguanine-Resistant Mutants of Cultured Human Fibroblasts

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12 December 2020

Incorporation of hypoxanthine by PHA-stimulated HPRT-deficient lymphocytes

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation

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12 December 2020

The measurement of proliferation in tissue cultures by enumeration of cell nuclei

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12 December 2020

Purine metabolism in heterozygous carriers of hypoxanthine-guanine phosphoribosyltransferase deficiency

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12 December 2020

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

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12 December 2020

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

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12 December 2020

The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker

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12 December 2020

Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome

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12 December 2020

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

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12 December 2020

Protein modification in aging cells

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12 December 2020

Identifiers

DOI

10.1007/BF00484400

1 reference

31 May 2018

1 reference

31 May 2018