Somatic cell mutation frequency at the HPRT, T-cell antigen receptor and glycophorin A loci in Cockayne syndrome.

No abstract is available for this paper.

• Publication year

  1995

• Venue

  Mutation research

• Publication date

  1995-07-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/0921-8777(95)00014-BPMID 7596357
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Somatic mutations at T-cell antigen receptor and glycophorin A loci in pediatric leukemia patients following chemotherapy: comparison with HPRT locus mutation.

  1994cited by this paper
• Molecular analysis of mutations in the hprt gene in circulating lymphocytes from normal and DNA-repair-deficient donors.

  1993cited by this paper
• Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.

  1993cited by this paper
• Frequencies of HPRT- lymphocytes and glycophorin A variants erythrocytes in Fanconi anemia patients, their parents and control donors.

  1993cited by this paper
• Analysis of hprt gene mutation following anti-cancer treatment in pediatric patients with acute leukemia.

  1993cited by this paper
• Enhanced hprt mutant frequency but no significant difference in mutation spectrum between a smoking and a non-smoking human population.

  1992cited by this paper
• Development of a flow-cytometric HLA-A locus mutation assay for human peripheral blood lymphocytes.

  1992cited by this paper
• Elevated hprt mutant frequency in circulating T-lymphocytes of xeroderma pigmentosum patients.

  1992cited by this paper
• Abnormal erythemal response and elevated T lymphocyte HRPT mutant frequency in Cockayne's syndrome

  1991cited by this paper
• Spontaneous loss and alteration of antigen receptor expression in mature CD4+ T cells

  1990cited by this paper
• Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophy.

  1990cited by this paper
• The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.

  1990cited by this paper
• Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus.

  1990cited by this paper
• Characterization of a splicing mutation in group A xeroderma pigmentosum.

  1990cited by this paper
• Cloning of in vivo-derived thioguanine-resistant human B cells.

  1989cited by this paper
• Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome.

  1989cited by this paper
• Detection of somatic mutations at the glycophorin A locus in erythrocytes of atomic bomb survivors using a single beam flow sorter.

  1989cited by this paper
• Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom's syndrome patients.

  1989cited by this paper
• Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasia.

  1989cited by this paper
• A further assessment of factors influencing measurements of thioguanine-resistant mutant frequency in circulating T-lymphocytes.

  1988cited by this paper
• Mutations in human lymphocytes studied by an HLA selection system.

  1988cited by this paper
• Increased somatic cell mutant frequency in atomic bomb survivors.

  1988cited by this paper
• Measurements of the frequency of human erythrocytes with gene expression loss phenotypes at the glycophorin A locus

  1986cited by this paper
• Somatic gene mutations in vivo as indicated by the 6-thioguanine-resistant T-lymphocytes in human blood.

  1985cited by this paper
• Monoclonal antibodies specific for the M- and N-forms of human glycophorin A.

  1983cited by this paper
• Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum.

  1982cited by this paper
• T-cell cloning to detect the mutant 6-thioguanine-resistant lymphocytes present in human peripheral blood.

  1982cited by this paper
• Cockayne's syndrome. An heredo-familial disorder of growth and development.

  1960cited by this paper

• Two Stories of Neurodevelopment: Exosome-Mediated Secretion of Sonic Hedgehog and Somatic Mutation in Disorders of DNA Damage Repair

  2016cites this paper
• Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency

  2016cites this paper
• Sources and consequences of oxidative damage from mitochondria and neurotransmitter signaling

  2016cites this paper
• Highly accurate RNA and DNA sequencing: Application to longstanding questions in aging and cancer

  2016cites this paper
• Oxidatively damaged DNA repair defect in cockayne syndrome and its complementation by heterologous repair proteins.

  2008cites this paper
• Elevated levels of somatic mutation in a manifesting BRCA1 mutation carrier

  2008cites this paper
• The current evidence for defective repair of oxidatively damaged DNA in Cockayne syndrome.

  2007cites this paper
• Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype

  2005cites this paper
• Somatic mutations and aging: a re-evaluation.

  2000cites this paper
• Cancer chemotherapy and somatic cell mutation.

  2000cites this paper
• The premature ageing syndromes: insights into the ageing process.

  1998cites this paper
• Evaluation of mutant frequencies at the hprt and the T-cell receptor loci in pediatric cancer patients before treatment.

  1998cites this paper
• Purine and Pyrimidine Metabolism in Man IX

  1998cites this paper
• Measurement of mutation frequency at the HPRT locus in peripheral lymphocytes. Is this a good method to evaluate a cancer risk in pediatric patients?

  1998cites this paper