Pig-a mutations in bone marrow erythroblasts of rats treated with 7,12-dimethyl-benz[a]anthracene
Author:
Funder
US FDA
Publisher
Elsevier BV
Subject
Health, Toxicology and Mutagenesis,Genetics
Reference33 articles.
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2. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals;Araten;Proc. Natl. Acad. Sci. U. S. A.,1999
3. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene;Bessler;EMBO J.,1994
4. Molecular genetics of paroxysmal nocturnal hemoglobinuria;Inoue;Int. J. Hematol.,2003
5. Paroxysmal nocturnal hemoglobinuria: an acquired genetic disease;Nishimura;Am. J. Hematol.,1999
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1. Lack of hydroxyurea‐associated mutagenesis in pediatric sickle cell disease patients;Environmental and Molecular Mutagenesis;2023-03
2. Recommendations for conducting the rodent erythrocyte Pig‐a assay: A report from the HESI GTTC Pig‐a Workgroup;Environmental and Molecular Mutagenesis;2021-03
3. CD59 ‐deficient bone marrow erythroid cells from rats treated with procarbazine and propyl‐nitrosourea have mutations in the Pig‐a gene;Environmental and Molecular Mutagenesis;2020-08-18
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