Frequent HPRT mutations in paroxysmal nocturnal haemoglobinuria reflect T cell clonal expansion, not genomic instability
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2004.04912.x/fullpdf
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4. Homologies between T cell receptor junctional sequences unique to multiple sclerosis and T cells mediating experimental allergic encephalomyelitis;Allegretta;Journal of Clinical Investigation,1994
5. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals;Araten;Proceedings of the National Acadamy of Sciences of the United States of America,1999
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1. Molecular characterization of hypoxanthine guanine phosphoribosyltransferase mutant T cells in human blood: The concept of surrogate selection for immunologically relevant cells;Mutation Research/Reviews in Mutation Research;2022-01
2. Analysis of TET2 mutations in paroxysmal nocturnal hemoglobinuria (PNH);Experimental Hematology & Oncology;2019-08-21
3. No evidence of hypermutability in red cells from patients with paroxysmal nocturnal hemoglobinuria using the XK gene;Haematologica;2014-05-09
4. The Role of Adaptive Immunity in Idiopathic Pulmonary Fibrosis: Hiding in Plain Sight;Idiopathic Pulmonary Fibrosis;2013-09-13
5. The mutation rate in PIG-A is normal in patients with paroxysmal nocturnal hemoglobinuria (PNH);Blood;2006-07-15
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