A new aspect of the molecular pathogenesis of paroxysmal nocturnal hemoglobinuria

Hematology

Volumn 7, Issue 4, 2002, Pages 211-227

  Schichishima, Tsutomu ^a   Noji, Hideyoshi ^a  

^a FUKUSHIMA MEDICAL UNIVERSITY   (Japan)

Author keywords

Bone marrow failure syndromes; Glycosylphosphatidylinositol (GPI) anchored membrane protein; Human leukocyte antigen (HLA) class II haplotype; Paroxysmal nocturnal hemoglobinuria (PNH); Phosphatidylinositol glycan class A (PIG A) gene; Wilms' tumor gene (WT1)

Indexed keywords

CD59 ANTIGEN; COMPLEMENT; DECAY ACCELERATING FACTOR; GLYCOSYLPHOSPHATIDYLINOSITOL; MEMBRANE PROTEIN; WT1 PROTEIN;

BONE MARROW DEPRESSION; CELL PROLIFERATION; CELL TYPE; CLINICAL FEATURE; CONTROLLED STUDY; CYTOPENIA; CYTOTOXIC T LYMPHOCYTE; ERYTHROCYTE; GENE EXPRESSION; GENE FUNCTION; GENE MUTATION; HEMATOPOIETIC STEM CELL; HEMOLYSIS; HLA SYSTEM; HUMAN; HYPOTHESIS; MOLECULAR CLONING; MOLECULAR GENETICS; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PATHOGENESIS; PATHOPHYSIOLOGY; PRELEUKEMIA; PRIORITY JOURNAL; REVIEW; VEIN THROMBOSIS;

ANEMIA, APLASTIC; ANTIGENS, CD55; ANTIGENS, CD59; BONE MARROW; CLONE CELLS; COMPLEMENT SYSTEM PROTEINS; GLYCOSYLPHOSPHATIDYLINOSITOLS; HEMATOPOIESIS; HEMOGLOBINURIA, PAROXYSMAL; HUMANS; MEMBRANE PROTEINS; MODELS, BIOLOGICAL; MUTATION; MYELODYSPLASTIC SYNDROMES; PANCYTOPENIA; PRELEUKEMIA; T-LYMPHOCYTES, CYTOTOXIC; WT1 PROTEINS;

EID: 0036439028     PISSN: 10245332     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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