Stem cells in paroxysmal nocturnal haemoglobinuria and aplastic anaemia: increasing evidence for overlap of haemopoietic defect-Reference-Cited by-同舟云学术

Stem cells in paroxysmal nocturnal haemoglobinuria and aplastic anaemia: increasing evidence for overlap of haemopoietic defect

Published:2003-12 Issue:6 Volume:13 Page:377-386
ISSN:0958-7578
Container-title:Transfusion Medicine
language:en
Short-container-title:

Author:

Marsh J. C. W.,Elebute M. O.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-3148.2003.00465.x/fullpdf

Reference88 articles.

1. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals;Araten;Proceedings of the National Academy of Sciences,1999

2. Affected paroxysmal nocturnal hemoglobinuria T lymphocytes harbor a common defect in assembly of N-acetyl-D-glucosamine inositol phospholipid corresponding to that in class A Thy-1-murine lymphoma mutants;Armstrong;Journal of Biological Chemistry,1992

3. CD59-deficient blood cells and PIG-A gene abnormalities in Japanese patients with aplastic anaemia;Azenishi;British Journal of Haematology,1999

4. Long-term marrow culture in patients with aplastic anemia compared with marrow transplant recipients and normal controls;Bacigalupo;Experimental Hematology,1992

5. Progressive telomere shortening in aplastic anaemia;Ball;Blood,1998

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