Advances in understanding the pathogenesis of acquired aplastic anaemia

Author:

Luzzatto Lucio1ORCID,Risitano Antonio M.2ORCID

Affiliation:

1. Muhimbili University of Health and Allied Sciences; Dar-es-Salaam Tanzania

2. Department of Clinical Medicine and Surgery; Federico II University; Naples Italy

Publisher

Wiley

Subject

Hematology

Reference151 articles.

1. ASXL1 mutations promote myeloid transformation through loss of PRC2-mediated gene repression;Abdel-Wahab;Cancer Cell,2012

2. Telomere length in inherited bone marrow failure syndromes;Alter;Haematologica,2015

3. Heterodimerization of TPO and IFNγ impairs human hematopoietic stem/progenitor cell signaling and survival in chronic inflammation;Alvarado;Blood,2017

4. Clonal cytogenetic abnormalities in patients with otherwise typical aplastic anemia;Appelbaum;Experimental Hematology,1987

5. 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 of the United States of America,1999

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