Origins of myelodysplastic syndromes after aplastic anemia.
暂无分享,去创建一个
S. Ogawa | J. Maciejewski | T. Yoshizato | Y. Nagata | R. Mahfouz | M. Sekeres | H. Makishima | A. Nazha | N. Hosono | T. Kuzmanovic | B. Przychodzen | C. Hirsch | M. Clemente | W. Shen | E. Negoro | Wenyi Shen
[1] S. Miyano,et al. Dynamics of clonal evolution in myelodysplastic syndromes , 2016, Nature Genetics.
[2] C. H. Bartlett,et al. Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia. , 2015, The New England journal of medicine.
[3] M. Heuser,et al. Genetic characterization of acquired aplastic anemia by targeted sequencing , 2014, Haematologica.
[4] G. Abel,et al. Low frequency clonal mutations recoverable by deep sequencing in patients with aplastic anemia , 2013, Leukemia.
[5] S. Ogawa,et al. Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia. , 2011, Blood.
[6] A. Jankowska,et al. Mutations of an E3 ubiquitin ligase c-Cbl but not TET2 mutations are pathogenic in juvenile myelomonocytic leukemia. , 2010, Blood.
[7] C. O'keefe,et al. Application of array‐based whole genome scanning technologies as a cytogenetic tool in haematological malignancies , 2009, British journal of haematology.
[8] C. O'keefe,et al. Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML. , 2008, Blood.
[9] N. Young,et al. Distinct clinical outcomes for cytogenetic abnormalities evolving from aplastic anemia. , 2002, Blood.
[10] N. Young,et al. Relationship between bone marrow failure syndromes and the presence of glycophosphatidyl inositol‐anchored protein‐deficient clones , 2001, British journal of haematology.
[11] N. Young,et al. Paroxysmal Nocturnal Hemoglobinuria Cells in Patients with Bone Marrow Failure Syndromes , 1999, Annals of Internal Medicine.
[12] A. Tichelli,et al. Malignant tumors occurring after treatment of aplastic anemia. European Bone Marrow Transplantation-Severe Aplastic Anaemia Working Party. , 1993, The New England journal of medicine.