RUNX1 gene mutation in primary myelodysplastic syndrome - the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome-Reference-Cited by-同舟云学术

RUNX1 gene mutation in primary myelodysplastic syndrome - the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome

Published:2007-10-01 Issue:3 Volume:139 Page:405-414
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Chen Chien-Yuan,Lin Liang-In,Tang Jih-Luh,Ko Bo-Sheng,Tsay Woei,Chou Wen-Chien,Yao Ming,Wu Shang-Ju,Tseng Mei-Hsuan,Tien Hwei-Fang

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2007.06811.x/fullpdf

Reference37 articles.

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2. Core-binding factors in haematopoiesis and immune function;De Bruijn;Oncogene,2004

3. SOCS1 methylation in patients with newly diagnosed acute myeloid leukemia;Chen;Genes, Chromosomes and Cancer,2003

4. Acquisition of JAK2, PTPN11, and RAS mutations during disease progression in primary myelodysplastic syndrome;Chen;Leukemia,2006

5. Nucleophosmin mutations in de novo acute myeloid leukemia: the age-dependent incidences and the stability during disease evolution;Chou;Cancer Research,2006

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