NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16)-Reference-Cited by-同舟云学术

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NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16)

Published:2009-04-24 Issue:1-2 Volume:56 Page:68-71
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:

Author:

Panagopoulos I.,Åman P.,Johansson B.,Malm C.,Lenhoff S.,Billström R.,Mitelman F.

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1996.tb00297.x/fullpdf

Reference22 articles.

1. ras genes;Barbacid;Annu Rev Biochem,1987

2. The ras gene family and human carcinogenesis;Bos;Mutat Res,1988

3. ras oncogenes in human cancer: a review;Bos;Cancer Res,1989

4. The incidence and prognostic significance of mutations in codon 13 of the N-RAS gene in acute myeloid leukemia;Coghlan;Leukemia,1994

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Implications of NRAS mutations in AML: a study of 2502 patients;Blood;2006-05-15

2. Acute myeloid leukemia with inv(16)(p13q22): Involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign;American Journal of Hematology;2002-09

3. The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex;British Journal of Haematology;2001-05

4. Deletions of CDKN1B and ETV6 in acute myeloid leukemia and myelodysplastic syndromes without cytogenetic evidence of 12p abnormalities;Genes, Chromosomes and Cancer;1997-06

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