c-FMS mutational analysis in acute myeloid leukaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2003.04681.x/fullpdf
Reference8 articles.
1. Mutational analysis of class III receptor tyrosine kinase genes (c-KIT, c-FMS, FLT3) in idiopathic myelofibrosis;Abu-Duhier;British Journal of Haematology,2003
2. Incidence and prognosis of c-KIT and FLT3 mutations in core binding factor (CBF) acute myeloid leukaemias;Care;British Journal of Haematology,2003
3. Activating mutations of RTK/ras signal transduction pathway in pediatric acute myeloid leukaemia;Meshinchi;Blood,2003
4. Genetic aberrations in the development and subsequent progression of myelodysplastic syndrome;Misawa;Leukemia,1997
5. FMS mutations in myelodysplastic, leukemic, and normal subjects;Ridge;Proceedings of the National Academy of Sciences of the United States of America,1990
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2. KIT Proto-oncogene Exon 8 Deletions at Codon 419 are Highly Frequent in Acute Myeloid Leukaemia with Inv(16) in Indian Population;Molecular Biotechnology;2012-07-24
3. Shooting the messenger: Targeting signal transduction pathways in leukemia and related disorders;Critical Reviews in Oncology/Hematology;2011-04
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