Integrative analysis of RUNX1 downstream pathways and target genes

BACKGROUND: The RUNX1 transcription factor gene is frequently mutated in sporadic myeloid and lymphoid leukemia through translocation, point mutation or amplification. It is also responsible for a familial platelet disorder with predisposition to acute myeloid leukemia (FPD-AML). The disruption of t...

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Detalhes bibliográficos
Main Authors: Michaud, Joëlle, Simpson, Ken M, Escher, Robert, Buchet-Poyau, Karine, Beissbarth, Tim, Carmichael, Catherine, Ritchie, Matthew E, Schütz, Frédéric, Cannon, Ping, Liu, Marjorie, Shen, Xiaofeng, Ito, Yoshiaki, Raskind, Wendy H, Horwitz, Marshall S, Osato, Motomi, Turner, David R, Speed, Terence P, Kavallaris, Maria, Smyth, Gordon K, Scott, Hamish S
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2008
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2529319/
https://ncbi.nlm.nih.gov/pubmed/18671852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-9-363
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