Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility

Two recent genome-wide association studies have independently identified a prostate cancer susceptibility locus on chromosome 10q11.2. The most significant single-nucleotide polymorphism (SNP) marker reported, rs10993994, is 57 bp centromeric of the first exon of the MSMB gene, which encodes β-micro...

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Detalhes bibliográficos
Main Authors: Lou, Hong, Yeager, Meredith, Li, Hongchuan, Bosquet, Jesus Gonzalez, Hayes, Richard B., Orr, Nick, Yu, Kai, Hutchinson, Amy, Jacobs, Kevin B., Kraft, Peter, Wacholder, Sholom, Chatterjee, Nilanjan, Feigelson, Heather Spencer, Thun, Michael J., Diver, W. Ryan, Albanes, Demetrius, Virtamo, Jarmo, Weinstein, Stephanie, Ma, Jing, Gaziano, J. Michael, Stampfer, Meir, Schumacher, Fredrick R., Giovannucci, Edward, Cancel-Tassin, Geraldine, Cussenot, Olivier, Valeri, Antoine, Andriole, Gerald L., Crawford, E. David, Anderson, Stephen K., Tucker, Margaret, Hoover, Robert N., Fraumeni, Joseph F., Thomas, Gilles, Hunter, David J., Dean, Michael, Chanock, Stephen J.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2009
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2671324/
https://ncbi.nlm.nih.gov/pubmed/19383797
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0902104106
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