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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محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: 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.
التنسيق: Artigo
اللغة:Inglês
منشور في: National Academy of Sciences 2009
الموضوعات:
Biological Sciences
الوصول للمادة أونلاين: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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