Common genetic variants in the 9p21 region and their associations with multiple tumours

BACKGROUND: The chromosome 9p21.3 region has been implicated in the pathogenesis of multiple cancers. METHODS: We systematically examined up to 203 tagging SNPs of 22 genes on 9p21.3 (19.9–32.8 Mb) in eight case–control studies: thyroid cancer, endometrial cancer (EC), renal cell carcinoma, colorect...

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Detalles Bibliográficos
Autores principales: Gu, F, Pfeiffer, R M, Bhattacharjee, S, Han, S S, Taylor, P R, Berndt, S, Yang, H, Sigurdson, A J, Toro, J, Mirabello, L, Greene, M H, Freedman, N D, Abnet, C C, Dawsey, S M, Hu, N, Qiao, Y-L, Ding, T, Brenner, A V, Garcia-Closas, M, Hayes, R, Brinton, L A, Lissowska, J, Wentzensen, N, Kratz, C, Moore, L E, Ziegler, R G, Chow, W-H, Savage, S A, Burdette, L, Yeager, M, Chanock, S J, Chatterjee, N, Tucker, M A, Goldstein, A M, Yang, X R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Genetics & Genomics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3619272/
https://www.ncbi.nlm.nih.gov/pubmed/23361049
http://dx.doi.org/10.1038/bjc.2013.7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3619272/
https://www.ncbi.nlm.nih.gov/pubmed/23361049
http://dx.doi.org/10.1038/bjc.2013.7

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