Cargando…
Single Nucleotide Polymorphisms in the Wnt and BMP Pathways and Colorectal Cancer Risk in a Spanish Cohort
BACKGROUND: Colorectal cancer (CRC) is considered a complex disease, and thus the majority of the genetic susceptibility is thought to lie in the form of low-penetrance variants following a polygenic model of inheritance. Candidate-gene studies have so far been one of the basic approaches taken to i...
Autores principales: | Fernández-Rozadilla, Ceres, de Castro, Luisa, Clofent, Juan, Brea-Fernández, Alejandro, Bessa, Xavier, Abulí, Anna, Andreu, Montserrat, Jover, Rodrigo, Xicola, Rosa, Llor, Xavier, Castells, Antoni, Castellví-Bel, Sergi, Carracedo, Angel, Ruiz-Ponte, Clara |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936577/ https://www.ncbi.nlm.nih.gov/pubmed/20844743 http://dx.doi.org/10.1371/journal.pone.0012673 |
Ejemplares similares
-
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12
por: Fernandez-Rozadilla, Ceres, et al.
Publicado: (2013) -
Case-control study for colorectal cancer genetic susceptibility in EPICOLON: previously identified variants and mucins
por: Abulí, Anna, et al.
Publicado: (2011) -
Pharmacogenomics of CRC treatments: putting bricks on the path to personalized medicine
por: Fernández-Rozadilla, Ceres, et al.
Publicado: (2014) -
Multiple Sporadic Colorectal Cancers Display a Unique Methylation Phenotype
por: Gonzalo, Victoria, et al.
Publicado: (2014) -
Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?
por: Gómez-Fernández, Nuria, et al.
Publicado: (2009)