Functional and clinical significance of variants localized to 8q24 in colon cancer.
about
Systematic meta-analyses and field synopsis of genetic association studies in colorectal cancerAssociation between polymorphisms in long non-coding RNA PRNCR1 in 8q24 and risk of colorectal cancerCharacterization of the association between 8q24 and colon cancer: gene-environment exploration and meta-analysisGenetic variants on chromosome 8q24 and colorectal neoplasia risk: a case-control study in China and a meta-analysis of the published literatureTen common genetic variants associated with colorectal cancer risk are not associated with survival after diagnosisColorectal cancer susceptibility loci in a population-based study: Associations with morphological parametersPolymorphisms on 8q24 are associated with lung cancer risk and survival in Han ChineseAssociation of eleven common, low-penetrance colorectal cancer susceptibility genetic variants at six risk loci with clinical outcome.A retrospective observational study of the relationship between single nucleotide polymorphisms associated with the risk of developing colorectal cancer and survival.Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.A LIN28B polymorphism predicts for colon cancer survival.Association between colorectal cancer susceptibility loci and survival time after diagnosis with colorectal cancer.Genome-wide association studies--a summary for the clinical gastroenterologist.Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.NDRG2 gene copy number is not altered in colorectal carcinoma.Association of 8q24.21 loci with the risk of colorectal cancer: a systematic review and meta-analysis.Infection and integration of high-risk human papillomavirus in HPV-associated cancer cells.A comprehensive meta-analysis of genetic associations between five key SNPs and colorectal cancer risk.Association between total number of deaths, diabetes mellitus, incident cancers, and haplotypes in chromosomal region 8q24 in a prospective study.Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats.Association between 8q24 rs6983267 polymorphism and cancer susceptibility: a meta-analysis involving 170,737 subjects.No evidence that associations of incident, sporadic colorectal adenoma with its major modifiable risk factors differ by chromosome 8q24 region rs6983267 genotype.Common variation rs6983267 at 8q24.1 and risk of colorectal adenoma and cancer: evidence based on 31 studies.Genetic variations are associated with lymph node metastasis in colorectal cancer patients.Effect of rs6983267 polymorphism in the 8q24 region and rs4444903 polymorphism in EGF gene on the risk of sporadic colorectal cancer in Iranian population.
P2860
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P2860
Functional and clinical significance of variants localized to 8q24 in colon cancer.
description
2009 nî lūn-bûn
@nan
2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Functional and clinical significance of variants localized to 8q24 in colon cancer.
@ast
Functional and clinical significance of variants localized to 8q24 in colon cancer.
@en
type
label
Functional and clinical significance of variants localized to 8q24 in colon cancer.
@ast
Functional and clinical significance of variants localized to 8q24 in colon cancer.
@en
prefLabel
Functional and clinical significance of variants localized to 8q24 in colon cancer.
@ast
Functional and clinical significance of variants localized to 8q24 in colon cancer.
@en
P2093
P2860
P1476
Functional and clinical significance of variants localized to 8q24 in colon cancer.
@en
P2093
Amy J French
Brian F Kabat
Daniel J Sargent
Gloria M Petersen
Hilary E Blair
James R Cerhan
Kevin C Halling
Lisa A Boardman
Mine S Cicek
Nathan R Foster
P2860
P304
P356
10.1158/1055-9965.EPI-09-0362
P577
2009-08-18T00:00:00Z