| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S00595-011-0038-Z |
| P698 | PubMed publication ID | 22127532 |
| P2093 | author name string | Masaki Mori | |
| Fumiaki Tanaka | |||
| Koshi Mimori | |||
| Kohei Shibata | |||
| P2860 | cites work | Multiple loci identified in a genome-wide association study of prostate cancer | Q28943507 |
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| Association between an 8q24 locus and the risk of colorectal cancer in Japanese | Q33512613 | ||
| Upregulation of c-MYC in cis through a large chromatin loop linked to a cancer risk-associated single-nucleotide polymorphism in colorectal cancer cells | Q33705050 | ||
| Long-range enhancers on 8q24 regulate c-Myc | Q33733965 | ||
| 8q24 prostate, breast, and colon cancer risk loci show tissue-specific long-range interaction with MYC. | Q34006369 | ||
| TCF4 and CDX2, major transcription factors for intestinal function, converge on the same cis-regulatory regions | Q34093875 | ||
| Association studies on 11 published colorectal cancer risk loci | Q34129391 | ||
| Genetic heterogeneity in colorectal cancer associations between African and European americans | Q37042039 | ||
| Association of common genetic variants in SMAD7 and risk of colon cancer | Q37214180 | ||
| Insulin-like growth factor-1 promoter polymorphisms and colorectal cancer: a functional genomics approach | Q37365062 | ||
| The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer | Q37390854 | ||
| Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. | Q37422744 | ||
| Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk | Q40034823 | ||
| Genetic variants in the 8q24 locus and risk of testicular germ cell tumors | Q44789708 | ||
| Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort | Q46856424 | ||
| Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. | Q50674084 | ||
| The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling. | Q51565310 | ||
| Genome-wide differences between microsatellite stable and unstable colorectal tumors. | Q53352742 | ||
| Genetic heterogeneity of 8q24 region in susceptibility to cancer. | Q54494898 | ||
| A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 | Q56436562 | ||
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| A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21 | Q57078703 | ||
| Susceptibility Genetic Variants Associated With Colorectal Cancer Risk Correlate With Cancer Phenotype | Q57083819 | ||
| A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk | Q57092250 | ||
| Common variants in mismatch repair genes and risk of colorectal cancer | Q57306185 | ||
| Lack of a relationship between the common 18q24 variant rs12953717 and risk of chronic lymphocytic leukemia | Q57319804 | ||
| Allelic Imbalance at rs6983267 Suggests Selection of the Risk Allele in Somatic Colorectal Tumor Evolution | Q57567520 | ||
| A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8 | Q57666866 | ||
| Common germline variation in mismatch repair genes and survival after a diagnosis of colorectal cancer | Q59654812 | ||
| Single nucleotide polymorphism in fibroblast growth factor receptor 4 at codon 388 is associated with prognosis in high‐grade soft tissue sarcoma | Q79256072 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | colorectal cancer | Q188874 |
| single-nucleotide polymorphism | Q501128 | ||
| P304 | page(s) | 215-219 | |
| P577 | publication date | 2011-11-30 | |
| P1433 | published in | Surgery Today | Q15765823 |
| P1476 | title | Review: Single nucleotide polymorphisms associated with the oncogenesis of colorectal cancer | |
| P478 | volume | 42 |
| Q39037289 | Allelic imbalance at an 8q24 oncogenic SNP is involved in activating MYC in human colorectal cancer |
| Q92591187 | Angiopoietin-2 gene polymorphisms are biomarkers for the development and progression of colorectal cancer in Han Chinese |
| Q47109441 | Association of rs6983267 at 8q24, HULC rs7763881 polymorphisms and serum lncRNAs CCAT2 and HULC with colorectal cancer in Egyptian patients |
| Q92838883 | Functional STR within PTPN11: a novel potential risk factor for colorectal cancer |
| Q45989122 | Gender-specific association of NFKBIA promoter polymorphisms with the risk of sporadic colorectal cancer. |
| Q26765344 | Single Nucleotide Polymorphisms as Prognostic and Predictive Factors of Adjuvant Chemotherapy in Colorectal Cancer of Stages I and II |
| Q51051659 | The Expression of CCAT2, a Novel Long Noncoding RNA Transcript, and rs6983267 Single-Nucleotide Polymorphism Genotypes in Colorectal Cancers. |
| Q48333531 | The Generation and Validation of a 20-Genes Model Influencing the Prognosis of Colorectal Cancer |
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