Pages that link to "Q49898831"
Jump to navigation
Jump to search
The following pages link to Daniel D Buchanan (Q49898831):
Displaying 50 items.
- Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndrome (Q26775022) (← links)
- Prediagnostic Physical Activity and Colorectal Cancer Survival: Overall and Stratified by Tumor Characteristics. (Q27347219) (← links)
- GSK3B polymorphisms alter transcription and splicing in Parkinson's disease (Q28116939) (← links)
- Colorectal carcinomas with KRAS mutation are associated with distinctive morphological and molecular features (Q28284149) (← links)
- Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations (Q28388475) (← links)
- Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer (Q30252873) (← links)
- Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer (Q30275554) (← links)
- Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer (Q30461804) (← links)
- Risks of Lynch syndrome cancers for MSH6 mutation carriers (Q30492977) (← links)
- Cancer risks for MLH1 and MSH2 mutation carriers (Q30563768) (← links)
- Improving identification of lynch syndrome patients: a comparison of research data with clinical records (Q30580847) (← links)
- Lessons from Lynch syndrome: a tumor biology-based approach to familial colorectal cancer. (Q33550512) (← links)
- Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases (Q33625221) (← links)
- Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinics (Q33641289) (← links)
- Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity (Q33700463) (← links)
- Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry (Q33767027) (← links)
- Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22. (Q33959070) (← links)
- Characterisation of familial colorectal cancer Type X, Lynch syndrome, and non-familial colorectal cancer (Q33994353) (← links)
- Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis (Q34048230) (← links)
- Cancer risks for the relatives of colorectal cancer cases with a methylated MLH1 promoter region: data from the Colorectal Cancer Family Registry (Q34092337) (← links)
- The intestinal epithelial cell differentiation marker intestinal alkaline phosphatase (ALPi) is selectively induced by histone deacetylase inhibitors (HDACi) in colon cancer cells in a Kruppel-like factor 5 (KLF5)-dependent manner (Q34139192) (← links)
- Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives (Q34266707) (← links)
- Genome-wide search for gene-gene interactions in colorectal cancer (Q34321689) (← links)
- Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome) (Q34351784) (← links)
- Association between molecular subtypes of colorectal cancer and patient survival (Q34759064) (← links)
- PIK3CA activating mutation in colorectal carcinoma: associations with molecular features and survival (Q34778710) (← links)
- Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome. (Q34785531) (← links)
- Quality assessment and correlation of microsatellite instability and immunohistochemical markers among population- and clinic-based colorectal tumors results from the Colon Cancer Family Registry (Q34801092) (← links)
- Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome). (Q35000837) (← links)
- Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patients (Q35034717) (← links)
- Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing. (Q35063442) (← links)
- High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry (Q35085756) (← links)
- Promoter methylation of Wnt antagonistsDKK1andSFRP1is associated with opposing tumor subtypes in two large populations of colorectal cancer patients (Q35117267) (← links)
- Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family history (Q35163670) (← links)
- A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer (Q35626744) (← links)
- Extensive DNA methylation in normal colorectal mucosa in hyperplastic polyposis. (Q35760876) (← links)
- Determining the familial risk distribution of colorectal cancer: a data mining approach. (Q35872667) (← links)
- Association between body mass index and mortality for colorectal cancer survivors: overall and by tumor molecular phenotype (Q35920915) (← links)
- Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study (Q35925149) (← links)
- Promoter methylation of ITF2, but not APC, is associated with microsatellite instability in two populations of colorectal cancer patients. (Q35925613) (← links)
- GWASeq: targeted re-sequencing follow up to GWAS. (Q38635553) (← links)
- Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinics (Q35965705) (← links)
- Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22. (Q36000794) (← links)
- Lynch syndrome and cervical cancer (Q36068742) (← links)
- Evidence for BRAF mutation and variable levels of microsatellite instability in a syndrome of familial colorectal cancer (Q36070164) (← links)
- Mutation deep within an intron of MSH2 causes Lynch syndrome (Q36087551) (← links)
- Methylation of Breast Cancer Predisposition Genes in Early-Onset Breast Cancer: Australian Breast Cancer Family Registry (Q36208014) (← links)
- Determining the frequency of de novo germline mutations in DNA mismatch repair genes (Q36217478) (← links)
- Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene. (Q36244730) (← links)
- Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome (Q36294966) (← links)