Found: 57
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Systemic Erdheim-Chester disease.
- Published in:
- 2008
- By:
- Publication type:
- journal article
MYH mutations are rare in prostate cancer.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2007, v. 133, n. 6, p. 373, doi. 10.1007/s00432-006-0181-x
- By:
- Publication type:
- Article
Prognostic value of molecular markers, sub-stage and European Organisation for the Research and Treatment of Cancer risk scores in primary T1 bladder cancer.
- Published in:
- BJU International, 2012, v. 110, n. 8, p. 1169, doi. 10.1111/j.1464-410X.2012.10996.x
- By:
- Publication type:
- Article
Exploring targets of TET2-mediated methylation reprogramming as potential discriminators of prostate cancer progression.
- Published in:
- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0651-z
- By:
- Publication type:
- Article
A urine-based DNA methylation assay, ProCUrE, to identify clinically significant prostate cancer.
- Published in:
- Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0575-z
- By:
- Publication type:
- Article
A germline mutation at the extreme 3′ end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 205, doi. 10.1034/j.1399-0004.2000.570306.x
- By:
- Publication type:
- Article
STK11/LKB1 germline mutations are not identified in most Peutz–Jeghers syndrome patients.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 2, p. 136, doi. 10.1034/j.1399-0004.1999.560207.x
- By:
- Publication type:
- Article
Combining CAPRA-S With Tumor IDC/C Features Improves the Prognostication of Biochemical Recurrence in Prostate Cancer Patients.
- Published in:
- Clinical Genitourinary Cancer, 2022, v. 20, n. 3, p. e217, doi. 10.1016/j.clgc.2022.01.003
- By:
- Publication type:
- Article
Association of rs2282679 A>C polymorphism in vitamin D binding protein gene with colorectal cancer risk and survival: effect modification by dietary vitamin D intake.
- Published in:
- 2018
- By:
- Publication type:
- journal article
A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 1, p. 37, doi. 10.1038/jhg.2009.119
- By:
- Publication type:
- Article
Distinct regions of frequent loss of heterozygosity of chromosome 5p and 5q in human esophageal cancer.
- Published in:
- International Journal of Cancer, 1998, v. 78, n. 5, p. 600, doi. 10.1002/(SICI)1097-0215(19981123)78:5<600::AID-IJC12>3.0.CO;2-1
- By:
- Publication type:
- Article
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
- Published in:
- Nature Genetics, 2000, v. 25, n. 4, p. 397, doi. 10.1038/78071
- By:
- Publication type:
- Article
A 38-gene model comprised of key TET2-associated genes shows additive utility to high-risk prostate cancer cases in the prognostication of biochemical recurrence.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Rac1 GTPase and the Rac1 exchange factor Tiam1 associate with Wnt-responsive promoters to enhance beta-catenin/TCF-dependent transcription in colorectal cancer cells.
- Published in:
- Molecular Cancer, 2008, v. 7, p. 1, doi. 10.1186/1476-4598-7-73
- By:
- Publication type:
- Article
MLH1 Region Polymorphisms Show a Significant Association with CpG Island Shore Methylation in a Large Cohort of Healthy Individuals.
- Published in:
- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051531
- By:
- Publication type:
- Article
Discovery of Novel Hypermethylated Genes in Prostate Cancer Using Genomic CpG Island Microarrays.
- Published in:
- PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004830
- By:
- Publication type:
- Article
Lynch syndrome in a predominantly Afrocentric population: a clinicopathological and genetic study.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Lynch syndrome in a predominantly Afrocentric population: a clinicopathological and genetic study.
- Published in:
- Canadian Journal of Surgery, 2012, v. 55, n. 5, p. 294, doi. 10.1503/cjs.037410
- By:
- Publication type:
- Article
Promoter methylation of ITF2, but not APC, is associated with microsatellite instability in two populations of colorectal cancer patients.
- Published in:
- 2016
- By:
- Publication type:
- journal article
A large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred.
- Published in:
- Human Genetics, 2008, v. 124, n. 5, p. 535, doi. 10.1007/s00439-008-0579-4
- By:
- Publication type:
- Article
Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium?
- Published in:
- Human Genetics, 2000, v. 107, n. 6, p. 623, doi. 10.1007/s004390000417
- By:
- Publication type:
- Article
Response.
- Published in:
- 2007
- By:
- Publication type:
- Letter
MLH1 -93G>A Promoter Polymorphism and the Risk of Microsatellite-Unstable Colorectal Cancer.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2007, v. 99, n. 6, p. 463, doi. 10.1093/jnci/djk095
- By:
- Publication type:
- Article
How to Deal with Batch Effect in Sequential Microarray Experiments?
- Published in:
- Molecular Informatics, 2010, v. 29, n. 5, p. 387
- By:
- Publication type:
- Article
Investigating Urinary Circular RNA Biomarkers for Improved Detection of Renal Cell Carcinoma.
- Published in:
- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2021.814228
- By:
- Publication type:
- Article
Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor).
- Published in:
- Oncogene, 1999, v. 18, n. 47, p. 6615, doi. 10.1038/sj.onc.1203041
- By:
- Publication type:
- Article
Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency: Familial Colorectal Cancer Type X.
- Published in:
- JAMA: Journal of the American Medical Association, 2005, v. 293, n. 16, p. 1979, doi. 10.1001/jama.293.16.1979
- By:
- Publication type:
- Article
Conversion Analysis for Mutation Detection in MLH1 and MSH2 in Patients With Colorectal Cancer.
- Published in:
- JAMA: Journal of the American Medical Association, 2005, v. 293, n. 7, p. 799, doi. 10.1001/jama.293.7.799
- By:
- Publication type:
- Article
Promoter methylation of Wnt antagonists DKK1 and SFRP1 is associated with opposing tumor subtypes in two large populations of colorectal cancer patients.
- Published in:
- Carcinogenesis, 2011, v. 32, n. 5, p. 741, doi. 10.1093/carcin/bgr020
- By:
- Publication type:
- Article
MSH2 118T>C and MSH6 159C>T promoter polymorphisms and the risk of colorectal cancer.
- Published in:
- Carcinogenesis, 2007, v. 28, n. 12, p. 2575, doi. 10.1093/carcin/bgm229
- By:
- Publication type:
- Article
Vitamin D receptor and calcium-sensing receptor polymorphisms and colorectal cancer survival in the Newfoundland population.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Development of a multivariable risk model integrating urinary cell DNA methylation and cell‐free RNA data for the detection of significant prostate cancer.
- Published in:
- Prostate, 2020, v. 80, n. 7, p. 547, doi. 10.1002/pros.23968
- By:
- Publication type:
- Article
Metformin Elicits Antitumor Effects and Downregulates the Histone Methyltransferase Multiple Myeloma SET Domain (MMSET) in Prostate Cancer Cells.
- Published in:
- Prostate, 2016, v. 76, n. 16, p. 1507, doi. 10.1002/pros.23235
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- Publication type:
- Article
Evaluation and prognostic significance of ACAT1 as a marker of prostate cancer progression.
- Published in:
- Prostate, 2014, v. 74, n. 4, p. 372, doi. 10.1002/pros.22758
- By:
- Publication type:
- Article
Distinct DNA methylation patterns associated with treatment resistance in metastatic castration resistant prostate cancer.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-85812-3
- By:
- Publication type:
- Article
Association of tissue promoter methylation levels of APC, TGFβ2, HOXD3 and RASSF1A with prostate cancer progression.
- Published in:
- International Journal of Cancer, 2011, v. 129, n. 10, p. 2454, doi. 10.1002/ijc.25908
- By:
- Publication type:
- Article
Parent of origin effects on age at colorectal cancer diagnosis.
- Published in:
- International Journal of Cancer, 2010, v. 127, n. 2, p. 361, doi. 10.1002/ijc.25037
- By:
- Publication type:
- Article
An association between the 4G polymorphism in the PAI-1 promoter and the development of aggressive fibromatosis (desmoid tumor) in familial adenomatous polyposis patients.
- Published in:
- Familial Cancer, 2007, v. 6, n. 1, p. 89, doi. 10.1007/s10689-006-9109-5
- By:
- Publication type:
- Article
FGFR3 mutations, but not FGFR3 expression and FGFR3 copy-number variations, are associated with favourable non-muscle invasive bladder cancer.
- Published in:
- Virchows Archiv: European Journal of Pathology, 2014, v. 465, n. 2, p. 207, doi. 10.1007/s00428-014-1596-4
- By:
- Publication type:
- Article
Novel Multiplex MethyLight Protocol for Detection of DNA Methylation in Patient Tissues and Bodily Fluids.
- Published in:
- Scientific Reports, 2014, p. 1, doi. 10.1038/srep04432
- By:
- Publication type:
- Article
Comparison of clinical schemas and morphologic features in predicting Lynch syndrome in mutation-positive patients with endometrial cancer encountered in the context of familial gastrointestinal cancer registries.
- Published in:
- Cancer (0008543X), 2012, v. 118, n. 3, p. 681, doi. 10.1002/cncr.26323
- By:
- Publication type:
- Article
Germline MYH mutations in a clinic-based series of Canadian multiple colorectal adenoma patients.
- Published in:
- Journal of Surgical Oncology, 2007, v. 95, n. 6, p. 499, doi. 10.1002/jso.20724
- By:
- Publication type:
- Article
Deciphering the colon cancer genes-report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010.
- Published in:
- Human Mutation, 2011, v. 32, n. 4, p. 491, doi. 10.1002/humu.21450
- By:
- Publication type:
- Article
High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families.
- Published in:
- Human Mutation, 2009, v. 30, n. 8, p. E797, doi. 10.1002/humu.21056
- By:
- Publication type:
- Article
Planning the Human Variome Project: The Spain report.
- Published in:
- Human Mutation, 2009, v. 30, n. 4, p. 496, doi. 10.1002/humu.20972
- By:
- Publication type:
- Article
The MLH1 variants p.Arg265Cys and p.Lys618Ala affect protein stability while p.Leu749Gln affects heterodimer formation.
- Published in:
- Human Mutation, 2008, v. 29, n. 2, p. 332, doi. 10.1002/humu.9523
- By:
- Publication type:
- Article
Distinct DNA methylation alterations are associated with cribriform architecture and intraductal carcinoma in Gleason pattern 4 prostate tumors.
- Published in:
- Oncology Letters, 2017, v. 14, n. 1, p. 390, doi. 10.3892/ol.2017.6140
- By:
- Publication type:
- Article
Dynamic interplay between locus-specific DNA methylation and hydroxymethylation regulates distinct biological pathways in prostate carcinogenesis.
- Published in:
- Clinical Epigenetics, 2016, v. 8, p. 1, doi. 10.1186/s13148-016-0195-4
- By:
- Publication type:
- Article
Suppression of nuclear Wnt signaling leads to stabilization of Rac1 isoforms
- Published in:
- FEBS Letters, 2007, v. 581, n. 25, p. 4850, doi. 10.1016/j.febslet.2007.09.013
- By:
- Publication type:
- Article
Characterization of two novel adenomatous polyposis coli ( APC) gene mutations in patients with familial adenomatous polyposis (FAP).
- Published in:
- Human Mutation, 1994, v. 4, n. 4, p. 253, doi. 10.1002/humu.1380040404
- By:
- Publication type:
- Article