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Clinical and Translational Gastroenterology|March 7, 2014
The association of telomere length with colorectal cancer differs by the age of cancer onsetLisa A Boardman, Kristin Litzelman, Songwon Seo, et al.Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Assessing Genotype-Phenotype Correlations with Deep Learning in Colorectal Cancer: A Multi-Centric StudyMarco Gustav, Marko van Treeck, Nic G Reitsam, et al.Gastroenterology|June 10, 2004
Relative frequency and morphology of cancers in STK11 mutation carriersWendy Lim, Sylviane Olschwang, Josbert J Keller, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 11, 2013
Telomere length varies by DNA extraction method: implications for epidemiologic researchJulie M Cunningham, Ruth A Johnson, Kristin Litzelman, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|August 20, 2009
Functional and clinical significance of variants localized to 8q24 in colon cancerMine S Cicek, Susan L Slager, Sara J Achenbach, et al.The Lancet. Digital Health|August 19, 2025
Assessing genotype-phenotype correlations in colorectal cancer with deep learning: a multicentre cohort studyMarco Gustav, Marko van Treeck, Nic G Reitsam, et al.JAMA|April 28, 2005
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type XNoralane M Lindor, Kari Rabe, Gloria M Petersen, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 31, 2018
Detection of Gastric Cancer with Novel Methylated DNA Markers: Discovery, Tissue Validation, and Pilot Testing in PlasmaBradley W Anderson, Yun-Suhk Suh, Boram Choi, et al.Scientific Reports|February 18, 2018
Molecular characterization of colorectal adenomas with and without malignancy reveals distinguishing genome, transcriptome and methylome alterationsBrooke R Druliner, Panwen Wang, Taejeong Bae, et al.Nature Genetics|May 3, 2011
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossChristopher J Klein, Maria-Victoria Botuyan, Yanhong Wu, et al.Pageof 9