Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D Buchanan

Showing results (641-650 of 884) with videos related to

Pageof 89
Sort By:
British Journal of Cancer|May 19, 2011
Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patientsJ B Rawson, M Mrkonjic, D Daftary, et al.
Gut|March 26, 2018
Assessing the ProMCol classifier as a prognostic marker for non-metastatic colorectal cancer within the Melbourne Collaborative Cohort StudyJihoon E Joo, Harindra Jayasekara, Ee Ming Wong, et al.
European Journal of Human Genetics : EJHG|November 30, 2006
Stability of BAT26 in Lynch syndrome colorectal tumoursLesley Jaskowski, Joanne Young, Leigh Jackson, et al.
Structure (London, England : 1993)|November 14, 2002
Structural studies of Salmonella typhimurium ArnB (PmrH) aminotransferase: a 4-amino-4-deoxy-L-arabinose lipopolysaccharide-modifying enzymeBrian W Noland, Janet M Newman, Jörg Hendle, et al.
Molecular Carcinogenesis|December 5, 2013
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 pathogenicityMichael T Parsons, Phillip J Whiley, Jonathan Beesley, et al.
Familial Cancer|June 3, 2017
RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancersLochlan J Fennell, Mark Clendenning, Diane M McKeone, et al.
Future Oncology (London, England)|February 6, 2016
Quantifying the utility of single nucleotide polymorphisms to guide colorectal cancer screeningMark A Jenkins, Enes Makalic, James G Dowty, et al.
Familial Cancer|January 5, 2013
Detection of large scale 3' deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?Mark Clendenning, Michael D Walsh, Judith Balmana Gelpi, et al.
Genes & Cancer|January 26, 2016
Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndromeAung Ko Win, Mark Clendenning, William Crawford, et al.
JAMA Oncology|June 19, 2015
Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family RegistryMatthew B Yurgelun, Serena Masciari, Victoria A Joshi, et al.
Pageof 89

Showing results (641-650 of 884) with videos related to

Sort By:
Pageof 89
British Journal of Cancer|May 19, 2011
Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patientsJ B Rawson, M Mrkonjic, D Daftary, et al.
Gut|March 26, 2018
Assessing the ProMCol classifier as a prognostic marker for non-metastatic colorectal cancer within the Melbourne Collaborative Cohort StudyJihoon E Joo, Harindra Jayasekara, Ee Ming Wong, et al.
European Journal of Human Genetics : EJHG|November 30, 2006
Stability of BAT26 in Lynch syndrome colorectal tumoursLesley Jaskowski, Joanne Young, Leigh Jackson, et al.
Structure (London, England : 1993)|November 14, 2002
Structural studies of Salmonella typhimurium ArnB (PmrH) aminotransferase: a 4-amino-4-deoxy-L-arabinose lipopolysaccharide-modifying enzymeBrian W Noland, Janet M Newman, Jörg Hendle, et al.
Molecular Carcinogenesis|December 5, 2013
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 pathogenicityMichael T Parsons, Phillip J Whiley, Jonathan Beesley, et al.
Familial Cancer|June 3, 2017
RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancersLochlan J Fennell, Mark Clendenning, Diane M McKeone, et al.
Future Oncology (London, England)|February 6, 2016
Quantifying the utility of single nucleotide polymorphisms to guide colorectal cancer screeningMark A Jenkins, Enes Makalic, James G Dowty, et al.
Familial Cancer|January 5, 2013
Detection of large scale 3' deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?Mark Clendenning, Michael D Walsh, Judith Balmana Gelpi, et al.
Genes & Cancer|January 26, 2016
Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndromeAung Ko Win, Mark Clendenning, William Crawford, et al.
JAMA Oncology|June 19, 2015
Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family RegistryMatthew B Yurgelun, Serena Masciari, Victoria A Joshi, et al.
Pageof 89