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Familial Cancer
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January 31, 2026
Germline MLH1 c.-42 C > T is a likely pathogenic variant predisposing to a reduced-penetrance/modified Lynch syndrome phenotype featuring MLH1-methylated cancers
Daniel D Buchanan, Rocio Alvarez, Khalid Mahmood, et al.
American Journal of Epidemiology
|
October 12, 2017
Association of DNA Methylation-Based Biological Age With Health Risk Factors and Overall and Cause-Specific Mortality
Pierre-Antoine Dugué, Julie K Bassett, JiHoon E Joo, et al.
JNCI Cancer Spectrum
|
April 30, 2021
Assessment of a Polygenic Risk Score for Colorectal Cancer to Predict Risk of Lynch Syndrome Colorectal Cancer
Mark A Jenkins, Daniel D Buchanan, John Lai, et al.
Familial Cancer
|
December 8, 2023
Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
James M Chan, Mark Clendenning, Sharelle Joseland, et al.
European Journal of Cancer (Oxford, England : 1990)
|
February 26, 2013
Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?
Aung Ko Win, John L Hopper, Daniel D Buchanan, et al.
Journal of Gastroenterology and Hepatology
|
June 9, 2016
Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts
Daniel D Buchanan, Mark Clendenning, Christophe Rosty, et al.
The Journal of Biological Chemistry
|
June 21, 2015
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
Joongho Shin, Azadeh Carr, Georgia A Corner, et al.
Cancer Communications (London, England)
|
June 11, 2026
<i>TGFBR1</i>*6A and Risk for Colorectal Cancer
Allan M Johansen, Julie T Ziegler, Kojo Agyemang, et al.
Familial Cancer
|
August 14, 2014
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry
Christophe Rosty, Michael D Walsh, Noralane M Lindor, et al.
Annals of Surgical Oncology
|
January 30, 2013
Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers
Aung Ko Win, Susan Parry, Bryan Parry, et al.
Page
of 30
Search research articles
Search
Showing results (141-150 of 299) with videos related to
Sort By:
Page
of 30
Familial Cancer
|
January 31, 2026
Germline MLH1 c.-42 C > T is a likely pathogenic variant predisposing to a reduced-penetrance/modified Lynch syndrome phenotype featuring MLH1-methylated cancers
Daniel D Buchanan, Rocio Alvarez, Khalid Mahmood, et al.
American Journal of Epidemiology
|
October 12, 2017
Association of DNA Methylation-Based Biological Age With Health Risk Factors and Overall and Cause-Specific Mortality
Pierre-Antoine Dugué, Julie K Bassett, JiHoon E Joo, et al.
JNCI Cancer Spectrum
|
April 30, 2021
Assessment of a Polygenic Risk Score for Colorectal Cancer to Predict Risk of Lynch Syndrome Colorectal Cancer
Mark A Jenkins, Daniel D Buchanan, John Lai, et al.
Familial Cancer
|
December 8, 2023
Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
James M Chan, Mark Clendenning, Sharelle Joseland, et al.
European Journal of Cancer (Oxford, England : 1990)
|
February 26, 2013
Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?
Aung Ko Win, John L Hopper, Daniel D Buchanan, et al.
Journal of Gastroenterology and Hepatology
|
June 9, 2016
Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts
Daniel D Buchanan, Mark Clendenning, Christophe Rosty, et al.
The Journal of Biological Chemistry
|
June 21, 2015
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
Joongho Shin, Azadeh Carr, Georgia A Corner, et al.
Cancer Communications (London, England)
|
June 11, 2026
<i>TGFBR1</i>*6A and Risk for Colorectal Cancer
Allan M Johansen, Julie T Ziegler, Kojo Agyemang, et al.
Familial Cancer
|
August 14, 2014
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry
Christophe Rosty, Michael D Walsh, Noralane M Lindor, et al.
Annals of Surgical Oncology
|
January 30, 2013
Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers
Aung Ko Win, Susan Parry, Bryan Parry, et al.
Page
of 30