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Journal of Medical Genetics
|
March 2, 2016
Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer
Karin Kast, Kerstin Rhiem, Barbara Wappenschmidt, et al.
International Journal of Cancer
|
May 14, 2019
Breast cancer risk in BRCA1/2 mutation carriers and noncarriers under prospective intensified surveillance
Christoph Engel, Christine Fischer, Silke Zachariae, et al.
NPJ Breast Cancer
|
May 13, 2021
Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects
Na Li, Magnus Zethoven, Simone McInerny, et al.
NEJM Evidence
|
June 12, 2024
A Patient-Level Meta-Analysis of Intensive Glucose Control in Critically Ill Adults
Derick Adigbli, Yang Li, Naomi Hammond, et al.
Cell Reports
|
November 2, 2022
Nuclear stabilization of p53 requires a functional nucleolar surveillance pathway
Katherine M Hannan, Priscilla Soo, Mei S Wong, et al.
Journal of the National Cancer Institute
|
June 27, 2023
Contralateral breast cancer risk in patients with breast cancer and a germline-BRCA1/2 pathogenic variant undergoing radiation
Mark van Barele, Delal Akdeniz, Bernadette A M Heemskerk-Gerritsen, et al.
Gut
|
February 15, 2013
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Hans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, et al.
Journal of Medical Genetics
|
August 15, 2012
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk
Amanda B Spurdle, Phillip J Whiley, Bryony Thompson, et al.
Gastroenterology
|
August 1, 2018
No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
Christoph Engel, Hans F Vasen, Toni Seppälä, et al.
Cancer Medicine
|
March 10, 2018
Gene panel testing of 5589 BRCA1/2-negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer
Jan Hauke, Judit Horvath, Eva Groß, et al.
Page
of 38
Search research articles
Search
Showing results (261-270 of 376) with videos related to
Sort By:
Page
of 38
Journal of Medical Genetics
|
March 2, 2016
Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer
Karin Kast, Kerstin Rhiem, Barbara Wappenschmidt, et al.
International Journal of Cancer
|
May 14, 2019
Breast cancer risk in BRCA1/2 mutation carriers and noncarriers under prospective intensified surveillance
Christoph Engel, Christine Fischer, Silke Zachariae, et al.
NPJ Breast Cancer
|
May 13, 2021
Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects
Na Li, Magnus Zethoven, Simone McInerny, et al.
NEJM Evidence
|
June 12, 2024
A Patient-Level Meta-Analysis of Intensive Glucose Control in Critically Ill Adults
Derick Adigbli, Yang Li, Naomi Hammond, et al.
Cell Reports
|
November 2, 2022
Nuclear stabilization of p53 requires a functional nucleolar surveillance pathway
Katherine M Hannan, Priscilla Soo, Mei S Wong, et al.
Journal of the National Cancer Institute
|
June 27, 2023
Contralateral breast cancer risk in patients with breast cancer and a germline-BRCA1/2 pathogenic variant undergoing radiation
Mark van Barele, Delal Akdeniz, Bernadette A M Heemskerk-Gerritsen, et al.
Gut
|
February 15, 2013
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Hans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, et al.
Journal of Medical Genetics
|
August 15, 2012
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk
Amanda B Spurdle, Phillip J Whiley, Bryony Thompson, et al.
Gastroenterology
|
August 1, 2018
No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
Christoph Engel, Hans F Vasen, Toni Seppälä, et al.
Cancer Medicine
|
March 10, 2018
Gene panel testing of 5589 BRCA1/2-negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer
Jan Hauke, Judit Horvath, Eva Groß, et al.
Page
of 38