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Scientific Reports|November 23, 2023
Nucleotide excision repair deficiency is a targetable therapeutic vulnerability in clear cell renal cell carcinomaAurel Prosz, Haohui Duan, Viktoria Tisza, et al.Science Translational Medicine|October 5, 2022
A germline SNP in BRMS1 predisposes patients with lung adenocarcinoma to metastasis and can be ameliorated by targeting c-fosYuan Liu, Neel Chudgar, Brooke Mastrogiacomo, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 11, 2010
Germline BRCA mutations denote a clinicopathologic subset of prostate cancerDavid J Gallagher, Mia M Gaudet, Prodipto Pal, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2022
Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndromeYing L Liu, Karen A Cadoo, Anna Maio, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 20, 2005
Breast cancer risk following bilateral oophorectomy in BRCA1 and BRCA2 mutation carriers: an international case-control studyAndrea Eisen, Jan Lubinski, Jan Klijn, et al.Biorxiv : the Preprint Server for Biology|February 17, 2023
Nucleotide excision repair deficiency is a targetable therapeutic vulnerability in clear cell renal cell carcinomaAurel Prosz, Haohui Duan, Viktoria Tisza, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 13, 2022
Genetic Predictors for Fecal Propionate and Butyrate-Producing Microbiome Pathway Are Not Associated with Colorectal Cancer Risk: A Mendelian Randomization AnalysisYujia Lu, Yu Chen Zhao, Jenny Chang-Claude, et al.Blood Advances|April 4, 2019
Germline deletion of ETV6 in familial acute lymphoblastic leukemiaEvadnie Rampersaud, David S Ziegler, Ilaria Iacobucci, et al.European Journal of Human Genetics : EJHG|March 9, 2019
Development of patient "profiles" to tailor counseling for incidental genomic sequencing resultsChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.Human Genetics|June 23, 2022
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findingsJordan Sam, Emma Reble, Rita Kodida, et al.Pageof 67