Showing results (21-30 of 30) with videos related to
Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Journal of Translational Medicine|May 3, 2017
Transcriptomic profiling and quantitative high-throughput (qHTS) drug screening of CDH1 deficient hereditary diffuse gastric cancer (HDGC) cells identify treatment leads for familial gastric cancerIna Chen, Lesley Mathews-Greiner, Dandan Li, et al.Human Genetics|May 6, 2015
Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large familyAnand Pathak, Alexander Pemov, Mary L McMaster, et al.Haematologica|January 2, 2016
Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large familyAnand Pathak, Katja Seipel, Alexander Pemov, et al.Journal of Medical Genetics|February 13, 2019
Associations of CDH1 germline variant location and cancer phenotype in families with hereditary diffuse gastric cancer (HDGC)Winifred Lo, Bin Zhu, Arvind Sabesan, et al.Haematologica|July 2, 2016
Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR geneMelissa Rotunno, Mary L McMaster, Joseph Boland, et al.Nature Communications|December 21, 2017
The evolutionary landscape of chronic lymphocytic leukemia treated with ibrutinib targeted therapyDan A Landau, Clare Sun, Daniel Rosebrock, et al.Papillomavirus Research (Amsterdam, Netherlands)|December 9, 2015
Deep sequencing of HPV16 genomes: A new high-throughput tool for exploring the carcinogenicity and natural history of HPV16 infectionMichael Cullen, Joseph F Boland, Mark Schiffman, et al.Plos Medicine|December 7, 2016
Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective StudyJianxin Shi, Xing Hua, Bin Zhu, et al.Science Translational Medicine|February 14, 2020
Mannose receptor (CD206) activation in tumor-associated macrophages enhances adaptive and innate antitumor immune responsesJesse M Jaynes, Rushikesh Sable, Michael Ronzetti, et al.Nature Genetics|April 2, 2014
Rare missense variants in POT1 predispose to familial cutaneous malignant melanomaJianxin Shi, Xiaohong R Yang, Bari Ballew, et al.Pageof 3