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Genome Biology|August 9, 2014
Biased estimates of clonal evolution and subclonal heterogeneity can arise from PCR duplicates in deep sequencing experimentsErin N Smith, Kristen Jepsen, Mahdieh Khosroheidari, et al.Genome Research|May 1, 1997
Computational and biological analysis of 680 kb of DNA sequence from the human 5q31 cytokine gene cluster regionK A Frazer, Y Ueda, Y Zhu, et al.Human Mutation|November 30, 2020
Detection and validation of novel mutations in MERTK in a simplex case of retinal degeneration using WGS and hiPSC-RPEs modelPooja Biswas, Shyamanga Borooah, Hiroko Matsui, et al.Journal of Thrombosis and Haemostasis : JTH|July 3, 2018
Discovery of novel plasma biomarkers for future incident venous thromboembolism by untargeted synchronous precursor selection mass spectrometry proteomicsS B Jensen, K Hindberg, T Solomon, et al.Haematologica|October 5, 2019
Fibrinogen gamma gene rs2066865 and risk of cancer-related venous thromboembolismBenedikte Paulsen, Hanne Skille, Erin N Smith, et al.Nature Communications|October 31, 2023
eQTL mapping in fetal-like pancreatic progenitor cells reveals early developmental insights into diabetes riskJennifer P Nguyen, Timothy D Arthur, Kyohei Fujita, et al.Plos One|March 26, 2013
Transcriptome sequencing of tumor subpopulations reveals a spectrum of therapeutic options for squamous cell lung cancerChristian L Barrett, Richard B Schwab, HyunChul Jung, et al.The Journal of Pharmacology and Experimental Therapeutics|July 3, 2004
Nicotine activates nuclear factor of activated T cells c2 (NFATc2) and prevents cell cycle entry in T cellsAshley A Frazer-Abel, Shairaz Baksh, Susan P Fosmire, et al.Stem Cell Research|June 25, 2025
Generation of a set of genetically modified long QT syndrome induced pluripotent stem cell lines carrying knock-in variants rs120074178 (KCNQ1 c.569G > A; p.Arg190Gln) and rs137854600 (SCN5A c.4865G > A; p.Arg1622Gln) and isogenic control linesNayara Sousa da Silva, Agnieszka D'Antonio-Chronowska, Reyna Hernandez-Benitez, et al.Genome Biology|December 22, 2011
Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencingOlivier Harismendy, Richard B Schwab, Lei Bao, et al.Pageof 38