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Plos Genetics|February 4, 2015
Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarctionAenne S Thormaehlen, Christian Schuberth, Hong-Hee Won, et al.Nature|August 10, 2017
Genome-scale activation screen identifies a lncRNA locus regulating a gene neighbourhoodJulia Joung, Jesse M Engreitz, Silvana Konermann, et al.Nature|September 22, 2017
Erratum: Genome-scale activation screen identifies a lncRNA locus regulating a gene neighbourhoodJulia Joung, Jesse M Engreitz, Silvana Konermann, et al.Human Genetics|December 20, 2005
Searching for signals of evolutionary selection in 168 genes related to immune functionEmily C Walsh, Pardis Sabeti, Holli B Hutcheson, et al.Nature Genetics|February 12, 2013
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Andreas Gnirke, David B Jaffe, et al.Bioorganic & Medicinal Chemistry Letters|April 17, 2012
Identification of a selective small molecule inhibitor of breast cancer stem cellsAndrew R Germain, Leigh C Carmody, Barbara Morgan, et al.Science (New York, N.Y.)|May 25, 2002
The structure of haplotype blocks in the human genomeStacey B Gabriel, Stephen F Schaffner, Huy Nguyen, et al.Plos Genetics|November 1, 2008
Genomewide analysis of PRC1 and PRC2 occupancy identifies two classes of bivalent domainsManching Ku, Richard P Koche, Esther Rheinbay, et al.Blood|June 4, 2014
Systematic identification of personal tumor-specific neoantigens in chronic lymphocytic leukemiaMohini Rajasagi, Sachet A Shukla, Edward F Fritsch, et al.Cell|July 23, 2025
SPIDR enables multiplexed mapping of RNA-protein interactions and uncovers a mechanism for selective translational suppression upon cell stressErica Wolin, Jimmy K Guo, Mario R Blanco, et al.Pageof 40