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Scientific Reports|August 18, 2016
Structural and functional characterization of endothelial microparticles released by cigarette smokeKarina A Serban, Samin Rezania, Daniela N Petrusca, et al.Science (New York, N.Y.)|August 5, 2017
UBE2O remodels the proteome during terminal erythroid differentiationAnthony T Nguyen, Miguel A Prado, Paul J Schmidt, et al.Cell Reports|August 30, 2018
Rapid and Integrative Discovery of Retina Regulatory MoleculesNicholas E Albrecht, Jonathan Alevy, Danye Jiang, et al.Disease Models & Mechanisms|November 2, 2012
Preclinical research in Rett syndrome: setting the foundation for translational successDavid M Katz, Joanne E Berger-Sweeney, James H Eubanks, et al.Plos Genetics|December 17, 2009
Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxinMelissa K Boles, Bonney M Wilkinson, Laurens G Wilming, et al.Genome Biology|September 16, 2011
Mutation discovery in mice by whole exome sequencingHeather Fairfield, Griffith J Gilbert, Mary Barter, et al.Nature Communications|June 27, 2017
Prevalence of sexual dimorphism in mammalian phenotypic traitsNatasha A Karp, Jeremy Mason, Arthur L Beaudet, et al.Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.Nature Genetics|June 27, 2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping ConsortiumTerrence F Meehan, Nathalie Conte, David B West, et al.American Journal of Human Genetics|July 2, 2013
TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensitiesWojciech Wiszniewski, Jill V Hunter, Neil A Hanchard, et al.Pageof 26