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American Journal of Human Genetics|June 5, 2002
Identification of microcephalin, a protein implicated in determining the size of the human brainAndrew P Jackson, Helen Eastwood, Sandra M Bell, et al.Thyroid : Official Journal of the American Thyroid Association|July 18, 2008
A human monoclonal autoantibody to the thyrotropin receptor with thyroid-stimulating blocking activityJane Sanders, Michele Evans, Corrado Betterle, et al.Nature Genetics|October 5, 2010
WDR62 is associated with the spindle pole and is mutated in human microcephalyAdeline K Nicholas, Maryam Khurshid, Julie Désir, et al.American Journal of Human Genetics|October 24, 2003
Protein-truncating mutations in ASPM cause variable reduction in brain sizeJacquelyn Bond, Sheila Scott, Daniel J Hampshire, et al.Journal of Neurovirology|January 6, 2016
Toxicity and in vitro activity of HIV-1 latency-reversing agents in primary CNS cellsLachlan R Gray, Hung On, Emma Roberts, et al.Nature|December 15, 2006
An SCN9A channelopathy causes congenital inability to experience painJames J Cox, Frank Reimann, Adeline K Nicholas, et al.Journal of Molecular Endocrinology|January 29, 2019
Crystal structure of a ligand-free stable TSH receptor leucine-rich repeat domainJennifer Miller-Gallacher, Paul Sanders, Stuart Young, et al.Journal of Medicinal Chemistry|January 9, 2025
Phenotype-Led Identification of IL-10 Upregulators in Human CD4<sup>+</sup> T-cells and Elucidation of Their Pharmacology as Highly Selective CDK8/CDK19 InhibitorsSimon Nicolle, Mike Barker, John Barrett, et al.Nature Genetics|March 29, 2005
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain sizeJacquelyn Bond, Emma Roberts, Kelly Springell, et al.Nature Genetics|May 27, 2003
Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix proteinLesley McGregor, Ville Makela, Susan M Darling, et al.Pageof 5