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The Journal of Biological Chemistry|March 4, 2000
The Hsp organizer protein hop enhances the rate of but is not essential for glucocorticoid receptor folding by the multiprotein Hsp90-based chaperone systemY Morishima, K C Kanelakis, A M Silverstein, et al.The Journal of Biological Chemistry|November 24, 1999
Differential effects of the hsp70-binding protein BAG-1 on glucocorticoid receptor folding by the hsp90-based chaperone machineryK C Kanelakis, Y Morishima, K D Dittmar, et al.American Journal of Medical Genetics|January 1, 1980
Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly--a new syndrome? Part I: clinical, causal, and pathogenetic considerationsJ G Hall, P D Pallister, S K Clarren, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 24, 2008
NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disordersM Estacion, S D Dib-Hajj, P J Benke, et al.The New England Journal of Medicine|October 3, 1985
Retinoic acid embryopathyE J Lammer, D T Chen, R M Hoar, et al.The Journal of Biological Chemistry|April 15, 1994
Characterization of the protein-protein interactions determining the heat shock protein (hsp90.hsp70.hsp56) heterocomplexM J Czar, J K Owens-Grillo, K D Dittmar, et al.Clinical Genetics|July 16, 2020
Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathyH K Robinson, E Zaklyazminskaya, I Povolotskaya, et al.American Journal of Human Genetics|June 13, 1998
OA1 mutations and deletions in X-linked ocular albinismR E Schnur, M Gao, P A Wick, et al.European Journal of Pediatrics|February 1, 2000
Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literatureC F Boerkoel, S O'Neill, J L André, et al.Pageof 5