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Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Intravitreous transplantation of encapsulated fibroblasts secreting the human fibroblast growth factor 2 delays photoreceptor cell degeneration in Royal College of Surgeons ratsY Uteza, J S Rouillot, A Kobetz, et al.
American Journal of Human Genetics|April 22, 2008
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndromeDaniel F Schorderet, Olivia Nichini, Gaëlle Boisset, et al.
Journal of Medical Genetics|May 12, 2000
A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 familiesP Dinçer, Z Akçören, E Demir, et al.
Journal of Medical Genetics|April 5, 2003
Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataractsE Nandrot, C Slingsby, A Basak, et al.
Circulation|May 22, 2015
Circulating Exosomes Induced by Cardiac Pressure Overload Contain Functional Angiotensin II Type 1 ReceptorsGianluigi Pironti, Ryan T Strachan, Dennis Abraham, et al.
Molecular Pharmacology|December 10, 2013
Regulation of β2-adrenergic receptor function by conformationally selective single-domain intrabodiesDean P Staus, Laura M Wingler, Ryan T Strachan, et al.
Molecular Vision|January 6, 2009
Analysis of partner of inscuteable (mPins) expression in the developing mouse eyeB Raji, A Dansault, V Vieira, et al.
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