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Progress in Retinal and Eye Research|August 2, 2003
Vitamin A metabolism in the retinal pigment epithelium: genes, mutations, and diseasesDebra A Thompson, Andreas GalDevelopments in Ophthalmology|July 25, 2003
Genetic defects in vitamin A metabolism of the retinal pigment epitheliumDebra A Thompson, Andreas GalMolecular Vision|November 17, 2005
Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophiesHanno Bolz, Inga Ebermann, Andreas GalThe Journal of Biological Chemistry|December 22, 2004
AlphaPIX associates with calpain 4, the small subunit of calpain, and has a dual role in integrin-mediated cell spreadingGeorg Rosenberger, Andreas Gal, Kerstin KutscheHuman Mutation|May 20, 2008
Does proximal myotonic myopathy show anticipation?Bernd Kruse, Doris Wöhrle, Peter Steinbach, et al.Human Molecular Genetics|December 25, 2002
Interaction of alphaPIX (ARHGEF6) with beta-parvin (PARVB) suggests an involvement of alphaPIX in integrin-mediated signalingGeorg Rosenberger, Inka Jantke, Andreas Gal, et al.American Journal of Medical Genetics. Part A|January 18, 2005
A novel 9 bp deletion in the filamin a gene causes an otopalatodigital-spectrum disorder with a variable, intermediate phenotypeMargarita Stefanova, Peter Meinecke, Andreas Gal, et al.Human Mutation|June 23, 2007
p.Gln200Glu, a putative constitutively active mutant of rod alpha-transducin (GNAT1) in autosomal dominant congenital stationary night blindnessViktoria Szabo, Hans-Jürgen Kreienkamp, Thomas Rosenberg, et al.Klinische Monatsblatter Fur Augenheilkunde|September 4, 2003
[Hereditary foveal hypoplasia - clinical differentiation]Hans Wolfgang Schroeder, Ulrike Orth, Eberhard Meyer-König, et al.Pediatric Neurology|March 31, 2005
Mucopolysaccharidosis type II in females: case report and review of literatureKarin Tuschl, Andreas Gal, Eduard Paschke, et al.Pageof 9