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Klinische Monatsblatter Fur Augenheilkunde|March 14, 2018
[The Usher Syndrome, a Human Ciliopathy]Uwe Wolfrum, Kerstin Nagel-WolfrumDevelopmental Cell|June 15, 2013
Vesicle transport and photoreceptor death: fishing for molecular linksKerstin Nagel-Wolfrum, Uwe WolfrumAdvances in Experimental Medicine and Biology|March 26, 2014
Therapy strategies for Usher syndrome Type 1C in the retinaKerstin Nagel-Wolfrum, Timor Baasov, Uwe WolfrumProgress in Retinal and Eye Research|May 16, 2017
Cilia - The sensory antennae in the eyeHelen May-Simera, Kerstin Nagel-Wolfrum, Uwe WolfrumVisual Neuroscience|June 11, 2014
Translational read-through as an alternative approach for ocular gene therapy of retinal dystrophies caused by in-frame nonsense mutationsKerstin Nagel-Wolfrum, Fabian Möller, Inessa Penner, et al.Investigative Ophthalmology & Visual Science|June 5, 2012
Gene repair of an Usher syndrome causing mutation by zinc-finger nuclease mediated homologous recombinationNora Overlack, Tobias Goldmann, Uwe Wolfrum, et al.Vision Research|October 10, 2007
SANS (USH1G) expression in developing and mature mammalian retinaNora Overlack, Tina Maerker, Martin Latz, et al.Advances in Experimental Medicine and Biology|March 26, 2014
Usher syndrome protein network functions in the retina and their relation to other retinal ciliopathiesNasrin Sorusch, Kirsten Wunderlich, Katharina Bauss, et al.Experimental Eye Research|March 21, 2006
Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher diseaseJan Reiners, Kerstin Nagel-Wolfrum, Karin Jürgens, et al.Biodrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy|February 18, 2016
Targeting Nonsense Mutations in Diseases with Translational Read-Through-Inducing Drugs (TRIDs)Kerstin Nagel-Wolfrum, Fabian Möller, Inessa Penner, et al.Pageof 18