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STAR Protocols|April 1, 2026
Protocol for the isolation, culturing, and evaluation of primary Müller glial cells from pig retina as cellular models in health and diseaseYesim Tütüncü, Jan Motlik, Nikolai Klymiuk, et al.
Basic & Clinical Pharmacology & Toxicology|April 1, 2023
The adhesion G protein-coupled receptor VLGR1/ADGRV1 controls autophagyJoshua Linnert, Baran E Güler, Jacek Krzysko, et al.
Visual 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.
Research Letters in Biochemistry|July 24, 2012
Dephosphorylation of Centrins by Protein Phosphatase 2C α and βMarie-Christin Thissen, Josef Krieglstein, Uwe Wolfrum, 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, 2006
Centrins, gatekeepers for the light-dependent translocation of transducin through the photoreceptor cell connecting ciliumAndreas Giessl, Philipp Trojan, Sebastian Rausch, et al.
Molecular Vision|June 2, 2005
Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C)Jan Reiners, Tina Märker, Karin Jürgens, et al.
Reproduction (Cambridge, England)|July 21, 2007
A novel pyruvate kinase (PK-S) from boar spermatozoa is localized at the fibrous sheath and the acrosomeSandra Feiden, Heike Stypa, 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.
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