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Plos One|March 24, 2015
The Leber congenital amaurosis protein AIPL1 and EB proteins co-localize at the photoreceptor ciliumJuan Hidalgo-de-Quintana, Nele Schwarz, Ingrid P Meschede, et al.
Investigative Ophthalmology & Visual Science|December 5, 2009
Association of whirlin with Cav1.3 (alpha1D) channels in photoreceptors, defining a novel member of the usher protein networkFerry F J Kersten, Erwin van Wijk, Jeroen van Reeuwijk, et al.
Pharmacological Reviews|February 26, 2015
International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptorsJörg Hamann, Gabriela Aust, Demet Araç, et al.
The EMBO Journal|December 18, 2002
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundleBatiste Boëda, Aziz El-Amraoui, Amel Bahloul, et al.
Molecular Biology of the Cell|November 24, 2021
The ARF GAPs ELMOD1 and ELMOD3 act at the Golgi and cilia to regulate ciliogenesis and ciliary protein trafficRachel E Turn, Yihan Hu, Skylar I Dewees, et al.
Human Molecular Genetics|November 26, 2008
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairmentEberhard Schneider, Tina Märker, Angelika Daser, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 17, 2009
Bone spicule pigment formation in retinitis pigmentosa: insights from a mouse modelGesine B Jaissle, Christian Albrecht May, Serge A van de Pavert, et al.
Human Mutation|December 31, 2013
A homozygous mutation in the TUB gene associated with retinal dystrophy and obesityArundhati Dev Borman, Laura R Pearce, Donna S Mackay, et al.
Human Molecular Genetics|December 15, 2010
A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosaFrançois Paquet-Durand, Susanne Beck, Stylianos Michalakis, et al.
Human Mutation|November 24, 2015
PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and MicrocephalyMaha S Zaki, Raoul Heller, Michaela Thoenes, et al.
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