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Human Gene Therapy|October 15, 2009
Adeno-associated virus-mediated rhodopsin replacement provides therapeutic benefit in mice with a targeted disruption of the rhodopsin geneArpad Palfi, Sophia Millington-Ward, Naomi Chadderton, et al.
Biomacromolecules|November 6, 2019
Tackling the Limitations of Copolymeric Small Interfering RNA Delivery Agents by a Combined Experimental-Computational ApproachIlja Tabujew, Maziar Heidari, Christoph Freidel, et al.
HGG Advances|September 1, 2023
<i>USH2A</i> variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoidsCarla Sanjurjo-Soriano, Carla Jimenez-Medina, Nejla Erkilic, et al.
Frontiers in Cellular Neuroscience|February 9, 2017
Deep Sequencing of the Human Retinae Reveals the Expression of Odorant ReceptorsNikolina Jovancevic, Kirsten A Wunderlich, Claudia Haering, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 13, 2011
Suppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosaSophia Millington-Ward, Naomi Chadderton, Mary O'Reilly, et al.
Human Molecular Genetics|June 26, 2014
Peripherin-2 couples rhodopsin to the CNG channel in outer segments of rod photoreceptorsElvir Becirovic, O N Phuong Nguyen, Christos Paparizos, et al.
Cellular and Molecular Life Sciences : CMLS|July 3, 2013
Light-dependent phosphorylation of Bardet-Biedl syndrome 5 in photoreceptor cells modulates its interaction with arrestin1Tyler S Smith, Benjamin Spitzbarth, Jian Li, et al.
European Journal of Human Genetics : EJHG|June 7, 2012
Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathyNaomi Chadderton, Arpad Palfi, Sophia Millington-Ward, et al.
Cilia|January 29, 2013
The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitoticallyFerry Fj Kersten, Erwin van Wijk, Lisette Hetterschijt, et al.
Human Molecular Genetics|May 17, 2014
Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degenerationMarcus Karlstetter, Nasrin Sorusch, Albert Caramoy, et al.
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