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Mathias W Seeliger

Showing results (61-70 of 128) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|April 5, 2008
Effect of late-stage therapy on disease progression in AAV-mediated rescue of photoreceptor cells in the retinoschisin-deficient mouseAndreas Janssen, Seok H Min, Laurie L Molday, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 7, 2006
Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 geneLeila El Matri, Aude Ambresin, Daniel F Schorderet, et al.
Human Molecular Genetics|January 8, 2016
Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsiaChristian Schön, Sabrina Asteriti, Susanne Koch, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 18, 2012
Light-driven calcium signals in mouse cone photoreceptorsTao Wei, Timm Schubert, François Paquet-Durand, et al.
Cell Communication and Signaling : CCS|February 2, 2024
T-type voltage-gated channels, Na<sup>+</sup>/Ca<sup>2+</sup>-exchanger, and calpain-2 promote photoreceptor cell death in inherited retinal degenerationJie Yan, Lan Wang, Qian-Lu Yang, et al.
Plos One|October 7, 2009
Vasoregression linked to neuronal damage in the rat with defect of polycystin-2Yuxi Feng, Yumei Wang, Oliver Stock, et al.
Advances in Experimental Medicine and Biology|March 19, 2010
Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophiesM Dominik Fischer, Naoyuki Tanimoto, Susanne C Beck, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Influence of the β2-Subunit of L-Type Voltage-Gated Cav Channels on the Structural and Functional Development of Photoreceptor Ribbon SynapsesRashmi Katiyar, Petra Weissgerber, Elisabeth Roth, et al.
The Journal of Clinical Investigation|April 9, 2013
Endothelial SRF/MRTF ablation causes vascular disease phenotypes in murine retinaeChristine Weinl, Heidemarie Riehle, Dongjeong Park, et al.
Investigative Ophthalmology & Visual Science|January 24, 2017
Murine Autoimmune Optic Neuritis Is Not Phenotypically Altered by the Retinal Degeneration 8 MutationAleksandar Stojic, Richard Fairless, Susanne C Beck, et al.
Pageof 13

Showing results (61-70 of 128) with videos related to

Sort By:
Pageof 13
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 5, 2008
Effect of late-stage therapy on disease progression in AAV-mediated rescue of photoreceptor cells in the retinoschisin-deficient mouseAndreas Janssen, Seok H Min, Laurie L Molday, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 7, 2006
Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 geneLeila El Matri, Aude Ambresin, Daniel F Schorderet, et al.
Human Molecular Genetics|January 8, 2016
Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsiaChristian Schön, Sabrina Asteriti, Susanne Koch, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 18, 2012
Light-driven calcium signals in mouse cone photoreceptorsTao Wei, Timm Schubert, François Paquet-Durand, et al.
Cell Communication and Signaling : CCS|February 2, 2024
T-type voltage-gated channels, Na<sup>+</sup>/Ca<sup>2+</sup>-exchanger, and calpain-2 promote photoreceptor cell death in inherited retinal degenerationJie Yan, Lan Wang, Qian-Lu Yang, et al.
Plos One|October 7, 2009
Vasoregression linked to neuronal damage in the rat with defect of polycystin-2Yuxi Feng, Yumei Wang, Oliver Stock, et al.
Advances in Experimental Medicine and Biology|March 19, 2010
Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophiesM Dominik Fischer, Naoyuki Tanimoto, Susanne C Beck, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Influence of the β2-Subunit of L-Type Voltage-Gated Cav Channels on the Structural and Functional Development of Photoreceptor Ribbon SynapsesRashmi Katiyar, Petra Weissgerber, Elisabeth Roth, et al.
The Journal of Clinical Investigation|April 9, 2013
Endothelial SRF/MRTF ablation causes vascular disease phenotypes in murine retinaeChristine Weinl, Heidemarie Riehle, Dongjeong Park, et al.
Investigative Ophthalmology & Visual Science|January 24, 2017
Murine Autoimmune Optic Neuritis Is Not Phenotypically Altered by the Retinal Degeneration 8 MutationAleksandar Stojic, Richard Fairless, Susanne C Beck, et al.
Pageof 13