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Vithiyanjali Sothilingam

Showing results (11-20 of 38) with videos related to

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Frontiers in Neuroscience|June 10, 2017
AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term EffectsRegine Mühlfriedel, Naoyuki Tanimoto, Christian Schön, 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.
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 European Journal of Neuroscience|January 29, 2013
Mice lacking Period 1 and Period 2 circadian clock genes exhibit blue cone photoreceptor defectsOuafa Ait-Hmyed, Marie-Paule Felder-Schmittbuhl, Marina Garcia-Garrido, 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.
Human Gene Therapy|December 8, 2017
Gene Therapy Successfully Delays Degeneration in a Mouse Model of <i>PDE6A</i>-Linked Retinitis Pigmentosa (RP43)Christian Schön, Vithiyanjali Sothilingam, Regine Mühlfriedel, et al.
Plos One|June 3, 2017
Long-term consequences of developmental vascular defects on retinal vessel homeostasis and function in a mouse model of Norrie diseaseSusanne C Beck, Yuxi Feng, Vithiyanjali Sothilingam, et al.
Plos One|September 10, 2014
Elk3 deficiency causes transient impairment in post-natal retinal vascular development and formation of tortuous arteries in adult murine retinaeChristine Weinl, Christine Wasylyk, Marina Garcia Garrido, et al.
Human Molecular Genetics|July 18, 2012
Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosaSusanne Koch, Vithiyanjali Sothilingam, Marina Garcia Garrido, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosaStylianos Michalakis, Susanne Koch, Vithiyanjali Sothilingam, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Frontiers in Neuroscience|June 10, 2017
AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term EffectsRegine Mühlfriedel, Naoyuki Tanimoto, Christian Schön, 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.
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 European Journal of Neuroscience|January 29, 2013
Mice lacking Period 1 and Period 2 circadian clock genes exhibit blue cone photoreceptor defectsOuafa Ait-Hmyed, Marie-Paule Felder-Schmittbuhl, Marina Garcia-Garrido, 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.
Human Gene Therapy|December 8, 2017
Gene Therapy Successfully Delays Degeneration in a Mouse Model of <i>PDE6A</i>-Linked Retinitis Pigmentosa (RP43)Christian Schön, Vithiyanjali Sothilingam, Regine Mühlfriedel, et al.
Plos One|June 3, 2017
Long-term consequences of developmental vascular defects on retinal vessel homeostasis and function in a mouse model of Norrie diseaseSusanne C Beck, Yuxi Feng, Vithiyanjali Sothilingam, et al.
Plos One|September 10, 2014
Elk3 deficiency causes transient impairment in post-natal retinal vascular development and formation of tortuous arteries in adult murine retinaeChristine Weinl, Christine Wasylyk, Marina Garcia Garrido, et al.
Human Molecular Genetics|July 18, 2012
Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosaSusanne Koch, Vithiyanjali Sothilingam, Marina Garcia Garrido, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosaStylianos Michalakis, Susanne Koch, Vithiyanjali Sothilingam, et al.
Pageof 4