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Bernd Wissinger

Showing results (61-70 of 196) with videos related to

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International Journal of Molecular Sciences|December 10, 2021
Oscillatory Potentials in Achromatopsia as a Tool for Understanding Cone Retinal FunctionsGiulia Righetti, Melanie Kempf, Christoph Braun, et al.
Investigative Ophthalmology & Visual Science|April 26, 2003
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retinaKatrin Pesch, Christina Zeitz, Julia E Fries, et al.
Experimental Neurology|October 10, 2009
Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyMarcel V Alavi, Nico Fuhrmann, Huu Phuc Nguyen, et al.
International Journal of Molecular Sciences|August 7, 2021
Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with <i>CNGA3</i>-Associated Autosomal Recessive AchromatopsiaSusanne Kohl, Britta Baumann, Francesca Dassie, et al.
Frontiers in Molecular Neuroscience|September 22, 2023
Genetic background modulates phenotypic expressivity in OPA1 mutated mice, relevance to DOA pathogenesisDjamaa Atamena, Venu Gurram, Petnoï Petsophonsakul, et al.
Human Mutation|August 11, 2017
CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patientsAnja K Mayer, Caroline Van Cauwenbergh, Christine Rother, et al.
Investigative Ophthalmology & Visual Science|March 29, 2007
The phenotype of early-onset retinal degeneration in persons with RDH12 mutationsAndreas Schuster, Andreas R Janecke, Robert Wilke, et al.
Investigative Ophthalmology & Visual Science|August 23, 2017
Subretinal Injection for Gene Therapy Does Not Cause Clinically Significant Outer Nuclear Layer Thinning in Normal Primate FoveaeG Alex Ochakovski, Tobias Peters, Stylianos Michalakis, et al.
Molecular Neurodegeneration|June 16, 2010
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophyNico Fuhrmann, Simone Schimpf, York Kamenisch, et al.
Journal of Neurochemistry|November 19, 2016
OPA1 haploinsufficiency induces a BNIP3-dependent decrease in mitophagy in neurons: relevance to Dominant Optic AtrophyManon F Moulis, Aurélie M Millet, Marlène Daloyau, et al.
Pageof 20

Showing results (61-70 of 196) with videos related to

Sort By:
Pageof 20
International Journal of Molecular Sciences|December 10, 2021
Oscillatory Potentials in Achromatopsia as a Tool for Understanding Cone Retinal FunctionsGiulia Righetti, Melanie Kempf, Christoph Braun, et al.
Investigative Ophthalmology & Visual Science|April 26, 2003
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retinaKatrin Pesch, Christina Zeitz, Julia E Fries, et al.
Experimental Neurology|October 10, 2009
Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyMarcel V Alavi, Nico Fuhrmann, Huu Phuc Nguyen, et al.
International Journal of Molecular Sciences|August 7, 2021
Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with <i>CNGA3</i>-Associated Autosomal Recessive AchromatopsiaSusanne Kohl, Britta Baumann, Francesca Dassie, et al.
Frontiers in Molecular Neuroscience|September 22, 2023
Genetic background modulates phenotypic expressivity in OPA1 mutated mice, relevance to DOA pathogenesisDjamaa Atamena, Venu Gurram, Petnoï Petsophonsakul, et al.
Human Mutation|August 11, 2017
CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patientsAnja K Mayer, Caroline Van Cauwenbergh, Christine Rother, et al.
Investigative Ophthalmology & Visual Science|March 29, 2007
The phenotype of early-onset retinal degeneration in persons with RDH12 mutationsAndreas Schuster, Andreas R Janecke, Robert Wilke, et al.
Investigative Ophthalmology & Visual Science|August 23, 2017
Subretinal Injection for Gene Therapy Does Not Cause Clinically Significant Outer Nuclear Layer Thinning in Normal Primate FoveaeG Alex Ochakovski, Tobias Peters, Stylianos Michalakis, et al.
Molecular Neurodegeneration|June 16, 2010
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophyNico Fuhrmann, Simone Schimpf, York Kamenisch, et al.
Journal of Neurochemistry|November 19, 2016
OPA1 haploinsufficiency induces a BNIP3-dependent decrease in mitophagy in neurons: relevance to Dominant Optic AtrophyManon F Moulis, Aurélie M Millet, Marlène Daloyau, et al.
Pageof 20