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Bernd Wissinger

Showing results (31-40 of 196) with videos related to

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Molecular Vision|March 28, 2015
Novel homozygous large deletion including the 5' part of the SPATA7 gene in a consanguineous Israeli Muslim Arab familyAnja-Kathrin Mayer, Muhammad Mahajnah, Ditta Zobor, et al.
JAMA Ophthalmology|January 31, 2020
Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye PhenotypesMark J Simcoe, Nicole Weisschuh, Bernd Wissinger, et al.
The Journal of Comparative Neurology|July 2, 2010
cGMP-dependent cone photoreceptor degeneration in the cpfl1 mouse retinaDragana Trifunović, Katja Dengler, Stylianos Michalakis, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 8, 2004
Blue cone monochromatism: clinical findings in patients with mutations in the red/green opsin gene clusterUlrich Kellner, Bernd Wissinger, Sabine Tippmann, et al.
Investigative Ophthalmology & Visual Science|November 24, 2004
Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutationsThomas Rosenberg, Britta Baumann, Susanne Kohl, et al.
Frontiers in Genetics|November 16, 2020
Gene and Protein Expression in Subjects With a Nystagmus-Associated AHR MutationNatalia Borovok, Celeste Weiss, Rajech Sharkia, et al.
Neuron|December 10, 2013
A tale of two retinal domains: near-optimal sampling of achromatic contrasts in natural scenes through asymmetric photoreceptor distributionTom Baden, Timm Schubert, Le Chang, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 13, 2024
S-cone contribution to oscillatory potentials in patients with blue cone monochromacyGiulia Righetti, Melanie Kempf, Susanne Kohl, et al.
BMC Medical Genetics|November 27, 2020
First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy - a case reportNicole Weisschuh, Pascale Mazzola, Tilman Heinrich, et al.
Molecular Therapy. Nucleic Acids|December 2, 2021
Autosomal dominant optic atrophy: A novel treatment for <i>OPA1</i> splice defects using U1 snRNA adaptionChristoph Jüschke, Thomas Klopstock, Claudia B Catarino, et al.
Pageof 20

Showing results (31-40 of 196) with videos related to

Sort By:
Pageof 20
Molecular Vision|March 28, 2015
Novel homozygous large deletion including the 5' part of the SPATA7 gene in a consanguineous Israeli Muslim Arab familyAnja-Kathrin Mayer, Muhammad Mahajnah, Ditta Zobor, et al.
JAMA Ophthalmology|January 31, 2020
Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye PhenotypesMark J Simcoe, Nicole Weisschuh, Bernd Wissinger, et al.
The Journal of Comparative Neurology|July 2, 2010
cGMP-dependent cone photoreceptor degeneration in the cpfl1 mouse retinaDragana Trifunović, Katja Dengler, Stylianos Michalakis, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 8, 2004
Blue cone monochromatism: clinical findings in patients with mutations in the red/green opsin gene clusterUlrich Kellner, Bernd Wissinger, Sabine Tippmann, et al.
Investigative Ophthalmology & Visual Science|November 24, 2004
Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutationsThomas Rosenberg, Britta Baumann, Susanne Kohl, et al.
Frontiers in Genetics|November 16, 2020
Gene and Protein Expression in Subjects With a Nystagmus-Associated AHR MutationNatalia Borovok, Celeste Weiss, Rajech Sharkia, et al.
Neuron|December 10, 2013
A tale of two retinal domains: near-optimal sampling of achromatic contrasts in natural scenes through asymmetric photoreceptor distributionTom Baden, Timm Schubert, Le Chang, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 13, 2024
S-cone contribution to oscillatory potentials in patients with blue cone monochromacyGiulia Righetti, Melanie Kempf, Susanne Kohl, et al.
BMC Medical Genetics|November 27, 2020
First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy - a case reportNicole Weisschuh, Pascale Mazzola, Tilman Heinrich, et al.
Molecular Therapy. Nucleic Acids|December 2, 2021
Autosomal dominant optic atrophy: A novel treatment for <i>OPA1</i> splice defects using U1 snRNA adaptionChristoph Jüschke, Thomas Klopstock, Claudia B Catarino, et al.
Pageof 20