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Bernd Wissinger

Showing results (81-90 of 196) with videos related to

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Investigative Ophthalmology & Visual Science|May 20, 2008
Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degenerationVeronique B D Kitiratschky, Robert Wilke, Agnes B Renner, et al.
Retina (Philadelphia, Pa.)|December 8, 2004
Morphology and functional characteristics in adult vitelliform macular dystrophyAgnes B Renner, Hilmar Tillack, Hannelore Kraus, et al.
Investigative Ophthalmology & Visual Science|October 3, 2009
Oligocone trichromacy: clinical and molecular genetic investigationsMette K G Andersen, Nynne L B Christoffersen, Birgit Sander, et al.
Investigative Ophthalmology & Visual Science|March 27, 2003
X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15Ingrid Bader, Oliver Brandau, Helene Achatz, et al.
Investigative Ophthalmology & Visual Science|May 9, 2022
Central Visual Function and Genotype-Phenotype Correlations in PDE6A-Associated Retinitis PigmentosaLaura Kuehlewein, Torsten Straßer, Gunnar Blumenstock, et al.
American Journal of Human Genetics|October 13, 2006
Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophyKatharina Agnes Wycisk, Christina Zeitz, Silke Feil, 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.
Human Mutation|May 28, 2010
Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channelKatja Koeppen, Peggy Reuter, Thomas Ladewig, et al.
Investigative Ophthalmology & Visual Science|April 21, 2018
Humoral Immune Response After Intravitreal But Not After Subretinal AAV8 in Primates and PatientsFelix F Reichel, Tobias Peters, Barbara Wilhelm, 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.
Pageof 20

Showing results (81-90 of 196) with videos related to

Sort By:
Pageof 20
Investigative Ophthalmology & Visual Science|May 20, 2008
Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degenerationVeronique B D Kitiratschky, Robert Wilke, Agnes B Renner, et al.
Retina (Philadelphia, Pa.)|December 8, 2004
Morphology and functional characteristics in adult vitelliform macular dystrophyAgnes B Renner, Hilmar Tillack, Hannelore Kraus, et al.
Investigative Ophthalmology & Visual Science|October 3, 2009
Oligocone trichromacy: clinical and molecular genetic investigationsMette K G Andersen, Nynne L B Christoffersen, Birgit Sander, et al.
Investigative Ophthalmology & Visual Science|March 27, 2003
X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15Ingrid Bader, Oliver Brandau, Helene Achatz, et al.
Investigative Ophthalmology & Visual Science|May 9, 2022
Central Visual Function and Genotype-Phenotype Correlations in PDE6A-Associated Retinitis PigmentosaLaura Kuehlewein, Torsten Straßer, Gunnar Blumenstock, et al.
American Journal of Human Genetics|October 13, 2006
Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophyKatharina Agnes Wycisk, Christina Zeitz, Silke Feil, 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.
Human Mutation|May 28, 2010
Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channelKatja Koeppen, Peggy Reuter, Thomas Ladewig, et al.
Investigative Ophthalmology & Visual Science|April 21, 2018
Humoral Immune Response After Intravitreal But Not After Subretinal AAV8 in Primates and PatientsFelix F Reichel, Tobias Peters, Barbara Wilhelm, 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.
Pageof 20