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Bernd Wissinger

Showing results (21-30 of 196) with videos related to

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Retina (Philadelphia, Pa.)|May 31, 2014
GUCY2D- or GUCA1A-related autosomal dominant cone-rod dystrophy: is there a phenotypic difference?Ditta Zobor, Eberhart Zrenner, Bernd Wissinger, et al.
Plos One|October 19, 2012
Rod and cone function in patients with KCNV2 retinopathyDitta Zobor, Susanne Kohl, Bernd Wissinger, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformationsNicole Weisschuh, Paul Dressler, Frank Schuettauf, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2Christoph Friedburg, Bernd Wissinger, Maria Schambeck, et al.
Ophthalmology|June 4, 2013
Cone dystrophy with supernormal rod response: novel KCNV2 mutations in an underdiagnosed phenotypeLina Zelinger, Bernd Wissinger, Dalia Eli, et al.
Investigative Ophthalmology & Visual Science|July 29, 2015
Influence of Opa1 Mutation on Survival and Function of Retinal Ganglion CellsIrene González-Menéndez, Katja Reinhard, Jorge Tolivia, et al.
The European Journal of Neuroscience|May 1, 2008
Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C)Katja Koeppen, Peggy Reuter, Susanne Kohl, et al.
Human Mutation|June 4, 2008
Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsiaPeggy Reuter, Katja Koeppen, Thomas Ladewig, et al.
Journal of Visualized Experiments : Jove|May 21, 2015
Imaging Ca2+ dynamics in cone photoreceptor axon terminals of the mouse retinaManoj Kulkarni, Timm Schubert, Tom Baden, et al.
BMC Genetics|January 30, 2010
Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German populationChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
Pageof 20

Showing results (21-30 of 196) with videos related to

Sort By:
Pageof 20
Retina (Philadelphia, Pa.)|May 31, 2014
GUCY2D- or GUCA1A-related autosomal dominant cone-rod dystrophy: is there a phenotypic difference?Ditta Zobor, Eberhart Zrenner, Bernd Wissinger, et al.
Plos One|October 19, 2012
Rod and cone function in patients with KCNV2 retinopathyDitta Zobor, Susanne Kohl, Bernd Wissinger, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformationsNicole Weisschuh, Paul Dressler, Frank Schuettauf, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2Christoph Friedburg, Bernd Wissinger, Maria Schambeck, et al.
Ophthalmology|June 4, 2013
Cone dystrophy with supernormal rod response: novel KCNV2 mutations in an underdiagnosed phenotypeLina Zelinger, Bernd Wissinger, Dalia Eli, et al.
Investigative Ophthalmology & Visual Science|July 29, 2015
Influence of Opa1 Mutation on Survival and Function of Retinal Ganglion CellsIrene González-Menéndez, Katja Reinhard, Jorge Tolivia, et al.
The European Journal of Neuroscience|May 1, 2008
Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C)Katja Koeppen, Peggy Reuter, Susanne Kohl, et al.
Human Mutation|June 4, 2008
Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsiaPeggy Reuter, Katja Koeppen, Thomas Ladewig, et al.
Journal of Visualized Experiments : Jove|May 21, 2015
Imaging Ca2+ dynamics in cone photoreceptor axon terminals of the mouse retinaManoj Kulkarni, Timm Schubert, Tom Baden, et al.
BMC Genetics|January 30, 2010
Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German populationChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.
Pageof 20