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E Zrenner

Showing results (251-260 of 284) with videos related to

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International Journal of Molecular Medicine|June 16, 2001
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disordersK Pesch, J Tomiuk, M Broghammer, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 1999
Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3M Biel, M Seeliger, A Pfeifer, et al.
Investigative Ophthalmology & Visual Science|February 7, 2001
Evaluation of the rhodopsin knockout mouse as a model of pure cone functionG B Jaissle, C A May, J Reinhard, et al.
The British Journal of Ophthalmology|July 30, 2008
Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patientsD Besch, H Sachs, P Szurman, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 15, 2016
[Transcorneal electrical stimulation in primary open angle glaucoma]T Röck, L Naycheva, G Willmann, et al.
Human Molecular Genetics|July 7, 2001
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritanceU E Pesch, B Leo-Kottler, S Mayer, et al.
Vision Research|July 9, 1999
Can subretinal microphotodiodes successfully replace degenerated photoreceptors?E Zrenner, A Stett, S Weiss, et al.
Human Genetics|November 1, 1992
Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosaM Horn, P Humphries, M Kunisch, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 1, 2002
Studies on the feasibility of a subretinal visual prosthesis: data from Yucatan micropig and rabbitH N Schwahn, F Gekeler, K Kohler, et al.
Nature Genetics|July 14, 1998
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channelS Kohl, T Marx, I Giddings, et al.
Pageof 29

Showing results (251-260 of 284) with videos related to

Sort By:
Pageof 29
International Journal of Molecular Medicine|June 16, 2001
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disordersK Pesch, J Tomiuk, M Broghammer, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 1999
Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3M Biel, M Seeliger, A Pfeifer, et al.
Investigative Ophthalmology & Visual Science|February 7, 2001
Evaluation of the rhodopsin knockout mouse as a model of pure cone functionG B Jaissle, C A May, J Reinhard, et al.
The British Journal of Ophthalmology|July 30, 2008
Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patientsD Besch, H Sachs, P Szurman, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 15, 2016
[Transcorneal electrical stimulation in primary open angle glaucoma]T Röck, L Naycheva, G Willmann, et al.
Human Molecular Genetics|July 7, 2001
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritanceU E Pesch, B Leo-Kottler, S Mayer, et al.
Vision Research|July 9, 1999
Can subretinal microphotodiodes successfully replace degenerated photoreceptors?E Zrenner, A Stett, S Weiss, et al.
Human Genetics|November 1, 1992
Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosaM Horn, P Humphries, M Kunisch, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 1, 2002
Studies on the feasibility of a subretinal visual prosthesis: data from Yucatan micropig and rabbitH N Schwahn, F Gekeler, K Kohler, et al.
Nature Genetics|July 14, 1998
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channelS Kohl, T Marx, I Giddings, et al.
Pageof 29