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M Seeliger

Showing results (1-10 of 10) with videos related to

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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|July 14, 2001
[Vitamin A metabolism and retinal degeneration]M Seeliger, H K Biesalski
Vision Research|January 20, 1999
Spatial cone activity distribution in diseases of the posterior pole determined by multifocal electroretinographyU Kretschmann, M Seeliger, K Ruether, et al.
Neuroscience|April 28, 2009
Detection of behavioral alterations and learning deficits in mice lacking synaptophysinU Schmitt, N Tanimoto, M Seeliger, et al.
American Journal of Ophthalmology|February 19, 1998
Multifocal electroretinography in retinitis pigmentosaM Seeliger, U Kretschmann, E Apfelstedt-Sylla, et al.
Advances in Experimental Medicine and Biology|November 9, 2006
Hypoxic preconditioning and erythropoietin protect retinal neurons from degenerationChristian Grimm, A Wenzel, N Acar, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|August 1, 1997
[Juvenile neuronal ceroid lipofuscinosis (Batten-Mayou) disease. Ophthalmologic diagnosis and findings]M Seeliger, K Rüther, E Apfelstedt-Sylla, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 20, 1999
Comparative study of visual, auditory, and olfactory function in Usher syndromeM Seeliger, M Pfister, K Gendo, 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.
Human Molecular Genetics|November 25, 2000
Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1B Incerti, K Cortese, A Pizzigoni, et al.
Nature Genetics|January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DH Bolz, B von Brederlow, A Ramírez, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|July 14, 2001
[Vitamin A metabolism and retinal degeneration]M Seeliger, H K Biesalski
Vision Research|January 20, 1999
Spatial cone activity distribution in diseases of the posterior pole determined by multifocal electroretinographyU Kretschmann, M Seeliger, K Ruether, et al.
Neuroscience|April 28, 2009
Detection of behavioral alterations and learning deficits in mice lacking synaptophysinU Schmitt, N Tanimoto, M Seeliger, et al.
American Journal of Ophthalmology|February 19, 1998
Multifocal electroretinography in retinitis pigmentosaM Seeliger, U Kretschmann, E Apfelstedt-Sylla, et al.
Advances in Experimental Medicine and Biology|November 9, 2006
Hypoxic preconditioning and erythropoietin protect retinal neurons from degenerationChristian Grimm, A Wenzel, N Acar, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|August 1, 1997
[Juvenile neuronal ceroid lipofuscinosis (Batten-Mayou) disease. Ophthalmologic diagnosis and findings]M Seeliger, K Rüther, E Apfelstedt-Sylla, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 20, 1999
Comparative study of visual, auditory, and olfactory function in Usher syndromeM Seeliger, M Pfister, K Gendo, 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.
Human Molecular Genetics|November 25, 2000
Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1B Incerti, K Cortese, A Pizzigoni, et al.
Nature Genetics|January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DH Bolz, B von Brederlow, A Ramírez, et al.
Pageof 1