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B Farber

Showing results (151-160 of 269) with videos related to

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Human Mutation|April 27, 2004
Molecular analysis of the ABCA4 gene in Turkish patients with Stargardt disease and retinitis pigmentosaRiza Köksal Ozgül, Hakan Durukan, Ayse Turan, et al.
Investigative Ophthalmology & Visual Science|January 1, 1988
The potential usefulness to research of retina obtained by biopsyA C Bird, D B Farber, A E Kreiger, et al.
The Journal of Biological Chemistry|March 23, 2005
Sp4 is expressed in retinal neurons, activates transcription of photoreceptor-specific genes, and synergizes with CrxLeonid E Lerner, Guang-Hua Peng, Yekaterina E Gribanova, et al.
Environmental Health Perspectives|June 15, 2000
Environmental agents that have the potential to trigger massive apoptotic neurodegeneration in the developing brainJ W Olney, N B Farber, D F Wozniak, et al.
Neurobiology of Disease|May 3, 2011
Glucocorticoid receptor stimulation and the regulation of neonatal cerebellar neural progenitor cell apoptosisKevin K Noguchi, Karen Lau, Derek J Smith, et al.
Cellular and Molecular Neurobiology|December 1, 1991
The potassium channel MBK1 (Kv1.1) is expressed in the mouse retinaD J Klumpp, D B Farber, C Bowes, et al.
Experimental Eye Research|June 13, 2006
Translational regulation of the rod photoreceptor cGMP-phosphodiesterase: the role of the 5'- and 3'-untranslated regionsNatik Piri, Emmanuel Mendoza, Jennifer Shih, et al.
Ophthalmology|January 5, 2005
A substitution of G to C in the cone cGMP-phosphodiesterase gamma subunit gene found in a distinctive form of cone dystrophyNatik Piri, Yong Qing Gao, Michael Danciger, et al.
Visual Neuroscience|February 14, 2006
Morphological characterization of the retinal degeneration in three strains of mice carrying the rd-3 mutationKenneth A Linberg, Robert N Fariss, John R Heckenlively, et al.
Nature|October 18, 1990
Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesteraseC Bowes, T Li, M Danciger, et al.
Pageof 27

Showing results (151-160 of 269) with videos related to

Sort By:
Pageof 27
Human Mutation|April 27, 2004
Molecular analysis of the ABCA4 gene in Turkish patients with Stargardt disease and retinitis pigmentosaRiza Köksal Ozgül, Hakan Durukan, Ayse Turan, et al.
Investigative Ophthalmology & Visual Science|January 1, 1988
The potential usefulness to research of retina obtained by biopsyA C Bird, D B Farber, A E Kreiger, et al.
The Journal of Biological Chemistry|March 23, 2005
Sp4 is expressed in retinal neurons, activates transcription of photoreceptor-specific genes, and synergizes with CrxLeonid E Lerner, Guang-Hua Peng, Yekaterina E Gribanova, et al.
Environmental Health Perspectives|June 15, 2000
Environmental agents that have the potential to trigger massive apoptotic neurodegeneration in the developing brainJ W Olney, N B Farber, D F Wozniak, et al.
Neurobiology of Disease|May 3, 2011
Glucocorticoid receptor stimulation and the regulation of neonatal cerebellar neural progenitor cell apoptosisKevin K Noguchi, Karen Lau, Derek J Smith, et al.
Cellular and Molecular Neurobiology|December 1, 1991
The potassium channel MBK1 (Kv1.1) is expressed in the mouse retinaD J Klumpp, D B Farber, C Bowes, et al.
Experimental Eye Research|June 13, 2006
Translational regulation of the rod photoreceptor cGMP-phosphodiesterase: the role of the 5'- and 3'-untranslated regionsNatik Piri, Emmanuel Mendoza, Jennifer Shih, et al.
Ophthalmology|January 5, 2005
A substitution of G to C in the cone cGMP-phosphodiesterase gamma subunit gene found in a distinctive form of cone dystrophyNatik Piri, Yong Qing Gao, Michael Danciger, et al.
Visual Neuroscience|February 14, 2006
Morphological characterization of the retinal degeneration in three strains of mice carrying the rd-3 mutationKenneth A Linberg, Robert N Fariss, John R Heckenlively, et al.
Nature|October 18, 1990
Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesteraseC Bowes, T Li, M Danciger, et al.
Pageof 27