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Patsy M Nishina

Showing results (51-60 of 80) with videos related to

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Plos One|October 31, 2014
Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAsRamani Soundararajan, Jungyeon Won, Timothy M Stearns, et al.
Molecular and Cellular Neurosciences|August 23, 2005
Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseasesYongsuk Lee, Shuhei Kameya, Gregory A Cox, et al.
Human Molecular Genetics|November 17, 2010
NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm developmentJungyeon Won, Caralina Marín de Evsikova, Richard S Smith, et al.
Molecular Vision|March 31, 2017
A mutagenesis-derived <i>Lrp5</i> mouse mutant with abnormal retinal vasculature and low bone mineral densityJeremy R Charette, Sarah E Earp, Brent A Bell, et al.
Advances in Experimental Medicine and Biology|October 3, 2015
A Chemical Mutagenesis Screen Identifies Mouse Models with ERG DefectsJeremy R Charette, Ivy S Samuels, Minzhong Yu, et al.
Plos One|September 1, 2017
Mouse models of human ocular disease for translational researchMark P Krebs, Gayle B Collin, Wanda L Hicks, et al.
The American Journal of Pathology|April 28, 2005
Spontaneous corneal hem- and lymphangiogenesis in mice with destrin-mutation depend on VEGFR3 signalingClaus Cursiefen, Sakae Ikeda, Patsy M Nishina, et al.
Human Molecular Genetics|September 26, 2015
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiationGayle B Collin, Dirk Hubmacher, Jeremy R Charette, et al.
Nature Genetics|April 10, 2002
Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndromeGayle B Collin, Jan D Marshall, Akihiro Ikeda, et al.
The Journal of Biological Chemistry|March 9, 2010
Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in miceEwa Budzynski, Alecia K Gross, Suzanne D McAlear, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
Plos One|October 31, 2014
Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAsRamani Soundararajan, Jungyeon Won, Timothy M Stearns, et al.
Molecular and Cellular Neurosciences|August 23, 2005
Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseasesYongsuk Lee, Shuhei Kameya, Gregory A Cox, et al.
Human Molecular Genetics|November 17, 2010
NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm developmentJungyeon Won, Caralina Marín de Evsikova, Richard S Smith, et al.
Molecular Vision|March 31, 2017
A mutagenesis-derived <i>Lrp5</i> mouse mutant with abnormal retinal vasculature and low bone mineral densityJeremy R Charette, Sarah E Earp, Brent A Bell, et al.
Advances in Experimental Medicine and Biology|October 3, 2015
A Chemical Mutagenesis Screen Identifies Mouse Models with ERG DefectsJeremy R Charette, Ivy S Samuels, Minzhong Yu, et al.
Plos One|September 1, 2017
Mouse models of human ocular disease for translational researchMark P Krebs, Gayle B Collin, Wanda L Hicks, et al.
The American Journal of Pathology|April 28, 2005
Spontaneous corneal hem- and lymphangiogenesis in mice with destrin-mutation depend on VEGFR3 signalingClaus Cursiefen, Sakae Ikeda, Patsy M Nishina, et al.
Human Molecular Genetics|September 26, 2015
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiationGayle B Collin, Dirk Hubmacher, Jeremy R Charette, et al.
Nature Genetics|April 10, 2002
Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndromeGayle B Collin, Jan D Marshall, Akihiro Ikeda, et al.
The Journal of Biological Chemistry|March 9, 2010
Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in miceEwa Budzynski, Alecia K Gross, Suzanne D McAlear, et al.
Pageof 8