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Marcel V Alavi

Showing results (11-20 of 22) with videos related to

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Investigative Ophthalmology & Visual Science|October 17, 2009
Electrophysiological and histologic assessment of retinal ganglion cell fate in a mouse model for OPA1-associated autosomal dominant optic atrophyPeter Heiduschka, Sven Schnichels, Nico Fuhrmann, et al.
Experimental Neurology|October 10, 2009
Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyMarcel V Alavi, Nico Fuhrmann, Huu Phuc Nguyen, et al.
Molecular Neurodegeneration|June 16, 2010
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophyNico Fuhrmann, Simone Schimpf, York Kamenisch, et al.
Investigative Ophthalmology & Visual Science|November 17, 2015
Strain-Dependent Anterior Segment Dysgenesis and Progression to Glaucoma in Col4a1 Mutant MiceMao Mao, Richard S Smith, Marcel V Alavi, et al.
Scientific Reports|January 28, 2016
Col4a1 mutations cause progressive retinal neovascular defects and retinopathyMarcel V Alavi, Mao Mao, Bradley T Pawlikowski, et al.
Investigative Ophthalmology & Visual Science|October 30, 2015
In Vivo Visualization of Endoplasmic Reticulum Stress in the Retina Using the ERAI Reporter MouseMarcel V Alavi, Wei-Chieh Chiang, Heike Kroeger, et al.
Experimental Eye Research|October 5, 2017
Long-term photoreceptor rescue in two rodent models of retinitis pigmentosa by adeno-associated virus delivery of Stanniocalcin-1Gavin W Roddy, Douglas Yasumura, Michael T Matthes, et al.
Cardiovascular Research|March 13, 2012
Down-regulation of OPA1 alters mouse mitochondrial morphology, PTP function, and cardiac adaptation to pressure overloadJerome Piquereau, Fanny Caffin, Marta Novotova, et al.
Brain : a Journal of Neurology|February 23, 2007
A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophyMarcel V Alavi, Stefanie Bette, Simone Schimpf, et al.
Human Molecular Genetics|February 26, 2011
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16Valerio Carelli, Simone Schimpf, Nico Fuhrmann, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Investigative Ophthalmology & Visual Science|October 17, 2009
Electrophysiological and histologic assessment of retinal ganglion cell fate in a mouse model for OPA1-associated autosomal dominant optic atrophyPeter Heiduschka, Sven Schnichels, Nico Fuhrmann, et al.
Experimental Neurology|October 10, 2009
Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyMarcel V Alavi, Nico Fuhrmann, Huu Phuc Nguyen, et al.
Molecular Neurodegeneration|June 16, 2010
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophyNico Fuhrmann, Simone Schimpf, York Kamenisch, et al.
Investigative Ophthalmology & Visual Science|November 17, 2015
Strain-Dependent Anterior Segment Dysgenesis and Progression to Glaucoma in Col4a1 Mutant MiceMao Mao, Richard S Smith, Marcel V Alavi, et al.
Scientific Reports|January 28, 2016
Col4a1 mutations cause progressive retinal neovascular defects and retinopathyMarcel V Alavi, Mao Mao, Bradley T Pawlikowski, et al.
Investigative Ophthalmology & Visual Science|October 30, 2015
In Vivo Visualization of Endoplasmic Reticulum Stress in the Retina Using the ERAI Reporter MouseMarcel V Alavi, Wei-Chieh Chiang, Heike Kroeger, et al.
Experimental Eye Research|October 5, 2017
Long-term photoreceptor rescue in two rodent models of retinitis pigmentosa by adeno-associated virus delivery of Stanniocalcin-1Gavin W Roddy, Douglas Yasumura, Michael T Matthes, et al.
Cardiovascular Research|March 13, 2012
Down-regulation of OPA1 alters mouse mitochondrial morphology, PTP function, and cardiac adaptation to pressure overloadJerome Piquereau, Fanny Caffin, Marta Novotova, et al.
Brain : a Journal of Neurology|February 23, 2007
A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophyMarcel V Alavi, Stefanie Bette, Simone Schimpf, et al.
Human Molecular Genetics|February 26, 2011
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16Valerio Carelli, Simone Schimpf, Nico Fuhrmann, et al.
Pageof 3