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Neena B Haider

Showing results (1-10 of 33) with videos related to

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International Ophthalmology Clinics|March 24, 2022
Microbiota, Microbiome, and Retinal DiseasesNakul Singh, Neena B Haider
Experimental Eye Research|May 11, 2010
Focus on molecules: nuclear hormone receptor Nr2e3: impact on retinal development and diseaseNissa Mollema, Neena B Haider
Journal of Experimental Neuroscience|May 12, 2016
Role of Nuclear Receptors in Central Nervous System Development and Associated DiseasesAna Maria Olivares, Oscar Andrés Moreno-Ramos, Neena B Haider
Human Molecular Genetics|May 17, 2002
Genetic modifiers of vision and hearingNeena B Haider, Akihiro Ikeda, Jürgen K Naggert, et al.
Plos One|December 17, 2009
Patterned neuroprotection in the Inpp4a(wbl) mutant mouse cerebellum correlates with the expression of Eaat4Andrew J Sachs, Samuel A David, Neena B Haider, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 3, 2008
A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinasArne M Nystuen, Andrew J Sachs, Yang Yuan, et al.
Bioengineering (Basel, Switzerland)|February 23, 2024
Seeing the Future: A Review of Ocular TherapyMaiya Whalen, Monica Akula, Shannon M McNamee, et al.
Neurogenetics|November 15, 2006
A null mutation in VAMP1/synaptobrevin is associated with neurological defects and prewean mortality in the lethal-wasting mouse mutantArne M Nystuen, Jamie K Schwendinger, Andrew J Sachs, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 16, 2007
The mouse mutants recoil wobbler and nmf373 represent a series of Grm1 mutationsAndrew J Sachs, Jamie K Schwendinger, Andy W Yang, et al.
Journal of Clinical Medicine|January 30, 2021
Interspecies Correlations between Human and Mouse <i>NR2E3</i>-Associated Recessive DiseaseAlessandro Iannaccone, Emily Brabbit, Christiaan Lopez-Miro, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
International Ophthalmology Clinics|March 24, 2022
Microbiota, Microbiome, and Retinal DiseasesNakul Singh, Neena B Haider
Experimental Eye Research|May 11, 2010
Focus on molecules: nuclear hormone receptor Nr2e3: impact on retinal development and diseaseNissa Mollema, Neena B Haider
Journal of Experimental Neuroscience|May 12, 2016
Role of Nuclear Receptors in Central Nervous System Development and Associated DiseasesAna Maria Olivares, Oscar Andrés Moreno-Ramos, Neena B Haider
Human Molecular Genetics|May 17, 2002
Genetic modifiers of vision and hearingNeena B Haider, Akihiro Ikeda, Jürgen K Naggert, et al.
Plos One|December 17, 2009
Patterned neuroprotection in the Inpp4a(wbl) mutant mouse cerebellum correlates with the expression of Eaat4Andrew J Sachs, Samuel A David, Neena B Haider, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 3, 2008
A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinasArne M Nystuen, Andrew J Sachs, Yang Yuan, et al.
Bioengineering (Basel, Switzerland)|February 23, 2024
Seeing the Future: A Review of Ocular TherapyMaiya Whalen, Monica Akula, Shannon M McNamee, et al.
Neurogenetics|November 15, 2006
A null mutation in VAMP1/synaptobrevin is associated with neurological defects and prewean mortality in the lethal-wasting mouse mutantArne M Nystuen, Jamie K Schwendinger, Andrew J Sachs, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 16, 2007
The mouse mutants recoil wobbler and nmf373 represent a series of Grm1 mutationsAndrew J Sachs, Jamie K Schwendinger, Andy W Yang, et al.
Journal of Clinical Medicine|January 30, 2021
Interspecies Correlations between Human and Mouse <i>NR2E3</i>-Associated Recessive DiseaseAlessandro Iannaccone, Emily Brabbit, Christiaan Lopez-Miro, et al.
Pageof 4