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Maureen Neitz

Showing results (41-50 of 94) with videos related to

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Visual Neuroscience|September 12, 2006
Topography of long- and middle-wavelength sensitive cone opsin gene expression in human and Old World monkey retinaMaureen Neitz, Shawn D Balding, Carrie McMahon, et al.
Acta Ophthalmologica|February 3, 2022
Limitation of standard pseudoisochromatic plates in identifying colour vision deficiencies when compared with genetic testingSolveig Arnegard, Rigmor C Baraas, Jay Neitz, et al.
Visual Neuroscience|July 5, 2008
Topography of the long- to middle-wavelength sensitive cone ratio in the human retina assessed with a wide-field color multifocal electroretinogramJames A Kuchenbecker, Manisha Sahay, Diane M Tait, et al.
Advances in Experimental Medicine and Biology|March 19, 2010
A multi-stage color model revisited: implications for a gene therapy cure for red-green colorblindnessKatherine Mancuso, Matthew C Mauck, James A Kuchenbecker, et al.
Visual Neuroscience|March 1, 2005
Photopigment optical density of the human foveola and a paradoxical senescent increase outside the foveaAgnes B Renner, Holger Knau, Maureen Neitz, et al.
Current Biology : CB|February 22, 2020
A Color Vision Circuit for Non-Image-Forming Vision in the Primate RetinaSara S Patterson, James A Kuchenbecker, James R Anderson, et al.
Visual Neuroscience|November 3, 2004
Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscopeMaureen Neitz, Joseph Carroll, Agnes Renner, et al.
Visual Neuroscience|May 8, 2014
S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variantScott H Greenwald, James A Kuchenbecker, Daniel K Roberson, et al.
Translational Vision Science & Technology|May 19, 2017
Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with <i>L</i>/<i>M</i> Opsin Interchange MutationsScott H Greenwald, James A Kuchenbecker, Jessica S Rowlan, et al.
Genes|June 24, 2022
Insight from <i>OPN1LW</i> Gene Haplotypes into the Cause and Prevention of MyopiaMaureen Neitz, Melissa Wagner-Schuman, Jessica S Rowlan, et al.
Pageof 10

Showing results (41-50 of 94) with videos related to

Sort By:
Pageof 10
Visual Neuroscience|September 12, 2006
Topography of long- and middle-wavelength sensitive cone opsin gene expression in human and Old World monkey retinaMaureen Neitz, Shawn D Balding, Carrie McMahon, et al.
Acta Ophthalmologica|February 3, 2022
Limitation of standard pseudoisochromatic plates in identifying colour vision deficiencies when compared with genetic testingSolveig Arnegard, Rigmor C Baraas, Jay Neitz, et al.
Visual Neuroscience|July 5, 2008
Topography of the long- to middle-wavelength sensitive cone ratio in the human retina assessed with a wide-field color multifocal electroretinogramJames A Kuchenbecker, Manisha Sahay, Diane M Tait, et al.
Advances in Experimental Medicine and Biology|March 19, 2010
A multi-stage color model revisited: implications for a gene therapy cure for red-green colorblindnessKatherine Mancuso, Matthew C Mauck, James A Kuchenbecker, et al.
Visual Neuroscience|March 1, 2005
Photopigment optical density of the human foveola and a paradoxical senescent increase outside the foveaAgnes B Renner, Holger Knau, Maureen Neitz, et al.
Current Biology : CB|February 22, 2020
A Color Vision Circuit for Non-Image-Forming Vision in the Primate RetinaSara S Patterson, James A Kuchenbecker, James R Anderson, et al.
Visual Neuroscience|November 3, 2004
Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscopeMaureen Neitz, Joseph Carroll, Agnes Renner, et al.
Visual Neuroscience|May 8, 2014
S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variantScott H Greenwald, James A Kuchenbecker, Daniel K Roberson, et al.
Translational Vision Science & Technology|May 19, 2017
Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with <i>L</i>/<i>M</i> Opsin Interchange MutationsScott H Greenwald, James A Kuchenbecker, Jessica S Rowlan, et al.
Genes|June 24, 2022
Insight from <i>OPN1LW</i> Gene Haplotypes into the Cause and Prevention of MyopiaMaureen Neitz, Melissa Wagner-Schuman, Jessica S Rowlan, et al.
Pageof 10