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Anthony T Moore

Showing results (211-220 of 277) with videos related to

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Ophthalmology|October 24, 2013
Retinal structure and function in achromatopsia: implications for gene therapyVenki Sundaram, Caroline Wilde, Jonathan Aboshiha, et al.
Ophthalmology|May 20, 2020
Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United KingdomNikolas Pontikos, Gavin Arno, Neringa Jurkute, et al.
American Journal of Human Genetics|June 29, 2010
X-linked cone dystrophy caused by mutation of the red and green cone opsinsJessica C Gardner, Tom R Webb, Naheed Kanuga, et al.
Retina (Philadelphia, Pa.)|October 17, 2024
THE FIGHT INHERITED RETINAL BLINDNESS! PROJECT: A New Treatment Outcome and Natural History Registry for Inherited Retinal DiseaseMatthew P Simunovic, Anthony T Moore, John Grigg, et al.
Brain : a Journal of Neurology|February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
European Journal of Human Genetics : EJHG|February 3, 2018
A clinical and molecular characterisation of CRB1-associated maculopathyKamron N Khan, Anthony Robson, Omar A R Mahroo, et al.
Investigative Ophthalmology & Visual Science|May 3, 2021
Expanding the FDXR-Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular FeatureNeringa Jurkute, Priya D Shanmugarajah, Marios Hadjivassiliou, et al.
Investigative Ophthalmology & Visual Science|May 1, 2023
IMI-Management and Investigation of High Myopia in Infants and Young ChildrenIan Flitcroft, John Ainsworth, Audrey Chia, et al.
American Journal of Human Genetics|January 28, 2014
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defectsKathleen A Williamson, Joe Rainger, James A B Floyd, et al.
Cell Stem Cell|May 7, 2016
Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic CupsDavid A Parfitt, Amelia Lane, Conor M Ramsden, et al.
Pageof 28

Showing results (211-220 of 277) with videos related to

Sort By:
Pageof 28
Ophthalmology|October 24, 2013
Retinal structure and function in achromatopsia: implications for gene therapyVenki Sundaram, Caroline Wilde, Jonathan Aboshiha, et al.
Ophthalmology|May 20, 2020
Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United KingdomNikolas Pontikos, Gavin Arno, Neringa Jurkute, et al.
American Journal of Human Genetics|June 29, 2010
X-linked cone dystrophy caused by mutation of the red and green cone opsinsJessica C Gardner, Tom R Webb, Naheed Kanuga, et al.
Retina (Philadelphia, Pa.)|October 17, 2024
THE FIGHT INHERITED RETINAL BLINDNESS! PROJECT: A New Treatment Outcome and Natural History Registry for Inherited Retinal DiseaseMatthew P Simunovic, Anthony T Moore, John Grigg, et al.
Brain : a Journal of Neurology|February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
European Journal of Human Genetics : EJHG|February 3, 2018
A clinical and molecular characterisation of CRB1-associated maculopathyKamron N Khan, Anthony Robson, Omar A R Mahroo, et al.
Investigative Ophthalmology & Visual Science|May 3, 2021
Expanding the FDXR-Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular FeatureNeringa Jurkute, Priya D Shanmugarajah, Marios Hadjivassiliou, et al.
Investigative Ophthalmology & Visual Science|May 1, 2023
IMI-Management and Investigation of High Myopia in Infants and Young ChildrenIan Flitcroft, John Ainsworth, Audrey Chia, et al.
American Journal of Human Genetics|January 28, 2014
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defectsKathleen A Williamson, Joe Rainger, James A B Floyd, et al.
Cell Stem Cell|May 7, 2016
Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic CupsDavid A Parfitt, Amelia Lane, Conor M Ramsden, et al.
Pageof 28