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Anthony T Moore

Showing results (121-130 of 277) with videos related to

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Investigative Ophthalmology & Visual Science|August 18, 2009
A mutant connexin50 with enhanced hemichannel function leads to cell deathPeter J Minogue, Jun-Jie Tong, Anita Arora, et al.
Investigative Ophthalmology & Visual Science|April 26, 2003
An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5Michel Michaelides, Samantha Johnson, Alok K Tekriwal, et al.
European Journal of Human Genetics : EJHG|February 14, 2013
Understanding the impact of genetic testing for inherited retinal dystrophyRyan Combs, Marion McAllister, Katherine Payne, et al.
European Journal of Medical Genetics|July 2, 2013
A clinical molecular genetic service for United Kingdom families with choroideraemiaSimon C Ramsden, Anna O'Grady, Tracy Fletcher, et al.
Ophthalmology|May 3, 2011
Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus)Panagiotis I Sergouniotis, Elliott H Sohn, Zheng Li, et al.
Vision Research|January 23, 2013
X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin geneMichelle McClements, Wayne I L Davies, Michel Michaelides, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Investigative Ophthalmology & Visual Science|August 29, 2013
ABCA4 gene screening by next-generation sequencing in a British cohortKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Investigative Ophthalmology & Visual Science|August 30, 2014
Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trialsJonathan Aboshiha, Vy Luong, Jill Cowing, et al.
Investigative Ophthalmology & Visual Science|December 23, 2008
Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficienciesRavikanth Metlapally, Michel Michaelides, Anuradha Bulusu, et al.
Pageof 28

Showing results (121-130 of 277) with videos related to

Sort By:
Pageof 28
Investigative Ophthalmology & Visual Science|August 18, 2009
A mutant connexin50 with enhanced hemichannel function leads to cell deathPeter J Minogue, Jun-Jie Tong, Anita Arora, et al.
Investigative Ophthalmology & Visual Science|April 26, 2003
An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5Michel Michaelides, Samantha Johnson, Alok K Tekriwal, et al.
European Journal of Human Genetics : EJHG|February 14, 2013
Understanding the impact of genetic testing for inherited retinal dystrophyRyan Combs, Marion McAllister, Katherine Payne, et al.
European Journal of Medical Genetics|July 2, 2013
A clinical molecular genetic service for United Kingdom families with choroideraemiaSimon C Ramsden, Anna O'Grady, Tracy Fletcher, et al.
Ophthalmology|May 3, 2011
Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus)Panagiotis I Sergouniotis, Elliott H Sohn, Zheng Li, et al.
Vision Research|January 23, 2013
X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin geneMichelle McClements, Wayne I L Davies, Michel Michaelides, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Investigative Ophthalmology & Visual Science|August 29, 2013
ABCA4 gene screening by next-generation sequencing in a British cohortKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Investigative Ophthalmology & Visual Science|August 30, 2014
Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trialsJonathan Aboshiha, Vy Luong, Jill Cowing, et al.
Investigative Ophthalmology & Visual Science|December 23, 2008
Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficienciesRavikanth Metlapally, Michel Michaelides, Anuradha Bulusu, et al.
Pageof 28