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Rando Allikmets

Showing results (91-100 of 180) with videos related to

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Investigative Ophthalmology & Visual Science|December 6, 2012
A1120, a nonretinoid RBP4 antagonist, inhibits formation of cytotoxic bisretinoids in the animal model of enhanced retinal lipofuscinogenesisNicoleta Dobri, Qiong Qin, Jian Kong, et al.
Investigative Ophthalmology & Visual Science|August 21, 2014
The external limiting membrane in early-onset Stargardt diseaseWinston Lee, Kalev Nõupuu, Maris Oll, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Genotypic spectrum and phenotype correlations of ABCA4-associated disease in patients of south Asian descentWinston Lee, Kaspar Schuerch, Jana Zernant, et al.
Ophthalmic Genetics|October 3, 2019
Modification of the <i>PROM1</i> disease phenotype by a mutation in <i>ABCA4</i>Winston Lee, Maarjaliis Paavo, Jana Zernant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 31, 2019
A case-control collapsing analysis identifies retinal dystrophy genes associated with ophthalmic disease in patients with no pathogenic ABCA4 variantsCharles J Wolock, Nicholas Stong, Chu Jian Ma, et al.
Translational Vision Science & Technology|May 1, 2023
Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus AutofluorescenceVivienne C Greenstein, David S Castillejos, Stephen H Tsang, et al.
American Journal of Ophthalmology|March 19, 2018
A Distinct Phenotype of Eyes Shut Homolog (EYS)-Retinitis Pigmentosa Is Associated With Variants Near the C-TerminusJesse D Sengillo, Winston Lee, Takayuki Nagasaki, et al.
European Journal of Ophthalmology|September 15, 2020
A mutation in <i>CRX</i> causing pigmented paravenous retinochoroidal atrophyJin Kyun Oh, Yan Nuzbrokh, Winston Lee, et al.
Cold Spring Harbor Molecular Case Studies|June 1, 2018
Extremely hypomorphic and severe deep intronic variants in the <i>ABCA4</i> locus result in varying Stargardt disease phenotypesJana Zernant, Winston Lee, Takayuki Nagasaki, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2011
Complement factor H 402H variant and reticular macular diseaseR Theodore Smith, Joanna E Merriam, Mahsa A Sohrab, et al.
Pageof 18

Showing results (91-100 of 180) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|December 6, 2012
A1120, a nonretinoid RBP4 antagonist, inhibits formation of cytotoxic bisretinoids in the animal model of enhanced retinal lipofuscinogenesisNicoleta Dobri, Qiong Qin, Jian Kong, et al.
Investigative Ophthalmology & Visual Science|August 21, 2014
The external limiting membrane in early-onset Stargardt diseaseWinston Lee, Kalev Nõupuu, Maris Oll, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Genotypic spectrum and phenotype correlations of ABCA4-associated disease in patients of south Asian descentWinston Lee, Kaspar Schuerch, Jana Zernant, et al.
Ophthalmic Genetics|October 3, 2019
Modification of the <i>PROM1</i> disease phenotype by a mutation in <i>ABCA4</i>Winston Lee, Maarjaliis Paavo, Jana Zernant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 31, 2019
A case-control collapsing analysis identifies retinal dystrophy genes associated with ophthalmic disease in patients with no pathogenic ABCA4 variantsCharles J Wolock, Nicholas Stong, Chu Jian Ma, et al.
Translational Vision Science & Technology|May 1, 2023
Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus AutofluorescenceVivienne C Greenstein, David S Castillejos, Stephen H Tsang, et al.
American Journal of Ophthalmology|March 19, 2018
A Distinct Phenotype of Eyes Shut Homolog (EYS)-Retinitis Pigmentosa Is Associated With Variants Near the C-TerminusJesse D Sengillo, Winston Lee, Takayuki Nagasaki, et al.
European Journal of Ophthalmology|September 15, 2020
A mutation in <i>CRX</i> causing pigmented paravenous retinochoroidal atrophyJin Kyun Oh, Yan Nuzbrokh, Winston Lee, et al.
Cold Spring Harbor Molecular Case Studies|June 1, 2018
Extremely hypomorphic and severe deep intronic variants in the <i>ABCA4</i> locus result in varying Stargardt disease phenotypesJana Zernant, Winston Lee, Takayuki Nagasaki, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2011
Complement factor H 402H variant and reticular macular diseaseR Theodore Smith, Joanna E Merriam, Mahsa A Sohrab, et al.
Pageof 18