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Jacque L Duncan

Showing results (81-90 of 170) with videos related to

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Clinical Ophthalmology (Auckland, N.Z.)|November 7, 2019
Quantifying choriocapillaris hypoperfusion in patients with choroidal neovascularization using swept-source OCT angiographyCathrine M Keiner, Hao Zhou, Qinqin Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2023
Disease modeling and pharmacological rescue of autosomal dominant Retinitis Pigmentosa associated with <i>RHO</i> copy number variationSangeetha Kandoi, Cassandra Martinez, Kevin Xu Chen, et al.
Genes|October 26, 2017
Correction: Gustafson et al., Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree. Genes 2017, 8, 210Kevin Gustafson, Jacque L Duncan, Pooja Biswas, et al.
Translational Vision Science & Technology|February 24, 2022
Choriocapillaris Changes in Myopic Macular DegenerationJonathan Li, Hao Zhou, Max Feinstein, et al.
Genes|August 25, 2017
Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish PedigreeKevin Gustafson, Jacque L Duncan, Pooja Biswas, et al.
Scientific Reports|January 28, 2016
Col4a1 mutations cause progressive retinal neovascular defects and retinopathyMarcel V Alavi, Mao Mao, Bradley T Pawlikowski, et al.
American Journal of Ophthalmology|August 26, 2021
Correlation Between Localized Choriocapillaris Perfusion and Macular Function in Eyes with Geographic AtrophyNicholas T Rinella, Hao Zhou, Jessica Wong, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 10, 2012
Identification of a novel mutation in the CDHR1 gene in a family with recessive retinal degenerationJacque L Duncan, Austin Roorda, Mili Navani, et al.
Research Square|December 11, 2025
Deep Learning Detection of Retinitis Pigmentosa Inheritance Forms through Synthetic Data Expansion of a Rare Disease DatasetElizabeth E Hwang, Max L Rivera, Lin Jia, et al.
Investigative Ophthalmology & Visual Science|November 27, 2019
Cone Structure Persists Beyond Margins of Short-Wavelength Autofluorescence in ChoroideremiaKatharina G Foote, Nicholas Rinella, Janette Tang, et al.
Pageof 17

Showing results (81-90 of 170) with videos related to

Sort By:
Pageof 17
Clinical Ophthalmology (Auckland, N.Z.)|November 7, 2019
Quantifying choriocapillaris hypoperfusion in patients with choroidal neovascularization using swept-source OCT angiographyCathrine M Keiner, Hao Zhou, Qinqin Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2023
Disease modeling and pharmacological rescue of autosomal dominant Retinitis Pigmentosa associated with <i>RHO</i> copy number variationSangeetha Kandoi, Cassandra Martinez, Kevin Xu Chen, et al.
Genes|October 26, 2017
Correction: Gustafson et al., Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree. Genes 2017, 8, 210Kevin Gustafson, Jacque L Duncan, Pooja Biswas, et al.
Translational Vision Science & Technology|February 24, 2022
Choriocapillaris Changes in Myopic Macular DegenerationJonathan Li, Hao Zhou, Max Feinstein, et al.
Genes|August 25, 2017
Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish PedigreeKevin Gustafson, Jacque L Duncan, Pooja Biswas, et al.
Scientific Reports|January 28, 2016
Col4a1 mutations cause progressive retinal neovascular defects and retinopathyMarcel V Alavi, Mao Mao, Bradley T Pawlikowski, et al.
American Journal of Ophthalmology|August 26, 2021
Correlation Between Localized Choriocapillaris Perfusion and Macular Function in Eyes with Geographic AtrophyNicholas T Rinella, Hao Zhou, Jessica Wong, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 10, 2012
Identification of a novel mutation in the CDHR1 gene in a family with recessive retinal degenerationJacque L Duncan, Austin Roorda, Mili Navani, et al.
Research Square|December 11, 2025
Deep Learning Detection of Retinitis Pigmentosa Inheritance Forms through Synthetic Data Expansion of a Rare Disease DatasetElizabeth E Hwang, Max L Rivera, Lin Jia, et al.
Investigative Ophthalmology & Visual Science|November 27, 2019
Cone Structure Persists Beyond Margins of Short-Wavelength Autofluorescence in ChoroideremiaKatharina G Foote, Nicholas Rinella, Janette Tang, et al.
Pageof 17