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Alex W Hewitt

Showing results (251-260 of 425) with videos related to

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Ophthalmology|March 5, 2013
Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registryEmmanuelle Souzeau, Kathryn P Burdon, Andrew Dubowsky, et al.
Plos One|October 11, 2012
The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucomaJaney L Wiggs, Alex W Hewitt, Bao Jian Fan, et al.
Ophthalmology|October 30, 2007
Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qGu Zhu, Alex W Hewitt, Jonathan B Ruddle, et al.
Molecular Vision|April 10, 2007
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgroundsAlex W Hewitt, John R Samples, R Rand Allingham, et al.
Scientific Reports|June 10, 2022
AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell modelsJiang-Hui Wang, Grace E Lidgerwood, Maciej Daniszewski, et al.
Scientific Reports|August 11, 2016
Enriched retinal ganglion cells derived from human embryonic stem cellsKatherine P Gill, Sandy S C Hung, Alexei Sharov, et al.
Scientific Reports|June 1, 2016
Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degenerationGabriel Cuellar-Partida, Jamie E Craig, Kathryn P Burdon, et al.
Clinical & Experimental Ophthalmology|February 8, 2020
Effect of phacoemulsification cataract surgery on intraocular pressure in early glaucoma: A prospective multi-site studyAyub Qassim, Mark J Walland, John Landers, et al.
NAR Genomics and Bioinformatics|February 12, 2021
Comparative performance of the BGI and Illumina sequencing technology for single-cell RNA-sequencingAnne Senabouth, Stacey Andersen, Qianyu Shi, et al.
G3 (Bethesda, Md.)|August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern AustraliaShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Pageof 43

Showing results (251-260 of 425) with videos related to

Sort By:
Pageof 43
Ophthalmology|March 5, 2013
Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registryEmmanuelle Souzeau, Kathryn P Burdon, Andrew Dubowsky, et al.
Plos One|October 11, 2012
The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucomaJaney L Wiggs, Alex W Hewitt, Bao Jian Fan, et al.
Ophthalmology|October 30, 2007
Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qGu Zhu, Alex W Hewitt, Jonathan B Ruddle, et al.
Molecular Vision|April 10, 2007
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgroundsAlex W Hewitt, John R Samples, R Rand Allingham, et al.
Scientific Reports|June 10, 2022
AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell modelsJiang-Hui Wang, Grace E Lidgerwood, Maciej Daniszewski, et al.
Scientific Reports|August 11, 2016
Enriched retinal ganglion cells derived from human embryonic stem cellsKatherine P Gill, Sandy S C Hung, Alexei Sharov, et al.
Scientific Reports|June 1, 2016
Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degenerationGabriel Cuellar-Partida, Jamie E Craig, Kathryn P Burdon, et al.
Clinical & Experimental Ophthalmology|February 8, 2020
Effect of phacoemulsification cataract surgery on intraocular pressure in early glaucoma: A prospective multi-site studyAyub Qassim, Mark J Walland, John Landers, et al.
NAR Genomics and Bioinformatics|February 12, 2021
Comparative performance of the BGI and Illumina sequencing technology for single-cell RNA-sequencingAnne Senabouth, Stacey Andersen, Qianyu Shi, et al.
G3 (Bethesda, Md.)|August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern AustraliaShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Pageof 43