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Ophthalmology
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March 5, 2013
Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registry
Emmanuelle 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 glaucoma
Janey 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 5q
Gu 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 backgrounds
Alex 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 models
Jiang-Hui Wang, Grace E Lidgerwood, Maciej Daniszewski, et al.
Scientific Reports
|
August 11, 2016
Enriched retinal ganglion cells derived from human embryonic stem cells
Katherine 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 degeneration
Gabriel 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 study
Ayub 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-sequencing
Anne 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 Australia
Shari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Page
of 43
Search research articles
Search
Showing results (251-260 of 425) with videos related to
Sort By:
Page
of 43
Ophthalmology
|
March 5, 2013
Higher prevalence of myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registry
Emmanuelle 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 glaucoma
Janey 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 5q
Gu 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 backgrounds
Alex 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 models
Jiang-Hui Wang, Grace E Lidgerwood, Maciej Daniszewski, et al.
Scientific Reports
|
August 11, 2016
Enriched retinal ganglion cells derived from human embryonic stem cells
Katherine 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 degeneration
Gabriel 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 study
Ayub 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-sequencing
Anne 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 Australia
Shari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Page
of 43