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W Hewitt

Showing results (461-470 of 648) with videos related to

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Genetic Epidemiology|October 27, 2015
Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization StudyGabriel Cuellar-Partida, Yi Lu, Pik Fang Kho, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 1, 2008
The Banff 2007 working classification of skin-containing composite tissue allograft pathologyL C Cendales, J Kanitakis, S Schneeberger, et al.
Hypertension (Dallas, Tex. : 1979)|August 19, 2009
Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye StudyCong Sun, Gu Zhu, Tien Y Wong, et al.
Ophthalmology|January 21, 2016
A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal ErosionsVerity F Oliver, Katherine A van Bysterveldt, Murray Cadzow, et al.
SLAS Technology|September 1, 2023
A semi-automated pipeline for quantifying drusen-like deposits in human induced pluripotent stem cell-derived retinal pigment epithelium cellsJenna Hall, Maciej Daniszewski, Shane Cheung, et al.
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.
Pageof 65

Showing results (461-470 of 648) with videos related to

Sort By:
Pageof 65
Genetic Epidemiology|October 27, 2015
Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization StudyGabriel Cuellar-Partida, Yi Lu, Pik Fang Kho, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 1, 2008
The Banff 2007 working classification of skin-containing composite tissue allograft pathologyL C Cendales, J Kanitakis, S Schneeberger, et al.
Hypertension (Dallas, Tex. : 1979)|August 19, 2009
Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye StudyCong Sun, Gu Zhu, Tien Y Wong, et al.
Ophthalmology|January 21, 2016
A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal ErosionsVerity F Oliver, Katherine A van Bysterveldt, Murray Cadzow, et al.
SLAS Technology|September 1, 2023
A semi-automated pipeline for quantifying drusen-like deposits in human induced pluripotent stem cell-derived retinal pigment epithelium cellsJenna Hall, Maciej Daniszewski, Shane Cheung, et al.
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.
Pageof 65