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H Fingert

Showing results (81-90 of 159) with videos related to

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Eye (London, England)|May 2, 2003
Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virusD A Mackey, J H Fingert, J Z Luzhansky, et al.
Ophthalmology. Glaucoma|August 28, 2025
Long term follow-up on a juvenile open angle glaucoma pedigree with a novel EFEMP1 mutation (c.1313, p.Tyr438Cys)Brian P Young, Angela W Nyunt, Molly A Clymer, et al.
Molecular Vision|April 13, 2017
LADD syndrome with glaucoma is caused by a novel geneAllie Simpson, Armin Avdic, Ben R Roos, et al.
Current Eye Research|January 5, 2013
Identification of proteins that interact with TANK binding kinase 1 and testing for mutations associated with glaucomaSeongjin Seo, Frances Solivan-Timpe, Ben R Roos, et al.
Molecular Vision|September 23, 2015
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmosDavid Khorram, Michael Choi, Ben R Roos, et al.
Ophthalmic Genetics|September 27, 2017
Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphismKathleen R Chirco, Carly J Lewis, Todd E Scheetz, et al.
Ophthalmic Genetics|September 25, 2012
Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United StatesJohn F Stamler, Ben R Roos, Michael D Wagoner, et al.
Ophthalmology. Glaucoma|May 24, 2023
Mutations in EFEMP1 in Patients with Juvenile Open-Angle GlaucomaAminatta Z Tejan-Kamara, Erin A Boese, Andrew E Pouw, et al.
Molecular Vision|December 23, 2016
MMP19 expression in the human optic nerveKathleen R Chirco, Ralph J Hazlewood, Kathy Miller, et al.
Ophthalmic Genetics|June 7, 2006
The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation glaucoma and primary open-angle glaucoma patients from IowaJohn H Fingert, Young H Kwon, Paula A Moore, et al.
Pageof 16

Showing results (81-90 of 159) with videos related to

Sort By:
Pageof 16
Eye (London, England)|May 2, 2003
Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virusD A Mackey, J H Fingert, J Z Luzhansky, et al.
Ophthalmology. Glaucoma|August 28, 2025
Long term follow-up on a juvenile open angle glaucoma pedigree with a novel EFEMP1 mutation (c.1313, p.Tyr438Cys)Brian P Young, Angela W Nyunt, Molly A Clymer, et al.
Molecular Vision|April 13, 2017
LADD syndrome with glaucoma is caused by a novel geneAllie Simpson, Armin Avdic, Ben R Roos, et al.
Current Eye Research|January 5, 2013
Identification of proteins that interact with TANK binding kinase 1 and testing for mutations associated with glaucomaSeongjin Seo, Frances Solivan-Timpe, Ben R Roos, et al.
Molecular Vision|September 23, 2015
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmosDavid Khorram, Michael Choi, Ben R Roos, et al.
Ophthalmic Genetics|September 27, 2017
Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphismKathleen R Chirco, Carly J Lewis, Todd E Scheetz, et al.
Ophthalmic Genetics|September 25, 2012
Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United StatesJohn F Stamler, Ben R Roos, Michael D Wagoner, et al.
Ophthalmology. Glaucoma|May 24, 2023
Mutations in EFEMP1 in Patients with Juvenile Open-Angle GlaucomaAminatta Z Tejan-Kamara, Erin A Boese, Andrew E Pouw, et al.
Molecular Vision|December 23, 2016
MMP19 expression in the human optic nerveKathleen R Chirco, Ralph J Hazlewood, Kathy Miller, et al.
Ophthalmic Genetics|June 7, 2006
The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation glaucoma and primary open-angle glaucoma patients from IowaJohn H Fingert, Young H Kwon, Paula A Moore, et al.
Pageof 16