Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Fingert

Showing results (31-40 of 159) with videos related to

Pageof 16
Sort By:
The New England Journal of Medicine|March 13, 2009
Primary open-angle glaucomaYoung H Kwon, John H Fingert, Markus H Kuehn, et al.
JAMA Ophthalmology|June 13, 2014
Thin central corneal thickness and early-onset glaucoma in lacrimo-auriculo-dento-digital syndromeAnamika Tandon, Shandiz Tehrani, Mark A Greiner, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Complement component C5a activates ICAM-1 expression on human choroidal endothelial cellsJessica M Skeie, John H Fingert, Stephen R Russell, et al.
Investigative Ophthalmology & Visual Science|August 27, 2010
Microarray analysis of iris gene expression in mice with mutations influencing pigmentationColleen M Trantow, Tryphena L Cuffy, John H Fingert, et al.
American Journal of Clinical Oncology|April 1, 1993
Cisplatin, cytosine arabinoside, and pentoxifylline in the treatment of squamous cell carcinoma of the head and neckD J Stewart, M C Cripps, H Fingert, et al.
Ophthalmic Genetics|December 28, 1999
Normal range of hearing associated with myocilin Thr377MetR M Simm, J H Fingert, J E Craig, et al.
Vision Research|August 16, 2024
Minimal phenotypes in transgenic mice with the human LOXL1/LOXL1-AS1 locus associated with exfoliation glaucomaKacie J Meyer, Hannah E Mercer, Ben R Roos, et al.
Molecular Vision|September 16, 2009
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern IndiaPeriasamy Sundaresan, P Vijayalakshmi, Stewart Thompson, et al.
Eye (London, England)|April 8, 2017
Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 geneM A Greiner, D C Terveen, J M Vislisel, et al.
American Journal of Ophthalmology|February 24, 2019
The Heritability of Pigment Dispersion Syndrome and Pigmentary GlaucomaAnamika Tandon, Ze Zhang, John H Fingert, et al.
Pageof 16

Showing results (31-40 of 159) with videos related to

Sort By:
Pageof 16
The New England Journal of Medicine|March 13, 2009
Primary open-angle glaucomaYoung H Kwon, John H Fingert, Markus H Kuehn, et al.
JAMA Ophthalmology|June 13, 2014
Thin central corneal thickness and early-onset glaucoma in lacrimo-auriculo-dento-digital syndromeAnamika Tandon, Shandiz Tehrani, Mark A Greiner, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Complement component C5a activates ICAM-1 expression on human choroidal endothelial cellsJessica M Skeie, John H Fingert, Stephen R Russell, et al.
Investigative Ophthalmology & Visual Science|August 27, 2010
Microarray analysis of iris gene expression in mice with mutations influencing pigmentationColleen M Trantow, Tryphena L Cuffy, John H Fingert, et al.
American Journal of Clinical Oncology|April 1, 1993
Cisplatin, cytosine arabinoside, and pentoxifylline in the treatment of squamous cell carcinoma of the head and neckD J Stewart, M C Cripps, H Fingert, et al.
Ophthalmic Genetics|December 28, 1999
Normal range of hearing associated with myocilin Thr377MetR M Simm, J H Fingert, J E Craig, et al.
Vision Research|August 16, 2024
Minimal phenotypes in transgenic mice with the human LOXL1/LOXL1-AS1 locus associated with exfoliation glaucomaKacie J Meyer, Hannah E Mercer, Ben R Roos, et al.
Molecular Vision|September 16, 2009
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern IndiaPeriasamy Sundaresan, P Vijayalakshmi, Stewart Thompson, et al.
Eye (London, England)|April 8, 2017
Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 geneM A Greiner, D C Terveen, J M Vislisel, et al.
American Journal of Ophthalmology|February 24, 2019
The Heritability of Pigment Dispersion Syndrome and Pigmentary GlaucomaAnamika Tandon, Ze Zhang, John H Fingert, et al.
Pageof 16