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

Adam P Deluca

Showing results (21-30 of 38) with videos related to

Pageof 4
Sort By:
Ophthalmology. Retina|April 25, 2019
Wide-Field Swept-Source OCT and Angiography in X-Linked RetinoschisisIan C Han, S Scott Whitmore, D Brice Critser, et al.
Ophthalmology Science|November 29, 2023
Using Goldmann Visual Field Volume to Track Disease Progression in ChoroideremiaAdam P DeLuca, S Scott Whitmore, Nicole J Tatro, et al.
Retinal Cases & Brief Reports|November 26, 2019
AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCYLuke A Wiley, Elaine M Binkley, Adam P DeLuca, et al.
Experimental Eye Research|March 19, 2013
Exon-level expression profiling of ocular tissuesAlex H Wagner, V Nikhil Anand, Wan-Heng Wang, et al.
Bioinformatics (Oxford, England)|August 16, 2014
Cordova: web-based management of genetic variation dataSean S Ephraim, Nikhil Anand, Adam P DeLuca, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2011
Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)Jing Zheng, Katharine K Miller, Tao Yang, et al.
Human Mutation|January 3, 2013
AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screeningKyle R Taylor, Adam P Deluca, A Eliot Shearer, et al.
Hearing Research|September 15, 2012
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesisRobert W Eppsteiner, A Eliot Shearer, Michael S Hildebrand, et al.
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
Stem Cells Translational Medicine|May 23, 2023
Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell ReplacementJessica A Cooke, Andrew P Voigt, Michael A Collingwood, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Ophthalmology. Retina|April 25, 2019
Wide-Field Swept-Source OCT and Angiography in X-Linked RetinoschisisIan C Han, S Scott Whitmore, D Brice Critser, et al.
Ophthalmology Science|November 29, 2023
Using Goldmann Visual Field Volume to Track Disease Progression in ChoroideremiaAdam P DeLuca, S Scott Whitmore, Nicole J Tatro, et al.
Retinal Cases & Brief Reports|November 26, 2019
AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCYLuke A Wiley, Elaine M Binkley, Adam P DeLuca, et al.
Experimental Eye Research|March 19, 2013
Exon-level expression profiling of ocular tissuesAlex H Wagner, V Nikhil Anand, Wan-Heng Wang, et al.
Bioinformatics (Oxford, England)|August 16, 2014
Cordova: web-based management of genetic variation dataSean S Ephraim, Nikhil Anand, Adam P DeLuca, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2011
Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)Jing Zheng, Katharine K Miller, Tao Yang, et al.
Human Mutation|January 3, 2013
AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screeningKyle R Taylor, Adam P Deluca, A Eliot Shearer, et al.
Hearing Research|September 15, 2012
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesisRobert W Eppsteiner, A Eliot Shearer, Michael S Hildebrand, et al.
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
Stem Cells Translational Medicine|May 23, 2023
Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell ReplacementJessica A Cooke, Andrew P Voigt, Michael A Collingwood, et al.
Pageof 4