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

R Charette

Showing results (21-30 of 31) with videos related to

Pageof 4
Sort By:
Plos One|October 31, 2014
Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAsRamani Soundararajan, Jungyeon Won, Timothy M Stearns, et al.
Advances in Experimental Medicine and Biology|October 3, 2015
A Chemical Mutagenesis Screen Identifies Mouse Models with ERG DefectsJeremy R Charette, Ivy S Samuels, Minzhong Yu, et al.
Molecular Vision|March 31, 2017
A mutagenesis-derived <i>Lrp5</i> mouse mutant with abnormal retinal vasculature and low bone mineral densityJeremy R Charette, Sarah E Earp, Brent A Bell, et al.
Plos One|September 1, 2017
Mouse models of human ocular disease for translational researchMark P Krebs, Gayle B Collin, Wanda L Hicks, et al.
Human Molecular Genetics|September 26, 2015
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiationGayle B Collin, Dirk Hubmacher, Jeremy R Charette, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Cell-type Specific Alteration of <i>Dicer1</i> Accelerates Tumor Progression in Mouse Models of KRAS-driven Lung AdenocarcinomaJulie Wells, Richard S Maser, Rosalinda Doty, et al.
Plos Genetics|June 8, 2022
Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse modelSonia M Weatherly, Gayle B Collin, Jeremy R Charette, et al.
International Journal of Molecular Sciences|February 26, 2022
A Splicing Mutation in <i>Slc4a5</i> Results in Retinal Detachment and Retinal Pigment Epithelium DysfunctionGayle B Collin, Lanying Shi, Minzhong Yu, et al.
The American Journal of Pathology|May 22, 2016
Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human DiseaseScott H Greenwald, Jeremy R Charette, Magdalena Staniszewska, et al.
Nature Genetics|December 23, 2015
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrityNicole T M Saksens, Mark P Krebs, Frederieke E Schoenmaker-Koller, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Plos One|October 31, 2014
Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAsRamani Soundararajan, Jungyeon Won, Timothy M Stearns, et al.
Advances in Experimental Medicine and Biology|October 3, 2015
A Chemical Mutagenesis Screen Identifies Mouse Models with ERG DefectsJeremy R Charette, Ivy S Samuels, Minzhong Yu, et al.
Molecular Vision|March 31, 2017
A mutagenesis-derived <i>Lrp5</i> mouse mutant with abnormal retinal vasculature and low bone mineral densityJeremy R Charette, Sarah E Earp, Brent A Bell, et al.
Plos One|September 1, 2017
Mouse models of human ocular disease for translational researchMark P Krebs, Gayle B Collin, Wanda L Hicks, et al.
Human Molecular Genetics|September 26, 2015
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiationGayle B Collin, Dirk Hubmacher, Jeremy R Charette, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Cell-type Specific Alteration of <i>Dicer1</i> Accelerates Tumor Progression in Mouse Models of KRAS-driven Lung AdenocarcinomaJulie Wells, Richard S Maser, Rosalinda Doty, et al.
Plos Genetics|June 8, 2022
Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse modelSonia M Weatherly, Gayle B Collin, Jeremy R Charette, et al.
International Journal of Molecular Sciences|February 26, 2022
A Splicing Mutation in <i>Slc4a5</i> Results in Retinal Detachment and Retinal Pigment Epithelium DysfunctionGayle B Collin, Lanying Shi, Minzhong Yu, et al.
The American Journal of Pathology|May 22, 2016
Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human DiseaseScott H Greenwald, Jeremy R Charette, Magdalena Staniszewska, et al.
Nature Genetics|December 23, 2015
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrityNicole T M Saksens, Mark P Krebs, Frederieke E Schoenmaker-Koller, et al.
Pageof 4