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Jeremy R Charette

Showing results (11-20 of 15) with videos related to

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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 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
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 2