Jeremy R Charette
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Explore the profile of Jeremy R Charette including associated specialties, affiliations and a list of published articles.
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14
Citations
249
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Recent Articles
1.
Lawal R, Mathis V, Barter M, Charette J, Garretson A, Dumont B
Sci Rep
. 2022 Dec;
12(1):20866.
PMID: 36460842
The house mouse species complex (Mus musculus) is comprised of three primary subspecies. A large number of secondary subspecies have also been suggested on the basis of divergent morphology and...
2.
Pandey R, Krebs M, Bolisetty M, Charette J, Naggert J, Robson P, et al.
Int J Mol Sci
. 2022 Sep;
23(18).
PMID: 36142331
Transcriptomic analysis of the mammalian retinal pigment epithelium (RPE) aims to identify cellular networks that influence ocular development, maintenance, function, and disease. However, available evidence points to RPE cell heterogeneity...
3.
Weatherly S, Collin G, Charette J, Stone L, Damkham N, Hyde L, et al.
PLoS Genet
. 2022 Jun;
18(6):e1009798.
PMID: 35675330
Mutations in the apicobasal polarity gene CRB1 lead to diverse retinal diseases, such as Leber congenital amaurosis, cone-rod dystrophy, retinitis pigmentosa (with and without Coats-like vasculopathy), foveal retinoschisis, macular dystrophy,...
4.
Collin G, Shi L, Yu M, Akturk N, Charette J, Hyde L, et al.
Int J Mol Sci
. 2022 Feb;
23(4).
PMID: 35216333
Fluid and solute transporters of the retinal pigment epithelium (RPE) are core components of the outer blood-retinal barrier. Characterizing these transporters and their role in retinal homeostasis may provide insights...
5.
Kong Y, Zhao L, Charette J, Hicks W, Stone L, Nishina P, et al.
Hum Mol Genet
. 2018 Jun;
27(19):3340-3352.
PMID: 29947801
Photoreceptor dysplasia, characterized by formation of folds and (pseudo-)rosettes in the outer retina, is associated with loss of functional nuclear receptor subfamily 2 group E member 3 (NR2E3) and neural...
6.
Krebs M, Collin G, Hicks W, Yu M, Charette J, Shi L, et al.
PLoS One
. 2017 Sep;
12(8):e0183837.
PMID: 28859131
Mouse models provide a valuable tool for exploring pathogenic mechanisms underlying inherited human disease. Here, we describe seven mouse models identified through the Translational Vision Research Models (TVRM) program, each...
7.
Charette J, Earp S, Bell B, Ackert-Bicknell C, Godfrey D, Rao S, et al.
Mol Vis
. 2017 Mar;
23:140-148.
PMID: 28356706
Purpose: Familial exudative vitreoretinopathy (FEVR) is caused by mutations in the genes encoding low-density lipoprotein receptor-related protein (LRP5) or its interacting partners, namely frizzled class receptor 4 (FZD4) and norrin...
8.
Greenwald S, Charette J, Staniszewska M, Shi L, Brown S, Stone L, et al.
Am J Pathol
. 2016 May;
186(7):1925-1938.
PMID: 27207593
The nicotinamide nucleotide adenylyltransferase 1 (NMNAT1) enzyme is essential for regenerating the nuclear pool of NAD(+) in all nucleated cells in the body, and mounting evidence also suggests that it...
9.
Saksens N, Krebs M, Schoenmaker-Koller F, Hicks W, Yu M, Shi L, et al.
Nat Genet
. 2015 Dec;
48(2):144-51.
PMID: 26691986
Butterfly-shaped pigment dystrophy is an eye disease characterized by lesions in the macula that can resemble the wings of a butterfly. Here we report the identification of heterozygous missense mutations...
10.
Charette J, Samuels I, Yu M, Stone L, Hicks W, Shi L, et al.
Adv Exp Med Biol
. 2015 Oct;
854:177-83.
PMID: 26427409
Mouse models provide important resources for many areas of vision research, pertaining to retinal development, retinal function and retinal disease. The Translational Vision Research Models (TVRM) program uses chemical mutagenesis...