Gayle B Collin
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Explore the profile of Gayle B Collin including associated specialties, affiliations and a list of published articles.
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42
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1245
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Recent Articles
1.
Gogna N, Hyde L, Collin G, Stone L, Naggert J, Nishina P
Adv Exp Med Biol
. 2023 Jul;
1415:27-36.
PMID: 37440010
Age-related macular degeneration (AMD) is the leading cause of blindness in the global aging population. Familial aggregation and genome-wide association (GWA) studies have identified gene variants associated with AMD, implying...
2.
Xue Y, Sun X, Wang S, Collin G, Kefalov V, Cepko C
Proc Natl Acad Sci U S A
. 2023 May;
120(23):e2217885120.
PMID: 37252956
Retinitis pigmentosa (RP) is an ocular disease characterized by the loss of night vision, followed by the loss of daylight vision. Daylight vision is initiated in the retina by cone...
3.
Naggert A, Collin G, Wang J, Krebs M, Chang B
Front Mol Neurosci
. 2023 Jan;
15:1080136.
PMID: 36698779
During routine screening of mouse strains and stocks by the Eye Mutant Resource at The Jackson Laboratory for genetic mouse models of human ocular disorders, we identified , a mouse...
4.
Hyde L, Kong Y, Zhao L, Ramachandra Rao S, Wang J, Stone L, et al.
Int J Mol Sci
. 2022 Oct;
23(19).
PMID: 36233305
Congenital disorders of glycosylation (CDG) are a heterogenous group of primarily autosomal recessive mendelian diseases caused by disruptions in the synthesis of lipid-linked oligosaccharides and their transfer to proteins. CDGs...
5.
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,...
6.
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...
7.
Gogna N, Weatherly S, Zhao F, Collin G, Pinkney J, Stone L, et al.
Int J Mol Sci
. 2022 Feb;
23(3).
PMID: 35163536
and mutant mice share similar eye disease characteristics. Previously, studies established a functional relationship of ADIPOR1 and MFRP proteins in maintaining retinal lipidome homeostasis and visual function. However, the independent...
8.
Collin G, Gogna N, Chang B, Damkham N, Pinkney J, Hyde L, et al.
Cells
. 2020 Apr;
9(4).
PMID: 32290105
Inherited retinal degeneration (RD) leads to the impairment or loss of vision in millions of individuals worldwide, most frequently due to the loss of photoreceptor (PR) cells. Animal models, particularly...
9.
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...
10.
Dotan G, Khetan V, Marshall J, Affel E, Armiger-George D, Naggert J, et al.
Ophthalmic Genet
. 2017 Jan;
38(5):440-445.
PMID: 28112973
Background: Alström syndrome is a multi-system recessive disorder caused by mutations in ALMS1 gene. The aim of this study was to characterize morphological retinal changes in Alström patients using spectral-domain...