J. Brett Stanton

University of Arizona — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

16h-index1.1kcitations33works1.02yr avg
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Research Topics

Retinal Development and Disorders(16), Retinal Diseases and Treatments(10), Neuroscience and Neuropharmacology Research(5), Connexins and lens biology(5), Glaucoma and retinal disorders(3)

Publications33 total

Key role of ERβ in estrogenic regulation of neuronal mitochondrial function
Alzheimer s & Dementia·2024· 1 citedOpen Access
In vitro characterization of neonatal, juvenile, and adult porcine islet oxygen demand, β‐cell function, and transcriptomes
Xenotransplantation·2018· 24 cited
Mutant Fibulin-3 Causes Proteoglycan Accumulation and Impaired Diffusion Across Bruch's Membrane
Investigative Ophthalmology & Visual Science·2017· 21 citedOpen Access
Deletion of Efemp1 Is Protective Against the Development of Sub-RPE Deposits in Mouse Eyes
Investigative Ophthalmology & Visual Science·2017· 29 citedOpen Access
Acute Ischemia Induced by High-Density Culture Increases Cytokine Expression and Diminishes the Function and Viability of Highly Purified Human Islets of Langerhans
Transplantation·2017· 27 citedOpen Access
Levodopa-Induced Morot Behavior Alterations in Dosophila Larvae
2017
Early AMD-like defects in the RPE and retinal degeneration in aged mice with RPE-specific deletion of <i>Atg5</i> or <i>Atg7</i>.
PubMed·2017· 59 cited
Levodopa-induced motor behavior alterations in Drosophila larvae
2016
RPE-specific deletion of murine Atg5 or Atg7 causes AMD-like features and retinal degeneration
2015
Bestrophin-1 influences transepithelial electrical properties and Ca2+ signaling in human retinal pigment epithelium.
PubMed·2015· 50 citedOpen Access
Diffusion across and proteoglycan content in Bruch’s membrane are altered in mice carrying an Efemp1 mutation.
Investigative Ophthalmology & Visual Science·2014
Differential effects of Best disease causing missense mutations on bestrophin-1 trafficking
Human Molecular Genetics·2013· 28 citedOpen Access
Characterization of Transgenic Mouse RPE Cultures
Investigative Ophthalmology & Visual Science·2011
Suppression of Ca2+ signaling in a mouse model of Best disease
Human Molecular Genetics·2010· 96 citedOpen Access
The OA1 Autocrine Loop: in vivo and in vitro
Investigative Ophthalmology & Visual Science·2009· 3 cited
Altered pH and Ca2+ Homeostasis in Mice Harboring the W93C Mutation in Bestrophin-1: Implications for the Pathogenesis of the Bestrophinopathies
Investigative Ophthalmology & Visual Science·2009
A Comparison of the Phenotypes of Bestrophin Knock-In and Knock-Out Mice: Implications for the Pathogenesis of Best Vitelliform Macular Degeneration
Investigative Ophthalmology & Visual Science·2008· 3 cited
Bestrophin-2 Is Involved in the Generation of Intraocular Pressure
Investigative Ophthalmology & Visual Science·2008· 61 citedOpen Access
The Bestrophin-2 Knock-Out Mouse: Histological and Functional Analysis
Investigative Ophthalmology & Visual Science·2007· 1 cited
Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2)
Experimental Eye Research·2007· 93 cited
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Frequent Co-authors

Alan D. Marmorstein(25), Lihua Y. Marmorstein(18), Neal S. Peachey(8), Benjamin Bakall(8), Brian S. McKay(5), Claes Wadelius(5), Precious J. McLaughlin(4), Youwen Zhang(4), Samuel D. Cross(4), Olaf Strauß(3), H. Criss Hartzell(3), Ronald M. Lynch(3), Jiang Wu(2), John Yocom(2), Kuai Yu(2), Roxana A. Radu(2), J. M. Burke(2), Tyson R. Kinnick(2), Adiv A. Johnson(2), Andrew F.X. Goldberg(2)