Neal S. Peachey, PhD
Affiliations: | Ophthalmology | Case Western Reserve University School of Medicine, Cleveland, OH, United States |
Area:
Visual System, ERGWebsite:
http://my.clevelandclinic.org/eye/research/labs/peachey.aspxGoogle:
"Neal Peachey"Mean distance: 15.97 (cluster 23) | S | N | B | C | P |
Parents
Sign in to add mentor| John Calvin Armington | grad student | 1979-1985 | Northeastern University |
| Kenneth Ross Alexander | post-doc | 1985-1990 | University of Illinois, Chicago |
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Publications
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| Tarchick MJ, Beight C, Bonezzi PB, et al. (2024) Photoreceptor deficits appear at eye opening in Rs1 mutant mouse models of X-linked retinoschisis. Experimental Eye Research. 242: 109872 |
| Eleftheriou CG, Corona C, Khattak S, et al. (2022) Retinoschisin deficiency induces persistent aberrant waves of activity affecting neuroglial signaling in the retina. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Collin GB, Shi L, Yu M, et al. (2022) A Splicing Mutation in Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction. International Journal of Molecular Sciences. 23 |
| Choi EH, Suh S, Einstein DE, et al. (2021) An inducible Cre mouse for studying roles of the RPE in retinal physiology and disease. Jci Insight |
| Han JYS, Kinoshita J, Bisetto S, et al. (2020) Role of monocarboxylate transporters in regulating metabolic homeostasis in the outer retina: Insight gained from cell-specific Bsg deletion. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology |
| Liu Y, Kinoshita J, Ivanova E, et al. (2019) Mouse models of X-linked juvenile retinoschisis have an early onset phenotype, the severity of which varies with genotype. Human Molecular Genetics |
| Sawant OB, Jidigam VK, Fuller RD, et al. (2019) The circadian clock gene is required to control the timing of retinal neurogenesis and lamination of Müller glia in the mouse retina. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201801832RR |
| Cho KI, Yoon D, Yu M, et al. (2019) Microglial activation in an amyotrophic lateral sclerosis-like model caused by Ranbp2 loss and nucleocytoplasmic transport impairment in retinal ganglion neurons. Cellular and Molecular Life Sciences : Cmls |
| Kiser PD, Kolesnikov AV, Kiser JZ, et al. (2019) Conditional deletion of Des1 in the mouse retina does not impair the visual cycle in cones. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201802493R |
| Scaramuzzi M, Kumar P, Peachey N, et al. (2018) Evidence of retinal degeneration in Wolfram syndrome. Ophthalmic Genetics. 40: 34-38 |