Catherine Morgans

Physiology and Pharmocology Oregon Health and Science University, Portland, OR 
The molecular events underlying synaptic transmissions in the retina
"Catherine Morgans"


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Gabriel Enrique Romero research assistant 2014-2014 OHSU (Neurotree)
Colin Wakeham grad student 2016-2022 OHSU (Neurotree)
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Yang P, Lockard R, Titus H, et al. (2020) Suppression of cGMP-Dependent Photoreceptor Cytotoxicity With Mycophenolate Is Neuroprotective in Murine Models of Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 61: 25
Varin J, Reynolds MM, Bouzidi N, et al. (2020) Identification and characterization of novel TRPM1 autoantibodies from serum of patients with melanoma-associated retinopathy. Plos One. 15: e0231750
Webster CM, Tworig J, Caval-Holme F, et al. (2020) Steroid activation of TRPM3 channels modulates spontaneous synaptic activity but not retinal waves in the developing retina. Eneuro
Wakeham CM, Ren G, Morgans CW. (2019) Expression and distribution of trophoblast glycoprotein in the mouse retina. The Journal of Comparative Neurology
Wakeham CM, Wilmarth PA, Cunliffe JM, et al. (2019) Identification of PKCα-dependent phosphoproteins in mouse retina. Journal of Proteomics. 103423
Guimarães-Souza EM, Perche O, Morgans CW, et al. (2015) Fragile X Mental Retardation Protein expression in the retina is regulated by light. Experimental Eye Research. 146: 72-82
Xiong WH, Pang JJ, Pennesi ME, et al. (2015) The Effect of PKCα on the Light Response of Rod Bipolar Cells in the Mouse Retina. Investigative Ophthalmology & Visual Science. 56: 4961-74
Neuillé M, Morgans CW, Cao Y, et al. (2015) LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation. The European Journal of Neuroscience. 42: 1966-75
Brown RL, Xiong WH, Peters JH, et al. (2015) TRPM3 expression in mouse retina. Plos One. 10: e0117615
Romero GE, Lockridge AD, Morgans CW, et al. (2014) The postnatal development of D-serine in the retinas of two mouse strains, including a mutant mouse with a deficiency in D-amino acid oxidase and a serine racemase knockout mouse. Acs Chemical Neuroscience. 5: 848-54
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