Shannon M. Conley, Ph.D.

Affiliations: 
2006 University of Arizona, Tucson, AZ 
Area:
Biomedical, Physiology, Ophthalmology
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"Shannon Conley"

Parents

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Muna Naash grad student (Neurotree)
W Daniel Stamer grad student 2006 University of Arizona
 (Selenium effects on the trabecular meshwork.)
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Publications

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Kakakhel M, Tebbe L, Makia MS, et al. (2020) Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survival. Proceedings of the National Academy of Sciences of the United States of America
Strayve D, Makia MM, Kakakhel M, et al. (2020) ROM1 contributes to phenotypic heterogeneity in PRPH2-associated retinal disease. Human Molecular Genetics
Genc AM, Makia MS, Sinha T, et al. (2020) Elimination of a Retinal Riboflavin Binding Protein Exacerbates Degeneration in a Model of Cone-Rod Dystrophy. Investigative Ophthalmology & Visual Science. 61: 17
Chakraborty D, Strayve DG, Makia MS, et al. (2020) Novel molecular mechanisms for Prph2-associated pattern dystrophy. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 34: 1211-1230
Conley SM, Al-Ubaidi MR, Naash MI. (2019) The Role of the Prph2 C-Terminus in Outer Segment Morphogenesis. Advances in Experimental Medicine and Biology. 1185: 495-499
Conley SM, Stuck MW, Watson JN, et al. (2018) Prph2 initiates outer segment morphogenesis but maturation requires Prph2/Rom1 oligomerization. Human Molecular Genetics
Agbaga MG, Merriman DK, Brush RS, et al. (2018) Differential Composition of DHA and Very Long Chain PUFAs in Rod and Cone Photoreceptors. Journal of Lipid Research
Zulliger R, Conley SM, Mwoyosvi ML, et al. (2018) Oligomerization of Prph2 and Rom1 is essential for photoreceptor outer segment formation. Human Molecular Genetics
Kelley RA, Conley SM, Makkia R, et al. (2018) DNA nanoparticles are safe and nontoxic in non-human primate eyes. International Journal of Nanomedicine. 13: 1361-1379
Conley SM, Stuck MW, Watson JN, et al. (2017) Rom1 converts Y141C-Prph2-associated pattern dystrophy to retinitis pigmentosa. Human Molecular Genetics
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