Cecinio C. Ronquillo, Ph.D.
Affiliations: | 2013 | Neuroscience | University of Utah, Salt Lake City, UT |
Area:
Ophthalmology, Neuroscience Biology, Molecular BiologyGoogle:
"Cecinio Ronquillo"Parents
Sign in to add mentor| Wolfgang Baehr | grad student | 2013 | University of Utah | |
| (Functional and morphological studies of an in vivo loss-of-function mouse model of nephrocystin-5: Insights into the retina-renal dystrophy, Senior-Loken syndrome.) | ||||
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Publications
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| Parra MM, Spoth E, Ronquillo CC, et al. (2022) Multimodal Retinal Imaging Findings in Two Cousins With VCAN-Related Vitreoretinopathy or Wagner Disease. Ophthalmic Surgery, Lasers & Imaging Retina. 53: 639-643 |
| Ronquillo CC, Sauer L, Morgan D, et al. (2019) ABSENCE OF MACULAR DEGENERATION IN A PATIENT WITH ACERULOPLASMINEMIA. Retina (Philadelphia, Pa.) |
| Ronquillo CC, Wegner K, Calvo CM, et al. (2018) Genetic Penetrance of Macular Telangiectasia Type 2. Jama Ophthalmology |
| Ronquillo CC, Hanke-Gogokhia C, Revelo MP, et al. (2016) Ciliopathy-associated IQCB1/NPHP5 protein is required for mouse photoreceptor outer segment formation. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology |
| Rao KN, Zhang W, Li L, et al. (2016) Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGR. Human Molecular Genetics |
| Jiang L, Wei Y, Ronquillo CC, et al. (2015) Heterotrimeric kinesin-2 (KIF3) mediates transition zone and axoneme formation of mouse photoreceptors. The Journal of Biological Chemistry. 290: 12765-78 |
| Ronquillo CC, Bernstein PS, Baehr W. (2012) Senior-Løken syndrome: a syndromic form of retinal dystrophy associated with nephronophthisis. Vision Research. 75: 88-97 |
| Tong Z, Yang Z, Patel S, et al. (2008) Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications. Proceedings of the National Academy of Sciences of the United States of America. 105: 6998-7003 |