Astra Dinculescu, Ph.D.
Affiliations: | 2002 | University of Florida, Gainesville, Gainesville, FL, United States |
Area:
Molecular BiologyGoogle:
"Astra Dinculescu"Mean distance: (not calculated yet)
Parents
Sign in to add mentorNigel G. J. Richards | grad student | 2002 | UF Gainesville | |
(Rhodopsin binding to visual arrestin: An insertional mutagenesis and immunochemical analysis.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Xu L, Ruddick WN, Bolch SN, et al. (2022) Distinct phenotypic consequences of pathogenic C1QTNF5 mutants associated with late-onset retinal degeneration. The American Journal of Pathology |
Nelson TS, Simpson C, Dyka FM, et al. (2022) A modified arrestin1 increases lactate production in the retina and slows retinal degeneration. Human Gene Therapy |
Dinculescu A, Link BA, Saperstein DA. (2021) Retinal Gene Therapy for Usher Syndrome: Current Developments, Challenges, and Perspectives. International Ophthalmology Clinics. 61: 109-124 |
Simpson CP, Bolch SN, Zhu P, et al. (2019) Systemic Delivery of Genes to Retina Using Adeno-Associated Viruses. Advances in Experimental Medicine and Biology. 1185: 109-112 |
Xu L, Bolch SN, Santiago CP, et al. (2019) Clarin-1 expression in adult mouse and human retina highlights a role of Müller glia in Usher syndrome. The Journal of Pathology |
Chekuri A, Sahu B, Chavali VRM, et al. (2018) The long-term effects of gene therapy in a novel mouse model of human MFRP-associated retinopathy. Human Gene Therapy |
Deng WT, Kolandaivelu S, Dinculescu A, et al. (2018) Cone Phosphodiesterase-6γ' Subunit Augments Cone PDE6 Holoenzyme Assembly and Stability in a Mouse Model Lacking Both Rod and Cone PDE6 Catalytic Subunits. Frontiers in Molecular Neuroscience. 11: 233 |
Dinculescu A, Dyka FM, Min SH, et al. (2018) Co-Expression of Wild-Type and Mutant S163R C1QTNF5 in Retinal Pigment Epithelium. Advances in Experimental Medicine and Biology. 1074: 61-66 |
Geng R, Omar A, Gopal SR, et al. (2017) Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III. Scientific Reports. 7: 13480 |
Mowat FM, Occelli LM, Bartoe JT, et al. (2017) Gene Therapy in a Large Animal Model of PDE6A-Retinitis Pigmentosa. Frontiers in Neuroscience. 11: 342 |