Astra Dinculescu, Ph.D.

Affiliations: 
2002 University of Florida, Gainesville, Gainesville, FL, United States 
Area:
Molecular Biology
Google:
"Astra Dinculescu"
Mean distance: (not calculated yet)
 

Parents

Sign in to add mentor
Nigel G. J. Richards grad student 2002 UF Gainesville
 (Rhodopsin binding to visual arrestin: An insertional mutagenesis and immunochemical analysis.)
BETA: Related publications

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
See more...