May Nour, Ph.D.
Affiliations: | 2003 | University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States |
Area:
Neuroscience Biology, Pathology, GeneticsGoogle:
"May Nour"Mean distance: 30533.1
Parents
Sign in to add mentor| Muna Naash | grad student | 2003 | University of Oklahoma Health Sciences Center | |
| (Therapeutic intervention in mouse models of retinal degeneration.) | ||||
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Publications
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| Nour M, Fliesler SJ, Naash MI. (2008) Genetic supplementation of RDS alleviates a loss-of-function phenotype in C214S model of retinitis pigmentosa. Advances in Experimental Medicine and Biology. 613: 129-38 |
| Conley S, Nour M, Fliesler SJ, et al. (2007) Late-onset cone photoreceptor degeneration induced by R172W mutation in Rds and partial rescue by gene supplementation. Investigative Ophthalmology & Visual Science. 48: 5397-407 |
| Naash MI, Wu TH, Chakraborty D, et al. (2004) Retinal abnormalities associated with the G90D mutation in opsin. The Journal of Comparative Neurology. 478: 149-63 |
| Nour M, Ding XQ, Stricker H, et al. (2004) Modulating expression of peripherin/rds in transgenic mice: critical levels and the effect of overexpression. Investigative Ophthalmology & Visual Science. 45: 2514-21 |
| Ding XQ, Nour M, Ritter LM, et al. (2004) The R172W mutation in peripherin/rds causes a cone-rod dystrophy in transgenic mice. Human Molecular Genetics. 13: 2075-87 |
| Nour M, Quiambao AB, Al-Ubaidi MR, et al. (2004) Absence of functional and structural abnormalities associated with expression of EGFP in the retina. Investigative Ophthalmology & Visual Science. 45: 15-22 |
| Nour M, Naash MI, Fliesler SJ. (2004) 231. Supplementation of Peripherin/rds Rescues Mutation-Associated Rod and Cone Photoreceptor Defects in Transgenic Mice Molecular Therapy. 9 |
| Naash MI, Wu TH, Chakraborty D, et al. (2004) Erratum: Retinal abnormalities associated with the G90D mutation in opsin (The Journal of Comparative Neurology (2004) 478 (149-163)) The Journal of Comparative Neurology. 480 |
| Nour M, Naash MI. (2003) Mouse models of human retinal disease caused by expression of mutant rhodopsin. A valuable tool for the assessment of novel gene therapies. Advances in Experimental Medicine and Biology. 533: 173-9 |
| Nour M, Quiambao AB, Peterson WM, et al. (2003) P2Y(2) receptor agonist INS37217 enhances functional recovery after detachment caused by subretinal injection in normal and rds mice. Investigative Ophthalmology & Visual Science. 44: 4505-14 |