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May Nour, Ph.D. - Publications

Affiliations: 
2003 University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States 
Area:
Neuroscience Biology, Pathology, Genetics
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10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2008 Nour M, Fliesler SJ, Naash MI. 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. PMID 18188937 DOI: 10.1007/978-0-387-74904-4_14  0.65
2007 Conley S, Nour M, Fliesler SJ, Naash MI. Late-onset cone photoreceptor degeneration induced by R172W mutation in Rds and partial rescue by gene supplementation. Investigative Ophthalmology & Visual Science. 48: 5397-407. PMID 18055786 DOI: 10.1167/Iovs.07-0663  0.704
2004 Naash MI, Wu TH, Chakraborty D, Fliesler SJ, Ding XQ, Nour M, Peachey NS, Lem J, Qtaishat N, Al-Ubaidi MR, Ripps H. Retinal abnormalities associated with the G90D mutation in opsin. The Journal of Comparative Neurology. 478: 149-63. PMID 15349976 DOI: 10.1002/Cne.20283  0.693
2004 Nour M, Ding XQ, Stricker H, Fliesler SJ, Naash MI. Modulating expression of peripherin/rds in transgenic mice: critical levels and the effect of overexpression. Investigative Ophthalmology & Visual Science. 45: 2514-21. PMID 15277471 DOI: 10.1167/Iovs.04-0065  0.592
2004 Ding XQ, Nour M, Ritter LM, Goldberg AF, Fliesler SJ, Naash MI. The R172W mutation in peripherin/rds causes a cone-rod dystrophy in transgenic mice. Human Molecular Genetics. 13: 2075-87. PMID 15254014 DOI: 10.1093/Hmg/Ddh211  0.701
2004 Nour M, Quiambao AB, Al-Ubaidi MR, Naash MI. Absence of functional and structural abnormalities associated with expression of EGFP in the retina. Investigative Ophthalmology & Visual Science. 45: 15-22. PMID 14691148 DOI: 10.1167/Iovs.03-0663  0.675
2004 Nour M, Naash MI, Fliesler SJ. 231. Supplementation of Peripherin/rds Rescues Mutation-Associated Rod and Cone Photoreceptor Defects in Transgenic Mice Molecular Therapy. 9. DOI: 10.1016/J.Ymthe.2004.06.179  0.624
2004 Naash MI, Wu TH, Chakraborty D, Fliesler SJ, Ding XQ, Nour M, Peachey NS, Lem J, Qtaishat N, Al-Ubaidi MR, Ripps H. 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. DOI: 10.1002/Cne.20373  0.539
2003 Nour M, Naash MI. 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. PMID 15180262 DOI: 10.1007/978-1-4615-0067-4_22  0.643
2003 Nour M, Quiambao AB, Peterson WM, Al-Ubaidi MR, Naash MI. 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. PMID 14507899 DOI: 10.1167/Iovs.03-0453  0.661
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