Naash MI - Search Results

1

Mouse models of human retinal disease caused by expression of mutant rhodopsin. A valuable tool for the assessment of novel gene therapies.

Nour M, Naash MI. Nour M, et al. Among authors: naash mi. Adv Exp Med Biol. 2003;533:173-9. doi: 10.1007/978-1-4615-0067-4_22. Adv Exp Med Biol. 2003. PMID: 15180262 Review. No abstract available.

2

The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1.

Tebbe L, Mwoyosvi ML, Crane R, Makia MS, Kakakhel M, Cosgrove D, Al-Ubaidi MR, Naash MI. Tebbe L, et al. Among authors: naash mi. Nat Commun. 2023 Feb 21;14(1):972. doi: 10.1038/s41467-023-36431-1. Nat Commun. 2023. PMID: 36810733 Free PMC article.

3

P2Y(2) receptor agonist INS37217 enhances functional recovery after detachment caused by subretinal injection in normal and rds mice.

Nour M, Quiambao AB, Peterson WM, Al-Ubaidi MR, Naash MI. Nour M, et al. Among authors: naash mi. Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4505-14. doi: 10.1167/iovs.03-0453. Invest Ophthalmol Vis Sci. 2003. PMID: 14507899 Free PMC article.

4

Absence of functional and structural abnormalities associated with expression of EGFP in the retina.

Nour M, Quiambao AB, Al-Ubaidi MR, Naash MI. Nour M, et al. Among authors: naash mi. Invest Ophthalmol Vis Sci. 2004 Jan;45(1):15-22. doi: 10.1167/iovs.03-0663. Invest Ophthalmol Vis Sci. 2004. PMID: 14691148 Free PMC article.

5

Peripherin/rds in skate retina.

Naash MI, Ding XQ, Li C, O'Brien J, Al-Ubaidi MR. Naash MI, et al. Adv Exp Med Biol. 2003;533:377-83. doi: 10.1007/978-1-4615-0067-4_48. Adv Exp Med Biol. 2003. PMID: 15180288 No abstract available.

6

The R172W mutation in peripherin/rds causes a cone-rod dystrophy in transgenic mice.

Ding XQ, Nour M, Ritter LM, Goldberg AF, Fliesler SJ, Naash MI. Ding XQ, et al. Among authors: naash mi. Hum Mol Genet. 2004 Sep 15;13(18):2075-87. doi: 10.1093/hmg/ddh211. Epub 2004 Jul 14. Hum Mol Genet. 2004. PMID: 15254014

7

Modulating expression of peripherin/rds in transgenic mice: critical levels and the effect of overexpression.

Nour M, Ding XQ, Stricker H, Fliesler SJ, Naash MI. Nour M, et al. Among authors: naash mi. Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2514-21. doi: 10.1167/iovs.04-0065. Invest Ophthalmol Vis Sci. 2004. PMID: 15277471 Free PMC article.

8

Retinal abnormalities associated with the G90D mutation in opsin.

Naash MI, Wu TH, Chakraborty D, Fliesler SJ, Ding XQ, Nour M, Peachey NS, Lem J, Qtaishat N, Al-Ubaidi MR, Ripps H. Naash MI, et al. J Comp Neurol. 2004 Oct 11;478(2):149-63. doi: 10.1002/cne.20283. J Comp Neurol. 2004. PMID: 15349976

9

Light/dark translocation of alphatransducin in mouse photoreceptor cells expressing G90D mutant opsin.

Nash ZA, Naash MI. Nash ZA, et al. Among authors: naash mi. Adv Exp Med Biol. 2006;572:125-31. doi: 10.1007/0-387-32442-9_19. Adv Exp Med Biol. 2006. PMID: 17249565 Free PMC article. No abstract available.

10

Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

Ding XQ, Naash MI. Ding XQ, et al. Among authors: naash mi. Adv Exp Med Biol. 2006;572:141-6. doi: 10.1007/0-387-32442-9_21. Adv Exp Med Biol. 2006. PMID: 17249567 Free PMC article. Review. No abstract available.

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