R56 EY010609/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1996	1
2003	2
2004	3
2005	2
2006	5
2007	3
2008	4
2009	2
2010	6
2011	4
2012	6
2013	3
2014	4
2015	2
2016	1
2017	1
2018	2
2019	1
2020	1
2021	1
2022	2
2023	4
2024	1

1

Gene therapy for PRPH2-associated ocular disease: challenges and prospects.

Conley SM, Naash MI. Conley SM, et al. Cold Spring Harb Perspect Med. 2014 Aug 28;4(11):a017376. doi: 10.1101/cshperspect.a017376. Cold Spring Harb Perspect Med. 2014. PMID: 25167981 Free PMC article. Review.

2

Nanoparticles for retinal gene therapy.

Conley SM, Naash MI. Conley SM, et al. Prog Retin Eye Res. 2010 Sep;29(5):376-97. doi: 10.1016/j.preteyeres.2010.04.004. Epub 2010 May 7. Prog Retin Eye Res. 2010. PMID: 20452457 Free PMC article. Review.

3

Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization.

Crane R, Tebbe L, Mwoyosvi ML, Al-Ubaidi MR, Naash MI. Crane R, et al. Commun Biol. 2023 Sep 12;6(1):933. doi: 10.1038/s42003-023-05296-x. Commun Biol. 2023. PMID: 37700068 Free PMC article.

4

Structural and functional relationships between photoreceptor tetraspanins and other superfamily members.

Conley SM, Stuck MW, Naash MI. Conley SM, et al. Cell Mol Life Sci. 2012 Apr;69(7):1035-47. doi: 10.1007/s00018-011-0736-0. Epub 2011 Jun 8. Cell Mol Life Sci. 2012. PMID: 21655915 Free PMC article. Review.

5

Novel molecular mechanisms for Prph2-associated pattern dystrophy.

Chakraborty D, Strayve DG, Makia MS, Conley SM, Kakahel M, Al-Ubaidi MR, Naash MI. Chakraborty D, et al. FASEB J. 2020 Jan;34(1):1211-1230. doi: 10.1096/fj.201901888R. Epub 2019 Nov 29. FASEB J. 2020. PMID: 31914632 Free PMC article.

6

ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims.

Lewis TR, Makia MS, Castillo CM, Hao Y, Al-Ubaidi MR, Skiba NP, Conley SM, Arshavsky VY, Naash MI. Lewis TR, et al. Elife. 2023 Nov 22;12:RP89444. doi: 10.7554/eLife.89444. Elife. 2023. PMID: 37991486 Free PMC article.

7

Differential distribution of proteins and lipids in detergent-resistant and detergent-soluble domains in rod outer segment plasma membranes and disks.

Elliott MH, Nash ZA, Takemori N, Fliesler SJ, McClellan ME, Naash MI. Elliott MH, et al. J Neurochem. 2008 Jan;104(2):336-52. doi: 10.1111/j.1471-4159.2007.04971.x. Epub 2007 Oct 18. J Neurochem. 2008. PMID: 17944869 Free PMC article.

8

Prph2 disease mutations lead to structural and functional defects in the RPE.

Tebbe L, Sakthivel H, Makia MS, Kakakhel M, Conley SM, Al-Ubaidi MR, Naash MI. Tebbe L, et al. FASEB J. 2022 May;36(5):e22284. doi: 10.1096/fj.202101562RR. FASEB J. 2022. PMID: 35344225 Free PMC article.

9

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

Ding XQ, Naash MI. Ding XQ, et al. 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.

10

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. Nat Commun. 2023 Feb 21;14(1):972. doi: 10.1038/s41467-023-36431-1. Nat Commun. 2023. PMID: 36810733 Free PMC article.

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