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
2025	0

1

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.

2

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.

3

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.

4

Downregulation of rhodopsin is an effective therapeutic strategy in ameliorating peripherin-2-associated inherited retinal disorders.

Rutan Woods CT, Makia MS, Lewis TR, Crane R, Zeibak S, Yu P, Kakakhel M, Castillo CM, Arshavsky VY, Naash MI, Al-Ubaidi MR. Rutan Woods CT, et al. Nat Commun. 2024 Jun 4;15(1):4756. doi: 10.1038/s41467-024-48846-5. Nat Commun. 2024. PMID: 38834544 Free PMC article.

5

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.

6

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.

7

AAV and compacted DNA nanoparticles for the treatment of retinal disorders: challenges and future prospects.

Han Z, Conley SM, Naash MI. Han Z, et al. Invest Ophthalmol Vis Sci. 2011 May 10;52(6):3051-9. doi: 10.1167/iovs.10-6916. Invest Ophthalmol Vis Sci. 2011. PMID: 21558483 Free PMC article. Review.

8

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.

9

Initiation of rod outer segment disc formation requires RDS.

Chakraborty D, Conley SM, Al-Ubaidi MR, Naash MI. Chakraborty D, et al. PLoS One. 2014 Jun 4;9(6):e98939. doi: 10.1371/journal.pone.0098939. eCollection 2014. PLoS One. 2014. PMID: 24897172 Free PMC article.

10

The K153Del PRPH2 mutation differentially impacts photoreceptor structure and function.

Chakraborty D, Conley SM, Zulliger R, Naash MI. Chakraborty D, et al. Hum Mol Genet. 2016 Aug 15;25(16):3500-3514. doi: 10.1093/hmg/ddw193. Epub 2016 Jun 29. Hum Mol Genet. 2016. PMID: 27365499 Free PMC article.

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