Sharon D - Search Results

1

A pipeline for identifying guide RNA sequences that promote RNA editing of nonsense mutations that cause inherited retinal diseases.

Schneider N, Steinberg R, Ben-David A, Valensi J, David-Kadoch G, Rosenwasser Z, Banin E, Levanon EY, Sharon D, Ben-Aroya S. Schneider N, et al. Among authors: sharon d. Mol Ther Nucleic Acids. 2024 Jan 30;35(1):102130. doi: 10.1016/j.omtn.2024.102130. eCollection 2024 Mar 12. Mol Ther Nucleic Acids. 2024. PMID: 38375504 Free PMC article.

2

Novel USH2A mutations in Israeli patients with retinitis pigmentosa and Usher syndrome type 2.

Kaiserman N, Obolensky A, Banin E, Sharon D. Kaiserman N, et al. Among authors: sharon d. Arch Ophthalmol. 2007 Feb;125(2):219-24. doi: 10.1001/archopht.125.2.219. Arch Ophthalmol. 2007. PMID: 17296898

3

A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa.

Banin E, Mizrahi-Meissonnier L, Neis R, Silverstein S, Magyar I, Abeliovich D, Roepman R, Berger W, Rosenberg T, Sharon D. Banin E, et al. Among authors: sharon d. Am J Med Genet A. 2007 Jun 1;143A(11):1150-8. doi: 10.1002/ajmg.a.31642. Am J Med Genet A. 2007. PMID: 17480003

4

A complex expression pattern of Pax6 in the pigeon retina.

Bandah D, Swissa T, Ben-Shlomo G, Banin E, Ofri R, Sharon D. Bandah D, et al. Among authors: sharon d. Invest Ophthalmol Vis Sci. 2007 Jun;48(6):2503-9. doi: 10.1167/iovs.06-1014. Invest Ophthalmol Vis Sci. 2007. PMID: 17525177

5

Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like disease.

Beit-Ya'acov A, Mizrahi-Meissonnier L, Obolensky A, Landau C, Blumenfeld A, Rosenmann A, Banin E, Sharon D. Beit-Ya'acov A, et al. Among authors: sharon d. Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4308-14. doi: 10.1167/iovs.07-0244. Invest Ophthalmol Vis Sci. 2007. PMID: 17724221

6

A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.

Auslender N, Sharon D, Abbasi AH, Garzozi HJ, Banin E, Ben-Yosef T. Auslender N, et al. Among authors: sharon d. Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5431-8. doi: 10.1167/iovs.07-0736. Invest Ophthalmol Vis Sci. 2007. PMID: 18055789

7

A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia.

Bandah D, Rosenmann A, Blumenfeld A, Averbukh E, Banin E, Sharon D. Bandah D, et al. Among authors: sharon d. Mol Vis. 2008 Jan 28;14:142-5. Mol Vis. 2008. PMID: 18334930 Free PMC article.

8

The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients.

Bandah D, Merin S, Ashhab M, Banin E, Sharon D. Bandah D, et al. Among authors: sharon d. Arch Ophthalmol. 2009 Mar;127(3):297-302. doi: 10.1001/archophthalmol.2008.615. Arch Ophthalmol. 2009. PMID: 19273793

9

Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array.

Mizrahi-Meissonnier L, Merin S, Banin E, Sharon D. Mizrahi-Meissonnier L, et al. Among authors: sharon d. Invest Ophthalmol Vis Sci. 2010 Aug;51(8):3884-92. doi: 10.1167/iovs.09-4592. Epub 2010 Mar 10. Invest Ophthalmol Vis Sci. 2010. PMID: 20220053

10

Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli population.

Bandah-Rozenfeld D, Littink KW, Ben-Yosef T, Strom TM, Chowers I, Collin RW, den Hollander AI, van den Born LI, Zonneveld MN, Merin S, Banin E, Cremers FP, Sharon D. Bandah-Rozenfeld D, et al. Among authors: sharon d. Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4387-94. doi: 10.1167/iovs.09-4732. Epub 2010 Apr 7. Invest Ophthalmol Vis Sci. 2010. PMID: 20375346 Free article.

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