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Subretinal gene therapy delays vision loss in a Bardet-Biedl Syndrome type 10 mouse model.
Hsu Y, Bhattarai S, Thompson JM, Mahoney A, Thomas J, Mayer SK, Datta P, Garrison J, Searby CC, Vandenberghe LH, Seo S, Sheffield VC, Drack AV. Hsu Y, et al. Among authors: bhattarai s. Mol Ther Nucleic Acids. 2022 Dec 12;31:164-181. doi: 10.1016/j.omtn.2022.12.007. eCollection 2023 Mar 14. Mol Ther Nucleic Acids. 2022. PMID: 36700052 Free PMC article.
Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1.
Seo S, Mullins RF, Dumitrescu AV, Bhattarai S, Gratie D, Wang K, Stone EM, Sheffield V, Drack AV. Seo S, et al. Among authors: bhattarai s. Invest Ophthalmol Vis Sci. 2013 Sep 11;54(9):6118-32. doi: 10.1167/iovs.13-11673. Invest Ophthalmol Vis Sci. 2013. PMID: 23900607 Free PMC article.
BBS mutations modify phenotypic expression of CEP290-related ciliopathies.
Zhang Y, Seo S, Bhattarai S, Bugge K, Searby CC, Zhang Q, Drack AV, Stone EM, Sheffield VC. Zhang Y, et al. Among authors: bhattarai s. Hum Mol Genet. 2014 Jan 1;23(1):40-51. doi: 10.1093/hmg/ddt394. Epub 2013 Aug 13. Hum Mol Genet. 2014. PMID: 23943788 Free PMC article.
Vitritis in pediatric genetic retinal disorders.
Stunkel M, Bhattarai S, Kemerley A, Stone EM, Wang K, Mullins RF, Drack AV. Stunkel M, et al. Among authors: bhattarai s. Ophthalmology. 2015 Jan;122(1):192-9. doi: 10.1016/j.ophtha.2014.07.037. Epub 2014 Sep 10. Ophthalmology. 2015. PMID: 25217415 Free PMC article.
α2δ-4 Is Required for the Molecular and Structural Organization of Rod and Cone Photoreceptor Synapses.
Kerov V, Laird JG, Joiner ML, Knecht S, Soh D, Hagen J, Gardner SH, Gutierrez W, Yoshimatsu T, Bhattarai S, Puthussery T, Artemyev NO, Drack AV, Wong RO, Baker SA, Lee A. Kerov V, et al. Among authors: bhattarai s. J Neurosci. 2018 Jul 4;38(27):6145-6160. doi: 10.1523/JNEUROSCI.3818-16.2018. Epub 2018 Jun 6. J Neurosci. 2018. PMID: 29875267 Free PMC article.
499 results