Obolensky A[Author] - Search Results

Year	Number of Results
2003	3
2005	3
2006	1
2007	4
2008	3
2009	3
2010	3
2011	2
2012	1
2013	1
2014	3
2015	3
2016	3
2017	6
2018	7
2019	1
2020	3
2021	3
2022	3
2023	4
2024	0

1

Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa.

Matsevich C, Gopalakrishnan P, Chang N, Obolensky A, Beryozkin A, Salameh M, Kostic C, Sharon D, Arsenijevic Y, Banin E. Matsevich C, et al. Among authors: obolensky a. Mol Ther. 2023 Oct 4;31(10):2948-2961. doi: 10.1016/j.ymthe.2023.08.011. Epub 2023 Aug 14. Mol Ther. 2023. PMID: 37580905

2

A new mouse model for retinal degeneration due to Fam161a deficiency.

Beryozkin A, Matsevich C, Obolensky A, Kostic C, Arsenijevic Y, Wolfrum U, Banin E, Sharon D. Beryozkin A, et al. Among authors: obolensky a. Sci Rep. 2021 Jan 21;11(1):2030. doi: 10.1038/s41598-021-81414-1. Sci Rep. 2021. PMID: 33479377 Free PMC article.

3

Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice.

Abu-Diab A, Gopalakrishnan P, Matsevich C, de Jong M, Obolensky A, Khalaileh A, Salameh M, Ejzenberg A, Gross M, Banin E, Sharon D, Khateb S. Abu-Diab A, et al. Among authors: obolensky a. Transl Vis Sci Technol. 2023 Mar 1;12(3):3. doi: 10.1167/tvst.12.3.3. Transl Vis Sci Technol. 2023. PMID: 36857066 Free PMC article.

4

Outer retinal transduction by AAV2-7m8 following intravitreal injection in a sheep model of CNGA3 achromatopsia.

Ross M, Obolensky A, Averbukh E, Desrosiers M, Ezra-Elia R, Honig H, Yamin E, Rosov A, Dvir H, Gootwine E, Banin E, Dalkara D, Ofri R. Ross M, et al. Among authors: obolensky a. Gene Ther. 2022 Nov;29(10-11):624-635. doi: 10.1038/s41434-021-00306-1. Epub 2021 Dec 2. Gene Ther. 2022. PMID: 34853444

5

Retinal Structure and Function in a Knock-in Mouse Model for the FAM161A-p.Arg523∗ Human Nonsense Pathogenic Variant.

Matsevich C, Gopalakrishnan P, Obolensky A, Banin E, Sharon D, Beryozkin A. Matsevich C, et al. Among authors: obolensky a. Ophthalmol Sci. 2022 Oct 3;3(1):100229. doi: 10.1016/j.xops.2022.100229. eCollection 2023 Mar. Ophthalmol Sci. 2022. PMID: 36420180 Free PMC article.

6

Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.

Kimchi A, Khateb S, Wen R, Guan Z, Obolensky A, Beryozkin A, Kurtzman S, Blumenfeld A, Pras E, Jacobson SG, Ben-Yosef T, Newman H, Sharon D, Banin E. Kimchi A, et al. Among authors: obolensky a. Ophthalmology. 2018 May;125(5):725-734. doi: 10.1016/j.ophtha.2017.11.014. Epub 2017 Dec 22. Ophthalmology. 2018. PMID: 29276052

7

Characterization of physiological defects in adult SIRT6-/- mice.

Peshti V, Obolensky A, Nahum L, Kanfi Y, Rathaus M, Avraham M, Tinman S, Alt FW, Banin E, Cohen HY. Peshti V, et al. Among authors: obolensky a. PLoS One. 2017 Apr 27;12(4):e0176371. doi: 10.1371/journal.pone.0176371. eCollection 2017. PLoS One. 2017. PMID: 28448551 Free PMC article.

8

Ocular phenotype analysis of a family with biallelic mutations in the BEST1 gene.

Sharon D, Al-Hamdani S, Engelsberg K, Mizrahi-Meissonnier L, Obolensky A, Banin E, Sander B, Jensen H, Larsen M, Schatz P. Sharon D, et al. Among authors: obolensky a. Am J Ophthalmol. 2014 Mar;157(3):697-709.e1-2. doi: 10.1016/j.ajo.2013.12.010. Epub 2013 Dec 15. Am J Ophthalmol. 2014. PMID: 24345323

9

The biologic effects and the therapeutic mechanism of action of electric and electromagnetic field stimulation on bone and cartilage: new findings and a review of earlier work.

Haddad JB, Obolensky AG, Shinnick P. Haddad JB, et al. Among authors: obolensky ag. J Altern Complement Med. 2007 Jun;13(5):485-90. doi: 10.1089/acm.2007.5270. J Altern Complement Med. 2007. PMID: 17604552 Review.

10

A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans.

Khateb S, Kowalewski B, Bedoni N, Damme M, Pollack N, Saada A, Obolensky A, Ben-Yosef T, Gross M, Dierks T, Banin E, Rivolta C, Sharon D. Khateb S, et al. Among authors: obolensky a. Genet Med. 2018 Sep;20(9):1004-1012. doi: 10.1038/gim.2017.227. Epub 2018 Jan 4. Genet Med. 2018. PMID: 29300381 Free article.

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