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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 2 |
Search Results
5 results
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Page 1
Blue cone monochromacy and gene therapy.
Vision Res. 2023 Jul;208:108221. doi: 10.1016/j.visres.2023.108221. Epub 2023 Mar 29.
Vision Res. 2023.
PMID: 37001420
Review.
Gene Therapy in Opn1mw-/-/Opn1sw-/- Mice and Implications for Blue Cone Monochromacy Patients with Deletion Mutations.
Ma X, Sechrest ER, Fajardo D, Zhu P, Dyka F, Wang Y, Lobanova E, Boye SE, Baehr W, Deng WT.
Ma X, et al.
Hum Gene Ther. 2022 Jul;33(13-14):708-718. doi: 10.1089/hum.2021.298. Epub 2022 May 16.
Hum Gene Ther. 2022.
PMID: 35272502
Free PMC article.
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Disease mechanisms of X-linked cone dystrophy caused by missense mutations in the red and green cone opsins.
Zhu P, Dyka F, Ma X, Yin L, Yu H, Baehr W, Hauswirth WW, Deng WT.
Zhu P, et al.
FASEB J. 2021 Oct;35(10):e21927. doi: 10.1096/fj.202101066R.
FASEB J. 2021.
PMID: 34547123
Free PMC article.
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Expression of red/green-cone opsin mutants K82E, P187S, M273K result in unique pathobiological perturbations to cone structure and function.
Sechrest ER, Barbera RJ, Ma X, Dyka F, Ahn J, Brothers BA, Cahill ME, Hall I, Baehr W, Deng WT.
Sechrest ER, et al.
Front Neurosci. 2024 Feb 12;18:1368089. doi: 10.3389/fnins.2024.1368089. eCollection 2024.
Front Neurosci. 2024.
PMID: 38410159
Free PMC article.
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Structural and functional rescue of cones carrying the most common cone opsin C203R missense mutation.
Sechrest ER, Ma X, Cahill ME, Barbera RJ, Wang Y, Deng WT.
Sechrest ER, et al.
JCI Insight. 2024 Jan 23;9(2):e172834. doi: 10.1172/jci.insight.172834.
JCI Insight. 2024.
PMID: 38060327
Free PMC article.
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