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Year | Number of Results |
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2015 | 1 |
2016 | 1 |
2017 | 1 |
2019 | 1 |
2024 | 0 |
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Calpain-5 gene expression in the mouse eye and brain.
BMC Res Notes. 2017 Nov 21;10(1):602. doi: 10.1186/s13104-017-2927-8.
BMC Res Notes. 2017.
PMID: 29157313
Free PMC article.
CAPN5 genetic inactivation phenotype supports therapeutic inhibition trials.
Wert KJ, Koch SF, Velez G, Hsu CW, Mahajan M, Bassuk AG, Tsang SH, Mahajan VB.
Wert KJ, et al.
Hum Mutat. 2019 Dec;40(12):2377-2392. doi: 10.1002/humu.23894. Epub 2019 Aug 26.
Hum Mutat. 2019.
PMID: 31403230
Free PMC article.
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Precision Medicine: Genetic Repair of Retinitis Pigmentosa in Patient-Derived Stem Cells.
Bassuk AG, Zheng A, Li Y, Tsang SH, Mahajan VB.
Bassuk AG, et al.
Sci Rep. 2016 Jan 27;6:19969. doi: 10.1038/srep19969.
Sci Rep. 2016.
PMID: 26814166
Free PMC article.
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CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model.
Wert KJ, Bassuk AG, Wu WH, Gakhar L, Coglan D, Mahajan M, Wu S, Yang J, Lin CS, Tsang SH, Mahajan VB.
Wert KJ, et al.
Hum Mol Genet. 2015 Aug 15;24(16):4584-98. doi: 10.1093/hmg/ddv189. Epub 2015 May 20.
Hum Mol Genet. 2015.
PMID: 25994508
Free PMC article.
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