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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2017 | 1 |
2018 | 1 |
2021 | 1 |
2022 | 2 |
2023 | 2 |
2024 | 1 |
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CRISPR-Cas9-Mediated Gene Therapy in Neurological Disorders.
Mol Neurobiol. 2022 Feb;59(2):968-982. doi: 10.1007/s12035-021-02638-w. Epub 2021 Nov 23.
Mol Neurobiol. 2022.
PMID: 34813019
Review.
Knockout of CTNNB1 by CRISPR-Cas9 technology inhibits cell proliferation through the Wnt/β-catenin signaling pathway.
Guan L, Zhu S, Han Y, Yang C, Liu Y, Qiao L, Li X, Li H, Lin J.
Guan L, et al.
Biotechnol Lett. 2018 Mar;40(3):501-508. doi: 10.1007/s10529-017-2491-2. Epub 2017 Dec 16.
Biotechnol Lett. 2018.
PMID: 29249062
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CRISPR-Cas9-Mediated NPC1 Gene Deletion Enhances HEK 293 T Cell Adhesion by Regulating E-Cadherin.
Jia Z, Yang M, Zhao Y, Li X, Yang C, Qiao L, Li H, Du J, Lin J, Guan L.
Jia Z, et al.
Mol Biotechnol. 2023 Feb;65(2):252-262. doi: 10.1007/s12033-022-00503-2. Epub 2022 May 19.
Mol Biotechnol. 2023.
PMID: 35587334
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Npc1 gene mutation abnormally activates the classical Wnt signalling pathway in mouse kidneys and promotes renal fibrosis.
Guan L, Jia Z, Xu K, Yang M, Li X, Qiao L, Liu Y, Lin J.
Guan L, et al.
Anim Genet. 2024 Feb;55(1):99-109. doi: 10.1111/age.13381. Epub 2023 Dec 12.
Anim Genet. 2024.
PMID: 38087834
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