Shu Y - Search Results

1

Treatment of autosomal recessive hearing loss via in vivo CRISPR/Cas9-mediated optimized homology-directed repair in mice.

Gu X, Hu X, Wang D, Xu Z, Wang F, Li D, Li GL, Yang H, Li H, Zuo E, Shu Y. Gu X, et al. Among authors: shu y. Cell Res. 2022 Jul;32(7):699-702. doi: 10.1038/s41422-022-00624-y. Epub 2022 Feb 23. Cell Res. 2022. PMID: 35197607 Free PMC article. No abstract available.

2

Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes.

Shu Y, Tao Y, Wang Z, Tang Y, Li H, Dai P, Gao G, Chen ZY. Shu Y, et al. Hum Gene Ther. 2016 Sep;27(9):687-99. doi: 10.1089/hum.2016.053. Epub 2016 Jun 24. Hum Gene Ther. 2016. PMID: 27342665 Free PMC article.

3

Mammalian Cochlear Hair Cell Regeneration and Ribbon Synapse Reformation.

Lu X, Shu Y, Tang M, Li H. Lu X, et al. Among authors: shu y. Neural Plast. 2016;2016:2523458. doi: 10.1155/2016/2523458. Epub 2016 Dec 29. Neural Plast. 2016. PMID: 28119785 Free PMC article. Review.

4

Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents.

Gao X, Tao Y, Lamas V, Huang M, Yeh WH, Pan B, Hu YJ, Hu JH, Thompson DB, Shu Y, Li Y, Wang H, Yang S, Xu Q, Polley DB, Liberman MC, Kong WJ, Holt JR, Chen ZY, Liu DR. Gao X, et al. Among authors: shu y. Nature. 2018 Jan 11;553(7687):217-221. doi: 10.1038/nature25164. Epub 2017 Dec 20. Nature. 2018. PMID: 29258297 Free PMC article.

5

[Analysis and treatment of postoperative blockage of tympanic ventilation tubes].

Shu YL, Li QZ, Li HW. Shu YL, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 May 5;31(9):697-699. doi: 10.13201/j.issn.1001-1781.2017.09.012. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017. PMID: 29871350 Chinese.

6

Transduction of Adeno-Associated Virus Vectors Targeting Hair Cells and Supporting Cells in the Neonatal Mouse Cochlea.

Gu X, Chai R, Guo L, Dong B, Li W, Shu Y, Huang X, Li H. Gu X, et al. Among authors: shu y. Front Cell Neurosci. 2019 Jan 24;13:8. doi: 10.3389/fncel.2019.00008. eCollection 2019. Front Cell Neurosci. 2019. PMID: 30733670 Free PMC article.

7

A humanized mouse model, demonstrating progressive hearing loss caused by MYO6 p.C442Y, is inherited in a semi-dominant pattern.

Wang J, Shen J, Guo L, Cheng C, Chai R, Shu Y, Li H. Wang J, et al. Among authors: shu y. Hear Res. 2019 Aug;379:79-88. doi: 10.1016/j.heares.2019.04.014. Epub 2019 Apr 26. Hear Res. 2019. PMID: 31103816

8

The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis.

Shu Y, Wang L, Cheng X, Tangshewinsirikul C, Shi W, Yuan Y, Yan Z, Li H, Shen J, Chen B, Zou W. Shu Y, et al. J Genet Genomics. 2019 Sep 20;46(9):445-449. doi: 10.1016/j.jgg.2019.09.003. Epub 2019 Sep 27. J Genet Genomics. 2019. PMID: 31628072 No abstract available.

9

Screened AAV variants permit efficient transduction access to supporting cells and hair cells.

Hu X, Wang J, Yao X, Xiao Q, Xue Y, Wang S, Shi L, Shu Y, Li H, Yang H. Hu X, et al. Among authors: shu y. Cell Discov. 2019 Oct 15;5:49. doi: 10.1038/s41421-019-0115-9. eCollection 2019. Cell Discov. 2019. PMID: 31636961 Free PMC article. No abstract available.

10

Prevention of acquired sensorineural hearing loss in mice by in vivo Htra2 gene editing.

Gu X, Wang D, Xu Z, Wang J, Guo L, Chai R, Li G, Shu Y, Li H. Gu X, et al. Among authors: shu y. Genome Biol. 2021 Mar 22;22(1):86. doi: 10.1186/s13059-021-02311-4. Genome Biol. 2021. PMID: 33752742 Free PMC article.

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