Wang D - Search Results

1

Engineering of the AAV-Compatible Hair Cell-Specific Small-Size Myo15 Promoter for Gene Therapy in the Inner Ear.

Hu SW, Lv J, Wang Z, Tang H, Wang H, Wang F, Wang D, Zhang J, Zhang L, Cao Q, Chen Y, Gao Z, Han Y, Wang W, Li GL, Shu Y, Li H. Hu SW, et al. Among authors: wang h, wang w, wang f, wang z, wang d. Research (Wash D C). 2024 Apr 25;7:0341. doi: 10.34133/research.0341. eCollection 2024. Research (Wash D C). 2024. PMID: 38665848 Free PMC article.

2

Effect of the house dust mite allergen Der p 1 on tryptase release from human mast cells.

Wang DQ, Shen YY, Xu JH, Tang H. Wang DQ, et al. Genet Mol Res. 2016 Jul 14;15(2). doi: 10.4238/gmr.15028284. Genet Mol Res. 2016. PMID: 27421012 Free article.

3

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: wang j, wang d. Genome Biol. 2021 Mar 22;22(1):86. doi: 10.1186/s13059-021-02311-4. Genome Biol. 2021. PMID: 33752742 Free PMC article.

4

Gene editing in a Myo6 semi-dominant mouse model rescues auditory function.

Xue Y, Hu X, Wang D, Li D, Li Y, Wang F, Huang M, Gu X, Xu Z, Zhou J, Wang J, Chai R, Shen J, Chen ZY, Li GL, Yang H, Li H, Zuo E, Shu Y. Xue Y, et al. Among authors: wang f, wang j, wang d. Mol Ther. 2022 Jan 5;30(1):105-118. doi: 10.1016/j.ymthe.2021.06.015. Epub 2021 Jun 24. Mol Ther. 2022. PMID: 34174443 Free PMC article.

5

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: wang f, wang d. 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.

6

Preventing autosomal-dominant hearing loss in Bth mice with CRISPR/CasRx-based RNA editing.

Zheng Z, Li G, Cui C, Wang F, Wang X, Xu Z, Guo H, Chen Y, Tang H, Wang D, Huang M, Chen ZY, Huang X, Li H, Li GL, Hu X, Shu Y. Zheng Z, et al. Among authors: wang x, wang f, wang d. Signal Transduct Target Ther. 2022 Mar 14;7(1):79. doi: 10.1038/s41392-022-00893-4. Signal Transduct Target Ther. 2022. PMID: 35283480 Free PMC article.

7

Rescue of mis-splicing of a common SLC26A4 mutant associated with sensorineural hearing loss by antisense oligonucleotides.

Feng P, Xu Z, Chen J, Liu M, Zhao Y, Wang D, Han L, Wang L, Wan B, Xu X, Li D, Shu Y, Hua Y. Feng P, et al. Among authors: wang l, wang d. Mol Ther Nucleic Acids. 2022 Mar 19;28:280-292. doi: 10.1016/j.omtn.2022.03.015. eCollection 2022 Jun 14. Mol Ther Nucleic Acids. 2022. PMID: 35433113 Free PMC article.

8

A humanized murine model, demonstrating dominant progressive hearing loss caused by a novel KCNQ4 mutation (p.G228D) from a large Chinese family.

Cui C, Zhang L, Qian F, Chen Y, Huang B, Wang F, Wang D, Lv J, Wang X, Yan Z, Guo L, Li GL, Shu Y, Liu D, Li H. Cui C, et al. Among authors: wang x, wang f, wang d. Clin Genet. 2022 Aug;102(2):149-154. doi: 10.1111/cge.14164. Epub 2022 May 28. Clin Genet. 2022. PMID: 35599357

9

Structural insights into Cas9 mismatch: promising for development of high-fidelity Cas9 variants.

Tang H, Wang D, Shu Y. Tang H, et al. Among authors: wang d. Signal Transduct Target Ther. 2022 Aug 4;7(1):271. doi: 10.1038/s41392-022-01139-z. Signal Transduct Target Ther. 2022. PMID: 35927241 Free PMC article. No abstract available.

10

Precise detection of CRISPR-Cas9 editing in hair cells in the treatment of autosomal dominant hearing loss.

Cui C, Wang D, Huang B, Wang F, Chen Y, Lv J, Zhang L, Han L, Liu D, Chen ZY, Li GL, Li H, Shu Y. Cui C, et al. Among authors: wang f, wang d. Mol Ther Nucleic Acids. 2022 Jul 20;29:400-412. doi: 10.1016/j.omtn.2022.07.016. eCollection 2022 Sep 13. Mol Ther Nucleic Acids. 2022. PMID: 36035752 Free PMC article.

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