Wang D - Search Results

1

AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial.

Lv J, Wang H, Cheng X, Chen Y, Wang D, Zhang L, Cao Q, Tang H, Hu S, Gao K, Xun M, Wang J, Wang Z, Zhu B, Cui C, Gao Z, Guo L, Yu S, Jiang L, Yin Y, Zhang J, Chen B, Wang W, Chai R, Chen ZY, Li H, Shu Y. Lv J, et al. Among authors: wang h, wang w, wang j, wang z, wang d. Lancet. 2024 May 25;403(10441):2317-2325. doi: 10.1016/S0140-6736(23)02874-X. Epub 2024 Jan 24. Lancet. 2024. PMID: 38280389 Clinical Trial.

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

An episomal vector-based CRISPR/Cas9 system for highly efficient gene knockout in human pluripotent stem cells.

Xie Y, Wang D, Lan F, Wei G, Ni T, Chai R, Liu D, Hu S, Li M, Li D, Wang H, Wang Y. Xie Y, et al. Among authors: wang h, wang y, wang d. Sci Rep. 2017 May 24;7(1):2320. doi: 10.1038/s41598-017-02456-y. Sci Rep. 2017. PMID: 28539611 Free PMC article.

4

Author Correction: An episomal vector-based CRISPR/Cas9 system for highly efficient gene knockout in human pluripotent stem cells.

Xie Y, Wang D, Lan F, Wei G, Ni T, Chai R, Liu D, Hu S, Li M, Li D, Wang H, Wang Y. Xie Y, et al. Among authors: wang h, wang y, wang d. Sci Rep. 2018 Dec 12;8(1):17900. doi: 10.1038/s41598-018-36738-w. Sci Rep. 2018. PMID: 30538257 Free PMC article.

5

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.

6

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.

7

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.

8

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.

9

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.

10

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

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