Wang H - Search Results

1

Preclinical Efficacy And Safety Evaluation of AAV-OTOF in DFNB9 Mouse Model And Nonhuman Primate.

Qi J, Zhang L, Tan F, Zhang Y, Zhou Y, Zhang Z, Wang H, Yu C, Jiang L, Liu J, Chen T, Wu L, Zhang S, Sun S, Sun S, Lu L, Wang Q, Chai R. Qi J, et al. Among authors: wang h, wang q. Adv Sci (Weinh). 2024 Jan;11(3):e2306201. doi: 10.1002/advs.202306201. Epub 2023 Nov 28. Adv Sci (Weinh). 2024. PMID: 38014592 Free PMC article.

2

Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han.

Li Q, Ji Y, Han B, Zong L, Lan L, Zhao Y, Wang H, Wang D, Wang Q. Li Q, et al. Among authors: wang h, wang d, wang q. Chin Med J (Engl). 2014;127(18):3233-7. Chin Med J (Engl). 2014. PMID: 25266519

3

Identification of Two Disease-causing Genes TJP2 and GJB2 in a Chinese Family with Unconditional Autosomal Dominant Nonsyndromic Hereditary Hearing Impairment.

Wang HY, Zhao YL, Liu Q, Yuan H, Gao Y, Lan L, Yu L, Wang DY, Guan J, Wang QJ. Wang HY, et al. Among authors: wang dy, wang qj. Chin Med J (Engl). 2015 Dec 20;128(24):3345-51. doi: 10.4103/0366-6999.171440. Chin Med J (Engl). 2015. PMID: 26668150 Free PMC article.

4

[Study of clinical characteristics and curative effects of sudden hearing loss patients with vertigo].

Gao Y, Wang D, Su Q, Wang H, Lan L, Yin Z, Yu L, Wu Z, Shan X, Xue X, Wang Q. Gao Y, et al. Among authors: wang h, wang d, wang q. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015 Jul;50(7):529-35. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015. PMID: 26695972 Chinese.

5

Understanding auditory neuropathy spectrum disorder: a systematic review in transgenic mouse models.

Wang L, Guan J, Wang H, Lan L, Zhang Q, Zong L, Du W, Xiong W, Li F, Wu K, Wang D, Wang Q. Wang L, et al. Among authors: wang h, wang d, wang q. Sci China Life Sci. 2016 May;59(5):480-6. doi: 10.1007/s11427-015-4985-2. Epub 2016 Jan 18. Sci China Life Sci. 2016. PMID: 26783139 Review.

6

[Advances in hereditary hearing loss caused by TMC1 mutations].

Wu K, Wang H, Wang Q. Wu K, et al. Among authors: wang h, wang q. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Mar;51(3):224-9. doi: 10.3760/cma.j.issn.1673-0860.2016.03.016. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016. PMID: 27033582 Chinese.

7

A novel dominant GJB2 (DFNA3) mutation in a Chinese family.

Wang H, Wu K, Yu L, Xie L, Xiong W, Wang D, Guan J, Wang Q. Wang H, et al. Among authors: wang d, wang q. Sci Rep. 2017 Jan 19;7:34425. doi: 10.1038/srep34425. Sci Rep. 2017. PMID: 28102197 Free PMC article.

8

Novel recessive PDZD7 biallelic mutations in two Chinese families with non-syndromic hearing loss.

Guan J, Wang H, Lan L, Wang L, Yang J, Xie L, Yin Z, Xiong W, Zhao L, Wang D, Wang Q. Guan J, et al. Among authors: wang h, wang l, wang d, wang q. Am J Med Genet A. 2018 Jan;176(1):99-106. doi: 10.1002/ajmg.a.38477. Epub 2017 Oct 19. Am J Med Genet A. 2018. PMID: 29048736 Free PMC article.

9

Delivery of Adeno-Associated Virus Vectors in Adult Mammalian Inner-Ear Cell Subtypes Without Auditory Dysfunction.

Tao Y, Huang M, Shu Y, Ruprecht A, Wang H, Tang Y, Vandenberghe LH, Wang Q, Gao G, Kong WJ, Chen ZY. Tao Y, et al. Among authors: wang h, wang q. Hum Gene Ther. 2018 Apr;29(4):492-506. doi: 10.1089/hum.2017.120. Epub 2018 Jan 22. Hum Gene Ther. 2018. PMID: 29130354 Free PMC article.

10

Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype-phenotype review for DFNA11.

Li L, Yuan H, Wang H, Guan J, Lan L, Wang D, Zong L, Liu Q, Han B, Huang D, Wang Q. Li L, et al. Among authors: wang h, wang d, wang q. Acta Otolaryngol. 2018 May;138(5):463-470. doi: 10.1080/00016489.2017.1397743. Epub 2018 Feb 5. Acta Otolaryngol. 2018. PMID: 29400105

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