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[Inner hair cells isolation and morphological observation].
Yang S, Shen J, Yamashita T, Yang W, Gu R, Han D. Yang S, et al. Among authors: yang w. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2002 Dec;37(6):462-4. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2002. PMID: 12966811 Chinese.
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family.
Cheng J, Han DY, Dai P, Sun HJ, Tao R, Sun Q, Yan D, Qin W, Wang HY, Ouyang XM, Yang SZ, Cao JY, Feng GY, Du LL, Zhang YZ, Zhai SQ, Yang WY, Liu XZ, He L, Yuan HJ. Cheng J, et al. Among authors: yang sz, yang wy. Clin Genet. 2007 Nov;72(5):471-7. doi: 10.1111/j.1399-0004.2007.00889.x. Epub 2007 Sep 14. Clin Genet. 2007. PMID: 17868390
Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.
Cheng J, Zhu Y, He S, Lu Y, Chen J, Han B, Petrillo M, Wrzeszczynski KO, Yang S, Dai P, Zhai S, Han D, Zhang MQ, Li W, Liu X, Li H, Chen ZY, Yuan H. Cheng J, et al. Among authors: yang s. Am J Hum Genet. 2011 Jul 15;89(1):56-66. doi: 10.1016/j.ajhg.2011.05.027. Epub 2011 Jun 30. Am J Hum Genet. 2011. PMID: 21722859 Free PMC article.
[Cochlear implantation with pericanal electrode insertion technique].
Cui T, Jiang H, Chen X, Feng G, Zhang Z, Li F, Zhao C, Gao Z, Han D, Yang S, Dai P, Li J, Xi X, Ma X, Dong Y, Yu P. Cui T, et al. Among authors: yang s. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 May;25(10):457-9. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011. PMID: 21809558 Chinese.
53,793 results
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