Kang DY - Search Results

1

Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing.

Gao X, Zhu QY, Song YS, Wang GJ, Yuan YY, Xin F, Huang SS, Kang DY, Han MY, Guan LP, Zhang JG, Dai P. Gao X, et al. Among authors: kang dy. J Transl Med. 2013 Nov 9;11:284. doi: 10.1186/1479-5876-11-284. J Transl Med. 2013. PMID: 24206587 Free PMC article.

2

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.

Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX. Dai P, et al. Biochem Biophys Res Commun. 2006 Feb 3;340(1):194-9. doi: 10.1016/j.bbrc.2005.11.156. Biochem Biophys Res Commun. 2006. PMID: 16375862 Clinical Trial.

3

[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients].

Dai P, Yu F, Kang DY, Zhang X, Liu X, Mi WZ, Cao JY, Yuan HJ, Yang WY, Wu BL, Han DY. Dai P, et al. Among authors: kang dy. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005 Oct;40(10):769-73. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005. PMID: 16408730 Chinese.

4

[Genotypic analysis of familial dilated vestibular aqueduct syndrome].

Dai P, Han D, Cao J, Zhai S, Kang D, Liu X, Yuan H, Zhang X, Li M, Liu L, Feng B, Yang W, Wu B. Dai P, et al. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006 Feb;20(4):147-50. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006. PMID: 16711435 Chinese.

5

[Patients suffered from enlarged vestibular aqueduct syndrome in Chifeng deaf and dumb school detected by Pendred's syndrome gene hot spot mutation screening].

Dai P, Zhu XH, Yuan YY, Zhu QW, Teng GC, Zhang X, Liu LX, Wang JL, Feng B, Zhai SQ, Kang DY, Liu X, Huang DL. Dai P, et al. Among authors: kang dy. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2006 Jul;41(7):497-500. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2006. PMID: 17007371 Chinese.

6

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population.

Dai P, Yu F, Han B, Yuan Y, Li Q, Wang G, Liu X, He J, Huang D, Kang D, Zhang X, Yuan H, Schmitt E, Han D, Wong LJ. Dai P, et al. Genet Med. 2007 May;9(5):283-9. doi: 10.1097/gim.0b013e31804d2371. Genet Med. 2007. PMID: 17505205 Free article.

7

[Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China].

Zhu Q, Liu X, Han D, Kang D, Zhang X, Jin Z, Li M, Dai P. Zhu Q, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 May;21(10):460-2. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17650818 Chinese.

8

[Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families].

Dai P, Han B, Yuan YY, Jin ZC, Wang Y, Xiang Y, Yu F, Liu X, Wang GJ, Kang DY, Zhang X, Li M, Zhai SQ, Huang DL, Han DY. Dai P, et al. Among authors: kang dy. Zhonghua Yi Xue Za Zhi. 2007 Apr 24;87(16):1088-92. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17672986 Chinese.

9

Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.

Yuan H, Chen J, Liu X, Cheng J, Wang X, Yang L, Yang S, Cao J, Kang D, Dai P, Zhai S, Han D, Young WY, Guan MX. Yuan H, et al. Biochem Biophys Res Commun. 2007 Oct 12;362(1):94-100. doi: 10.1016/j.bbrc.2007.07.161. Epub 2007 Aug 8. Biochem Biophys Res Commun. 2007. PMID: 17698030

10

[Genetic counseling and instruction for deaf couples directed by genetic testing].

Han B, Dai P, Wang GJ, Kang DY, Zhang X, Yuan YY, Zhu QW, Jin ZC, Li M, Zhai SQ, Huang DL, Han DY. Han B, et al. Among authors: kang dy. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Jul;42(7):499-503. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17886676 Chinese.

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