Liu X - Search Results

1

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss.

Dai P, Li Q, Huang D, Yuan Y, Kang D, Miller DT, Shao H, Zhu Q, He J, Yu F, Liu X, Han B, Yuan H, Platt OS, Han D, Wu BL. Dai P, et al. Among authors: liu x. Genet Med. 2008 Aug;10(8):586-92. doi: 10.1097/gim.0b013e31817d2ef1. Genet Med. 2008. PMID: 18641518

2

[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: liu x. 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.

3

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.

Dai P, Yuan Y, Huang D, Qian Y, Liu X, Han D, Yuan H, Wang X, Young WY, Guan MX. Dai P, et al. Among authors: liu x. Biochem Biophys Res Commun. 2006 Sep 15;348(1):200-5. doi: 10.1016/j.bbrc.2006.07.031. Epub 2006 Jul 17. Biochem Biophys Res Commun. 2006. PMID: 16875663

4

The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.

Han D, Dai P, Zhu Q, Liu X, Huang D, Yuan Y, Yuan H, Wang X, Qian Y, Young WY, Guan MX. Han D, et al. Among authors: liu x. Biochem Biophys Res Commun. 2007 Jun 1;357(2):554-60. doi: 10.1016/j.bbrc.2007.03.199. Epub 2007 Apr 9. Biochem Biophys Res Commun. 2007. PMID: 17434445

5

[GJB6 gene mutation analysis in Chinese nonsyndromic deaf population].

Yuan Y, Huang D, Dai P, Zhu Q, Liu X, Wang G, Li Q, Wu B. Yuan Y, et al. Among authors: liu x. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Jan;21(1):3-6. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17438853 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. Among authors: liu x. 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. Among authors: liu x. 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

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. Among authors: liu x. 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

9

[Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China].

Dai P, Yuan YY, Kang DY, Li Q, Zhu QW, Zhang X, Liu LX, Liu X, Huang DL. Dai P, et al. Among authors: liu x, liu lx. Zhonghua Yi Xue Za Zhi. 2007 Sep 25;87(36):2521-5. Zhonghua Yi Xue Za Zhi. 2007. PMID: 18067822 Chinese.

10

[Mutation of GJB2 gene in nonsyndromic hearing impairment patients: analysis of 1190 cases].

Yu F, Han DY, Dai P, Kang DY, Zhang X, Liu X, Zhu QW, Yuan YY, Sun Q, Xue DD, Li M, Liu J, Yuan HJ, Yang WY. Yu F, et al. Among authors: liu j, liu x. Zhonghua Yi Xue Za Zhi. 2007 Oct 30;87(40):2814-9. Zhonghua Yi Xue Za Zhi. 2007. PMID: 18167282 Chinese.

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