Yuan HJ - Search Results

1

[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: yuan hj. 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.

2

[Screening for mitochondrial 1555(G) mutation in patients with aminoglycoside antibiotic-induced deafness].

Yuan H, Jiang S, Yang W, Guo W, Cao J, Dai P. Yuan H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1999 Jun;16(3):141-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1999. PMID: 10359861 Chinese.

3

[Screening for the 1555G mutation in mitochondrial DNA in pedigrees with aminoglycoside antibiotic induced deafness].

Yuan H, Jiang S, Yang W. Yuan H, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 1998 Apr;33(2):67-70. Zhonghua Er Bi Yan Hou Ke Za Zhi. 1998. PMID: 11498854 Chinese.

4

[Sequence analysis of mtDNA 12S rRNA, tRNA(Leu(UUR)),tRNA(Ser(UCN))and 16S rRNA gene of 12 nonsyndromic inherited deafness pedigrees].

Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S. Li W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001 Dec;18(6):415-20. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001. PMID: 11774206 Chinese.

5

[Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].

Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S. Li W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Feb;19(1):64-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 11836692 Chinese.

6

Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusis.

Dai P, Yang W, Jiang S, Gu R, Yuan H, Han D, Guo W, Cao J. Dai P, et al. Acta Otolaryngol. 2004 Mar;124(2):130-6. doi: 10.1080/00016480410016586. Acta Otolaryngol. 2004. PMID: 15072414

7

[Pedigree analysis and sequence analysis of mtDNA 12srRNA, tRNA(Leu(UUR)), tRNA(Ser(UCN)) gene in nonsyndromic inherited deafness pedigrees].

Li W, Han D, Yuan H, Cao J. Li W, et al. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2004 Oct;18(10):582-5, 589. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2004. PMID: 15620132 Chinese.

8

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.

Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX. Yuan H, et al. Am J Med Genet A. 2005 Oct 1;138A(2):133-40. doi: 10.1002/ajmg.a.30952. Am J Med Genet A. 2005. PMID: 16152638 Free PMC article.

9

[Clinical features of a Chinese pedigree with Waardenburg syndrome type 2].

Yang SZ, Yuan HJ, Bai LN, Cao JY, Xu Y, Shen WD, Ji F, Yang WY. Yang SZ, et al. Among authors: yuan hj. Zhonghua Yi Xue Za Zhi. 2005 Oct 12;85(38):2686-90. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16324295 Chinese.

10

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.

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