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Journal Abstract Search

193 related items for PubMed ID: 16796900

  • 1. [Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].
    Liu X, Dai P, Huang DL, Yuan HJ, Li WM, Cao JY, Yu F, Zhang RN, Lin HY, Zhu XH, He Y, Yu YJ, Yao K.
    Zhonghua Yi Xue Za Zhi; 2006 May 23; 86(19):1318-22. PubMed ID: 16796900
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  • 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.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862
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  • 3. [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.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun 03; 16(3):141-4. PubMed ID: 10359861
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  • 15. Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.
    Jin L, Yang A, Zhu Y, Zhao J, Wang X, Yang L, Sun D, Tao Z, Tsushima A, Wu G, Xu L, Chen C, Yi B, Cai J, Tang X, Wang J, Li D, Yuan Q, Liao Z, Chen J, Li Z, Lu J, Guan MX.
    Biochem Biophys Res Commun; 2007 Sep 14; 361(1):133-9. PubMed ID: 17659260
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  • 17. [Aminoglycoside ototoxicity associated with mitochondrial DNA mutation].
    Ke X, Qi Y, Gu Z, Zhang Z, Zhang W, Jiang S, Liu J.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 1999 May 14; 13(5):195-7. PubMed ID: 12563999
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