검색결과 : 7건
No. | Article |
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1 |
Discrimination of A1555G and C1494T Point Mutations in the Mitochondrial 12S rRNA Gene by On/Off Switch Guo ZF, Guo WS, Xiao L, Gao GQ, Lan F, Lu XG, Li K, Liao DF Applied Biochemistry and Biotechnology, 166(1), 234, 2012 |
2 |
A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment Chaig MR, Zernotti ME, Soria NW, Romero OF, Romero MF, Gerez NM Biochemical and Biophysical Research Communications, 368(3), 631, 2008 |
3 |
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 DY, Qian YP, Huang DL, Yuan HJ, Li WM, Yu F, Zhang RN, Lin HY, He Y, Yu YJ, Sun QZ, Qin HY, Li RH, Zhang X, Kang DY, Cao JY, Young WY, Guan MX Biochemical and Biophysical Research Communications, 340(1), 194, 2006 |
4 |
Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation Wang QJ, Li QZ, Han DY, Zhao YL, Zhao LD, Qian YP, Yuan H, Li RH, Zhai SQ, Young WY, Guan MX Biochemical and Biophysical Research Communications, 340(2), 583, 2006 |
5 |
Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations Yan QF, Bykhovskaya Y, Li RH, Mengesha E, Shohat M, Estivill X, Fischel-Ghodsian N, Guan MX Biochemical and Biophysical Research Communications, 342(4), 1130, 2006 |
6 |
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families Dai P, Yuan YI, Huang DL, Qian YP, Liu X, Han DY, Yuan HJ, Wang XJ, Young WY, Guan MX Biochemical and Biophysical Research Communications, 348(1), 200, 2006 |
7 |
Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss Zhao LD, Wang QJ, Qian YP, Li RH, Cao JY, Hart LC, Zhai SQ, Han DY, Young WY, Guan MX Biochemical and Biophysical Research Communications, 336(3), 967, 2005 |