화학공학소재연구정보센터
검색결과 : 5건
No. Article
1 Mitochondrial tRNA(Ser(UCN)) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss
Jin LJ, Yang AF, Zhu Y, Zhao JY, Wang XJ, Yang L, Sun DM, Tao ZH, Tsushima A, Wu GM, Xu LM, Chen CX, Yi B, Cai JX, Tang XW, Wang J, Li D, Yuan Q, Liao ZS, Chen JF, Li ZY, Lu JX, Guan MX
Biochemical and Biophysical Research Communications, 361(1), 133, 2007
2 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
3 Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation
Young WY, Zhao LD, Qian YP, Wang QJ, Li N, Greinwald JH, Guan MX
Biochemical and Biophysical Research Communications, 328(4), 1244, 2005
4 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
5 Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation
Zhao LD, Young WY, Li R, Wang QJ, Qian YP, Guan MX
Biochemical and Biophysical Research Communications, 325(4), 1503, 2004