검색결과 : 8건
| No. | Article |
|---|---|
| 1 |
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 DY, Dai P, Zhu QW, Lin X, Huang DL, Yuan YY, Yuan HJ, Wang XJ, Qian YP, Young WY, Guan MX Biochemical and Biophysical Research Communications, 357(2), 554, 2007 |
| 2 |
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, Llu X, Cheng J, Wang X, Yang L, Yang S, Cao J, Kang D, Dal P, Zhai S, Han D, Young WY, Guan MX Biochemical and Biophysical Research Communications, 362(1), 94, 2007 |
| 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 |
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 |
| 6 |
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 |
| 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 |
| 8 |
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 |