검색결과 : 10건
| No. | Article |
|---|---|
| 1 |
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy Elstner M, Schmidt C, Zingler VC, Prokisch H, Bettecken T, Elson JL, Rudolph G, Bender A, Halmagyi GM, Brandt T, Strupp M, Klopstock T Biochemical and Biophysical Research Communications, 377(2), 379, 2008 |
| 2 |
Co-segregation of the T1095C with the A1555G mutation of the mitochondrial 12S rRNA gene in a patient with non-syndromic hearing loss Dai DC, Lu YJ, Chen ZB, Wei QJ, Cao X, Xing GQ Biochemical and Biophysical Research Communications, 377(4), 1152, 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 |
Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene Bravo O, Ballana E, Estivill X Biochemical and Biophysical Research Communications, 344(2), 511, 2006 |
| 6 |
Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family Xing GQ, Chen ZB, Wei QJ, Tian HQ, Li XL, Zhou AD, Bu XK, Cao X Biochemical and Biophysical Research Communications, 344(4), 1253, 2006 |
| 7 |
Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity Xing GQ, Chen ZB, Wei QJ, Tian HQ, Li XL, Zhou AD, Bu XK, Cao X Biochemical and Biophysical Research Communications, 346(4), 1131, 2006 |
| 8 |
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 |
| 9 |
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 |
| 10 |
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 |