| 1 |
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families
Zhang JJ, Zhou XT, Zhou JA, Li CW, Zhao FX, Wang Y, Meng YZ, Wang JY, Yuan MX, Cai WS, Tong Y, Sun YH, Yang L, Qu J, Guan MX
Biochemical and Biophysical Research Communications, 399(4), 647, 2010 |
| 2 |
The mitochondrial ND1 T3308C mutation in a Chinese family with the secondary hypertension
Liu YQ, Li ZB, Yang L, Wang S, Guan MX
Biochemical and Biophysical Research Communications, 368(1), 18, 2008 |
| 3 |
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 |
| 4 |
The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss
Wei QP, Zhou XT, Yang L, Sun YH, Zhou J, Li G, Jiang R, Lu F, Qu J, Guan MX
Biochemical and Biophysical Research Communications, 357(4), 910, 2007 |
| 5 |
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 |
| 6 |
Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNA (Ser(UCN)) genes in two Chinese families
Zhu Y, Qian YP, Tang XW, Wang JD, Yang L, Liao ZS, Li RH, Ji JZ, Li ZY, Chen JF, Choo DI, Lu JX, Guan MX
Biochemical and Biophysical Research Communications, 342(3), 843, 2006 |
| 7 |
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 |
| 8 |
Mutation scanning-coupled analysis of haplotypic variability in mitochondrial DNA regions reveals low gene flow between human and porcine Ascaris in endemic regions of China
Peng WD, Yuan K, Hu M, Zhou XM, Gasser RB
Electrophoresis, 26(22), 4317, 2005 |
| 9 |
Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome
Ruppert V, Nolte D, Aschenbrenner T, Pankuweit S, Funck R, Maisch B
Biochemical and Biophysical Research Communications, 318(2), 535, 2004 |
| 10 |
Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations
Fauser S, Luberichs J, Besch D, Leo-Kottler B
Biochemical and Biophysical Research Communications, 295(2), 342, 2002 |
