검색결과 : 11건
| No. | Article |
|---|---|
| 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 |
Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation Liang M, Guan MQ, Zhao FX, Zhou XT, Yuan MX, Tong Y, Yang L, Wei QP, Sun YH, Lu F, Qu J, Guan MX Biochemical and Biophysical Research Communications, 383(3), 286, 2009 |
| 3 |
Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation Zhao FX, Guan MQ, Zhou XT, Yuan MX, Liang M, Liu Q, Liu Y, Zhang YM, Yang L, Tong Y, Wei QP, Sun YH, Qu J, Guan MX Biochemical and Biophysical Research Communications, 389(3), 466, 2009 |
| 4 |
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy Petruzzella V, Tessa A, Torraco A, Fattori F, Dotti MT, Bruno C, Cardaioli E, Papa S, Federico A, Santorelli FM Biochemical and Biophysical Research Communications, 355(1), 181, 2007 |
| 5 |
Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families Zhou XT, Wei QP, Yang L, Tong Y, Zhao FX, Lu CJ, Qian YP, Sun YH, Lu F, Qu J, Guan MX Biochemical and Biophysical Research Communications, 340(1), 69, 2006 |
| 6 |
Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families Sun YH, Wei QP, Zhou X, Qian Y, Zhou J, Lu F, Qu J, Guan MX Biochemical and Biophysical Research Communications, 347(1), 221, 2006 |
| 7 |
Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation Qu J, Li RH, Tong Y, Hu YW, Zhou XT, Qian YP, Lu F, Guan MX Biochemical and Biophysical Research Communications, 328(4), 1139, 2005 |
| 8 |
A novel mtDNA ND6 gene mutation associated with LHON in a Caucasian family Zhadanov SI, Atamanov VV, Zhadanov NI, Oleinikov OV, Osipova LP, Schurr TG Biochemical and Biophysical Research Communications, 332(4), 1115, 2005 |
| 9 |
GUG is an efficient initiation codon to translate the human mitochondrial ATP6 gene Dubot A, Godinot C, Dumur V, Sablonniere B, Stojkovic T, Cuisset JM, Vojtiskova A, Pecina P, Jesina P, Houstek J Biochemical and Biophysical Research Communications, 313(3), 687, 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 |