검색결과 : 13건
| No. | Article |
|---|---|
| 1 |
The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations Zou Y, Jia XY, Zhang AM, Wang WZ, Li SQ, Guo XM, Kong QP, Zhang QJ, Yao YG Biochemical and Biophysical Research Communications, 399(2), 179, 2010 |
| 2 |
mtDNA m.3635G > A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population Jia XY, Li SQ, Wang PF, Guo XM, Zhang QJ Biochemical and Biophysical Research Communications, 403(2), 237, 2010 |
| 3 |
Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation Yang JH, Zhu YH, Tong Y, Chen L, Liu LJ, Zhang ZQ, Wang XY, Huang DG, Qiu WT, Zhuang SL, Ma X Biochemical and Biophysical Research Communications, 386(1), 50, 2009 |
| 4 |
Mitochondrial DNA mutation m.3635G > A may be associated with Leber hereditary optic neuropathy in Chinese Zhang AM, Zou Y, Guo XM, Jia XY, Zhang QJ, Yao YG Biochemical and Biophysical Research Communications, 386(2), 392, 2009 |
| 5 |
Novel A14841G mutation is associated with high penetrance of LHON/C4171A family Yang JH, Zhu YH, Chen L, Zhang HX, Tong Y, Huang DG, Zhang ZQ, Chen S, Han XL, Ma X Biochemical and Biophysical Research Communications, 386(4), 693, 2009 |
| 6 |
Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber's hereditary optic neuropathy Zhang AM, Jia XY, Yao YG, Zhang QJ Biochemical and Biophysical Research Communications, 376(1), 221, 2008 |
| 7 |
High penetrance of sequencing errors and interpretative shortcomings in mtDNA sequence analysis of LHON patients Bandelt HJ, Yao YG, Salas A, Kivisild T, Bravi CM Biochemical and Biophysical Research Communications, 352(2), 283, 2007 |
| 8 |
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 |
| 9 |
The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy Tong Y, Mao YJ, Zhou XT, Yang L, Zhang JJ, Cai WS, Zhao FX, Wang XJ, Lu F, Qu J, Guan MX Biochemical and Biophysical Research Communications, 357(2), 524, 2007 |
| 10 |
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 |