검색결과 : 39건
| No. | Article |
|---|---|
| 1 |
Effect of mitochondrial tRNA(LYs) mutation on the clinical and biochemical characteristics of Chinese essential hypertensive subjects Lu Y, Xiao TH, Zhang F, Chen YM, Liu YQ, Li Y, Chen YD, Li ZB, Guan MX Biochemical and Biophysical Research Communications, 454(4), 500, 2014 |
| 2 |
A novel OPA1 mutation in a Chinese family with autosomal dominant optic atrophy Zhang JJ, Yuan YM, Lin B, Feng H, Li Y, Dai XN, Zhou HH, Dong XJ, Liu XL, Guan MX Biochemical and Biophysical Research Communications, 419(4), 670, 2012 |
| 3 |
Four Novel Cellulose Synthase (CESA) Genes from Birch (Betula platyphylla Suk.) Involved in Primary and Secondary Cell Wall Biosynthesis Liu XM, Wang QY, Chen PF, Song FN, Guan MX, Jin LH, Wang YC, Yang C International Journal of Molecular Sciences, 13(10), 12195, 2012 |
| 4 |
Voltage-dependent anion channel involved in the mitochondrial calcium cycle of cell lines carrying the mitochondrial DNA A4263G mutation Liu YQ, Gao L, Xue QA, Li ZB, Wang L, Chen R, Liu M, Wen Y, Guan MX, Li Y, Wang SW Biochemical and Biophysical Research Communications, 404(1), 364, 2011 |
| 5 |
The effect of the mtDNA4834 deletion on hearing (vol 344, pg 425, 2006) Kong WJ, Hu YJ, Wang QO, Wang Y, Han YC, Cheng HM, Kong W, Guan MX Biochemical and Biophysical Research Communications, 398(4), 791, 2010 |
| 6 |
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 |
| 7 |
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 |
| 8 |
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 |
| 9 |
Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family Li ZB, Liu Y, Yang L, Wang SW, Guan MX Biochemical and Biophysical Research Communications, 367(4), 906, 2008 |
| 10 |
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 |