검색결과 : 7건
| No. | Article |
|---|---|
| 1 |
G7731A mutation in mouse mitochondrial tRNA(LYs) regulates late-onset disorders in transmitochondrial mice Shimizu A, Mito T, Hashizume O, Yonekawa H, Ishikawa K, Nakada K, Hayashi J Biochemical and Biophysical Research Communications, 459(1), 66, 2015 |
| 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 |
Identification of a new mtDNA mutation (14724G > A) associated with mitochondrial leukoencephalopathy Pereira C, Nogueira C, Barbot C, Tessa A, Soares C, Fattori F, Guimaraes A, Santorelli FM, Vilarinho L Biochemical and Biophysical Research Communications, 354(4), 937, 2007 |
| 4 |
Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations Yan QF, Bykhovskaya Y, Li RH, Mengesha E, Shohat M, Estivill X, Fischel-Ghodsian N, Guan MX Biochemical and Biophysical Research Communications, 342(4), 1130, 2006 |
| 5 |
Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy Qian YP, Zhou XT, Hu YW, Tong Y, Li RH, Lu F, Yang HM, Mo JQ, Qu J, Guan MX Biochemical and Biophysical Research Communications, 332(2), 614, 2005 |
| 6 |
Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations Da Pozzo P, Cardaioli E, Radi E, Federico A Biochemical and Biophysical Research Communications, 324(1), 360, 2004 |
| 7 |
Detection of mitochondrial DNA mutations using temporal temperature gradient gel electrophoresis Wong LJC, Chen TJ, Tan DJ Electrophoresis, 25(15), 2602, 2004 |