검색결과 : 16건
| No. | Article |
|---|---|
| 1 |
Lipidomic profiling of plasma samples from patients with mitochondrial disease Ren CX, Liu J, Zhou JT, Liang H, Zhu YZ, Wang QQ, Leng YL, Zhang Z, Yuan Y, Wang ZX, Yin YX Biochemical and Biophysical Research Communications, 500(2), 124, 2018 |
| 2 |
Myoclonus epilepsy, retinitis pigmentosa, leukoencephalopathy and cerebral calcifications associated with a novel m.5513G>A mutation in the MT-TW gene Cardaioli E, Mignarri A, Cantisani TA, Malandrini A, Nesti C, Rubegni A, Funel N, Federico A, Santorelli FM, Dotti MT Biochemical and Biophysical Research Communications, 500(2), 158, 2018 |
| 3 |
A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrorne Mordel P, Schaeffer S, Dupas Q, Laville MA, Gerard M, Chapon F, Allouche S Biochemical and Biophysical Research Communications, 494(1-2), 133, 2017 |
| 4 |
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 |
| 5 |
Mitochondrial tRNA cleavage by tRNA-targeting ribonuclease causes mitochondrial dysfunction observed in mitochondrial disease Ogawa T, Shimizu A, Takahashi K, Hidaka M, Masaki H Biochemical and Biophysical Research Communications, 451(1), 131, 2014 |
| 6 |
Nitric Oxide Synthesis Is Increased in Cybrid Cells with m.3243A > G Mutation Gamba J, Gamba LT, Rodrigues GS, Kiyomoto BH, Moraes CT, Tengan CH International Journal of Molecular Sciences, 14(1), 394, 2013 |
| 7 |
Nitric Oxide in Skeletal Muscle: Role on Mitochondrial Biogenesis and Function Tengan CH, Rodrigues GS, Godinho RO International Journal of Molecular Sciences, 13(12), 17160, 2012 |
| 8 |
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation Ronchi D, Bordoni A, Cosi A, Rizzuti M, Fassone E, Di Fonzo A, Servida M, Sciacco M, Collotta M, Ronzoni M, Lucchini V, Mattioli M, Moggio M, Bresolin N, Corti S, Comi GP Biochemical and Biophysical Research Communications, 412(2), 245, 2011 |
| 9 |
A novel mutation in the mitochondrial tRNA(Asn) gene associated with a lethal disease Coulbault L, Herlicoviez D, Chapon F, Read MH, Penniello MJ, Reynier P, Fayet G, Lombes A, Jauzac P, Allouche S Biochemical and Biophysical Research Communications, 329(3), 1152, 2005 |
| 10 |
Low "penetrance" of phylogenetic knowledge in mitochondrial disease studies Bandelt HJ, Achilli A, Kong QP, Salas A, Lutz-Bonengel S, Sun C, Zhang YP, Torroni A, Yao YG Biochemical and Biophysical Research Communications, 333(1), 122, 2005 |