(6 articles were found) |
| 1 | Acta Diabetol | 1 | J Appl Genet |
| 1 | Biochem Biophys Res Commun | 1 | J Cell Biol |
| 1 | FEBS Lett | 1 | Schizophr Res |
| Reda E, et al. The carnitine system and body composition. | |
| Acta Diabetol 2003 Oct;40 Suppl 1:S106-13. | |
| Tomitsuka E, et al. Direct evidence for expression of Type II flavoprotein subunit in human complex II (succinate-ubiquinone reductase). | |
| Biochem Biophys Res Commun 2003 Nov 21;311(3):774-9. | |
| Wang L, et al. Mitochondrial deoxyguanosine kinase mutations and mitochondrial DNA depletion syndrome. | |
| FEBS Lett 2003 Nov 20;554(3):319-22. | |
| MROCZEK-TONSKA K, et al. Leber hereditary optic neuropathy - a disease with a known molecular basis but a mysterious mechanism of pathology. | |
| J Appl Genet 2003;44(4):529-538. | |
| Atorino L, et al. Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. | |
| J Cell Biol 2003 Nov 17;. | |
| Marchbanks RM, et al. A mitochondrial DNA sequence variant associated with schizophrenia and oxidative stress. | |
| Schizophr Res 2003 Dec 1;65(1):33-8. | |
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