(69 articoli trovati) |
| Kiens B, et al. Utilization of long-chain fatty acids in human skeletal muscle during exercise. | |
| Acta Physiol Scand 2003 Aug;178(4):391-6. | |
| Barret B, et al. Persistent mitochondrial dysfunction in HIV-1-exposed but uninfected infants: clinical screening in a large prospective cohort. | |
| AIDS 2003 Aug 15;17(12):1769-1785. | |
| Zand DJ, et al. In Vivo Pyruvate Detected by MR Spectroscopy in Neonatal Pyruvate Dehydrogenase Deficiency. | |
| AJNR Am J Neuroradiol 2003 Aug;24(7):1471-1474. | |
| Keyser-Tracqui C, et al. Nuclear and mitochondrial DNA analysis of a 2,000-year-old necropolis in the egyin gol valley of mongolia. | |
| Am J Hum Genet 2003 Aug;73(2):247-60. | |
| Boles RG, et al. Maternal inheritance in cyclic vomiting syndrome with neuromuscular disease. | |
| Am J Med Genet 2003 Aug 1;120A(4):474-82. | |
| Strauss KA, et al. Type I glutaric aciduria, part 1: Natural history of 77 patients. | |
| Am J Med Genet 2003 Aug 15;121C(1):38-52. | |
| Sadun AA, et al. Extensive investigation of a large Brazilian pedigree of 11778/haplogroup J Leber hereditary optic neuropathy. | |
| Am J Ophthalmol 2003 Aug;136(2):231-8. | |
| Wang H, et al. Uncoupling Protein 2 Polymorphisms in Type 2 Diabetes, Obesity, and Insulin Secretion. | |
| Am J Physiol Endocrinol Metab 2003 Aug 12;. | |
| Shukla A, et al. Asbestos Induces Mitochondrial DNA Damage and Dysfunction Linked to the Development of Apoptosis. | |
| Am J Physiol Lung Cell Mol Physiol 2003 Aug 8;. | |
| Kuznetsov AV, et al. Cryopreservation of mitochondria and mitochondrial function in cardiac and skeletal muscle fibers. | |
| Anal Biochem 2003 Aug 15;319(2):296-303. | |
| Gerschenson M. Mitochondria and lipodystrophy: where are we now? | |
| Antivir Ther 2003 Aug;8(4):261-3. | |
| Cossarizza A, et al. Increased mitochondrial DNA content in peripheral blood lymphocytes from HIV-infected patients with lipodystrophy. | |
| Antivir Ther 2003 Aug;8(4):315-21. | |
| Pace CS, et al. Mitochondrial proliferation, DNA depletion and adipocyte differentiation in subcutaneous adipose tissue of HIV-positive HAART recipients. | |
| Antivir Ther 2003 Aug;8(4):323-31. | |
| Miro O, et al. Mitochondrial DNA depletion and respiratory chain enzyme deficiencies are present in peripheral blood mononuclear cells of HIV-infected patients with HAART-related lipodystrophy. | |
| Antivir Ther 2003 Aug;8(4):333-8. | |
| Thirlwall AS, et al. Phenotypic characterization of hereditary hearing impairment linked to DFNA25. | |
| Arch Otolaryngol Head Neck Surg 2003 Aug;129(8):830-5. | |
| Westermann B. Mitochondrial membrane fusion. | |
| Biochim Biophys Acta 2003 Aug 18;1641(2-3):195-202. | |
| Overman RG, et al. The human mitochondrial translation initiation factor 2 gene (MTIF2): transcriptional analysis and identification of a pseudogene. | |
| Biochim Biophys Acta 2003 Aug 25;1628(3):195-205. | |
| Liu VW, et al. High frequency of mitochondrial genome instability in human endometrial carcinomas. | |
| Br J Cancer 2003 Aug 18;89(4):697-701. | |
| Taimor G. Mitochondria as common endpoints in early and late preconditioning. | |
| Cardiovasc Res 2003 Aug 1;59(2):266-7. | |
| Searcy DG. Metabolic integration during the evolutionary origin of mitochondria. | |
| Cell Res 2003 Aug;13(4):229-38. | |
| Liu Y, et al. Mitochondrial Sources of H2O2 Generation Play a Key Role in Flow-Mediated Dilation in Human Coronary Resistance Arteries. | |
| Circ Res 2003 Aug 14;. | |
| Weiss JN, et al. Role of the mitochondrial permeability transition in myocardial disease. | |
| Circ Res 2003 Aug 22;93(4):292-301. | |
| Chabi B, et al. Quantification of Mitochondrial DNA Deletion, Depletion, and Overreplication: Application to Diagnosis. | |
| Clin Chem 2003 Aug;49(8):1309-1317. | |
| Kroemer G. The mitochondrial permeability transition pore complex as a pharmacological target. An introduction. | |
| Curr Med Chem 2003 Aug;10(16):1469-72. | |
| Halestrap AP, et al. The adenine nucleotide translocase: a central component of the mitochondrial permeability transition pore and key player in cell death. | |
| Curr Med Chem 2003 Aug;10(16):1507-25. | |
| Fischel-Ghodsian N. Mitochondrial deafness. | |
| Ear Hear 2003 Aug;24(4):303-13. | |
| Grafakou O, et al. Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation. | |
| Eur J Pediatr 2003 Aug 19;. | |
| Salpietro CD, et al. A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting. | |
| Eur J Pediatr 2003 Aug 2;. | |
| Jauslin ML, et al. Mitochondria-targeted antioxidants protect Friedreich Ataxia fibroblasts from endogenous oxidative stress più effectively than untargeted antioxidants. | |
| FASEB J 2003 Aug 15;. | |
| Okura T, et al. Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population. | |
| Hum Genet 2003 Aug 2;. | |
| Taanman JW, et al. Mitochondrial DNA depletion can be prevented by dGMP and dAMP supplementation in a resting culture of deoxyguanosine kinase-deficient fibroblasts. | |
| Hum Mol Genet 2003 Aug 1;12(15):1839-45. | |
| Hofmann S, et al. Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene product. | |
| Hum Mol Genet 2003 Aug 15;12(16):2003-12. | |
| Jacobs HT. Disorders of mitochondrial protein synthesis. | |
| Hum Mol Genet 2003 Aug 19;. | |
| Antonicka H, et al. Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early onset clinical phenotypes associated with isolated COX deficiency. | |
| Hum Mol Genet 2003 Aug 19;. | |
| Liu VW, et al. Mitochondrial DNA variant 16189T>C is associated with susceptibility to endometrial cancer. | |
| Hum Mutat 2003 Aug;22(2):173-4. | |
| Man Chiu P, et al. Detection of mitochondrial DNA mutations in gestational trophoblastic disease. | |
| Hum Mutat 2003 Aug;22(2):177. | |
| Brandstatter A, et al. Rapid screening of mtDNA coding region SNPs for the identification of west European Caucasian haplogroups. | |
| Int J Legal Med 2003 Aug 21;. | |
| Marriage B, et al. Nutritional cofactor treatment in mitochondrial disorders. | |
| J Am Diet Assoc 2003 Aug;103(8):1029-1038. | |
| Guery B, et al. The Spectrum of Systemic Involvement in Adults Presenting with Renal Lesion and Mitochondrial tRNA(Leu) Gene Mutation. | |
| J Am Soc Nephrol 2003 Aug;14(8):2099-108. | |
| Tomitsuka E, et al. Direct Evidence for Two Distinct Forms of the Flavoprotein Subunit of Human Mitochondrial Complex II (Succinate-Ubiquinone Reductase). | |
| J Biochem (Tokyo) 2003 Aug;134(2):191-5. | |
| Horie C, et al. Targeting and assembly of mitochondrial tail-anchored protein Tom5 to the TOM complex depend on a signal distinct from that of tail-anchored proteins dispersed in the membrane. | |
| J Biol Chem 2003 Aug 1;. | |
| Waizenegger T, et al. Signal-anchor domains of proteins of the outer membrane of mitochondria: structural and functional characteristics. | |
| J Biol Chem 2003 Aug 13;. | |
| Antonicka H, et al. Identification and characterization of a common set of complex I assembly intermediates in mitochondria from patients with complex I deficiency. | |
| J Biol Chem 2003 Aug 26;. | |
| Scacco S, et al. Pathological mutations of the human NDUFS4 gene of the 18 kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complex. | |
| J Biol Chem 2003 Aug 27;. | |
| Csordas G, et al. Plasticity of mitochondrial calcium signalling. | |
| J Biol Chem 2003 Aug 7;. | |
| Endo T, et al. Functional cooperation and separation of translocators in protein import into mitochondria, the double-membrane bounded organelles. | |
| J Cell Sci 2003 Aug 15;116(Pt 16):3259-67. | |
| Ohsawa I, et al. Genetic deficiency of a mitochondrial aldehyde dehydrogenase increases serum lipid peroxides in community-dwelling females. | |
| J Hum Genet 2003 Aug 7;. | |
| Del Castillo FJ, et al. Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss. | |
| J Med Genet 2003 Aug;40(8):632-636. | |
| Miura T, et al. Depletion of mitochondrial DNA in HIV-1-infected patients and its amelioration by antiretroviral therapy. | |
| J Med Virol 2003 Aug;70(4):497-505. | |
| Remes AM, et al. Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome. | |
| J Neurol Neurosurg Psychiatry 2003 Aug;74(8):1158-1159. | |
| Von Kleist-Retzow JC, et al. Antenatal manifestations of mitochondrial respiratory chain deficiency. | |
| J Pediatr 2003 Aug;143(2):208-212. | |
| Bruton JD, et al. Mitochondrial function in intact skeletal muscle fibres of creatine kinase deficient mice. | |
| J Physiol 2003 Aug 15;. | |
| Turrens JF. Mitochondrial Formation of Reactive Oxygen Species. | |
| J Physiol 2003 Aug 22;. | |
| Takahashi K, et al. Temporal Bone Histopathological and Quantitative Analysis of Mitochondrial DNA in MELAS. | |
| Laryngoscope 2003 Aug;113(8):1362-8. | |
| Carew JS, et al. Mitochondrial DNA mutations in primary leukemia cells after chemotherapy: clinical significance and therapeutic implications. | |
| Leukemia 2003 Aug;17(8):1437-47. | |
| Moilanen JS, et al. Lineage-Specific Selection in Human mtDNA: Lack of Polymorphisms in a Segment of MTND5 Gene in Haplogroup J. | |
| Mol Biol Evol 2003 Aug 29;. | |
| Bhattacharyya SN, et al. "Ping-Pong" Interactions between Mitochondrial tRNA Import Receptors within a Multiprotein Complex. | |
| Mol Cell Biol 2003 Aug;23(15):5217-24. | |
| Camacho JA, et al. Cloning and characterization of human ORNT2: a second mitochondrial ornithine transporter that can rescue a defective ORNT1 in patients with the hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a urea cycle disorder. | |
| Mol Genet Metab 2003 Aug;79(4):257-71. | |
| Leshinsky-Silver E, et al. Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiency. | |
| Mol Genet Metab 2003 Aug;79(4):288-93. | |
| Phillips MJ, et al. The root of the mammalian tree inferred from whole mitochondrial genomes. | |
| Mol Phylogenet Evol 2003 Aug;28(2):171-85.; Review | |
| Hudelot C, et al. RNA-based phylogenetic methods: application to mammalian mitochondrial RNA sequences. | |
| Mol Phylogenet Evol 2003 Aug;28(2):241-52. | |
| Murata Y, et al. Afrotherian phylogeny as inferred from complete mitochondrial genomes. | |
| Mol Phylogenet Evol 2003 Aug;28(2):253-60. | |
| Sawyer DE, et al. Quantitative analysis of gene-specific DNA damage in human spermatozoa. | |
| Mutat Res 2003 Aug 28;529(1-2):21-34. | |
| Bayona-Bafaluy MP, et al. A chemical enucleation method for the transfer of mitochondrial DNA to rho(o) cells. | |
| Nucleic Acids Res 2003 Aug 15;31(16):e98. | |
| Isashiki Y, et al. Phylogenetic Assessment of the Mitochondrial DNA Displacement Loop Haplotype in Japanese Patients with Leber's Hereditary Optic Neuropathy Harboring the Mitochondrial DNA G11778A Mutation. | |
| Ophthalmic Res 2003 Aug;35(4):224-31. | |
| Greenamyre JT, et al. The rotenone model of Parkinson's disease: genes, environment and mitochondria. | |
| Parkinsonism Relat Disord 2003 Aug;9 Suppl 2:59-64. | |
| Piganeau G, et al. Estimating the distribution of fitness effects from DNA sequence data: Implications for the molecular clock. | |
| Proc Natl Acad Sci U S A 2003 Aug 18;. | |
| Hiendleder S, et al. The mitochondrial genome in embryo technologies. | |
| Reprod Domest Anim 2003 Aug;38(4):290-304. | |
| Bogenhagen DF, et al. Concluding remarks: The mitochondrial DNA replication bubble has not burst. | |
| Trends Biochem Sci 2003 Aug;28(8):404-5. | |
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