(62 articoli trovati) |
| Jacobs HT. The mitochondrial theory of aging: dead or alive? | |
| Aging Cell 2003 Feb;2(1):11-7. | |
| Pak JW, et al. Mitochondrial DNA mutations as a fundamental mechanism in physiological declines associated with aging. | |
| Aging Cell 2003 Feb;2(1):1-7. | |
| Pak JW, et al. Rebuttal to Jacobs: the mitochondrial theory of aging: alive and well. | |
| Aging Cell 2003 Feb;2(1):9-10; discussion 19-20. | |
| Arai T, et al. Age-related mitochondrial DNA deletion in human heart: its relationship with cardiovascular diseases. | |
| Aging Clin Exp Res 2003 Feb;15(1):1-5. | |
| Diehl S, et al. Mitochondrial DNA and sperm quality in patients under antiretroviral therapy. | |
| AIDS 2003 Feb 14;17(3):450-1. | |
| Martin AM, et al. Accumulation of Mitochondrial DNA Mutations in Human Immunodeficiency Virus-Infected Patients Treated with Nucleoside-Analogue Reverse-Transcriptase Inhibitors. | |
| Am J Hum Genet 2003 Feb 13;72(3). | |
| Torroni A, et al. Mitochondrial DNA Haplogroups Do Not Play a Role in the Variable Phenotypic Presentation of the A3243G Mutation. | |
| Am J Hum Genet 2003 Feb 24;72(4). | |
| Van Der Walt JM, et al. Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease. | |
| Am J Hum Genet 2003 Feb 28;72(4). | |
| Howell N, et al. The Pedigree Rate of Sequence Divergence in the Human Mitochondrial Genome: There Is a Difference Between Phylogenetic and Pedigree Rates. | |
| Am J Hum Genet 2003 Feb 4;72(3). | |
| Shekhawat PS, et al. Human Placenta Metabolizes Fatty Acids: Implications for Fetal Fatty Acid Oxidation Disorders and Maternal Liver Diseases. | |
| Am J Physiol Endocrinol Metab 2003 Feb 11;. | |
| Qi X, et al. Suppression of complex I gene expression induces optic neuropathy. | |
| Ann Neurol 2003 Feb;53(2):198-205. | |
| McCully JD, et al. The mitochondrial K(ATP) channel and cardioprotection. | |
| Ann Thorac Surg 2003 Feb;75(2):S667-73. | |
| Dessole S, et al. Postpartum hemorrhage and emergency hysterectomy in a patient with mitochondrial myopathy: a case report. | |
| Arch Gynecol Obstet 2003 Feb;267(4):247-9. | |
| Newman-Toker DE, et al. Clinicopathologic reports, case reports, and small case series: recurrent visual loss in leber hereditary optic neuropathy. | |
| Arch Ophthalmol 2003 Feb;121(2):288-91. | |
| Park H, et al. The Pathogenic A3243G Mutation in Human Mitochondrial tRNA(Leu(UUR)) Decreases the Efficiency of Aminoacylation. | |
| Biochemistry 2003 Feb 4;42(4):958-64. | |
| Taivassalo T, et al. The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients. | |
| Brain 2003 Feb;126(Pt 2):413-423. | |
| Lai LP, et al. Atrial fibrillation is associated with accumulation of aging-related common type mitochondrial DNA deletion mutation in human atrial tissue. | |
| Chest 2003 Feb;123(2):539-44. | |
| Minchenko J, et al. Adaptation of a Mitochondrial Complex III Assay for Automation: Examination of Reproducibility and Precision. | |
| Clin Chem 2003 Feb;49(2):330-2. | |
| Fuller KM, et al. Advances in the analysis of single mitochondria. | |
| Curr Opin Biotechnol 2003 Feb;14(1):35-41. | |
| Biousse V, et al. Neuro-ophthalmology of mitochondrial diseases. | |
| Curr Opin Neurol 2003 Feb;16(1):35-43. | |
| Muranyi M, et al. Diabetes activates cell death pathway after transient focal cerebral ischemia. | |
| Diabetes 2003 Feb;52(2):481-6. | |
| Lynn S, et al. Heteroplasmic ratio of the A3243G mitochondrial DNA mutation in single pancreatic beta cells. | |
| Diabetologia 2003 Feb;46(2):296-9. | |
| Bindoff L. Mitochondria and the heart. | |
| Eur Heart J 2003 Feb;24(3):221-4. | |
| Holmgren D, et al. Cardiomyopathy in children with mitochondrial disease. Clinical course and cardiological findings. | |
| Eur Heart J 2003 Feb;24(3):280-8. | |
| Schwab KO, et al. Complete deficiency of mitochondrial trifunctional protein due to a novel mutation within the beta-subunit of the mitochondrial trifunctional protein gene leads to failure of long-chain fatty acid beta-oxidation with fatal outcome. | |
| Eur J Pediatr 2003 Feb;162(2):90-5. | |
| Gajewski CD, et al. Mitochondrial DNA from platelets of sporadic ALS patients restores normal respiratory functions in rho(0) cells. | |
| Exp Neurol 2003 Feb;179(2):229-35. | |
| Richardson D. Friedreich's ataxia: iron chelators that target the mitochondrion as a therapeutic strategy? | |
| Expert Opin Investig Drugs 2003 Feb;12(2):235-245. | |
| Kenchappa RS, et al. Glutaredoxin is essential for maintenance of brain mitochondrial complex I: studies with MPTP. | |
| FASEB J 2003 Feb 19;. | |
| Wilding M, et al. Chaotic mosaicism in human preimplantation embryos is correlated with a low mitochondrial membrane potential. | |
| Fertil Steril 2003 Feb;79(2):340-6. | |
| Stewart VC, et al. Nitric oxide-induced mitochondrial dysfunction: implications for neurodegeneration. | |
| Free Radic Biol Med 2003 Feb 1;34(3):287-303. | |
| Blazej RG, et al. Polymorphism ratio sequencing: a new approach for single nucleotide polymorphism discovery and genotyping. | |
| Genome Res 2003 Feb;13(2):287-93. | |
| Mashima Y, et al. Optic disc excavation in the atrophic stage of Leber's hereditary optic neuropathy: comparison with normal tension glaucoma. | |
| Graefes Arch Clin Exp Ophthalmol 2003 Feb;241(2):75-80. | |
| Caldovic L, et al. Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. | |
| Hum Genet 2003 Feb 20;. | |
| Hortnagel K, et al. An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria. | |
| Hum Mol Genet 2003 Feb 1;12(3):321-327. | |
| Acin-Perez R, et al. An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA. | |
| Hum Mol Genet 2003 Feb 1;12(3):329-39. | |
| Agostino A, et al. Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice. | |
| Hum Mol Genet 2003 Feb 15;12(4):399-413. | |
| Barrientos A. Yeast models of human mitochondrial diseases. | |
| IUBMB Life 2003 Feb;55(2):83-95. | |
| Bach D, et al. Mitofusin-2 determines mitochondrial network architecture and mitochondrial metabolism: a novel regulatory mechanism altered in obesity. | |
| J Biol Chem 2003 Feb 21;. | |
| Bedogni B, et al. Redox regulation of CREB and induction of manganous superoxide dismutase in NGF-dependent cell survival. | |
| J Biol Chem 2003 Feb 27;. | |
| Zoll J, et al. Quantitative and qualitative adaptation of skeletal muscle mitochondria to increased physical activity. | |
| J Cell Physiol 2003 Feb;194(2):186-93. | |
| Hesselink MK, et al. Increased uncoupling protein 3 content does not affect mitochondrial function in human skeletal muscle in vivo. | |
| J Clin Invest 2003 Feb 15;111(4):479-486. | |
| Schon EA, et al. Neuronal degeneration and mitochondrial dysfunction. | |
| J Clin Invest 2003 Feb;111(3):303-12. | |
| Tolomeo M, et al. Mitochondrial disruption and apoptosis in lymphocytes of an HIV infected patient affected by lactic acidosis after treatment with highly active antiretroviral therapy. | |
| J Clin Pathol 2003 Feb;56(2):147-151. | |
| Fossati G, et al. The mitochondrial network of human neutrophils: role in chemotaxis, phagocytosis, respiratory burst activation, and commitment to apoptosis. | |
| J Immunol 2003 Feb 15;170(4):1964-72. | |
| Hoglinger GU, et al. Chronic systemic complex I inhibition induces a hypokinetic multisystem degeneration in rats. | |
| J Neurochem 2003 Feb;84(3):491-502. | |
| Djouadi F, et al. Characterization of fatty acid oxidation in human muscle mitochondria and myoblasts. | |
| Mol Genet Metab 2003 Feb;78(2):112-8. | |
| Sieb JP, et al. Iatrogenic and toxic myopathies. | |
| Muscle Nerve 2003 Feb;27(2):142-56. | |
| Ozawa T, et al. A genetic approach to identifying mitochondrial proteins. | |
| Nat Biotechnol 2003 Feb 10;. | |
| Penninger JM, et al. Mitochondria, AIF and caspases - rivaling for cell death execution. | |
| Nat Cell Biol 2003 Feb;5(2):97-9. | |
| Dennis C. Error reports threaten to unravel databases of mitochondrial DNA. | |
| Nature 2003 Feb 20;421(6925):773-4. | |
| Van Goethem G, et al. Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. | |
| Neuromuscul Disord 2003 Feb;13(2):133-42. | |
| Reimann J, et al. Mitochondrial dysfunction in myofibrillar myopathy. | |
| Neuropathol Appl Neurobiol 2003 Feb;29(1):45-51. | |
| Van Der Westhuizen FH, et al. Human mitochondrial complex I deficiency: investigating transcriptional responses by microarray. | |
| Neuropediatrics 2003 Feb;34(1):14-22. | |
| Ohkusu Y, et al. Quantitative assessment of the total myocardial uptake ratio of 123I-BMIPP by using the Ishii-MacIntyre method is useful for predicting cardiac complications in patients with mitochondrial encephalomyopathy or myotonic dystrophy. | |
| Nucl Med Commun 2003 Feb;24(2):183-90. | |
| Mason PA, et al. Mismatch repair activity in mammalian mitochondria. | |
| Nucleic Acids Res 2003 Feb 1;31(3):1052-8. | |
| Sacconi S, et al. Mutation Screening in Patients With Isolated Cytochrome c Oxidase Deficiency. | |
| Pediatr Res 2003 Feb;53(2):224-230. | |
| Krippeit-Drews P, et al. Phosphocreatine as a determinant of K(ATP) channel activity in pancreatic beta-cells. | |
| Pflugers Arch 2003 Feb;445(5):556-62. | |
| Russell P, et al. UCP3 protein expression is lower in type I, IIa and IIx muscle fiber types of endurance-trained compared to untrained subjects. | |
| Pflugers Arch 2003 Feb;445(5):563-9. | |
| Mambo E, et al. Electrophile and oxidant damage of mitochondrial DNA leading to rapid evolution of homoplasmic mutations. | |
| Proc Natl Acad Sci U S A 2003 Feb 10;. | |
| Lescuyer P, et al. Progress in the definition of a reference human mitochondrial proteome. | |
| Proteomics 2003 Feb;3(2):157-67. | |
| Chinnery PF. Searching for nuclear-mitochondrial genes. | |
| Trends Genet 2003 Feb;19(2):60-2. | |
| Hagelberg E. Recombination or mutation rate heterogeneity? Implications for Mitochondrial Eve. | |
| Trends Genet 2003 Feb;19(2):84-90. | |
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