1 Giu 2003 - 30 Giu 2003 |
(47 articoli trovati) |
| Nolan D, et al. Mitochondrial DNA depletion and morphologic changes in adipocytes associated with nucleoside reverse transcriptase inhibitor therapy. | |
| AIDS 2003 Jun 13;17(9):1329-38. | |
| Howell N, et al. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background. | |
| Am J Med Genet 2003 Jun 1;119A(2):147-51. | |
| Fiskum G, et al. Mitochondrial mechanisms of neural cell death and neuroprotective interventions in Parkinson's disease. | |
| Ann N Y Acad Sci 2003 Jun;991:111-9. | |
| Beal MF. Mitochondria, oxidative damage, and inflammation in Parkinson's disease. | |
| Ann N Y Acad Sci 2003 Jun;991:120-31. | |
| Mari;n-Hernandez A, et al. Toxic effects of copper-based antineoplastic drugs (Casiopeinas((R))) on mitochondrial functions. | |
| Biochem Pharmacol 2003 Jun 15;65(12):1979-1989. | |
| Kadenbach B. Intrinsic and extrinsic uncoupling of oxidative phosphorylation. | |
| Biochim Biophys Acta 2003 Jun 5;1604(2):77-94. | |
| Leary SC, et al. Mitochondrial biogenesis: Which part of "NO" do we understand? | |
| Bioessays 2003 Jun;25(6):538-41. | |
| Van Noord PA. An alternative, non-intrauterine hypothesis, based on maternal mitochondrial oocyte inheritance, to explain inconsistent findings of birth weight on (breast) cancer risk. | |
| Br J Cancer 2003 Jun 2;88(11):1817-8. | |
| Binder J, et al. Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene. | |
| Brain 2003 Jun 4;. | |
| Johnson PR, et al. Non-uniform distribution of mitochondria in pancreatic acinar cells. | |
| Cell Tissue Res 2003 Jun 28;. | |
| Greenberger JS, et al. Radioprotective gene therapy. | |
| Curr Gene Ther 2003 Jun;3(3):183-95. | |
| Stacpoole PW, et al. The pyruvate dehydrogenase complex as a target for gene therapy. | |
| Curr Gene Ther 2003 Jun;3(3):239-45. | |
| Zeviani M, et al. Nuclear genes in mitochondrial disorders. | |
| Curr Opin Genet Dev 2003 Jun;13(3):262-70. | |
| Evangeliou A, et al. Carnitine Metabolism and Deficit - When Supplementation is Necessary? | |
| Curr Pharm Biotechnol 2003 Jun;4(3):211-9. | |
| van der Bliek AM, et al. A mitochondrial rhomboid protease. | |
| Dev Cell 2003 Jun;4(6):769-70. | |
| Suzuki Y, et al. Multiple Tumors in Mitochondrial Diabetes Associated With tRNA(Leu(UUR)) Mutation at Position 3264. | |
| Diabetes Care 2003 Jun;26(6):1942-1943. | |
| Wedel T, et al. Mitochondrial myopathy (complex I deficiency) associated with chronic intestinal pseudo-obstruction. | |
| Eur J Pediatr Surg 2003 Jun;13(3):201-5. | |
| Jendrossek V, et al. Celecoxib activates a novel mitochondrial apoptosis signaling pathway. | |
| FASEB J 2003 Jun 17;. | |
| Tan DJ, et al. Novel heteroplasmic frameshift and missense somatic mitochondrial DNA mutations in oral cancer of betel quid chewers. | |
| Genes Chromosomes Cancer 2003 Jun;37(2):186-94. | |
| Lehtonen MS, et al. Increased variation in mtDNA in patients with familial sensorineural hearing impairment. | |
| Hum Genet 2003 Jun 12;. | |
| Benit P, et al. Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophic cardiomyopathy and encephalopathy. | |
| Hum Mutat 2003 Jun;21(6):582-6. | |
| Brandstatter A, et al. Mitochondrial DNA heteroplasmy or artefacts-a matter of the amplification strategy? | |
| Int J Legal Med 2003 Jun;117(3):180-4. | |
| Marin-Garcia J. Mitochondrial dysfunction in heart failure. | |
| J Am Coll Cardiol 2003 Jun 18;41(12):2299; author reply 2299. | |
| Fiermonte G, et al. The mitochondrial ornithine transporter: bacterial expression,reconstitution, functional characterization, and tissuedistribution of two human isoforms. | |
| J Biol Chem 2003 Jun 13;. | |
| Speer O, et al. Rapid suppression of mitochondrial permeability transition by methylglyoxal. Role of reversible arginine modification. | |
| J Biol Chem 2003 Jun 18;. | |
| Wang WL, et al. PICK1: An anchoring protein that specifically targets PKCalpha to mitochondria selectively upon serum stimulation in NIH 3T3 cells. | |
| J Biol Chem 2003 Jun 25;. | |
| Brookes PS, et al. Control of mitochondrial respiration by NO, effects of low oxygen and respiratory state. | |
| J Biol Chem 2003 Jun 4;. | |
| Punter FA, et al. Mutagenesis reveals a specific role for Cox17p in copper transport to cytochrome oxidase. | |
| J Biol Chem 2003 Jun 4;. | |
| Nishigaki Y, et al. Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency. | |
| J Clin Invest 2003 Jun 15;111(12):1913-1921. | |
| Collins TJ, et al. Mitochondria are morphologically heterogeneous within cells. | |
| J Exp Biol 2003 Jun;206(Pt 12):1993-2000. | |
| Nishioka T, et al. Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia. | |
| J Hum Genet 2003 Jun 24;. | |
| Regula KM, et al. Mitochondria-assisted cell suicide: a license to kill. | |
| J Mol Cell Cardiol 2003 Jun;35(6):559-67. | |
| Karlic H, et al. Downregulation of carnitine acyltransferases and organic cation transporter OCTN2 in mononuclear cells in healthy elderly and patients with myelodysplastic syndromes. | |
| J Mol Med 2003 Jun 12;. | |
| den Boer ME, et al. Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement. | |
| J Pediatr 2003 Jun;142(6):684-9. | |
| Read CY. The demands of biochemical genetic disorders: A survey of mothers of children with mitochondrial disease or phenylketonuria. | |
| J Pediatr Nurs 2003 Jun;18(3):181-6. | |
| Ogedegbe AE, et al. Hyperlactataemia syndromes associated with HIV therapy. | |
| Lancet Infect Dis 2003 Jun;3(6):329-37. | |
| Kokaze A, et al. Longevity-associated mitochondrial DNA 5178 A/C polymorphism influences effects of cigarette smoking on serum protein fraction levels in Japanese men. | |
| Mech Ageing Dev 2003 Jun;124(6):765-70. | |
| Privette JD, et al. Fatty acid oxidation by skeletal muscle homogenates from morbidly obese black and white American women. | |
| Metabolism 2003 Jun;52(6):735-8. | |
| Fuselli S, et al. Mitochondrial DNA Diversity in South America and the Genetic History of Andean Highlanders. | |
| Mol Biol Evol 2003 Jun 27;. | |
| Das AM. Regulation of the mitochondrial ATP-synthase in health and disease. | |
| Mol Genet Metab 2003 Jun;79(2):71-82. | |
| Peng Y, et al. Spasmodic dysphonia in a patient with the A to G transition at nucleotide 8344 in mitochondrial DNA. | |
| Mov Disord 2003 Jun;18(6):716-8. | |
| DiMauro S, et al. Mitochondrial respiratory-chain diseases. | |
| N Engl J Med 2003 Jun 26;348(26):2656-68. | |
| Campos Y, et al. Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypes. | |
| Neuromuscul Disord 2003 Jun;13(5):416-420. | |
| Mayer B, et al. Mitochondrial regulation of apoptosis. | |
| News Physiol Sci 2003 Jun;18:89-94.; Review | |
| Miller FJ, et al. Precise determination of mitochondrial DNA copy number in human skeletal and cardiac muscle by a PCR-based assay: lack of change of copy number with age. | |
| Nucleic Acids Res 2003 Jun 1;31(11):e61. | |
| Bolton P, et al. Anaesthesia for an adolescent with mitochondrial encephalomyopathy-lactic acidosis-stroke-like episodes syndrome. | |
| Paediatr Anaesth 2003 Jun;13(5):453-6. | |
| Petris MJ. The SLC31 (Ctr) copper transporter family. | |
| Pflugers Arch 2003 Jun 24;. | |
Ritorno a Fonama.org Home Page
