(44 articoli trovati) |
| Reidla M, et al. Origin and Diffusion of mtDNA Haplogroup X. | |
| Am J Hum Genet 2003 Nov;73(6):1178-90. | |
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| Am J Physiol Cell Physiol 2003 Nov 5;. | |
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| Am J Physiol Endocrinol Metab 2003 Nov 12;. | |
| Cooper MA, et al. Anesthesia for Corrective Spinal Surgery in a Patient with Leigh's Disease. | |
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| Ann Neurol 2003 Nov;54(5):665-9. | |
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| 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. | |
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| Clin Chem 2003 Nov 21;. | |
| Perez-Martinez X, et al. Mss51p promotes mitochondrial Cox1p synthesis and interacts with newly synthesized Cox1p. | |
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| Lin PH, et al. Oxidative damage to mitochondrial DNA in atrial muscle of patients with atrial fibrillation. | |
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| Hum Mol Genet 2003 Nov 12;. | |
| Maxfield AB, et al. Cox17 is functional when tethered to the mitochondrial inner membrane. | |
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| 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. | |
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| J Cell Biol 2003 Nov 24;163(4):707-13. | |
| Suomalainen L, et al. Sphingosine-1-phosphate in inhibition of male germ cell apoptosis in the human testis. | |
| J Clin Endocrinol Metab 2003 Nov;88(11):5572-9. | |
| Taylor RW, et al. Mitochondrial DNA mutations in human colonic crypt stem cells. | |
| J Clin Invest 2003 Nov;112(9):1351-60. | |
| Puoti G, et al. Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son. | |
| J Med Genet 2003 Nov;40(11):858-63. | |
| Moraes CT, et al. Techniques and pitfalls in the detection of pathogenic mitochondrial DNA mutations. | |
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| Douwes Dekker P, et al. SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology. | |
| J Pathol 2003 Nov;201(3):480-486. | |
| Fernstrom M, et al. Effects of acute and chronic endurance exercise on mitochondrial uncoupling in human skeletal muscle. | |
| J Physiol 2003 Nov 21;. | |
| Taylor RW, et al. Mitochondrial DNA mutations in the haematopoietic system. | |
| Leukemia 2003 Nov 13;. | |
| Gattermann N. Mitochondrial DNA mutations in the hematopoietic system. | |
| Leukemia 2003 Nov 13;. | |
| Tzen CY, et al. Melas with point mutations involving tRNALeu (A3243G) and tRNAGlu(A14693g). | |
| Muscle Nerve 2003 Nov;28(5):575-81. | |
| Delsite RL, et al. Mitochondrial impairment is accompanied by impaired oxidative DNA repair in the nucleus. | |
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| Iizuka T, et al. Slowly progressive spread of the stroke-like lesions in MELAS. | |
| Neurology 2003 Nov 11;61(9):1238-44. | |
| Chinnery PF, et al. 116th ENMC international workshop: the treatment of mitochondrial disorders, 14th-16th March 2003, Naarden, The Netherlands. | |
| Neuromuscul Disord 2003 Nov;13(9):757-64. | |
| Hiyama T, et al. Somatic mutation in mitochondrial DNA and nuclear microsatellite instability in gastric cancer. | |
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| Pediatr Res 2003 Nov 19;. | |
| Palmieri F. The mitochondrial transporter family (SLC25): physiological and pathological implications. | |
| Pflugers Arch 2003 Nov 4;. | |
| Klaidman L, et al. Nicotinamide Offers Multiple Protective Meccanismi in Stroke as a Precursor for NAD(+), as a PARP Inhibitor and by Partial Restoration of Mitochondrial Function. | |
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| Vekemans BC, et al. Prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency in chorionic villi: a novel approach. | |
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| Trends Biochem Sci 2003 Nov;28(11):605-11. | |
| Boirie Y. Insulin regulation of mitochondrial proteins and oxidative phosphorylation in human muscle. | |
| Trends Endocrinol Metab 2003 Nov;14(9):393-4. | |
