1 Mar  2003  -  31 Mar  2003

(60 articoli trovati)

 

1 Acta Neuropathol (Berl) 3 J Biol Chem
1 Acta Psychiatr Scand 1 J Clin Immunol
1 Am J Ophthalmol 1 J Intern Med
1 Am J Otolaryngol 1 J Med Genet
1 Am J Phys Anthropol 1 J Nephrol
1 Amino Acids 2 J Neuroophthalmol
1 Anesthesiology 1 J Neuropathol Exp Neurol
1 Biochem Biophys Res Commun 1 J Physiol
1 Biol Reprod 1 J Surg Oncol
1 Chem Biol Interact 2 Leg Med (Tokyo)
1 Clin Exp Nephrol 1 Mech Ageing Dev
1 Diabetes Care 1 Mol Cell
1 Diabetes Res Clin Pract 1 Mol Genet Metab
2 Eur J Biochem 1 Muscle Nerve
1 Eur J Pediatr 1 Nat Genet
1 Exp Hematol 1 Nat Rev Cancer
1 FEBS Lett 1 Neuromuscul Disord
1 Fertil Steril 1 Neuroreport
1 Free Radic Biol Med 2 Nucleic Acids Res
1 Hum Gene Ther 1 Oncogene
1 Hum Genet 1 Ophthalmologe
1 Hum Mol Genet 1 Pediatr Pathol Mol Med
1 Hum Reprod 2 Pediatr Res
1 Invest Ophthalmol Vis Sci 1 Pediatrics
2 IUBMB Life 1 Theor Popul Biol
1 J Am Coll Cardiol 1 Traffic

 

Acta Neuropathol (Berl)

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Berger A, et al. Severe depletion of mitochondrial DNA in spinal muscular atrofia.
Acta Neuropathol (Berl) 2003 Mar;105(3):245-51.  

 

Acta Psychiatr Scand

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Gardner A, et al. Alterations of rCBF and mitochondrial dysfunction in major depressive disorder: a case report.
Acta Psychiatr Scand 2003 Mar;107(3):233-239.  

 

Am J Ophthalmol

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Grossniklaus EB. Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy. Guy J,* Qi X, Pallotti F, Schon EA, Manfredi G, Carelli V, Martinuzzi A, Hauswirth WW, Lewin AS. Ann Neurol 2002;52:534-542.
Am J Ophthalmol 2003 Mar;135(3):422.  

 

Am J Otolaryngol

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Kaidar-Person O, et al. Rapidly progressive bilateral sensory neural hearing loss as a presentation of mitochondrial neurogastrointestinal encephalomyopathy.
Am J Otolaryngol 2003 Mar-Apr;24(2):128-30.  

 

Am J Phys Anthropol

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Pakendorf B, et al. Mitochondrial DNA evidence for admixed origins of central Siberian populations.
Am J Phys Anthropol 2003 Mar;120(3):211-24.  

 

Amino Acids

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Nocera S, et al. New perspectives on the role of amine oxidases in physiopathology.
Amino Acids 2003 Mar;24(1-2):13-7.  

 

Anesthesiology

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Ludwig LM, et al. Morphine Enhances Pharmacological Preconditioning by Isoflurane: Role of Mitochondrial KATP Channels and Opioid Receptors.
Anesthesiology 2003 Mar;98(3):705-711.  

 

Biochem Biophys Res Commun

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Tomikura Y, et al. Coordinate induction of AMP deaminase in human atrium with mitochondrial DNA deletion.
Biochem Biophys Res Commun 2003 Mar 7;302(2):372-6.  

 

Biol Reprod

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Thompson WE, et al. Ubiquitination of Prohibitin in Mammalian Sperm Mitochondria: Possible Roles in The Regulation of Mitochondrial Inheritance and Sperm Quality Control.
Biol Reprod 2003 Mar 19;.  

 

Chem Biol Interact

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Muraoka S, et al. Inactivation of mitochondrial succinate dehydrogenase by adriamycin activated by horseradish peroxidase and hydrogen peroxide.
Chem Biol Interact 2003 Mar 6;145(1):67-75.  

 

Clin Exp Nephrol

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Takebayashi S, et al. Mitochondrial DNA deletion of proximal tubules is the result of itai-itai disease.
Clin Exp Nephrol 2003 Mar;7(1):18-26.  

 

Diabetes Care

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Hattori Y, et al. Heteroplasmic Mitochondrial DNA 3310 Mutation in NADH Dehydrogenase Subunit 1 Associated With Type 2 Diabetes, Hypertrophic Cardiomyopathy, and Mental Retardation in a Single Patient.
Diabetes Care 2003 Mar;26(3):952-953.  

 

Diabetes Res Clin Pract

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Suzuki S, et al. Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A-G) mutation in Japanese: Maternal inheritance and mitochondria-related complications.
Diabetes Res Clin Pract 2003 Mar;59(3):207-17.  

 

Eur J Biochem

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Vijayasarathy C, et al. Adaptive changes in the expression of nuclear and mitochondrial encoded subunits of cytochrome c oxidase and the catalytic activity during hypoxia.
Eur J Biochem 2003 Mar;270(5):871-9.  
Bratton M, et al. Disease-related mutations in cytochrome c oxidase studied in yeast and bacterial models.
Eur J Biochem 2003 Mar;270(6):1222-30.  

 

Eur J Pediatr

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Tekin M, et al. Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey.
Eur J Pediatr 2003 Mar;162(3):154-8.  

 

Exp Hematol

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Dror Y. The role of mitochondrial-mediated apoptosis in a myelodysplastic syndrome secondary to congenital deletion of the short arm of chromosome 4.
Exp Hematol 2003 Mar;31(3):211-7.  

 

FEBS Lett

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Mattenberger Y, et al. Fusion of mitochondria in mammalian cells is dependent on the mitochondrial inner membrane potential and independent of microtubules or actin.
FEBS Lett 2003 Mar 13;538(1-3):53-9.  

 

Fertil Steril

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O'Connell M, et al. Differences in mitochondrial and nuclear DNA status of high-density and low-density sperm fractions after density centrifugation preparation.
Fertil Steril 2003 Mar;79(3 Suppl 1):754-62.  

 

Free Radic Biol Med

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Borras C, et al. Mitochondria from females exhibit higher antioxidant gene expression and lower oxidative damage than males.
Free Radic Biol Med 2003 Mar 1;34(5):546-52.  

 

Hum Gene Ther

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Herraiz M, et al. Liver failure caused by herpes simplex virus thymidine kinase plus ganciclovir therapy is associated with mitochondrial dysfunction and mitochondrial DNA depletion.
Hum Gene Ther 2003 Mar 20;14(5):463-72.  

 

Hum Genet

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Benit P, et al. Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome.
Hum Genet 2003 Mar 4;.  

 

Hum Mol Genet

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Schroder R, et al. On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria.
Hum Mol Genet 2003 Mar 15;12(6):657-669.  

 

Hum Reprod

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May-Panloup P, et al. Increased sperm mitochondrial DNA content in male infertility.
Hum Reprod 2003 Mar;18(3):550-556.  

 

Invest Ophthalmol Vis Sci

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Qi X, et al. Optic neuropathy induced by reductions in mitochondrial superoxide dismutase.
Invest Ophthalmol Vis Sci 2003 Mar;44(3):1088-96.  

 

IUBMB Life

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Wang ZC, et al. Detection of mitochondrial DNA deletion by a modified PCR method in a 60Co radiation-exposed patient.
IUBMB Life 2003 Mar;55(3):133-7.  
Wang ZC, et al. Search for difference in aminoacylation of mitochondrial DNA-encoded wild-type and mutant human tRNALeu (UUR).
IUBMB Life 2003 Mar;55(3):139-44.  

 

J Am Coll Cardiol

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Monteiro P, et al. Trimetazidine-mediated cardioprotection during ischemia is mediated by mitochondrial respiratory chain's complex I activity.
J Am Coll Cardiol 2003 Mar 19;41(6 Suppl B):373.  

 

J Biol Chem

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Jazayeri M, et al. Inducible expression of a dominant negative DNA polymerase-gamma depletes mitochondrial DNA and produces a rho0 phenotype.
J Biol Chem 2003 Mar 14;278(11):9823-30.  
Tomari Y, et al. Decreased CCA-addition in human mitochondrial tRNAs bearing a pathogenic A4317G or A10044G mutation.
J Biol Chem 2003 Mar 5;.  
Dolder M, et al. Inhibition of the mitochondrial permeability transition by creatine kinase substrates: requirement for microcompartmentation.
J Biol Chem 2003 Mar 5;.  

 

J Clin Immunol

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Brenner C, et al. Insights into the mitochondrial signaling pathway: what lessons for chemotherapy?
J Clin Immunol 2003 Mar;23(2):73-80.  

 

J Intern Med

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Garcia-Velasco A, et al. Intestinal pseudo-obstruction and urinary retention: cardinal features of a mitochondrial DNA-related disease.
J Intern Med 2003 Mar;253(3):381-5.  

 

J Med Genet

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Chol M, et al. The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.
J Med Genet 2003 Mar;40(3):188-91.  

 

J Nephrol

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Rotig A. Renal disease and mitochondrial genetics.
J Nephrol 2003 Mar-Apr;16(2):286-92.  

 

J Neuroophthalmol

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Vaphiades MS, et al. Optic nerve and chiasmal enhancement in leber hereditary optic neuropathy.
J Neuroophthalmol 2003 Mar;23(1):104-5.  
Batioglu F, et al. Chiasmal high signal on magnetic resonance imaging in the atrophic phase of leber hereditary optic neuropathy.
J Neuroophthalmol 2003 Mar;23(1):28-30.  

 

J Neuropathol Exp Neurol

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Oldfors A, et al. Mitochondrial encephalomyopathies.
J Neuropathol Exp Neurol 2003 Mar;62(3):217-27.  

 

J Physiol

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Ward JP. Mitochondria and oxygen sensing: fuelling the controversy.
J Physiol 2003 Mar 7;.  

 

J Surg Oncol

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Tong BC, et al. Mitochondrial DNA alterations in thyroid cancer.
J Surg Oncol 2003 Mar;82(3):170-3.  

 

Leg Med (Tokyo)

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von Wurmb-Schwark N, et al. Extraction and amplification of nuclear and mitochondrial DNA from ancient and artificially aged bones.
Leg Med (Tokyo) 2003 Mar;5 Suppl:S169-72.  
Wittig H, et al. Variability of mitochondrial DNA in a population sample from Iceland.
Leg Med (Tokyo) 2003 Mar;5 Suppl:S173-6.  

 

Mech Ageing Dev

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Waters DL, et al. Skeletal muscle mitochondrial function and lean body mass in healthy exercising elderly.
Mech Ageing Dev 2003 Mar;124(3):301-9.  

 

Mol Cell

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Mihara M, et al. p53 Has a Direct Apoptogenic Role at the Mitochondria.
Mol Cell 2003 Mar;11(3):577-90.  

 

Mol Genet Metab

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Brivet M, et al. Impaired mitochondrial pyruvate importation in a patient and a fetus at risk.
Mol Genet Metab 2003 Mar;78(3):186-92.  

 

Muscle Nerve

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Tarnopolsky M, et al. Diagnostic utility of a modified forearm ischemic exercise test and technical issues relevant to exercise testing.
Muscle Nerve 2003 Mar;27(3):359-66.  

 

Nat Genet

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Cavalli-Sforza LL, et al. The application of molecular genetic approaches to the study of human evolution.
Nat Genet 2003 Mar;33 Suppl:266-75.  

 

Nat Rev Cancer

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Eng C, et al. A role for mitochondrial enzymes in inherited neoplasia and beyond.
Nat Rev Cancer 2003 Mar;3(3):193-202.  

 

Neuromuscul Disord

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Koga A, et al. Increased mitochondrial processing intermediates associated with three tRNA(Leu(UUR)) gene mutations.
Neuromuscul Disord 2003 Mar;13(3):259-62.  

 

Neuroreport

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McDermott CJ, et al. Investigation of mitochondrial function in hereditary spastic paraparesis.
Neuroreport 2003 Mar 3;14(3):485-8.  

 

Nucleic Acids Res

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Yoon YG, et al. Efficient cloning and engineering of entire mitochondrial genomes in Escherichia coli and transfer into transcriptionally active mitochondria.
Nucleic Acids Res 2003 Mar 1;31(5):1407-15.  
Alam TI, et al. Human mitochondrial DNA is packaged with TFAM.
Nucleic Acids Res 2003 Mar 15;31(6):1640-5.  

 

Oncogene

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Benn DE, et al. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.
Oncogene 2003 Mar 6;22(9):1358-64.  

 

Ophthalmologe

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Staudt S, et al. [Pigmented retinopathy as a presenting sign of mitochondrial encephalomyopathy without external ophthalmoplegia]
Ophthalmologe 2003 Mar;100(3):234-7.  

 

Pediatr Pathol Mol Med

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Kurup RK, et al. The isoprenoid pathway and the pathogenesis of reye's syndrome.
Pediatr Pathol Mol Med 2003 Mar-Apr;22(2):159-70.  

 

Pediatr Res

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Rizzo C, et al. Characteristic Acylcarnitine Profiles in Inherited Defects of Peroxisome Biogenesis: A Novel Tool for Screening Diagnosis Using Tandem Mass Spectrometry.
Pediatr Res 2003 Mar 19;.  
Jones PM, et al. Accumulation of 3-Hydroxy-Fatty Acids in the Culture Medium of Long-Chain L-3-Hydroxyacyl CoA Dehydrogenase (LCHAD) and Mitochondrial Trifunctional Protein-Deficient Skin Fibroblasts: Implications for Medium Chain Triglyceride Dietary Treatment of LCHAD Deficiency.
Pediatr Res 2003 Mar 5;.  

 

Pediatrics

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Uusimaa J, et al. A Mutation in Mitochondrial DNA-Encoded Cytochrome c Oxidase II Gene in a Child With Alpers-Huttenlocher-Like Disease.
Pediatrics 2003 Mar;111(3):E262-8.  

 

Theor Popul Biol

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Matessi C, et al. Mother's mitochondria and optimal offspring sex ratio.
Theor Popul Biol 2003 Mar;63(2):147-57.  

 

Traffic

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Leuenberger D, et al. The Role of Tim9p in the Assembly of the TIM22 Import Complexes.
Traffic 2003 Mar;4(3):144-52.  

 

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