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Academic Journal

Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases.

  • Authors : Filosto M; Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Policlinico G.B. Rossi, p. le L.A. Scuro 10, 37134 Verona, Italy.; Tonin P

Subjects: Antioxidants/Antioxidants/Antioxidants/*metabolism ; Free Radical Scavengers/Free Radical Scavengers/Free Radical Scavengers/*immunology ; Free Radical Scavengers/Free Radical Scavengers/Free Radical Scavengers/*metabolism

  • Source: Acta neuropathologica [Acta Neuropathol] 2002 Mar; Vol. 103 (3), pp. 215-20. Date of Electronic Publication: 2001 Nov 16.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 0412041 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Allotopic expression of ATP6 in the mouse as a transgenic model of mitochondrial disease.

  • Authors : Dunn DA; Department of Biological Sciences, State University of New York, Oswego, NY, USA.; Pinkert CA

Subjects: Gene Expression*; Mitochondrial Diseases/Mitochondrial Diseases/Mitochondrial Diseases/*genetics ; Mitochondrial Proton-Translocating ATPases/Mitochondrial Proton-Translocating ATPases/Mitochondrial Proton-Translocating ATPases/*genetics

  • Source: Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2015; Vol. 1265, pp. 255-69.Publisher: Humana Press Country of Publication: United States NLM ID: 9214969 Publication Model: Print Cited Medium: Internet ISSN: 1940-6029

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Academic Journal

Melanopsin-expressing retinal ganglion cells are resistant to cell injury, but not always.

  • Authors : Georg B; Department of Clinical Biochemistry, Bispebjerg and Frederiksberg Hospital, Faculty Health Sciences, University of Copenhagen, Denmark.; Ghelli A

Subjects: Gene Expression* ; Stress, Physiological*; Mitochondrial Diseases/Mitochondrial Diseases/Mitochondrial Diseases/*pathology

  • Source: Mitochondrion [Mitochondrion] 2017 Sep; Vol. 36, pp. 77-84. Date of Electronic Publication: 2017 Apr 12.Publisher: Elsevier Science Country of Publication: Netherlands NLM ID: 100968751 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Induction of mitochondrial biogenesis is a maladaptive mechanism in mitochondrial cardiomyopathies.

  • Authors : Sebastiani M; Dipartimento di Medicina Sperimentale, Polo Pontino, Sapienza, Università di Roma, Rome, Italy.; Giordano C

Subjects: Gene Expression*; Cardiomyopathies/Cardiomyopathies/Cardiomyopathies/*genetics ; Cardiomyopathies/Cardiomyopathies/Cardiomyopathies/*pathology

  • Source: Journal of the American College of Cardiology [J Am Coll Cardiol] 2007 Oct 02; Vol. 50 (14), pp. 1362-9. Date of Electronic Publication: 2007 Sep 17.Publisher: Elsevier Biomedical Country of Publication: United States NLM ID: 8301365 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

OXPHOS gene expression and control in mitochondrial disorders.

  • Authors : Reinecke F; Centre for Human Metabonomics, School for Physical and Chemical Sciences, North-West University, Hoffman street, Potchefstroom 2531, South Africa.; Smeitink JA

Subjects: Oxidative Phosphorylation*; Gene Expression/Gene Expression/Gene Expression/*physiology ; Genes, Mitochondrial/Genes, Mitochondrial/Genes, Mitochondrial/*genetics

  • Source: Biochimica et biophysica acta [Biochim Biophys Acta] 2009 Dec; Vol. 1792 (12), pp. 1113-21. Date of Electronic Publication: 2009 Apr 21.Publisher: Elsevier Pub. Co Country of Publication: Netherlands NLM ID: 0217513 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

[Gene expression profiling of classic mitochondrial disorders. Its value in finding therapeutic strategies].

  • Authors : Mende S; Klinik und Poliklinik für Neurologie, Technische Universität Dresden. ; Storch A

Subjects: Gene Expression Profiling*; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; Gene Expression/Gene Expression/Gene Expression/*physiology

  • Source: Der Nervenarzt [Nervenarzt] 2007 Oct; Vol. 78 (10), pp. 1155-9.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 0400773 Publication Model: Print Cited Medium: Print ISSN: 0028-2804 (Print)

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Academic Journal

Gene expression in a Drosophila model of mitochondrial disease.

  • Authors : Fernández-Ayala DJ; Institute of Medical Technology and Tampere University Hospital, University of Tampere, Tampere, Finland.; Chen S

Subjects: Disease Models, Animal* ; Gene Expression*; Drosophila/Drosophila/Drosophila/*genetics

  • Source: PloS one [PLoS One] 2010 Jan 06; Vol. 5 (1), pp. e8549. Date of Electronic Publication: 2010 Jan 06.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Electronic Cited Medium: Internet

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Academic Journal

Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation.

  • Authors : Desguerre I; Service de Neuropédiatrie, Hôpital Saint Vincent de Paul, 74 Avenue Denfert-Rochereau, 75014 Paris, France. ; Pinton F

Subjects: Magnetic Resonance Imaging*; Adenosine Triphosphatases/Adenosine Triphosphatases/Adenosine Triphosphatases/*genetics ; Basal Ganglia/Basal Ganglia/Basal Ganglia/*pathology

  • Source: Neuropediatrics [Neuropediatrics] 2003 Jun; Vol. 34 (5), pp. 265-9.Publisher: Hippokrates Verlag Country of Publication: Germany NLM ID: 8101187 Publication Model: Print Cited Medium: Print ISSN: 0174-304X

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Academic Journal

Over-expression of the catalytic core of mitochondrial DNA (mtDNA) polymerase in the nervous system of Drosophila melanogaster reduces median life span by inducing mtDNA depletion.

  • Authors : Martínez-Azorín F; Departamento de Bioquímica, Instituto de Investigaciones Biomédicas Alberto Sols CSIC-UAM, Facultad de Medicina CIBERER ISCIII, Universidad Autónoma de Madrid, Madrid, Spain. ; Calleja M

Subjects: Catalytic Domain/Catalytic Domain/Catalytic Domain/*physiology ; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*chemistry ; Gene Expression/Gene Expression/Gene Expression/*physiology

  • Source: Journal of neurochemistry [J Neurochem] 2008 Apr; Vol. 105 (1), pp. 165-76. Date of Electronic Publication: 2007 Nov 12.Publisher: Wiley on behalf of the International Society for Neurochemistry Country of Publication: England NLM ID: 2985190R Publication Model: Print-Electronic

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Academic Journal

A novel mutation, P126R, in a Japanese patient with HHH syndrome.

  • Authors : Miyamoto T; Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP, 4-1-1 Ogawahigashi, Kodaira, Tokyo 187-8502, Japan.; Kanazawa N

Subjects: Gene Expression/Gene Expression/Gene Expression/*genetics ; Metabolism, Inborn Errors/Metabolism, Inborn Errors/Metabolism, Inborn Errors/*genetics ; Metabolism, Inborn Errors/Metabolism, Inborn Errors/Metabolism, Inborn Errors/*metabolism

  • Source: Pediatric neurology [Pediatr Neurol] 2002 Jan; Vol. 26 (1), pp. 65-7.Publisher: Elsevier Science Publishing Country of Publication: United States NLM ID: 8508183 Publication Model: Print Cited Medium: Print ISSN:

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  • 1-10 of  974 results for ""Mitochondrial Diseases""