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المساهمون: University of Zurich, Murgia, Marta
المصدر: International Journal of Molecular Sciences, Vol 22, Iss 11080, p 11080 (2021)
International Journal of Molecular Sciences
International journal of molecular sciences 22(20), 11080 (2021). doi:10.3390/ijms222011080 special issue: "Novel Molecular Approaches to Skeletal Muscle Disease and Disuse"
Int. J. Mol. Sci. 22:11080 (2021)
Volume 22
Issue 20مصطلحات موضوعية: Male, Ophthalmoplegia, Chronic Progressive External, skeletal muscle, mtDNA deletions, transcriptomics, proteomics, myopathy, disease models, Muscle Fibers, Skeletal, Respiratory chain, 1607 Spectroscopy, Proteomics, Transcriptome, genetics [Ophthalmoplegia, Chronic Progressive External], Gene Regulatory Networks, Biology (General), Spectroscopy, Laser capture microdissection, General Medicine, genetics [DNA, Mitochondrial], Computer Science Applications, Cell biology, ddc, Succinate Dehydrogenase, Chemistry, Proteome, ddc:540, Female, 1606 Physical and Theoretical Chemistry, Mitochondrial DNA, genetics [Mitochondria, Muscle], 1503 Catalysis, QH301-705.5, pathology [Mitochondria, Muscle], 610 Medicine & health, Laser Capture Microdissection, Biology, genetics [NADPH Dehydrogenase], DNA, Mitochondrial, Catalysis, Article, Inorganic Chemistry, Electron Transport Complex IV, metabolism [Succinate Dehydrogenase], medicine, 1312 Molecular Biology, 1706 Computer Science Applications, Humans, Physical and Theoretical Chemistry, Molecular Biology, QD1-999, metabolism [NADPH Dehydrogenase], 1604 Inorganic Chemistry, metabolism [Electron Transport Complex IV], Gene Expression Profiling, Organic Chemistry, NADPH Dehydrogenase, pathology [Ophthalmoplegia, Chronic Progressive External], medicine.disease, Mitochondria, Muscle, Disease Models, Mtdna Deletions, Myopathy, Skeletal Muscle, Transcriptomics, 10054 Clinic for Psychiatry, Psychotherapy, and Psychosomatics, Translational elongation, pathology [Muscle Fibers, Skeletal], methods [Proteomics], Chronic progressive external ophthalmoplegia, 1605 Organic Chemistry
وصف الملف: application/pdf; application/zip; ijms_22_11080_v2.pdf - application/pdf
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المؤلفون: Irina Minin, Reinhard Dengler, Viktoriya Peeva, Grazyna Debska-Vielhaber, Gábor Zsurka, Wolfram S. Kunz, Katja Kollewe, Cornelia Kornblum, Susanne Schoeler, Werner Zuschratter, Alexei P. Kudin, Stefan Vielhaber, Stefanie Schreiber
المصدر: Acta neuropathologica 125(2), 245-256 (2012). doi:10.1007/s00401-012-1036-y
مصطلحات موضوعية: Male, DNA Repair, Muscle Fibers, Skeletal, MFN2, Respiratory chain, Gene Dosage, Cell Separation, GTP Phosphohydrolases, MFN2 protein, human, Charcot-Marie-Tooth Disease, Cells, Cultured, physiology [Muscle, Skeletal], physiology [Fibroblasts], Mitochondria, physiology [Electron Transport], metabolism [Citrate (si)-Synthase], Succinate Dehydrogenase, Mitochondrial respiratory chain, physiology [Muscle Fibers, Skeletal], Female, genetics [Mitochondrial Proteins], genetics [Charcot-Marie-Tooth Disease], Adult, Mitochondrial DNA, genetics [GTP Phosphohydrolases], DNA repair, Blotting, Western, genetics [Mutation], Oxidative phosphorylation, Citrate (si)-Synthase, Biology, DNA, Mitochondrial, Pathology and Forensic Medicine, Electron Transport, metabolism [Succinate Dehydrogenase], Mitochondrial Proteins, Electron Transport Complex IV, Cellular and Molecular Neuroscience, Mitofusin-2, Young Adult, Oxygen Consumption, Cytochrome c oxidase, Humans, physiology [Mitochondria], ddc:610, Muscle, Skeletal, metabolism [Electron Transport Complex IV], physiology [Oxygen Consumption], Fibroblasts, genetics [Electron Transport], Molecular biology, physiology [DNA, Mitochondrial], Microscopy, Electron, Mutation, biology.protein, Neurology (clinical), genetics [Mitochondria]