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Experimental Dermatology, ISSN 0906-6705, 09/2014, Volume 23, Issue 9, pp. 607 - 614
Aberrant mitochondrial structure and function influence tissue homeostasis and thereby contribute to multiple human disorders and ageing. Ten per cent of... 
skin | OXPHOS | mitochondria | energy metabolism | respiratory chain | Energy metabolism | Mitochondria | Respiratory chain | Skin | OXIDATIVE-PHOSPHORYLATION | EPIDERMOLYSIS-BULLOSA SIMPLEX | SYSTEMIC-LUPUS-ERYTHEMATOSUS | BIRT-HOGG-DUBE | COCKAYNE-SYNDROME | KEARNS-SAYRE SYNDROME | DERMATOLOGY | CYTOCHROME-C-OXIDASE | AICARDI-GOUTIERES-SYNDROME | DNA MUTATIONS | PHOSPHORYLATED IN-VIVO | Intermediate Filaments - genetics | Intermediate Filaments - pathology | Skin Diseases - genetics | Humans | Mitochondrial Diseases - metabolism | Mitochondrial Proteins - genetics | Cockayne Syndrome - etiology | Autoimmune Diseases - etiology | Intermediate Filaments - metabolism | MAP Kinase Signaling System | Autoimmune Diseases - genetics | Mitochondrial Diseases - complications | DNA, Mitochondrial - genetics | Mitochondria - genetics | Heme - biosynthesis | Iron-Sulfur Proteins - biosynthesis | Skin Aging - physiology | Autoimmune Diseases - metabolism | Fatty Acids - metabolism | Mitochondrial Diseases - genetics | DNA, Mitochondrial - metabolism | Skin Diseases - metabolism | Cockayne Syndrome - metabolism | Oxidative Phosphorylation | Mitochondria - metabolism | Mitochondria - pathology | Genes, Mitochondrial | Skin Neoplasms - metabolism | Skin Diseases - etiology | Energy Metabolism | Deoxyribonucleotides - metabolism | DNA Repair | Skin Neoplasms - genetics | Cockayne Syndrome - genetics | Skin Aging - genetics | Skin Neoplasms - etiology | Mutation | Physiological aspects | Skin diseases | Mitochondrial DNA | Intermediate filament proteins | Fatty acids
Journal Article
Molecular and Cellular Proteomics, ISSN 1535-9476, 04/2011, Volume 10, Issue 4, p. M110.002964
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2015, Volume 92, Issue Pt A, pp. 55 - 63
Journal Article
Journal of Neurology, ISSN 0340-5354, 3/2003, Volume 250, Issue 3, pp. 267 - 277
Mitochondrial cytopathies represent a heterogeneous group of multisystem disorders which preferentially affect the muscle and nervous systems. They are caused... 
lactic acidosis | ragged-red fibres | mtDNA | respiratory chain | mitochondrial cytopathy | Mitochondrial cytopathy | MtDNA | Respiratory chain | Lactic acidosis | Ragged-red fibres | COMPLEX I | RESPIRATORY-CHAIN | SPERM MITOCHONDRIA | CLINICAL NEUROLOGY | CYTOCHROME-C-OXIDASE | MULTIPLE DELETIONS | EXTERNAL OPHTHALMOPLEGIA | HEREDITARY OPTIC NEUROPATHY | PREEXCITATION SYNDROME | RAGGED-RED FIBERS | PRENATAL-DIAGNOSIS | Mitochondrial Myopathies - metabolism | Humans | Ophthalmoplegia - physiopathology | Optic Atrophy, Hereditary, Leber - genetics | Leigh Disease - metabolism | Mitochondrial Myopathies - therapy | MELAS Syndrome - genetics | Kearns-Sayre Syndrome - physiopathology | Kearns-Sayre Syndrome - metabolism | DNA, Mitochondrial - genetics | MERRF Syndrome - genetics | Optic Atrophy, Hereditary, Leber - metabolism | Mitochondrial Myopathies - diagnosis | Optic Atrophy, Hereditary, Leber - physiopathology | Leigh Disease - physiopathology | Kearns-Sayre Syndrome - genetics | MERRF Syndrome - physiopathology | MELAS Syndrome - metabolism | MELAS Syndrome - physiopathology | MERRF Syndrome - metabolism | Mitochondrial Myopathies - physiopathology | Leigh Disease - genetics | Mitochondrial Myopathies - genetics | Animals | Ophthalmoplegia - genetics | Ophthalmoplegia - metabolism | Causes of | Genetic aspects | Mitochondrial DNA | Mitochondrial myopathies | Research
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 2014, Volume 9, Issue 1, p. 217
Journal Article
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2018, Volume 13, Issue 6, p. e0199258
Journal Article