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Volumn 256, Issue SUPPL. 1, 2009, Pages 9-17
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The pathogenesis of Friedreich ataxia and the structure and function of frataxin
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Author keywords
Iron metabolism; Mitochondria; Oxidative stress
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Indexed keywords
ASPARTIC ACID;
CHAPERONE;
FRATAXIN;
GLUTAMIC ACID;
GLUTATHIONE;
GLUTATHIONE TRANSFERASE;
IRON;
IRON REGULATORY PROTEIN 1;
IRON REGULATORY PROTEIN 2;
REACTIVE OXYGEN METABOLITE;
SULFUR;
SULFUR AMINO ACID;
AMINO TERMINAL SEQUENCE;
BETA SHEET;
CARBOXY TERMINAL SEQUENCE;
CELL STRESS;
CELLULAR STRESS RESPONSE;
ENERGY METABOLISM;
EUKARYOTE;
FRIEDREICH ATAXIA;
HEME SYNTHESIS;
HUMAN;
IRON BINDING CAPACITY;
IRON METABOLISM;
METABOLIC DISORDER;
MITOCHONDRION;
NEUROPATHOLOGY;
NONHUMAN;
ORTHOLOGY;
OXIDATIVE STRESS;
PRIORITY JOURNAL;
PROTEIN BINDING;
PROTEIN FUNCTION;
PROTEIN STABILITY;
PROTEIN STRUCTURE;
REVIEW;
SEQUENCE ALIGNMENT;
SEQUENCE HOMOLOGY;
ANIMALS;
FRIEDREICH ATAXIA;
HUMANS;
IRON-BINDING PROTEINS;
METABOLIC DISEASES;
MODELS, MOLECULAR;
PROTEIN BINDING;
PROTEIN FOLDING;
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EID: 62549093116
PISSN: 03405354
EISSN: 14321459
Source Type: Journal
DOI: 10.1007/s00415-009-1003-2 Document Type: Review |
Times cited : (209)
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References (76)
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