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Volumn 19, Issue 13, 2005, Pages 1851-1853
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Functional relevance of ceruloplasmin mutations in Parkinson's disease
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Author keywords
[No Author keywords available]
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Indexed keywords
CERULOPLASMIN;
GLYCOSYLPHOSPHATIDYLINOSITOL;
PROTEIN ANTIBODY;
ARTICLE;
DEGENERATIVE DISEASE;
DOPAMINERGIC NERVE CELL;
ENDOPLASMIC RETICULUM;
ENZYME GLYCOSYLATION;
GENE MUTATION;
HUMAN;
IRON METABOLISM;
MISSENSE MUTATION;
NEUROLOGIC DISEASE;
OXIDATIVE STRESS;
PARKINSON DISEASE;
PRIORITY JOURNAL;
PROTEIN LOCALIZATION;
SERUM;
SUBSTANTIA NIGRA;
ALLELES;
CELL LINE;
CERULOPLASMIN;
ENDOPLASMIC RETICULUM;
EPITHELIAL CELLS;
FERRITINS;
FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT;
GLYCOSYLATION;
GLYCOSYLPHOSPHATIDYLINOSITOLS;
HETEROZYGOTE;
HUMANS;
IMMUNOPRECIPITATION;
IRON;
KIDNEY;
MICROSCOPY, FLUORESCENCE;
MUTATION;
MUTATION, MISSENSE;
NEURODEGENERATIVE DISEASES;
OXIDATIVE STRESS;
PARKINSON DISEASE;
PROTEIN DENATURATION;
PROTEIN FOLDING;
PROTEIN ISOFORMS;
SUBSTANTIA NIGRA;
TRANSFECTION;
TRANSFERRIN;
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EID: 27744446323
PISSN: 08926638
EISSN: None
Source Type: Journal
DOI: 10.1096/fj.04-3486fje Document Type: Article |
Times cited : (77)
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References (0)
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