Amyloid associated proteins in Alzheimer's and prion disease

Current Drug Targets: CNS and Neurological Disorders

Volumn 4, Issue 3, 2005, Pages 235-248

  Veerhuis, R ^a,b   Boshuizen, R S ^c   Familian, A ^a,b  

^a Institute for Clinical and Experimental Neurosciences ICEN   (Netherlands)

^b VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^c Pepscan Systems   (Netherlands)

Author keywords

Acute phase proteins; Alzheimer's disease; Amyloid (A ); Complement; Fibril formation; Microglia; Prion disease; Prion peptide

Indexed keywords

ACUTE PHASE PROTEIN; ADVANCED GLYCATION END PRODUCT RECEPTOR; ALPHA 1 ANTICHYMOTRYPSIN; ALPHA 2 MACROGLOBULIN; AMYLOID BETA PROTEIN; AMYLOID PRECURSOR PROTEIN; AMYLOID PROTEIN; APOLIPOPROTEIN E; C REACTIVE PROTEIN; CATHEPSIN G; CLUSTERIN; COMPLEMENT COMPONENT C1Q; COMPLEMENT COMPONENT C3D; COMPLEMENT COMPONENT C4D; CYSTATIN C; DERMATAN SULFATE; ENOXAPARIN; FC RECEPTOR; INTERLEUKIN 1ALPHA; INTERLEUKIN 6; KERATAN SULFATE; KININOGEN; LOW MOLECULAR WEIGHT HEPARIN; PENTRAXIN; PRION PROTEIN; PROTEOCHONDROITIN SULFATE; PROTEOHEPARAN SULFATE; SERUM AMYLOID P; TRANSFORMING GROWTH FACTOR BETA; TUMOR NECROSIS FACTOR ALPHA;

ALZHEIMER DISEASE; CELL ACTIVATION; CLINICAL FEATURE; CLINICAL TRIAL; COMPLEMENT SYSTEM; CREUTZFELDT JAKOB DISEASE; DISEASE COURSE; DRUG PROTEIN BINDING; DRUG TARGETING; GERSTMANN STRAUSSLER SCHEINKER SYNDROME; HUMAN; IMMUNOHISTOCHEMISTRY; MICROGLIA; NERVE DEGENERATION; NEUROTOXICITY; NONHUMAN; PATHOGENESIS; PRION DISEASE; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; REVIEW; SCRAPIE;

ALZHEIMER DISEASE; AMYLOID; ANIMALS; COMPLEMENT SYSTEM PROTEINS; HUMANS; MICE; MICE, TRANSGENIC; MICROGLIA; NEURODEGENERATIVE DISEASES; PRION DISEASES; PRIONS; SERUM AMYLOID P-COMPONENT;

EID: 19944414648     PISSN: 1568007X     EISSN: None     Source Type: Journal    
DOI: 10.2174/1568007054038184     Document Type: Review

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