Metalloproteinase shedding of fas ligand regulates β-amyloid neurotoxicity

Current Biology

Volumn 12, Issue 18, 2002, Pages 1595-1600

  Ethell, Douglas W ^a,b   Kinloch, Ross ^c   Green, Douglas R ^a  

^a LA JOLLA INSTITUTE FOR ALLERGY AND IMMUNOLOGY   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c PFIZER GLOBAL RESEARCH AND DEVELOPMENT   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID BETA PROTEIN; AMYLOID BETA PROTEIN[1-40]; DIPEPTIDE; FAS LIGAND; FASL PROTEIN, MOUSE; FASLG PROTEIN, HUMAN; ILOMASTAT; MATRILYSIN; MEMBRANE PROTEIN; METALLOPROTEINASE; PEPTIDE FRAGMENT; PROTEINASE INHIBITOR;

ALZHEIMER DISEASE; ANIMAL; APOPTOSIS; ARTICLE; C3H MOUSE; C57BL MOUSE; CELL CULTURE; CONGENIC STRAIN; DRUG ANTAGONISM; DRUG EFFECT; HUMAN; METABOLISM; MOUSE; NERVE CELL; PATHOLOGY;

ALZHEIMER DISEASE; AMYLOID BETA-PROTEIN; ANIMALS; ANIMALS, CONGENIC; APOPTOSIS; CELLS, CULTURED; DIPEPTIDES; FAS LIGAND PROTEIN; HUMANS; MATRIX METALLOPROTEINASE 7; MEMBRANE GLYCOPROTEINS; METALLOENDOPEPTIDASES; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; NEURONS; PEPTIDE FRAGMENTS; PROTEASE INHIBITORS;

ANIMALIA;

EID: 0037125956     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-9822(02)01140-5     Document Type: Article

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