Assembly of hereditary amyloid β-protein variants in the presence of favorable gangliosides

FEBS Letters

Volumn 579, Issue 10, 2005, Pages 2185-2190

  Yamamoto, Naoki ^a   Hirabayashi, Yoshio ^b   Amari, Masakuni ^c   Yamaguchi, Haruyasu ^d   Romanov, Galina ^e   Van Nostrand, William E ^e   Yanagisawa, Katsuhiko ^a  

^a NATIONAL CENTER FOR GERIATRICS AND GERONTOLOGY   (Japan)

^b RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^c GERIATRICS RESEARCH INSTITUTE AND HOSPITAL   (Japan)

^d GUNMA UNIVERSITY   (Japan)

^e STONY BROOK UNIVERSITY   (United States)

Author keywords

Alzheimer's disease; Amyloid; Amyloid protein; Cerebral amyloid angiopathy; Ganglioside; Seed

Indexed keywords

AMYLOID BETA PROTEIN; GANGLIOSIDE GD3; GANGLIOSIDE GM3;

ARTICLE; BRAIN BLOOD VESSEL; CELL CULTURE; CHEMICAL REACTION KINETICS; COCULTURE; ENDOTHELIUM CELL; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN ASSEMBLY; SMOOTH MUSCLE FIBER; UPREGULATION;

EID: 16344382167     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2005.03.013     Document Type: Article

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