Ontology highlight
ABSTRACT:
SUBMITTER: Solomon A
PROVIDER: S-EPMC1894569 | biostudies-literature | 2007 Jun
REPOSITORIES: biostudies-literature
Solomon Alan A Richey Tina T Murphy Charles L CL Weiss Deborah T DT Wall Jonathan S JS Westermark Gunilla T GT Westermark Per P
Proceedings of the National Academy of Sciences of the United States of America 20070619 26
The human cerebral and systemic amyloidoses and prion-associated spongiform encephalopathies are acquired or inherited protein folding disorders in which normally soluble proteins or peptides are converted into fibrillar aggregates. This is a nucleation-dependent process that can be initiated or accelerated by fibril seeds formed from homologous or heterologous amyloidogenic precursors that serve as an amyloid enhancing factor (AEF) and has pathogenic significance in that disease may be transmit ...[more]