Transthyretin Amyloidosis: Chaperone Concentration Changes and Increased Proteolysis in the Pathway to Disease.
Transthyretin amyloidosis is a conformational pathology characterized by the extracellular formation of amyloid deposits and the progressive impairment of the peripheral nervous system. Point mutations in this tetrameric plasma protein decrease its stability and are linked to disease onset and progr...
Main Authors: | Gonçalo da Costa, Cristina Ribeiro-Silva, Raquel Ribeiro, Samuel Gilberto, Ricardo A Gomes, António Ferreira, Élia Mateus, Eduardo Barroso, Ana V Coelho, Ana Ponces Freire, Carlos Cordeiro |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2015-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC4492746?pdf=render |
Similar Items
-
Beyond genetic factors in familial amyloidotic polyneuropathy: protein glycation and the loss of fibrinogen's chaperone activity.
by: Gonçalo da Costa, et al.
Published: (2011-01-01) -
Hereditary transthyretin amyloidosis
by: T. A. Adyan, et al.
Published: (2020-01-01) -
Management of transthyretin amyloidosis
by: Adalgisa Condoluci, et al.
Published: (2021-10-01) -
The Role of Proteolysis in Amyloidosis
by: Laura Acquasaliente, et al.
Published: (2022-12-01) -
Erratum to: Management of transthyretin amyloidosis
by: Swiss Medical Weekly
Published: (2021-11-01)