The molecular lifecycle of amyloid – Mechanism of assembly, mesoscopic organisation, polymorphism, suprastructures, and biological consequences-Reference-Cited by-同舟云学术

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The molecular lifecycle of amyloid – Mechanism of assembly, mesoscopic organisation, polymorphism, suprastructures, and biological consequences

Published:2019-11 Issue:11 Volume:1867 Page:140257
ISSN:1570-9639
Container-title:Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics

Author:

Lutter Liisa,Serpell Christopher J.,Tuite Mick F.,Xue Wei-Feng

Funder

Biotechnology and Biological Sciences Research Council (BBSRC), UK

Engineering and Physical Sciences Research Council (EPSRC), UK DTP

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry,Biophysics,Analytical Chemistry

Reference175 articles.

1. Unfolding the role of protein misfolding in neurodegenerative diseases;Soto;Nat. Rev. Neurosci.,2003

2. Pathophysiology and treatment of cardiac amyloidosis;Gertz;Nat. Rev. Cardiol.,2015

3. Systemic immunoglobulin light chain amyloidosis;Merlini;Nat. Rev. Dis. Primers,2018

4. Type 2 diabetes as a protein misfolding disease;Mukherjee;Trends Mol. Med.,2015

5. Protein misfolding, functional amyloid, and human disease;Chiti;Annu. Rev. Biochem.,2006

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