Related references
Note: Only part of the references are listed.Amyotrophic Lateral Sclerosis and Organ Donation: Is There Risk of Disease Transmission?
Brandon B. Holmes et al.
ANNALS OF NEUROLOGY (2012)
Transmissible Proteins: Expanding the Prion Heresy
Claudio Soto
CELL (2012)
Can regional spreading of amyotrophic lateral sclerosis motor symptoms be explained by prion-like propagation?
Tadashi Kanouchi et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)
The Seeds of Neurodegeneration: Prion-like Spreading in ALS
Magdalini Polymenidou et al.
CELL (2011)
A Seeding Reaction Recapitulates Intracellular Formation of Sarkosyl-insoluble Transactivation Response Element (TAR) DNA-binding Protein-43 Inclusions
Yoshiaki Furukawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Intermolecular transmission of superoxide dismutase 1 misfolding in living cells
Leslie I. Grad et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Prion-like propagation of mutant superoxide dismutase-1 misfolding in neuronal cells
Christian Muench et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Mutation-dependent Polymorphism of Cu,Zn-Superoxide Dismutase Aggregates in the Familial Form of Amyotrophic Lateral Sclerosis
Yoshiaki Furukawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Nonamyloid Aggregates Arising from Mature Copper/Zinc Superoxide Dismutases Resemble Those Observed in Amyotrophic Lateral Sclerosis
Young-Mi Hwang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Exposure of Hydrophobic Surfaces Initiates Aggregation of Diverse ALS-Causing Superoxide Dismutase-1 Mutants
Christian Muench et al.
JOURNAL OF MOLECULAR BIOLOGY (2010)
Superoxide Dismutase 1 and tgSOD1G93A Mouse Spinal Cord Seed Fibrils, Suggesting a Propagative Cell Death Mechanism in Amyotrophic Lateral Sclerosis
Ruth Chia et al.
PLOS ONE (2010)
ALS motor phenotype heterogeneity, focality, and spread Deconstructing motor neuron degeneration
John M. Ravits et al.
NEUROLOGY (2009)
Complete loss of post-translational modifications triggers fibrillar aggregation of SOD1 in the familial form of amyotrophic lateral sclerosis
Yoshiaki Furukawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Protein aggregation and protein instability govern familial amyotrophic lateral sclerosis patient survival
Qi Wang et al.
PLOS BIOLOGY (2008)
Protein aggregation and neurodegenerative disease
CA Ross et al.
NATURE MEDICINE (2004)
Unraveling the mechanisms involved in motor neuron degeneration in ALS
LI Bruijn et al.
ANNUAL REVIEW OF NEUROSCIENCE (2004)
Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis show enhanced formation of aggregates in vitro
PB Stathopulos et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Familial amyotrophic lateral sclerosis mutants of copper/zinc superoxide dismutase are susceptible to disulfide reduction
A Tiwari et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Copper-binding-site-null SOD1 causes ALS in transgenic mice: aggregates of non-native SOD1 delineate a common feature
J Wang et al.
HUMAN MOLECULAR GENETICS (2003)
Fibrillar inclusions and motor neuron degeneration in transgenic mice expressing superoxide dismutase 1 with a disrupted copper-binding site
J Wang et al.
NEUROBIOLOGY OF DISEASE (2002)
Decreased metallation and activity in subsets of mutant superoxide dismutases associated with familial amyotrophic lateral sclerosis
LJ Hayward et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Review: History of the amyloid fibril
JD Sipe et al.
JOURNAL OF STRUCTURAL BIOLOGY (2000)