相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Spinal cord homogenates from SOD1 familial amyotrophic lateral sclerosis induce SOD1 aggregation in living cells
Edward Pokrishevsky et al.
PLOS ONE (2017)
Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathways
Jacob I. Ayers et al.
ACTA NEUROPATHOLOGICA (2016)
Distinct conformers of transmissible misfolded SOD1 distinguish human SOD1-FALS from other forms of familial and sporadic ALS
Jacob I. Ayers et al.
ACTA NEUROPATHOLOGICA (2016)
Two superoxide dismutase prion strains transmit amyotrophic lateral sclerosis-like disease
Elaheh Ekhtiari Bidhendi et al.
JOURNAL OF CLINICAL INVESTIGATION (2016)
Mammalian prions and their wider relevance in neurodegenerative diseases
John Collinge
NATURE (2016)
Age-related myelin degradation burdens the clearance function of microglia during aging
Shima Safaiyan et al.
NATURE NEUROSCIENCE (2016)
A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration
Dominic M. Walsh et al.
NATURE REVIEWS NEUROSCIENCE (2016)
Low autophagy capacity implicated in motor system vulnerability to mutant superoxide dismutase
Eiichi Tokuda et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2016)
Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping
Johan Bergh et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Experimental transmissibility of mutant SOD1 motor neuron disease
Jacob I. Ayers et al.
ACTA NEUROPATHOLOGICA (2014)
Rodent models of amyotrophic lateral sclerosis
Philip McGoldrick et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2013)
Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis
Karin S. Graffmo et al.
HUMAN MOLECULAR GENETICS (2013)
Composition of Soluble Misfolded Superoxide Dismutase-1 in Murine Models of Amyotrophic Lateral Sclerosis
Per Zetterstrom et al.
NEUROMOLECULAR MEDICINE (2013)
Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in mice
Kelvin C. Luk et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2012)
Prion-like acceleration of a synucleinopathy in a transgenic mouse model
Anne-Laure Mougenot et al.
NEUROBIOLOGY OF AGING (2012)
Fibrillation precursor of superoxide dismutase 1 revealed by gradual tuning of the protein-folding equilibrium
Lisa Lang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Glial nuclear aggregates of superoxide dismutase-1 are regularly present in patients with amyotrophic lateral sclerosis
Karin Forsberg et al.
ACTA NEUROPATHOLOGICA (2011)
Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
Peter M. Andersen et al.
NATURE REVIEWS NEUROLOGY (2011)
Novel Antibodies Reveal Inclusions Containing Non-Native SOD1 in Sporadic ALS Patients
Karin Forsberg et al.
PLOS ONE (2010)
Transmission and spreading of tauopathy in transgenic mouse brain
Florence Clavaguera et al.
NATURE CELL BIOLOGY (2009)
Superoxide dismutase in amyotrophic lateral sclerosis patients homozygous for the D90A mutation
P. Andreas Jonsson et al.
NEUROBIOLOGY OF DISEASE (2009)
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
Richard Wroe et al.
AMYOTROPHIC LATERAL SCLEROSIS (2008)
Inclusions of amyotrophic lateral sclerosis-linked superoxide dismutase in ventral horns, liver, and kidney
P. Andreas Jonsson et al.
ANNALS OF NEUROLOGY (2008)
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)
Initiation and elongation in fibrillation of ALS-linked superoxide dismutase
Madhuri Chattopadhyay et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models
Per Zetterstrom et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Motor neuron disease in mice expressing the wild type-like D90A mutant superoxide dismutase-1
P. Andreas Jonsson et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2006)
Exogenous induction of cerebral β-amyloidogenesis is governed by agent and host
Melanie Meyer-Luehmann et al.
SCIENCE (2006)
Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis models
PA Jonsson et al.
BRAIN (2006)
New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: Inclusions containing SOD1 in neurons and astrocytes
S Kato et al.
AMYOTROPHIC LATERAL SCLEROSIS (2000)