(Q77892135)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

review article

1 reference

title

The genetic and molecular mechanisms of motor neuron disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference

P C Wong

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

J D Rothstein

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

D L Price

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

publication date

1 December 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

Current Opinion in Neurobiology

9 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

page(s)

791-799

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

Lewy body-like hyaline inclusions in sporadic motor neuron disease are ubiquitinated

9 December 2019

cites work

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7 January 2021

Clarke's column in sporadic amyotrophic lateral sclerosis

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7 January 2021

Morphometric and biochemical studies of peripheral nerves in amyotrophic lateral sclerosis

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7 January 2021

New pathological findings in amyotrophic lateral sclerosis

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7 January 2021

Mutant superoxide dismutase-1-linked familial amyotrophic lateral sclerosis: molecular mechanisms of neuronal death and protection

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7 January 2021

Neurofilaments and motor neuron disease

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7 January 2021

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

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7 January 2021

Amyotrophic lateral sclerosis. Insights from genetics

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7 January 2021

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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7 January 2021

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

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7 January 2021

Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.

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7 January 2021

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

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7 January 2021

Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis

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7 January 2021

Analysis of the KSP repeat of the neurofilament heavy subunit in familiar amyotrophic lateral sclerosis

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7 January 2021

Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis

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7 January 2021

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

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7 January 2021

Age-dependent penetrance of disease in a transgenic mouse model of familial amyotrophic lateral sclerosis

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7 January 2021

The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease

1 reference

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7 January 2021

Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1

1 reference

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7 January 2021

Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions

1 reference

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7 January 2021

Neurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutation

1 reference

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7 January 2021

A low expressor line of transgenic mice carrying a mutant human Cu,Zn superoxide dismutase (SOD1) gene develops pathological changes that most closely resemble those in human amyotrophic lateral sclerosis

1 reference

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7 January 2021

Benefit of vitamin E, riluzole, and gabapentin in a transgenic model of familial amyotrophic lateral sclerosis

1 reference

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7 January 2021

The copper chelator d-penicillamine delays onset of disease and extends survival in a transgenic mouse model of familial amyotrophic lateral sclerosis

1 reference

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7 January 2021

Bcl-2: prolonging life in a transgenic mouse model of familial amyotrophic lateral sclerosis

1 reference

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7 January 2021

Inhibition of ICE slows ALS in mice

1 reference

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7 January 2021

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

1 reference

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7 January 2021

Axonal transport of mutant superoxide dismutase 1 and focal axonal abnormalities in the proximal axons of transgenic mice.

1 reference

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7 January 2021

Neurofilament-deficient axons and perikaryal aggregates in viable transgenic mice expressing a neurofilament-beta-galactosidase fusion protein

1 reference

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7 January 2021

Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis

1 reference

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7 January 2021

Pathogenesis of two axonopathies does not require axonal neurofilaments.

1 reference

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7 January 2021

Protective effect of neurofilament heavy gene overexpression in motor neuron disease induced by mutant superoxide dismutase

1 reference

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7 January 2021

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

1 reference

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7 January 2021

Absence of neurofilaments reduces the selective vulnerability of motor neurons and slows disease caused by a familial amyotrophic lateral sclerosis-linked superoxide dismutase 1 mutant

1 reference

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7 January 2021

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

1 reference

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7 January 2021

Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis

1 reference

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7 January 2021

Time course of neuropathology in the spinal cord of G86R superoxide dismutase transgenic mice

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7 January 2021

Quantitative immunocytochemical analysis of the spinal cord in G86R superoxide dismutase transgenic mice: neurochemical correlates of selective vulnerability

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7 January 2021

Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity

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7 January 2021

Superoxide dismutase 1 subunits with mutations linked to familial amyotrophic lateral sclerosis do not affect wild-type subunit function.

1 reference

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7 January 2021

Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cells

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7 January 2021

Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

1 reference

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7 January 2021

Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury

1 reference

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7 January 2021

ALS, SOD and peroxynitrite

1 reference

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7 January 2021

Decreased zinc affinity of amyotrophic lateral sclerosis-associated superoxide dismutase mutants leads to enhanced catalysis of tyrosine nitration by peroxynitrite

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7 January 2021

Increased 3-nitrotyrosine in both sporadic and familial amyotrophic lateral sclerosis

1 reference

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7 January 2021

Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitration as an aberrant in vivo property of one familial ALS-linked superox

1 reference

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7 January 2021

Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis.

1 reference

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7 January 2021

Genetic and molecular basis for copper toxicity

1 reference

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7 January 2021

Metal ion chaperone function of the soluble Cu(I) receptor Atx1.

1 reference

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7 January 2021

Delivering copper inside yeast and human cells

1 reference

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7 January 2021

The copper chaperone for superoxide dismutase

1 reference

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7 January 2021

The copper chaperone CCS directly interacts with copper/zinc superoxide dismutase

1 reference

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7 January 2021

Chaperone-facilitated copper binding is a property common to several classes of familial amyotrophic lateral sclerosis-linked superoxide dismutase mutants

1 reference

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7 January 2021

Excitotoxicity in ALS.

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7 January 2021

Excitotoxicity hypothesis

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7 January 2021

Selective loss of glial glutamate transporter GLT‐1 in amyotrophic lateral sclerosis

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7 January 2021

Abnormal excitatory amino acid metabolism in amyotrophic lateral sclerosis

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7 January 2021

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

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7 January 2021

Aberrant RNA splicing in sporadic amyotrophic lateral sclerosis

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7 January 2021

Splicing regulation in neurons: tinkering with cell-specific control

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7 January 2021

Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate

1 reference

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7 January 2021

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

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7 January 2021

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

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7 January 2021

Advances in hereditary spastic paraplegia.

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7 January 2021

Pure hereditary spastic paraplegia.

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7 January 2021

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

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7 January 2021

The neurobiology of childhood spinal muscular atrophy.

1 reference

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7 January 2021

Identification and characterization of a spinal muscular atrophy-determining gene

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7 January 2021

The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

1 reference

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7 January 2021

Identification and characterization of a mouse homologue of the spinal muscular atrophy-determining gene, survival motor neuron.

1 reference

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7 January 2021

Deletion and conversion in spinal muscular atrophy patients: is there a relationship to severity?

1 reference

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7 January 2021

Correlation between severity and SMN protein level in spinal muscular atrophy

1 reference

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7 January 2021

Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

1 reference

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7 January 2021

From transcript to protein

1 reference

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7 January 2021

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0959-4388%2898%2980123-2

7 January 2021

Suppression of apoptosis in mammalian cells by NAIP and a related family of IAP genes

1 reference

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7 January 2021

A novel nuclear structure containing the survival of motor neurons protein

1 reference

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7 January 2021

10.1016/S0959-4388(98)80123-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914243%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference