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Neurofilaments and motor neuron disease
scientific article published on June 1997
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scholarly article
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Europe PubMed Central
PubMed ID
17708953
retrieved
17 August 2017
title
Neurofilaments and motor neuron disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17708953
retrieved
17 August 2017
author name string
Julien JP
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
17708953
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17 August 2017
publication date
1 June 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
17708953
retrieved
17 August 2017
published in
Trends in Cell Biology
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stated in
Europe PubMed Central
PubMed ID
17708953
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17 August 2017
volume
7
1 reference
stated in
Europe PubMed Central
PubMed ID
17708953
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17 August 2017
issue
6
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stated in
Europe PubMed Central
PubMed ID
17708953
retrieved
17 August 2017
page(s)
243-249
1 reference
stated in
Europe PubMed Central
PubMed ID
17708953
retrieved
17 August 2017
cites work
The slow component of axonal transport. Identification of major structural polypeptides of the axon and their generality among mammalian neurons
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Neurofilament-deficient axons and perikaryal aggregates in viable transgenic mice expressing a neurofilament-beta-galactosidase fusion protein
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Assembly of type IV neuronal intermediate filaments in nonneuronal cells in the absence of preexisting cytoplasmic intermediate filaments
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Neurofilaments are obligate heteropolymers in vivo
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Molecular and cellular biology of intermediate filaments
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Molecular architecture of the neurofilament. II. Reassembly process of neurofilament L protein in vitro
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Sequence and structure of the mouse gene coding for the largest neurofilament subunit.
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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The structure and organization of the human heavy neurofilament subunit (NF-H) and the gene encoding it
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7 January 2021
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Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Modulation of axon diameter and neurofilaments by hypomyelinating Schwann cells in transgenic mice
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7 January 2021
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Proximal axonal enlargement in motor neuron disease.
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis
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Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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A mutant neurofilament subunit causes massive, selective motor neuron death: implications for the pathogenesis of human motor neuron disease
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Intermediate filaments and disease: mutations that cripple cell strength
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Increasing neurofilament subunit NF-M expression reduces axonal NF-H, inhibits radial growth, and results in neurofilamentous accumulation in motor neurons.
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Abnormal perikaryal accumulation of neurofilament light protein in the brain of mice transgenic for the human protein: sequence of postnatal development
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Age-associated and cell-type-specific neurofibrillary pathology in transgenic mice expressing the human midsized neurofilament subunit
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Neurofilament subunit NF-H modulates axonal diameter by selectively slowing neurofilament transport
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Neurofilament phosphorylation
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Early upregulation of medium neurofilament gene expression in developing spinal cord of the wobbler mouse mutant.
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7 January 2021
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Impairment of fast axonal transport in the proximal axons of anterior horn neurons in amyotrophic lateral sclerosis
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Cytoskeletal disorganization induced by local application of beta, beta'-iminodipropionitrile and 2,5-hexanedione
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Retardation in the slow axonal transport of cytoskeletal elements during maturation and aging
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An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments.
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Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis
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Analysis of the KSP repeat of the neurofilament heavy subunit in familiar amyotrophic lateral sclerosis
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7 January 2021
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Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis
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Inhibition of growth factor-induced protein synthesis by a selective MEK inhibitor in aortic smooth muscle cells
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Amyotrophic lateral sclerosis: recent insights from genetics and transgenic mice
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
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Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury
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ALS, SOD and peroxynitrite
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis
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Superoxide dismutase protects calcineurin from inactivation.
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7 January 2021
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SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Colocalization of NOS and SOD1 in neurofilament accumulation within motor neurons of amyotrophic lateral sclerosis: an immunohistochemical study
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Carbonyl-related posttranslational modification of neurofilament protein in the neurofibrillary pathology of Alzheimer's disease
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7 January 2021
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Neurofilament light and polyadenylated mRNA levels are decreased in amyotrophic lateral sclerosis motor neurons
1 reference
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Aggregation of neurofilaments in NF-L transfected neuronal cells: regeneration of the filamentous network by a protein kinase C inhibitor
1 reference
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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Aluminum neurotoxicity: an experimental approach to the induction of neurofilamentous inclusions.
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https://api.crossref.org/works/10.1016%2FS0962-8924%2897%2901049-0
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7 January 2021
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Identifiers
DOI
10.1016/S0962-8924(97)01049-0
1 reference
stated in
Europe PubMed Central
PubMed ID
17708953
retrieved
17 August 2017
PubMed ID
17708953
1 reference
stated in
Europe PubMed Central
PubMed ID
17708953
retrieved
17 August 2017
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