(Q24306886)

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Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis

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title

Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis (English)

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main subject

amyotrophic lateral sclerosis

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Neurofilament heavy

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stated in

GOA release 2020-03-11

regulation of organelle transport along microtubule

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GOA release 2020-03-11

author name string

J F Collard

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1

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F Côté

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2

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J P Julien

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3

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language of work or name

English

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publication date

4 May 1995

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published in

Nature

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volume

375

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issue

6526

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page(s)

61-4

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cites work

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

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https://api.crossref.org/works/10.1038%2F375061A0

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7 January 2021

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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/10.1038%2F375061A0

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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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7 January 2021

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

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The slow component of axonal transport. Identification of major structural polypeptides of the axon and their generality among mammalian neurons

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7 January 2021

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Neurofibrillary axonal swellings and amyotrophic lateral sclerosis

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7 January 2021

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Slow Axonal Transport of Neurofilament Proteins: Impairment of β,β′-Iminodipropionitrile Administration

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https://api.crossref.org/works/10.1038%2F375061A0

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7 January 2021

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Axonal transport in neurological disease

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7 January 2021

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Cytotypic differences in the protein composition of the axonally transported cytoskeleton in mammalian neurons

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7 January 2021

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Retardation in the slow axonal transport of cytoskeletal elements during maturation and aging

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https://api.crossref.org/works/10.1038%2F375061A0

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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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7 January 2021

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(Q24306886)

Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis

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