(Q60220472)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

3

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16 January 2020

author name string

San Pun

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Alexandre Ferrão Santos

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Lan Xu

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Pico Caroni

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

language of work or name

English

0 references

publication date

12 February 2006

1 reference

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16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

page(s)

408-419

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nn1653

16 January 2020

exact match

0 references

cites work

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Early and selective loss of neuromuscular synapse subtypes with low sprouting competence in motoneuron diseases

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Accumulation of SOD1 mutants in postnatal motoneurons does not cause motoneuron pathology or motoneuron disease

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Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice

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Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria

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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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7 January 2021

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

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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

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7 January 2021

Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons

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7 January 2021

Motor unit behavior in canine motor neuron disease

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7 January 2021

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

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7 January 2021

Bcl-2 overexpression prevents motoneuron cell body loss but not axonal degeneration in a mouse model of a neurodegenerative disease

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7 January 2021

Altered axonal architecture by removal of the heavily phosphorylated neurofilament tail domains strongly slows superoxide dismutase 1 mutant-mediated ALS.

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7 January 2021

Differential effects of neurotrophic factors on motoneuron retrograde labeling in a murine model of motoneuron disease.

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7 January 2021

AMPA receptors regulate dynamic equilibrium of presynaptic terminals in mature hippocampal networks.

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Axonopathy and transport deficits early in the pathogenesis of Alzheimer's disease

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Polyglutamine diseases and transport problems: deadly traffic jams on neuronal highways.

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Pre-existing pathways promote precise projection patterns

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Axon pruning during Drosophila metamorphosis: evidence for local degeneration and requirement of the ubiquitin-proteasome system

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7 January 2021

Involvement of the ubiquitin-proteasome system in the early stages of wallerian degeneration

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7 January 2021

Axonal self-destruction and neurodegeneration

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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.

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7 January 2021

Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease

1 reference

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

7 January 2021

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

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7 January 2021

Ciliary neurotrophic factor and stress stimuli activate the Jak-STAT pathway in retinal neurons and glia

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7 January 2021

Cellular mechanisms associated with spontaneous and ciliary neurotrophic factor-cAMP-induced survival and axonal regeneration of adult retinal ganglion cells

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7 January 2021

NF-kappaB-mediated up-regulation of Bcl-x and Bfl-1/A1 is required for CD40 survival signaling in B lymphocytes

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7 January 2021

Motor unit function during evolution of proximal axonal swellings.

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7 January 2021

Disruption of dynein/dynactin inhibits axonal transport in motor neurons causing late-onset progressive degeneration.

1 reference

7 January 2021

Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A.

1 reference

7 January 2021

Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosis

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7 January 2021

Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene

1 reference

7 January 2021

A compensatory subpopulation of motor neurons in a mouse model of amyotrophic lateral sclerosis

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7 January 2021

Properties of slow- and fast-twitch muscle fibres in a mouse model of amyotrophic lateral sclerosis.

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7 January 2021

Motoneuron death triggered by a specific pathway downstream of Fas. potentiation by ALS-linked SOD1 mutations.

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7 January 2021

Amyotrophic lateral sclerosis: macro-EMG and twitch forces of single motor units

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7 January 2021

Contractile properties in single muscle fibres from chronically overused motor units in relation to motoneuron firing properties in prior polio patients.

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7 January 2021

Reduction of axonal caliber does not alleviate motor neuron disease caused by mutant superoxide dismutase 1

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7 January 2021

Ca2+, mitochondria and selective motoneuron vulnerability: implications for ALS.

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7 January 2021

Hyperexcitability of cultured spinal motoneurons from presymptomatic ALS mice.

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7 January 2021

Disruption of axonal transport and neuronal viability by amyloid precursor protein mutations in Drosophila.

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7 January 2021

Disruption of Axonal Transport by Loss of Huntingtin or Expression of Pathogenic PolyQ Proteins in Drosophila

1 reference

7 January 2021

Restoration of cognitive and motor functions by ciliary neurotrophic factor in a primate model of Huntington's disease.

1 reference

7 January 2021

Identifiers

DOI

10.1038/NN1653

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16474388%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference