(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

1 reference

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16 January 2020

San Pun

1 reference

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16 January 2020

Alexandre Ferrão Santos

series ordinal

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

series ordinal

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

series ordinal

1 reference

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16 January 2020

language of work or name

English

0 references

publication date

12 February 2006

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16 January 2020

1 reference

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16 January 2020

volume

1 reference

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16 January 2020

issue

1 reference

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16 January 2020

page(s)

408-419

1 reference

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

Synaptic slaughter in Alzheimer's disease

16 January 2020

cites work

1 reference

7 January 2021

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

1 reference

7 January 2021

Unraveling the mechanisms involved in motor neuron degeneration in ALS

1 reference

7 January 2021

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

1 reference

7 January 2021

Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria.

1 reference

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

7 January 2021

Motor unit behavior in canine motor neuron disease

1 reference

7 January 2021

Bcl-2: Prolonging Life in a Transgenic Mouse Model of Familial Amyotrophic Lateral Sclerosis

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Pre-existing pathways promote precise projection patterns

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Axonal self-destruction and neurodegeneration

1 reference

7 January 2021

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

1 reference

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Motor unit function during evolution of proximal axonal swellings.

1 reference

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

1 reference

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Hyperexcitability of cultured spinal motoneurons from presymptomatic ALS mice.

1 reference

7 January 2021

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

1 reference

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

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