(Q45923964)

English

Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice.

scientific article published in August 2011

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scholarly article

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice. (English)

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

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amyotrophic lateral sclerosis

1 reference

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author name string

Mehdi Hossaini

1

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Sebastian Cardona Cano

2

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Vera van Dis

3

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Elize D Haasdijk

4

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Casper C Hoogenraad

5

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Jan C Holstege

6

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Dick Jaarsma

7

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

publication date

1 August 2011

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Journal of Neuropathology & Experimental Neurology

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Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

70

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

8

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

662-677

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

1 reference

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21 January 2018

Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene

1 reference

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21 January 2018

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

1 reference

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21 January 2018

Mutations of optineurin in amyotrophic lateral sclerosis

1 reference

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21 January 2018

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

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21 January 2018

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

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21 January 2018

How do ALS-associated mutations in superoxide dismutase 1 promote aggregation of the protein?

1 reference

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21 January 2018

Superoxide dismutase-1 and other proteins in inclusions from transgenic amyotrophic lateral sclerosis model mice.

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21 January 2018

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

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21 January 2018

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

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21 January 2018

A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity

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21 January 2018

Recent advances in motor neuron disease.

1 reference

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21 January 2018

A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice

1 reference

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21 January 2018

ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration

1 reference

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21 January 2018

Cortical selective vulnerability in motor neuron disease: a morphometric study.

1 reference

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21 January 2018

Widespread loss of neuronal populations in the spinal ventral horn in sporadic motor neuron disease. A morphometric study.

1 reference

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21 January 2018

Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Motor neuron disease clinically limited to the lower motor neuron is a diffuse TDP-43 proteinopathy

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Clinicopathological characteristics of FTLD-TDP showing corticospinal tract degeneration but lacking lower motor neuron loss

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Progression of cortical and spinal dysfunctions over time in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

The motor cortex and amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Amyotrophic lateral sclerosis: lower motor neuron disease spreading to upper motor neurons

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Focality of upper and lower motor neuron degeneration at the clinical onset of ALS.

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Wild-type microglia extend survival in PU.1 knockout mice with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Onset and progression in inherited ALS determined by motor neurons and microglia

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

The effect of mutant SOD1 dismutase activity on non-cell autonomous degeneration in familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Spinal interneuronal networks in the cat: elementary components

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Measured motion: searching for simplicity in spinal locomotor networks

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

The role of excitotoxicity in the pathogenesis of amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Evidence for sequential degeneration of the neurons in the intermediate zone of the spinal cord in amyotrophic lateral sclerosis: a topographic and quantitative investigation

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Motor neuron degeneration in amyotrophic lateral sclerosis mutant superoxide dismutase-1 transgenic mice: mechanisms of mitochondriopathy and cell death.

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Glycinergic innervation of motoneurons is deficient in amyotrophic lateral sclerosis mice: a quantitative confocal analysis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Progressive changes in synaptic inputs to motoneurons in adult sacral spinal cord of a mouse model of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

The use of transgenic mouse models of amyotrophic lateral sclerosis in preclinical drug studies

1 reference

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21 January 2018

Induction of c-Jun immunoreactivity in spinal cord and brainstem neurons in a transgenic mouse model for amyotrophic lateral sclerosis.

1 reference

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21 January 2018

Glycinergic neurons expressing enhanced green fluorescent protein in bacterial artificial chromosome transgenic mice

1 reference

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21 January 2018

Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mut

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Distribution of glycinergic neuronal somata in the rat spinal cord.

1 reference

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21 January 2018

Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice

1 reference

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21 January 2018

Distribution and colocalisation of glutamate decarboxylase isoforms in the rat spinal cord

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21 January 2018

Transient increase in expression of GAD65 and GAD67 mRNAs during postnatal development of rat spinal cord.

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21 January 2018

Postnatal phenotype and localization of spinal cord V1 derived interneurons

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21 January 2018

Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria

1 reference

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21 January 2018

An examination of wild-type SOD1 in modulating the toxicity and aggregation of ALS-associated mutant SOD1

1 reference

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21 January 2018

Imbalanced excitatory to inhibitory synaptic input precedes motor neuron degeneration in an animal model of amyotrophic lateral sclerosis

1 reference

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21 January 2018

Defining the mechanisms that underlie cortical hyperexcitability in amyotrophic lateral sclerosis

1 reference

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21 January 2018

Changes in cortically induced inhibition in amyotrophic lateral sclerosis with time

1 reference

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21 January 2018

Microglia in ALS: the good, the bad, and the resting

1 reference

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21 January 2018

Microglia in neurodegenerative disease

1 reference

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The transcellular spread of cytosolic amyloids, prions, and prionoids

1 reference

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21 January 2018

Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis

1 reference

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21 January 2018

Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

Progressive motor weakness in transgenic mice expressing human TDP-43.

1 reference

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21 January 2018

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1097%2FNEN.0B013E31822581AC

21 January 2018

TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration

1 reference

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21 January 2018

Identifiers

10.1097/NEN.0B013E31822581AC

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/21760539

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