Wild-type microglia extend survival in PU.1 knockout mice with familial amyotrophic lateral sclerosis (Q35094527)

6 August 2017

title

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

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amyotrophic lateral sclerosis

6 August 2017

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9

Stanley H Appel

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6 August 2017

David R Beers

1

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6 August 2017

Jenny S Henkel

2

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6 August 2017

Qin Xiao

3

1 reference

6 August 2017

Weihua Zhao

4

1 reference

6 August 2017

Jinghong Wang

5

1 reference

6 August 2017

Albert A Yen

6

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6 August 2017

Laszlo Siklos

7

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6 August 2017

Scott R McKercher

8

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6 August 2017

language of work or name

English

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publication date

16 October 2006

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Proceedings of the National Academy of Sciences of the United States of America

6 August 2017

published in

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6 August 2017

volume

103

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6 August 2017

issue

43

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6 August 2017

page(s)

16021-16026

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

6 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1613228

CD4-positive T cell-mediated neuroprotection requires dual compartment antigen presentation

9 July 2018

1 reference

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Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS).

9 July 2018

1 reference

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From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

9 July 2018

1 reference

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Microglial activation and dopaminergic cell injury: an in vitro model relevant to Parkinson's disease.

9 July 2018

1 reference

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Turning blood into brain: cells bearing neuronal antigens generated in vivo from bone marrow

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1613228

Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1613228

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

9 July 2018

1 reference

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

9 July 2018

1 reference

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Towards gene therapy for adenosine deaminase deficiency

9 July 2018

1 reference

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The efficiency of systematic sampling in stereology and its prediction.

9 July 2018

1 reference

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Origin and distribution of bone marrow-derived cells in the central nervous system in a mouse model of amyotrophic lateral sclerosis

9 July 2018

1 reference

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Wild-type bone marrow cells ameliorate the phenotype of SOD1-G93A ALS mice and contribute to CNS, heart and skeletal muscle tissues.

27 September 2018

1 reference

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Activated microglia initiate motor neuron injury by a nitric oxide and glutamate-mediated mechanism

27 September 2018

1 reference

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

27 September 2018

1 reference

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Retrograde viral delivery of IGF-1 prolongs survival in a mouse ALS model.

27 September 2018

1 reference

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

27 September 2018

1 reference

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Adverse effect of a presenilin-1 mutation in microglia results in enhanced nitric oxide and inflammatory cytokine responses to immune challenge in the brain

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1613228

Neuron-specific expression of mutant superoxide dismutase 1 in transgenic mice does not lead to motor impairment.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1613228

Expression of human adenosine deaminase in murine haematopoietic progenitor cells following retroviral transfer

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1613228

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

27 September 2018

1 reference

12 December 2020

Assessing disease onset and progression in the SOD1 mouse model of ALS

1 reference

12 December 2020

Early activation of microglia as antigen-presenting cells correlates with T cell-mediated protection and repair of the injured central nervous system

1 reference

12 December 2020

Increased cytotoxic potential of microglia from ALS-transgenic mice

1 reference

12 December 2020

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

1 reference

12 December 2020

Tissue-type plasminogen activator is not required for kainate-induced motoneuron death in vitro

1 reference

12 December 2020

Restricted expression of G86R Cu/Zn superoxide dismutase in astrocytes results in astrocytosis but does not cause motoneuron degeneration

1 reference

12 December 2020

Immune reactivity in a mouse model of familial ALS correlates with disease progression

1 reference

12 December 2020

Parvalbumin overexpression alters immune-mediated increases in intracellular calcium, and delays disease onset in a transgenic model of familial amyotrophic lateral sclerosis

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0607423103

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6 August 2017

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6 August 2017

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