Axonal mitochondrial clusters containing mutant SOD1 in transgenic models of ALS. (Q33742751)

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25 January 2020

title

Axonal mitochondrial clusters containing mutant SOD1 in transgenic models of ALS (English)

1 reference

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amyotrophic lateral sclerosis

25 January 2020

main subject

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José Roberto Sotelo-Silveira

inferred from title

author

1

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25 January 2020

Laura Martínez-Palma

6

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25 January 2020

author name string

Paola Lepanto

2

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25 January 2020

Victoria Elizondo

3

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25 January 2020

Sofia Horjales

4

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25 January 2020

Florencia Palacios

5

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25 January 2020

Monica Marin

7

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25 January 2020

Joseph S Beckman

8

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25 January 2020

Luis Barbeito

9

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25 January 2020

publication date

1 July 2009

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Antioxidants & Redox Signaling

25 January 2020

published in

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25 January 2020

volume

11

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25 January 2020

issue

7

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25 January 2020

page(s)

1535-1545

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Selective association of misfolded ALS-linked mutant SOD1 with the cytoplasmic face of mitochondria.

25 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content

21 June 2018

1 reference

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p62 accumulates and enhances aggregate formation in model systems of familial amyotrophic lateral sclerosis

21 June 2018

1 reference

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

21 June 2018

1 reference

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Mitochondria in amyotrophic lateral sclerosis: a trigger and a target

21 June 2018

1 reference

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RNA trafficking in axons.

21 June 2018

1 reference

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

21 June 2018

1 reference

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Differential transport and local translation of cytoskeletal, injury-response, and neurodegeneration protein mRNAs in axons

21 June 2018

1 reference

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Myosin Va and kinesin II motor proteins are concentrated in ribosomal domains (periaxoplasmic ribosomal plaques) of myelinated axons

21 June 2018

1 reference

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

21 June 2018

1 reference

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Unraveling the mechanisms involved in motor neuron degeneration in ALS

21 June 2018

1 reference

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Automatic and quantitative measurement of protein-protein colocalization in live cells.

21 June 2018

1 reference

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Superoxide dismutase and the death of motoneurons in ALS.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

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

21 June 2018

1 reference

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Genetics of sporadic ALS.

21 June 2018

1 reference

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Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Neurofilaments and Orthograde Transport Are Reduced in Ventral Root Axons of Transgenic Mice that Express Human SOD1 with a G93A Mutation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitration as an aberrant in vivo property of one familial ALS-linked superox

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Isolation of native Mauthner cell axoplasm and an analysis of organelle movement in non-aqueous and aqueous media

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Myelinated axons contain beta-actin mRNA and ZBP-1 in periaxoplasmic ribosomal plaques and depend on cyclic AMP and F-actin integrity for in vitro translation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Accumulation of human SOD1 and ubiquitinated deposits in the spinal cord of SOD1G93A mice during motor neuron disease progression correlates with a decrease of proteasome.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Inactivation of human Cu,Zn superoxide dismutase by peroxynitrite and formation of histidinyl radical.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Axonal mitochondrial transport and potential are correlated

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2842590

Cryptic peripheral ribosomal domains distributed intermittently along mammalian myelinated axons

30 October 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Impairment of axonal transport in the axon hillock and the initial segment of anterior horn neurons in transgenic mice with a G93A mutant SOD1 gene

1 reference

12 December 2020

Insoluble Mutant SOD1 Is Partly Oligoubiquitinated in Amyotrophic Lateral Sclerosis Mice

1 reference

12 December 2020

Fine structural study of neurofibrillary changes in a family with amyotrophic lateral sclerosis

1 reference

12 December 2020

A regional analysis of alpha-spectrin in the isolated Mauthner neuron and in isolated axons of the goldfish and rabbit

1 reference

12 December 2020

1 reference

12 December 2020

Induction of nitrotyrosine-like immunoreactivity in the lower motor neuron of amyotrophic lateral sclerosis

1 reference

12 December 2020

Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1

1 reference

12 December 2020

Identifiers

DOI

10.1089/ARS.2009.2614

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19344250%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

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25 January 2020

PubMed publication ID

19344250

1 reference