(Q35103318)

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Dysregulation of stathmin, a microtubule-destabilizing protein, and up-regulation of Hsp25, Hsp27, and the antioxidant peroxiredoxin 6 in a mouse model of familial amyotrophic lateral sclerosis

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Europe PubMed Central

PubMed publication ID

6 August 2017

Dysregulation of stathmin, a microtubule-destabilizing protein, and up-regulation of Hsp25, Hsp27, and the antioxidant peroxiredoxin 6 in a mouse model of familial amyotrophic lateral sclerosis (English)

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Europe PubMed Central

PubMed publication ID

6 August 2017

amyotrophic lateral sclerosis

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author name string

Christoph W Strey

1

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Daniel Spellman

2

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Europe PubMed Central

PubMed publication ID

6 August 2017

Anna Stieber

3

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Jacqueline O Gonatas

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Xiaosong Wang

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

John D Lambris

6

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Nicholas K Gonatas

7

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Europe PubMed Central

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6 August 2017

language of work or name

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publication date

1 November 2004

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Europe PubMed Central

PubMed publication ID

6 August 2017

The American Journal of Pathology

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Europe PubMed Central

PubMed publication ID

6 August 2017

165

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Europe PubMed Central

PubMed publication ID

6 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

1701-1718

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Dorfin prevents cell death by reducing mitochondrial localizing mutant superoxide dismutase 1 in a neuronal cell model of familial amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

Mitochondrial dysfunction and oxidative damage in parkin-deficient mice

1 reference

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9 July 2018

Expression of the small heat-shock protein alphaB-crystallin in tauopathies with glial pathology

1 reference

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9 July 2018

Mice with targeted mutation of peroxiredoxin 6 develop normally but are susceptible to oxidative stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

Misfolded CuZnSOD and amyotrophic lateral sclerosis

1 reference

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9 July 2018

Aberrant expression of peroxiredoxin subtypes in neurodegenerative disorders

1 reference

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9 July 2018

Analysis of the cytosolic proteome in a cell culture model of familial amyotrophic lateral sclerosis reveals alterations to the proteasome, antioxidant defenses, and nitric oxide synthetic pathways

1 reference

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9 July 2018

Differential gene expression in a cell culture model of SOD1-related familial motor neurone disease

1 reference

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Chaperoning brain degeneration

1 reference

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Discordant protein and mRNA expression in lung adenocarcinomas

1 reference

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9 July 2018

Amyotrophic lateral sclerosis: a proposed mechanism

1 reference

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9 July 2018

Stathmin-deficient mice develop an age-dependent axonopathy of the central and peripheral nervous systems

1 reference

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9 July 2018

Decreased protein levels of stathmin in adult brains with Down syndrome and Alzheimer's disease

1 reference

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9 July 2018

Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays

1 reference

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9 July 2018

Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded

1 reference

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The mitotic phosphorylation cycle of the cis-Golgi matrix protein GM130

1 reference

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9 July 2018

Down-regulation of the stathmin/Op18 and FKBP25 genes following p53 induction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

The stathmin phosphoprotein family: intracellular localization and effects on the microtubule network

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

1 reference

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9 July 2018

Major DNA fragmentation is a late event in apoptosis

1 reference

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9 July 2018

Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron disease

1 reference

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9 July 2018

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

1 reference

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9 July 2018

The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

In Alzheimer's disease the Golgi apparatus of a population of neurons without neurofibrillary tangles is fragmented and atrophic.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

Rous-Whipple Award Lecture. Contributions to the physiology and pathology of the Golgi apparatus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

Intracellular substrates for extracellular signaling. Characterization of a ubiquitous, neuron-enriched phosphoprotein (stathmin)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

MG-160. A novel sialoglycoprotein of the medial cisternae of the Golgi apparatus [published eeratum appears in J Biol Chem 1989 Mar 5;264(7):4264]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

9 July 2018

Immunocytochemical visualization of the Golgi apparatus in several species, including human, and tissues with an antiserum against MG-160, a sialoglycoprotein of rat Golgi apparatus

1 reference

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9 July 2018

Developmental tissue expression and phylogenetic conservation of stathmin, a phosphoprotein associated with cell regulations

1 reference

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

1 reference

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9 July 2018

Disruption of the structure of the Golgi apparatus and the function of the secretory pathway by mutants G93A and G85R of Cu, Zn superoxide dismutase (SOD1) of familial amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

27 September 2018

Reduction of detyrosinated microtubules and Golgi fragmentation are linked to tau-induced degeneration in astrocytes.

1 reference

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27 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

27 September 2018

Mice lacking phosphatidylinositol transfer protein-alpha exhibit spinocerebellar degeneration, intestinal and hepatic steatosis, and hypoglycemia

1 reference

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Antioxidant protein 2 prevents methemoglobin formation in erythrocyte hemolysates

1 reference

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Altered levels and distribution of microtubule-associated proteins before disease onset in a mouse model of amyotrophic lateral sclerosis

1 reference

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1 reference

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Regulation and subcellular localization of the microtubule-destabilizing stathmin family phosphoproteins in cortical neurons

1 reference

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Neurobiology. Chaperones take flight

1 reference

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1 reference

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

27 September 2018

Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1: gene multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

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Neurofibrillary tangle-associated alteration of stathmin in Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1618651

27 September 2018

A hypothesis on the traffic of MG160, a medial Golgi sialoglycoprotein, from the trans-Golgi network to the Golgi cisternae.

1 reference

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1 reference

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

1 reference

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HISTOCHEMICAL AND ULTRASTRUCTURAL STUDIES ON HELA CELL CULTURES EXPOSED TO SPINDLE INHIBITORS WITH SPECIAL REFERENCE TO THE INTERPHASE CELL

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

7 January 2021

Fragmentation of the Golgi apparatus of the anterior horn cells in patients with familial amyotrophic lateral sclerosis with SOD1 mutations and posterior column involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

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The neuronal Golgi apparatus is fragmented in transgenic mice expressing a mutant human SOD1, but not in mice expressing the human NF-H gene

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

7 January 2021

Effect of protein application mode and acrylamide concentration on the resolution of protein spots separated by two-dimensional gel electrophoresis.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

7 January 2021

Increased apolipoprotein E expression correlates with the onset of neuronal degeneration in the spinal cord of G93A-SOD1 mice

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

7 January 2021

New genes reveal major role for iron in neurodegeneration

1 reference

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7 January 2021

Aggregation of ubiquitin and a mutant ALS-linked SOD1 protein correlate with disease progression and fragmentation of the Golgi apparatus

1 reference

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SOD1 aggregates in ALS: cause, correlate or consequence?

1 reference

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Modulation of HSP25 expression during anterior horn motor neuron degeneration in the paralysé mouse mutant

1 reference

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7 January 2021

Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cord

1 reference

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Differential expression of inflammation- and apoptosis-related genes in spinal cords of a mutant SOD1 transgenic mouse model of familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

7 January 2021

Aggregates of mutant protein appear progressively in dendrites, in periaxonal processes of oligodendrocytes, and in neuronal and astrocytic perikarya of mice expressing the SOD1(G93A) mutation of familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963426-8

7 January 2021

Truncations of the C-terminal cytoplasmic domain of MG160, a medial Golgi sialoglycoprotein, result in its partial transport to the plasma membrane and filopodia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15509539

12 December 2020

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10.1016/S0002-9440(10)63426-8

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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