Axonal mitochondrial clusters containing mutant SOD1 in transgenic models of ALS. - Wikidata - awgldk - TriplyDB

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

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

http://www.wikidata.org/entity/Q33742751

about

Effects of ALS-related SOD1 mutants on dynein- and KIF5-mediated retrograde and anterograde axonal transport A Case for Microtubule Vulnerability in Amyotrophic Lateral Sclerosis: Altered Dynamics During Disease ALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the disease Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models.Abnormalities of Mitochondrial Dynamics in Neurodegenerative Diseases.Misfolded SOD1 associated with motor neuron mitochondria alters mitochondrial shape and distribution prior to clinical onset.ALS-linked mutant SOD1 damages mitochondria by promoting conformational changes in Bcl-2.Mitochondrial dysfunction and intracellular calcium dysregulation in ALS SOD1 targeted to the mitochondrial intermembrane space prevents motor neuropathy in the Sod1 knockout mouse.Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice.Rodent models of TDP-43 proteinopathy: investigating the mechanisms of TDP-43-mediated neurodegeneration Activation of the endoplasmic reticulum stress response in skeletal muscle of G93A*SOD1 amyotrophic lateral sclerosis mice.Fluoxetine increases plasticity and modulates the proteomic profile in the adult mouse visual cortex.Early and gender-specific differences in spinal cord mitochondrial function and oxidative stress markers in a mouse model of ALS Mitochondrial dynamic abnormalities in amyotrophic lateral sclerosis.Elimination Rate of Serum Lactate is Correlated with Amyotrophic Lateral Sclerosis Progression.Mitochondrial dysfunction in amyotrophic lateral sclerosis.SOD1 and TDP-43 animal models of amyotrophic lateral sclerosis: recent advances in understanding disease toward the development of clinical treatments.Mitochondrial dysfunction in familial amyotrophic lateral sclerosis.Misfolded SOD1 and ALS: zeroing in on mitochondria.Human TDP-43 and FUS selectively affect motor neuron maturation and survival in a murine cell model of ALS by non-cell-autonomous mechanisms.Defining peripheral nervous system dysfunction in the SOD-1G93A transgenic rat model of amyotrophic lateral sclerosis.S-nitrosylated protein disulfide isomerase contributes to mutant SOD1 aggregates in amyotrophic lateral sclerosis.Amyotrophic lateral sclerosis: a dying motor unit?Implications of white matter damage in amyotrophic lateral sclerosis (Review).An antibody-based affinity chromatography tool to assess Cu, Zn superoxide dismutase (SOD) G93A structural complexity in vivo.Energy metabolism in ALS: an underappreciated opportunity?

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P2860

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

http://www.wikidata.org/entity/Q33742751

description

2009 nî lūn-bûn

@nan

2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

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

@ast

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

@en

type

label

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

@ast

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

@en

prefLabel

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

@ast

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

@en

P1433

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P1433

Antioxidants & Redox Signaling

P1476

Axonal mitochondrial clusters containing mutant SOD1 in transgenic models of ALS

@en

P2093

Florencia Palacios

http://www.w3.org/2001/XMLSchema#string

Joseph S Beckman

http://www.w3.org/2001/XMLSchema#string

Luis Barbeito

http://www.w3.org/2001/XMLSchema#string

Monica Marin

http://www.w3.org/2001/XMLSchema#string

Paola Lepanto

http://www.w3.org/2001/XMLSchema#string

Sofia Horjales

http://www.w3.org/2001/XMLSchema#string

Victoria Elizondo

http://www.w3.org/2001/XMLSchema#string

P2860

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

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

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

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

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

Unraveling the mechanisms involved in motor neuron degeneration in ALS

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

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

Genetics of sporadic ALS.

Superoxide dismutase and the death of motoneurons in ALS.

P304

1535-1545

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scholarly article

P356

10.1089/ARS.2009.2614

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P433

7

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P478

11

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José Roberto Sotelo-Silveira

Laura Martínez-Palma

P577

2009-07-01T00:00:00Z

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P698

19344250

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P921

amyotrophic lateral sclerosis

P932

2842590

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