Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis. - Wikidata - wikimedia - TriplyDB

Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q37936558

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Mechanisms, models and biomarkers in amyotrophic lateral sclerosis SOD1 oxidation and formation of soluble aggregates in yeast: relevance to sporadic ALS development.Model systems of motor neuron diseases as a platform for studying pathogenic mechanisms and searching for therapeutic agents.Mitochondrion-mediated cell death: dissecting yeast apoptosis for a better understanding of neurodegeneration.Ubiquitin-dependent proteolysis in yeast cells expressing neurotoxic proteins.Unraveling protein misfolding diseases using model systems ALS Yeast Models—Past Success Stories and New Opportunities

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Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q37936558

description

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article scientifique

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artikel ilmiah

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artículo científico

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name

Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

@en

Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

@nl

type

label

Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

@en

Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

@nl

prefLabel

Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

@en

Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.

@nl

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Biochemical Society Transactions

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Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis

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Emma L Bastow

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P2860

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

Suppressors of superoxide dismutase (SOD1) deficiency in Saccharomyces cerevisiae. Identification of proteins predicted to mediate iron-sulfur cluster assembly.

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

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

Glutaredoxins: glutathione-dependent redox enzymes with functions far beyond a simple thioredoxin backup system

Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice

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

Riluzole increases the amount of latent HSF1 for an amplified heat shock response and cytoprotection

Copper, zinc superoxide dismutase catalyzes hydroxyl radical production from hydrogen peroxide

A yeast model of FUS/TLS-dependent cytotoxicity.

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1482-1487

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scholarly article

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10.1042/BST0391482

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5

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39

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Campbell W. Gourlay

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2011-10-01T00:00:00Z

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51660610

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21936838

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amyotrophic lateral sclerosis