Modification of superoxide dismutase 1 (SOD1) properties by a GFP tag--implications for research into amyotrophic lateral sclerosis (ALS) - Wikidata - awgldk - TriplyDB

Modification of superoxide dismutase 1 (SOD1) properties by a GFP tag--implications for research into amyotrophic lateral sclerosis (ALS)

Modification of superoxide dismutase 1 (SOD1) properties by a GFP tag--implications for research into amyotrophic lateral sclerosis (ALS)

http://www.wikidata.org/entity/Q28473111

about

Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis Screening of Drugs Inhibiting In vitro Oligomerization of Cu/Zn-Superoxide Dismutase with a Mutation Causing Amyotrophic Lateral Sclerosis Suppressing mutation-induced protein aggregation in mammalian cells by mutating residues significantly displaced upon the original mutation A revisited folding reporter for quantitative assay of protein misfolding and aggregation in mammalian cells.The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease.Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleus.An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function.Induction of cell stress in neurons from transgenic mice expressing yellow fluorescent protein: implications for neurodegeneration research.50nm-scale localization of single unmodified, isotopically enriched, proteins in cells.An analysis of interactions between fluorescently-tagged mutant and wild-type SOD1 in intracellular inclusions Large-scale production and structural and biophysical characterizations of the human hepatitis B virus polymerase.N-terminal truncations of human bHLH transcription factor Twist1 leads to the formation of aggresomes.Polyanion binding accelerates the formation of stable and low-toxic aggregates of ALS-linked SOD1 mutant A4V.Extracellular aggregated Cu/Zn superoxide dismutase activates microglia to give a cytotoxic phenotype.Structural and aggregation behavior of the human γD-crystallin mutant E107A, associated with congenital nuclear cataract Spinal cord homogenates from SOD1 familial amyotrophic lateral sclerosis induce SOD1 aggregation in living cells.Features of wild-type human SOD1 limit interactions with misfolded aggregates of mouse G86R Sod1.Marinesco-Sjögren syndrome protein SIL1 regulates motor neuron subtype-selective ER stress in ALS.Implications of fALS Mutations on Sod1 Function and Oligomerization in Cell Models.Relationship between mutant Cu/Zn superoxide dismutase 1 maturation and inclusion formation in cell models.In vivo genome editing improves motor function and extends survival in a mouse model of ALS.Genetic validation of a therapeutic target in a mouse model of ALS.A theoretical study on Zn binding loop mutants instigating destabilization and metal binding loss in human SOD1 protein.Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes

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P2860

Modification of superoxide dismutase 1 (SOD1) properties by a GFP tag--implications for research into amyotrophic lateral sclerosis (ALS)

http://www.wikidata.org/entity/Q28473111

description

2010 nî lūn-bûn

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2010 թուականի Մարտին հրատարակուած գիտական յօդուած

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2010 թվականի մարտին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Modification of superoxide dis ...... rophic lateral sclerosis (ALS)

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Modification of superoxide dis ...... rophic lateral sclerosis (ALS)

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Modification of superoxide dis ...... rophic lateral sclerosis (ALS)

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James C Stevens

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Jan van Minnen

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Joanne E Martin

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Ruth Chia

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Virginie Bros-Facer

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William T Hendriks

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P2860

SOD1 and amyotrophic lateral sclerosis: mutations and oligomerization

Copper,zinc superoxide dismutase is primarily a cytosolic protein in human cells

Modern analytical ultracentrifugation in protein science: a tutorial review

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

Size-Distribution Analysis of Macromolecules by Sedimentation Velocity Ultracentrifugation and Lamm Equation Modeling

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

In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector

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

The use of differential scanning fluorimetry to detect ligand interactions that promote protein stability

Loss of metal ions, disulfide reduction and mutations related to familial ALS promote formation of amyloid-like aggregates from superoxide dismutase.

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Elizabeth M. C. Fisher

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amyotrophic lateral sclerosis

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