Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis - Test2 - elhamkhani - TriplyDB

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

http://www.wikidata.org/entity/Q24605104

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Altered ribostasis: RNA-protein granules in degenerative disorders Inside out: the role of nucleocytoplasmic transport in ALS and FTLD Mechanisms of FUS mutations in familial amyotrophic lateral sclerosis Engineering and Evolution of Molecular Chaperones and Protein Disaggregases with Enhanced Activity Prion-like domains as epigenetic regulators, scaffolds for subcellular organization, and drivers of neurodegenerative disease FUS-mediated regulation of alternative RNA processing in neurons: insights from global transcriptome analysis RNA-Binding Proteins in the Regulation of miRNA Activity: A Focus on Neuronal Functions Chaperones in Neurodegeneration Yeast prions and human prion-like proteins: sequence features and prediction methods Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis The function of RNA-binding proteins at the synapse: implications for neurodegeneration Structural and energetic basis of ALS-causing mutations in the atypical proline–tyrosine nuclear localization signal of the Fused in Sarcoma protein (FUS)Emerging mechanisms of molecular pathology in ALS Engineering enhanced protein disaggregases for neurodegenerative disease Drosophila as an In Vivo Model for Human Neurodegenerative Disease Oxr1 improves pathogenic cellular features of ALS-associated FUS and TDP-43 mutations Gene expression responses to FUS, EWS, and TAF15 reduction and stress granule sequestration analyses identifies FET-protein non-redundant functions.Iron and restless legs syndrome: treatment, genetics and pathophysiology.The ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction.Molecular network analysis suggests a logical hypothesis for the pathological role of c9orf72 in amyotrophic lateral sclerosis/frontotemporal dementia.Assemblages: functional units formed by cellular phase separation The emerging role of guanine nucleotide exchange factors in ALS and other neurodegenerative diseases.Potentiated Hsp104 variants suppress toxicity of diverse neurodegenerative disease-linked proteins.Targeted exon capture and sequencing in sporadic amyotrophic lateral sclerosis.Profilin 1 associates with stress granules and ALS-linked mutations alter stress granule dynamics.Genetic interaction of hnRNPA2B1 and DNAJB6 in a Drosophila model of multisystem proteinopathy.Interaction of tau with the RNA-Binding Protein TIA1 Regulates tau Pathophysiology and Toxicity.Sequence Determinants of Intracellular Phase Separation by Complex Coacervation of a Disordered Protein.The RNA-binding protein fused in sarcoma (FUS) functions downstream of poly(ADP-ribose) polymerase (PARP) in response to DNA damage Aberrant RNA homeostasis in amyotrophic lateral sclerosis: potential for new therapeutic targets?Therapeutic modulation of eIF2α phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models.Gene expression signatures in motor neurone disease fibroblasts reveal dysregulation of metabolism, hypoxia-response and RNA processing functions Increasing prion propensity by hydrophobic insertion.Network analyses reveal novel aspects of ALS pathogenesis A fruitful endeavor: modeling ALS in the fruit fly Linking RNA Dysfunction and Neurodegeneration in Amyotrophic Lateral Sclerosis.Calcium-responsive transactivator (CREST) protein shares a set of structural and functional traits with other proteins associated with amyotrophic lateral sclerosis.Prion-like domains in RNA binding proteins are essential for building subnuclear paraspeckles.Severe respiratory changes at end stage in a FUS-induced disease state in adult rats.Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs.

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

http://www.wikidata.org/entity/Q24605104

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2012 nî lūn-bûn

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2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

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Cecilia E Kim

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Dana Clay-Falcone

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Fadia Ibrahim

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Jelena Mojsilovic-Petrovic

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

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

Rules for nuclear localization sequence recognition by karyopherin beta 2

Exome sequencing identifies the cause of a mendelian disorder

Targeted capture and massively parallel sequencing of 12 human exomes

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

A systematic survey identifies prions and illuminates sequence features of prionogenic proteins

Transformation of intact yeast cells treated with alkali cations

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