FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
about
Immunoprecipitation and mass spectrometry defines an extensive RBM45 protein-protein interaction networkEngineering enhanced protein disaggregases for neurodegenerative diseaseRNA Polymerase II C-Terminal Domain: Tethering Transcription to Transcript and TemplateFrontotemporal Dementia.FUS is phosphorylated by DNA-PK and accumulates in the cytoplasm after DNA damageThe ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction.Potentiated Hsp104 variants suppress toxicity of diverse neurodegenerative disease-linked proteins.Coaggregation of RNA-binding proteins in a model of TDP-43 proteinopathy with selective RGG motif methylation and a role for RRM1 ubiquitinationTargeting RNA binding proteins involved in neurodegeneration.Aberrant RNA homeostasis in amyotrophic lateral sclerosis: potential for new therapeutic targets?Linking RNA Dysfunction and Neurodegeneration in Amyotrophic Lateral Sclerosis.A Systematic Analysis of Factors Localized to Damaged Chromatin Reveals PARP-Dependent Recruitment of Transcription FactorsALS mutations in TLS/FUS disrupt target gene expression.Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS.Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS.Disease mutations in the prion-like domains of hnRNPA1 and hnRNPA2/B1 introduce potent steric zippers that drive excess RNP granule assembly.Targeting TDP-43 in neurodegenerative diseases.The role of FUS gene variants in neurodegenerative diseases.Genetics of FTLD: overview and what else we can expect from genetic studies.Physiological functions and pathobiology of TDP-43 and FUS/TLS proteins.Role of FET proteins in neurodegenerative disorders.Comparative protein interactomics of neuroglobin and myoglobin.Identification of in vivo, conserved, TAF15 RNA binding sites reveals the impact of TAF15 on the neuronal transcriptome.RNA Granules and Diseases: A Case Study of Stress Granules in ALS and FTLDFUS regulates genes coding for RNA-binding proteins in neurons by binding to their highly conserved introns.Biology and Pathobiology of TDP-43 and Emergent Therapeutic Strategies.Fused in Sarcoma Neuropathology in Neurodegenerative Disease.Genetic Ablation of EWS RNA Binding Protein 1 (EWSR1) Leads to Neuroanatomical Changes and Motor Dysfunction in Mice.
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FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
@en
FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
@nl
type
label
FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
@en
FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
@nl
prefLabel
FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
@en
FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
@nl
P1433
P1476
FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.
@en
P2093
Ian R A Mackenzie
P356
10.1016/J.BRAINRES.2011.12.010
P407
P577
2011-12-13T00:00:00Z