The function of RNA-binding proteins at the synapse: implications for neurodegeneration - Test2 - elhamkhani - TriplyDB

The function of RNA-binding proteins at the synapse: implications for neurodegeneration

The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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Alphaherpesvirus Subversion of Stress-Induced Translational Arrest Adducin at the Neuromuscular Junction in Amyotrophic Lateral Sclerosis: Hanging on for Dear Life Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision Medicine RNA binding motif protein 3: a potential biomarker in cancer and therapeutic target in neuroprotection.Co-regulation of mRNA translation by TDP-43 and Fragile X Syndrome protein FMRP Modelling FUS Mislocalisation in an In Vitro Model of Innervated Human Muscle.Screening the Molecular Framework Underlying Local Dendritic mRNA Translation.Tyrosine kinase inhibition reverses TDP-43 effects on synaptic protein expression, astrocytic function and amino acid dis-homeostasis.Protein Kinase C Activation as a Potential Therapeutic Strategy in Alzheimer's Disease: Is there a Role for Embryonic Lethal Abnormal Vision-like Proteins?Physiological functions and pathobiology of TDP-43 and FUS/TLS proteins.Extracellular vesicles and intercellular communication within the nervous system.Neurodegeneration and RNA-binding proteins.TDP-43/FUS in motor neuron disease: Complexity and challenges.Synapse Dysfunction of Layer V Pyramidal Neurons Precedes Neurodegeneration in a Mouse Model of TDP-43 Proteinopathies.Energy Homeostasis and Abnormal RNA Metabolism in Amyotrophic Lateral Sclerosis TDP-43 in the spectrum of MND-FTLD pathologies.Hepatitis C virus plays with fire and yet avoids getting burned. A review for clinicians on processing bodies and stress granules.Major hnRNP proteins act as general TDP-43 functional modifiers both in Drosophila and human neuronal cells.Do Low Serum UCH-L1 and TDP-43 Levels Indicate Disturbed Ubiquitin-Proteosome System in Autism Spectrum Disorder?In Vivo Translatome Profiling in Spinal Muscular Atrophy Reveals a Role for SMN Protein in Ribosome Biology.RNA-binding proteins in neurodegeneration: mechanisms in aggregate.Synaptic dysfunction and altered excitability in C9ORF72 ALS/FTD.FUS Phase Separation Is Modulated by a Molecular Chaperone and Methylation of Arginine Cation-π Interactions.Synaptic Paths to Neurodegeneration: The Emerging Role of TDP-43 and FUS in Synaptic Functions.Linking hnRNP Function to ALS and FTD Pathology.Importance of Functional Loss of FUS in FTLD/ALS.The physiological and pathological biophysics of phase separation and gelation of RNA binding proteins in amyotrophic lateral sclerosis and fronto-temporal lobar degeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

http://www.wikidata.org/entity/Q26991684

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2015 nî lūn-bûn

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2015 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2015 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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Gang Yu

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

Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules

FUS stimulates microRNA biogenesis by facilitating co-transcriptional Drosha recruitment

TRBP recruits the Dicer complex to Ago2 for microRNA processing and gene silencing

The Microprocessor complex mediates the genesis of microRNAs

Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs

Mammalian Smaug is a translational repressor that forms cytoplasmic foci similar to stress granules

The composition of Staufen-containing RNA granules from human cells indicates their role in the regulated transport and translation of messenger RNAs

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

Identification of hnRNP P2 as TLS/FUS using electrospray mass spectrometry.

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