Deficiency of the Survival of Motor Neuron Protein Impairs mRNA Localization and Local Translation in the Growth Cone of Motor Neurons.
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Emerging therapies and challenges in spinal muscular atrophyBioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy.Disruption of the Axonal Trafficking of Tyrosine Hydroxylase mRNA Impairs Catecholamine Biosynthesis in the Axons of Sympathetic NeuronsThe Survival of Motor Neuron Protein Acts as a Molecular Chaperone for mRNP AssemblyAltered mRNA Splicing in SMN-Depleted Motor Neuron-Like Cells.Dysregulation of mRNA Localization and Translation in Genetic DiseaseRecombinant hNeuritin Promotes Structural and Functional Recovery of Sciatic Nerve Injury in Rats.Advances in understanding the role of disease-associated proteins in spinal muscular atrophy.Astrocyte-produced miR-146a as a mediator of motor neuron loss in spinal muscular atrophy.Diverse role of survival motor neuron protein.Spatially and temporally regulating translation via mRNA-binding proteins in cellular and neuronal function.Expanding Axonal Transcriptome Brings New Functions for Axonally Synthesized Proteins in Health and Disease.Smn-Deficiency Increases the Intrinsic Excitability of Motoneurons.SECIS-binding protein 2 interacts with the SMN complex and the methylosome for selenoprotein mRNP assembly and translation.Impaired spliceosomal UsnRNP assembly leads to Sm mRNA down-regulation and Sm protein degradation.In Vivo Translatome Profiling in Spinal Muscular Atrophy Reveals a Role for SMN Protein in Ribosome Biology.To the end of the line: Axonal mRNA transport and local translation in health and neurodegenerative disease.HuD and the Survival Motor Neuron Protein Interact in Motoneurons and Are Essential for Motoneuron Development, Function, and mRNA Regulation.SMN regulation in SMA and in response to stress: new paradigms and therapeutic possibilities.Overview of Current Drugs and Molecules in Development for Spinal Muscular Atrophy Therapy.mRNP assembly, axonal transport, and local translation in neurodegenerative diseases.Neurochondrin interacts with the SMN protein suggesting a novel mechanism for Spinal Muscular Atrophy pathology.Axon outgrowth and neuronal differentiation defects after a-SMN and FL-SMN silencing in primary hippocampal cultures.Unraveling the Pathways to Neuronal Homeostasis and Disease: Mechanistic Insights into the Role of RNA-Binding Proteins and Associated Factors
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P2860
Deficiency of the Survival of Motor Neuron Protein Impairs mRNA Localization and Local Translation in the Growth Cone of Motor Neurons.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Deficiency of the Survival of ...... Growth Cone of Motor Neurons.
@ast
Deficiency of the Survival of ...... Growth Cone of Motor Neurons.
@en
type
label
Deficiency of the Survival of ...... Growth Cone of Motor Neurons.
@ast
Deficiency of the Survival of ...... Growth Cone of Motor Neurons.
@en
prefLabel
Deficiency of the Survival of ...... Growth Cone of Motor Neurons.
@ast
Deficiency of the Survival of ...... Growth Cone of Motor Neurons.
@en
P2860
P50
P1476
Deficiency of the Survival of ...... e Growth Cone of Motor Neurons
@en
P2093
Gary J Bassell
Jeremy P Rouanet
P2860
P304
P356
10.1523/JNEUROSCI.2396-15.2016
P407
P577
2016-03-01T00:00:00Z