Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
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Golgi Fragmentation in ALS Motor Neurons. New Mechanisms Targeting Microtubules, Tethers, and Transport VesiclesSpinal muscular atrophy: from gene discovery to clinical trialsThe Microtubule Regulatory Protein Stathmin Is Required to Maintain the Integrity of Axonal Microtubules in DrosophilaThe spinal muscular atrophy disease protein SMN is linked to the Golgi networkChondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophyThe intricate relationship between microtubules and their associated motor proteins during axon growth and maintenance.Epothilone D prevents binge methamphetamine-mediated loss of striatal dopaminergic markers.Proteomic assessment of a cell model of spinal muscular atrophyAbnormalities of Mitochondrial Dynamics in Neurodegenerative Diseases.Autophagy dysregulation in cell culture and animals models of spinal muscular atrophy.SMN requirement for synaptic vesicle, active zone and microtubule postnatal organization in motor nerve terminalsSOD1 targeted to the mitochondrial intermembrane space prevents motor neuropathy in the Sod1 knockout mouse.Stathmin is required for stability of the Drosophila neuromuscular junction.Mitochondrial dynamic abnormalities in amyotrophic lateral sclerosis.Spinal muscular atrophy: the role of SMN in axonal mRNA regulation.Placental development in a mouse model of spinal muscular atrophy.A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutationsStathmin 1/2-triggered microtubule loss mediates Golgi fragmentation in mutant SOD1 motor neurons.Is SOD1 loss of function involved in amyotrophic lateral sclerosis?cAMP-dependent protein kinase and c-Jun N-terminal kinase mediate stathmin phosphorylation for the maintenance of interphase microtubules during osmotic stress.Developments in the discovery of drugs for spinal muscular atrophy: successful beginnings and future prospects.Advances in understanding the role of disease-associated proteins in spinal muscular atrophy.Dilysine motifs in exon 2b of SMN protein mediate binding to the COPI vesicle protein α-COP and neurite outgrowth in a cell culture model of spinal muscular atrophy.Hypothermia improves disease manifestations in SMA mice via SMN augmentation.Diverse role of survival motor neuron protein.Nanomolar naloxone attenuates neurotoxicity induced by oxidative stress and survival motor neuron protein deficiency.Alpha-synuclein loss in spinal muscular atrophyExonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder.TBCD may be a causal gene in progressive neurodegenerative encephalopathy with atypical infantile spinal muscular atrophy.MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretion.Solving the puzzle of spinal muscular atrophy: what are the missing pieces?Axon outgrowth and neuronal differentiation defects after a-SMN and FL-SMN silencing in primary hippocampal cultures.
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P2860
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
description
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մայիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2010
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im Mai 2010 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
@en
vedecký článok (publikovaný 2010/05/01)
@sk
vědecký článek publikovaný v roce 2010
@cs
wetenschappelijk artikel (gepubliceerd op 2010/05/01)
@nl
наукова стаття, опублікована в травні 2010
@uk
مقالة علمية (نشرت في مايو 2010)
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name
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@ast
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@en
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@nl
type
label
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@ast
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@en
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@nl
prefLabel
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@ast
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@en
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@nl
P2093
P921
P3181
P356
P1476
Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy
@en
P2093
Chen-Hung Ting
Hsin-Lan Wen
Hsiu Mei Hsieh-Li
Sue Lin-Chao
Yuan-Ta Lin
P304
P3181
P356
10.1093/HMG/DDQ058
P577
2010-05-01T00:00:00Z