Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS).
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The genetics and neuropathology of frontotemporal lobar degenerationGenotype-phenotype correlations of amyotrophic lateral sclerosisPhenotypic Heterogeneity of Monogenic Frontotemporal DementiaUltrastructural studies of ALS mitochondria connect altered function and permeability with defects of mitophagy and mitochondriogenesisMouse models of frontotemporal dementiaConverging mechanisms in ALS and FTD: disrupted RNA and protein homeostasisState of play in amyotrophic lateral sclerosis geneticsDifferentiating lower motor neuron syndromesFrontotemporal dementia: a bridge between dementia and neuromuscular diseaseAutophagosome dynamics in neurodegeneration at a glanceModeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neuronsAmyotrophic lateral sclerosis, gene deregulation in the anterior horn of the spinal cord and frontal cortex area 8: implications in frontotemporal lobar degenerationProtein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities?Deregulated expression of cytoskeleton related genes in the spinal cord and sciatic nerve of presymptomatic SOD1(G93A) Amyotrophic Lateral Sclerosis mouse model.Amyotrophic lateral sclerosis patient iPSC-derived astrocytes impair autophagy via non-cell autonomous mechanisms.The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement.The emerging roles of microRNAs in the pathogenesis of frontotemporal dementia-amyotrophic lateral sclerosis (FTD-ALS) spectrum disordersPathogenic role of BECN1/Beclin 1 in the development of amyotrophic lateral sclerosis.Biosignatures for Parkinson's disease and atypical parkinsonian disorders patients.Genetic overlap between apparently sporadic motor neuron diseases.Population-specific regulation of Chmp2b by Lbx1 during onset of synaptogenesis in lateral association interneurons.Alterations in microRNA-124 and AMPA receptors contribute to social behavioral deficits in frontotemporal dementia.Regulation of autophagy by mTOR-dependent and mTOR-independent pathways: autophagy dysfunction in neurodegenerative diseases and therapeutic application of autophagy enhancers.Downregulation of microRNA-9 in iPSC-derived neurons of FTD/ALS patients with TDP-43 mutations.A network of RNA and protein interactions in Fronto Temporal Dementia.Rab8, POSH, and TAK1 regulate synaptic growth in a Drosophila model of frontotemporal dementiaMotor and Sensory Deficits in the teetering Mice Result from Mutation of the ESCRT Component HGSNeuronal Functions of ESCRTsLysosomal and phagocytic activity is increased in astrocytes during disease progression in the SOD1 (G93A) mouse model of amyotrophic lateral sclerosis.Significant expansion of the REST/NRSF cistrome in human versus mouse embryonic stem cells: potential implications for neural developmentCause or Effect: Misregulation of microRNA Pathways in Neurodegeneration.Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis.Potential contribution of exosomes to the prion-like propagation of lesions in Alzheimer's disease.The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrumα-Synuclein interferes with the ESCRT-III complex contributing to the pathogenesis of Lewy body disease.Transcriptome Profiling Following Neuronal and Glial Expression of ALS-Linked SOD1 in Drosophila.The wobbler mouse, an ALS animal model.The Enemy within: Innate Surveillance-Mediated Cell Death, the Common Mechanism of Neurodegenerative Disease.Genetics of amyotrophic lateral sclerosis: an update.Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15
P2860
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P2860
Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS).
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Mutations in CHMP2B in lower m ...... ophic lateral sclerosis (ALS).
@ast
Mutations in CHMP2B in lower m ...... ophic lateral sclerosis (ALS).
@en
type
label
Mutations in CHMP2B in lower m ...... ophic lateral sclerosis (ALS).
@ast
Mutations in CHMP2B in lower m ...... ophic lateral sclerosis (ALS).
@en
prefLabel
Mutations in CHMP2B in lower m ...... ophic lateral sclerosis (ALS).
@ast
Mutations in CHMP2B in lower m ...... ophic lateral sclerosis (ALS).
@en
P2093
P2860
P50
P1433
P1476
Mutations in CHMP2B in lower m ...... ophic lateral sclerosis (ALS).
@en
P2093
Adrian Higginbottom
Alice Brockington
Christine E Burness
Hannah C Hollinger
Judith A Hartley
Karen E Morrison
Laura E Cox
Paul R Heath
Stephen B Wharton
P2860
P356
10.1371/JOURNAL.PONE.0009872
P407
P50
P577
2010-03-24T00:00:00Z