Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not.
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Association of Long Runs of Homozygosity With Alzheimer Disease Among African American IndividualsCharacterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.Pathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substrates.Frontotemporal dementia and its subtypes: a genome-wide association study.Identical twins with the C9orf72 repeat expansion are discordant for ALSMutation analysis of patients with neurodegenerative disorders using NeuroX arrayRab8, POSH, and TAK1 regulate synaptic growth in a Drosophila model of frontotemporal dementiaWhole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.Special Issue on amyotrophic lateral sclerosis.miR-132/212 deficiency impairs tau metabolism and promotes pathological aggregation in vivo.Low autophagy capacity implicated in motor system vulnerability to mutant superoxide dismutaseTDP-43 functions within a network of hnRNP proteins to inhibit the production of a truncated human SORT1 receptor.Pathological TDP-43 changes in Betz cells differ from those in bulbar and spinal α-motoneurons in sporadic amyotrophic lateral sclerosis.Microarray gene and miRNA expression studies: looking for new therapeutic targets for frontotemporal lobar degeneration.Disease origin and progression in amyotrophic lateral sclerosis: an immunology perspective.Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysisInflammatory role of dendritic cells in Amyotrophic Lateral Sclerosis revealed by an analysis of patients' peripheral blood.Physiological functions and pathobiology of TDP-43 and FUS/TLS proteins.TDP-43 in the spectrum of MND-FTLD pathologies.Isoform-specific antibodies reveal distinct subcellular localizations of C9orf72 in amyotrophic lateral sclerosis.DNA methylation age-acceleration is associated with disease duration and age at onset in C9orf72 patientsThe minor spliceosome could be the major key for FUS/TLS mutants in ALSJump from pre-mutation to pathologic expansion in C9orf72.Dementia in motor neuron disease: Reviewing the role of MRI in diagnosis.Unaffected mosaic C9orf72 case: RNA foci, dipeptide proteins, but upregulated C9orf72 expression.TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics.OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia.The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.Synaptic Failure: Focus in an Integrative View of ALS.A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
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P2860
Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
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2013年學術文章
@zh-hant
name
Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not.
@en
type
label
Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not.
@en
prefLabel
Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not.
@en
P1476
Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not.
@en
P356
10.1016/J.EXPNEUROL.2013.11.006
P407
P478
P577
2013-11-15T00:00:00Z