Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
about
Micro spies from the brain to the periphery: new clues from studies on microRNAs in neuropsychiatric disordersGenome-wide association study of Tourette's syndromeThe FTLD risk factor TMEM106B and MAP6 control dendritic trafficking of lysosomesIncreased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathologyFrequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyThe genetics and neuropathology of frontotemporal lobar degenerationChromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyExpanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSA hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDFrontotemporal Lobar Degeneration and MicroRNAsPhenotypic Heterogeneity of Monogenic Frontotemporal DementiaMechanisms of granulin deficiency: lessons from cellular and animal modelsConverging mechanisms in ALS and FTD: disrupted RNA and protein homeostasisTherapeutic and diagnostic challenges for frontotemporal dementiaPotential roles of microglial cell progranulin in HIV-associated CNS pathologies and neurocognitive impairmentProgranulin: at the interface of neurodegenerative and metabolic diseasesLower plasma apolipoprotein A1 levels are found in Parkinson's disease and associate with apolipoprotein A1 genotypeFrontotemporal dementia: a bridge between dementia and neuromuscular diseaseLysosome size, motility and stress response regulated by fronto-temporal dementia modifier TMEM106BGenome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPC9orf72 binds SMCR8, localizes to lysosomes, and regulates mTORC1 signaling.Identification of genes associated with dissociation of cognitive performance and neuropathological burden: Multistep analysis of genetic, epigenetic, and transcriptional dataGenetic and clinical features of progranulin-associated frontotemporal lobar degenerationGenome-wide estimate of the heritability of Multiple System AtrophyChronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank.The genetics of dementia.Evidence of the innate antiviral and neuroprotective properties of progranulin.TMEM106B expression is reduced in Alzheimer's disease brainsIdentification of misdiagnosed fronto-temporal dementia using APOE genotype and phenotype-genotype correlation analyses.Regulated intramembrane proteolysis of the frontotemporal lobar degeneration risk factor, TMEM106B, by signal peptide peptidase-like 2a (SPPL2a).Biomarkers in frontotemporal lobar degenerations--progress and challenges.Progranulin protein levels are differently regulated in plasma and CSF.Frontotemporal dementia and its subtypes: a genome-wide association study.C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisRNA-protein interactions in unstable microsatellite diseases.Genetics of dementia.Transmembrane protein 106A is silenced by promoter region hypermethylation and suppresses gastric cancer growth by inducing apoptosisThe emerging roles of microRNAs in the pathogenesis of frontotemporal dementia-amyotrophic lateral sclerosis (FTD-ALS) spectrum disordersThe widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype.A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy
P2860
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P2860
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին 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
Common variants at 7p21 are as ...... ration with TDP-43 inclusions.
@ast
Common variants at 7p21 are as ...... ration with TDP-43 inclusions.
@en
type
label
Common variants at 7p21 are as ...... ration with TDP-43 inclusions.
@ast
Common variants at 7p21 are as ...... ration with TDP-43 inclusions.
@en
prefLabel
Common variants at 7p21 are as ...... ration with TDP-43 inclusions.
@ast
Common variants at 7p21 are as ...... ration with TDP-43 inclusions.
@en
P2093
P2860
P50
P356
P1433
P1476
Common variants at 7p21 are as ...... ration with TDP-43 inclusions.
@en
P2093
Ainhoa Alzualde
Albert Lladó
Alice Chen-Plotkin
Allan I Levey
Andrew P Lieberman
Ann C McKee
Bernardino Ghetti
Bradley F Boeve
Bryan K Woodruff
Carl W Cotman
P2860
P2888
P304
P356
10.1038/NG.536
P407
P50
P577
2010-02-14T00:00:00Z
P5875
P6179
1011035298