Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
about
What we truly know about occupation as a risk factor for ALS: A critical and systematic reviewChromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyGenome-wide association studies in neurological disordersA two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisToward precision medicine in amyotrophic lateral sclerosisState of play in amyotrophic lateral sclerosis geneticsAmyotrophic Lateral Sclerosis: An update for 2013 Clinical Features, Pathophysiology, Management and Therapeutic TrialsKv4.2 and accessory dipeptidyl peptidase-like protein 10 (DPP10) subunit preferentially form a 4:2 (Kv4.2:DPP10) channel complexDPP6 establishes the A-type K(+) current gradient critical for the regulation of dendritic excitability in CA1 hippocampal neuronsAugmentation of Kv4.2-encoded currents by accessory dipeptidyl peptidase 6 and 10 subunits reflects selective cell surface Kv4.2 protein stabilizationDipeptidyl peptidase-like protein 6 is required for normal electrophysiological properties of cerebellar granule cellsA high-density genome-wide association screen of sporadic ALS in US veteransThe prion protein modulates A-type K+ currents mediated by Kv4.2 complexes through dipeptidyl aminopeptidase-like protein 6Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosisScreening for replication of genome-wide SNP associations in sporadic ALSAge of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.A HapMap harvest of insights into the genetics of common diseaseENDEAVOUR update: a web resource for gene prioritization in multiple speciesThe role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathology.Beyond Parkinson disease: amyotrophic lateral sclerosis and the axon guidance pathwayCopy number variations play important roles in heredity of common diseases: a novel method to calculate heritability of a polymorphism.Markov Models for inferring copy number variations from genotype data on Illumina platformsWeighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patientsGenome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis.The Analysis of Two BDNF Polymorphisms G196A/C270T in Chinese Sporadic Amyotrophic Lateral Sclerosis.The landscape of human genes involved in the immune response to parasitic wormsTargeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansionMicroarray analysis of peripheral blood lymphocytes from ALS patients and the SAFE detection of the KEGG ALS pathway.Global similarity with local differences in linkage disequilibrium between the Dutch and HapMap-CEU populations.Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisMapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.Neuronal voltage-gated K+ (Kv) channels function in macromolecular complexes.Incorporation of DPP6a and DPP6K variants in ternary Kv4 channel complex reconstitutes properties of A-type K current in rat cerebellar granule cells.Joint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power.DPP6 domains responsible for its localization and function.Identification of active loci of a human endogenous retrovirus in neurons of patients with amyotrophic lateral sclerosis.Genome-wide association studies in neurology.A new TASK for Dipeptidyl Peptidase-like Protein 6.
P2860
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P2860
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Genetic variation in DPP6 is a ...... amyotrophic lateral sclerosis.
@en
type
label
Genetic variation in DPP6 is a ...... amyotrophic lateral sclerosis.
@en
prefLabel
Genetic variation in DPP6 is a ...... amyotrophic lateral sclerosis.
@en
P2093
P50
P356
P1433
P1476
Genetic variation in DPP6 is a ...... amyotrophic lateral sclerosis.
@en
P2093
Anna Birve
Bryan J Traynor
Christiaan G J Saris
Helenius J Schelhaas
Hylke M Blauw
Jennifer C Schymick
John H J Wokke
Michael A van Es
Paul W J van Vught
Roel A Ophoff
P2888
P356
10.1038/NG.2007.52
P407
P50
P577
2007-12-16T00:00:00Z
P5875
P6179
1023923852