Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.
about
Impaired spatial learning and defective theta burst induced LTP in mice lacking fibroblast growth factor 14Human-specific transcriptional regulation of CNS development genes by FOXP2Crystal Structure of a Fibroblast Growth Factor Homologous Factor (FHF) Defines a Conserved Surface on FHFs for Binding and Modulation of Voltage-gated Sodium ChannelsModulation, Plasticity and Pathophysiology of the Parallel Fiber-Purkinje Cell Synapse.Integrative biological analysis for neuropsychopharmacologyIntracellular Fibroblast Growth Factor 14: Emerging Risk Factor for Brain Disorders.FGF14 N-terminal splice variants differentially modulate Nav1.2 and Nav1.6-encoded sodium channels.Role of the axonal initial segment in psychiatric disorders: function, dysfunction, and interventionBrain pathology of spinocerebellar ataxias.Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxiaThe Fibroblast Growth Factor signaling pathwayThe fibroblast growth factor 14·voltage-gated sodium channel complex is a new target of glycogen synthase kinase 3 (GSK3).Fibroblast growth factors: from molecular evolution to roles in development, metabolism and disease.Dual transgene expression in murine cerebellar Purkinje neurons by viral transduction in vivoIntracellular FGF14 (iFGF14) Is Required for Spontaneous and Evoked Firing in Cerebellar Purkinje Neurons and for Motor Coordination and BalanceIdentifying a kinase network regulating FGF14:Nav1.6 complex assembly using split-luciferase complementation.Bioluminescence methodology for the detection of protein-protein interactions within the voltage-gated sodium channel macromolecular complexFibroblast Growth Factor Homologous Factors: New Roles in Neuronal Health and Disease.Restoration of Central Programmed Movement Pattern by Temporal Electrical Stimulation-Assisted Training in Patients with Spinal Cerebellar Atrophy.Microarray Analyses Reveal Marked Differences in Growth Factor and Receptor Expression Between 8-Cell Human Embryos and Pluripotent Stem CellsOn autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.CK2 activity is required for the interaction of FGF14 with voltage-gated sodium channels and neuronal excitabilityProteomic analysis of native cerebellar iFGF14 complexes.FGF14 regulates the intrinsic excitability of cerebellar Purkinje neurons.FGF14 localization and organization of the axon initial segmentMolecular pathology of the fibroblast growth factor family.A programmable Cas9-serine recombinase fusion protein that operates on DNA sequences in mammalian cellsPhysiologic alterations in ataxia: channeling changes into novel therapies.Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.The inherited ataxias: genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics.Roles of intracellular fibroblast growth factors in neural development and functions.The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability.Non-Ataxic Presenting Symptoms of Dominant Ataxias.Fibroblast Growth Factor 14 Modulates the Neurogenesis of Granule Neurons in the Adult Dentate Gyrus.PPARgamma agonists rescue increased phosphorylation of FGF14 at S226 in the Tg2576 mouse model of Alzheimer's disease.Cerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathways.Genetic deletion of fibroblast growth factor 14 recapitulates phenotypic alterations underlying cognitive impairment associated with schizophrenia.Parallel fiber to Purkinje cell synaptic impairment in a mouse model of spinocerebellar ataxia type 27.Polyglutamine spinocerebellar ataxias - from genes to potential treatments.Functional Modulation of Voltage-Gated Sodium Channels by a FGF14-Based Peptidomimetic.
P2860
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P2860
Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.
description
2006 nî lūn-bûn
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2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Spinocerebellar ataxia associa ...... gene (SCA27): A new phenotype.
@ast
Spinocerebellar ataxia associa ...... gene (SCA27): A new phenotype.
@en
Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene
@nl
type
label
Spinocerebellar ataxia associa ...... gene (SCA27): A new phenotype.
@ast
Spinocerebellar ataxia associa ...... gene (SCA27): A new phenotype.
@en
Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene
@nl
prefLabel
Spinocerebellar ataxia associa ...... gene (SCA27): A new phenotype.
@ast
Spinocerebellar ataxia associa ...... gene (SCA27): A new phenotype.
@en
Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene
@nl
P2093
P2860
P356
P1433
P1476
Spinocerebellar ataxia associa ...... gene (SCA27): A new phenotype.
@en
P2093
Anneke Maat-Kievit
Ben A Oostra
Esther Brusse
Inge de Koning
John C van Swieten
P2860
P304
P356
10.1002/MDS.20708
P407
P577
2006-03-01T00:00:00Z