Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.
about
Functional MAPT haplotypes: bridging the gap between genotype and neuropathologyFrontotemporal lobar degeneration: old knowledge and new insight into the pathogenetic mechanisms of tau mutationsGenetics Underlying Atypical Parkinsonism and Related Neurodegenerative DisordersGenetics of Progressive Supranuclear PalsyInvited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimagingClosing the tau loop: the missing tau mutation.Tau isoform regulation is region- and cell-specific in mouse brain.A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects.Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.Alternative splicing of exon 10 in the tau gene as a target for treatment of tauopathies.Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.Development of a grape seed polyphenolic extract with anti-oligomeric activity as a novel treatment in progressive supranuclear palsy and other tauopathiesThe cytoskeleton in neurodegenerative diseases.Hereditary frontotemporal dementia caused by Tau gene mutations.Novel L284R MAPT mutation in a family with an autosomal dominant progressive supranuclear palsy syndrome.Genetics of parkinsonism.Disordered proteins in dementia.Neuropathology of frontotemporal lobar degeneration-tau (FTLD-tau).Structural and mechanistic commonalities of amyloid-β and the prion proteinIdentification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStudy on LOC426217 as a candidate gene for beak deformity in chickenAppoptosin-Mediated Caspase Cleavage of Tau Contributes to Progressive Supranuclear Palsy Pathogenesis.Tau alternative splicing and frontotemporal dementia.Clinical and molecular aspects of frontotemporal dementia.Phenotypic variation of autosomal-dominant corticobasal degeneration.Progressive supranuclear palsy: pathology and genetics.The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family.The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease.Back to the tubule: microtubule dynamics in Parkinson's disease.Rational therapeutic approaches to progressive supranuclear palsy.Visual signs and symptoms of progressive supranuclear palsy.Mitochondrial dysfunction as a therapeutic target in progressive supranuclear palsy."Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.Tau mis-splicing in the pathogenesis of neurodegenerative disorders.Genetics of Frontotemporal Dementia.Glycogen synthase kinase-3beta and tau genes interact in Alzheimer's disease.Monitoring tau-tubulin interactions utilizing second harmonic generation in living neurons.Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy.
P2860
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P2860
Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Progressive supranuclear palsy ...... caused by tau gene mutations.
@en
Progressive supranuclear palsy ...... caused by tau gene mutations.
@nl
type
label
Progressive supranuclear palsy ...... caused by tau gene mutations.
@en
Progressive supranuclear palsy ...... caused by tau gene mutations.
@nl
prefLabel
Progressive supranuclear palsy ...... caused by tau gene mutations.
@en
Progressive supranuclear palsy ...... caused by tau gene mutations.
@nl
P2093
P2860
P50
P356
P1433
P1476
Progressive supranuclear palsy ...... e caused by tau gene mutations
@en
P2093
C E Storey
J G Morris
M J Fulham
P M Stanford
P2860
P304
P356
10.1093/BRAIN/123.5.880
P407
P478
123 ( Pt 5)
P577
2000-05-01T00:00:00Z