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「"Dickson DW "[Author]」の検索結果

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TLR5 decoy receptor as a novel anti-amyloid therapeutic for Alzheimer's disease.

ε4 is associated with severity of Lewy body pathology independent of Alzheimer pathology.

Identification and functional characterization of novel mutations including frameshift mutation in exon 4 of CSF1R in patients with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.

Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy.

"Minimal change" multiple system atrophy with limbic-predominant α-synuclein pathology.

Long-read sequencing across the C9orf72 'GGGGCC' repeat expansion: implications for clinical use and genetic discovery efforts in human disease.

Association study between multiple system atrophy and TREM2 p.R47H.

Epigenome-wide DNA methylation profiling in Progressive Supranuclear Palsy reveals major changes at DLX1.

Poly-GR dipeptide repeat polymers correlate with neurodegeneration and Clinicopathological subtypes in C9ORF72-related brain disease.

TDP-43 and Alzheimer's Disease Pathologic Subtype in Non-Amnestic Alzheimer's Disease Dementia.

Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci.

Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patients.

TMEM106B haplotypes have distinct gene expression patterns in aged brain.

Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease.

Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis.

Genetic fine-mapping of the Iowan gene triplication in a patient with Parkinson's disease.

Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype.

Diffuse Lewy body disease manifesting as corticobasal syndrome: A rare form of Lewy body disease.

Loss of Tmem106b is unable to ameliorate frontotemporal dementia-like phenotypes in an AAV mouse model of C9ORF72-repeat induced toxicity.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

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