about
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTDRare coding variants in the phospholipase D3 gene confer risk for Alzheimer's diseaseUBAP1 is a component of an endosome-specific ESCRT-I complex that is essential for MVB sortingFrequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyA hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDHeterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotypeMutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17CHMP2B mutations are not a common cause of frontotemporal lobar degenerationProgranulin and frontotemporal lobar degenerationIdentification of a truncated IL-18R beta mRNA: a putative regulator of IL-18 expressed in rat brainThe extended haplotype of the microtubule associated protein tau gene is not associated with Pick's disease.Apolipoprotein E epsilon4 allele has no effect on age at onset or duration of disease in cases of frontotemporal dementia with pick- or microvacuolar-type histology.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.Frontotemporal dementia and its subtypes: a genome-wide association study.Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsyMutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.Sporadic Pick's disease: a tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matter.The tau gene locus and frontotemporal dementia.Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies.Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.The complex aetiology of frontotemporal lobar degeneration.Small deletion in C9orf72 hides a proportion of expansion carriers in FTLD.Prominent phenotypic variability associated with mutations in ProgranulinA polymorphic variation in the interleukin 1A gene increases brain microglial cell activity in Alzheimer's diseaseAssociation between apolipoprotein E e4 allele and arteriosclerosis, cerebral amyloid angiopathy, and cerebral white matter damage in Alzheimer's diseaseAntisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy.Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutationsAmyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease.Chromosome 9 ALS and FTD locus is probably derived from a single founderPlasma levels of progranulin and interleukin-6 in frontotemporal lobar degeneration.Genetic associations between cathepsin D exon 2 C-->T polymorphism and Alzheimer's disease, and pathological correlations with genotypeThe apolipoprotein E epsilon4 allele selectively increases the risk of frontotemporal lobar degeneration in males.Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 geneNext generation sequencing of CLU, PICALM and CR1: pitfalls and potential solutions.Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases.Pathological tau deposition in Motor Neurone Disease and frontotemporal lobar degeneration associated with TDP-43 proteinopathy
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
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name
Stuart Pickering-Brown
@ast
Stuart Pickering-Brown
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Stuart Pickering-Brown
@es
Stuart Pickering-Brown
@fr
Stuart Pickering-Brown
@nl
Stuart Pickering-Brown
@sl
type
label
Stuart Pickering-Brown
@ast
Stuart Pickering-Brown
@en
Stuart Pickering-Brown
@es
Stuart Pickering-Brown
@fr
Stuart Pickering-Brown
@nl
Stuart Pickering-Brown
@sl
prefLabel
Stuart Pickering-Brown
@ast
Stuart Pickering-Brown
@en
Stuart Pickering-Brown
@es
Stuart Pickering-Brown
@fr
Stuart Pickering-Brown
@nl
Stuart Pickering-Brown
@sl
P106
P1153
7003642804
P21
P31
P496
0000-0003-1561-6054
P569
2000-01-01T00:00:00Z