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Misfolded proteinase K-resistant hyperphosphorylated alpha-synuclein in aged transgenic mice with locomotor deterioration and in human alpha-synucleinopathiesAbundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion diseaseALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear importA harmonized classification system for FTLD-TDP pathologyA new subtype of frontotemporal lobar degeneration with FUS pathologyUbiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosisFUS pathology in basophilic inclusion body diseaseTDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementiaTDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron diseaseCommon variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.Knockdown of transactive response DNA-binding protein (TDP-43) downregulates histone deacetylase 6The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegenerationThe amyloid-beta (Abeta) peptide pattern in cerebrospinal fluid in Alzheimer's disease: evidence of a novel carboxyterminally elongated Abeta peptide.Mitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43.Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar DegenerationA mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition.Transactive response DNA-binding protein 43 burden in familial Alzheimer disease and Down syndromeFUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97.Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update.Distinct pathological subtypes of FTLD-FUS.FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations.Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene.PART is part of Alzheimer disease.FAS-dependent cell death in α-synuclein transgenic oligodendrocyte models of multiple system atrophyStructure/function of alpha-synuclein in health and disease: rational development of animal models for Parkinson's and related diseases.Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies.Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutationTDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions.Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUS.Mechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effectsDifferential sialylation of serpin A1 in the early diagnosis of Parkinson's disease dementia.Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS.TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysisEnrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosisLength of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotypeAdvances in understanding the molecular basis of frontotemporal dementia.Concomitant TAR-DNA-binding protein 43 pathology is present in Alzheimer disease and corticobasal degeneration but not in other tauopathies.Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS.TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis: protein misfolding diseases without amyloidosis.
P50
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P50
name
Manuela Neumann
@ast
Manuela Neumann
@en
Manuela Neumann
@nl
type
label
Manuela Neumann
@ast
Manuela Neumann
@en
Manuela Neumann
@nl
prefLabel
Manuela Neumann
@ast
Manuela Neumann
@en
Manuela Neumann
@nl