Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration - Wikidata - wikimedia - TriplyDB

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

http://www.wikidata.org/entity/Q33830991

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The genetics and neuropathology of frontotemporal lobar degeneration Aging and Autophagic Function Influences the Progressive Decline of Adult Drosophila Behaviors FUS transgenic rats develop the phenotypes of amyotrophic lateral sclerosis and frontotemporal lobar degeneration Frontotemporal dementia: a bridge between dementia and neuromuscular disease A 43-kDa TDP-43 species is present in aggregates associated with frontotemporal lobar degeneration Clinical characterization of bvFTD due to FUS neuropathology.Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion.Recent advances in the imaging of frontotemporal dementia.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.Distinct pathological subtypes of FTLD-FUS.Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management.The diagnosis of young-onset dementia.Nuclear localization sequence of FUS and induction of stress granules by ALS mutants.An algorithm for genetic testing of frontotemporal lobar degeneration Neuroimaging in frontotemporal dementia.p62, Ref(2)P and ubiquitinated proteins are conserved markers of neuronal aging, aggregate formation and progressive autophagic defects.Rodent models of TDP-43 proteinopathy: investigating the mechanisms of TDP-43-mediated neurodegeneration Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations Advances in neuroimaging in frontotemporal dementia.Mechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effects Entorhinal cortical neurons are the primary targets of FUS mislocalization and ubiquitin aggregation in FUS transgenic rats.Nuclear carrier and RNA-binding proteins in frontotemporal lobar degeneration associated with fused in sarcoma (FUS) pathological changes.The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum Chorea as a clinical feature of the basophilic inclusion body disease subtype of fused-in-sarcoma-associated frontotemporal lobar degeneration FTD and ALS: a tale of two diseases Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS-FTD-linked UBQLN2 mutations.TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration.Visual spatial cognition in neurodegenerative disease Frontotemporal dementia caused by CHMP2B mutations.Behavioural variant frontotemporal dementia--defining genetic and pathological subtypes.Novel types of frontotemporal lobar degeneration: beyond tau and TDP-43.Neuropathological background of phenotypical variability in frontotemporal dementia.Neuroimaging in frontotemporal lobar degeneration--predicting molecular pathology.Frontotemporal dementia: implications for understanding Alzheimer disease.Genetics of dementia: update and guidelines for the clinician.Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management.Progress in frontotemporal dementia research.Schizophrenia and frontotemporal dementia: shared causation?From frontotemporal lobar degeneration pathology to frontotemporal lobar degeneration biomarkers.Clinical Subtypes of Frontotemporal Dementia.

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P2860

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

http://www.wikidata.org/entity/Q33830991

description

2009 nî lūn-bûn

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2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Frequency of ubiquitin and FUS ...... ntotemporal lobar degeneration

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Frequency of ubiquitin and FUS ...... ntotemporal lobar degeneration

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type

label

Frequency of ubiquitin and FUS ...... ntotemporal lobar degeneration

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Frequency of ubiquitin and FUS ...... ntotemporal lobar degeneration

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prefLabel

Frequency of ubiquitin and FUS ...... ntotemporal lobar degeneration

@ast

Frequency of ubiquitin and FUS ...... ntotemporal lobar degeneration

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Journal of Neurology

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Frequency of ubiquitin and FUS ...... ntotemporal lobar degeneration

@en

P2093

Aad van der Lugt

http://www.w3.org/2001/XMLSchema#string

Annemieke J M Rozemuller

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Asma Azmani

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Harro Seelaar

http://www.w3.org/2001/XMLSchema#string

Inge de Koning

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Kirsten Y Klijnsma

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Wang Zheng Chiu

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P2860

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

A new subtype of frontotemporal lobar degeneration with FUS pathology

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

The neuropathology and clinical phenotype of FTD with progranulin mutations

The Clinical Dementia Rating (CDR): current version and scoring rules

Psychotic symptoms in frontotemporal dementia: prevalence and review.

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies.

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

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747-753

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10.1007/S00415-009-5404-Z

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5

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257

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John Van Swieten

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2009-11-28T00:00:00Z

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40039915

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1031245034

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19946779

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