Reappraisal of TDP-43 pathology in FTLD-U subtypes. - Wikidata - awgldk - TriplyDB

Reappraisal of TDP-43 pathology in FTLD-U subtypes.

Reappraisal of TDP-43 pathology in FTLD-U subtypes.

http://www.wikidata.org/entity/Q48202306

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TDP-43 in the spectrum of MND-FTLD pathologies.Neuron loss and degeneration in the progression of TDP-43 in frontotemporal lobar degeneration.Intracellular Proteolysis of Progranulin Generates Stable, Lysosomal Granulins that Are Haploinsufficient in Patients with Frontotemporal Dementia Caused by GRN Mutations.Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis.Clinical and neuropathological features of ALS/FTD with TIA1 mutations.Possible concurrence of TDP-43, tau and other proteins in amyotrophic lateral sclerosis/frontotemporal lobar degeneration.Protein astrogliopathies in human neurodegenerative diseases and aging.Towards a TDP-43-Based Biomarker for ALS and FTLD.Disruption of ER-mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis.Dissecting the pathobiology of altered MRI signal in amyotrophic lateral sclerosis: A post mortem whole brain sampling strategy for the integration of ultra-high-field MRI and quantitative neuropathology.Patient-derived frontotemporal lobar degeneration brain extracts induce formation and spreading of TDP-43 pathology in vivo

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Reappraisal of TDP-43 pathology in FTLD-U subtypes.

http://www.wikidata.org/entity/Q48202306

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Reappraisal of TDP-43 pathology in FTLD-U subtypes.

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Reappraisal of TDP-43 pathology in FTLD-U subtypes.

@nl

type

label

Reappraisal of TDP-43 pathology in FTLD-U subtypes.

@en

Reappraisal of TDP-43 pathology in FTLD-U subtypes.

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prefLabel

Reappraisal of TDP-43 pathology in FTLD-U subtypes.

@en

Reappraisal of TDP-43 pathology in FTLD-U subtypes.

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Reappraisal of TDP-43 pathology in FTLD-U subtypes.

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Ian R Mackenzie

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P2860

Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

A harmonized classification system for FTLD-TDP pathology

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

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

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

Neuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysis

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scholarly article

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1

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Manuela Neumann

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