Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration - Wikidata - awgldk - TriplyDB

Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration

Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration

http://www.wikidata.org/entity/Q24676458

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Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments Characteristics of Tau and Its Ligands in PET Imaging Tau Protein Hyperphosphorylation and Aggregation in Alzheimer's Disease and Other Tauopathies, and Possible Neuroprotective Strategies Clinicopathologic assessment and imaging of tauopathies in neurodegenerative dementias The fluorescent Congo red derivative, (trans, trans)-1-bromo-2,5-bis-(3-hydroxycarbonyl-4-hydroxy)styrylbenzene (BSB), labels diverse beta-pleated sheet structures in postmortem human neurodegenerative disease brains Tau-mediated synaptic damage in Alzheimer's disease Zebrafish models of Tauopathy Detailed immunohistochemical characterization of temporal and spatial progression of Alzheimer's disease-related pathologies in male triple-transgenic mice Filamentous nerve cell inclusions in neurodegenerative diseases: tauopathies and alpha-synucleinopathies.Characterization of tau fibrillization in vitro.Human Tau isoforms assemble into ribbon-like fibrils that display polymorphic structure and stability.Neurofibrillary degeneration in amyotrophic lateral sclerosis/parkinsonism-dementia complex of Guam. Immunochemical characterization of tau proteins.Ultrastructural differences in pretangles between Alzheimer disease and corticobasal degeneration revealed by comparative light and electron microscopy.The feasibility of white matter volume reduction analysis using SPM8 plus DARTEL for the diagnosis of patients with clinically diagnosed corticobasal syndrome and Richardson's syndrome.Signature tau neuropathology in gray and white matter of corticobasal degeneration Ultrastructural instability of paired helical filaments from corticobasal degeneration as examined by scanning transmission electron microscopy.Biochemical analysis of tau proteins in argyrophilic grain disease, Alzheimer's disease, and Pick's disease : a comparative study Selective tau tyrosine nitration in non-AD tauopathies.Tau isoform composition influences rate and extent of filament formation Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.Brain homogenates from human tauopathies induce tau inclusions in mouse brain Soluble phospho-tau from Alzheimer's disease hippocampus drives microglial degeneration.Tau prions from Alzheimer's disease and chronic traumatic encephalopathy patients propagate in cultured cells.Potential mechanisms and implications for the formation of tau oligomeric strains.Distinct binding of PET ligands PBB3 and AV-1451 to tau fibril strains in neurodegenerative tauopathies.Haplotype-specific expression of the N-terminal exons 2 and 3 at the human MAPT locus.Tau protein assembles into isoform- and disulfide-dependent polymorphic fibrils with distinct structural properties.Are tau aggregates toxic or protective in tauopathies?Ferritin is associated with the aberrant tau filaments present in progressive supranuclear palsy.Glial fibrillary tangles and JAK/STAT-mediated glial and neuronal cell death in a Drosophila model of glial tauopathy.The tauopathies: toward an experimental animal model.Conformation determines the seeding potencies of native and recombinant Tau aggregates.Protein astrogliopathies in human neurodegenerative diseases and aging.

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Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration

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1994 nî lūn-bûn

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1994 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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1994 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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1994年の論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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Ultrastructure and biochemical ...... s in corticobasal degeneration

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The American Journal of Pathology

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Ultrastructure and biochemical ...... s in corticobasal degeneration

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D W Dickson

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H Ksiezak-Reding

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K Morgan

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P2860

Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

Identification of the major multiphosphorylation site in mammalian neurofilaments

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

Distribution and degradation of biotin-containing carboxylases in human cell lines

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology

The distribution of tau in the mammalian central nervous system

Structural characterization of the core of the paired helical filament of Alzheimer disease.

A preparation of Alzheimer paired helical filaments that displays distinct tau proteins by polyacrylamide gel electrophoresis.

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