Signature tau neuropathology in gray and white matter of corticobasal degeneration - Wikidata - wikimedia - TriplyDB

Signature tau neuropathology in gray and white matter of corticobasal degeneration

Signature tau neuropathology in gray and white matter of corticobasal degeneration

http://www.wikidata.org/entity/Q35747931

about

Neuropathologic, biochemical, and molecular characterization of the frontotemporal dementias.Characterization of tau fibrillization in vitro.Multiparametric MRI to distinguish early onset Alzheimer's disease and behavioural variant of frontotemporal dementia A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition.Myelin oligodendrocyte basic protein and prognosis in behavioral-variant frontotemporal dementia.Dementia induces correlated reductions in white matter integrity and cortical thickness: a multivariate neuroimaging study with sparse canonical correlation analysis.Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.Tau PET imaging: present and future directions.Shape analysis of the corpus callosum in Alzheimer's disease and frontotemporal lobar degeneration subtypes White matter disease contributes to apathy and disinhibition in behavioral variant frontotemporal dementia.Differential induction and spread of tau pathology in young PS19 tau transgenic mice following intracerebral injections of pathological tau from Alzheimer's disease or corticobasal degeneration brains Expression of the small heat-shock protein alphaB-crystallin in tauopathies with glial pathology.Tau depletion prevents progressive blood-brain barrier damage in a mouse model of tauopathy Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.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.Patterns of gray matter atrophy in atypical parkinsonism syndromes: a VBM meta-analysis Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy White matter imaging contributes to the multimodal diagnosis of frontotemporal lobar degeneration.The non-fluent/agrammatic variant of primary progressive aphasia.Too much to count on: impaired very small numbers in corticobasal degeneration Linking white matter integrity loss to associated cortical regions using structural connectivity information in Alzheimer's disease and fronto-temporal dementia: the Loss in Connectivity (LoCo) score.Progression of Microstructural Degeneration in Progressive Supranuclear Palsy and Corticobasal Syndrome: A Longitudinal Diffusion Tensor Imaging Study.Patterns of MRI atrophy in tau positive and ubiquitin positive frontotemporal lobar degeneration Criteria for the diagnosis of corticobasal degeneration Disruption of large-scale neural networks in non-fluent/agrammatic variant primary progressive aphasia associated with frontotemporal degeneration pathology.Imaging in-vivo tau pathology in Alzheimer's disease with THK5317 PET in a multimodal paradigm.White matter imaging helps dissociate tau from TDP-43 in frontotemporal lobar degeneration Comparative survey of the topographical distribution of signature molecular lesions in major neurodegenerative diseases.Genetic and neuroanatomic associations in sporadic frontotemporal lobar degeneration.Other dementias.Dystonia in corticobasal degeneration: a review of the literature on 404 pathologically proven cases.MRI signatures of the frontotemporal lobar degeneration continuum.Atypical association of semantic dementia, corticobasal syndrome, and 4R tauopathy.Diffusion tensor magnetic resonance imaging for single subject diagnosis in neurodegenerative diseases.Multimodal imaging evidence of pathology-mediated disease distribution in corticobasal syndrome.Cholinergic imaging in corticobasal syndrome, progressive supranuclear palsy and frontotemporal dementia.Cellular tau pathology and immunohistochemical study of tau isoforms in sporadic tauopathies.From progressive nonfluent aphasia to corticobasal syndrome: a case report of corticobasal degeneration.PET Imaging of Tau Pathology and Relationship to Amyloid, Longitudinal MRI, and Cognitive Change in Down Syndrome: Results from the Down Syndrome Biomarker Initiative (DSBI).Clinicopathologic analysis of progressive non-fluent aphasia and corticobasal degeneration: Case report and review.

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P2860

Signature tau neuropathology in gray and white matter of corticobasal degeneration

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2002 nî lūn-bûn

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Signature tau neuropathology in gray and white matter of corticobasal degeneration

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Signature tau neuropathology in gray and white matter of corticobasal degeneration

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Signature tau neuropathology in gray and white matter of corticobasal degeneration

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The American Journal of Pathology

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Signature tau neuropathology in gray and white matter of corticobasal degeneration

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P2093

Catherine Bergeron

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Chris Clark

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Mark S Forman

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Steven S-M Chin

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Victoria Zhukareva

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Virginia M-Y Lee

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P2860

A protein factor essential for microtubule assembly

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

Regulated phosphorylation and dephosphorylation of tau protein: effects on microtubule interaction, intracellular trafficking and neurodegeneration

Hyperphosphorylation induces self-assembly of tau into tangles of paired helical filaments/straight filaments

Identification of the major multiphosphorylation site in mammalian neurofilaments

Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration

Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease

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

Neurodegenerative tauopathies

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

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2045-2053

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12057909

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1850831

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