Filamentous tau in oligodendrocytes and astrocytes of transgenic mice expressing the human tau isoform with the P301L mutation. - Wikidata - awgldk - TriplyDB

Filamentous tau in oligodendrocytes and astrocytes of transgenic mice expressing the human tau isoform with the P301L mutation.

Filamentous tau in oligodendrocytes and astrocytes of transgenic mice expressing the human tau isoform with the P301L mutation.

http://www.wikidata.org/entity/Q35748867

about

Rapid neurofibrillary tangle formation after localized gene transfer of mutated tau CSF T-Tau/Aβ42 predicts white matter microstructure in healthy adults at risk for Alzheimer's disease Tau deposition drives neuropathological, inflammatory and behavioral abnormalities independently of neuronal loss in a novel mouse model Alzheimer disease with amygdala Lewy bodies: a distinct form of alpha-synucleinopathy.Optineurin immunoreactivity in neuronal and glial intranuclear inclusions in adult-onset neuronal intranuclear inclusion disease.Tau gene transfer, but not alpha-synuclein, induces both progressive dopamine neuron degeneration and rotational behavior in the rat.Role for glyoxalase I in Alzheimer's disease.The role of tau (MAPT) in frontotemporal dementia and related tauopathies.Glial cell inclusions and the pathogenesis of neurodegenerative diseases Cortical neuronal and glial pathology in TgTauP301L transgenic mice: neuronal degeneration, memory disturbance, and phenotypic variation.Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72 Sensitive quantitative assays for tau and phospho-tau in transgenic mouse models Obesity, diabetes, and leptin resistance promote tau pathology in a mouse model of disease.Pin1 has opposite effects on wild-type and P301L tau stability and tauopathy Animal models of tauopathies.A decade of tau transgenic animal models and beyond.Knock-out and transgenic mouse models of tauopathies.Tauopathy models and human neuropathology: similarities and differences.The cytoskeleton in oligodendrocytes. Microtubule dynamics in health and disease.Structural abnormalities in the cortex of the rTg4510 mouse model of tauopathy: a light and electron microscopy study.TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease.Coexisting cholinergic and parahippocampal degeneration: a key to memory loss in dementia and a challenge for transgenic models?Reduced early hypoxic/ischemic brain damage is associated with increased GLT-1 levels in mice expressing mutant (P301L) human tau.A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration Structure-activity relationship of cyanine tau aggregation inhibitors.Misfolded tau protein and disease modifying pathways in transgenic rodent models of human tauopathies.De novo prion aggregates trigger autophagy in skeletal muscle.Review: tauopathy in the retina and optic nerve: does it shadow pathological changes in the brain?Mutations in MAPT give rise to aneuploidy in animal models of tauopathy.Accumulation of filamentous tau in the cerebral cortex of human tau R406W transgenic mice Robust cytoplasmic accumulation of phosphorylated TDP-43 in transgenic models of tauopathy.Truncated Tau with the Fyn-binding domain and without the microtubule-binding domain hinders the myelinating capacity of an oligodendrocyte cell line.Ultrastructural localization of TDP-43 in filamentous neuronal inclusions in various neurodegenerative diseases.Diversity of pathological features other than Lewy bodies in familial Parkinson's disease due to SNCA mutations.Hereditary diffuse leukoencephalopathy with spheroids: ultrastructural and immunoelectron microscopic studies.Astrocytes in mouse models of tauopathies acquire early deficits and lose neurosupportive functions.Atypical progressive supranuclear palsy with corticospinal tract degeneration.Progressive white matter pathology in the spinal cord of transgenic mice expressing mutant (P301L) human tau.Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions

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P2860

Filamentous tau in oligodendrocytes and astrocytes of transgenic mice expressing the human tau isoform with the P301L mutation.

http://www.wikidata.org/entity/Q35748867

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2003 nî lūn-bûn

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Filamentous tau in oligodendro ...... oform with the P301L mutation.

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Filamentous tau in oligodendro ...... oform with the P301L mutation.

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Filamentous tau in oligodendro ...... oform with the P301L mutation.

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Filamentous tau in oligodendro ...... oform with the P301L mutation.

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Filamentous tau in oligodendro ...... oform with the P301L mutation.

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Filamentous tau in oligodendro ...... oform with the P301L mutation.

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The American Journal of Pathology

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Filamentous tau in oligodendro ...... oform with the P301L mutation.

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P2093

Dennis W Dickson

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Jada Lewis

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Michael Hutton

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Shu-Hui Yen

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Wen-Lang Lin

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P2860

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

Neurodegenerative tauopathies

The distribution of tau in the mammalian central nervous system

Tau filament formation in transgenic mice expressing P301L tau.

REVIEW: tau protein pathology in Alzheimer's disease and related disorders.

Functional implications for the microtubule-associated protein tau: localization in oligodendrocytes.

Neuropathologic overlap of progressive supranuclear palsy, Pick's disease and corticobasal degeneration.

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands

Hydrated autoclave pretreatment enhances tau immunoreactivity in formalin-fixed normal and Alzheimer's disease brain tissues.

Transgenic expression of the shortest human tau affects its compartmentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease

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