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tauopathy


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'tauopathy' can also refer to...

tauopathy

Is Huntington's disease a tauopathy?

Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy‐like tauopathy

The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family

Acetylated tau, a novel pathological signature in Alzheimer's disease and other tauopathies

Stimulation of autophagy reduces neurodegeneration in a mouse model of human tauopathy

Genetic suppression of β2-adrenergic receptors ameliorates tau pathology in a mouse model of tauopathies

Functional genomic screen and network analysis reveal novel modifiers of tauopathy dissociated from tau phosphorylation

Inhibition of tau aggregation in a novel Caenorhabditis elegans model of tauopathy mitigates proteotoxicity

Kinesin-1 transport reductions enhance human tau hyperphosphorylation, aggregation and neurodegeneration in animal models of tauopathies

Absence of ALOX5 gene prevents stress-induced memory deficits, synaptic dysfunction and tauopathy in a mouse model of Alzheimer's disease

Liquid Chromatography–Tandem Mass Spectrometry Method for Determination of Homocysteine in Rat Plasma: Application to the Study of a Rat Model for Tauopathies

Fractalkine activates NRF2/NFE2L2 and heme oxygenase 1 to restrain tauopathy-induced microgliosis

NMNAT suppresses Tau-induced neurodegeneration by promoting clearance of hyperphosphorylated Tau oligomers in a Drosophila model of tauopathy

MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies

Tauopathy induced by low level expression of a human brain-derived tau fragment in mice is rescued by phenylbutyrate

Generation of a transgenic zebrafish model of Tauopathy using a novel promoter element derived from the zebrafish eno2 gene

Ca2+/calmodulin-dependent protein kinase II promotes neurodegeneration caused by tau phosphorylated at Ser262/356 in a transgenic Drosophila model of tauopathy

CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy

 

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Any neuropathy in which there are brain lesions with an excess of tau protein. In Alzheimer's disease the neuronal cytoskeleton is progressively disrupted and replaced by neurofibrillary tangles of paired helical filaments (PHFs) composed mainly of hyperphosphorylated forms of tau. Mutations in tau are associated with familial frontotemporal dementia with parkinsonism, and with Pick's disease.

Subjects: Medicine and Health.


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