(Q33792966)

29 July 2017

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title

Neurodegenerative tauopathies: human disease and transgenic mouse models (English)

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29 July 2017

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Trojanowski JQ

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29 July 2017

Lee VM

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29 July 2017

language of work or name

English

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publication date

1 November 1999

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29 July 2017

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29 July 2017

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29 July 2017

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29 July 2017

page(s)

507-510

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

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Alzheimer-type neuropathology in transgenic mice overexpressing V717F β-amyloid precursor protein

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https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Tau mutations cause frontotemporal dementias

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https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments

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https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Human tau becomes phosphorylated and forms filamentous deposits when overexpressed in lamprey central neurons in situ.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Correlative Memory Deficits, Abeta Elevation, and Amyloid Plaques in Transgenic Mice

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Abeta deposition is associated with neuropil changes, but not with overt neuronal loss in the human amyloid precursor protein V717F (PDAPP) transgenic mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Age-Dependent Emergence and Progression of a Tauopathy in Transgenic Mice Overexpressing the Shortest Human Tau Isoform

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Mutant genes in familial Alzheimer's disease and transgenic models

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2981106-X

7 January 2021

10.1016/S0896-6273(00)81106-X

Identifiers

DOI

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29 July 2017

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