(Q33750074)

29 July 2017

1 reference

title

Transgenic models of tauopathies and synucleinopathies (English)

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29 July 2017

1 reference

1 reference

1

Trojanowski JQ

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29 July 2017

Lee VM

2

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29 July 2017

1 October 1999

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29 July 2017

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29 July 2017

9

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29 July 2017

4

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29 July 2017

733-739

1 reference

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

The tauopathies: toward an experimental animal model

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

Increased vulnerability of NFH-LacZ transgenic mouse to traumatic brain injury-induced behavioral deficits and cortical damage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

Alpha-synuclein in Lewy bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1999.TB00554.X

10.1111/J.1750-3639.1999.TB00554.X

21 January 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference

PubMed ID

10517511