(Q27919715)

18037885

26 November 2016

title

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11. (English)

1 reference

PubMed

26 November 2016

0 references

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spinocerebellar ataxia

1 reference

Erratum: Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11

inferred from title

corrigendum / erratum

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author

Janice Holton

9

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Henry Houlden

1

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Paola Giunti

12

0 references

Nicholas W. Wood

Nicholas W Wood

14

0 references

Andrew Singleton

7

Andrew B Singleton

0 references

Tammaryn Lashley

4

Tammaryn Lashley

0 references

Dena G. Hernandez

5

Christopher Gardner-Thorpe

Dena Hernandez

0 references

3

Christopher Gardner-Thorpe

0 references

Paolo Giunti

13

Paolo Giunti

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author name string

Tamas Revesz

10

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Paul Worth

6

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Mary B Davis

11

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Janel Johnson

2

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David A Hilton

Trinucleotide Repeat Disorders

8

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language of work or name

English

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publication date

December 2007

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1 reference

39

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issue

12

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page(s)

1434-6

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG.2007.43

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG.2007.43

A novel tau-tubulin kinase from bovine brain

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG.2007.43

Tau-mediated neurodegeneration in Alzheimer's disease and related disorders

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

Dominantly inherited, non-coding microsatellite expansion disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

Tau-tubulin kinase 1 (TTBK1), a neuron-specific tau kinase candidate, is involved in tau phosphorylation and aggregation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

Expression, purification and crystallization of a human tau-tubulin kinase 2 that phosphorylates tau protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

Inhibition of glycogen synthase kinase-3 by lithium correlates with reduced tauopathy and degeneration in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

The prevalence of Alzheimer neuropathologic lesions is similar in blacks and whites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

7 January 2021

inferred from DOI database lookup

A morphological analysis of senile plaques in the brains of non-demented persons of different ages using silver, immunocytochemical and lectin histochemical staining techniques.

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

7 January 2021

inferred from DOI database lookup

Molecular pathways that influence human tau-induced pathology in Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.43

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.2007.43

0 references

Dimensions Publication ID

1027518951

0 references

Fatcat ID

release_qvyosr7vu5flxdnpnosifcyque

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/qvyosr7vu5flxdnpnosifcyque

24 November 2022

mapped directly with Wikidata item

18037885

1 reference

PubMed

18037885