(Q40293550)

English

Cellular localization of 17 natural mutant variants of ALADIN protein in triple A syndrome - shedding light on an unexpected splice mutation

scientific article published on April 2006

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Statements

scholarly article

1 reference

Europe PubMed Central

19 September 2017

Cellular localization of 17 natural mutant variants of ALADIN protein in triple A syndrome - shedding light on an unexpected splice mutation (English)

1 reference

Europe PubMed Central

19 September 2017

author name string

Krumbholz M

1

1 reference

Europe PubMed Central

19 September 2017

Koehler K

2

1 reference

Europe PubMed Central

19 September 2017

Huebner A

3

1 reference

Europe PubMed Central

19 September 2017

publication date

1 April 2006

1 reference

Europe PubMed Central

19 September 2017

Biochemistry and Cell Biology

1 reference

Europe PubMed Central

19 September 2017

84

1 reference

Europe PubMed Central

19 September 2017

243-249

1 reference

Europe PubMed Central

19 September 2017

2

1 reference

Europe PubMed Central

19 September 2017

Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

Proteomic analysis of the mammalian nuclear pore complex

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

Structural analysis of the p62 complex, an assembly of O-linked glycoproteins that localizes near the central gated channel of the nuclear pore complex

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

Clinical and genetic characterization of families with triple A (Allgrove) syndrome.

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

Triple A syndrome--clinical aspects and molecular genetics

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

The ancient regulatory-protein family of WD-repeat proteins

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

The WD repeat: a common architecture for diverse functions

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

Mutant WD-repeat protein in triple-A syndrome

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

The WD-repeat protein superfamily in Arabidopsis: conservation and divergence in structure and function

1 reference

https://api.crossref.org/works/10.1139%2FO05-198

21 January 2018

Identifiers

10.1139/O05-198

1 reference

Europe PubMed Central

19 September 2017

1 reference

Europe PubMed Central

19 September 2017

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