(Q46966676)

English

Isoform-specific increase of spastin stability by N-terminal missense variants including intragenic modifiers of SPG4 hereditary spastic paraplegia

scientific article published on 3 October 2007

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scholarly article

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

Isoform-specific increase of spastin stability by N-terminal missense variants including intragenic modifiers of SPG4 hereditary spastic paraplegia (English)

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

Wolfgang Dubiel

9

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

Christian Beetz

object named as

C Beetz

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T Deufel

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author name string

J Schickel

1

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

T Pamminger

2

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

A Ehrsam

3

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

S Münch

4

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

X Huang

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1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

T Klopstock

6

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

G Kurlemann

7

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

P Hemmerich

8

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

publication date

3 October 2007

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

European Journal of Neurology

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

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26 December 2017

http://europepmc.org/abstract/MED/17916079

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

1322-1328

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

The hereditary spastic paraplegias.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Recognition of C-terminal amino acids in tubulin by pore loops in Spastin is important for microtubule severing

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Unexpected pathogenic mechanism of a novel mutation in the coding sequence of SPG4 (spastin).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

PEST sequences and regulation by proteolysis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

AAA+ proteins and substrate recognition, it all depends on their partner in crime

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Identification of nuclear localisation sequences in spastin (SPG4) using a novel Tetra-GFP reporter system

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Eight Novel Mutations in SPG4 in a Large Sample of Patients With Hereditary Spastic Paraplegia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01971.X

21 January 2018

Identifiers

10.1111/J.1468-1331.2007.01971.X

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17916079

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