Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners (Q33229002)

24 July 2017

title

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

1 reference

hereditary spastic paraplegia

24 July 2017

main subject

1 reference

Thomas L Edwards

3

0 references

Evan Reid

object named as

Evan Reid

8

0 references

author name string

Christopher M Sanderson

1

1 reference

24 July 2017

James W Connell

2

1 reference

24 July 2017

Nicholas A Bright

4

1 reference

24 July 2017

Simon Duley

5

1 reference

24 July 2017

Amanda Thompson

6

1 reference

24 July 2017

J Paul Luzio

7

1 reference

24 July 2017

publication date

8 December 2005

1 reference

24 July 2017

published in

Human Molecular Genetics

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24 July 2017

volume

15

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24 July 2017

issue

2

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24 July 2017

page(s)

307-318

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

24 July 2017

cites work

1 reference

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The Drosophila homologue of the hereditary spastic paraplegia protein, spastin, severs and disassembles microtubules

14 July 2018

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

14 July 2018

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Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

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

14 July 2018

1 reference

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p97 and close encounters of every kind: a brief review

14 July 2018

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Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Multiple binding proteins suggest diverse functions for the N-ethylmaleimide sensitive factor

14 July 2018

1 reference

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Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation

14 July 2018

1 reference

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SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)

14 July 2018

1 reference

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Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation

14 July 2018

1 reference

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The hereditary spastic paraplegias: nine genes and counting

14 July 2018

1 reference

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Identification of mammalian Vps24p as an effector of phosphatidylinositol 3,5-bisphosphate-dependent endosome compartmentalization

14 July 2018

1 reference

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The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

SPG3A: An additional family carrying a new atlastin mutation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Basic local alignment search tool

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Neuroblastoma x spinal cord (NSC) hybrid cell lines resemble developing motor neurons

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Hereditary spastic paraplegia

14 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDI447

The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2443951

Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16339213

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Dense core lysosomes can fuse with late endosomes and are re-formed from the resultant hybrid organelles

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16339213

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDI447

1 reference

24 July 2017

1 reference

24 July 2017

1 reference