Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance (Q24295258)

2

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Karen Pavur

3

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Kristen Glasgow

4

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Bryan Conn

5

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Brett Lauring

Proceedings of the National Academy of Sciences of the United States of America

6

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language of work or name

English

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publication date

11 July 2006

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published in

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volume

103

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issue

28

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page(s)

10666-71

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cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

19 March 2017

1 reference

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

19 March 2017

1 reference

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Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

19 March 2017

1 reference

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Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

Alsin is a Rab5 and Rac1 guanine nucleotide exchange factor

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

SPG3A: An additional family carrying a new atlastin mutation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

A lentivirus-based system to functionally silence genes in primary mammalian cells, stem cells and transgenic mice by RNA interference

19 March 2017

1 reference

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1502289

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

27 September 2017

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0510863103

Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0510863103

Early-onset ALS with long-term survival associated with spastin gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0510863103

The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0510863103

Hereditary spastic paraplegia: the pace quickens

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16815977

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0510863103

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ADS bibcode

2006PNAS..10310666E

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Fatcat ID

release_rkl6akcfwnac5kjhqq7rzn4yym

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rkl6akcfwnac5kjhqq7rzn4yym