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English
Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation.
scholarly article
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scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
title
Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation
(English)
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
author
William T Dauer
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
Rose E Goodchild
series ordinal
1
object named as
Rose E Goodchild
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
language of work or name
English
0 references
publication date
7 January 2004
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
number of pages
6
1 reference
based on heuristic
inferred from page(s)
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
volume
101
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
page(s)
847-852
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
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12 July 2018
TorsinA in PC12 cells: localization in the endoplasmic reticulum and response to stress
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PubMed Central
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The inner nuclear membrane
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12 July 2018
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12 July 2018
Torsin A and its torsion dystonia-associated mutant forms are lumenal glycoproteins that exhibit distinct subcellular localizations
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Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells
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The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function
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The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
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12 July 2018
N-ethylmaleimide-sensitive fusion protein: a trimeric ATPase whose hydrolysis of ATP is required for membrane fusion
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26 September 2018
The Caenorhabditis elegans polarity gene ooc-5 encodes a Torsin-related protein of the AAA ATPase superfamily
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PubMed Central
reference URL
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Mutations in ooc-5 and ooc-3 disrupt oocyte formation and the reestablishment of asymmetric PAR protein localization in two-cell Caenorhabditis elegans embryos
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26 September 2018
Concurrent chaperone and protease activities of ClpAP and the requirement for the N-terminal ClpA ATP binding site for chaperone activity
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14711988
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based on heuristic
inferred from PubMed ID database lookup
ClpA and ClpP remain associated during multiple rounds of ATP-dependent protein degradation by ClpAP protease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14711988
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14711988
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.0304375101
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
ADS bibcode
2004PNAS..101..847G
0 references
PMCID
321769
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
PubMed ID
14711988
1 reference
stated in
Europe PubMed Central
PMCID
321769
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14711988%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
ResearchGate publication ID
8928599
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