TOR1A protein, human

Known as: torsin, dystonia 1, torsion (autosomal dominant; torsin A) protein, human, torsin family 1, member A (torsin A) protein, human 
 

Topic mentions per year

Topic mentions per year

2001-2016
0246820012016

Papers overview

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2014
2014
Lamina-associated polypeptide 1 (LAP1) resides at the nuclear envelope and interacts with Torsins, poorly understood endoplasmic… (More)
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2014
2014
Torsins are membrane-associated ATPases whose activity is dependent on two activating cofactors, lamina-associated polypeptide 1… (More)
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2008
2008
A subgroup of the AAA+ proteins that reside in the endoplasmic reticulum and the nuclear envelope including human torsinA, a… (More)
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2006
2006
Early-onset torsion dystonia is a dominant motor disorder linked to mutations in torsinA. TorsinA is weakly related to a… (More)
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Highly Cited
2005
Highly Cited
2005
Parkinson's disease (PD) is linked genetically to proteins that function in the management of cellular stress resulting from… (More)
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2004
2004
TorsinA is a novel protein identified in the search for mutations underlying the human neurologic movement disorder, early onset… (More)
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2003
2003
Most cases of early-onset torsion dystonia are caused by deletion of GAG in the coding region of the DYT1 gene encoding torsinA… (More)
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2003
2003
Torsion dystonia is an autosomal dominant movement disorder characterized by involuntary, repetitive muscle contractions and… (More)
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Highly Cited
2003
Highly Cited
2003
Familial, early onset, generalized torsion dystonia is the most common and severe primary dystonia. Most cases are caused by a 3… (More)
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2001
2001
BACKGROUND Early-onset torsion dystonia is a hyperkinetic movement disorder caused by a deletion of 1 glutamic acid residue in… (More)
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