Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

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Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia?A cell autonomous torsinA requirement for cholinergic neuron survival and motor control

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P2860

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

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http://www.wikidata.org/entity/Q42351211

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

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2016年论文

@wuu

2016年论文

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2016年论文

@zh-cn

name

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

@en

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

@nl

type

Item

label

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

@en

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

@nl

prefLabel

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

@en

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

@nl

P1476

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia

@en

P2093

Abhik Ray-Chaudhury

http://www.w3.org/2001/XMLSchema#string

Drew Pratt

http://www.w3.org/2001/XMLSchema#string

Mark Hallett

http://www.w3.org/2001/XMLSchema#string

Nancy A Edwards

http://www.w3.org/2001/XMLSchema#string

Shervin Rahimpour

http://www.w3.org/2001/XMLSchema#string

Sule Tinaz

http://www.w3.org/2001/XMLSchema#string

P2860

TorsinA in PC12 cells: localization in the endoplasmic reticulum and response to stress

Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells

Striatal cholinergic dysfunction as a unifying theme in the pathophysiology of dystonia

TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration

Current Gaps in the Understanding of the Subcellular Distribution of Exogenous and Endogenous Protein TorsinA.

Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.

Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions.

Spread of symptoms in idiopathic torsion dystonia.

Inherited isolated dystonia: clinical genetics and gene function.

P2888

s40478-016-0362-z

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scholarly article

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10.1186/S40478-016-0362-Z

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P478

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Brian D Berman

Karin Mente

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2016-08-17T00:00:00Z

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1035949115

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Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

about

P2860

P2860

Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932