Identifying the genetic components underlying the pathophysiology of movement disorders.

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Identifying the genetic components underlying the pathophysiology of movement disorders.

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2011 nî lūn-bûn

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2011年の論文

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2011年論文

@yue

2011年論文

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2011年論文

@zh-hk

2011年論文

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2011年論文

@zh-tw

2011年论文

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2011年论文

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2011年论文

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Identifying the genetic components underlying the pathophysiology of movement disorders.

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Item

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Identifying the genetic components underlying the pathophysiology of movement disorders.

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Identifying the genetic components underlying the pathophysiology of movement disorders.

@en

P1476

Identifying the genetic components underlying the pathophysiology of movement disorders.

@en

P2093

Maria J Marti

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Mario Ezquerra

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Yaroslau Compta

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P2860

The TOR1A (DYT1) gene family and its role in early onset torsion dystonia

The complete genome of an individual by massively parallel DNA sequencing

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

Dystonia-causing mutant torsinA inhibits cell adhesion and neurite extension through interference with cytoskeletal dynamics

The THAP domain of THAP1 is a large C2CH module with zinc-dependent sequence-specific DNA-binding activity

The THAP-zinc finger protein THAP1 regulates endothelial cell proliferation through modulation of pRB/E2F cell-cycle target genes

The dystonia-associated protein torsinA modulates synaptic vesicle recycling

The early onset dystonia protein torsinA interacts with kinesin light chain 1

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

TorsinA binds the KASH domain of nesprins and participates in linkage between nuclear envelope and cytoskeleton

P304

81-92

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P31

scholarly article

P356

10.2147/TACG.S7333

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P478

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

P577

2011-06-23T00:00:00Z

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P698

23776369

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P932

3681180

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