Suppression of Trim32 Enhances Motor Function Repair after Traumatic Brain Injury Associated with Antiapoptosis.

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Suppression of Trim32 Enhances Motor Function Repair after Traumatic Brain Injury Associated with Antiapoptosis.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Suppression of Trim32 Enhances ...... Associated with Antiapoptosis.

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Suppression of Trim32 Enhances ...... Associated with Antiapoptosis.

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Suppression of Trim32 Enhances ...... Associated with Antiapoptosis.

@en

Suppression of Trim32 Enhances ...... Associated with Antiapoptosis.

@nl

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Suppression of Trim32 Enhances ...... Associated with Antiapoptosis.

@en

Suppression of Trim32 Enhances ...... Associated with Antiapoptosis.

@nl

P1476

Suppression of Trim32 Enhances ...... Associated with Antiapoptosis.

@en

P2093

Bin-Tuan Lu

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

Hui-Xiang Zhang

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Liu-Lin Xiong

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

Piao Zhang

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

Ting-Hua Wang

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

Zi-Bin Zhang

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P2860

Cloning and characterization of a novel RING finger protein that interacts with class V myosins

The interaction of Piasy with Trim32, an E3-ubiquitin ligase mutated in limb-girdle muscular dystrophy type 2H, promotes Piasy degradation and regulates UVB-induced keratinocyte apoptosis through NFkappaB

Tripartite motif protein 32 facilitates cell growth and migration via degradation of Abl-interactor 2

TRIM family proteins: retroviral restriction and antiviral defence

Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene

Regulation of the psoriatic chemokine CCL20 by E3 ligases Trim32 and Piasy in keratinocytes

The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype

Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin

Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers

The neural stem cell fate determinant TRIM32 regulates complex behavioral traits.

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scholarly article

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10.1177/0963689717716510

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P478

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2017-07-01T00:00:00Z

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28933219

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5657740

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