Postnatal Gene Therapy Improves Spatial Learning Despite the Presence of Neuronal Ectopia in a Model of Neuronal Migration Disorder.

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Postnatal Gene Therapy Improves Spatial Learning Despite the Presence of Neuronal Ectopia in a Model of Neuronal Migration Disorder.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

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2016年學術文章

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name

Postnatal Gene Therapy Improve ...... f Neuronal Migration Disorder.

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Postnatal Gene Therapy Improve ...... f Neuronal Migration Disorder.

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Item

label

Postnatal Gene Therapy Improve ...... f Neuronal Migration Disorder.

@en

Postnatal Gene Therapy Improve ...... f Neuronal Migration Disorder.

@nl

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Postnatal Gene Therapy Improve ...... f Neuronal Migration Disorder.

@en

Postnatal Gene Therapy Improve ...... f Neuronal Migration Disorder.

@nl

P1476

Postnatal Gene Therapy Improve ...... f Neuronal Migration Disorder.

@en

P2093

Huaiyu Hu

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

Kevin Bampoe

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

Miao Yu

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

Yonglin He

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

Yu Liu

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

P2860

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE

Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

Pikachurin interaction with dystroglycan is diminished by defective O-mannosyl glycosylation in congenital muscular dystrophy models and rescued by LARGE overexpression

Post-translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localization

P31

scholarly article

P356

10.3390/GENES7120105

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P433

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

P478

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

P577

2016-11-29T00:00:00Z

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P698

27916859

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P921

gene therapy

P932

5192481

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