MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

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Rescue of hyperexcitability in hippocampal CA1 neurons from Mecp2 (-/y) mouse through surface potential neutralization.

P2860

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MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

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http://www.wikidata.org/entity/Q42372796

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

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name

MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

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MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

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Item

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MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

@en

MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

@nl

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MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

@en

MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

@nl

P1476

MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

@en

P2093

Lan Xiao

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

Xing-Shu Chen

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

Xu-Rui Jin

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

P2860

Neuregulin and BDNF induce a switch to NMDA receptor-dependent myelination by oligodendrocytes

Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation

CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

Astrocytes control breathing through pH-dependent release of ATP

Developmental Dynamics of Rett Syndrome

Excitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum Disorders

Sodium-coupled neutral amino acid (System N/A) transporters of the SLC38 gene family

The story of Rett syndrome: from clinic to neurobiology

MeCP2 mutation causes distinguishable phases of acute and chronic defects in synaptogenesis and maintenance, respectively

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316

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scholarly article

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10.3389/FNMOL.2017.00316

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P478

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

P577

2017-10-04T00:00:00Z

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

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29046627

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

P921

glia

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5632713

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

MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

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P2860

MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

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P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P921

P932