Structural and functional differences in the barrel cortex of Mecp2 null mice.

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Common Defects of Spine Dynamics and Circuit Function in Neurodevelopmental Disorders: A Systematic Review of Findings From in Vivo Optical Imaging of Mouse Models.

P2860

Q55474439-69219827-93A4-4290-A6EA-01D44BF14276

P2860

Structural and functional differences in the barrel cortex of Mecp2 null mice.

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http://www.wikidata.org/entity/Q47878842

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2017 nî lūn-bûn

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2017年の論文

@ja

2017年学术文章

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2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

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@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Structural and functional differences in the barrel cortex of Mecp2 null mice.

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Structural and functional differences in the barrel cortex of Mecp2 null mice.

@nl

type

Item

label

Structural and functional differences in the barrel cortex of Mecp2 null mice.

@en

Structural and functional differences in the barrel cortex of Mecp2 null mice.

@nl

prefLabel

Structural and functional differences in the barrel cortex of Mecp2 null mice.

@en

Structural and functional differences in the barrel cortex of Mecp2 null mice.

@nl

P1476

Structural and functional differences in the barrel cortex of Mecp2 null mice

@en

P2093

Li-Jen Lee

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

Reha S Erzurumlu

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

Vassiliy Tsytsarev

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

P2860

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome

The impact of MeCP2 loss- or gain-of-function on synaptic plasticity

Refinement of thalamocortical arbors and emergence of barrel domains in the primary somatosensory cortex: a study of normal and monoamine oxidase a knock-out mice

MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions

Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations

The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells

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3951-3961

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scholarly article

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10.1002/CNE.24315

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English

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

P478

525

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Li-Jen Lee

Vassiliy Tsytsarev

Reha S Erzurumlu

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2017-09-15T00:00:00Z

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28857161

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5994756

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Structural and functional differences in the barrel cortex of Mecp2 null mice.

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P2860

P2860

Structural and functional differences in the barrel cortex of Mecp2 null mice.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932