Rett syndrome from bench to bedside: recent advances.

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Rett syndrome from bench to bedside: recent advances.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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2018年學術文章

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Rett syndrome from bench to bedside: recent advances.

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Rett syndrome from bench to bedside: recent advances.

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Rett syndrome from bench to bedside: recent advances.

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Rett syndrome from bench to bedside: recent advances.

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Rett syndrome from bench to bedside: recent advances.

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Rett syndrome from bench to bedside: recent advances.

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P1476

Rett syndrome from bench to bedside: recent advances

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Valerie Matagne

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Yann Ehinger

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

Rett syndrome: revised diagnostic criteria and nomenclature

Structure-specific binding of MeCP2 to four-way junction DNA through its methyl CpG-binding domain

MECP2 disorders: from the clinic to mice and back

BDNF deregulation in Rett syndrome

Illness Severity, Social and Cognitive Ability, and EEG Analysis of Ten Patients with Rett Syndrome Treated with Mecasermin (Recombinant Human IGF-1).

GABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient mice

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor

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398

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scholarly article

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10.12688/F1000RESEARCH.14056.1

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P478

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Laurent Villard

J C Roux

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2018-03-26T00:00:00Z

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29636907

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5871944

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