Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome

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Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome

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2017 nî lūn-bûn

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2017年論文

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2017年論文

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2017年論文

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Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome

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Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome

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prefLabel

Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome

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P1476

Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome

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P2093

Hiroshi Kida

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Keiichiro Nakamura

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Ken-Ichiro Kosai

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Masaki Okamoto

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Munetsugu Hara

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Satoko Okayama

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Takashi Kinoshita

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Takayuki Taniwaki

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Tomoyuki Takahashi

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Toyojiro Matsuishi

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P2860

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

Rett syndrome: revised diagnostic criteria and nomenclature

Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome

Rett Syndrome: Crossing the Threshold to Clinical Translation

Role of the dorsal medulla in the neurogenesis of airway protection

Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

The story of Rett syndrome: from clinic to neurobiology

Alveolar surfactant homeostasis and the pathogenesis of pulmonary disease

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

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

P2888

s41598-017-12293-8

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12032

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scholarly article

P356

10.1038/S41598-017-12293-8

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P407

English

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P478

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P577

2017-09-20T00:00:00Z

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P698

28931890

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P932

5607245

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