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Impaired CO(2) sensitivity of astrocytes in a mouse model of Rett syndrome

Rett syndrome, a prototypical neurological disorder caused by loss of function of the transcriptional regulator methyl-CpG-binding protein 2 (MeCP2) gene, is associated with a severely disordered breathing pattern and reduced ventilatory CO(2) sensitivity. In a mouse model of Rett syndrome (MeCP2 kn...

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Detalhes bibliográficos
Publicado no:J Physiol
Main Authors: Turovsky, Egor, Karagiannis, Anastassios, Abdala, Ana Paula, Gourine, Alexander V
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Ltd 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4532534/
https://ncbi.nlm.nih.gov/pubmed/25981852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/JP270369
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