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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Detalles Bibliográficos
Autores principales: Turovsky, Egor, Karagiannis, Anastassios, Abdala, Ana Paula, Gourine, Alexander V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Respiratory
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532534/
https://www.ncbi.nlm.nih.gov/pubmed/25981852
http://dx.doi.org/10.1113/JP270369

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532534/
https://www.ncbi.nlm.nih.gov/pubmed/25981852
http://dx.doi.org/10.1113/JP270369

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