טוען...
Remodelling of the respiratory network in a mouse model of Rett syndrome depends on brain-derived neurotrophic factor regulated slow calcium buffering
Rett syndrome caused by MeCP2 mutations is a devastating neurodevelopmental disorder accompanied by severe breathing irregularities. Using transduction of organotypic slices from model MeCP2–/y mice with neuron-specific calcium sensor protein D3cpv, we examined the slow calcium buffering in neurons...
שמור ב:
| Main Authors: | , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Blackwell Science Inc
2009
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2714014/ https://ncbi.nlm.nih.gov/pubmed/19359374 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2009.169805 |
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