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Astrocytes in Atp1a2‐deficient heterozygous mice exhibit hyperactivity after induction of cortical spreading depression
The ATP1A2 coding α2 subunit of Na,K‐ATPase, which is predominantly located in astrocytes, is a causative gene of familial hemiplegic migraine type 2 (FHM2). FHM2 model mice (Atp1a2(tmCKwk/+)) are susceptible to cortical spreading depression (CSD), which is profoundly related to migraine aura and he...
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| Publicado en: | FEBS Open Bio |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7262908/ https://ncbi.nlm.nih.gov/pubmed/32237043 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/2211-5463.12848 |
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