Φορτώνει......
Familial hemiplegic migraine Ca(V)2.1 channel mutation R192Q enhances ATP-gated P2X(3 )receptor activity of mouse sensory ganglion neurons mediating trigeminal pain
BACKGROUND: The R192Q mutation of the CACNA1A gene, encoding for the α1 subunit of voltage-gated P/Q Ca(2+ )channels (Ca(v)2.1), is associated with familial hemiplegic migraine-1. We investigated whether this gain-of-function mutation changed the structure and function of trigeminal neuron P2X(3 )re...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2010
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2940876/ https://ncbi.nlm.nih.gov/pubmed/20735819 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-8069-6-48 |
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