M Channel KCNQ2 Subunits Are Localized to Key Sites for Control of Neuronal Network Oscillations and Synchronization in Mouse Brain

Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy. In heterologous cells, KCNQ2 expression yields voltage-gated potassium channels that activate slowly (τ, ∼0.1 sec) at subthreshold membrane potentials....

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Bibliografiset tiedot
Julkaisussa:J Neurosci
Päätekijät: Cooper, Edward C., Harrington, Emily, Jan, Yuh Nung, Jan, Lily Y.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Society for Neuroscience 2001
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Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6763050/
https://ncbi.nlm.nih.gov/pubmed/11739564
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.21-24-09529.2001
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