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Pathophysiological Consequences of KATP Channel Overactivity and Pharmacological Response to Glibenclamide in Skeletal Muscle of a Murine Model of Cantù Syndrome
Cantù syndrome (CS) arises from mutations in ABCC9 and KCNJ8 genes that lead to gain of function (GOF) of ATP-sensitive potassium (KATP) channels containing SUR2A and Kir6.1 subunits, respectively, of KATP channels. Pathological consequences of CS have been reported for cardiac and smooth muscle cel...
Autores principales: | Scala, Rosa, Maqoud, Fatima, Zizzo, Nicola, Mele, Antonietta, Camerino, Giulia Maria, Zito, Francesco Alfredo, Ranieri, Girolamo, McClenaghan, Conor, Harter, Theresa M., Nichols, Colin G., Tricarico, Domenico |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734337/ https://www.ncbi.nlm.nih.gov/pubmed/33329006 http://dx.doi.org/10.3389/fphar.2020.604885 |
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