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Structural nucleotide analogs are potent activators/inhibitors of pancreatic β cell KATP channels: an emerging mechanism supporting their use as antidiabetic drugs.
Tricarico D, Rolland JF, Cannone G, Mele A, Cippone V, Laghezza A, Carbonara G, Fracchiolla G, Tortorella P, Loiodice F, Conte Camerino D. Tricarico D, et al. Among authors: conte camerino d. J Pharmacol Exp Ther. 2012 Feb;340(2):266-76. doi: 10.1124/jpet.111.185835. Epub 2011 Oct 25. J Pharmacol Exp Ther. 2012. PMID: 22028392
Investigations of pharmacologic properties of the renal CLC-K1 chloride channel co-expressed with barttin by the use of 2-(p-Chlorophenoxy)propionic acid derivatives and other structurally unrelated chloride channels blockers.
Liantonio A, Pusch M, Picollo A, Guida P, De Luca A, Pierno S, Fracchiolla G, Loiodice F, Tortorella P, Conte Camerino D. Liantonio A, et al. Among authors: conte camerino d. J Am Soc Nephrol. 2004 Jan;15(1):13-20. doi: 10.1097/01.asn.0000103226.28798.ea. J Am Soc Nephrol. 2004. PMID: 14694153
Emerging role of calcium-activated potassium channel in the regulation of cell viability following potassium ions challenge in HEK293 cells and pharmacological modulation.
Tricarico D, Mele A, Calzolaro S, Cannone G, Camerino GM, Dinardo MM, Latorre R, Conte Camerino D. Tricarico D, et al. Among authors: camerino gm, conte camerino d. PLoS One. 2013 Jul 16;8(7):e69551. doi: 10.1371/journal.pone.0069551. Print 2013. PLoS One. 2013. PMID: 23874973 Free PMC article.
113 results