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Pharmacological Targeting of Neuronal Kv7.2/3 Channels: A Focus on Chemotypes and Receptor Sites.
Curr Med Chem. 2018;25(23):2637-2660. doi: 10.2174/0929867324666171012122852.
Curr Med Chem. 2018.
PMID: 29022505
Review.
Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphate.
Soldovieri MV, Ambrosino P, Mosca I, De Maria M, Moretto E, Miceli F, Alaimo A, Iraci N, Manocchio L, Medoro A, Passafaro M, Taglialatela M.
Soldovieri MV, et al. Among authors: manocchio l.
Sci Rep. 2016 Dec 1;6:38167. doi: 10.1038/srep38167.
Sci Rep. 2016.
PMID: 27905566
Free PMC article.
Item in Clipboard
Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP2-Dependent K+ Channel Gating.
Ambrosino P, Freri E, Castellotti B, Soldovieri MV, Mosca I, Manocchio L, Gellera C, Canafoglia L, Franceschetti S, Salis B, Iraci N, Miceli F, Ragona F, Granata T, DiFrancesco JC, Taglialatela M.
Ambrosino P, et al. Among authors: manocchio l.
Mol Neurobiol. 2018 Aug;55(8):7009-7024. doi: 10.1007/s12035-018-0883-5. Epub 2018 Jan 30.
Mol Neurobiol. 2018.
PMID: 29383681
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Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin.
Ambrosino P, Alaimo A, Bartollino S, Manocchio L, De Maria M, Mosca I, Gomis-Perez C, Alberdi A, Scambia G, Lesca G, Villarroel A, Taglialatela M, Soldovieri MV.
Ambrosino P, et al. Among authors: manocchio l.
Biochim Biophys Acta. 2015 Sep;1852(9):1856-66. doi: 10.1016/j.bbadis.2015.06.012. Epub 2015 Jun 12.
Biochim Biophys Acta. 2015.
PMID: 26073431
Free article.
Item in Clipboard
Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels.
Miceli F, Soldovieri MV, Ambrosino P, De Maria M, Manocchio L, Medoro A, Taglialatela M.
Miceli F, et al. Among authors: manocchio l.
Front Cell Neurosci. 2015 Jul 15;9:259. doi: 10.3389/fncel.2015.00259. eCollection 2015.
Front Cell Neurosci. 2015.
PMID: 26236192
Free PMC article.
Review.
Item in Clipboard
Characterization of two de novoKCNT1 mutations in children with malignant migrating partial seizures in infancy.
Rizzo F, Ambrosino P, Guacci A, Chetta M, Marchese G, Rocco T, Soldovieri MV, Manocchio L, Mosca I, Casara G, Vecchi M, Taglialatela M, Coppola G, Weisz A.
Rizzo F, et al. Among authors: manocchio l.
Mol Cell Neurosci. 2016 Apr;72:54-63. doi: 10.1016/j.mcn.2016.01.004. Epub 2016 Jan 16.
Mol Cell Neurosci. 2016.
PMID: 26784557
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De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy.
Ambrosino P, Soldovieri MV, Bast T, Turnpenny PD, Uhrig S, Biskup S, Döcker M, Fleck T, Mosca I, Manocchio L, Iraci N, Taglialatela M, Lemke JR.
Ambrosino P, et al. Among authors: manocchio l.
Ann Neurol. 2018 Jun;83(6):1198-1204. doi: 10.1002/ana.25248.
Ann Neurol. 2018.
PMID: 29740868
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