IMBRICI, Paola

IMBRICI, Paola  

DIPARTIMENTO DI FARMACIA-SCIENZE DEL FARMACO  

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Titolo Data di pubblicazione Autore(i) File
All atom molecular dynamics simulation of the K+ Channel Chimera Kv1.2/2.1 1-gen-2010 Grottesi, A; Imbrici, Paola; Chillemi, G; Pessia, M.
Alteration of stim1/orai1-mediated soce in skeletal muscle: Impact in genetic muscle diseases and beyond 1-gen-2021 Conte, E.; Imbrici, P.; Mantuano, P.; Coppola, M. A.; Camerino, G. M.; De Luca, A.; Liantonio, A.
Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability 1-gen-2020 Imbrici, P.; Nematian-Ardestani, E.; Hasan, S.; Pessia, M.; Tucker, S. J.; D'Adamo, M. C.
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within CBS2 domain and C-terminal peptide of ClC-1 channel 1-gen-2018 Altamura, Concetta; Lucchiari, Sabrina; Sahbani, Dalila; Ulzi, Gianna; Comi, Giacomo P; D'Ambrosio, Paola; Petillo, Roberta; Politano, Luisa; Vercelli, Liliana; Mongini, Tiziana; Dotti, Maria Teresa; Cardani, Rosanna; Meola, Giovanni; Lo Monaco, Mauro; Matthews, Emma; Hanna, Michael G; Carratù, Maria Rosaria; Conte, Diana; Imbrici, Paola; Desaphy, Jean-François
Andersen-Tawil syndrome: New potassium channel mutations and possible phenotypic variation 1-gen-2005 Davies, N. P.; Imbrici, Paola; Fialho, D.; Herd, C.; Bilsland, L. G.; Weber, A.; Mueller, R.; Hilton Jones, D.; Ealing, J.; Boothman, B. R.; Giunti, P.; Parsons, L. M.; Thomas, M.; Manzur, A. Y.; Jurkat Rott, K.; Lehmann Horn, F.; Chinnery, P. F.; Rose, M.; Kullmann, D. M.; Hanna, M. G.
ATP Sensitive Potassium Channels in the Skeletal Muscle Function: Involvement of the KCNJ11(Kir6.2) Gene in the Determination of Mechanical Warner Bratzer Shear Force 1-gen-2016 Tricarico, Domenico; Selvaggi, Maria; Passantino, Giuseppe; De Palo, Pasquale; Dario, Cataldo; Centoducati, Pasquale; Tateo, Alessandra; Curci, Angela; Maqoud, Fatima; Mele, Antonietta; Camerino, Giulia M.; Liantonio, Antonella; Imbrici, Paola; Zizzo, Nicola
Autism with seizure and intellectual disability: possible causative role of gain-of-function of the Inwardly-Rectifying K+ Channel Kir4.1 1-gen-2011 Sicca, F; Imbrici, Paola; D'Adamo, Mc; Moro, F; Bonatti, F; Brovedani, P; Grottesi, A; Guerrini, R; Masi, G; Santorelli, Fm; Pessia, M.
Changes in Expression and Cellular Localization of Rat Skeletal Muscle ClC-1 Chloride Channel in Relation to Age, Myofiber Phenotype and PKC Modulation 1-gen-2020 Conte, E.; Fonzino, A.; Cibelli, A.; De Benedictis, V.; Imbrici, P.; Nicchia, G. P.; Pierno, S.; Camerino, G. M.
Chaperone activity of niflumic acid on ClC-1 chloride channel mutants causing myotonia congenita 1-gen-2022 Altamura, Concetta; Conte, Elena; Campanale, Carmen; Laghetti, Paola; Saltarella, Ilaria; Camerino, Giulia Maria; Imbrici, Paola; Desaphy, Jean-Francois
Characterization of Student Drinking Behaviors at the Beginning of the First Academic Year at One University in Southern Italy 1-gen-2019 De Salvia, Maria Antonietta; Dʼuggento, Angela Maria; Aquilino, Giovanni; Tattoli, Maria; Finelli, Carmine; Imbrici, Paola; Desaphy, Jean Francois; Giustino, Arcangela
ClC-1 chloride channels: state-of-the-art research and future challenges 1-gen-2015 Imbrici, Paola; Altamura, C; Pessia, M; Mantegazza, R; Desaphy, Jean Francois; Conte, Diana
ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype-phenotype correlation 1-gen-2015 Imbrici, P; Maggi, L; Mangiatordi, G F; Dinardo, M M; Altamura, Concetta; Brugnoni, R; Alberga, D; Pinter, G L; Ricci, G; Siciliano, G; Micheli, R; Annicchiarico, G; Lattanzi, G; Nicolotti, O; Morandi, L; Bernasconi, P; Desaphy, J-F; Mantegazza, R; Camerino, D C
Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita 1-gen-2015 Portaro, Simona; Altamura, Concetta; Licata, Norma; Camerino, GIULIA MARIA; Imbrici, Paola; Musumeci, Olimpia; Rodolico, Carmelo; Conte, Diana; Toscano, Antonio; Desaphy, Jean Francois
Coexistence of CLCN1 and SCN4A mutations in one family suffering from myotonia 1-gen-2017 Maggi, Lorenzo; Ravaglia, Sabrina; Farinato, Alessandro; Brugnoni, Raffaella; Altamura, Concetta; Imbrici, Paola; Conte, Diana; Padovani, Alessandro; Mantegazza, Renato; Bernasconi, Pia; Desaphy, Jean-François; Filosto, Massimiliano
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties 1-gen-2009 Imbrici, Paola; A., Grottesi; Mc, D'Adamo; Sj, Tucker; M., Pessia
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties 1-gen-2009 Imbrici, Paola; Grottesi, A; D'Adamo, Mc; Mannucci, R; Tucker, Sj; Pessia, M.
Copertina della rivista Neuroscience 157 (3). A novel mutation identified in an Italian family displaying episodic ataxia, neuromyotonia and epilepsy 1-gen-2008 Imbrici, Paola; Gualandi, F.; D’Adamo, M. C.; Taddei Masieri, M.; Cudia, P.; De Grandis, D.; Ferlini, A.; Pessia, M.
Copertina della rivista The Journal of Physiology 1-gen-2001 Pessia, M.; Imbrici, Paola; D'Adamo, M. C.; Salvatore, L.; Tucker, S. J.
Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1 1-gen-2001 M., Pessia; Imbrici, Paola; M. C., D'Adamo; L., Salvatore; S. J., Tucker
Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1 1-gen-2001 Pessia, M; Imbrici, Paola; D'Adamo, Mc; Salvatore, L; Tucker, Sj