Torthaí cuardaigh - CAMPIANI, GIUSEPPE

Allosteric Modulation of Ionotropic Glutamate Receptors: An Outlook on New Therapeutic Approaches To Treat Central Nervous System Disorders de réir Brogi, Simone, Campiani, Giuseppe, Brindisi, Margherita, Butini, Stefania

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Broad inhibition of plasmodium falciparum cytoadherence by (+)-epigallocatechin gallate de réir Patil, Pradeep R, Gemma, Sandra, Campiani, Giuseppe, Craig, Alister G

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Computer-Driven Development of an in Silico Tool for Finding Selective Histone Deacetylase 1 Inhibitors de réir Sirous, Hajar, Campiani, Giuseppe, Brogi, Simone, Calderone, Vincenzo, Chemi, Giulia

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Computational Tool for Fast in silico Evaluation of hERG K(+) Channel Affinity de réir Chemi, Giulia, Gemma, Sandra, Campiani, Giuseppe, Brogi, Simone, Butini, Stefania, Brindisi, Margherita

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Endocannabinoid Modulation of Predator Stress-Induced Long-Term Anxiety in Rats de réir Lim, James, Igarashi, Miki, Jung, Kwang-Mook, Butini, Stefania, Campiani, Giuseppe, Piomelli, Daniele

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The FAAH inhibitor URB597 suppresses hippocampal maximal dentate afterdischarges and restores seizure-induced impairment of short and long-term synaptic plasticity de réir Colangeli, Roberto, Pierucci, Massimo, Benigno, Arcangelo, Campiani, Giuseppe, Butini, Stefania, Di Giovanni, Giuseppe

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Author Correction: The FAAH inhibitor URB597 suppresses hippocampal maximal dentate afterdischarges and restores seizure-induced impairment of short and long-term synaptic plastici... de réir Colangeli, Roberto, Pierucci, Massimo, Benigno, Arcangelo, Campiani, Giuseppe, Butini, Stefania, Di Giovanni, Giuseppe

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Author Correction: The FAAH inhibitor URB597 suppresses hippocampal maximal dentate afterdischarges and restores seizure-induced impairment of short and long-term synaptic plastici... de réir Colangeli, Roberto, Pierucci, Massimo, Benigno, Arcangelo, Campiani, Giuseppe, Butini, Stefania, Di Giovanni, Giuseppe

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Dopamine D3 Receptor Antagonists as Potential Therapeutics for the Treatment of Neurological Diseases de réir Maramai, Samuele, Gemma, Sandra, Brogi, Simone, Campiani, Giuseppe, Butini, Stefania, Stark, Holger, Brindisi, Margherita

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A Repurposing Approach for Uncovering the Anti-Tubercular Activity of FDA-Approved Drugs with Potential Multi-Targeting Profiles de réir Battah, Basem, Chemi, Giulia, Butini, Stefania, Campiani, Giuseppe, Brogi, Simone, Delogu, Giovanni, Gemma, Sandra

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Covalent Reversible Inhibitors of Cysteine Proteases Containing the Nitrile Warhead: Recent Advancement in the Field of Viral and Parasitic Diseases de réir Brogi, Simone, Ibba, Roberta, Rossi, Sara, Butini, Stefania, Calderone, Vincenzo, Gemma, Sandra, Campiani, Giuseppe

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The Structural Evolution of β-Secretase Inhibitors: A Focus on the Development of Small-Molecule Inhibitors de réir Butini, Stefania, Brogi, Simone, Novellino, Ettore, Campiani, Giuseppe, Ghosh, Arun K., Brindisi, Margherita, Gemma, Sandra

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Polypharmacological Approaches for CNS Diseases: Focus on Endocannabinoid Degradation Inhibition de réir Papa, Alessandro, Pasquini, Silvia, Contri, Chiara, Gemma, Sandra, Campiani, Giuseppe, Butini, Stefania, Varani, Katia, Vincenzi, Fabrizio

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In silico study of subtilisin-like protease 1 (SUB1) from different Plasmodium species in complex with peptidyl-difluorostatones and characterization of potent pan-SUB1 inhibitors de réir Brogi, Simone, Giovani, Simone, Brindisi, Margherita, Gemma, Sandra, Novellino, Ettore, Campiani, Giuseppe, Blackman, Michael J., Butini, Stefania

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Effects of Drug Resistance Mutations L100I and V106A on the Binding of Pyrrolobenzoxazepinone Nonnucleoside Inhibitors to the Human Immunodeficiency Virus Type 1 Reverse Transcript... de réir Locatelli, Giada A., Campiani, Giuseppe, Cancio, Reynel, Morelli, Elena, Ramunno, Anna, Gemma, Sandra, Hübscher, Ulrich, Spadari, Silvio, Maga, Giovanni

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A non-toxic, reversibly released imaging probe for oral cancer that is derived from natural compounds de réir Ghanim, Magda, Relitti, Nicola, McManus, Gavin, Butini, Stefania, Cappelli, Andrea, Campiani, Giuseppe, Mok, K. H., Kelly, Vincent P.

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The Ca(2+)-ATPase (SERCA1) Is Inhibited by 4-Aminoquinoline Derivatives through Interference with Catalytic Activation by Ca(2+), Whereas the ATPase E(2) State Remains Functional de réir Bartolommei, Gianluca, Tadini-Buoninsegni, Francesco, Moncelli, Maria Rosa, Gemma, Sandra, Camodeca, Caterina, Butini, Stefania, Campiani, Giuseppe, Lewis, David, Inesi, Giuseppe

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The pyrrolo-1,5-benzoxazepine, PBOX-15, enhances TRAIL-induced apoptosis by upregulation of DR5 and downregulation of core cell survival proteins in acute lymphoblastic leukaemia c... de réir NATHWANI, SEEMA-MARIA, GREENE, LISA M., BUTINI, STEFANIA, CAMPIANI, GIUSEPPE, WILLIAMS, D. CLIVE, SAMALI, AFSHIN, SZEGEZDI, EVA, ZISTERER, DANIELA M.

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Pyrrolo-1,5-Benzoxazepines Induce Apoptosis in Chronic Myeloid Leukemia (CML) Cells by Bypassing the Apoptotic Suppressor BCR-ABL de réir Mc Gee, Margaret M., Campiani, Giuseppe, Ramunno, Anna, Fattorusso, Caterina, Nacci, Vito, Lawler, Mark, Williams, D. Clive, Zisterer, Daniela M.

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Selective Histone Deacetylase 6 Inhibitors Restore Cone Photoreceptor Vision or Outer Segment Morphology in Zebrafish and Mouse Models of Retinal Blindness de réir Sundaramurthi, Husvinee, Roche, Sarah L., Grice, Guinevere L., Moran, Ailis, Dillion, Eugene T., Campiani, Giuseppe, Nathan, James A., Kennedy, Breandán N.

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