Rezultati - CAMPIANI, GIUSEPPE

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

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Broad inhibition of plasmodium falciparum cytoadherence by (+)-epigallocatechin gallate od 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 od 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 od 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 od 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 od 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... od 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... od 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 od 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 od 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 od 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 od 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 od 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 od 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... od 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 od 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 od 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... od 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 od 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 od 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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