نتائج البحث - "Sara Passacantilli"

1

دورية أكاديمية

Immunogenicity and reactogenicity of modified vaccinia Ankara pre-exposure vaccination against mpox according to previous smallpox vaccine exposure and HIV infection: prospective cohort studyResearch in context

المؤلفون: Valentina Mazzotta, Alessandro Cozzi Lepri, Giulia Matusali, Eleonora Cimini, Pierluca Piselli, Camilla Aguglia, Simone Lanini, Francesca Colavita, Stefania Notari, Alessandra Oliva, Silvia Meschi, Rita Casetti, Vanessa Mondillo, Alessandra Vergori, Aurora Bettini, Germana Grassi, Carmela Pinnetti, Daniele Lapa, Eleonora Tartaglia, Paola Gallì, Annalisa Mondi, Giulia Montagnari, Roberta Gagliardini, Emanuele Nicastri, Miriam Lichtner, Loredana Sarmati, Enrica Tamburrini, Claudio Mastroianni, Christof Stingone, Andrea Siddu, Alessandra Barca, Carla Fontana, Chiara Agrati, Enrico Girardi, Francesco Vaia, Fabrizio Maggi, Andrea Antinori, Enza Anzalone, Marta Camici, Fabio Cannone, Priscilla Caputi, Claudia Cimaglia, Rita Corso, Flavia Cristofanelli, Stefania Cruciani, Nicola De Marco, Chiara De Ponte, Giulia Del Duca, Paolo Faccendini, Francesca Faraglia, Augusto Faticoni, Marisa Fusto, Saba Gebremeskel, Maria Letizia Giancola, Giuseppina Giannico, Simona Gili, Maria Rosaria Iannella, Angela Junea, Alessandra Lamonaca, Alessandra Marani, Erminia Masone, Ilaria Mastrorosa, Stefania Mazzotta, Alessandra Nappo, Giorgia Natalini, Alfredo Parisi, Sara Passacantilli, Jessica Paulicelli, Maria Maddalena Plazzi, Adriano Possi, Gianni Preziosi, Silvia Rosati, Marika Rubino, Pietro Scanzano, Laura Scorzolini, Virginia Tomassi, Maurizio Vescovo, Serena Vita, Luciano Caterini, Luigi Coppola, Dimitra Kontogiannis, Gabriella D'Ettorre, Marco Ridolfi, Simona Di Giambenedetto, Damiano Farinacci, Alessandra Latini, Mauro Marchili, Raffaella Marocco

المصدر: EClinicalMedicine, Vol 68, Iss , Pp 102420- (2024)

مصطلحات موضوعية: mpox, MVA-BN immunogenicity, Reactogenicity, Cellular response, Humoral response, HIV, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2589537023005977; https://doaj.org/toc/2589-5370

URL الوصول: https://doaj.org/article/ca4f7789ccd24dc59dd11b518dd6da6b

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A Negative Allosteric Modulator of WNT Receptor Frizzled 4 Switches into an Allosteric Agonist

المؤلفون: Giuseppe La Regina, Mariano Stornaiuolo, Antonella Accardo, Giovanni Battista Rossi, Sara Bottone, Nadia Badolati, Romano Silvestri, Ettore Novellino, Sara Passacantilli, Monica Dentice, Gennaro Riccio

المساهمون: Riccio, Gennaro, Bottone, Sara, Giuseppe La, Regina‡, Badolati, Nadia, Sara, Passacantilli‡, Giovanni Battista, Rossi§, Accardo, Antonella, Dentice, Monica, Silvestri, Romano, Novellino, Ettore, Stornaiuolo, Mariano

مصطلحات موضوعية: 0301 basic medicine, Models, Molecular, Frizzled, Allosteric modulator, Protein Conformation, Allosteric regulation, Primary Cell Culture, Biochemistry, Wnt-5a Protein, Small Molecule Libraries, 03 medical and health sciences, Phosphatidylinositol 3-Kinases, Structure-Activity Relationship, Allosteric Regulation, Heterotrimeric G protein, Cell Line, Tumor, Humans, Computer Simulation, Receptor, Wnt Signaling Pathway, Tissue homeostasis, Chemistry, Wnt signaling pathway, Small molecule, Heterotrimeric GTP-Binding Proteins, Endocytosis, Frizzled Receptors, Recombinant Proteins, Cell biology, wnt receptor frizzled 4, allosteric agonist, colon cancer cells, 030104 developmental biology, HEK293 Cells, Adenomatous Polyposis Coli, Culture Media, Conditioned, Neoplastic Stem Cells

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c99cf17602a918d56c6d278eabc913ad
http://hdl.handle.net/11588/703535

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Pharmacological folding chaperones act as allosteric ligands of Frizzled4

المؤلفون: Agostino Bruno, Salvatore Di Maro, Serena F Generoso, Mariano Stornaiuolo, Mariateresa Giustiniano, Massimo Mallardo, Ettore Novellino, Daniela Sarnataro, Luciana Marinelli, Giuseppe La Regina, Sara Passacantilli, Sara Bottone, Romano Silvestri, Stefano Bonatti, Monica Dentice, Hilde Cassese

المساهمون: Generoso, Serena F, Giustiniano, Mariateresa, La Regina, Giuseppe, Bottone, Sara, Passacantilli, Sara, DI MARO, Salvatore, Cassese, Hilde, Bruno, Agostino, Mallardo, Massimo, Dentice, Monica, Silvestri, Romano, Marinelli, Luciana, Sarnataro, Daniela, Bonatti, Stefano, Novellino, Ettore, Stornaiuolo, Mariano

المصدر: Nature Chemical Biology. 11:280-286

مصطلحات موضوعية: Glycerol, Molecular Chaperone, Protein Folding, Chemistry, Pharmaceutical, Amino Acid Motifs, Plasma protein binding, Protein aggregation, Ligands, HeLa Cell, cell-surface expression, Mutagenesi, Receptors, G-Protein-Coupled, HEK293 Cell, drosophila-melanogaster, Effector, Medicine (all), Frizzled Receptor, Cell biology, Co-chaperone, Amino Acid Motif, Protein folding, dishevelled dep domain, Allosteric Site, Human, Protein Binding, signaling pathway, Molecular Sequence Data, Allosteric regulation, Ligand, Biology, Cell Line, Tumor, Humans, Molecular Biology, G protein-coupled receptor, Base Sequence, Dose-Response Relationship, Drug, colorectal-cancer, endoplasmic-reticulum, structural basis, Cell Biology, Frizzled Receptors, HEK293 Cells, ephrogenic diabetes-insipidus, Microscopy, Fluorescence, Structural biology, Mutagenesis, Drug Design, mass-spectrometry data, receptor mutants, HeLa Cells, Molecular Chaperones

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76aaa5c743b54dcbb43c66b31fdebe1b
https://doi.org/10.1038/nchembio.1770

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4

3-Aroyl-1,4-diarylpyrroles inhibit chronic myeloid leukemia cell growth through an interaction with tubulin

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31abffa3386350904eea1af92e307fdb
http://hdl.handle.net/11573/954246

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5

New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including hedgehog-dependent cancer

المساهمون: Giuseppe La Regina, Ruoli, Bai, Antonio, Coluccia, Valeria, Famiglini, Pelliccia, Sveva, Sara, Passacantilli, Carmela, Mazzoccoli, Vitalba, Ruggieri, Lorenza, Sisinni, Alessio, Bolognesi, Whilelmina Maria Rensen, Andrea, Miele, Marianna, Nalli, Romina, Alfonsi, Lucia Di Marcotullio, Alberto, Gulino, Andrea, Brancale, Novellino, Ettore, Giulio, Dondio, Stefania, Vultaggio, Mario, Varasi, Ciro, Mercurio, Ernest, Hamel, Patrizia, Lavia, Romano, Silvestri

المصدر: Journal of medicinal chemistry 57 (2014): 6531–6552. doi:10.1021/jm500561a
info:cnr-pdr/source/autori:La Regina, Giuseppe; Bai, Ruoli; Coluccia, Antonio; Famiglini, Valeria; Pelliccia, Sveva; Passacantilli, Sara; Mazzoccoli, Carmela; Ruggieri, Vitalba; Sisinni, Lorenza; Bolognesi, Alessio; Rensen, Whilelmina Maria; Miele, Andrea; Nalli, Marianna; Alfonsi, Romina; Di Marcotullio, Lucia; Gulino, Alberto; Brancale, Andrea; Novellino, Ettore; Dondio, Giulio; Vultaggio, Stefania; Varasi, Mario; Mercurio, Ciro; Hamel, Ernest; Lavia, Patrizia; Silvestri, Romano/titolo:New Pyrrole Derivatives with Potent Tubulin Polymerization Inhibiting Activity As Anticancer Agents Including Hedgehog-Dependent Cancer/doi:10.1021%2Fjm500561a/rivista:Journal of medicinal chemistry/anno:2014/pagina_da:6531/pagina_a:6552/intervallo_pagine:6531–6552/volume:57

مصطلحات موضوعية: Cell Membrane Permeability, drug design, Cell Survival, Antineoplastic Agents, Guanidines, Article, RS, Polymerization, Mice, Structure-Activity Relationship, hedgehog pathway, Tubulin, Cell Line, Tumor, Neoplasms, Drug Discovery, Animals, Humans, Hedgehog Proteins, Pyrroles, Hedgehog, Cell Proliferation, Aniline Compounds, biology, Cell Death, Chemistry, Cell growth, Tubulin Modulators, tubulin-binding drugs, cancer growth inhibition, Hedgehog signaling pathway, Molecular Docking Simulation, Biochemistry, Cell culture, Cancer cell, biology.protein, Molecular Medicine, M Phase Cell Cycle Checkpoints, Signal transduction, Drug Screening Assays, Antitumor, Colchicine, Protein Binding, Signal Transduction

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0415ed9efa3f7456b5dcb3a529131644
https://pubmed.ncbi.nlm.nih.gov/25025991

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6

New inhibitors of indoleamine 2,3-dioxygenase 1: molecular modeling studies, synthesis, and biological evaluation

المؤلفون: Sara Passacantilli, Valeria Famiglini, Giuseppe La Regina, Rino Ragno, Romano Silvestri, Lorenza Sisinni, Osamu Takikawa, Manuela Sabatino, Antonio Coluccia, Carmela Mazzoccoli, Alexandros Patsilinakos, Alato Okuno

مصطلحات موضوعية: 0301 basic medicine, Models, Molecular, Molecular model, Stereochemistry, Antineoplastic Agents, tryptophan degradation, ido1 inhibitors, tubulin polymerization, substrate recognition, chemical-structures, dendritic cells, t-cells, cancer, expression, algorithm, 03 medical and health sciences, chemistry.chemical_compound, Structure-Activity Relationship, 0302 clinical medicine, Cell Line, Tumor, Drug Discovery, Humans, Indoleamine-Pyrrole 2,3,-Dioxygenase, Enzyme Inhibitors, Indoleamine 2,3-dioxygenase, IC50, Biological evaluation, Cell Proliferation, Virtual screening, Dose-Response Relationship, Drug, Molecular Structure, Biological activity, 030104 developmental biology, chemistry, Biochemistry, 030220 oncology & carcinogenesis, Molecular Medicine, Growth inhibition, Derivative (chemistry)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9616da1985d9ed4ac2ca11eb07bdcc5c
http://hdl.handle.net/11573/897502

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New indole tubulin assembly inhibitors cause stable arrest of mitotic progression, enhanced stimulation of natural killer cell cytotoxic activity, and repression of hedgehog-dependent cancer

المساهمون: La Regina, Giuseppe, Bai, Ruoli, Coluccia, Antonio, Famiglini, Valeria, Pelliccia, Sveva, Passacantilli, Sara, Mazzoccoli, Carmela, Ruggieri, Vitalba, Verrico, Annalisa, Miele, Andrea, Monti, Ludovica, Nalli, Marianna, Alfonsi, Romina, Di Marcotullio, Lucia, Gulino, Alberto, Ricci, Biancamaria, Soriani, Alessandra, Santoni, Angela, Caraglia, Michele, Porto, Stefania, Da Pozzo, Eleonora, Martini, Claudia, Brancale, Andrea, Marinelli, Luciana, Novellino, Ettore, Vultaggio, Stefania, Varasi, Mario, Mercurio, Ciro, Bigogno, Chiara, Dondio, Giulio, Hamel, Ernest, Lavia, Patrizia, Silvestri, Romano

المصدر: Journal of medicinal chemistry 58 (2015): 5789–5807. doi:10.1021/acs.jmedchem.5b00310
info:cnr-pdr/source/autori:La Regina, Giuseppe; Bai, Ruoli; Coluccia, Antonio; Farniglini, Valeria; Pelliccia, Sveva; Passacantilli, Sara; Mazzoccoli, Carmela; Ruggieri, Vitalba; Verrico, Annalisa; Miele, Andrea; Monti, Ludovica; Nalli, Marianna; Alfonsi, Romina; Di Marcotullio, Lucia; Gulino, Alberto; Ricci, Biancamaria; Soriani, Alessandra; Santoni, Angela; Caraglia, Michele; Porto, Stefania; Da Pozzo, Eleonora; Martini, Claudia; Brancale, Andrea; Marinelli, Luciana; Novellino, Ettore; Vultaggio, Stefania; Varasi, Mario; Mercurio, Ciro; Bigogno, Chiara; Dondio, Giulio; Hamel, Ernest; Lavia, Patrizia; Silvestri, Romano/titolo:New Indole Tubulin Assembly Inhibitors Cause Stable Arrest of Mitotic Progression, Enhanced Stimulation of Natural Killer Cell Cytotoxic Activity, and Repression of Hedgehog-Dependent Cancer/doi:10.1021%2Facs.jmedchem.5b00310/rivista:Journal of medicinal chemistry/anno:2015/pagina_da:5789/pagina_a:5807/intervallo_pagine:5789–5807/volume:58

مصطلحات موضوعية: Cytotoxicity, Immunologic, Indoles, Cell cycle checkpoint, HeLa, Mice, Tubulin, Neoplasms, Drug Discovery, Cytotoxic T cell, 2-phenylindole, tubulin, tubulin polymerization, NIH 3T3 Cell, Cancer, biology, Chemistry, Medicine (all), Cell cycle, Mitosi, Hedgehog signaling pathway, Cell biology, Killer Cells, Natural, tubulin polymerization, medicine.anatomical_structure, mitotic progression, Hedgehog signaling activation, tubulin polymerization, cancer cell growth, Molecular Medicine, Hedgehog Protein, Cell Division, Human, RM, Mitosis, cancer cell growth, Article, Natural killer cell, RC0254, Cell Line, Tumor, medicine, Animals, Humans, Hedgehog Proteins, Hedgehog signaling activation, Animal, Drug Discovery3003 Pharmaceutical Science, Tubulin inhbitors, mitotic progression, biology.organism_classification, Cell culture, Drug Resistance, Neoplasm, Indole, Cancer cell, NIH 3T3 Cells, Neoplasm, Hedgehog