Search Results - Barbara Mandriani

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  1. 1
    Cutting Edge: The NLRP3 Inflammasome Links Complement-Mediated Inflammation and IL-1β Release

    Cutting Edge: The NLRP3 Inflammasome Links Complement-Mediated Inflammation and IL-1β Release by Federica Laudisi, Roberto Spreafico, Maximilien Evrard, Timothy R. Hughes, Barbara Mandriani, Matheswaran Kandasamy, B. Paul Morgan, Baalasubramanian Sivasankar, Alessandra Mortellaro

    Published 2013
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  2. 2
    gene2drug: a computational tool for pathway-based rational drug repositioning

    gene2drug: a computational tool for pathway-based rational drug repositioning by Francesco Napolitano, Diego Carrella, Barbara Mandriani, Sandra Pisonero‐Vaquero, Francesco Sirci, Diego L. Medina, Nicola Brunetti‐Pierri, Diego di Bernardo

    Published 2017
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  3. 3
    Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits

    Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits by Carmela Fusco, Lucia Micale, Bartolomeo Augello, Maria Teresa Pellico, Deny Menghini, Paolo Alfieri, M. Cristina Digilio, Barbara Mandriani, Massimo Carella, Orazio Palumbo, Stefano Vicari, Giuseppe Merla

    Published 2013
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  4. 4
    DAXX mutations as potential genomic markers of malignant evolution in small nonfunctioning pancreatic neuroendocrine tumors

    DAXX mutations as potential genomic markers of malignant evolution in small nonfunctioning pancreatic neuroendocrine tumors by Mauro Cives, Stefano Partelli, Raffaele Palmirotta, Domenica Lovero, Barbara Mandriani, Davide Quaresmini, Eleonora Pellè, Valentina Andreasi, M. Paola Castelli, Jonathan Strosberg, Giuseppe Zamboni, Massimo Falconi, Franco Silvestris

    Published 2019
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  5. 5
    Dissecting KMT2D missense mutations in Kabuki syndrome patients

    Dissecting KMT2D missense mutations in Kabuki syndrome patients by Dario Cocciadiferro, Bartolomeo Augello, Pasquelena De Nittis, Jiyuan Zhang, Barbara Mandriani, Natascia Malerba, Gabriella Maria Squeo, Alessandro Romano, Barbara Piccinni, Tiziano Verri, Lucia Micale, Laura Pasqualucci, Giuseppe Merla

    Published 2018
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  6. 6
    Development of anti-somatostatin receptors CAR T cells for treatment of neuroendocrine tumors

    Development of anti-somatostatin receptors CAR T cells for treatment of neuroendocrine tumors by Barbara Mandriani, Eleonora Pellè, Francesco Mannavola, Antonio J. Palazzo, René Massimiliano Marsano, Giuseppe Ingravallo, Gerardo Cazzato, María C. Ramello, Camillo Porta, Jonathan Strosberg, Daniel Abate‐Daga, Mauro Cives

    Published 2022
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  7. 7
    TRIM50 regulates Beclin 1 proautophagic activity

    TRIM50 regulates Beclin 1 proautophagic activity by Carmela Fusco, Barbara Mandriani, Martina Di Rienzo, Lucia Micale, Natascia Malerba, Dario Cocciadiferro, Eva Sjøttem, Bartolomeo Augello, Gabriella Maria Squeo, Maria Teresa Pellico, Ashish Jain, Terje Johansen, Gian María Fimia, Giuseppe Merla

    Published 2018
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  8. 8
    TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survival

    TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survival by Lucia Micale, Carmela Fusco, Andrea Fontana, Raffaela Barbano, Bartolomeo Augello, Pasquelena De Nittis, Massimiliano Copetti, Maria Teresa Pellico, Barbara Mandriani, Dario Cocciadiferro, Paola Parrella, Vito Michele Fazio, Lucia Dimitri, Vincenzo D’Angelo, Chiara Novielli, Lidia Larizza, Antonio Daga, Giuseppe Merla

    Published 2015
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  9. 9
    Autophagy induction in atrophic muscle cells requires ULK1 activation by TRIM32 through unanchored K63-linked polyubiquitin chains

    Autophagy induction in atrophic muscle cells requires ULK1 activation by TRIM32 through unanchored K63-linked polyubiquitin chains by Martina Di Rienzo, Manuela Antonioli, Carmela Fusco, Yuangang Liu, Muriel Mari, Idil Orhon, Giulia Refolo, F. Germani, Marco Corazzari, Alessandra Romagnoli, Fabiola Ciccosanti, Barbara Mandriani, Maria Teresa Pellico, R. De La Torre, Hao Ding, Monica Dentice, Marcella Neri, Alessandra Ferlini, Fulvio Reggiori, Molly Kulesz‐Martin, Mauro Piacentini, Giuseppe Merla, Gian María Fimia

    Published 2019
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  10. 10
    <i>BRF1</i> mutations alter RNA polymerase III–dependent transcription and cause neurodevelopmental anomalies

    <i>BRF1</i> mutations alter RNA polymerase III–dependent transcription and cause neurodevelopmental anomalies by Guntram Borck, Friederike Hög, Maria Lisa Dentici, Perciliz L. Tan, Nadine Sowada, Ana Medeira, Lucie Gueneau, Hölger Thiele, Maria Kousi, Francesca Romana Lepri, Larissa Wenzeck, Ian Blumenthal, A. Radicioni, Tito Livio Schwarzenberg, Barbara Mandriani, Rita Fischetto, Deborah Morris‐Rosendahl, Janine Altmüller, Alexandre Reymond, Peter Nürnberg, Giuseppe Merla, Bruno Dallapiccola, Nicholas Katsanis, Patrick Cramer, Christian Kubisch

    Published 2015
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  11. 11
    Molecular Analysis, Pathogenic Mechanisms, and Readthrough Therapy on a Large Cohort of<scp>K</scp>abuki Syndrome Patients

    Molecular Analysis, Pathogenic Mechanisms, and Readthrough Therapy on a Large Cohort of<scp>K</scp>abuki Syndrome Patients by Lucia Micale, Bartolomeo Augello, Claudia Maffeo, Angelo Selicorni, Federica Zucchetti, Carmela Fusco, Pasquelena De Nittis, Maria Teresa Pellico, Barbara Mandriani, Rita Fischetto, Loredana Boccone, Margherita Silengo, Elisa Biamino, Chiara Perrìa, Stefano Sotgiu, Gigliola Serra, Elisabetta Lapi, Marcella Neri, Alessandra Ferlini, Maria Luigia Cavaliere, Pietro Chiurazzi, Matteo Della Monica, Gioacchino Scarano, Francesca Faravelli, Paola Ferrari, Laura Mazzanti, Alba Pilotta, Maria Grazia Patricelli, Maria Francesca Bedeschi, Francesco Benedicenti, Paolo Prontera, Benedetta Toschi, Leonardo Salviati, Daniela Melis, E. Di Battista, Alessandra Vancini, Livia Garavelli, Leopoldo Zelante, Giuseppe Merla

    Published 2014
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  12. 12
    GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability

    GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability by Elisabeth M. Lodder, Pasquelena De Nittis, Charlotte D. Koopman, Wojciech Wiszniewski, Carolina Fischinger Moura de Souza, Najim Lahrouchi, Nicolas Guex, Valerio Napolioni, Federico Tessadori, Leander Beekman, Eline A. Nannenberg, Lamiae Boualla, Nico A. Blom, Wim de Graaff, Maarten Kamermans, Dario Cocciadiferro, Natascia Malerba, Barbara Mandriani, Zeynep H. Coban Akdemir, Richard J. Fish, Mohammad K. Eldomery, Ilham Ratbi, Arthur A.M. Wilde, Teun P. de Boer, William F. Simonds, Marguerite Neerman‐Arbez, V. Reid Sutton, Fernando Kok, James R. Lupski, Alexandre Reymond, Connie R. Bezzina, Jeroen Bakkers, Giuseppe Merla

    Published 2016
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