Výsledky vyhledávání - Barbara Mandriani
- Zobrazuji výsledky 1 - 11 z 11
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Cutting Edge: The NLRP3 Inflammasome Links Complement-Mediated Inflammation and IL-1β Release Autor Federica Laudisi, Roberto Spreafico, Maximilien Evrard, Timothy R. Hughes, Barbara Mandriani, Matheswaran Kandasamy, B. Paul Morgan, Baalasubramanian Sivasankar, Alessandra Mortellaro
Vydáno 2013Artigo -
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3
Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits Autor 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
Vydáno 2013Artigo -
4
Dissecting KMT2D missense mutations in Kabuki syndrome patients Autor 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
Vydáno 2018Artigo -
5
Development of anti-somatostatin receptors CAR T cells for treatment of neuroendocrine tumors Autor 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
Vydáno 2022Artigo -
6
TRIM50 regulates Beclin 1 proautophagic activity Autor 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
Vydáno 2018Artigo -
7
TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survival Autor 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
Vydáno 2015Artigo -
8
Autophagy induction in atrophic muscle cells requires ULK1 activation by TRIM32 through unanchored K63-linked polyubiquitin chains Autor 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
Vydáno 2019Artigo -
9
<i>BRF1</i> mutations alter RNA polymerase III–dependent transcription and cause neurodevelopmental anomalies Autor 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
Vydáno 2015Errata/Corrigenda -
10
Molecular Analysis, Pathogenic Mechanisms, and Readthrough Therapy on a Large Cohort of<scp>K</scp>abuki Syndrome Patients Autor 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
Vydáno 2014Artigo -
11
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability Autor 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
Vydáno 2016Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Cell biology
Chemistry
Missense mutation
Mutation
Phenotype
AMPK
Apoptosis
Autophagy
Biochemistry
Cancer research
Haploinsufficiency
Immune system
Immunology
Internal medicine
Kabuki syndrome
Pharmacology
Protein kinase A
ULK1
Acetylation
Allele
Anaphylatoxin
Atrophy
BAG3
Bioinformatics
Carcinogenesis
Caspase 1