Výsledky vyhledávání - Gabriele, Michele

From enhanceropathies to the epigenetic manifold underlying human cognition Autor Vitriolo, Alessandro, Gabriele, Michele, Testa, Giuseppe

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KMT2B and Neuronal Transdifferentiation: Bridging Basic Chromatin Mechanisms to Disease Actionability Autor Barbagiovanni, Giulia, Gabriele, Michele, Testa, Giuseppe

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Tracking and interpreting long-range chromatin interactions with super-resolution live-cell imaging Autor Brandão, Hugo B., Gabriele, Michele, Hansen, Anders S.

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Dynamics of CTCF and cohesin mediated chromatin looping revealed by live-cell imaging Autor Gabriele, Michele, Brandão, Hugo B., Grosse-Holz, Simon, Jha, Asmita, Dailey, Gina M., Cattoglio, Claudia, Hsieh, Tsung-Han S., Mirny, Leonid, Zechner, Christoph, Hansen, Anders S.

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ANMCO/SIC Consensus Document: cardiology networks for outpatient heart failure care Autor Aspromonte, Nadia, Gulizia, Michele Massimo, Di Lenarda, Andrea, Mortara, Andrea, Battistoni, Ilaria, De Maria, Renata, Gabriele, Michele, Iacoviello, Massimo, Navazio, Alessandro, Pini, Daniela, Di Tano, Giuseppe, Marini, Marco, Ricci, Renato Pietro, Alunni, Gianfranco, Radini, Donatella, Metra, Marco, Romeo, Francesco

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High-throughput screening identifies histone deacetylase inhibitors that modulate GTF2I expression in 7q11.23 microduplication autism spectrum disorder patient-derived cortical neu... Autor Cavallo, Francesca, Troglio, Flavia, Fagà, Giovanni, Fancelli, Daniele, Shyti, Reinald, Trattaro, Sebastiano, Zanella, Matteo, D’Agostino, Giuseppe, Hughes, James M., Cera, Maria Rosaria, Pasi, Maurizio, Gabriele, Michele, Lazzarin, Maddalena, Mihailovich, Marija, Kooy, Frank, Rosa, Alessandro, Mercurio, Ciro, Varasi, Mario, Testa, Giuseppe

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Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders Autor Linda, Katrin, Lewerissa, Elly I., Verboven, Anouk H. A., Gabriele, Michele, Frega, Monica, Klein Gunnewiek, Teun M., Devilee, Lynn, Ulferts, Edda, Hommersom, Marina, Oudakker, Astrid, Schoenmaker, Chantal, van Bokhoven, Hans, Schubert, Dirk, Testa, Giuseppe, Koolen, David A., de Vries, Bert B.A., Nadif Kasri, Nael

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction Autor Gabriele, Michele, Vulto-van Silfhout, Anneke T., Germain, Pierre-Luc, Vitriolo, Alessandro, Kumar, Raman, Douglas, Evelyn, Haan, Eric, Kosaki, Kenjiro, Takenouchi, Toshiki, Rauch, Anita, Steindl, Katharina, Frengen, Eirik, Misceo, Doriana, Pedurupillay, Christeen Ramane J., Stromme, Petter, Rosenfeld, Jill A., Shao, Yunru, Craigen, William J., Schaaf, Christian P., Rodriguez-Buritica, David, Farach, Laura, Friedman, Jennifer, Thulin, Perla, McLean, Scott D., Nugent, Kimberly M., Morton, Jenny, Nicholl, Jillian, Andrieux, Joris, Stray-Pedersen, Asbjørg, Chambon, Pascal, Patrier, Sophie, Lynch, Sally A., Kjaergaard, Susanne, Tørring, Pernille M., Brasch-Andersen, Charlotte, Ronan, Anne, van Haeringen, Arie, Anderson, Peter J., Powis, Zöe, Brunner, Han G., Pfundt, Rolph, Schuurs-Hoeijmakers, Janneke H.M., van Bon, Bregje W.M., Lelieveld, Stefan, Gilissen, Christian, Nillesen, Willy M., Vissers, Lisenka E.L.M., Gecz, Jozef, Koolen, David A., Testa, Giuseppe, de Vries, Bert B.A.

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