Suchergebnisse - Gabriele, Michele

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

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

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Tracking and interpreting long-range chromatin interactions with super-resolution live-cell imaging von 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 von 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 von 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... von 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 von 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 von 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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