Search Results - Vitriolo, Alessandro
- Showing 1 - 8 results of 8
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An Acidic Loop and Cognate Phosphorylation Sites Define a Molecular Switch That Modulates Ubiquitin Charging Activity in Cdc34-Like Enzymes by Papaleo, Elena, Ranzani, Valeria, Tripodi, Farida, Vitriolo, Alessandro, Cirulli, Claudia, Fantucci, Piercarlo, Alberghina, Lilia, Vanoni, Marco, De Gioia, Luca, Coccetti, Paola
Published 2011Text -
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The guanine nucleotide exchange factor Arhgef7/βPix promotes axon formation upstream of TC10 by López Tobón, Alejandro, Suresh, Megalakshmi, Jin, Jing, Vitriolo, Alessandro, Pietralla, Thorben, Tedford, Kerry, Bossenz, Michael, Mahnken, Kristina, Kiefer, Friedemann, Testa, Giuseppe, Fischer, Klaus-Dieter, Püschel, Andreas W.
Published 2018Text -
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Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication by Zanella, Matteo, Vitriolo, Alessandro, Andirko, Alejandro, Martins, Pedro Tiago, Sturm, Stefanie, O’Rourke, Thomas, Laugsch, Magdalena, Malerba, Natascia, Skaros, Adrianos, Trattaro, Sebastiano, Germain, Pierre-Luc, Mihailovic, Marija, Merla, Giuseppe, Rada-Iglesias, Alvaro, Boeckx, Cedric, Testa, Giuseppe
Published 2019Text -
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DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes by Choufani, Sanaa, Gibson, William T., Turinsky, Andrei L., Chung, Brian H.Y., Wang, Tianren, Garg, Kopal, Vitriolo, Alessandro, Cohen, Ana S.A., Cyrus, Sharri, Goodman, Sarah, Chater-Diehl, Eric, Brzezinski, Jack, Brudno, Michael, Ming, Luk Ho, White, Susan M., Lynch, Sally Ann, Clericuzio, Carol, Temple, I. Karen, Flinter, Frances, McConnell, Vivienne, Cushing, Tom, Bird, Lynne M., Splitt, Miranda, Kerr, Bronwyn, Scherer, Stephen W., Machado, Jerry, Imagawa, Eri, Okamoto, Nobuhiko, Matsumoto, Naomichi, Testa, Guiseppe, Iascone, Maria, Tenconi, Romano, Caluseriu, Oana, Mendoza-Londono, Roberto, Chitayat, David, Cytrynbaum, Cheryl, Tatton-Brown, Katrina, Weksberg, Rosanna
Published 2020Text -
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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction by 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.
Published 2017Text