Resultados de procura - Vitriolo, Alessandro

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

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Temporal mapping of derived high-frequency gene variants supports the mosaic nature of the evolution of Homo sapiens por Andirkó, Alejandro, Moriano, Juan, Vitriolo, Alessandro, Kuhlwilm, Martin, Testa, Giuseppe, Boeckx, Cedric

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RNAontheBENCH: computational and empirical resources for benchmarking RNAseq quantification and differential expression methods por Germain, Pierre-Luc, Vitriolo, Alessandro, Adamo, Antonio, Laise, Pasquale, Das, Vivek, Testa, Giuseppe

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An Acidic Loop and Cognate Phosphorylation Sites Define a Molecular Switch That Modulates Ubiquitin Charging Activity in Cdc34-Like Enzymes por Papaleo, Elena, Ranzani, Valeria, Tripodi, Farida, Vitriolo, Alessandro, Cirulli, Claudia, Fantucci, Piercarlo, Alberghina, Lilia, Vanoni, Marco, De Gioia, Luca, Coccetti, Paola

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The guanine nucleotide exchange factor Arhgef7/βPix promotes axon formation upstream of TC10 por 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.

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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 por 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

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DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes por 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

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction por 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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