Výsledky vyhledávání - Vitriolo, Alessandro

From enhanceropathies to the epigenetic manifold underlying human cognition Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 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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