Risultati della ricerca - Aksoy, Irène
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Oct4 switches partnering from Sox2 to Sox17 to reinterpret the enhancer code and specify endoderm di Aksoy, Irene, Jauch, Ralf, Chen, Jiaxuan, Dyla, Mateusz, Divakar, Ushashree, Bogu, Gireesh K, Teo, Roy, Leng Ng, Calista Keow, Herath, Wishva, Lili, Sun, Hutchins, Andrew P, Robson, Paul, Kolatkar, Prasanna R, Stanton, Lawrence W
Pubblicazione 2013testo -
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Murine AGM single-cell profiling identifies a continuum of hemogenic endothelium differentiation marked by ACE di Fadlullah, Muhammad Zaki Hidayatullah, Neo, Wen Hao, Lie-a-ling, Michael, Thambyrajah, Roshana, Patel, Rahima, Mevel, Renaud, Aksoy, Irène, Do Khoa, Nam, Savatier, Pierre, Fontenille, Laura, Baker, Syed Murtuza, Rattray, Magnus, Kouskoff, Valerie, Lacaud, Georges
Pubblicazione 2022testo -
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Apoptosis, G1 Phase Stall, and Premature Differentiation Account for Low Chimeric Competence of Human and Rhesus Monkey Naive Pluripotent Stem Cells di Aksoy, Irène, Rognard, Cloé, Moulin, Anaïs, Marcy, Guillaume, Masfaraud, Etienne, Wianny, Florence, Cortay, Véronique, Bellemin-Ménard, Angèle, Doerflinger, Nathalie, Dirheimer, Manon, Mayère, Chloé, Bourillot, Pierre-Yves, Lynch, Cian, Raineteau, Olivier, Joly, Thierry, Dehay, Colette, Serrano, Manuel, Afanassieff, Marielle, Savatier, Pierre
Pubblicazione 2020testo -
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Reinforcement of STAT3 activity reprogrammes human embryonic stem cells to naive-like pluripotency di Chen, Hongwei, Aksoy, Irène, Gonnot, Fabrice, Osteil, Pierre, Aubry, Maxime, Hamela, Claire, Rognard, Cloé, Hochard, Arnaud, Voisin, Sophie, Fontaine, Emeline, Mure, Magali, Afanassieff, Marielle, Cleroux, Elouan, Guibert, Sylvain, Chen, Jiaxuan, Vallot, Céline, Acloque, Hervé, Genthon, Clémence, Donnadieu, Cécile, De Vos, John, Sanlaville, Damien, Guérin, Jean- François, Weber, Michael, Stanton, Lawrence W, Rougeulle, Claire, Pain, Bertrand, Bourillot, Pierre-Yves, Savatier, Pierre
Pubblicazione 2015testo -
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The FunGenES Database: A Genomics Resource for Mouse Embryonic Stem Cell Differentiation di Schulz, Herbert, Kolde, Raivo, Adler, Priit, Aksoy, Irène, Anastassiadis, Konstantinos, Bader, Michael, Billon, Nathalie, Boeuf, Hélène, Bourillot, Pierre-Yves, Buchholz, Frank, Dani, Christian, Doss, Michael Xavier, Forrester, Lesley, Gitton, Murielle, Henrique, Domingos, Hescheler, Jürgen, Himmelbauer, Heinz, Hübner, Norbert, Karantzali, Efthimia, Kretsovali, Androniki, Lubitz, Sandra, Pradier, Laurent, Rai, Meena, Reimand, Jüri, Rolletschek, Alexandra, Sachinidis, Agapios, Savatier, Pierre, Stewart, Francis, Storm, Mike P., Trouillas, Marina, Vilo, Jaak, Welham, Melanie J., Winkler, Johannes, Wobus, Anna M., Hatzopoulos, Antonis K.
Pubblicazione 2009testo -
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Detection of Chromosomal Breakpoints in Patients with Developmental Delay and Speech Disorders di Utami, Kagistia H., Hillmer, Axel M., Aksoy, Irene, Chew, Elaine G. Y., Teo, Audrey S. M., Zhang, Zhenshui, Lee, Charlie W. H., Chen, Pauline J., Seng, Chan Chee, Ariyaratne, Pramila N., Rouam, Sigrid L., Soo, Lim Seong, Yousoof, Saira, Prokudin, Ivan, Peters, Gregory, Collins, Felicity, Wilson, Meredith, Kakakios, Alyson, Haddad, Georges, Menuet, Arnaud, Perche, Olivier, Tay, Stacey Kiat Hong, Sung, Ken W. K., Ruan, Xiaoan, Ruan, Yijun, Liu, Edison T., Briault, Sylvain, Jamieson, Robyn V., Davila, Sonia, Cacheux, Valere
Pubblicazione 2014testo