نتائج البحث - Notarangelo, Giulia
- يعرض 1 - 6 نتائج من 6
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Defective respiration and one-carbon metabolism contribute to impaired naïve T cell activation in aged mice حسب Ron-Harel, Noga, Notarangelo, Giulia, Ghergurovich, Jonathan M., Paulo, Joao A., Sage, Peter T., Santos, Daniel, Satterstrom, F. Kyle, Gygi, Steven P., Rabinowitz, Joshua D., Sharpe, Arlene H., Haigis, Marcia C.
منشور في 2018نص -
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Magnesium transporter 1 (MAGT1) deficiency causes selective defects in N-linked glycosylation and expression of immune-response genes حسب Matsuda-Lennikov, Mami, Biancalana, Matthew, Zou, Juan, Ravell, Juan C., Zheng, Lixin, Kanellopoulou, Chrysi, Jiang, Ping, Notarangelo, Giulia, Jing, Huie, Masutani, Evan, Oler, Andrew J., Olano, Lisa Renee, Schulz, Benjamin L., Lenardo, Michael J.
منشور في 2019نص -
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SIRT4 is an early regulator of branched-chain amino acid catabolism that promotes adipogenesis حسب Zaganjor, Elma, Yoon, Haejin, Spinelli, Jessica B., Nunn, Elizabeth R., Laurent, Gaëlle, Keskinidis, Paulina, Sivaloganathan, Suganja, Joshi, Shakchhi, Notarangelo, Giulia, Mulei, Stacy, Chvasta, Mathew T., Tucker, Sarah A., Kalafut, Krystle, van de Ven, Robert A.H., Clish, Clary B., Haigis, Marcia C.
منشور في 2021نص -
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Mitochondrial reprogramming underlies resistance to BCL-2 inhibition in lymphoid Malignancies حسب Guièze, Romain, Liu, Vivian M., Rosebrock, Daniel, Jourdain, Alexis A., Hernández-Sánchez, María, Zurita, Aina Martinez, Sun, Jing, Hacken, Elisa Ten, Baranowski, Kaitlyn, Thompson, Philip A., Heo, Jin-Mi, Cartun, Zachary, Aygün, Ozan, Iorgulescu, J. Bryan, Zhang, Wandi, Notarangelo, Giulia, Livitz, Dimitri, Li, Shuqiang, Davids, Matthew S., Biran, Anat, Fernandes, Stacey M., Brown, Jennifer R., Lako, Ana, Ciantra, Zoe B, Lawlor, Matthew A, Keskin, Derin B., Udeshi, Namrata D., Wierda, William G., Livak, Kenneth J, Letai, Anthony G., Neuberg, Donna, Wade Harper, J., Carr, Steven A., Piccioni, Federica, Ott, Christopher J., Leshchiner, Ignaty, Johannessen, Cory M., Doench, John, Mootha, Vamsi K., Getz, Gad, Wu, Catherine J.
منشور في 2019نص -
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Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease حسب Ravell, Juan C., Matsuda-Lennikov, Mami, Chauvin, Samuel D., Zou, Juan, Biancalana, Matthew, Deeb, Sally J., Price, Susan, Su, Helen C., Notarangelo, Giulia, Jiang, Ping, Morawski, Aaron, Kanellopoulou, Chrysi, Binder, Kyle, Mukherjee, Ratnadeep, Anibal, James T., Sellers, Brian, Zheng, Lixin, He, Tingyan, George, Alex B., Pittaluga, Stefania, Powers, Astin, Kleiner, David E., Kapuria, Devika, Ghany, Marc, Hunsberger, Sally, Cohen, Jeffrey I., Uzel, Gulbu, Bergerson, Jenna, Wolfe, Lynne, Toro, Camilo, Gahl, William, Folio, Les R., Matthews, Helen, Angelus, Pam, Chinn, Ivan K., Orange, Jordan S., Trujillo-Vargas, Claudia M., Franco, Jose Luis, Orrego-Arango, Julio, Gutiérrez-Hincapié, Sebastian, Patel, Niraj Chandrakant, Raymond, Kimiyo, Patiroglu, Turkan, Unal, Ekrem, Karakukcu, Musa, Day, Alexandre G.R., Mehta, Pankaj, Masutani, Evan, De Ravin, Suk S., Malech, Harry L., Altan-Bonnet, Grégoire, Rao, V. Koneti, Mann, Matthias, Lenardo, Michael J.
منشور في 2019نص