TACI and BAFF-R mediate isotype switching in B cells

por Castigli, Emanuela, Wilson, Stephen A., Scott, Sumi, Dedeoglu, Fatma, Xu, Shengli, Lam, Kong-Peng, Bram, Richard J., Jabara, Haifa, Geha, Raif S.
Publicado 2005

Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBα

por Mooster, Jana L., Le Bras, Severine, Massaad, Michel J., Jabara, Haifa, Yoon, Juhan, Galand, Claire, Heesters, Balthasar A., Burton, Oliver T., Mattoo, Hamid, Manis, John, Geha, Raif S.
Publicado 2015

DOCK8 functions as an adaptor that links Toll-like receptor–MyD88 signaling to B cell activation

por Jabara, Haifa H., McDonald, Douglas R., Janssen, Erin, Massaad, Michel J., Ramesh, Narayanaswamy, Borzutzky, Arturo, Rauter, Ingrid, Benson, Halli, Schneider, Lynda, Baxi, Sachin, Recher, Mike, Notarangelo, Luigi, Wakim, Rima, Dbaibo, Ghassan, Dasouki, Majed, Al-Herz, Waleed, Barlan, Isil, Baris, Safa, Kutukculer, Necil, Ochs, Hans, Plebani, Alessandro, Kanariou, Maria, Lefranc, Gerard, Reisli, Ismail, Fitzgerald, Kate, Golenbock, Douglas, Manis, John, Keles, Sevgi, Ceja, Reuben, Chatila, Talal, Geha, Raif S.
Publicado 2012

A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

por Jabara, Haifa H., Boyden, Steven E., Chou, Janet, Ramesh, Narayanaswamy, Massaad, Michel J., Benson, Halli, Bainter, Wayne, Fraulino, David, Rahimov, Fedik, Sieff, Colin, Liu, Zhi-Jian, Alshemmari, Salem H., Al-Ramadi, Basel K., Al-Dhekri, Hasan, Arnaout, Rand, Abu-Shukair, Mohammad, Vatsayan, Anant, Silver, Eli, Ahuja, Sanjay, Davies, E. Graham, Sola-Visner, Martha, Ohsumi, Toshiro K., Andrews, Nancy C., Notarangelo, Luigi D., Fleming, Mark D., Al-Herz, Waleed, Kunkel, Louis M., Geha, Raif S.
Publicado 2015