The Yeast Split-Ubiquitin Membrane Protein Two-Hybrid Screen Identifies BAP31 as a Regulator of the Turnover of Endoplasmic Reticulum-Associated Protein Tyrosine Phosphatase-Like B

Por Wang, Bing, Pelletier, Jerry, Massaad, Michel J., Herscovics, Annette, Shore, Gordon C.
Publicado em 2004

Platelet-associated IgAs and impaired GPVI responses in platelets lacking WIP

Por Falet, Hervé, Marchetti, Michael P., Hoffmeister, Karin M., Massaad, Michel J., Geha, Raif S., Hartwig, John H.
Publicado em 2009

Successful engraftment of donor marrow following allogeneic hematopoietic cell transplantation in autosomal recessive Hyper IgE syndrome due to DOCK8 deficiency

Por McDonald, Douglas R., Massaad, Michel J., Johnston, Alicia, Keles, Sevgi, Chatila, Talal, Geha, Raif S., Pai, Sung-Yun
Publicado em 2010

Binding of the WASP/N-WASP-Interacting Protein WIP to Actin Regulates Focal Adhesion Assembly and Adhesion

Por Ramesh, Narayanaswamy, Massaad, Michel J., Kumar, Lalit, Koduru, Suresh, Sasahara, Yoji, Anton, Ines, Bhasin, Manoj, Libermann, Towia, Geha, Raif
Publicado em 2014

The Rho GTPase Cdc42 Is Essential for the Activation and Function of Mature B Cells

Por Gerasimcik, Natalija, Dahlberg, Carin I. M., Baptista, Marisa A. P., Massaad, Michel J., Geha, Raif S., Westerberg, Lisa S., Severinson, Eva
Publicado no J Immunol (2015)

A WIP peptide restores WASP levels and actin cytoskeleton reorganization in lymphocytes from patients with WAS mutations that disrupt WIP binding

Por Massaad, Michel J., Ramesh, Narayanaswamy, Bras, Severine Le, Giliani, Silvia, Notarangelo, Lucia D., Al-Herz, Waleed, Notarangelo, Luigi D., Geha, Raif S.
Publicado em 2011

Binding of WIP to Actin Is Essential for T Cell Actin Cytoskeleton Integrity and Tissue Homing

Por Massaad, Michel J., Oyoshi, Michiko K., Kane, Jennifer, Koduru, Suresh, Alcaide, Pilar, Nakamura, Fumihiko, Ramesh, Narayanaswamy, Luscinskas, Francis W., Hartwig, John, Geha, Raif S.
Publicado no Mol Cell Biol (2014)

Clinical, Immunologic and Genetic Profile of DOCK8-Deficient Patients in Kuwait

Por Al-Herz, Waleed, Ragupathy, Raj, Massaad, Michel J., Al-Attiyah, Raja’a, Nanda, Arti, Engelhardt, Karin R., Grimbacher, Bodo, Notarangelo, Luigi, Chatila, Talal, Geha, Raif S.
Publicado em 2012

LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency

Por Alangari, Abdullah, Alsultan, Abdulrahman, Adly, Nouran, Massaad, Michel J., Kiani, Iram Shakir, Aljebreen, Abdulrahman, Raddaoui, Emad, Almomen, Abdul-Kareem, Al-Muhsen, Saleh, Geha, Raif S., Alkuraya, Fowzan S.
Publicado em 2012

Lessons in gene hunting: a RAG1 mutation presenting with agammaglobulinemia and absence of B cells

Por Hedayat, Mona, Massaad, Michel J., Lee, Yu Nee, Conley, Mary Ellen, Orange, Jordan S., Ohsumi, Toshiro K., Al-Herz, Waleed, Notarangelo, Luigi D., Geha, Raif S., Chou, Janet
Publicado em 2014

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 no J Exp Med (2015)

Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association

Por Yee, Christina S., Massaad, Michel J., Bainter, Wayne, Ohsumi, Toshiro K., Föger, Niko, Chan, Andrew C., Akarsu, Nurten A., Aytekin, Caner, Ayvaz, Deniz Çagdas, Tezcan, Ilhan, Sanal, Özden, Geha, Raif S., Chou, Janet
Publicado no J Allergy Clin Immunol (2015)

Intronic SH2D1A mutation with impaired SAP expression and agammaglobulinemia

Por Recher, Mike, Fried, Ari J., Massaad, Michel J., Kim, Hye Young, Rizzini, Michela, Frugoni, Francesco, Walter, Jolan E., Mathew, Divij, Eibel, Hermann, Hess, Christoph, Giliani, Silvia, Umetsu, Dale T., Notarangelo, Luigi D., Geha, Raif S.
Publicado em 2012

A novel homozygous mutation in Recombination Activating Gene 2 in two relatives with different clinical phenotypes: Omenn syndrome and Hyper-IgM syndrome

Por Chou, Janet, Hanna-Wakim, Rima, Tirosh, Irit, Kane, Jennifer, Fraulino, David, Lee, Yu Nee, Ghanem, Soha, Mahfouz, Iman, Mégarbané, André, Lefranc, Gérard, Inati, Adlette, Dbaibo, Ghassan, Giliani, Silvia, Notarangelo, Luigi D., Geha, Raif S., Massaad, Michel J.
Publicado em 2012

Regulatory T Cell Deficiency and Immune dysregulation, Polyendocrinopathy, Enteropathy, X-Linked-Like Disorder Due to Loss of Function Mutations in LRBA

Por Charbonnier, Louis-Marie, Janssen, Erin, Chou, Janet, Ohsumi, Toshiro K., Keles, Sevgi, Hsu, Joyce T., Massaad, Michel J., Garcia-Lloret, Maria, Hanna-Wakim, Rima, Dbaibo, Ghassan, Alangari, Abdullah A., Alsultan, Abdulrahman, Al-Zahrani, Daifulah, Geha, Raif S., Chatila, Talal A.
Publicado no J Allergy Clin Immunol (2014)

Cdc42 interacting protein 4 (CIP4) is essential for integrin-dependent T-cell trafficking

Por Koduru, Suresh, Kumar, Lalit, Massaad, Michel J., Ramesh, Narayanaswamy, Le Bras, Séverine, Ozcan, Esra, Oyoshi, Michiko K., Kaku, Mayumi, Fujiwara, Yuko, Kremer, Leonor, King, Sandra, Fuhlbrigge, Robert, Rodig, Scott, Sage, Peter, Carman, Chris, Alcaide, Pilar, Luscinskas, Francis W., Geha, Raif S.
Publicado em 2010

A Homozygous mucosa-associated ly 1 mphoid tissue 1 (MALT1) mutation in a family with 2 combined immunodeficiency

Por Jabara, Haifa H., Ohsumi, Toshiro, Chou, Janet, Massaad, Michel J., Benson, Halli, Megarbane, Andre, Chouery, Eliane, Mikhael, Raymond, Gorka, Oliver, Gewies, Andreas, Portales, Pierre, Nakayama, Toshinori, Hosokawa, Hiroyuki, Revy, Patrick, Herrod, Henry, Deist, Francoise Le, Lefranc, Gerard, Ruland, Jürgen, Geha, Raif S.
Publicado em 2013

A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP

Por Lanzi, Gaetana, Moratto, Daniele, Vairo, Donatella, Masneri, Stefania, Delmonte, Ottavia, Paganini, Tiziana, Parolini, Silvia, Tabellini, Giovanna, Mazza, Cinzia, Savoldi, Gianfranco, Montin, Davide, Martino, Silvana, Tovo, Pierangelo, Pessach, Itai M., Massaad, Michel J., Ramesh, Narayanaswamy, Porta, Fulvio, Plebani, Alessandro, Notarangelo, Luigi D., Geha, Raif S., Giliani, Silvia
Publicado em 2012

A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton

Por Janssen, Erin, Tohme, Mira, Hedayat, Mona, Leick, Marion, Kumari, Sudha, Ramesh, Narayanaswamy, Massaad, Michel J., Ullas, Sumana, Azcutia, Veronica, Goodnow, Christopher C., Randall, Katrina L., Qiao, Qi, Wu, Hao, Al-Herz, Waleed, Cox, Dianne, Hartwig, John, Irvine, Darrell J., Luscinskas, Francis W., Geha, Raif S.
Publicado no J Clin Invest (2016)

Hematopoietic Stem Cell Transplantation Outcomes for 11 Patients with Dedicator of Cytokinesis 8 (DOCK8) Deficiency

Por Al-Herz, Waleed, Chu, Julia I., van der Spek, Jet, Raghupathy, Raj, Massaad, Michel J., Keles, Sevgi, Biggs, Catherine M., Cockerton, Lucinda, Chou, Janet, Dbaibo, Ghassan, Elisofon, Scott A., Hanna-Wakim, Rima, Kim, Heung Bae, Lehmann, Leslie E., McDonald, Douglas R., Notarangelo, Luigi D., Veys, Paul, Chatila, Talal, Geha, Raif S., Gaspar, H. Bobby, Pai, Sung-Yun
Publicado no J Allergy Clin Immunol (2016)