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J Massaad

Showing results (31-40 of 73) with videos related to

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Clinical Immunology (Orlando, Fla.)|April 12, 2016
Combined immunodeficiency due to a homozygous mutation in ORAI1 that deletes the C-terminus that interacts with STIM 1Yousef R Badran, Michel J Massaad, Wayne Bainter, et al.
Molecular and Cellular Biology|September 24, 2014
Binding of WIP to actin is essential for T cell actin cytoskeleton integrity and tissue homingMichel J Massaad, Michiko K Oyoshi, Jennifer Kane, et al.
Clinical Immunology (Orlando, Fla.)|April 27, 2012
Clinical, immunologic and genetic profiles of DOCK8-deficient patients in KuwaitWaleed Al-Herz, Raj Ragupathy, Michel J Massaad, et al.
Clinical Immunology (Orlando, Fla.)|September 7, 2025
Clinical, biochemical, and genetic characterization of Lebanese patients with chronic granulomatous disease due to NCF2 pathogenic variantsYoumna El-Orfali, Hagop Mardirossian, Habib Al-Kalamouni, et al.
The Journal of Allergy and Clinical Immunology|May 20, 2019
Combined immunodeficiency in a patient with c-Rel deficiencySarah Beaussant-Cohen, Faris Jaber, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|October 13, 2015
Autoimmune lymphoproliferative syndrome caused by a homozygous FasL mutation that disrupts FasL assemblyAli Sobh, Elena Crestani, Brittney Cangemi, et al.
Frontiers in Immunology|January 31, 2019
Comprehensive Genetic Results for Primary Immunodeficiency Disorders in a Highly Consanguineous PopulationWaleed Al-Herz, Janet Chou, Ottavia Maria Delmonte, et al.
Clinical Immunology (Orlando, Fla.)|April 15, 2015
Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in EgyptSafa Meshaal, Rabab El Hawary, Marwa Elsharkawy, et al.
The Journal of Experimental Medicine|January 21, 2015
Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBαJana L Mooster, Severine Le Bras, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|July 3, 2014
Lessons in gene hunting: a RAG1 mutation presenting with agammaglobulinemia and absence of B cellsMona Hedayat, Michel J Massaad, Yu Nee Lee, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Clinical Immunology (Orlando, Fla.)|April 12, 2016
Combined immunodeficiency due to a homozygous mutation in ORAI1 that deletes the C-terminus that interacts with STIM 1Yousef R Badran, Michel J Massaad, Wayne Bainter, et al.
Molecular and Cellular Biology|September 24, 2014
Binding of WIP to actin is essential for T cell actin cytoskeleton integrity and tissue homingMichel J Massaad, Michiko K Oyoshi, Jennifer Kane, et al.
Clinical Immunology (Orlando, Fla.)|April 27, 2012
Clinical, immunologic and genetic profiles of DOCK8-deficient patients in KuwaitWaleed Al-Herz, Raj Ragupathy, Michel J Massaad, et al.
Clinical Immunology (Orlando, Fla.)|September 7, 2025
Clinical, biochemical, and genetic characterization of Lebanese patients with chronic granulomatous disease due to NCF2 pathogenic variantsYoumna El-Orfali, Hagop Mardirossian, Habib Al-Kalamouni, et al.
The Journal of Allergy and Clinical Immunology|May 20, 2019
Combined immunodeficiency in a patient with c-Rel deficiencySarah Beaussant-Cohen, Faris Jaber, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|October 13, 2015
Autoimmune lymphoproliferative syndrome caused by a homozygous FasL mutation that disrupts FasL assemblyAli Sobh, Elena Crestani, Brittney Cangemi, et al.
Frontiers in Immunology|January 31, 2019
Comprehensive Genetic Results for Primary Immunodeficiency Disorders in a Highly Consanguineous PopulationWaleed Al-Herz, Janet Chou, Ottavia Maria Delmonte, et al.
Clinical Immunology (Orlando, Fla.)|April 15, 2015
Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in EgyptSafa Meshaal, Rabab El Hawary, Marwa Elsharkawy, et al.
The Journal of Experimental Medicine|January 21, 2015
Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBαJana L Mooster, Severine Le Bras, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|July 3, 2014
Lessons in gene hunting: a RAG1 mutation presenting with agammaglobulinemia and absence of B cellsMona Hedayat, Michel J Massaad, Yu Nee Lee, et al.
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