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J Massaad

Showing results (51-60 of 73) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 1, 2010
Cdc42 interacting protein 4 (CIP4) is essential for integrin-dependent T-cell traffickingSuresh Koduru, Lalit Kumar, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|December 4, 2014
Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBALouis-Marie Charbonnier, Erin Janssen, Janet Chou, et al.
The Journal of Allergy and Clinical Immunology|June 4, 2013
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiencyHaifa H Jabara, Toshiro Ohsumi, Janet Chou, et al.
The Journal of Clinical Investigation|September 7, 2016
A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeletonErin Janssen, Mira Tohme, Mona Hedayat, et al.
The Journal of Experimental Medicine|January 11, 2012
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIPGaetana Lanzi, Daniele Moratto, Donatella Vairo, et al.
The Journal of Allergy and Clinical Immunology|February 9, 2023
Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6Safa Baris, Mehdi Benamar, Qian Chen, et al.
The Journal of Allergy and Clinical Immunology|May 1, 2016
Hematopoietic stem cell transplantation outcomes for 11 patients with dedicator of cytokinesis 8 deficiencyWaleed Al-Herz, Julia I Chu, Jet van der Spek, et al.
The Journal of Allergy and Clinical Immunology|June 21, 2017
Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiencyDaniel Petersheim, Michel J Massaad, Saetbyul Lee, et al.
The Journal of Clinical Investigation|February 2, 2021
Combined immunodeficiency due to a mutation in the γ1 subunit of the coat protein I complexWayne Bainter, Craig D Platt, Seung-Yeol Park, et al.
The Journal of Clinical Investigation|November 2, 2016
Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunityMichel J Massaad, Jia Zhou, Daisuke Tsuchimoto, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Proceedings of the National Academy of Sciences of the United States of America|September 1, 2010
Cdc42 interacting protein 4 (CIP4) is essential for integrin-dependent T-cell traffickingSuresh Koduru, Lalit Kumar, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|December 4, 2014
Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBALouis-Marie Charbonnier, Erin Janssen, Janet Chou, et al.
The Journal of Allergy and Clinical Immunology|June 4, 2013
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiencyHaifa H Jabara, Toshiro Ohsumi, Janet Chou, et al.
The Journal of Clinical Investigation|September 7, 2016
A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeletonErin Janssen, Mira Tohme, Mona Hedayat, et al.
The Journal of Experimental Medicine|January 11, 2012
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIPGaetana Lanzi, Daniele Moratto, Donatella Vairo, et al.
The Journal of Allergy and Clinical Immunology|February 9, 2023
Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6Safa Baris, Mehdi Benamar, Qian Chen, et al.
The Journal of Allergy and Clinical Immunology|May 1, 2016
Hematopoietic stem cell transplantation outcomes for 11 patients with dedicator of cytokinesis 8 deficiencyWaleed Al-Herz, Julia I Chu, Jet van der Spek, et al.
The Journal of Allergy and Clinical Immunology|June 21, 2017
Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiencyDaniel Petersheim, Michel J Massaad, Saetbyul Lee, et al.
The Journal of Clinical Investigation|February 2, 2021
Combined immunodeficiency due to a mutation in the γ1 subunit of the coat protein I complexWayne Bainter, Craig D Platt, Seung-Yeol Park, et al.
The Journal of Clinical Investigation|November 2, 2016
Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunityMichel J Massaad, Jia Zhou, Daisuke Tsuchimoto, et al.
Pageof 8