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Showing results (61-70 of 73) with videos related to

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Nature Immunology|June 1, 2026
Editorial Expression of Concern: DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Immunology|March 25, 2022
Author Correction: DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Immunology|May 15, 2012
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Genetics|December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiencyHaifa H Jabara, Steven E Boyden, Janet Chou, et al.
The Journal of Clinical Investigation|March 13, 2020
Inherited human IFN-γ deficiency underlies mycobacterial diseaseGaspard Kerner, Jérémie Rosain, Antoine Guérin, et al.
The Journal of Allergy and Clinical Immunology|December 22, 2019
Hypomorphic variants in AK2 reveal the contribution of mitochondrial function to B-cell activationJanet Chou, Anas M Alazami, Faris Jaber, et al.
The Journal of Allergy and Clinical Immunology|December 3, 2013
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiencyYu Nee Lee, Francesco Frugoni, Kerry Dobbs, et al.
Blood|February 4, 2012
B cell-intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in miceMike Recher, Siobhan O Burns, Miguel A de la Fuente, et al.
The New England Journal of Medicine|June 18, 2015
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive InfectionsKerry Dobbs, Cecilia Domínguez Conde, Shen-Ying Zhang, et al.
The Journal of Allergy and Clinical Immunology|March 1, 2015
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiencyKarin R Engelhardt, Michael E Gertz, Sevgi Keles, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Nature Immunology|June 1, 2026
Editorial Expression of Concern: DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Immunology|March 25, 2022
Author Correction: DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Immunology|May 15, 2012
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activationHaifa H Jabara, Douglas R McDonald, Erin Janssen, et al.
Nature Genetics|December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiencyHaifa H Jabara, Steven E Boyden, Janet Chou, et al.
The Journal of Clinical Investigation|March 13, 2020
Inherited human IFN-γ deficiency underlies mycobacterial diseaseGaspard Kerner, Jérémie Rosain, Antoine Guérin, et al.
The Journal of Allergy and Clinical Immunology|December 22, 2019
Hypomorphic variants in AK2 reveal the contribution of mitochondrial function to B-cell activationJanet Chou, Anas M Alazami, Faris Jaber, et al.
The Journal of Allergy and Clinical Immunology|December 3, 2013
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiencyYu Nee Lee, Francesco Frugoni, Kerry Dobbs, et al.
Blood|February 4, 2012
B cell-intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in miceMike Recher, Siobhan O Burns, Miguel A de la Fuente, et al.
The New England Journal of Medicine|June 18, 2015
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive InfectionsKerry Dobbs, Cecilia Domínguez Conde, Shen-Ying Zhang, et al.
The Journal of Allergy and Clinical Immunology|March 1, 2015
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiencyKarin R Engelhardt, Michael E Gertz, Sevgi Keles, et al.
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