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Stuart G Tangye

Showing results (191-200 of 284) with videos related to

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The Journal of Experimental Medicine|June 23, 2021
High Th2 cytokine levels and upper airway inflammation in human inherited T-bet deficiencyRui Yang, Marc Weisshaar, Federico Mele, et al.
Journal of Clinical Immunology|December 12, 2017
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of ImmunityCapucine Picard, H Bobby Gaspar, Waleed Al-Herz, et al.
Journal of Clinical Immunology|March 7, 2019
Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil DysfunctionLeen Moens, Mieke Gouwy, Barbara Bosch, et al.
The Journal of Allergy and Clinical Immunology|August 25, 2016
Dedicator of cytokinesis 8-deficient CD4<sup>+</sup> T cells are biased to a T<sub>H</sub>2 effector fate at the expense of T<sub>H</sub>1 and T<sub>H</sub>17 cellsStuart G Tangye, Bethany Pillay, Katrina L Randall, et al.
Journal of Clinical Immunology|June 21, 2020
Everolimus-Induced Remission of Classic Kaposi's Sarcoma Secondary to Cryptic Splicing Mediated CTLA4 HaploinsufficiencyJin Yan Yap, Brian Gloss, Marcel Batten, et al.
Science Translational Medicine|February 16, 2018
Circulating T<sub>FH</sub> cells, serological memory, and tissue compartmentalization shape human influenza-specific B cell immunityMarios Koutsakos, Adam K Wheatley, Liyen Loh, et al.
Journal of Clinical Immunology|October 17, 2021
Intrinsic Defects in B Cell Development and Differentiation, T Cell Exhaustion and Altered Unconventional T Cell Generation Characterize Human Adenosine Deaminase Type 2 DeficiencyJin Yan Yap, Leen Moens, Ming-Wei Lin, et al.
Journal of Clinical Immunology|September 19, 2024
Correction to: A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented AncestriesAimee Huynh, Paul E Gray, Anna Sullivan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2019
A deep intronic splice mutation of <i>STAT3</i> underlies hyper IgE syndrome by negative dominanceJoëlle Khourieh, Geetha Rao, Tanwir Habib, et al.
Journal of Clinical Immunology|December 12, 2017
The 2017 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Capucine Picard, et al.
Pageof 29

Showing results (191-200 of 284) with videos related to

Sort By:
Pageof 29
The Journal of Experimental Medicine|June 23, 2021
High Th2 cytokine levels and upper airway inflammation in human inherited T-bet deficiencyRui Yang, Marc Weisshaar, Federico Mele, et al.
Journal of Clinical Immunology|December 12, 2017
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of ImmunityCapucine Picard, H Bobby Gaspar, Waleed Al-Herz, et al.
Journal of Clinical Immunology|March 7, 2019
Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil DysfunctionLeen Moens, Mieke Gouwy, Barbara Bosch, et al.
The Journal of Allergy and Clinical Immunology|August 25, 2016
Dedicator of cytokinesis 8-deficient CD4<sup>+</sup> T cells are biased to a T<sub>H</sub>2 effector fate at the expense of T<sub>H</sub>1 and T<sub>H</sub>17 cellsStuart G Tangye, Bethany Pillay, Katrina L Randall, et al.
Journal of Clinical Immunology|June 21, 2020
Everolimus-Induced Remission of Classic Kaposi's Sarcoma Secondary to Cryptic Splicing Mediated CTLA4 HaploinsufficiencyJin Yan Yap, Brian Gloss, Marcel Batten, et al.
Science Translational Medicine|February 16, 2018
Circulating T<sub>FH</sub> cells, serological memory, and tissue compartmentalization shape human influenza-specific B cell immunityMarios Koutsakos, Adam K Wheatley, Liyen Loh, et al.
Journal of Clinical Immunology|October 17, 2021
Intrinsic Defects in B Cell Development and Differentiation, T Cell Exhaustion and Altered Unconventional T Cell Generation Characterize Human Adenosine Deaminase Type 2 DeficiencyJin Yan Yap, Leen Moens, Ming-Wei Lin, et al.
Journal of Clinical Immunology|September 19, 2024
Correction to: A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented AncestriesAimee Huynh, Paul E Gray, Anna Sullivan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2019
A deep intronic splice mutation of <i>STAT3</i> underlies hyper IgE syndrome by negative dominanceJoëlle Khourieh, Geetha Rao, Tanwir Habib, et al.
Journal of Clinical Immunology|December 12, 2017
The 2017 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Capucine Picard, et al.
Pageof 29