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The Journal of Experimental Medicine
|
June 17, 2021
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
Takaki Asano, Joëlle Khourieh, Peng Zhang, et al.
The Journal of Experimental Medicine
|
August 26, 2018
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency
Nicholas Hernandez, Isabelle Melki, Huie Jing, et al.
The Journal of Allergy and Clinical Immunology
|
March 2, 2019
F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects
Enrica Calzoni, Craig D Platt, Sevgi Keles, et al.
Biorxiv : the Preprint Server for Biology
|
August 12, 2024
Mechanism of neurodegeneration mediated by clonal inflammatory microglia
Rocio Vicario, Stamatina Fragkogianni, Maria Pokrovskii, et al.
Science Immunology
|
July 22, 2022
Human T-bet governs the generation of a distinct subset of CD11c<sup>high</sup>CD21<sup>low</sup> B cells
Rui Yang, Danielle T Avery, Katherine J L Jackson, et al.
Neuron
|
March 13, 2025
Role of clonal inflammatory microglia in histiocytosis-associated neurodegeneration
Rocio Vicario, Stamatina Fragkogianni, Maria Pokrovskii, et al.
The Journal of Experimental Medicine
|
September 2, 2021
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency
Juan Li, Wei-Te Lei, Peng Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 4, 2018
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated <i>RPSA</i> exons
Alexandre Bolze, Bertrand Boisson, Barbara Bosch, et al.
Cell Reports
|
May 14, 2020
Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions
Marta Martin-Fernandez, María Bravo García-Morato, Conor Gruber, et al.
Journal of Human Immunity
|
November 26, 2025
Novel genotypes, phenotypes, and triggers in humans with OTULIN haploinsufficiency
Tristan J van der Linden, Rob J W Arts, Catherine M Biggs, et al.
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of 16
Search research articles
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Showing results (101-110 of 154) with videos related to
Sort By:
Page
of 16
The Journal of Experimental Medicine
|
June 17, 2021
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
Takaki Asano, Joëlle Khourieh, Peng Zhang, et al.
The Journal of Experimental Medicine
|
August 26, 2018
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency
Nicholas Hernandez, Isabelle Melki, Huie Jing, et al.
The Journal of Allergy and Clinical Immunology
|
March 2, 2019
F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects
Enrica Calzoni, Craig D Platt, Sevgi Keles, et al.
Biorxiv : the Preprint Server for Biology
|
August 12, 2024
Mechanism of neurodegeneration mediated by clonal inflammatory microglia
Rocio Vicario, Stamatina Fragkogianni, Maria Pokrovskii, et al.
Science Immunology
|
July 22, 2022
Human T-bet governs the generation of a distinct subset of CD11c<sup>high</sup>CD21<sup>low</sup> B cells
Rui Yang, Danielle T Avery, Katherine J L Jackson, et al.
Neuron
|
March 13, 2025
Role of clonal inflammatory microglia in histiocytosis-associated neurodegeneration
Rocio Vicario, Stamatina Fragkogianni, Maria Pokrovskii, et al.
The Journal of Experimental Medicine
|
September 2, 2021
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency
Juan Li, Wei-Te Lei, Peng Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 4, 2018
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated <i>RPSA</i> exons
Alexandre Bolze, Bertrand Boisson, Barbara Bosch, et al.
Cell Reports
|
May 14, 2020
Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions
Marta Martin-Fernandez, María Bravo García-Morato, Conor Gruber, et al.
Journal of Human Immunity
|
November 26, 2025
Novel genotypes, phenotypes, and triggers in humans with OTULIN haploinsufficiency
Tristan J van der Linden, Rob J W Arts, Catherine M Biggs, et al.
Page
of 16