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The Journal of Allergy and Clinical Immunology
|
April 26, 2022
STAT5B restrains human B-cell differentiation to maintain humoral immune homeostasis
Simon J Pelham, Maria Soledad Caldirola, Danielle T Avery, et al.
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
|
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.
The Journal of Experimental Medicine
|
November 3, 2022
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis
Masato Ogishi, Rui Yang, Rémy Rodriguez, et al.
The Journal of Allergy and Clinical Immunology
|
July 12, 2015
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies
Cindy S Ma, Natalie Wong, Geetha Rao, et al.
Science Immunology
|
May 30, 2025
Human LY9 governs CD4<sup>+</sup> T cell IFN-γ immunity to <i>Mycobacterium tuberculosis</i>
Masato Ogishi, Julia Puchan, Rui Yang, et al.
Nature Medicine
|
June 29, 2021
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child
Masato Ogishi, Rui Yang, Caner Aytekin, et al.
Science Immunology
|
June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
Vivien Béziat, Juan Li, Jian-Xin Lin, et al.
Immunity
|
November 27, 2024
Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling
Masato Ogishi, Koji Kitaoka, Kim L Good-Jacobson, et al.
Nature
|
August 28, 2024
Tuberculosis in otherwise healthy adults with inherited TNF deficiency
Andrés A Arias, Anna-Lena Neehus, Masato Ogishi, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
The Journal of Allergy and Clinical Immunology
|
April 26, 2022
STAT5B restrains human B-cell differentiation to maintain humoral immune homeostasis
Simon J Pelham, Maria Soledad Caldirola, Danielle T Avery, et al.
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
|
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.
The Journal of Experimental Medicine
|
November 3, 2022
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis
Masato Ogishi, Rui Yang, Rémy Rodriguez, et al.
The Journal of Allergy and Clinical Immunology
|
July 12, 2015
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies
Cindy S Ma, Natalie Wong, Geetha Rao, et al.
Science Immunology
|
May 30, 2025
Human LY9 governs CD4<sup>+</sup> T cell IFN-γ immunity to <i>Mycobacterium tuberculosis</i>
Masato Ogishi, Julia Puchan, Rui Yang, et al.
Nature Medicine
|
June 29, 2021
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child
Masato Ogishi, Rui Yang, Caner Aytekin, et al.
Science Immunology
|
June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
Vivien Béziat, Juan Li, Jian-Xin Lin, et al.
Immunity
|
November 27, 2024
Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling
Masato Ogishi, Koji Kitaoka, Kim L Good-Jacobson, et al.
Nature
|
August 28, 2024
Tuberculosis in otherwise healthy adults with inherited TNF deficiency
Andrés A Arias, Anna-Lena Neehus, Masato Ogishi, et al.
Page
of 3