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Blood
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April 27, 2016
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
Julie Toubiana, Satoshi Okada, Julia Hiller, et al.
The Journal of Experimental Medicine
|
September 21, 2016
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations
Yi Wang, Cindy S Ma, Yun Ling, 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
|
December 5, 2025
Autoantibodies neutralizing type I IFNs in patients with fulminant herpes simplex virus hepatitis
Adrian Gervais, Astrid Marchal, Soraya Boucherit, et al.
The Journal of Experimental Medicine
|
September 24, 2024
Autoantibodies neutralizing type I IFNs underlie severe tick-borne encephalitis in ∼10% of patients
Adrian Gervais, Astrid Marchal, Andrea Fortova, et al.
The Journal of Experimental Medicine
|
March 10, 2026
The STING HAQ haplotype and clinical non-penetrance in COPA syndrome
Clémence David, Tifenn Wauquier, Alix de Becdelièvre, et al.
The Journal of Allergy and Clinical Immunology
|
February 24, 2015
Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species-induced meningoencephalitis, colitis, or both
Fanny Lanternier, Seyed Alireza Mahdaviani, Elisa Barbati, 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.
The Journal of Experimental Medicine
|
November 1, 2024
Auto-Abs neutralizing type I IFNs in patients with severe Powassan, Usutu, or Ross River virus disease
Adrian Gervais, Paul Bastard, Lucy Bizien, et al.
Journal of Clinical Immunology
|
July 12, 2018
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency
Jérémie Rosain, Carmen Oleaga-Quintas, Caroline Deswarte, et al.
Page
of 30
Search research articles
Search
Showing results (221-230 of 296) with videos related to
Sort By:
Page
of 30
Blood
|
April 27, 2016
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
Julie Toubiana, Satoshi Okada, Julia Hiller, et al.
The Journal of Experimental Medicine
|
September 21, 2016
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations
Yi Wang, Cindy S Ma, Yun Ling, 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
|
December 5, 2025
Autoantibodies neutralizing type I IFNs in patients with fulminant herpes simplex virus hepatitis
Adrian Gervais, Astrid Marchal, Soraya Boucherit, et al.
The Journal of Experimental Medicine
|
September 24, 2024
Autoantibodies neutralizing type I IFNs underlie severe tick-borne encephalitis in ∼10% of patients
Adrian Gervais, Astrid Marchal, Andrea Fortova, et al.
The Journal of Experimental Medicine
|
March 10, 2026
The STING HAQ haplotype and clinical non-penetrance in COPA syndrome
Clémence David, Tifenn Wauquier, Alix de Becdelièvre, et al.
The Journal of Allergy and Clinical Immunology
|
February 24, 2015
Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species-induced meningoencephalitis, colitis, or both
Fanny Lanternier, Seyed Alireza Mahdaviani, Elisa Barbati, 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.
The Journal of Experimental Medicine
|
November 1, 2024
Auto-Abs neutralizing type I IFNs in patients with severe Powassan, Usutu, or Ross River virus disease
Adrian Gervais, Paul Bastard, Lucy Bizien, et al.
Journal of Clinical Immunology
|
July 12, 2018
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency
Jérémie Rosain, Carmen Oleaga-Quintas, Caroline Deswarte, et al.
Page
of 30