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Aziz Bousfiha

Showing results (121-130 of 152) with videos related to

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The Journal of Experimental Medicine|March 8, 2022
A partial form of inherited human USP18 deficiency underlies infection and inflammationMarta Martin-Fernandez, Sofija Buta, Tom Le Voyer, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2016
Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variantsReiko Kagawa, Ryoji Fujiki, Miyuki Tsumura, et al.
Expert Review of Clinical Immunology|July 29, 2020
Global systematic review of primary immunodeficiency registriesHassan Abolhassani, Gholamreza Azizi, Laleh Sharifi, et al.
Journal of Clinical Immunology|March 3, 2016
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK MutationsZahra Aadam, Nadia Kechout, Abdelhamid Barakat, et al.
BMC Infectious Diseases|April 26, 2026
Etiology, prevalence, and mortality of sepsis among children under five years in Africa: a systematic review and meta-analysisCheickna Hamallah Dicko, Deprince Nakensy N'Dri, Malak Snoussi, et al.
The Journal of Experimental Medicine|December 5, 2025
Autoantibodies neutralizing type I IFNs in patients with fulminant herpes simplex virus hepatitisAdrian Gervais, Astrid Marchal, Soraya Boucherit, et al.
Blood|April 27, 2016
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotypeJulie Toubiana, Satoshi Okada, Julia Hiller, et al.
Genome Medicine|October 15, 2025
A human YEATS4 variant confers resistance to TST and IGRA conversion despite Mycobacterium tuberculosis exposureClément Conil, Jonathan Bohlen, Elouise E Kroon, et al.
The Journal of Experimental Medicine|September 21, 2016
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutationsYi 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 dominanceTakaki Asano, Joëlle Khourieh, Peng Zhang, et al.
Pageof 16

Showing results (121-130 of 152) with videos related to

Sort By:
Pageof 16
The Journal of Experimental Medicine|March 8, 2022
A partial form of inherited human USP18 deficiency underlies infection and inflammationMarta Martin-Fernandez, Sofija Buta, Tom Le Voyer, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2016
Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variantsReiko Kagawa, Ryoji Fujiki, Miyuki Tsumura, et al.
Expert Review of Clinical Immunology|July 29, 2020
Global systematic review of primary immunodeficiency registriesHassan Abolhassani, Gholamreza Azizi, Laleh Sharifi, et al.
Journal of Clinical Immunology|March 3, 2016
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK MutationsZahra Aadam, Nadia Kechout, Abdelhamid Barakat, et al.
BMC Infectious Diseases|April 26, 2026
Etiology, prevalence, and mortality of sepsis among children under five years in Africa: a systematic review and meta-analysisCheickna Hamallah Dicko, Deprince Nakensy N'Dri, Malak Snoussi, et al.
The Journal of Experimental Medicine|December 5, 2025
Autoantibodies neutralizing type I IFNs in patients with fulminant herpes simplex virus hepatitisAdrian Gervais, Astrid Marchal, Soraya Boucherit, et al.
Blood|April 27, 2016
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotypeJulie Toubiana, Satoshi Okada, Julia Hiller, et al.
Genome Medicine|October 15, 2025
A human YEATS4 variant confers resistance to TST and IGRA conversion despite Mycobacterium tuberculosis exposureClément Conil, Jonathan Bohlen, Elouise E Kroon, et al.
The Journal of Experimental Medicine|September 21, 2016
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutationsYi 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 dominanceTakaki Asano, Joëlle Khourieh, Peng Zhang, et al.
Pageof 16