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Showing results (591-600 of 613) with videos related to

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The Journal of Experimental Medicine|April 23, 2021
Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1Paul Bastard, Elizaveta Orlova, Leila Sozaeva, et al.
The Journal of Experimental Medicine|September 12, 2022
Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiencyMasato Ogishi, Andrés Augusto Arias, Rui Yang, et al.
The Journal of Experimental Medicine|September 16, 2022
Autoantibodies against type I IFNs in patients with critical influenza pneumoniaQian Zhang, Andrés Pizzorno, Lisa Miorin, et al.
Cell|May 3, 2024
FLT3L governs the development of partially overlapping hematopoietic lineages in humans and miceMana Momenilandi, Romain Lévy, Steicy Sobrino, et al.
Cell|December 29, 2023
Human inherited CCR2 deficiency underlies progressive polycystic lung diseaseAnna-Lena Neehus, Brenna Carey, Marija Landekic, et al.
The Journal of Experimental Medicine|December 14, 2022
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiencyRomain Lévy, Florian Gothe, Mana Momenilandi, et al.
The Journal of Clinical Investigation|October 1, 2024
IL-7-dependent and -independent lineages of IL-7R-dependent human T cellsCarlos A Arango-Franco, Masato Ogishi, Susanne Unger, et al.
Nature Immunology|January 16, 2026
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and functionTaja Vatovec, Anna-Lena Neehus, Katherine J L Jackson, et al.
Nature|August 28, 2024
Tuberculosis in otherwise healthy adults with inherited TNF deficiencyAndrés A Arias, Anna-Lena Neehus, Masato Ogishi, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Homozygosity for rare or common hypomorphic <i>IL23R</i> variants confers a predisposition to tuberculosis in humansDiana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.
Pageof 62

Showing results (591-600 of 613) with videos related to

Sort By:
Pageof 62
The Journal of Experimental Medicine|April 23, 2021
Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1Paul Bastard, Elizaveta Orlova, Leila Sozaeva, et al.
The Journal of Experimental Medicine|September 12, 2022
Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiencyMasato Ogishi, Andrés Augusto Arias, Rui Yang, et al.
The Journal of Experimental Medicine|September 16, 2022
Autoantibodies against type I IFNs in patients with critical influenza pneumoniaQian Zhang, Andrés Pizzorno, Lisa Miorin, et al.
Cell|May 3, 2024
FLT3L governs the development of partially overlapping hematopoietic lineages in humans and miceMana Momenilandi, Romain Lévy, Steicy Sobrino, et al.
Cell|December 29, 2023
Human inherited CCR2 deficiency underlies progressive polycystic lung diseaseAnna-Lena Neehus, Brenna Carey, Marija Landekic, et al.
The Journal of Experimental Medicine|December 14, 2022
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiencyRomain Lévy, Florian Gothe, Mana Momenilandi, et al.
The Journal of Clinical Investigation|October 1, 2024
IL-7-dependent and -independent lineages of IL-7R-dependent human T cellsCarlos A Arango-Franco, Masato Ogishi, Susanne Unger, et al.
Nature Immunology|January 16, 2026
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and functionTaja Vatovec, Anna-Lena Neehus, Katherine J L Jackson, et al.
Nature|August 28, 2024
Tuberculosis in otherwise healthy adults with inherited TNF deficiencyAndrés A Arias, Anna-Lena Neehus, Masato Ogishi, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Homozygosity for rare or common hypomorphic <i>IL23R</i> variants confers a predisposition to tuberculosis in humansDiana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.
Pageof 62