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Anne Puel

Showing results (181-190 of 296) with videos related to

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Journal of Clinical Immunology|June 21, 2023
Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE SyndromeTiphaine Arlabosse, Marie Materna, Orbicia Riccio, et al.
Frontiers in Immunology|November 16, 2018
A <i>CARD9</i> Founder Mutation Disrupts NF-κB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome FormationMarieke De Bruyne, Levi Hoste, Delfien J Bogaert, et al.
The Journal of Clinical Investigation|November 14, 2018
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiencyBertrand Boisson, Yoshitaka Honda, Masahiko Ajiro, et al.
The Journal of Experimental Medicine|June 5, 2023
Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunityKunihiko Moriya, Tomohiro Nakano, Yoshitaka Honda, et al.
Journal of Clinical Immunology|June 24, 2020
Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down SyndromeXiao-Fei Kong, Lisa Worley, Darawan Rinchai, et al.
The Journal of Infectious Diseases|July 25, 2014
Inherited CARD9 deficiency in 2 unrelated patients with invasive Exophiala infectionFanny Lanternier, Elisa Barbati, Ulrich Meinzer, et al.
Science (New York, N.Y.)|September 16, 2006
Herpes simplex virus encephalitis in human UNC-93B deficiencyArmanda Casrouge, Shen-Ying Zhang, Céline Eidenschenk, 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.
Journal of Clinical Immunology|September 29, 2018
Early-Onset Invasive Infection Due to Corynespora cassiicola Associated with Compound Heterozygous CARD9 Mutations in a Colombian PatientCarlos A Arango-Franco, Marcela Moncada-Vélez, Claudia Patricia Beltrán, et al.
Cell|March 12, 2017
Systemic Human ILC Precursors Provide a Substrate for Tissue ILC DifferentiationAi Ing Lim, Yan Li, Silvia Lopez-Lastra, et al.
Pageof 30

Showing results (181-190 of 296) with videos related to

Sort By:
Pageof 30
Journal of Clinical Immunology|June 21, 2023
Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE SyndromeTiphaine Arlabosse, Marie Materna, Orbicia Riccio, et al.
Frontiers in Immunology|November 16, 2018
A <i>CARD9</i> Founder Mutation Disrupts NF-κB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome FormationMarieke De Bruyne, Levi Hoste, Delfien J Bogaert, et al.
The Journal of Clinical Investigation|November 14, 2018
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiencyBertrand Boisson, Yoshitaka Honda, Masahiko Ajiro, et al.
The Journal of Experimental Medicine|June 5, 2023
Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunityKunihiko Moriya, Tomohiro Nakano, Yoshitaka Honda, et al.
Journal of Clinical Immunology|June 24, 2020
Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down SyndromeXiao-Fei Kong, Lisa Worley, Darawan Rinchai, et al.
The Journal of Infectious Diseases|July 25, 2014
Inherited CARD9 deficiency in 2 unrelated patients with invasive Exophiala infectionFanny Lanternier, Elisa Barbati, Ulrich Meinzer, et al.
Science (New York, N.Y.)|September 16, 2006
Herpes simplex virus encephalitis in human UNC-93B deficiencyArmanda Casrouge, Shen-Ying Zhang, Céline Eidenschenk, 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.
Journal of Clinical Immunology|September 29, 2018
Early-Onset Invasive Infection Due to Corynespora cassiicola Associated with Compound Heterozygous CARD9 Mutations in a Colombian PatientCarlos A Arango-Franco, Marcela Moncada-Vélez, Claudia Patricia Beltrán, et al.
Cell|March 12, 2017
Systemic Human ILC Precursors Provide a Substrate for Tissue ILC DifferentiationAi Ing Lim, Yan Li, Silvia Lopez-Lastra, et al.
Pageof 30