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Anne Puel

Showing results (131-140 of 296) with videos related to

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Biorxiv : the Preprint Server for Biology|January 14, 2021
SARS-CoV-2 induces human plasmacytoid pre-dendritic cell diversification via UNC93B and IRAK4Fanny Onodi, Lucie Bonnet-Madin, Laurent Meertens, et al.
The Pediatric Infectious Disease Journal|February 19, 2008
Cutaneous infection with Metarhizium anisopliae in a patient with hypohidrotic ectodermal dysplasia and immune deficiencyRebecca A Marsh, Anne W Lucky, Thomas J Walsh, et al.
American Journal of Human Genetics|March 15, 2006
The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translationAnne Puel, Janine Reichenbach, Jacinta Bustamante, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 2022
Genome-wide detection of human variants that disrupt intronic branchpointsPeng Zhang, Quentin Philippot, Weicheng Ren, et al.
Journal of Clinical Immunology|March 11, 2016
Chronic and Invasive Fungal Infections in a Family with CARD9 DeficiencyAna Karina Alves de Medeiros, Evelyn Lodewick, Delfien J A Bogaert, et al.
Journal of Clinical Immunology|February 9, 2021
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic SiblingsYusuke Imanaka, Maki Taniguchi, Takehiko Doi, et al.
Journal of Clinical Immunology|October 21, 2020
IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 ReactivationShiho Nishimura, Yoshiyuki Kobayashi, Hidenori Ohnishi, et al.
Journal of Clinical Immunology|April 27, 2016
Erratum to: Chronic and Invasive Fungal Infections in a Family with CARD9 DeficiencyAna Karina Alves de Medeiros, Evelyn Lodewick, Delfien J A Bogaert, et al.
Intensive Care Medicine Experimental|November 26, 2025
Impaired serum neutralization and death in Omicron-infected critically ill patients: insights from the French SEVARVIR prospective, multicenter cohort studyTimothée Bruel, Isabelle Staropoli, Pierre Bay, et al.
American Journal of Human Genetics|November 27, 2010
Whole-exome-sequencing-based discovery of human FADD deficiencyAlexandre Bolze, Minji Byun, David McDonald, et al.
Pageof 30

Showing results (131-140 of 296) with videos related to

Sort By:
Pageof 30
Biorxiv : the Preprint Server for Biology|January 14, 2021
SARS-CoV-2 induces human plasmacytoid pre-dendritic cell diversification via UNC93B and IRAK4Fanny Onodi, Lucie Bonnet-Madin, Laurent Meertens, et al.
The Pediatric Infectious Disease Journal|February 19, 2008
Cutaneous infection with Metarhizium anisopliae in a patient with hypohidrotic ectodermal dysplasia and immune deficiencyRebecca A Marsh, Anne W Lucky, Thomas J Walsh, et al.
American Journal of Human Genetics|March 15, 2006
The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translationAnne Puel, Janine Reichenbach, Jacinta Bustamante, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 2022
Genome-wide detection of human variants that disrupt intronic branchpointsPeng Zhang, Quentin Philippot, Weicheng Ren, et al.
Journal of Clinical Immunology|March 11, 2016
Chronic and Invasive Fungal Infections in a Family with CARD9 DeficiencyAna Karina Alves de Medeiros, Evelyn Lodewick, Delfien J A Bogaert, et al.
Journal of Clinical Immunology|February 9, 2021
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic SiblingsYusuke Imanaka, Maki Taniguchi, Takehiko Doi, et al.
Journal of Clinical Immunology|October 21, 2020
IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 ReactivationShiho Nishimura, Yoshiyuki Kobayashi, Hidenori Ohnishi, et al.
Journal of Clinical Immunology|April 27, 2016
Erratum to: Chronic and Invasive Fungal Infections in a Family with CARD9 DeficiencyAna Karina Alves de Medeiros, Evelyn Lodewick, Delfien J A Bogaert, et al.
Intensive Care Medicine Experimental|November 26, 2025
Impaired serum neutralization and death in Omicron-infected critically ill patients: insights from the French SEVARVIR prospective, multicenter cohort studyTimothée Bruel, Isabelle Staropoli, Pierre Bay, et al.
American Journal of Human Genetics|November 27, 2010
Whole-exome-sequencing-based discovery of human FADD deficiencyAlexandre Bolze, Minji Byun, David McDonald, et al.
Pageof 30