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Anne Puel

Showing results (201-210 of 296) with videos related to

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Nature|January 1, 2025
Monoallelic expression can govern penetrance of inborn errors of immunityO'Jay Stewart, Conor Gruber, Haley E Randolph, et al.
Nature Communications|August 1, 2023
Genetic inhibition of CARD9 accelerates the development of atherosclerosis in mice through CD36 dependent-defective autophagyYujiao Zhang, Marie Vandestienne, Jean-Rémi Lavillegrand, et al.
Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.
Science (New York, N.Y.)|March 15, 2003
Pyogenic bacterial infections in humans with IRAK-4 deficiencyCapucine Picard, Anne Puel, Marion Bonnet, et al.
Journal of Clinical Immunology|March 9, 2016
Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive SurveyTracy A Briggs, Gillian I Rice, Navid Adib, et al.
Nature Immunology|February 1, 2011
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial diseaseJacinta Bustamante, Andres A Arias, Guillaume Vogt, et al.
Science (New York, N.Y.)|September 18, 2007
TLR3 deficiency in patients with herpes simplex encephalitisShen-Ying Zhang, Emmanuelle Jouanguy, Sophie Ugolini, et al.
The New England Journal of Medicine|October 18, 2013
Deep dermatophytosis and inherited CARD9 deficiencyFanny Lanternier, Saad Pathan, Quentin B Vincent, et al.
Nature Immunology|October 30, 2012
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiencyBertrand Boisson, Emmanuel Laplantine, Carolina Prando, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulationQuentin Riller, Boris Sorin, Charline Courteille, et al.
Pageof 30

Showing results (201-210 of 296) with videos related to

Sort By:
Pageof 30
Nature|January 1, 2025
Monoallelic expression can govern penetrance of inborn errors of immunityO'Jay Stewart, Conor Gruber, Haley E Randolph, et al.
Nature Communications|August 1, 2023
Genetic inhibition of CARD9 accelerates the development of atherosclerosis in mice through CD36 dependent-defective autophagyYujiao Zhang, Marie Vandestienne, Jean-Rémi Lavillegrand, et al.
Nature Communications|June 22, 2023
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signalingCristiane J Nunes-Santos, HyeSun Kuehn, Brigette Boast, et al.
Science (New York, N.Y.)|March 15, 2003
Pyogenic bacterial infections in humans with IRAK-4 deficiencyCapucine Picard, Anne Puel, Marion Bonnet, et al.
Journal of Clinical Immunology|March 9, 2016
Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive SurveyTracy A Briggs, Gillian I Rice, Navid Adib, et al.
Nature Immunology|February 1, 2011
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial diseaseJacinta Bustamante, Andres A Arias, Guillaume Vogt, et al.
Science (New York, N.Y.)|September 18, 2007
TLR3 deficiency in patients with herpes simplex encephalitisShen-Ying Zhang, Emmanuelle Jouanguy, Sophie Ugolini, et al.
The New England Journal of Medicine|October 18, 2013
Deep dermatophytosis and inherited CARD9 deficiencyFanny Lanternier, Saad Pathan, Quentin B Vincent, et al.
Nature Immunology|October 30, 2012
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiencyBertrand Boisson, Emmanuel Laplantine, Carolina Prando, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulationQuentin Riller, Boris Sorin, Charline Courteille, et al.
Pageof 30