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Anne Durandy

Showing results (91-100 of 104) with videos related to

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Blood|October 26, 2013
IL-21 signalling via STAT3 primes human naive B cells to respond to IL-2 to enhance their differentiation into plasmablastsLucinda J Berglund, Danielle T Avery, Cindy S Ma, et al.
The Journal of Clinical Investigation|October 5, 2016
Decreased somatic hypermutation induces an impaired peripheral B cell tolerance checkpointTineke Cantaert, Jean-Nicolas Schickel, Jason M Bannock, et al.
The Journal of Allergy and Clinical Immunology|July 9, 2013
Signal transducer and activator of transcription 3 (STAT3) mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8(+) T-cell memory formation and functionMegan L Ives, Cindy S Ma, Umaimainthan Palendira, et al.
The Journal of Allergy and Clinical Immunology|July 14, 2016
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) geneChantal Lagresle-Peyrou, Sonia Luce, Farid Ouchani, et al.
The Journal of Experimental Medicine|November 13, 2013
Naive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cellsElissa K Deenick, Danielle T Avery, Anna Chan, et al.
Journal of Clinical Immunology|April 30, 2021
Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor DeficiencyDeniz Cagdas, Daniel Mayr, Safa Baris, et al.
The Journal of Experimental Medicine|July 5, 2006
X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 productionOrchidée Filipe-Santos, Jacinta Bustamante, Margje H Haverkamp, et al.
The Journal of Allergy and Clinical Immunology|December 14, 2011
Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemiaRomain Micol, Samer Kayal, Nizar Mahlaoui, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2016
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort studyElodie Elkaim, Benedicte Neven, Julie Bruneau, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
Blood|October 26, 2013
IL-21 signalling via STAT3 primes human naive B cells to respond to IL-2 to enhance their differentiation into plasmablastsLucinda J Berglund, Danielle T Avery, Cindy S Ma, et al.
The Journal of Clinical Investigation|October 5, 2016
Decreased somatic hypermutation induces an impaired peripheral B cell tolerance checkpointTineke Cantaert, Jean-Nicolas Schickel, Jason M Bannock, et al.
The Journal of Allergy and Clinical Immunology|July 9, 2013
Signal transducer and activator of transcription 3 (STAT3) mutations underlying autosomal dominant hyper-IgE syndrome impair human CD8(+) T-cell memory formation and functionMegan L Ives, Cindy S Ma, Umaimainthan Palendira, et al.
The Journal of Allergy and Clinical Immunology|July 14, 2016
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) geneChantal Lagresle-Peyrou, Sonia Luce, Farid Ouchani, et al.
The Journal of Experimental Medicine|November 13, 2013
Naive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cellsElissa K Deenick, Danielle T Avery, Anna Chan, et al.
Journal of Clinical Immunology|April 30, 2021
Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor DeficiencyDeniz Cagdas, Daniel Mayr, Safa Baris, et al.
The Journal of Experimental Medicine|July 5, 2006
X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 productionOrchidée Filipe-Santos, Jacinta Bustamante, Margje H Haverkamp, et al.
The Journal of Allergy and Clinical Immunology|December 14, 2011
Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemiaRomain Micol, Samer Kayal, Nizar Mahlaoui, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2016
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort studyElodie Elkaim, Benedicte Neven, Julie Bruneau, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Pageof 11