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Anne Durandy

Showing results (61-70 of 104) with videos related to

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Blood|May 6, 2011
Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LGStéphanie Rigaud, Eduardo Lopez-Granados, Sophie Sibéril, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 29, 2008
Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patientsChantal Lagresle-Peyrou, Fatine Benjelloun, Christophe Hue, et al.
Cell|January 28, 2006
Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephalyDietke Buck, Laurent Malivert, Régina de Chasseval, et al.
The Journal of Allergy and Clinical Immunology|April 5, 2014
Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndromeSven Kracker, James Curtis, Mohammad A A Ibrahim, et al.
The Journal of Allergy and Clinical Immunology|August 4, 2014
The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiencyStuart E Turvey, Anne Durandy, Alain Fischer, et al.
Blood|December 31, 2005
Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiencyKlaus Warnatz, Lukas Bossaller, Ulrich Salzer, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2011
Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humansGreta Meyers, Yen-Shing Ng, Jason M Bannock, et al.
The Journal of Experimental Medicine|March 14, 2023
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiencyRomane Thouenon, Loïc Chentout, Nidia Moreno-Corona, et al.
The Journal of Allergy and Clinical Immunology|May 2, 2015
Mild B-cell lymphocytosis in patients with a CARD11 C49Y mutationDavid Buchbinder, Jeffrey R Stinson, Diane J Nugent, 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.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
Blood|May 6, 2011
Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LGStéphanie Rigaud, Eduardo Lopez-Granados, Sophie Sibéril, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 29, 2008
Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patientsChantal Lagresle-Peyrou, Fatine Benjelloun, Christophe Hue, et al.
Cell|January 28, 2006
Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephalyDietke Buck, Laurent Malivert, Régina de Chasseval, et al.
The Journal of Allergy and Clinical Immunology|April 5, 2014
Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndromeSven Kracker, James Curtis, Mohammad A A Ibrahim, et al.
The Journal of Allergy and Clinical Immunology|August 4, 2014
The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiencyStuart E Turvey, Anne Durandy, Alain Fischer, et al.
Blood|December 31, 2005
Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiencyKlaus Warnatz, Lukas Bossaller, Ulrich Salzer, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2011
Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humansGreta Meyers, Yen-Shing Ng, Jason M Bannock, et al.
The Journal of Experimental Medicine|March 14, 2023
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiencyRomane Thouenon, Loïc Chentout, Nidia Moreno-Corona, et al.
The Journal of Allergy and Clinical Immunology|May 2, 2015
Mild B-cell lymphocytosis in patients with a CARD11 C49Y mutationDavid Buchbinder, Jeffrey R Stinson, Diane J Nugent, 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.
Pageof 11