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Sven Kracker

Showing results (41-50 of 66) with videos related to

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Cell|February 21, 2012
Immune surveillance and therapy of lymphomas driven by Epstein-Barr virus protein LMP1 in a mouse modelBaochun Zhang, Sven Kracker, Tomoharu Yasuda, et al.
The Journal of Allergy and Clinical Immunology|October 15, 2014
An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complexSven Kracker, Michela Di Virgilio, Jeremy Schwartzentruber, et al.
Blood|March 5, 2020
Topoisomerase 2β mutation impairs early B-cell developmentOlivier Papapietro, Anita Chandra, Davide Eletto, et al.
Journal of Clinical Immunology|September 26, 2022
Lymphoma as an Exclusion Criteria for CVID Diagnosis RevisitedVincent Allain, Virginie Grandin, Véronique Meignin, et al.
The Journal of Clinical Investigation|December 7, 2018
Loss of ARHGEF1 causes a human primary antibody deficiencyAmine Bouafia, Sébastien Lofek, Julie Bruneau, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 12, 2017
IgG1 Is Required for Optimal Protection after Immunization with the Purified Porin OmpD from <i>Salmonella</i> TyphimuriumYang Zhang, Coral Dominguez-Medina, Nicola J Cumley, et al.
The Journal of Allergy and Clinical Immunology|May 12, 2015
Early-onset hypogammaglobulinemia: A survey of 44 patientsAnne C Brignier, Nizar Mahlaoui, Christian Reimann, et al.
Haematologica|April 22, 2017
Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)Lucie Heurtier, Hicham Lamrini, Loïc Chentout, et al.
Journal of Clinical Immunology|February 16, 2024
A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 SyndromeErika Della Mina, Katherine J L Jackson, Alexander J I Crawford, et al.
Blood Advances|January 27, 2019
Successful in utero stem cell transplantation in X-linked severe combined immunodeficiencyAlessandra Magnani, Jean-Marie Jouannic, Jérémie Rosain, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Cell|February 21, 2012
Immune surveillance and therapy of lymphomas driven by Epstein-Barr virus protein LMP1 in a mouse modelBaochun Zhang, Sven Kracker, Tomoharu Yasuda, et al.
The Journal of Allergy and Clinical Immunology|October 15, 2014
An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complexSven Kracker, Michela Di Virgilio, Jeremy Schwartzentruber, et al.
Blood|March 5, 2020
Topoisomerase 2β mutation impairs early B-cell developmentOlivier Papapietro, Anita Chandra, Davide Eletto, et al.
Journal of Clinical Immunology|September 26, 2022
Lymphoma as an Exclusion Criteria for CVID Diagnosis RevisitedVincent Allain, Virginie Grandin, Véronique Meignin, et al.
The Journal of Clinical Investigation|December 7, 2018
Loss of ARHGEF1 causes a human primary antibody deficiencyAmine Bouafia, Sébastien Lofek, Julie Bruneau, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 12, 2017
IgG1 Is Required for Optimal Protection after Immunization with the Purified Porin OmpD from <i>Salmonella</i> TyphimuriumYang Zhang, Coral Dominguez-Medina, Nicola J Cumley, et al.
The Journal of Allergy and Clinical Immunology|May 12, 2015
Early-onset hypogammaglobulinemia: A survey of 44 patientsAnne C Brignier, Nizar Mahlaoui, Christian Reimann, et al.
Haematologica|April 22, 2017
Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1)Lucie Heurtier, Hicham Lamrini, Loïc Chentout, et al.
Journal of Clinical Immunology|February 16, 2024
A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 SyndromeErika Della Mina, Katherine J L Jackson, Alexander J I Crawford, et al.
Blood Advances|January 27, 2019
Successful in utero stem cell transplantation in X-linked severe combined immunodeficiencyAlessandra Magnani, Jean-Marie Jouannic, Jérémie Rosain, et al.
Pageof 7