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Ulrich Salzer

Showing results (111-120 of 121) with videos related to

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The New England Journal of Medicine|November 6, 2009
Inflammatory bowel disease and mutations affecting the interleukin-10 receptorErik-Oliver Glocker, Daniel Kotlarz, Kaan Boztug, et al.
American Journal of Human Genetics|May 22, 2012
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunityGabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarström, et al.
Blood|November 5, 2008
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromesUlrich Salzer, Chiara Bacchelli, Sylvie Buckridge, et al.
The Journal of Experimental Medicine|May 21, 2024
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
The Journal of Experimental Medicine|May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
Nature Medicine|October 21, 2014
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutationsDesirée Schubert, Claudia Bode, Rupert Kenefeck, et al.
Nature Communications|April 21, 2015
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cellsJin Li, Silje F Jørgensen, S Melkorka Maggadottir, et al.
Blood Cancer Journal|July 15, 2025
Age-dependent phenotypic and molecular evolution of pediatric MDS arising from GATA2 deficiencyLili Kotmayer, Emilia J Kozyra, Guolian Kang, et al.
Science Immunology|October 8, 2021
The expansion of human T-bet<sup>high</sup>CD21<sup>low</sup> B cells is T cell dependentBaerbel Keller, Valentina Strohmeier, Ina Harder, et al.
The Journal of Allergy and Clinical Immunology|May 7, 2018
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjectsCharlotte Schwab, Annemarie Gabrysch, Peter Olbrich, et al.
Pageof 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
The New England Journal of Medicine|November 6, 2009
Inflammatory bowel disease and mutations affecting the interleukin-10 receptorErik-Oliver Glocker, Daniel Kotlarz, Kaan Boztug, et al.
American Journal of Human Genetics|May 22, 2012
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunityGabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarström, et al.
Blood|November 5, 2008
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromesUlrich Salzer, Chiara Bacchelli, Sylvie Buckridge, et al.
The Journal of Experimental Medicine|May 21, 2024
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
The Journal of Experimental Medicine|May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
Nature Medicine|October 21, 2014
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutationsDesirée Schubert, Claudia Bode, Rupert Kenefeck, et al.
Nature Communications|April 21, 2015
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cellsJin Li, Silje F Jørgensen, S Melkorka Maggadottir, et al.
Blood Cancer Journal|July 15, 2025
Age-dependent phenotypic and molecular evolution of pediatric MDS arising from GATA2 deficiencyLili Kotmayer, Emilia J Kozyra, Guolian Kang, et al.
Science Immunology|October 8, 2021
The expansion of human T-bet<sup>high</sup>CD21<sup>low</sup> B cells is T cell dependentBaerbel Keller, Valentina Strohmeier, Ina Harder, et al.
The Journal of Allergy and Clinical Immunology|May 7, 2018
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjectsCharlotte Schwab, Annemarie Gabrysch, Peter Olbrich, et al.
Pageof 13