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Astrid Bergbreiter

Showing results (1-10 of 6) with videos related to

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Expert Review of Clinical Immunology|May 19, 2010
Common variable immunodeficiency: a multifaceted and puzzling disorderAstrid Bergbreiter, Ulrich Salzer
Journal of Clinical Immunology|July 25, 2009
Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiencyJavad Mohammadi, Chonghai Liu, Asghar Aghamohammadi, et al.
Human Molecular Genetics|August 30, 2008
Genetic and physical interaction between the NPHP5 and NPHP6 gene productsTobias Schäfer, Michael Pütz, Soeren Lienkamp, et al.
European Journal of Medical Genetics|January 24, 2021
Recurrent necrotizing cellulitis, multi-organ autoimmune disease and humoral immunodeficiency due to a novel NFKB1 frameshift mutationAstrid Bergbreiter, Teresa Jaeger, Antje Karle, et al.
The Journal of Allergy and Clinical Immunology|November 1, 2011
Genetic CD21 deficiency is associated with hypogammaglobulinemiaJens Thiel, Lucas Kimmig, Ulrich Salzer, 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.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Expert Review of Clinical Immunology|May 19, 2010
Common variable immunodeficiency: a multifaceted and puzzling disorderAstrid Bergbreiter, Ulrich Salzer
Journal of Clinical Immunology|July 25, 2009
Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiencyJavad Mohammadi, Chonghai Liu, Asghar Aghamohammadi, et al.
Human Molecular Genetics|August 30, 2008
Genetic and physical interaction between the NPHP5 and NPHP6 gene productsTobias Schäfer, Michael Pütz, Soeren Lienkamp, et al.
European Journal of Medical Genetics|January 24, 2021
Recurrent necrotizing cellulitis, multi-organ autoimmune disease and humoral immunodeficiency due to a novel NFKB1 frameshift mutationAstrid Bergbreiter, Teresa Jaeger, Antje Karle, et al.
The Journal of Allergy and Clinical Immunology|November 1, 2011
Genetic CD21 deficiency is associated with hypogammaglobulinemiaJens Thiel, Lucas Kimmig, Ulrich Salzer, 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.
Pageof 1