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Ulrich Salzer

Showing results (91-100 of 121) with videos related to

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Blood|July 22, 2018
A novel disease-causing synonymous exonic mutation in <i>GATA2</i> affecting RNA splicingClaudia Wehr, Katja Grotius, Silvia Casadei, 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.
BMC Immunology|February 8, 2008
Screening of functional and positional candidate genes in families with common variable immunodeficiencyUlrich Salzer, Carla Neumann, Jens Thiel, et al.
Journal of Thrombosis and Thrombolysis|December 14, 2021
Complement system component dysregulation is a distinctive feature of COVID-19 disease: a prospective and comparative analysis of patients admitted to the emergency department for suspected COVID-19 diseaseNadine Gauchel, Marina Rieder, Krystin Krauel, et al.
Journal of Clinical Immunology|June 16, 2021
Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell TransplantationAndrea Meinhardt, Paula C Ramos, R Jürgen Dohmen, et al.
EMBO Reports|September 14, 2014
Direct interaction of actin filaments with F-BAR protein pacsin2Julius Kostan, Ulrich Salzer, Albina Orlova, et al.
Nature Genetics|May 2, 2006
Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive diseaseTony Roscioli, Simon T Cliffe, Donald B Bloch, et al.
Blood|October 17, 2015
Gray platelet syndrome can mimic autoimmune lymphoproliferative syndromeAnne Rensing-Ehl, Ulrich Pannicke, Stefanie-Yvonne Zimmermann, et al.
The New England Journal of Medicine|October 30, 2009
A homozygous CARD9 mutation in a family with susceptibility to fungal infectionsErik-Oliver Glocker, Andre Hennigs, Mohammad Nabavi, et al.
The Journal of Allergy and Clinical Immunology|February 24, 2015
β2-Microglobulin deficiency causes a complex immunodeficiency of the innate and adaptive immune systemÖmür Ardeniz, Susanne Unger, Hüseyin Onay, et al.
Pageof 13

Showing results (91-100 of 121) with videos related to

Sort By:
Pageof 13
Blood|July 22, 2018
A novel disease-causing synonymous exonic mutation in <i>GATA2</i> affecting RNA splicingClaudia Wehr, Katja Grotius, Silvia Casadei, 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.
BMC Immunology|February 8, 2008
Screening of functional and positional candidate genes in families with common variable immunodeficiencyUlrich Salzer, Carla Neumann, Jens Thiel, et al.
Journal of Thrombosis and Thrombolysis|December 14, 2021
Complement system component dysregulation is a distinctive feature of COVID-19 disease: a prospective and comparative analysis of patients admitted to the emergency department for suspected COVID-19 diseaseNadine Gauchel, Marina Rieder, Krystin Krauel, et al.
Journal of Clinical Immunology|June 16, 2021
Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell TransplantationAndrea Meinhardt, Paula C Ramos, R Jürgen Dohmen, et al.
EMBO Reports|September 14, 2014
Direct interaction of actin filaments with F-BAR protein pacsin2Julius Kostan, Ulrich Salzer, Albina Orlova, et al.
Nature Genetics|May 2, 2006
Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive diseaseTony Roscioli, Simon T Cliffe, Donald B Bloch, et al.
Blood|October 17, 2015
Gray platelet syndrome can mimic autoimmune lymphoproliferative syndromeAnne Rensing-Ehl, Ulrich Pannicke, Stefanie-Yvonne Zimmermann, et al.
The New England Journal of Medicine|October 30, 2009
A homozygous CARD9 mutation in a family with susceptibility to fungal infectionsErik-Oliver Glocker, Andre Hennigs, Mohammad Nabavi, et al.
The Journal of Allergy and Clinical Immunology|February 24, 2015
β2-Microglobulin deficiency causes a complex immunodeficiency of the innate and adaptive immune systemÖmür Ardeniz, Susanne Unger, Hüseyin Onay, et al.
Pageof 13