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Mathijs Willemsen

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Frontiers in Immunology|June 3, 2024
OTULIN haploinsufficiency predisposes to environmentally directed inflammationFrederik Staels, Leoni Bücken, Leana De Vuyst, et al.
Journal of Cachexia, Sarcopenia and Muscle|June 10, 2022
A disease-associated missense mutation in CYP4F3 affects the metabolism of leukotriene B4 via disruption of electron transferElien Smeets, Shengyun Huang, Xiao Yin Lee, et al.
The Journal of Allergy and Clinical Immunology|February 25, 2023
Homozygous DBF4 mutation as a cause of severe congenital neutropeniaMathijs Willemsen, John S Barber, Erika Van Nieuwenhove, et al.
Frontiers in Immunology|October 7, 2022
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous <i>NFKB1</i> mutationsFrederik Staels, Kerstin De Keukeleere, Matias Kinnunen, et al.
Cellular & Molecular Immunology|December 5, 2022
Author Correction: Disrupted Ca<sup>2+</sup> homeostasis and immunodeficiency in patients with functional IP<sub>3</sub> receptor subtype 3 defectsJulika Neumann, Erika Van Nieuwenhove, Lara E Terry, et al.
Cellular & Molecular Immunology|October 27, 2022
Disrupted Ca<sup>2+</sup> homeostasis and immunodeficiency in patients with functional IP<sub>3</sub> receptor subtype 3 defectsJulika Neumann, Erika Van Nieuwenhove, Lara E Terry, et al.
Journal of Clinical Immunology|December 15, 2023
Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn SyndromeMaria Rodrigo Riestra, Bethany A Pillay, Mathijs Willemsen, et al.
NPJ Vaccines|July 2, 2025
Systems vaccinology identifies immunological correlates of SARS-CoV-2 vaccine response in solid organ transplant recipientsNicolas Gemander, Julika Neumann, Rafael Veiga, et al.
The Journal of Allergy and Clinical Immunology|April 24, 2020
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropeniaErika Van Nieuwenhove, John S Barber, Julika Neumann, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Frontiers in Immunology|June 3, 2024
OTULIN haploinsufficiency predisposes to environmentally directed inflammationFrederik Staels, Leoni Bücken, Leana De Vuyst, et al.
Journal of Cachexia, Sarcopenia and Muscle|June 10, 2022
A disease-associated missense mutation in CYP4F3 affects the metabolism of leukotriene B4 via disruption of electron transferElien Smeets, Shengyun Huang, Xiao Yin Lee, et al.
The Journal of Allergy and Clinical Immunology|February 25, 2023
Homozygous DBF4 mutation as a cause of severe congenital neutropeniaMathijs Willemsen, John S Barber, Erika Van Nieuwenhove, et al.
Frontiers in Immunology|October 7, 2022
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous <i>NFKB1</i> mutationsFrederik Staels, Kerstin De Keukeleere, Matias Kinnunen, et al.
Cellular & Molecular Immunology|December 5, 2022
Author Correction: Disrupted Ca<sup>2+</sup> homeostasis and immunodeficiency in patients with functional IP<sub>3</sub> receptor subtype 3 defectsJulika Neumann, Erika Van Nieuwenhove, Lara E Terry, et al.
Cellular & Molecular Immunology|October 27, 2022
Disrupted Ca<sup>2+</sup> homeostasis and immunodeficiency in patients with functional IP<sub>3</sub> receptor subtype 3 defectsJulika Neumann, Erika Van Nieuwenhove, Lara E Terry, et al.
Journal of Clinical Immunology|December 15, 2023
Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn SyndromeMaria Rodrigo Riestra, Bethany A Pillay, Mathijs Willemsen, et al.
NPJ Vaccines|July 2, 2025
Systems vaccinology identifies immunological correlates of SARS-CoV-2 vaccine response in solid organ transplant recipientsNicolas Gemander, Julika Neumann, Rafael Veiga, et al.
The Journal of Allergy and Clinical Immunology|April 24, 2020
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropeniaErika Van Nieuwenhove, John S Barber, Julika Neumann, et al.
Pageof 3