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Mira Marie Laustsen

Showing results (1-10 of 5) with videos related to

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HLA|June 23, 2022
The novel HLA class I allele, HLA-B*14:110, identified by next-generation sequencingMira Marie Laustsen, Maja Nørgaard, Marie Quach Lam, et al.
Cancer Genetics|May 9, 2026
Novel truncating WT1 germline variant in a case of familial Wilms tumorMira Marie Laustsen, Ulrik Kristoffer Stoltze, Karen Bonde Larsen, et al.
Journal of Clinical Immunology|June 2, 2025
Genetics in a Danish Common Variable Immunodeficiency CohortCamilla Heldbjerg Drabe, Mira Marie Laustsen, Hanne Vibeke Marquart, et al.
Frontiers in Immunology|January 19, 2026
Case Report: Possible C3 nephritic factor-driven complement-mediated severe hemolytic anemia and acute kidney injury in a child with <i>Bordetella parapertussis</i> infectionSteffen Ullitz Thorsen, Anne Todsen Hansen, Hans Jakob Hartling, et al.
Journal of Clinical Immunology|June 8, 2026
Novel Partial Loss-of-function STAT3-variant as Cause of Hyper-IgE-Syndrome in a Danish Family with Variable ExpressivityCamilla Heldbjerg Drabe, Jonathan Gehrig, Jens Magnus Bernth Jensen, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
HLA|June 23, 2022
The novel HLA class I allele, HLA-B*14:110, identified by next-generation sequencingMira Marie Laustsen, Maja Nørgaard, Marie Quach Lam, et al.
Cancer Genetics|May 9, 2026
Novel truncating WT1 germline variant in a case of familial Wilms tumorMira Marie Laustsen, Ulrik Kristoffer Stoltze, Karen Bonde Larsen, et al.
Journal of Clinical Immunology|June 2, 2025
Genetics in a Danish Common Variable Immunodeficiency CohortCamilla Heldbjerg Drabe, Mira Marie Laustsen, Hanne Vibeke Marquart, et al.
Frontiers in Immunology|January 19, 2026
Case Report: Possible C3 nephritic factor-driven complement-mediated severe hemolytic anemia and acute kidney injury in a child with <i>Bordetella parapertussis</i> infectionSteffen Ullitz Thorsen, Anne Todsen Hansen, Hans Jakob Hartling, et al.
Journal of Clinical Immunology|June 8, 2026
Novel Partial Loss-of-function STAT3-variant as Cause of Hyper-IgE-Syndrome in a Danish Family with Variable ExpressivityCamilla Heldbjerg Drabe, Jonathan Gehrig, Jens Magnus Bernth Jensen, et al.
Pageof 1