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Alexandra F Freeman

Showing results (231-240 of 268) with videos related to

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Nature|August 20, 2025
TCF1 and LEF1 promote B-1a cell homeostasis and regulatory functionQian Shen, Hao Wang, Jonathan A Roco, et al.
The Journal of Allergy and Clinical Immunology|March 1, 2026
Allogeneic hematopoietic cell transplantation for partial RAG deficiency in children and adults: excellent outcomes with a reduced intensity, posttransplantation cyclophosphamide-based approachDimana Dimitrova, Marita Bosticardo, Ottavia M Delmonte, et al.
The Journal of Clinical Investigation|June 9, 2026
Aberrant STAT signaling and T cell dysregulation define a targetable pediatric sepsis endotypeRobert B Lindell, Samir U Sayed, Jose S Campos Duran, et al.
Blood|April 20, 2021
SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulationOttavia M Delmonte, Jenna R E Bergerson, Tomoki Kawai, et al.
Blood Advances|June 20, 2025
Allogeneic hematopoietic stem cell transplantation for STAT3 hyper-IgE syndrome: a worldwide studyChristo Tsilifis, Johannes Raedler, Joanna Renke, et al.
Genome Medicine|January 26, 2023
The genomic landscape of rare disorders in the Middle EastMaha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, et al.
The Journal of Experimental Medicine|September 2, 2021
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiencyJuan Li, Wei-Te Lei, Peng Zhang, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|September 8, 2019
Prospective Study of a Novel, Radiation-Free, Reduced-Intensity Bone Marrow Transplantation Platform for Primary Immunodeficiency DiseasesDimana Dimitrova, Juan Gea-Banacloche, Seth M Steinberg, et al.
The Journal of Allergy and Clinical Immunology|February 28, 2026
Additive effects of common and rare genetic variants on inflammatory bowel disease risk in a cohort with immunodeficiencySruthi Srinivasan, Wenjia Cao, Morgan N Similuk, et al.
Frontiers in Immunology|May 22, 2023
Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunityBreanna J Beers, Morgan N Similuk, Rajarshi Ghosh, et al.
Pageof 27

Showing results (231-240 of 268) with videos related to

Sort By:
Pageof 27
Nature|August 20, 2025
TCF1 and LEF1 promote B-1a cell homeostasis and regulatory functionQian Shen, Hao Wang, Jonathan A Roco, et al.
The Journal of Allergy and Clinical Immunology|March 1, 2026
Allogeneic hematopoietic cell transplantation for partial RAG deficiency in children and adults: excellent outcomes with a reduced intensity, posttransplantation cyclophosphamide-based approachDimana Dimitrova, Marita Bosticardo, Ottavia M Delmonte, et al.
The Journal of Clinical Investigation|June 9, 2026
Aberrant STAT signaling and T cell dysregulation define a targetable pediatric sepsis endotypeRobert B Lindell, Samir U Sayed, Jose S Campos Duran, et al.
Blood|April 20, 2021
SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulationOttavia M Delmonte, Jenna R E Bergerson, Tomoki Kawai, et al.
Blood Advances|June 20, 2025
Allogeneic hematopoietic stem cell transplantation for STAT3 hyper-IgE syndrome: a worldwide studyChristo Tsilifis, Johannes Raedler, Joanna Renke, et al.
Genome Medicine|January 26, 2023
The genomic landscape of rare disorders in the Middle EastMaha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, et al.
The Journal of Experimental Medicine|September 2, 2021
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiencyJuan Li, Wei-Te Lei, Peng Zhang, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|September 8, 2019
Prospective Study of a Novel, Radiation-Free, Reduced-Intensity Bone Marrow Transplantation Platform for Primary Immunodeficiency DiseasesDimana Dimitrova, Juan Gea-Banacloche, Seth M Steinberg, et al.
The Journal of Allergy and Clinical Immunology|February 28, 2026
Additive effects of common and rare genetic variants on inflammatory bowel disease risk in a cohort with immunodeficiencySruthi Srinivasan, Wenjia Cao, Morgan N Similuk, et al.
Frontiers in Immunology|May 22, 2023
Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunityBreanna J Beers, Morgan N Similuk, Rajarshi Ghosh, et al.
Pageof 27