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The Journal of Experimental Medicine
|
March 25, 2020
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome
Vivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
Nucleic Acids Research
|
November 27, 2018
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, et al.
The Journal of Clinical Investigation
|
November 15, 2022
Human Dectin-1 deficiency impairs macrophage-mediated defense against phaeohyphomycosis
Rebecca A Drummond, Jigar V Desai, Amy P Hsu, et al.
The Journal of Allergy and Clinical Immunology
|
April 13, 2020
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
Tiziana Lorenzini, Manfred Fliegauf, Nils Klammer, et al.
The Journal of Allergy and Clinical Immunology
|
February 7, 2026
Targeted deep sequencing identifies mosaicism in patients with immune dysregulation
Elizabeth G Schmitz, Alexander J Paul, Rajarshi Ghosh, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology
|
April 5, 2026
2025 Inborn errors of immunity practice parameter: Guidance from the Joint Task Force on Practice Parameters, the American Academy of Allergy, Asthma & Immunology (AAAAI), the American College of Allergy, Asthma and Immunology (ACAAI) and the Clinical Immunology Society (CIS)
Jordan S Orange, Javier Chinen, Caroline C Horner, et al.
Science (New York, N.Y.)
|
September 19, 2024
Germline mutations in a G protein identify signaling cross-talk in T cells
Hyoungjun Ham, Huie Jing, Ian T Lamborn, et al.
Science Immunology
|
January 10, 2025
Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature
Marita Bosticardo, Kerry Dobbs, Ottavia M Delmonte, et al.
Page
of 27
Search research articles
Search
Showing results (261-270 of 268) with videos related to
Sort By:
Page
of 27
You have reached the last page of results.
This site can display upto 268 results.
The Journal of Experimental Medicine
|
March 25, 2020
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome
Vivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
Nucleic Acids Research
|
November 27, 2018
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, et al.
The Journal of Clinical Investigation
|
November 15, 2022
Human Dectin-1 deficiency impairs macrophage-mediated defense against phaeohyphomycosis
Rebecca A Drummond, Jigar V Desai, Amy P Hsu, et al.
The Journal of Allergy and Clinical Immunology
|
April 13, 2020
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
Tiziana Lorenzini, Manfred Fliegauf, Nils Klammer, et al.
The Journal of Allergy and Clinical Immunology
|
February 7, 2026
Targeted deep sequencing identifies mosaicism in patients with immune dysregulation
Elizabeth G Schmitz, Alexander J Paul, Rajarshi Ghosh, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology
|
April 5, 2026
2025 Inborn errors of immunity practice parameter: Guidance from the Joint Task Force on Practice Parameters, the American Academy of Allergy, Asthma & Immunology (AAAAI), the American College of Allergy, Asthma and Immunology (ACAAI) and the Clinical Immunology Society (CIS)
Jordan S Orange, Javier Chinen, Caroline C Horner, et al.
Science (New York, N.Y.)
|
September 19, 2024
Germline mutations in a G protein identify signaling cross-talk in T cells
Hyoungjun Ham, Huie Jing, Ian T Lamborn, et al.
Science Immunology
|
January 10, 2025
Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature
Marita Bosticardo, Kerry Dobbs, Ottavia M Delmonte, et al.
Page
of 27