Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Janet Chou

Showing results (141-150 of 152) with videos related to

Pageof 16
Sort By:
Frontiers in Immunology|October 19, 2017
Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin ContentKerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
The Journal of Allergy and Clinical Immunology|April 19, 2021
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiencyStefano Vavassori, Janet Chou, Laura Eva Faletti, et al.
Frontiers in Immunology|August 4, 2017
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin ContentKerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
The Journal of Allergy and Clinical Immunology|September 17, 2017
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiencyHassan Abolhassani, Janet Chou, Wayne Bainter, et al.
Science Immunology|June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activityVivien Béziat, Juan Li, Jian-Xin Lin, et al.
The Journal of Clinical Investigation|October 13, 2015
Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiencyJolan E Walter, Lindsey B Rosen, Krisztian Csomos, et al.
The Journal of Clinical Investigation|November 2, 2016
Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiencyJolan E Walter, Lindsey B Rosen, Krisztian Csomos, et al.
The Journal of Allergy and Clinical Immunology|October 5, 2016
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantationM Teresa de la Morena, David Leonard, Troy R Torgerson, et al.
Cell|August 13, 2024
High expression of oleoyl-ACP hydrolase underpins life-threatening respiratory viral diseasesXiaoxiao Jia, Jeremy Chase Crawford, Deborah Gebregzabher, 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 mutationsTiziana Lorenzini, Manfred Fliegauf, Nils Klammer, et al.
Pageof 16

Showing results (141-150 of 152) with videos related to

Sort By:
Pageof 16
Frontiers in Immunology|October 19, 2017
Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin ContentKerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
The Journal of Allergy and Clinical Immunology|April 19, 2021
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiencyStefano Vavassori, Janet Chou, Laura Eva Faletti, et al.
Frontiers in Immunology|August 4, 2017
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin ContentKerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
The Journal of Allergy and Clinical Immunology|September 17, 2017
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiencyHassan Abolhassani, Janet Chou, Wayne Bainter, et al.
Science Immunology|June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activityVivien Béziat, Juan Li, Jian-Xin Lin, et al.
The Journal of Clinical Investigation|October 13, 2015
Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiencyJolan E Walter, Lindsey B Rosen, Krisztian Csomos, et al.
The Journal of Clinical Investigation|November 2, 2016
Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiencyJolan E Walter, Lindsey B Rosen, Krisztian Csomos, et al.
The Journal of Allergy and Clinical Immunology|October 5, 2016
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantationM Teresa de la Morena, David Leonard, Troy R Torgerson, et al.
Cell|August 13, 2024
High expression of oleoyl-ACP hydrolase underpins life-threatening respiratory viral diseasesXiaoxiao Jia, Jeremy Chase Crawford, Deborah Gebregzabher, 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 mutationsTiziana Lorenzini, Manfred Fliegauf, Nils Klammer, et al.
Pageof 16