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Raz Somech

Showing results (191-200 of 200) with videos related to

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Immunity|May 6, 2014
Interleukin-10 receptor signaling in innate immune cells regulates mucosal immune tolerance and anti-inflammatory macrophage functionDror S Shouval, Amlan Biswas, Jeremy A Goettel, et al.
Blood|September 11, 2019
CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesisIdo Somekh, Marini Thian, David Medgyesi, et al.
Science Immunology|August 8, 2017
Characterization of T and B cell repertoire diversity in patients with RAG deficiencyYu Nee Lee, Francesco Frugoni, Kerry Dobbs, et al.
American Journal of Human Genetics|March 19, 2024
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndromeCaspar I van der Made, Simone Kersten, Odelia Chorin, et al.
Blood|September 27, 2018
T-cell defects in patients with <i>ARPC1B</i> germline mutations account for combined immunodeficiencyImmacolata Brigida, Matteo Zoccolillo, Maria Pia Cicalese, et al.
The Journal of Experimental Medicine|April 1, 2024
Helper T cell immunity in humans with inherited CD4 deficiencyAntoine Guérin, Marcela Moncada-Vélez, Katherine Jackson, et al.
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.
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 Experimental Medicine|December 14, 2022
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiencyRomain Lévy, Florian Gothe, Mana Momenilandi, et al.
Science Immunology|January 10, 2025
Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signatureMarita Bosticardo, Kerry Dobbs, Ottavia M Delmonte, et al.
Pageof 20

Showing results (191-200 of 200) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 200 results.
Immunity|May 6, 2014
Interleukin-10 receptor signaling in innate immune cells regulates mucosal immune tolerance and anti-inflammatory macrophage functionDror S Shouval, Amlan Biswas, Jeremy A Goettel, et al.
Blood|September 11, 2019
CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesisIdo Somekh, Marini Thian, David Medgyesi, et al.
Science Immunology|August 8, 2017
Characterization of T and B cell repertoire diversity in patients with RAG deficiencyYu Nee Lee, Francesco Frugoni, Kerry Dobbs, et al.
American Journal of Human Genetics|March 19, 2024
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndromeCaspar I van der Made, Simone Kersten, Odelia Chorin, et al.
Blood|September 27, 2018
T-cell defects in patients with <i>ARPC1B</i> germline mutations account for combined immunodeficiencyImmacolata Brigida, Matteo Zoccolillo, Maria Pia Cicalese, et al.
The Journal of Experimental Medicine|April 1, 2024
Helper T cell immunity in humans with inherited CD4 deficiencyAntoine Guérin, Marcela Moncada-Vélez, Katherine Jackson, et al.
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.
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 Experimental Medicine|December 14, 2022
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiencyRomain Lévy, Florian Gothe, Mana Momenilandi, et al.
Science Immunology|January 10, 2025
Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signatureMarita Bosticardo, Kerry Dobbs, Ottavia M Delmonte, et al.
Pageof 20