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Capucine Picard

Showing results (201-210 of 400) with videos related to

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The Journal of Allergy and Clinical Immunology|November 21, 2017
ORAI1 mutations abolishing store-operated Ca<sup>2+</sup> entry cause anhidrotic ectodermal dysplasia with immunodeficiencyJayson Lian, Mario Cuk, Sascha Kahlfuss, et al.
Blood|May 31, 2011
New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO proteinMarjorie Hubeau, Flora Ngadjeua, Anne Puel, et al.
Clinical Immunology (Orlando, Fla.)|July 19, 2015
SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signalingFabian Hauck, Britta Blumenthal, Sebastian Fuchs, et al.
The Journal of Clinical Investigation|November 18, 2014
Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestationsNadia Jeremiah, Bénédicte Neven, Matteo Gentili, et al.
Nature Immunology|October 27, 2014
A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4Laia Alsina, Elisabeth Israelsson, Matthew C Altman, et al.
The Journal of Pediatrics|December 5, 2017
Burden of Poor Health Conditions and Quality of Life in 656 Children with Primary ImmunodeficiencyVincent Barlogis, Nizar Mahlaoui, Pascal Auquier, et al.
The Journal of Allergy and Clinical Immunology|May 12, 2015
Early-onset hypogammaglobulinemia: A survey of 44 patientsAnne C Brignier, Nizar Mahlaoui, Christian Reimann, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|March 17, 2019
Haploidentical Hematopoietic Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immunodeficiencies and Inherited Disorders in ChildrenBénédicte Neven, Jean-Sébastien Diana, Martin Castelle, et al.
Journal of Human Immunity|January 29, 2026
Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert CommitteeM Cecilia Poli, Ivona Aksentijevich, Ahmed Aziz Bousfiha, et al.
The Journal of Clinical Investigation|December 25, 2010
Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulationAude Magerus-Chatinet, Bénédicte Neven, Marie-Claude Stolzenberg, et al.
Pageof 40

Showing results (201-210 of 400) with videos related to

Sort By:
Pageof 40
The Journal of Allergy and Clinical Immunology|November 21, 2017
ORAI1 mutations abolishing store-operated Ca<sup>2+</sup> entry cause anhidrotic ectodermal dysplasia with immunodeficiencyJayson Lian, Mario Cuk, Sascha Kahlfuss, et al.
Blood|May 31, 2011
New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO proteinMarjorie Hubeau, Flora Ngadjeua, Anne Puel, et al.
Clinical Immunology (Orlando, Fla.)|July 19, 2015
SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signalingFabian Hauck, Britta Blumenthal, Sebastian Fuchs, et al.
The Journal of Clinical Investigation|November 18, 2014
Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestationsNadia Jeremiah, Bénédicte Neven, Matteo Gentili, et al.
Nature Immunology|October 27, 2014
A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4Laia Alsina, Elisabeth Israelsson, Matthew C Altman, et al.
The Journal of Pediatrics|December 5, 2017
Burden of Poor Health Conditions and Quality of Life in 656 Children with Primary ImmunodeficiencyVincent Barlogis, Nizar Mahlaoui, Pascal Auquier, et al.
The Journal of Allergy and Clinical Immunology|May 12, 2015
Early-onset hypogammaglobulinemia: A survey of 44 patientsAnne C Brignier, Nizar Mahlaoui, Christian Reimann, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|March 17, 2019
Haploidentical Hematopoietic Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immunodeficiencies and Inherited Disorders in ChildrenBénédicte Neven, Jean-Sébastien Diana, Martin Castelle, et al.
Journal of Human Immunity|January 29, 2026
Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert CommitteeM Cecilia Poli, Ivona Aksentijevich, Ahmed Aziz Bousfiha, et al.
The Journal of Clinical Investigation|December 25, 2010
Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulationAude Magerus-Chatinet, Bénédicte Neven, Marie-Claude Stolzenberg, et al.
Pageof 40