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Stephan Ehl

Showing results (201-210 of 239) with videos related to

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Haematologica|July 16, 2013
Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopeniaAnne Rensing-Ehl, Ales Janda, Myriam R Lorenz, et al.
Haematologica|May 30, 2015
The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesisSebastian Fn Bode, Sandra Ammann, Waleed Al-Herz, et al.
The Journal of Experimental Medicine|May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
The Journal of Experimental Medicine|May 21, 2024
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
Nature Medicine|October 21, 2014
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutationsDesirée Schubert, Claudia Bode, Rupert Kenefeck, et al.
Journal of Human Immunity|May 15, 2026
FAS-controlled T cells drive lymphoproliferation through glycolysis without effector differentiationMaria Elena Maccari, Christoph König, Geoffroy Andrieux, et al.
The Journal of Allergy and Clinical Immunology|September 24, 2016
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysisCarsten Speckmann, Sam Doerken, Alessandro Aiuti, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2009
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndromeKarin R Engelhardt, Sean McGhee, Sabine Winkler, et al.
The Journal of Allergy and Clinical Immunology|April 2, 2023
Autoimmunity and immunodeficiency associated with monoallelic LIG4 mutations via haploinsufficiencyAnnaïse J Jauch, Olivier Bignucolo, Sayuri Seki, et al.
The Journal of Experimental Medicine|September 26, 2007
Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunityCheng-Lung Ku, Horst von Bernuth, Capucine Picard, et al.
Pageof 24

Showing results (201-210 of 239) with videos related to

Sort By:
Pageof 24
Haematologica|July 16, 2013
Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopeniaAnne Rensing-Ehl, Ales Janda, Myriam R Lorenz, et al.
Haematologica|May 30, 2015
The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesisSebastian Fn Bode, Sandra Ammann, Waleed Al-Herz, et al.
The Journal of Experimental Medicine|May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
The Journal of Experimental Medicine|May 21, 2024
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
Nature Medicine|October 21, 2014
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutationsDesirée Schubert, Claudia Bode, Rupert Kenefeck, et al.
Journal of Human Immunity|May 15, 2026
FAS-controlled T cells drive lymphoproliferation through glycolysis without effector differentiationMaria Elena Maccari, Christoph König, Geoffroy Andrieux, et al.
The Journal of Allergy and Clinical Immunology|September 24, 2016
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysisCarsten Speckmann, Sam Doerken, Alessandro Aiuti, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2009
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndromeKarin R Engelhardt, Sean McGhee, Sabine Winkler, et al.
The Journal of Allergy and Clinical Immunology|April 2, 2023
Autoimmunity and immunodeficiency associated with monoallelic LIG4 mutations via haploinsufficiencyAnnaïse J Jauch, Olivier Bignucolo, Sayuri Seki, et al.
The Journal of Experimental Medicine|September 26, 2007
Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunityCheng-Lung Ku, Horst von Bernuth, Capucine Picard, et al.
Pageof 24