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Stephan Ehl

Showing results (161-170 of 239) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|February 9, 2011
ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysisAndrea Maul-Pavicic, Samuel C C Chiang, Anne Rensing-Ehl, et al.
The Journal of Experimental Medicine|August 20, 2020
Rapid identification and characterization of infected cells in blood during chronic active Epstein-Barr virus infectionBenjamin Fournier, David Boutboul, Julie Bruneau, et al.
Blood|March 28, 2012
Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)Julia Pagel, Karin Beutel, Kai Lehmberg, et al.
Immunology and Cell Biology|May 24, 2018
CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndromePaola Cura Daball, Monica Sofia Ventura Ferreira, Sandra Ammann, et al.
Pediatric Blood & Cancer|July 4, 2020
Risk factors for mixed chimerism in children with hemophagocytic lymphohistiocytosis after reduced toxicity conditioningKatharina Wustrau, Johann Greil, Karl-Walter Sykora, et al.
Journal of Clinical Immunology|September 29, 2021
Reduced-Intensity/Reduced-Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute GVHDDanielle E Arnold, Rofida Nofal, Connor Wakefield, et al.
The Journal of Allergy and Clinical Immunology|January 9, 2023
Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutationsMaria Elena Maccari, Pascal Schneider, Cristian Roberto Smulski, et al.
Blood|January 9, 2016
Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndromeSandra Ammann, Ansgar Schulz, Ingeborg Krägeloh-Mann, et al.
Clinical Immunology (Orlando, Fla.)|November 27, 2019
Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunitySabine Jägle, Maximilian Heeg, Sarah Grün, et al.
Frontiers in Immunology|May 2, 2017
Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome PatientsSamuel C C Chiang, Stephanie M Wood, Bianca Tesi, et al.
Pageof 24

Showing results (161-170 of 239) with videos related to

Sort By:
Pageof 24
Proceedings of the National Academy of Sciences of the United States of America|February 9, 2011
ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysisAndrea Maul-Pavicic, Samuel C C Chiang, Anne Rensing-Ehl, et al.
The Journal of Experimental Medicine|August 20, 2020
Rapid identification and characterization of infected cells in blood during chronic active Epstein-Barr virus infectionBenjamin Fournier, David Boutboul, Julie Bruneau, et al.
Blood|March 28, 2012
Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)Julia Pagel, Karin Beutel, Kai Lehmberg, et al.
Immunology and Cell Biology|May 24, 2018
CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndromePaola Cura Daball, Monica Sofia Ventura Ferreira, Sandra Ammann, et al.
Pediatric Blood & Cancer|July 4, 2020
Risk factors for mixed chimerism in children with hemophagocytic lymphohistiocytosis after reduced toxicity conditioningKatharina Wustrau, Johann Greil, Karl-Walter Sykora, et al.
Journal of Clinical Immunology|September 29, 2021
Reduced-Intensity/Reduced-Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute GVHDDanielle E Arnold, Rofida Nofal, Connor Wakefield, et al.
The Journal of Allergy and Clinical Immunology|January 9, 2023
Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutationsMaria Elena Maccari, Pascal Schneider, Cristian Roberto Smulski, et al.
Blood|January 9, 2016
Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndromeSandra Ammann, Ansgar Schulz, Ingeborg Krägeloh-Mann, et al.
Clinical Immunology (Orlando, Fla.)|November 27, 2019
Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunitySabine Jägle, Maximilian Heeg, Sarah Grün, et al.
Frontiers in Immunology|May 2, 2017
Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome PatientsSamuel C C Chiang, Stephanie M Wood, Bianca Tesi, et al.
Pageof 24