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Stephan Ehl

Showing results (171-180 of 239) with videos related to

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Cell Stem Cell|May 14, 2026
Genotoxicity profiling reveals distinct platform-and cell type-specific effects in therapeutic gene editing for genetic hyperinflammationLei Lei, Masako M Kaufmann, Jessica Lao, et al.
Blood|June 5, 2014
Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiencyAnne Rensing-Ehl, Simon Völkl, Carsten Speckmann, et al.
Blood Advances|May 9, 2020
Targeted busulfan-based reduced-intensity conditioning and HLA-matched HSCT cure hemophagocytic lymphohistiocytosisMatthias Felber, Colin G Steward, Karim Kentouche, et al.
Clinical Immunology (Orlando, Fla.)|February 19, 2019
Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestationsInga Tometten, Kerstin Felgentreff, Manfred Hönig, et al.
Blood|April 22, 2016
Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndromeSimon Völkl, Anne Rensing-Ehl, Andrea Allgäuer, et al.
Blood|March 16, 2025
Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variantsOliver Wegehaupt, Oleg Borisov, Elena Sieni, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 29, 2020
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension StudiesNieves Diaz, Maria Juarez, Caterina Cancrini, et al.
Journal of Human Immunity|April 13, 2026
Dominant-negative PSMB10 disrupts immunoproteasome assembly and leads to transient T lymphopeniaSujal Ghosh, Yuqin Wang, Christoph Schultheiss, et al.
The Journal of Allergy and Clinical Immunology|March 10, 2018
A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentationBianca Tesi, Jelena Rascon, Samuel C C Chiang, et al.
The Journal of Allergy and Clinical Immunology|December 21, 2019
Erythropoiesis defect observed in STAT3 GOF patients with severe anemiaAndrea A Mauracher, Julia J M Eekels, Janine Woytschak, et al.
Pageof 24

Showing results (171-180 of 239) with videos related to

Sort By:
Pageof 24
Cell Stem Cell|May 14, 2026
Genotoxicity profiling reveals distinct platform-and cell type-specific effects in therapeutic gene editing for genetic hyperinflammationLei Lei, Masako M Kaufmann, Jessica Lao, et al.
Blood|June 5, 2014
Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiencyAnne Rensing-Ehl, Simon Völkl, Carsten Speckmann, et al.
Blood Advances|May 9, 2020
Targeted busulfan-based reduced-intensity conditioning and HLA-matched HSCT cure hemophagocytic lymphohistiocytosisMatthias Felber, Colin G Steward, Karim Kentouche, et al.
Clinical Immunology (Orlando, Fla.)|February 19, 2019
Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestationsInga Tometten, Kerstin Felgentreff, Manfred Hönig, et al.
Blood|April 22, 2016
Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndromeSimon Völkl, Anne Rensing-Ehl, Andrea Allgäuer, et al.
Blood|March 16, 2025
Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variantsOliver Wegehaupt, Oleg Borisov, Elena Sieni, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 29, 2020
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension StudiesNieves Diaz, Maria Juarez, Caterina Cancrini, et al.
Journal of Human Immunity|April 13, 2026
Dominant-negative PSMB10 disrupts immunoproteasome assembly and leads to transient T lymphopeniaSujal Ghosh, Yuqin Wang, Christoph Schultheiss, et al.
The Journal of Allergy and Clinical Immunology|March 10, 2018
A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentationBianca Tesi, Jelena Rascon, Samuel C C Chiang, et al.
The Journal of Allergy and Clinical Immunology|December 21, 2019
Erythropoiesis defect observed in STAT3 GOF patients with severe anemiaAndrea A Mauracher, Julia J M Eekels, Janine Woytschak, et al.
Pageof 24