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Stephan Ehl

Showing results (51-60 of 239) with videos related to

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Blood|November 30, 2012
Hemophagocytic lymphohistiocytosis in syntaxin-11-deficient mice: T-cell exhaustion limits fatal diseaseTamara Kögl, Jürgen Müller, Birthe Jessen, et al.
Clinical Immunology (Orlando, Fla.)|December 17, 2013
Severe eczema and Hyper-IgE in Loeys-Dietz-syndrome - contribution to new findings of immune dysregulation in connective tissue disordersKerstin Felgentreff, Matthias Siepe, Stefan Kotthoff, et al.
Cellular Immunology|October 2, 2007
Recombinant Sendai virus induces T cell immunity against respiratory syncytial virus that is protective in the absence of antibodiesBrigitte Voges, Simone Vallbracht, Gert Zimmer, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2013
Syntaxin binding mechanism and disease-causing mutations in Munc18-2Yvonne Hackmann, Stephen C Graham, Stephan Ehl, et al.
Blood|November 23, 2013
Platelet secretion defect in a patient with stromal interaction molecule 1 deficiencyLea Nakamura, Kirstin Sandrock-Lang, Carsten Speckmann, et al.
Frontiers in Pediatrics|November 16, 2020
Tuberculosis-Associated HLH in an 8-Month-Old Infant: A Case Report and ReviewHolger Hauch, Susanne Skrzypek, Wilhelm Woessmann, et al.
Blood Advances|March 31, 2026
Digenic and Multigenic Heterozygous FHL Genotypes Are Common but Clinically Silent in the General PopulationOleg Borisov, Jasmin Mann, Kevin Kim Walz, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|August 29, 2018
Stephan Ehl, Christian Bogdan, Tim Niehues, et al.
The Journal of Clinical Investigation|October 8, 2005
A variant of SCID with specific immune responses and predominance of gamma delta T cellsStephan Ehl, Klaus Schwarz, Anselm Enders, et al.
Frontiers in Pharmacology|February 7, 2022
Hermansky-Pudlak Syndrome: Identification of <i>Novel</i> Variants in the Genes <i>HPS3</i>, <i>HPS5,</i> and <i>DTNBP1</i> (HPS-7)Doris Boeckelmann, Mira Wolter, Katharina Neubauer, et al.
Pageof 24

Showing results (51-60 of 239) with videos related to

Sort By:
Pageof 24
Blood|November 30, 2012
Hemophagocytic lymphohistiocytosis in syntaxin-11-deficient mice: T-cell exhaustion limits fatal diseaseTamara Kögl, Jürgen Müller, Birthe Jessen, et al.
Clinical Immunology (Orlando, Fla.)|December 17, 2013
Severe eczema and Hyper-IgE in Loeys-Dietz-syndrome - contribution to new findings of immune dysregulation in connective tissue disordersKerstin Felgentreff, Matthias Siepe, Stefan Kotthoff, et al.
Cellular Immunology|October 2, 2007
Recombinant Sendai virus induces T cell immunity against respiratory syncytial virus that is protective in the absence of antibodiesBrigitte Voges, Simone Vallbracht, Gert Zimmer, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2013
Syntaxin binding mechanism and disease-causing mutations in Munc18-2Yvonne Hackmann, Stephen C Graham, Stephan Ehl, et al.
Blood|November 23, 2013
Platelet secretion defect in a patient with stromal interaction molecule 1 deficiencyLea Nakamura, Kirstin Sandrock-Lang, Carsten Speckmann, et al.
Frontiers in Pediatrics|November 16, 2020
Tuberculosis-Associated HLH in an 8-Month-Old Infant: A Case Report and ReviewHolger Hauch, Susanne Skrzypek, Wilhelm Woessmann, et al.
Blood Advances|March 31, 2026
Digenic and Multigenic Heterozygous FHL Genotypes Are Common but Clinically Silent in the General PopulationOleg Borisov, Jasmin Mann, Kevin Kim Walz, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|August 29, 2018
Stephan Ehl, Christian Bogdan, Tim Niehues, et al.
The Journal of Clinical Investigation|October 8, 2005
A variant of SCID with specific immune responses and predominance of gamma delta T cellsStephan Ehl, Klaus Schwarz, Anselm Enders, et al.
Frontiers in Pharmacology|February 7, 2022
Hermansky-Pudlak Syndrome: Identification of <i>Novel</i> Variants in the Genes <i>HPS3</i>, <i>HPS5,</i> and <i>DTNBP1</i> (HPS-7)Doris Boeckelmann, Mira Wolter, Katharina Neubauer, et al.
Pageof 24