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Karin R Engelhardt

Showing results (11-20 of 32) with videos related to

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Frontiers in Immunology|September 2, 2017
14 Years after Discovery: Clinical Follow-up on 15 Patients with Inducible Co-Stimulator DeficiencyJohanna Schepp, Janet Chou, Andrea Skrabl-Baumgartner, et al.
Journal of Clinical Immunology|September 25, 2015
Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and HepatitisNic Robertson, Karin R Engelhardt, Neil V Morgan, et al.
The Journal of Allergy and Clinical Immunology|December 6, 2020
Defective neutrophil development and specific granule deficiency caused by a homozygous splice-site mutation in SMARCD2Ina Schim van der Loeff, Evelien G G Sprenkeler, Anton T J Tool, et al.
Blood|February 2, 2012
The phenotype of human STK4 deficiencyHengameh Abdollahpour, Giridharan Appaswamy, Daniel Kotlarz, et al.
The Journal of Allergy and Clinical Immunology|November 20, 2012
Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantationKarin R Engelhardt, Neil Shah, Intan Faizura-Yeop, et al.
Journal of Clinical Immunology|January 24, 2016
Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 DeficiencyTarana Singh Dang, Joseph D P Willet, Helen R Griffin, et al.
Journal of Clinical Immunology|November 4, 2016
Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome SequencingKarin R Engelhardt, Yaobo Xu, Angela Grainger, et al.
Science Translational Medicine|October 2, 2015
Human IFNAR2 deficiency: Lessons for antiviral immunityChristopher J A Duncan, Siti M B Mohamad, Dan F Young, et al.
Blood|June 11, 2020
Germline TET2 loss of function causes childhood immunodeficiency and lymphomaJarmila Stremenova Spegarova, Dylan Lawless, Siti Mardhiana Binti Mohamad, et al.
The Journal of Experimental Medicine|May 2, 2019
Human interleukin-2 receptor β mutations associated with defects in immunity and peripheral toleranceZinan Zhang, Florian Gothe, Perrine Pennamen, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Frontiers in Immunology|September 2, 2017
14 Years after Discovery: Clinical Follow-up on 15 Patients with Inducible Co-Stimulator DeficiencyJohanna Schepp, Janet Chou, Andrea Skrabl-Baumgartner, et al.
Journal of Clinical Immunology|September 25, 2015
Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and HepatitisNic Robertson, Karin R Engelhardt, Neil V Morgan, et al.
The Journal of Allergy and Clinical Immunology|December 6, 2020
Defective neutrophil development and specific granule deficiency caused by a homozygous splice-site mutation in SMARCD2Ina Schim van der Loeff, Evelien G G Sprenkeler, Anton T J Tool, et al.
Blood|February 2, 2012
The phenotype of human STK4 deficiencyHengameh Abdollahpour, Giridharan Appaswamy, Daniel Kotlarz, et al.
The Journal of Allergy and Clinical Immunology|November 20, 2012
Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantationKarin R Engelhardt, Neil Shah, Intan Faizura-Yeop, et al.
Journal of Clinical Immunology|January 24, 2016
Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 DeficiencyTarana Singh Dang, Joseph D P Willet, Helen R Griffin, et al.
Journal of Clinical Immunology|November 4, 2016
Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome SequencingKarin R Engelhardt, Yaobo Xu, Angela Grainger, et al.
Science Translational Medicine|October 2, 2015
Human IFNAR2 deficiency: Lessons for antiviral immunityChristopher J A Duncan, Siti M B Mohamad, Dan F Young, et al.
Blood|June 11, 2020
Germline TET2 loss of function causes childhood immunodeficiency and lymphomaJarmila Stremenova Spegarova, Dylan Lawless, Siti Mardhiana Binti Mohamad, et al.
The Journal of Experimental Medicine|May 2, 2019
Human interleukin-2 receptor β mutations associated with defects in immunity and peripheral toleranceZinan Zhang, Florian Gothe, Perrine Pennamen, et al.
Pageof 4