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E D Renner

Showing results (21-30 of 27) with videos related to

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Annals of Internal Medicine|April 1, 1979
Legionnaires' disease in pneumonia patients in Iowa. A retrospective seroepidemiologic study, 1972-1977E D Renner, C M Helms, W J Hierholzer, et al.
Cytokine|May 29, 2024
Staphylococcus aureus Serine protease-like protein A (SplA) induces IL-8 by keratinocytes and synergizes with IL-17AD P De Donato, R Effner, M Nordengrün, et al.
Rheumatology (Oxford, England)|June 20, 2006
Classification of non-bacterial osteitis: retrospective study of clinical, immunological and genetic aspects in 89 patientsA Jansson, E D Renner, J Ramser, et al.
Journal of Clinical Immunology|September 1, 2005
No indication for a defect in toll-like receptor signaling in patients with hyper-IgE syndromeE D Renner, I Pawlita, F Hoffmann, et al.
Klinische Padiatrie|November 9, 2010
Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantationT C Bittner, U Pannicke, E D Renner, et al.
Allergy|June 6, 2014
Atopic dermatitis, STAT3- and DOCK8-hyper-IgE syndromes differ in IgE-based sensitization patternA C Boos, B Hagl, A Schlesinger, et al.
American Journal of Human Genetics|August 12, 1999
Genetic linkage of hyper-IgE syndrome to chromosome 4B Grimbacher, A A Schäffer, S M Holland, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Annals of Internal Medicine|April 1, 1979
Legionnaires' disease in pneumonia patients in Iowa. A retrospective seroepidemiologic study, 1972-1977E D Renner, C M Helms, W J Hierholzer, et al.
Cytokine|May 29, 2024
Staphylococcus aureus Serine protease-like protein A (SplA) induces IL-8 by keratinocytes and synergizes with IL-17AD P De Donato, R Effner, M Nordengrün, et al.
Rheumatology (Oxford, England)|June 20, 2006
Classification of non-bacterial osteitis: retrospective study of clinical, immunological and genetic aspects in 89 patientsA Jansson, E D Renner, J Ramser, et al.
Journal of Clinical Immunology|September 1, 2005
No indication for a defect in toll-like receptor signaling in patients with hyper-IgE syndromeE D Renner, I Pawlita, F Hoffmann, et al.
Klinische Padiatrie|November 9, 2010
Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantationT C Bittner, U Pannicke, E D Renner, et al.
Allergy|June 6, 2014
Atopic dermatitis, STAT3- and DOCK8-hyper-IgE syndromes differ in IgE-based sensitization patternA C Boos, B Hagl, A Schlesinger, et al.
American Journal of Human Genetics|August 12, 1999
Genetic linkage of hyper-IgE syndrome to chromosome 4B Grimbacher, A A Schäffer, S M Holland, et al.
Pageof 3