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D Renner

Showing results (131-140 of 158) with videos related to

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Pediatric Hematology and Oncology|August 18, 2012
Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimenHeidrun Boztug, Cäcilia Karitnig-Weiß, Bernd Ausserer, et al.
Journal of the American Society of Nephrology : JASN|February 11, 2014
Stat3 programs Th17-specific regulatory T cells to control GNMalte A Kluger, Michael Luig, Claudia Wegscheid, et al.
Neurology|December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteriaM K Bruno, M Hallett, K Gwinn-Hardy, et al.
Journal of Clinical Immunology|April 16, 2013
Lung parenchyma surgery in autosomal dominant hyper-IgE syndromeAlexandra F Freeman, Ellen D Renner, Carolyn Henderson, et al.
Scientific Reports|November 15, 2018
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutationBeate Hagl, Benedikt D Spielberger, Silvia Thoene, 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.
Allergy|April 8, 2021
Electrical impedance spectroscopy for the characterization of skin barrier in atopic dermatitisArturo O Rinaldi, Angelica Korsfeldt, Siobhan Ward, et al.
Science (New York, N.Y.)|April 3, 2025
Tissue-like multicellular development triggered by mechanical compression in archaeaTheopi Rados, Olivia S Leland, Pedro Escudeiro, et al.
Allergy|July 4, 2019
Impaired memory B-cell development and antibody maturation with a skewing toward IgE in patients with STAT3 hyper-IgE syndromeWillem van de Veen, Carolin E Krätz, Craig I McKenzie, et al.
The Journal of Allergy and Clinical Immunology|July 8, 2008
Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndromeEllen D Renner, Stacey Rylaarsdam, Stephanie Anover-Sombke, et al.
Pageof 16

Showing results (131-140 of 158) with videos related to

Sort By:
Pageof 16
Pediatric Hematology and Oncology|August 18, 2012
Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimenHeidrun Boztug, Cäcilia Karitnig-Weiß, Bernd Ausserer, et al.
Journal of the American Society of Nephrology : JASN|February 11, 2014
Stat3 programs Th17-specific regulatory T cells to control GNMalte A Kluger, Michael Luig, Claudia Wegscheid, et al.
Neurology|December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteriaM K Bruno, M Hallett, K Gwinn-Hardy, et al.
Journal of Clinical Immunology|April 16, 2013
Lung parenchyma surgery in autosomal dominant hyper-IgE syndromeAlexandra F Freeman, Ellen D Renner, Carolyn Henderson, et al.
Scientific Reports|November 15, 2018
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutationBeate Hagl, Benedikt D Spielberger, Silvia Thoene, 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.
Allergy|April 8, 2021
Electrical impedance spectroscopy for the characterization of skin barrier in atopic dermatitisArturo O Rinaldi, Angelica Korsfeldt, Siobhan Ward, et al.
Science (New York, N.Y.)|April 3, 2025
Tissue-like multicellular development triggered by mechanical compression in archaeaTheopi Rados, Olivia S Leland, Pedro Escudeiro, et al.
Allergy|July 4, 2019
Impaired memory B-cell development and antibody maturation with a skewing toward IgE in patients with STAT3 hyper-IgE syndromeWillem van de Veen, Carolin E Krätz, Craig I McKenzie, et al.
The Journal of Allergy and Clinical Immunology|July 8, 2008
Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndromeEllen D Renner, Stacey Rylaarsdam, Stephanie Anover-Sombke, et al.
Pageof 16