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Dirk Roos

Showing results (51-60 of 146) with videos related to

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Human Genetics|September 1, 2004
Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cellsClara Bionda, Xing Jun Li, Robin van Bruggen, et al.
Journal of Clinical Immunology|January 17, 2023
A Novel Deletion in FERMT3 Causes LAD-III in a Turkish FamilyNezihe Köker, İhsan Deveci, Karin van Leeuwen, et al.
International Archives of Allergy and Immunology|March 25, 2019
Common Infections and Target Organs Associated with Chronic Granulomatous Disease in IranEsmaeil Mortaz, Elham Azempour, Davood Mansouri, et al.
Blood|March 17, 2005
Hematologic abnormalities in Shwachman Diamond syndrome: lack of genotype-phenotype relationshipTaco W Kuijpers, Mariel Alders, Anton T J Tool, et al.
Clinical Nutrition (Edinburgh, Scotland)|August 7, 2004
Lipid effects on neutrophil calcium signaling induced by opsonized particles: platelet activating factor is only part of the storyGeert Wanten, Anneke Kusters, Sjenet E van Emst-de Vries, et al.
Plos One|October 7, 2009
Inherited glutathione reductase deficiency and Plasmodium falciparum malaria--a case studyValentina Gallo, Evelin Schwarzer, Stefan Rahlfs, et al.
Blood|March 11, 2006
Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infectionsTom Sprong, Dirk Roos, Corry Weemaes, et al.
American Journal of Human Genetics|July 3, 2002
Evidence consistent with human L1 retrotransposition in maternal meiosis IBrook Brouha, Christof Meischl, Eric Ostertag, et al.
Journal of Clinical Immunology|May 24, 2011
Two X-linked chronic granulomatous disease patients with unusual NADPH oxidase propertiesBaruch Wolach, Arnon Broides, Tal Zeeli, et al.
Acta Dermato-Venereologica|July 5, 2014
Recurrent pyoderma gangrenosum and cystic acne associated with leucocyte adhesion deficiency due to novel mutations in ITGB2: successful treatment with infliximab and adalimumabAnders Vahlquist, Lena Douhan Håkansson, Lars Rönnblom, et al.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
Human Genetics|September 1, 2004
Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cellsClara Bionda, Xing Jun Li, Robin van Bruggen, et al.
Journal of Clinical Immunology|January 17, 2023
A Novel Deletion in FERMT3 Causes LAD-III in a Turkish FamilyNezihe Köker, İhsan Deveci, Karin van Leeuwen, et al.
International Archives of Allergy and Immunology|March 25, 2019
Common Infections and Target Organs Associated with Chronic Granulomatous Disease in IranEsmaeil Mortaz, Elham Azempour, Davood Mansouri, et al.
Blood|March 17, 2005
Hematologic abnormalities in Shwachman Diamond syndrome: lack of genotype-phenotype relationshipTaco W Kuijpers, Mariel Alders, Anton T J Tool, et al.
Clinical Nutrition (Edinburgh, Scotland)|August 7, 2004
Lipid effects on neutrophil calcium signaling induced by opsonized particles: platelet activating factor is only part of the storyGeert Wanten, Anneke Kusters, Sjenet E van Emst-de Vries, et al.
Plos One|October 7, 2009
Inherited glutathione reductase deficiency and Plasmodium falciparum malaria--a case studyValentina Gallo, Evelin Schwarzer, Stefan Rahlfs, et al.
Blood|March 11, 2006
Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infectionsTom Sprong, Dirk Roos, Corry Weemaes, et al.
American Journal of Human Genetics|July 3, 2002
Evidence consistent with human L1 retrotransposition in maternal meiosis IBrook Brouha, Christof Meischl, Eric Ostertag, et al.
Journal of Clinical Immunology|May 24, 2011
Two X-linked chronic granulomatous disease patients with unusual NADPH oxidase propertiesBaruch Wolach, Arnon Broides, Tal Zeeli, et al.
Acta Dermato-Venereologica|July 5, 2014
Recurrent pyoderma gangrenosum and cystic acne associated with leucocyte adhesion deficiency due to novel mutations in ITGB2: successful treatment with infliximab and adalimumabAnders Vahlquist, Lena Douhan Håkansson, Lars Rönnblom, et al.
Pageof 15