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D Roos

Showing results (301-310 of 422) with videos related to

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Journal of Clinical Pathology|July 31, 2002
NADPH oxidase(s): new source(s) of reactive oxygen species in the vascular system?L Van Heerebeek, C Meischl, W Stooker, et al.
Blood Cells, Molecules & Diseases|February 13, 2001
Hematologically important mutations: X-linked chronic granulomatous disease (second update)P G Heyworth, J T Curnutte, J Rae, et al.
Fertility and Sterility|June 17, 2000
Association of histologic features and cytogenetic abnormalities in ectopic pregnanciesM Goddijn, D Roos, M van Wely, et al.
Immunological Investigations|January 1, 1995
Neutrophil antigens, from bench to bedsideA E von dem Borne, M de Haas, D Roos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 22, 1998
Triple role of platelet-activating factor in eosinophil migration across monolayers of lung epithelial cells: eosinophil chemoattractant and priming agent and epithelial cell activatorL Liu, A E Zuurbier, F P Mul, et al.
Journal of the American College of Cardiology|December 19, 2003
NAD(P)H oxidase in the failing human heartP A J Krijnen, C Meischl, C A Visser, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 30, 1998
Nicotinamide-adenine dinucleotide phosphate oxidase assembly and activation in EBV-transformed B lymphoblastoid cell lines of normal and chronic granulomatous disease patientsS Dusi, K A Nadalini, M Donini, et al.
European Journal of Clinical Investigation|April 20, 2006
Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one familyM Y Köker, O Sanal, M de Boer, et al.
The Journal of Clinical Investigation|March 1, 1985
Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridizationR S Weening, L Corbeel, M de Boer, et al.
American Journal of Human Genetics|November 1, 1992
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)M de Boer, A de Klein, J P Hossle, et al.
Pageof 43

Showing results (301-310 of 422) with videos related to

Sort By:
Pageof 43
Journal of Clinical Pathology|July 31, 2002
NADPH oxidase(s): new source(s) of reactive oxygen species in the vascular system?L Van Heerebeek, C Meischl, W Stooker, et al.
Blood Cells, Molecules & Diseases|February 13, 2001
Hematologically important mutations: X-linked chronic granulomatous disease (second update)P G Heyworth, J T Curnutte, J Rae, et al.
Fertility and Sterility|June 17, 2000
Association of histologic features and cytogenetic abnormalities in ectopic pregnanciesM Goddijn, D Roos, M van Wely, et al.
Immunological Investigations|January 1, 1995
Neutrophil antigens, from bench to bedsideA E von dem Borne, M de Haas, D Roos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 22, 1998
Triple role of platelet-activating factor in eosinophil migration across monolayers of lung epithelial cells: eosinophil chemoattractant and priming agent and epithelial cell activatorL Liu, A E Zuurbier, F P Mul, et al.
Journal of the American College of Cardiology|December 19, 2003
NAD(P)H oxidase in the failing human heartP A J Krijnen, C Meischl, C A Visser, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 30, 1998
Nicotinamide-adenine dinucleotide phosphate oxidase assembly and activation in EBV-transformed B lymphoblastoid cell lines of normal and chronic granulomatous disease patientsS Dusi, K A Nadalini, M Donini, et al.
European Journal of Clinical Investigation|April 20, 2006
Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one familyM Y Köker, O Sanal, M de Boer, et al.
The Journal of Clinical Investigation|March 1, 1985
Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridizationR S Weening, L Corbeel, M de Boer, et al.
American Journal of Human Genetics|November 1, 1992
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)M de Boer, A de Klein, J P Hossle, et al.
Pageof 43