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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 pregnancies
M Goddijn, D Roos, M van Wely, et al.
Immunological Investigations
|
January 1, 1995
Neutrophil antigens, from bench to bedside
A 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 activator
L 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 heart
P 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 patients
S 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 family
M 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 hybridization
R 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.
Page
of 43
Search research articles
Search
Showing results (301-310 of 422) with videos related to
Sort By:
Page
of 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 pregnancies
M Goddijn, D Roos, M van Wely, et al.
Immunological Investigations
|
January 1, 1995
Neutrophil antigens, from bench to bedside
A 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 activator
L 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 heart
P 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 patients
S 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 family
M 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 hybridization
R 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.
Page
of 43