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European Journal of Clinical Investigation|July 24, 2009
Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutationsM Y Köker, O Sanal, K van Leeuwen, et al.
The Journal of Experimental Medicine|December 1, 1994
156Pro-->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phoxJ H Leusen, B G Bolscher, P M Hilarius, et al.
Molecular Microbiology|January 6, 2011
Functional characterization of Rho GTPases in Aspergillus niger uncovers conserved and diverged roles of Rho proteins within filamentous fungiMin Jin Kwon, Mark Arentshorst, Eelke D Roos, et al.
Clinical and Experimental Dermatology|June 1, 2011
Chronic granulomatous disease of childhood: an unusual cause of recurrent uncommon infections in a 61-year-old manG Isman-Nelkenbaum, B Wolach, R Gavrieli, et al.
Blood|January 15, 1994
Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriersM de Boer, P M Hilarius-Stokman, J P Hossle, et al.
Blood|September 15, 1992
Splice site mutations are a common cause of X-linked chronic granulomatous diseaseM de Boer, B G Bolscher, M C Dinauer, et al.
Blood|August 1, 1997
Expression and intracellular localization of the human N-acetylmuramyl-L-alanine amidase, a bacterial cell wall-degrading enzymeM A Hoijer, M J Melief, J Calafat, et al.
European Journal of Clinical Investigation|March 19, 2009
Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous diseaseM Y Köker, K van Leeuwen, M de Boer, et al.
Journal of Clinical Pathology|March 1, 2003
Increased Nox2 expression in human cardiomyocytes after acute myocardial infarctionP A J Krijnen, C Meischl, C E Hack, et al.
The Journal of Clinical Investigation|October 6, 1997
Leukocyte adhesion deficiency type 1 (LAD-1)/variant. A novel immunodeficiency syndrome characterized by dysfunctional beta2 integrinsT W Kuijpers, R A Van Lier, D Hamann, et al.
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