Genetic studies of three Japanese patients with p22‐phox‐deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and …
M Yamada, T Ariga, N Kawamura… - British journal of …, 2000 - Wiley Online Library
Chronic granulomatous disease (CGD) is a disorder caused by defects in the NADPH
oxidase responsible for superoxide generation in phagocytes. Cytochrome b558, an …
oxidase responsible for superoxide generation in phagocytes. Cytochrome b558, an …
Gene therapy for chronic granulomatous disease
WS Goebel, MC Dinauer - Acta haematologica, 2003 - karger.com
Identification of gene mutations responsible for leukocyte dysfunction along with the
application of gene transfer technology has made genetic correction of such disorders …
application of gene transfer technology has made genetic correction of such disorders …
Chronic granulomatous disease
PG Heyworth, AR Cross, JT Curnutte - Current opinion in immunology, 2003 - Elsevier
Chronic granulomatous disease (CGD) is a primary immunodeficiency that affects
phagocytes of the innate immune system and is characterized by a greatly increased …
phagocytes of the innate immune system and is characterized by a greatly increased …
Very early-onset inflammatory manifestations of X-linked chronic granulomatous disease
R Labrosse, J Abou-Diab, A Blincoe, G Cros… - Frontiers in …, 2017 - frontiersin.org
Chronic granulomatous disease (CGD) is a rare primary immune deficiency caused by
mutations in genes coding for components of the nicotinamide adenine dinucleotide …
mutations in genes coding for components of the nicotinamide adenine dinucleotide …
Diagnostic modalities based on flow cytometry for chronic granulomatous disease: a multicenter study in a well-defined cohort
Background Chronic granulomatous disease (CGD) is characterized by defective microbial
killing due to mutations affecting subunits of the nicotinamide adenine dinucleotide …
killing due to mutations affecting subunits of the nicotinamide adenine dinucleotide …
Immunological aspects of X-linked chronic granulomatous disease female carriers
M Chiriaco, I Salfa, GM Ursu, C Cifaldi, S Di Cesare… - Antioxidants, 2021 - mdpi.com
X-linked Granulomatous Disease (XL-CGD) carriers were previously thought to be clinically
healthy because random X-chromosome inactivation (XCI) allows approximately half of their …
healthy because random X-chromosome inactivation (XCI) allows approximately half of their …
Focus on FOCIS: the continuing diagnostic challenge of autosomal recessive chronic granulomatous disease
G Yu, DK Hong, KY Dionis, J Rae, PG Heyworth… - Clinical …, 2008 - Elsevier
Chronic granulomatous disease (CGD) is a primary immunodeficiency of defective
neutrophil oxidative burst activity due to mutations in the genes CYBA, NCF-1, NCF-2, and …
neutrophil oxidative burst activity due to mutations in the genes CYBA, NCF-1, NCF-2, and …
[引用][C] Molecular genetics of chronic granulomatous disease
SH Orkin - Annual review of immunology, 1989 - annualreviews.org
Chronic granulomatous disease (COD) is an uncommon inherited disorder in which
phagocytic cells (neutrophils, monocytes, macrophages, and eosinophils) fail to produce …
phagocytic cells (neutrophils, monocytes, macrophages, and eosinophils) fail to produce …
Chronic granulomatous disease: a comprehensive review
Chronic granulomatous disease (CGD) is a primary immunodeficiency of phagocyte function
due to defective NADPH oxidase (phox). Compared with the common types of CYBB/gp91 …
due to defective NADPH oxidase (phox). Compared with the common types of CYBB/gp91 …
Infections associated with chronic granulomatous disease: linking genetics to phenotypic expression
J Ben-Ari, O Wolach, R Gavrieli… - Expert review of anti …, 2012 - Taylor & Francis
Chronic granulomatous disease (CGD) is an inherited primary immunodeficiency
characterized by the absence or malfunction of the NADPH oxidase in phagocytic cells. As a …
characterized by the absence or malfunction of the NADPH oxidase in phagocytic cells. As a …