(Q37176109)

18 August 2017

1 reference

title

Genetics and immunopathology of chronic granulomatous disease (English)

1 reference

18 August 2017

Marie José Stasia

1

1 reference

18 August 2017

Xing Jun Li

series ordinal

2

1 reference

18 August 2017

publication date

29 May 2008

1 reference

Seminars in Immunopathology

18 August 2017

published in

1 reference

18 August 2017

volume

30

1 reference

18 August 2017

issue

3

1 reference

18 August 2017

page(s)

209-235

1 reference

Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease

18 August 2017

cites work

1 reference

12 December 2020

Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia

1 reference

12 December 2020

X-CGDbase: a database of X-CGD-causing mutations

1 reference

12 December 2020

Cellular and molecular effects of recombinant interferon gamma in chronic granulomatous disease

1 reference

12 December 2020

A new X-linked variant of chronic granulomatous disease characterized by the existence of a normal clone of respiratory burst-competent phagocytic cells.

1 reference

12 December 2020

Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phox

1 reference

12 December 2020

Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.

1 reference

12 December 2020

Neutrophil nicotinamide adenine dinucleotide phosphate oxidase assembly. Translocation of p47-phox and p67-phox requires interaction between p47-phox and cytochrome b558.

1 reference

12 December 2020

High-level reconstitution of respiratory burst activity in a human X-linked chronic granulomatous disease (X-CGD) cell line and correction of murine X-CGD bone marrow cells by retroviral-mediated gene transfer of human gp91phox

1 reference

12 December 2020

Prolonged production of NADPH oxidase-corrected granulocytes after gene therapy of chronic granulomatous disease

1 reference

12 December 2020

Mutations in the promoter region of the gene for gp91-phox in X-linked chronic granulomatous disease with decreased expression of cytochrome b558.

1 reference

12 December 2020

Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing

1 reference

12 December 2020

Immunodeficiency mutation databases (IDbases).

1 reference

12 December 2020

Molecular and functional characterization of a new X-linked chronic granulomatous disease variant (X91+) case with a double missense mutation in the cytosolic gp91phox C-terminal tail.

1 reference

12 December 2020

Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

1 reference

12 December 2020

[On the nature of neutrophilic granules]

1 reference

12 December 2020

Interaction of Rac with p67phox and regulation of phagocytic NADPH oxidase activity

1 reference

12 December 2020

Cytochrome b-245 is a flavocytochrome containing FAD and the NADPH-binding site of the microbicidal oxidase of phagocytes

1 reference

12 December 2020

An unusual case of sarcoidosis

1 reference

12 December 2020

Assembly and activation of the phagocyte NADPH oxidase. Specific interaction of the N-terminal Src homology 3 domain of p47phox with p22phox is required for activation of the NADPH oxidase

1 reference

12 December 2020

Two-exon skipping due to a point mutation in p67-phox--deficient chronic granulomatous disease

1 reference

12 December 2020

Novel cytochrome b system in phagocytic vacuoles of human granulocytes

1 reference

12 December 2020

Genomic structure of the human p47-phox (NCF1) gene

1 reference

12 December 2020

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (first update).

1 reference

12 December 2020

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 cells

1 reference

12 December 2020

CHANGES IN THE METABOLIC PATTERN OF POLYMORPHO-NUCLEAR LEUCOCYTES DURING PHAGOCYTOSIS

1 reference

12 December 2020

The X-linked chronic granulomatous disease gene codes for the beta-chain of cytochrome b-245

1 reference

12 December 2020

X-linked chronic granulomatous disease: correction of NADPH oxidase defect by retrovirus-mediated expression of gp91-phox

1 reference

12 December 2020

Preliminary characterisation of the promoter of the human p22(phox) gene: identification of a new polymorphism associated with hypertension

1 reference

12 December 2020

In vitro molecular reconstitution of the respiratory burst in B lymphoblasts from p47-phox-deficient chronic granulomatous disease

1 reference

12 December 2020

Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes

1 reference

12 December 2020

Progress in gene therapy for chronic granulomatous disease

1 reference

12 December 2020

Activation of SHP2 protein-tyrosine phosphatase increases HoxA10-induced repression of the genes encoding gp91(PHOX) and p67(PHOX)

1 reference

12 December 2020

The biochemical basis of phagocytosis. I. Metabolic changes during the ingestion of particles by polymorphonuclear leukocytes

1 reference

12 December 2020

Allogeneic bone marrow transplantation with reduced intensity conditioning for chronic granulomatous disease complicated by invasive Aspergillus infection

1 reference

12 December 2020

Gene therapy for chronic granulomatous disease

1 reference

12 December 2020

Functional analysis of NADPH oxidase in granulocytic cells expressing a delta488-497 gp91(phox) deletion mutant.

1 reference

12 December 2020

The association of nonsense codons with exon skipping

1 reference

12 December 2020

Cloning of a 67-kD neutrophil oxidase factor with similarity to a noncatalytic region of p60c-src

1 reference

12 December 2020

Regulation and termination of NADPH oxidase activity

1 reference

12 December 2020

Unsaturated fatty acids stimulate NADPH-dependent superoxide production by cell-free system derived from macrophages

1 reference

12 December 2020

Processing and Maturation of Flavocytochromeb558Include Incorporation of Heme as a Prerequisite for Heterodimer Assembly

1 reference

12 December 2020

Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers.

1 reference

12 December 2020

A fatal granulomatous disease of childhood; the clinical, pathological, and laboratory features of a new syndrome.

1 reference

12 December 2020

Adenovirus-mediated gene transfer into monocyte-derived macrophages of patients with X-linked chronic granulomatous disease: ex vivo correction of deficient respiratory burst

1 reference

12 December 2020

Mechanisms of insertional mutagenesis in human genes causing genetic disease

1 reference

12 December 2020

Molecular analysis in three cases of X91- variant chronic granulomatous disease

1 reference

12 December 2020

Long-term correction of phagocyte NADPH oxidase activity by retroviral-mediated gene transfer in murine X-linked chronic granulomatous disease.

1 reference

12 December 2020

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

1 reference

12 December 2020

A syndrome of recurrent infection and infiltration of viscera by pigmented lipid histiocytes

1 reference

12 December 2020

A new cytochrome in neurophilic granules of rabbit leucocyte.

1 reference

12 December 2020

Recruitment of CREB-binding protein by PU.1, IFN-regulatory factor-1, and the IFN consensus sequence-binding protein is necessary for IFN-gamma-induced p67phox and gp91phox expression.

1 reference

12 December 2020

Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23

1 reference

12 December 2020

Gene transfer to primary chronic granulomatous disease monocytes

1 reference

12 December 2020

Recombinant interferon gamma augments phagocyte superoxide production and X-chronic granulomatous disease gene expression in X-linked variant chronic granulomatous disease

1 reference

12 December 2020

Progress toward effective gene therapy for chronic granulomatous disease.

1 reference

12 December 2020

Generation of recombinant adeno-associated virus (rAAV) from an adenoviral vector and functional reconstitution of the NADPH-oxidase

1 reference

12 December 2020

Prospects for gene therapy of neutrophil defects

1 reference

12 December 2020

In vitro bactericidal capacity of human polymorphonuclear leukocytes: diminished activity in chronic granulomatous disease of childhood

1 reference

12 December 2020

Restitution of superoxide generation in autosomal cytochrome-negative chronic granulomatous disease (A22(0) CGD)-derived B lymphocyte cell lines by transfection with p22phax cDNA.

1 reference

12 December 2020

The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology

1 reference

12 December 2020

Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter study

1 reference

12 December 2020

CD34+ peripheral blood progenitors as a target for genetic correction of the two flavocytochrome b558 defective forms of chronic granulomatous disease.

1 reference

12 December 2020

Two novel point mutations in the cytochrome b 558 heavy chain gene, detected in two Japanese patients with X-linked chronic granulomatous disease

1 reference

12 December 2020

A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox

1 reference

12 December 2020

A novel mutation at a probable heme-binding ligand in neutrophil cytochrome b558 in atypical X-linked chronic granulomatous disease

1 reference

12 December 2020

Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient

1 reference

12 December 2020

Retroviral-mediated gene transfer and nonmyeloablative conditioning: studies in a murine X-linked chronic granulomatous disease model

1 reference

12 December 2020

A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease

1 reference

12 December 2020

Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)

1 reference

12 December 2020

Gene therapy for chronic granulomatous disease

1 reference

12 December 2020

Peripheral blood progenitors as a target for genetic correction of p47phox-deficient chronic granulomatous disease

1 reference

12 December 2020

A variant X-linked chronic granulomatous disease patient (X91+) with partially functional cytochrome b

1 reference

12 December 2020

Disturbed interaction of p21-rac with mutated p67-phox causes chronic granulomatous disease

1 reference

12 December 2020

Characterisation of the enzyme defect in chronic granulomatous disease

1 reference

12 December 2020

Attempt to treat a case of chronic familial granulomatous disease by allogenic bone marrow transplantation

1 reference

12 December 2020

Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion: significance for A47 degrees chronic granulomatous disease carrier detection

1 reference

12 December 2020

Detection of gp91-phox precursor protein in B-cell lines from patients with X-linked chronic granulomatous disease as an indicator for mutations impairing cytochrome b558 biosynthesis

1 reference

12 December 2020

Allogeneic stem cell transplant from HLA-identical sibling for chronic granulomatous disease and review of the literature.

1 reference

12 December 2020

Absence of cytochrome b-245 in chronic granulomatous disease. A multicenter European evaluation of its incidence and relevance

1 reference

12 December 2020

Structure of the TPR domain of p67phox in complex with Rac.GTP

1 reference

12 December 2020

Correction of respiratory burst activity in X-linked chronic granulomatous cells to therapeutically relevant levels after gene transfer into bone marrow CD34+ cells

1 reference

12 December 2020

Recombinant human interferon-gamma in patients with chronic granulomatous disease —European follow up study

1 reference

12 December 2020

Cloning of the cDNA and functional expression of the 47-kilodalton cytosolic component of human neutrophil respiratory burst oxidase

1 reference

12 December 2020

Human peripheral eosinophils have a specific mechanism to express gp91-phox, the large subunit of cytochrome b558

1 reference

12 December 2020

Eosinophil-specific regulation of gp91(phox) gene expression by transcription factors GATA-1 and GATA-2.

1 reference

12 December 2020

The active N-terminal region of p67phox. Structure at 1.8 A resolution and biochemical characterizations of the A128V mutant implicated in chronic granulomatous disease

1 reference

12 December 2020

Characterization of six novel mutations in the CYBB gene leading to different sub-types of X-linked chronic granulomatous disease

1 reference

12 December 2020

Relationship of glycolytic and oxidative metabolism to particle entry and destruction in phagocytosing cells

1 reference

12 December 2020

Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients

1 reference

12 December 2020

Two cytosolic neutrophil oxidase components absent in autosomal chronic granulomatous disease

1 reference

12 December 2020

Binding of pleomorphic adenoma gene-like 2 to the tumor necrosis factor (TNF)-alpha-responsive region of the NCF2 promoter regulates p67(phox) expression and NADPH oxidase activity

1 reference

12 December 2020

Characterization of a new human diploid myeloid leukemia cell line (PLB-985) with granulocytic and monocytic differentiating capacity.

1 reference

12 December 2020

Genetic analysis of 13 families with X-linked chronic granulomatous disease reveals a low proportion of sporadic patients and a high proportion of sporadic carriers

1 reference

12 December 2020

Retroviral-mediated gene transfer of gp91phox into bone marrow cells rescues defect in host defense against Aspergillus fumigatus in murine X-linked chronic granulomatous disease

1 reference

12 December 2020

Absence of both the 91kD and 22kD subunits of human neutrophil cytochrome b in two genetic forms of chronic granulomatous disease

1 reference

12 December 2020

Restoration of superoxide generation to a chronic granulomatous disease-derived B-cell line by retrovirus mediated gene transfer

1 reference

12 December 2020

Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous disease

1 reference

12 December 2020

Genetic correction of p67phox deficient chronic granulomatous disease using peripheral blood progenitor cells as a target for retrovirus mediated gene transfer

1 reference

12 December 2020

Simian immunodeficiency virus lentivector corrects human X-linked chronic granulomatous disease in the NOD/SCID mouse xenograft

1 reference

12 December 2020

Treatment of chronic granulomatous disease with nonmyeloablative conditioning and a T-cell-depleted hematopoietic allograft

1 reference

12 December 2020

Chronic Granulomatous Disease Presenting in a 69-Year-Old Man

1 reference

12 December 2020

Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase

1 reference

12 December 2020

Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease

1 reference

12 December 2020

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

1 reference

12 December 2020

Regulation of phagocyte oxygen radical production by the GTP-binding protein Rac 2

1 reference

12 December 2020

Variable correction of host defense following gene transfer and bone marrow transplantation in murine X-linked chronic granulomatous disease

1 reference

12 December 2020

Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiency

1 reference

12 December 2020

Severe Clinical Forms of Cytochromeb–Negative Chronic Granulomatous Disease (X91−) in 3 Brothers with a Point Mutation in the Promoter Region ofCYBB

1 reference

12 December 2020

Reconstitution of NADPH oxidase activity in human X-linked chronic granulomatous disease myeloid cells after stable gene transfer using a recombinant adeno-associated virus 2 vector

1 reference

12 December 2020

NADPH-binding component of the superoxide-generating oxidase in unstimulated neutrophils and the neutrophils from the patients with chronic granulomatous disease

1 reference

12 December 2020

Dominant negative mutation of the hematopoietic-specific Rho GTPase, Rac2, is associated with a human phagocyte immunodeficiency

1 reference

12 December 2020

Probing the role of the carboxyl terminus of the gp91phox subunit of neutrophil flavocytochrome b558 using site-directed mutagenesis

1 reference

12 December 2020

Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase

1 reference

12 December 2020

Long-term itraconazole prophylaxis against Aspergillus infections in thirty-two patients with chronic granulomatous disease.

1 reference

12 December 2020

Oxidative killing of microbes by neutrophils

1 reference

12 December 2020

Activation of the NADPH oxidase involves the small GTP-binding protein p21rac1

1 reference

12 December 2020

Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat

1 reference

12 December 2020

Hematologically important mutations: X-linked chronic granulomatous disease (second update).

1 reference

12 December 2020

Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1.

1 reference

12 December 2020

Chronic granulomatous disease. Report on a national registry of 368 patients

1 reference

12 December 2020

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

1 reference

12 December 2020

Itraconazole to prevent fungal infections in chronic granulomatous disease

1 reference

12 December 2020

Modern management of chronic granulomatous disease

1 reference

12 December 2020

Genetic, biochemical, and clinical features of chronic granulomatous disease.

1 reference

12 December 2020

A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease

1 reference

12 December 2020

Advances in the treatment of Chronic Granulomatous Disease by gene therapy.

1 reference

12 December 2020

Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000

1 reference

12 December 2020

The search for a genetic defect in Polish patients with chronic granulomatous disease.

1 reference

12 December 2020

A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency

1 reference

12 December 2020

Treatment of chronic granulomatous disease with myeloablative conditioning and an unmodified hemopoietic allograft: a survey of the European experience, 1985-2000.

1 reference

12 December 2020

A newly recognized point mutation in the cytochrome b558 heavy chain gene replacing alanine57 by glutamic acid, in a patient with cytochrome b positive X-linked chronic granulomatous disease

1 reference

12 December 2020

AG dinucleotide insertion in a patient with chronic granulomatous disease lacking cytosolic 67-kD protein.

1 reference

12 December 2020

Activation of neutrophil NADPH oxidase in a cell-free system. Partial purification of components and characterization of the activation process

1 reference

12 December 2020

A structural model for the nucleotide binding domains of the flavocytochrome b-245 beta-chain

1 reference

12 December 2020

Follow up of patients with chronic granulomatous disease diagnosed since 1990

1 reference

12 December 2020

A 1.1-kb duplication in the p67-phox gene causes chronic granulomatous disease

1 reference

12 December 2020

IFN-gamma is effective in reducing infections in the mouse model of chronic granulomatous disease (CGD).

1 reference

12 December 2020

Spectroscopic identification of the heme axial ligation of cytochrome b558 in the NADPH oxidase of porcine neutrophils

1 reference

12 December 2020

Leukocyte oxidase: defective activity in chronic granulomatous disease

1 reference

12 December 2020

Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease

1 reference

12 December 2020

Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase

1 reference

12 December 2020

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-phox

1 reference

12 December 2020

Molecular characterization of autosomal recessive chronic granulomatous disease caused by a defect of the nicotinamide adenine dinucleotide phosphate (reduced form) oxidase component p67-phox

1 reference

12 December 2020

A bicistronic retrovirus vector containing a picornavirus internal ribosome entry site allows for correction of X-linked CGD by selection for MDR1 expression.

1 reference

12 December 2020

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease.

1 reference

12 December 2020

Complementation of NADPH oxidase in p67-phox-deficient CGD patients

1 reference

12 December 2020

A donor splice site mutation in intron 1 of CYBA, leading to chronic granulomatous disease

1 reference

12 December 2020

NOX enzymes and the biology of reactive oxygen

1 reference

12 December 2020

Crucial role of two potential cytosolic regions of Nox2, 191TSSTKTIRRS200 and 484DESQANHFAVHHDEEKD500, on NADPH oxidase activation

1 reference

12 December 2020

A Controlled Trial of Interferon Gamma to Prevent Infection in Chronic Granulomatous Disease

1 reference

12 December 2020

Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation

1 reference

12 December 2020

PU.1 as an essential activator for the expression of gp91(phox) gene in human peripheral neutrophils, monocytes, and B lymphocytes

1 reference

12 December 2020

Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease

1 reference

12 December 2020

Chronic granulomatous disease

1 reference

12 December 2020

DNA linkage analysis of X chromosome-linked chronic granulomatous disease

1 reference

12 December 2020

Chronic granulomatous disease with partial deficiency of cytochrome b558 and incomplete respiratory burst: variants of the X-linked, cytochrome b558-negative form of the disease

1 reference

12 December 2020

Genotoxicity of retroviral integration in hematopoietic cells.

1 reference

12 December 2020

Inherited Neutrophil Disorders: Molecular Basis and New Therapies

1 reference

12 December 2020

The genetic basis of chronic granulomatous disease

1 reference

12 December 2020

Long-term interferon-gamma therapy for patients with chronic granulomatous disease

1 reference

12 December 2020

Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox)

1 reference

12 December 2020

A new mutation in exon 12 of the gp91-phox gene leading to cytochrome b-positive X-linked chronic granulomatous disease

1 reference

12 December 2020

Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase: consequences for oxidase assembly

1 reference

12 December 2020

Two forms of autosomal chronic granulomatous disease lack distinct neutrophil cytosol factors.

1 reference

12 December 2020

Nicotinamide-adenine dinucleotide phosphate oxidase assembly and activation in EBV-transformed B lymphoblastoid cell lines of normal and chronic granulomatous disease patients.

1 reference

12 December 2020

[The X+ chronic granulomatous disease as a fabulous model to study the NADPH oxidase complex activation]

1 reference

12 December 2020

A novel and unusual case of chronic granulomatous disease in a child with a homozygous 36-bp deletion in the CYBA gene (A22(0)) leading to the activation of a cryptic splice site in intron 4.

1 reference

12 December 2020

Enhanced host defense after gene transfer in the murine p47phox-deficient model of chronic granulomatous disease

1 reference

12 December 2020

Homologous dinucleotide (GT or TG) deletion in Japanese patients with chronic granulomatous disease with p47-phox deficiency

1 reference

12 December 2020

Human Gene Mutation Database (HGMD): 2003 update

1 reference

12 December 2020

Concentrated RD114-pseudotyped MFGS-gp91phox vector achieves high levels of functional correction of the chronic granulomatous disease oxidase defect in NOD/SCID/beta -microglobulin-/- repopulating mobilized human peripheral blood CD34+ cells

1 reference

12 December 2020

Point mutations in the promoter region of the CYBB gene leading to mild chronic granulomatous disease

1 reference

12 December 2020

Stimulated neutrophils from patients with autosomal recessive chronic granulomatous disease fail to phosphorylate a Mr-44,000 protein

1 reference

12 December 2020

The phagocyte 47-kilodalton cytosolic oxidase protein is an early reactant in activation of the respiratory burst

1 reference

12 December 2020

Atomic structure of ferredoxin-NADP+ reductase: prototype for a structurally novel flavoenzyme family

1 reference

12 December 2020

A mutation located at the 5' splice junction sequence of intron 3 in the p67phox gene causes the lack of p67phox mRNA in a patient with chronic granulomatous disease

1 reference

12 December 2020

Relationships of p40(phox) with p67(phox) in the activation and expression of the human respiratory burst NADPH oxidase

1 reference

12 December 2020

Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis

1 reference

12 December 2020

X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.

1 reference

12 December 2020

Leu505 of Nox2 is crucial for optimal p67phox-dependent activation of the flavocytochrome b558 during phagocytic NADPH oxidase assembly.

1 reference

12 December 2020

Identification of a donor splice site mutation leading to loss of p22-phox exon 5 in autosomal chronic granulomatous disease

1 reference

12 December 2020

Prevalence, genetics and clinical presentation of chronic granulomatous disease in Sweden.

1 reference

12 December 2020

Bone marrow transplantation for chronic granulomatous disease: long-term follow-up and review of literature

1 reference

12 December 2020

Enhancer-deleted retroviral vectors restore high levels of superoxide generation in a mouse model of CGD.

1 reference

12 December 2020

Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes

1 reference

12 December 2020

Drug-selected complete restoration of superoxide generation in Epstein-Barr virus-transformed B cells from p47phox-deficient chronic granulomatous disease patients by using a bicistronic retrovirus vector encoding a human multi-drug resistance gene

1 reference

12 December 2020

The superoxide-generating NADPH oxidase: structural aspects and activation mechanism

1 reference

12 December 2020

Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1)

1 reference

12 December 2020

Trimethoprim-sulfamethoxazole prophylaxis in the management of chronic granulomatous disease

1 reference

12 December 2020

Fatal granulomatous disease of childhood. An inborn abnormality of phagocytic function

1 reference

12 December 2020

Complementation of NADPH oxidase in p67-phox-deficient CGD patients p67-phox/p40-phox interaction

1 reference

12 December 2020

10.1007/S00281-008-0121-8

Identifiers

DOI

1 reference

18 August 2017

1 reference