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Phosphorylation of the oxidase-related 48K phosphoprotein family in the unusual autosomal cytochrome-negative and X-linked cytochrome-positive types of chronic granulomatous disease

Data up to Jan 2025

Published1988
Citations76
References27

Total Citations Per Year

Abstract

References (27)

Glucose-6-phosphate Dehydrogenase

1974 • 1,219 citations

Subcellular localization of the b-cytochrome component of the human neutrophil microbicidal oxidase: translocation during activation.

1983 • 938 citations

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

1987 • 459 citations

Chemiluminescence and superoxide production by myeloperoxidase-deficient leukocytes.

1976 • 373 citations

Absence of Cytochrome b-245in Chronic Granulomatous Disease

1983 • 300 citations

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

1985 • 286 citations

Chronic Granulomatous Disease

1983 • 266 citations

NADPH oxidase deficiency in X-linked chronic granulomatous disease.

1975 • 251 citations

Effects of free fatty acids on release of superoxide and on change of shape by human neutrophils. Reversibility by albumin.

1984 • 230 citations

Chronic Granulomatous Disease

1987 • 204 citations

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

1987 • 202 citations

Gastrointestinal Manifestations of Chronic Granulomatous Disease

1973 • 188 citations

Subcellular localization of the human neutrophil NADPH oxidase. b-Cytochrome and associated flavoprotein.

1984 • 187 citations

Relationship of protein phosphorylation to the activation of the respiratory burst in human neutrophils. Defects in the phosphorylation of a group of closely related 48-kDa proteins in two forms of chronic granulomatous disease.

1988 • 181 citations

Quantitative Leukocyte Iodination

1971 • 180 citations

The NBT slide test: A simple screening method for detecting chronic granulomatous disease and female carriers

1973 • 171 citations

Defect in Pyridine Nucleotide Dependent Superoxide Production by a Particulate Fraction from the Granulocytes of Patients with Chronic Granulomatous Disease

1975 • 148 citations

Purified protein kinase C phosphorylates a 47-kDa protein in control neutrophil cytoplasts but not in neutrophil cytoplasts from patients with the autosomal form of chronic granulomatous disease.

1988 • 127 citations

Mechanism of the superoxide-producing oxidase of neutrophils. O2 is necessary for the fast reduction of cytochrome b-245 by NADPH

1985 • 126 citations

Chronic granulomatous disease due to a defect in the cytosolic factor required for nicotinamide adenine dinucleotide phosphate oxidase activation.

1988 • 103 citations

Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridization.

1985 • 88 citations

Deficient flavoprotein component of the NADPH-dependent O2-.-generating oxidase in the neutrophils from three male patients with chronic granulomatous disease.

1984 • 67 citations

A study of 25 patients with chronic granulomatous disease: A new classification by correlating respiratory burst, cytochrome b, and flavoprotein

1986 • 63 citations

Changes in the subcellular distribution of the cytochrome b-245 on stimulation of human neutrophils

1984 • 51 citations

Involvement of protein kinase C in the phosphorylation of 46 kDa proteins which are phosphorylated in parallel with activation of NADPH oxidase in intact guinea-pig polymorphonuclear leukocytes

1986 • 45 citations

Quantitation of superoxide production in human polymorphonuclear leukocytes from normals and 3 types of chronic granulomatous disease

1979 • 40 citations

Phosphoproteins and the activation of the neutrophil respiratory burst oxidase

1987 • 2 citations

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Phosphorylation of the oxidase-related 48K phosphoprotein family in the unusual autosomal… (1988) – Blood | Metascience Observatory Explorer