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

The structure of the tetratricopeptide repeats of protein phosphatase 5: implications for TPR-mediated protein-protein interactions

1998 • 820 citations

Assembly of the phagocyte NADPH oxidase: molecular interaction of oxidase proteins

1996 • 534 citations

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

1996 • 424 citations

Novel domains in NADPH oxidase subunits, sorting nexins, and PtdIns 3‐kinases: Binding partners of SH3 domains?

1996 • 304 citations

Rac translocates independently of the neutrophil NADPH oxidase components p47phox and p67phox. Evidence for its interaction with flavocytochrome b558.

1994 • 260 citations

The Tetratricopeptide Repeat Domain of Protein Phosphatase 5 Mediates Binding to Glucocorticoid Receptor Heterocomplexes and Acts as a Dominant Negative Mutant

1996 • 224 citations

X-Linked Chronic Granulomatous Disease: Mutations in the CYBB Gene Encoding the gp91-phox Component of Respiratory-Burst Oxidase

1998 • 207 citations

The Cytosolic Component p47 Is Not a Sine Qua Non Participant in the Activation of NADPH Oxidase but Is Required for Optimal Superoxide Production

1996 • 150 citations

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

1997 • 138 citations

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

1991 • 119 citations

The NADPH oxidase complex of phagocytic leukocytes: a biochemical and cytochemical view

1995 • 103 citations

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

1995 • 97 citations

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

1996 • 87 citations

Simultaneous Presence of p47 and Flavocytochrome b −245 Are Required for the Activation of NADPH Oxidase by Anionic Amphiphiles

1999 • 54 citations

The cytosolic subunit p67phox contains an NADPH-binding site that participates in catalysis by the leukocyte NADPH oxidase.

1996 • 49 citations

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

1994 • 49 citations

Characterization of the p67phox gene: genomic organization and restriction fragment length polymorphism analysis for prenatal diagnosis in chronic granulomatous disease

1993 • 38 citations

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

1995 • 34 citations

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

1996 • 26 citations

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

1995 • 25 citations

Identification of a Double Mutation (D160V-K161E) in the p67phox Gene of a Chronic Granulomatous Disease Patient

1997 • 18 citations

A new quantitative nitroblue tetrazolium reduction assay based on kinetic colorimetry

1990 • 14 citations

Deleted Work

1955 • 0 citations