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Items: 1 to 20 of 97

1.

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

Leto TL, Lomax KJ, Volpp BD, Nunoi H, Sechler JM, Nauseef WM, Clark RA, Gallin JI, Malech HL.

Science. 1990 May 11;248(4956):727-30.

PMID:
1692159
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3.

The p67-phox cytosolic peptide of the respiratory burst oxidase from human neutrophils. Functional aspects.

Okamura N, Babior BM, Mayo LA, Peveri P, Smith RM, Curnutte JT.

J Clin Invest. 1990 May;85(5):1583-7.

4.

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

Leusen JH, Meischl C, Eppink MH, Hilarius PM, de Boer M, Weening RS, Ahlin A, Sanders L, Goldblatt D, Skopczynska H, Bernatowska E, Palmblad J, Verhoeven AJ, van Berkel WJ, Roos D.

Blood. 2000 Jan 15;95(2):666-73.

5.

Recombinant 47-kilodalton cytosol factor restores NADPH oxidase in chronic granulomatous disease.

Lomax KJ, Leto TL, Nunoi H, Gallin JI, Malech HL.

Science. 1989 Jul 28;245(4916):409-12. Erratum in: Science 1989 Nov 24;246(4933):987.

PMID:
2547247
6.

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.

Leusen JH, de Boer M, Bolscher BG, Hilarius PM, Weening RS, Ochs HD, Roos D, Verhoeven AJ.

J Clin Invest. 1994 May;93(5):2120-6.

7.

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.

Dinauer MC, Pierce EA, Erickson RW, Muhlebach TJ, Messner H, Orkin SH, Seger RA, Curnutte JT.

Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11231-5.

8.

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

Volpp BD, Nauseef WM, Donelson JE, Moser DR, Clark RA.

Proc Natl Acad Sci U S A. 1989 Sep;86(18):7195-9. Erratum in: Proc Natl Acad Sci U S A 1989 Dec;86(23):9563.

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

Vergnaud S, Paclet MH, El Benna J, Pocidalo MA, Morel F.

Eur J Biochem. 2000 Feb;267(4):1059-67.

16.

Role of p67-phox SH3 domains in assembly of the NADPH oxidase system.

de Mendez I, Garrett MC, Adams AG, Leto TL.

J Biol Chem. 1994 Jun 10;269(23):16326-32.

17.

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

de Boer M, Hilarius-Stokman PM, Hossle JP, Verhoeven AJ, Graf N, Kenney RT, Seger R, Roos D.

Blood. 1994 Jan 15;83(2):531-6.

18.

Identification of the defective NADPH-oxidase component in chronic granulomatous disease: a study of 57 European families.

Casimir C, Chetty M, Bohler MC, Garcia R, Fischer A, Griscelli C, Johnson B, Segal AW.

Eur J Clin Invest. 1992 Jun;22(6):403-6.

PMID:
1633835
19.

Chronic granulomatous disease. Molecular genetics.

Dinauer MC, Orkin SH.

Hematol Oncol Clin North Am. 1988 Jun;2(2):225-40. Review.

PMID:
3292508
20.

Two cytosolic neutrophil oxidase components absent in autosomal chronic granulomatous disease.

Volpp BD, Nauseef WM, Clark RA.

Science. 1988 Dec 2;242(4883):1295-7.

PMID:
2848318

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