recent publications

• academic article

  • Chanock, S. J., Roesler, J., Zhan, S. X., Hopkins, P., Lee, P., Barrett, D. T., Christensen, B. L., Curnutte, J. T., Gorlach, A. Genomic structure of the human p47-phox (ncf1) gene Blood Cells Molecules and Diseases  2000 26:37-46  DOI:10.1006/bcmd.2000.0274  PMID:10772875
  • Gorlach, A., Lee, P. L., Roesler, J., Hopkins, P. J., Christensen, B., Green, E. D., Chanock, S. J., Curnutte, J. T. A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease Journal of Clinical Investigation  1997 100:1907-1918  DOI:10.1172/jci119721  PMID:9329953
  • Maly, F. E., Schuerermaly, C. C., Quilliam, L., Cochrane, C. G., Newburger, P. E., Curnutte, J. T., Gifford, M., Dinauer, M. C. Restitution of superoxide generation in autosomal cytochrome-negative chronic granulomatous disease (A22(0) CGD)-derived B lymphocyte cell lines by transfection with p22phax cDNA Journal of Experimental Medicine  1993 178:2047-2053  DOI:10.1084/jem.178.6.2047  PMID:8245781  PMCID:PMC2191282
  • Heyworth, P. G., Curnutte, J. T., Nauseef, W. M., Volpp, B. D., Pearson, D. W., Rosen, H., Clark, R. A. Neutrophil nicotinamide adenine-dinucleotide phosphate oxidase assembly - translocation of p47-phox and p67-phox requires interaction between p47-phox and cytochrome-b558 Journal of Clinical Investigation  1991 87:352-356  DOI:10.1172/jci114993  PMID:1985107
  • Hurst, J. K., Loehr, T. M., Curnutte, J. T., Rosen, H. Resonance raman and electron-paramagnetic resonance structural investigations of neutrophil cytochrome-b558 Journal of Biological Chemistry  1991 266:1627-1634  PMID:1846361
  • Dinauer, M. C., Curnutte, J. T., Rosen, H., Orkin, S. H. A missense mutation in the neutrophil cytochrome-b heavy-chain in cytochrome-positive x-linked chronic granulomatous-disease Journal of Clinical Investigation  1989 84:2012-2016  DOI:10.1172/jci114393  PMID:2556453
  • Okamura, N., Malawista, S. E., Roberts, R. L., Rosen, H., Ochs, H. D., Babior, B. M., Curnutte, J. T. Phosphorylation of the oxidase-related k-48 phosphoprotein family in the unusual autosomal cytochrome-negative and x-linked cytochrome-positive types of chronic granulomatous-disease Blood  1988 72:811-816  PMID:3401601