Vote for your favorite mineral in #MinCup25! - Titanite vs. Thortveitite
It's a pair of T-minerals with as versatile #titanite faces off against the home of rare earth elements #thortveitite.
Log InRegister
Quick Links : The Mindat ManualThe Rock H. Currier Digital LibraryMindat Newsletter [Free Download]
Home PageAbout MindatThe Mindat ManualHistory of MindatCopyright StatusWho We AreContact UsAdvertise on Mindat
Donate to MindatCorporate SponsorshipSponsor a PageSponsored PagesMindat AdvertisersAdvertise on Mindat
Learning CenterWhat is a mineral?The most common minerals on earthInformation for EducatorsMindat ArticlesThe ElementsThe Rock H. Currier Digital LibraryGeologic Time
Minerals by PropertiesMinerals by ChemistryAdvanced Locality SearchRandom MineralRandom LocalitySearch by minIDLocalities Near MeSearch ArticlesSearch GlossaryMore Search Options
Search For:
Mineral Name:
Locality Name:
Keyword(s):
 
The Mindat ManualAdd a New PhotoRate PhotosLocality Edit ReportCoordinate Completion ReportAdd Glossary Item
Mining CompaniesStatisticsUsersMineral MuseumsClubs & OrganizationsMineral Shows & EventsThe Mindat DirectoryDevice SettingsThe Mineral Quiz
Photo SearchPhoto GalleriesSearch by ColorNew Photos TodayNew Photos YesterdayMembers' Photo GalleriesPast Photo of the Day GalleryPhotography

Dinauer, M. C., Pierce, E. A., Erickson, R. W., Muhlebach, T. J., Messner, H., Orkin, S. H., Seger, R. A., Curnutte, J. T. (1991) 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. Proceedings of the National Academy of Sciences, 88 (24) 11231-11235 doi:10.1073/pnas.88.24.11231

Advanced
   -   Only viewable:
Reference TypeJournal (article/letter/editorial)
TitlePoint mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.
JournalProceedings of the National Academy of Sciences
AuthorsDinauer, M. C.Author
Pierce, E. A.Author
Erickson, R. W.Author
Muhlebach, T. J.Author
Messner, H.Author
Orkin, S. H.Author
Seger, R. A.Author
Curnutte, J. T.Author
Year1991 (December 15)Volume88
Issue24
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.88.24.11231Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1504245Long-form Identifiermindat:1:5:1504245:7
GUID0
Full ReferenceDinauer, M. C., Pierce, E. A., Erickson, R. W., Muhlebach, T. J., Messner, H., Orkin, S. H., Seger, R. A., Curnutte, J. T. (1991) 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. Proceedings of the National Academy of Sciences, 88 (24) 11231-11235 doi:10.1073/pnas.88.24.11231
Plain TextDinauer, M. C., Pierce, E. A., Erickson, R. W., Muhlebach, T. J., Messner, H., Orkin, S. H., Seger, R. A., Curnutte, J. T. (1991) 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. Proceedings of the National Academy of Sciences, 88 (24) 11231-11235 doi:10.1073/pnas.88.24.11231
In(1991, December) Proceedings of the National Academy of Sciences Vol. 88 (24) Proceedings of the National Academy of Sciences

See Also

These are possibly similar items as determined by title/reference text matching only.

Archer, S. L., Reeve, H. L., Michelakis, E., Puttagunta, L., Waite, R., Nelson, D. P., Dinauer, M. C., Weir, E. K. (1999) O2 sensing is preserved in mice lacking the gp91 phox subunit of NADPH oxidase. Proceedings of the National Academy of Sciences, 96 (14) 7944-7949 doi:10.1073/pnas.96.14.7944
Yu, L., Quinn, M. T., Cross, A. R., Dinauer, M. C. (1998) Gp91phox is the heme binding subunit of the superoxide-generating NADPH oxidase. Proceedings of the National Academy of Sciences, 95 (14) 7993-7998 doi:10.1073/pnas.95.14.7993
Parkos, C. A., Dinauer, M. C., Walker, L. E., Allen, R. A., Jesaitis, A. J., Orkin, S. H. (1988) Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b. Proceedings of the National Academy of Sciences, 85 (10) 3319-3323 doi:10.1073/pnas.85.10.3319
Dinauer, Mary C., Orkin, Stuart H., Brown, Robin, Jesaitis, Algirdas J., Parkos, Charles A. (1987) The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex. Nature, 327 (6124). 717-720 doi:10.1038/327717a0
Nanda, A., Grinstein, S., Curnutte, J. T. (1993) Abnormal activation of H+ conductance in NADPH oxidase-defective neutrophils. Proceedings of the National Academy of Sciences, 90 (2) 760-764 doi:10.1073/pnas.90.2.760
Zhen, L., King, A. A., Xiao, Y., Chanock, S. J., Orkin, S. H., Dinauer, M. C. (1993) Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phox. Proceedings of the National Academy of Sciences, 90 (21) 9832-9836 doi:10.1073/pnas.90.21.9832
Curnutte, J. T., Scott, P. J., Mayo, L. A. (1989) Cytosolic components of the respiratory burst oxidase: resolution of four components, two of which are missing in complementing types of chronic granulomatous disease. Proceedings of the National Academy of Sciences, 86 (3) 825-829 doi:10.1073/pnas.86.3.825
Rae, Julie, Newburger, Peter E., Dinauer, Mary C., Noack, Deborah, Hopkins, Penelope J., Kuruto, Ryoko, Curnutte, John T. (1998) X-Linked Chronic Granulomatous Disease: Mutations in the CYBB Gene Encoding the gp91-phox Component of Respiratory-Burst Oxidase. The American Journal of Human Genetics, 62 (6) 1320-1331 doi:10.1086/301874
Jacob, C. O., Eisenstein, M., Dinauer, M. C., Ming, W., Liu, Q., John, S., Quismorio, F. P., Reiff, A., Myones, B. L., Kaufman, K. M., McCurdy, D., Harley, J. B., Silverman, E., Kimberly, R. P., Vyse, T. J., Gaffney, P. M., Moser, K. L., Klein-Gitelman, M., Wagner-Weiner, L., Langefeld, C. D., Armstrong, D. L., Zidovetzki, R. (2012) Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase. Proceedings of the National Academy of Sciences, 109 (2) doi:10.1073/pnas.1113251108
Baehner, R. L., Kunkel, L. M., Monaco, A. P., Haines, J. L., Conneally, P. M., Palmer, C., Heerema, N., Orkin, S. H. (1986) DNA linkage analysis of X chromosome-linked chronic granulomatous disease. Proceedings of the National Academy of Sciences, 83 (10) 3398-3401 doi:10.1073/pnas.83.10.3398
Malech, H. L., Maples, P. B., Whiting-Theobald, N., Linton, G. F., Sekhsaria, S., Vowells, S. J., Li, F., Miller, J. A., DeCarlo, E., Holland, S. M., Leitman, S. F., Carter, C. S., Butz, R. E., Read, E. J., Fleisher, T. A., Schneiderman, R. D., Van Epps, D. E., Spratt, S. K., Maack, C. A., Rokovich, J. A., Cohen, L. K., Gallin, J. I. (1997) Prolonged production of NADPH oxidase-corrected granulocytes after gene therapy of chronic granulomatous disease. Proceedings of the National Academy of Sciences, 94 (22) 12133-12138 doi:10.1073/pnas.94.22.12133
 
and/or  
Mindat.org is an outreach project of the Hudson Institute of Mineralogy, a 501(c)(3) not-for-profit organization.
Copyright © mindat.org and the Hudson Institute of Mineralogy 1993-2025, except where stated. Most political location boundaries are Β© OpenStreetMap contributors. Mindat.org relies on the contributions of thousands of members and supporters. Founded in 2000 by Jolyon Ralph.
To cite: Ralph, J., Von Bargen, D., Martynov, P., Zhang, J., Que, X., Prabhu, A., Morrison, S. M., Li, W., Chen, W., & Ma, X. (2025). Mindat.org: The open access mineralogy database to accelerate data-intensive geoscience research. American Mineralogist, 110(6), 833–844. doi:10.2138/am-2024-9486.
Privacy Policy - Terms & Conditions - Contact Us / DMCA issues - Report a bug/vulnerability Current server date and time: September 11, 2025 09:31:39
Go to top of page