| 1 | NCF1, NCF1D
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| Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects.
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| Chiriaco M, Salfa I, Di Matteo G, Rossi P, Finocchi A.
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| Pediatr Allergy Immunol 27(3):242-53. doi: 10.1111/pai.12527. Review.
2016
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| 2 | CYBB, NCF1
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| Direct Comparison of a Natural Loss-Of-Function Single Nucleotide Polymorphism with a Targeted Deletion in the Ncf1 Gene Reveals Different Phenotypes.
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| Sareila O, Hagert C, Rantakari P, Poutanen M, Holmdahl R.
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| PLoS One 10(11):e0141974. doi: 10.1371/journal.pone.0141974.
2015
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| 3 | NCF1
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| p47phox-Nox2-dependent ROS Signaling Inhibits Early Bone Development in Mice but Protects against Skeletal Aging.
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| Chen JR, Lazarenko OP, Blackburn ML, Mercer KE, Badger TM, Ronis MJ.
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| J Biol Chem 290(23):14692-704. doi: 10.1074/jbc.M114.633461.
2015
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| 4 | MAPK14, NCF1, PIN1, TLR8
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| TLR8, but not TLR7, induces the priming of the NADPH oxidase activation in human neutrophils.
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| Makni-Maalej K, Marzaioli V, Boussetta T, Belambri SA, Gougerot-Pocidalo MA, Hurtado-Nedelec M, Dang PM, El-Benna J.
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| J Leukoc Biol 97(6):1081-7. doi: 10.1189/jlb.2A1214-623R.
2015
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| 5 | ANGPT1, NCF1
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| Angiopoietin-1 requires oxidant signaling through p47phox to promote endothelial barrier defense.
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| Ghosh CC, Mukherjee A, David S, Milam KE, Hunter JT, Parikh SM.
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| PLoS One 10(3):e0119577. doi: 10.1371/journal.pone.0119577.
2015
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| 6 | NCF1, NMRAL1
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| HSCARG, a novel regulator of H2A ubiquitination by downregulating PRC1 ubiquitin E3 ligase activity, is essential for cell proliferation.
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| Hu B, Li S, Zhang X, Zheng X.
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| Nucleic Acids Res 42(9):5582-93. doi: 10.1093/nar/gku230. Epub 2014 Apr 7.
2014
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| 7 | NCF1
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| Molecular insights of p47phox phosphorylation dynamics in the regulation of NADPH oxidase activation and superoxide production.
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| Meijles DN, Fan LM, Howlin BJ, Li JM.
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| J Biol Chem 289(33):22759-70. doi: 10.1074/jbc.M114.561159.
2014
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| 8 | CYBB, NCF1
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| Nox2 and p47(phox) modulate compensatory growth of primary collateral arteries.
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| DiStasi MR, Unthank JL, Miller SJ.
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| Am J Physiol Heart Circ Physiol 306(10):H1435-43. doi: 10.1152/ajpheart.00828.2013.
2014
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| 9 | NCF1, RAC2
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| The recruitment of p47(phox) and Rac2G12V at the phagosome is transient and phosphatidylserine dependent.
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| Faure MC, Sulpice JC, Delattre M, Lavielle M, Prigent M, Cuif MH, Melchior C, Tschirhart E, Nüße O, Dupré-Crochet S.
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| Biol Cell 105(11):501-18. doi: 10.1111/boc.201300010.
2013
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| 10 | NCF1
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| Female mice lacking p47phox have altered adipose tissue gene expression and are protected against high fat-induced obesity.
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| Ronis MJ, Sharma N, Vantrease J, Borengasser SJ, Ferguson M, Mercer KE, Cleves MA, Gomez-Acevedo H, Badger TM.
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| Physiol Genomics 45(9):351-66. doi: 10.1152/physiolgenomics.00148.2012.
2013
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| 11 | CYBB, NCF1
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| Loss of p47phox subunit enhances susceptibility to biomechanical stress and heart failure because of dysregulation of cortactin and actin filaments.
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| Patel VB, Wang Z, Fan D, Zhabyeyev P, Basu R, Das SK, Wang W, Desaulniers J, Holland SM, Kassiri Z, Oudit GY.
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| Circ Res 112(12):1542-56. doi: 10.1161/CIRCRESAHA.111.300299.
2013
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| 12 | NCF1
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| p47(phox) is required for afferent arteriolar contractile responses to angiotensin II and perfusion pressure in mice.
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| Lai EY, Solis G, Luo Z, Carlstrom M, Sandberg K, Holland S, Wellstein A, Welch WJ, Wilcox CS.
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| Hypertension 59(2):415-20. doi: 10.1161/HYPERTENSIONAHA.111.184291.
2012
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| 13 | NCF1
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| Copy number variation of the gene NCF1 is associated with rheumatoid arthritis.
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| Olsson LM, Nerstedt A, Lindqvist AK, Johansson SC, Medstrand P, Olofsson P, Holmdahl R.
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| Antioxid Redox Signal 16(1):71-8. doi: 10.1089/ars.2011.4013.
2012
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| 14 | NCF1
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| Ncf1 (p47phox) is essential for direct regulatory T cell mediated suppression of CD4+ effector T cells.
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| Efimova O, Szankasi P, Kelley TW.
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| PLoS One 6(1):e16013. doi: 10.1371/journal.pone.0016013.
2011
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| 15 | NCF1, NCF1B
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| A copy number variation in human NCF1 and its pseudogenes.
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| Brunson T, Wang Q, Chambers I, Song Q.
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| BMC Genet 11:13.PMID: 20178640 2010
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| 16 | NCF1, NCF1D
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| Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update).
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| Roos D, Kuhns DB, Maddalena A, Bustamante J, Kannengiesser C, de Boer M, van Leeuwen K, Köker MY, Wolach B, Roesler J, Malech HL, Holland SM, Gallin JI, Stasia MJ.
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| Blood Cells Mol Dis 44(4):291-9. Epub 2010 Feb 18. Review.PMID: 20167518 2010
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| 17 | NCF1, NCF1D
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| A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation.
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| van de Vosse E, van Wengen A, van Geelen JA, de Boer M, Roos D, van Dissel JT.
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| J Hum Genet 54(6):313-6. Epub 2009 Mar 27.PMID: 19329991 2009
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| 18 | NCF1
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| NCF1 gene and pseudogene pattern: association with parasitic infection and autoimmunity.
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| Greve B, Hoffmann P, Vonthein R, Kun J, Lell B, Mycko MP, Selmaj KW, Berger K, Weissert R, Kremsner PG.
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| Malar J 7:251.PMID: 19077231 2008
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| 19 | NCF1, NCF1D
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| Autosomal recessive chronic granulomatous disease, IgA deficiency and refractory autoimmune thrombocytopenia responding to Anti-CD20 monoclonal antibody.
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| Shamsian BS, Mansouri D, Pourpak Z, Rezaei N, Chavoshzadeh Z, Jadali F, Gharib A, Alavi S, Eghbali A, Arzanian MT.
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| Iran J Allergy Asthma Immunol 7(3):181-4.PMID: 18780954 2008
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| 20 | WBS, NCF1
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| Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension.
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| Del Campo M, Antonell A, Magano LF, Munoz FJ, Flores R, Bayes M, Perez Jurado LA.
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| Am J Hum Genet 78(4):533-42. Epub 2006 Jan 31. 2006
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| 21 | NCF1
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| Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase.
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| Roos D, de Boer M, Koker MY, Dekker J, Singh-Gupta V, Ahlin A, Palmblad J, Sanal O, Kurenko-Deptuch M, Jolles S, Wolach B.
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| Hum Mutat 27(12):1218-29. 2006
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| 22 | GTF2I, NCF1, POM121, EIF4H, MLXIPL, WBS
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| Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.
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| DeSilva U, Elnitski L, Idol JR, Doyle JL, Gan W, Thomas JW, Schwartz S, Dietrich NL, Beckstrom-Sternberg SM, McDowell JC, Blakesley RW, Bouffard GG, Thomas PJ, Touchman JW, Miller W, Green ED.
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| Genome Res 12(1):3-15. 2002
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| 23 | NCF1
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| Genomic structure of the human p47-phox (NCF1) gene.
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| Chanock SJ, Roesler J, Zhan S, Hopkins P, Lee P, Barrett DT, Christensen BL, Curnutte JT, Gorlach A.
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| Blood Cells Mol Dis 26(1):37-46. 2000
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| 24 | NCF1, NCF1B
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| A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease.
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| Gorlach A, Lee PL, Roesler J, Hopkins PJ, Christensen B, Green ED, Chanock SJ, Curnutte JT.
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| J Clin Invest 100(8):1907-18. 1997
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| 25 | NCF1, NCF2, NCF4, PIK3C2G, SNX1
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| Novel domains in NADPH oxidase subunits, sorting nexins, and PtdIns 3-kinases : binding partners of SH3 domains ?
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| Ponting CP.
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| Protein Sci 5 : 2353-2357. 1996
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| 26 | CYBA, CYBB, NCF1
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| Role of Src homology 3 domains in assembly and activation of the phagocyte NADPH oxidase.
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| Sumimoto H, Kage Y, Nunoi H, Sasaki H, Nose T, Fukumaki Y, Ohno M, Minakami S, Takeshige K.
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| Proc Natl Acad Sci U S A 91(12):5345-9. 1994
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| 27 | NCF1
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| Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat.
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| Casimir CM, et al.
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| Proc Natl Acad Sci U S A 88 : 2753-2757. 1991
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| 28 | GDCC2, NCF1, NCF2
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| Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1).
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| Francke U, et al.
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| Am J Hum Genet 47 : 483-492. 1990
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| 29 | CYBA, CYBB, GDCC2, NCF1, NCF2
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| Genetic variants of chronic granulomatous disease : prevalence of deficiencies of two cytosolic components of the NADPH oxidase system.
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| Clark RA, et al.
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| N Engl J Med 321 : 647-652. 1989
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| 30 | NCF1
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| Cloning of the cDNA and functional expression of the 47-kilodalton cytosolic component of human neutrophil respiratory burst oxidase.
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| Volpp BD, et al.
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| Proc Natl Acad Sci U S A 86 : 7195-7199. 1989
|