| 1 | NCF2, VAV1
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| Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase.
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| Jacob CO, Eisenstein M, Dinauer MC, Ming W, Liu Q, John S, Quismorio FP Jr, Reiff A, Myones BL, Kaufman KM, McCurdy D, Harley JB, Silverman E, Kimberly RP, Vyse TJ, Gaffney PM, Moser KL, Klein-Gitelman M, Wagner-Weiner L, Langefeld CD, Armstrong DL, Zidovetzki R.
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| Proc Natl Acad Sci U S A 109(2):E59-67. doi: 10.1073/pnas.1113251108. Epub 2011 Dec 27. 2012
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| 2 | MED15, NCF2, PLAGL2, SPI1
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| Modulation of PLAGL2 transactivation by positive cofactor 2 (PC2), a component of the ARC/Mediator complex.
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| Wezensky SJ, Hanks TS, Wilkison MJ, Ammons MC, Siemsen DW, Gauss KA.
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| Gene 452(1):22-34. Epub 2009 Dec 16. 2010
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| 3 | NCF2
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| A single nucleotide polymorphism in the promoter region of theNCF-2 gene.
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| Gomez LA, Patino PJ, Novaira HJ, Morales MM, Condino-Neto A.
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| Am J Hematol 82(12):1124-5. No abstract available. 2007
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| 4 | NCF2
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| Variants of the 5'-untranslated region of human NCF2: expression and translational efficiency.
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| Gauss KA, Bunger PL, Crawford MA, McDermott BE, Swearingen R, Nelson-Overton LK, Siemsen DW, Kobayashi SD, Deleo FR, Quinn MT.
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| Gene 366(1):169-79. Epub 2005 Nov 28. 2006
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| 5 | CYBA, CYBB, NCF2
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| Assembly of the neutrophil respiratory burst oxidase: A direct interaction between p67PHOX and cytochrome b558.
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| Dang PM, Cross AR, Babior BM.
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| Proc Natl Acad Sci U S A 98(6):3001-5. 2001
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| 6 | GDCC2, NCF2
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| A 1.1-kb duplication in the p67-phox gene causes chronic granulomatous disease.
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| Borgato L, Bonizzato A, Lunardi C, Dusi S, Andrioli G, Scarperi A, Corrocher R.
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| Hum Genet 108(6):504-10. 2001
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| 7 | GDCC2, NCF2
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| Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase.
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| Noack D, Rae J, Cross AR, Munoz J, Salmen S, Mendoza JA, Rossi N, Curnutte JT, Heyworth PG.
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| Hum Genet 105(5):460-7 1999
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| 8 | GDCC2, NCF2
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| Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient.
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| Bonizzato A, et al.
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| Biochem Biophys Res Commun 231 : 861-863. 1997
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| 9 | GDCC2, NCF2
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| Two-exon skipping due to a point mutation in p67-phox-deficient chronic granulomatous disease.
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| Aoshima M, et al.
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| Blood 88 : 1841-1845. 1996
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| 10 | 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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| 11 | GDCC2, NCF2
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| 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.
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| Cohen Tanugi-Cholley L, et al.
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| Blood 85 : 242-249. 1995
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| 12 | GDCC2, NCF2
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| Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component : identification of mutation and detection of carriers.
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| De Boer M, et al.
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| Blood 83 : 531-536. 1994
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| 13 | NCF2
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| Characterization of the p67phox gene : genomic organization and restriction fragment length polymorphism analysis for prenatal diagnosis in chronic granulomatous disease.
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| Kenney RT, et al.
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| Blood 82 : 3739-3744. 1993
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| 14 | 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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| 15 | NCF2
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| A HindIII polymorphism in the human NCF2 gene.
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| Kenney RT, et al.
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| Nucleic Acids Res 18 : 7193. 1990
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| 16 | 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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