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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1997 1
1998 2
1999 1
2000 3
2001 3
2002 3
2005 1
2006 2
2007 4
2008 5
2009 4
2010 2
2011 6
2012 11
2013 8
2014 5
2015 7
2016 12
2017 9
2018 14
2019 13
2020 7
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105 results
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Page 1
Chronic Granulomatous Disease.
Roos D. Roos D. Methods Mol Biol. 2019;1982:531-542. doi: 10.1007/978-1-4939-9424-3_32. Methods Mol Biol. 2019. PMID: 31172494 Review.
Inherited p40phox deficiency differs from classic chronic granulomatous disease.
van de Geer A, Nieto-Patlán A, Kuhns DB, Tool AT, Arias AA, Bouaziz M, de Boer M, Franco JL, Gazendam RP, van Hamme JL, van Houdt M, van Leeuwen K, Verkuijlen PJ, van den Berg TK, Alzate JF, Arango-Franco CA, Batura V, Bernasconi AR, Boardman B, Booth C, Burns SO, Cabarcas F, Bensussan NC, Charbit-Henrion F, Corveleyn A, Deswarte C, Azcoiti ME, Foell D, Gallin JI, Garcés C, Guedes M, Hinze CH, Holland SM, Hughes SM, Ibañez P, Malech HL, Meyts I, Moncada-Velez M, Moriya K, Neves E, Oleastro M, Perez L, Rattina V, Oleaga-Quintas C, Warner N, Muise AM, López JS, Trindade E, Vasconcelos J, Vermeire S, Wittkowski H, Worth A, Abel L, Dinauer MC, Arkwright PD, Roos D, Casanova JL, Kuijpers TW, Bustamante J. van de Geer A, et al. J Clin Invest. 2018 Aug 31;128(9):3957-3975. doi: 10.1172/JCI97116. Epub 2018 Aug 6. J Clin Invest. 2018. PMID: 29969437 Free PMC article.
Biallelic loss-of-function (LOF) mutations of the NCF4 gene, encoding the p40phox subunit of the phagocyte NADPH oxidase, have been described in only 1 patient. ...These patients display 8 different in-frame or out-of-frame mutations of NCF4 that are homozygous in 1 …
Biallelic loss-of-function (LOF) mutations of the NCF4 gene, encoding the p40phox subunit of the phagocyte NADPH oxidase, have been d …
Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects.
Chiriaco M, Salfa I, Di Matteo G, Rossi P, Finocchi A. Chiriaco M, et al. Pediatr Allergy Immunol. 2016 May;27(3):242-53. doi: 10.1111/pai.12527. Epub 2016 Jan 21. Pediatr Allergy Immunol. 2016. PMID: 26680691 Review.
CGD is a genetically heterogeneous disease with an X-linked recessive (XR-CGD) form caused by mutations in the CYBB gene encoding the gp91(phox) protein, and an autosomal recessive (AR-CGD) form caused by mutations in the CYBA, NCF1, NCF2, or NCF4 genes encoding p22(phox) …
CGD is a genetically heterogeneous disease with an X-linked recessive (XR-CGD) form caused by mutations in the CYBB gene encoding the gp91(p …
NADPH oxidase activation in neutrophils: Role of the phosphorylation of its subunits.
Belambri SA, Rolas L, Raad H, Hurtado-Nedelec M, Dang PM, El-Benna J. Belambri SA, et al. Eur J Clin Invest. 2018 Nov;48 Suppl 2:e12951. doi: 10.1111/eci.12951. Epub 2018 Jun 3. Eur J Clin Invest. 2018. PMID: 29757466 Review.
Macrophages target Salmonella by Lc3-associated phagocytosis in a systemic infection model.
Masud S, Prajsnar TK, Torraca V, Lamers GEM, Benning M, Van Der Vaart M, Meijer AH. Masud S, et al. Autophagy. 2019 May;15(5):796-812. doi: 10.1080/15548627.2019.1569297. Epub 2019 Jan 24. Autophagy. 2019. PMID: 30676840 Free PMC article.
Abbreviations: ATG: autophagy related gene; BECN1: Beclin 1; CFU: colony forming units; CYBA/P22PHOX: cytochrome b-245, alpha chain; CYBB/NOX2: cytochrome b-245 beta chain; dpf: days post fertilization; EGFP: enhanced green fluorescent protein; GFP: green fluorescent protein; hfp …
Abbreviations: ATG: autophagy related gene; BECN1: Beclin 1; CFU: colony forming units; CYBA/P22PHOX: cytochrome b-245, alpha chain; CYBB/NO …
Recommendations for genetic testing to reduce the incidence of anthracycline-induced cardiotoxicity.
Aminkeng F, Ross CJ, Rassekh SR, Hwang S, Rieder MJ, Bhavsar AP, Smith A, Sanatani S, Gelmon KA, Bernstein D, Hayden MR, Amstutz U, Carleton BC; CPNDS Clinical Practice Recommendations Group. Aminkeng F, et al. Br J Clin Pharmacol. 2016 Sep;82(3):683-95. doi: 10.1111/bcp.13008. Epub 2016 Jun 30. Br J Clin Pharmacol. 2016. PMID: 27197003 Free PMC article. Review.
Genetic variants in ABCC1, ABCC2, ABCC5, ABCB1, ABCB4, CBR3, RAC2, NCF4, CYBA, GSTP1, CAT, SULT2B1, POR, HAS3, SLC22A7, SCL22A17, HFE and NOS3 have also been associated with ACT, but require additional validation. ...
Genetic variants in ABCC1, ABCC2, ABCC5, ABCB1, ABCB4, CBR3, RAC2, NCF4, CYBA, GSTP1, CAT, SULT2B1, POR, HAS3, SLC22A7, SCL22A17, HFE …
Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility.
Ju Z, Wang C, Wang X, Yang C, Sun Y, Jiang Q, Wang F, Li M, Zhong J, Huang J. Ju Z, et al. PLoS One. 2015 Nov 24;10(11):e0143705. doi: 10.1371/journal.pone.0143705. eCollection 2015. PLoS One. 2015. PMID: 26600390 Free PMC article.
To determine whether NCF4-TV could be due to the g.18174 A>G mutation, we constructed two mini-gene expression vectors with the wild-type or mutant NCF4 g.18174 A>G fragment. ...NCF4 expression was also regulated by alternative splicing. This study prop …
To determine whether NCF4-TV could be due to the g.18174 A>G mutation, we constructed two mini-gene expression vectors with the wi …
A Reduction in Intracellular Reactive Oxygen Species Due to a Mutation in NCF4 Promotes Autoimmune Arthritis in Mice.
Winter S, Hultqvist Hopkins M, Laulund F, Holmdahl R. Winter S, et al. Antioxid Redox Signal. 2016 Dec 20;25(18):983-996. doi: 10.1089/ars.2016.6675. Epub 2016 Jul 8. Antioxid Redox Signal. 2016. PMID: 27231144
To address the impact of NCF4 and selective changes in intracellular ROS production on autoimmune inflammation, we studied collagen-induced arthritis (CIA) and mannan-induced psoriatic arthritis-like disease (MIP) in mice lacking NCF4 and mice with a mutation in the …
To address the impact of NCF4 and selective changes in intracellular ROS production on autoimmune inflammation, we studied collagen-i …
The effect of the SNP g.18475 A>G in the 3'UTR of NCF4 on mastitis susceptibility in dairy cattle.
Ju Z, Wang C, Wang X, Yang C, Zhang Y, Sun Y, Jiang Q, Li R, Li J, Zhong J, Huang J. Ju Z, et al. Cell Stress Chaperones. 2018 May;23(3):385-391. doi: 10.1007/s12192-017-0848-z. Epub 2018 Feb 23. Cell Stress Chaperones. 2018. PMID: 29476341 Free PMC article.
To explore the variability of the NCF4 gene and the susceptibility of cows to mastitis, NCF4 functional single nucleotide polymorphism (SNP) of the 3' untranslated region (3'UTR) and its targeted microRNA (miRNA) were identified. ...NCF4 expression was regula …
To explore the variability of the NCF4 gene and the susceptibility of cows to mastitis, NCF4 functional single nucleotide poly …
NOX2 in autoimmunity, tumor growth and metastasis.
Martner A, Aydin E, Hellstrand K. Martner A, et al. J Pathol. 2019 Feb;247(2):151-154. doi: 10.1002/path.5175. Epub 2018 Nov 29. J Pathol. 2019. PMID: 30270440 Free PMC article.
Recent research published in the Journal of Pathology showed that genetic depletion of any of the NOX2 subunits Cyba, Cybb, Ncf1, Ncf2 and Ncf4 reduced the formation of lung metastases following intravenous injection of murine tumor cells. ...
Recent research published in the Journal of Pathology showed that genetic depletion of any of the NOX2 subunits Cyba, Cybb, Ncf1, Ncf2 and …
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