162 related articles for article (PubMed ID: 33892719)
21. Clinical, Immunological, and Molecular Findings of Patients with p47
Kulkarni M; Desai M; Gupta M; Dalvi A; Taur P; Terrance A; Bhat S; Manglani M; Raj R; Shah I; Madkaikar M
J Clin Immunol; 2016 Nov; 36(8):774-784. PubMed ID: 27699571
[TBL] [Abstract][Full Text] [Related]
22. NCF1-dependent production of ROS protects against lupus by regulating plasmacytoid dendritic cell development and functions.
Luo H; Urbonaviciute V; Saei AA; Lyu H; Gaetani M; Végvári Á; Li Y; Zubarev RA; Holmdahl R
JCI Insight; 2023 Apr; 8(7):. PubMed ID: 36853827
[TBL] [Abstract][Full Text] [Related]
23. 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.
Roos D; de Boer M; Köker MY; Dekker J; Singh-Gupta V; Ahlin A; Palmblad J; Sanal O; Kurenko-Deptuch M; Jolles S; Wolach B
Hum Mutat; 2006 Dec; 27(12):1218-29. PubMed ID: 16972229
[TBL] [Abstract][Full Text] [Related]
24. Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(phox)-deficient chronic granulomatous disease.
Hayrapetyan A; Dencher PC; van Leeuwen K; de Boer M; Roos D
Biochim Biophys Acta; 2013 Oct; 1832(10):1662-72. PubMed ID: 23688784
[TBL] [Abstract][Full Text] [Related]
25. Genetic and molecular findings of 38 Iranian patients with chronic granulomatous disease caused by p47-phox defect.
Tajik S; Badalzadeh M; Fazlollahi MR; Houshmand M; Bazargan N; Movahedi M; Mahlouji Rad M; Mahdaviani SA; Mamishi S; Khotaei GT; Mansouri D; Zandieh F; Pourpak Z
Scand J Immunol; 2019 Jul; 90(1):e12767. PubMed ID: 30963593
[TBL] [Abstract][Full Text] [Related]
26. Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A).
Wolach B; Gavrieli R; de Boer M; van Leeuwen K; Wolach O; Grisaru-Soen G; Broides A; Etzioni A; Somech R; Roos D
J Clin Immunol; 2018 Feb; 38(2):193-203. PubMed ID: 29411231
[TBL] [Abstract][Full Text] [Related]
27. Neutrophil Cytosolic Factor-1 Genotyping in Acne Vulgaris.
Bakry O; Shoeib M; Soliman S; Kamal L
Skin Pharmacol Physiol; 2021; 34(1):51-56. PubMed ID: 33596590
[TBL] [Abstract][Full Text] [Related]
28. A novel mutation in NCF2 associated with autoimmune disease and a solitary late-onset infection.
Chou J; Hsu JT; Bainter W; Al-Attiyah R; Al-Herz W; Geha RS
Clin Immunol; 2015 Dec; 161(2):128-30. PubMed ID: 26272171
[TBL] [Abstract][Full Text] [Related]
29. Whole Exome Sequencing in Early-onset Systemic Lupus Erythematosus.
Batu ED; Koşukcu C; Taşkıran E; Sahin S; Akman S; Sözeri B; Ünsal E; Bilginer Y; Kasapcopur O; Alikaşifoğlu M; Ozen S
J Rheumatol; 2018 Dec; 45(12):1671-1679. PubMed ID: 30008451
[TBL] [Abstract][Full Text] [Related]
30. Loss-of-function variants in
Xu L; Zhao J; Sun Q; Xu X; Wang L; Liu T; Wu Y; Zhu J; Geng L; Deng Y; Awgulewitsch A; Kamen DL; Oates JC; Raj P; Wakeland EK; Scofield RH; Guthridge JM; James JA; Hahn BH; McCurdy DK; Wang F; Zhang M; Tan W; Gilkeson GS; Tsao BP
Ann Rheum Dis; 2022 Dec; 81(12):1712-1721. PubMed ID: 35977808
[TBL] [Abstract][Full Text] [Related]
31. Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes.
Vázquez N; Lehrnbecher T; Chen R; Christensen BL; Gallin JI; Malech H; Holland S; Zhu S; Chanock SJ
Exp Hematol; 2001 Feb; 29(2):234-43. PubMed ID: 11166463
[TBL] [Abstract][Full Text] [Related]
32. Identification of a pathogenic variant in TREX1 in early-onset cerebral systemic lupus erythematosus by Whole-exome sequencing.
Ellyard JI; Jerjen R; Martin JL; Lee AY; Field MA; Jiang SH; Cappello J; Naumann SK; Andrews TD; Scott HS; Casarotto MG; Goodnow CC; Chaitow J; Pascual V; Hertzog P; Alexander SI; Cook MC; Vinuesa CG
Arthritis Rheumatol; 2014 Dec; 66(12):3382-6. PubMed ID: 25138095
[TBL] [Abstract][Full Text] [Related]
33. Genetic heterogeneity of pediatric systemic lupus erythematosus with lymphoproliferation.
Li G; Li Y; Liu H; Shi Y; Guan W; Zhang T; Yao W; Wu B; Xu H; Sun L
Medicine (Baltimore); 2020 May; 99(20):e20232. PubMed ID: 32443356
[TBL] [Abstract][Full Text] [Related]
34. Variants in nicotinamide adenine dinucleotide phosphate oxidase complex components determine susceptibility to very early onset inflammatory bowel disease.
Dhillon SS; Fattouh R; Elkadri A; Xu W; Murchie R; Walters T; Guo C; Mack D; Huynh HQ; Baksh S; Silverberg MS; Griffiths AM; Snapper SB; Brumell JH; Muise AM
Gastroenterology; 2014 Sep; 147(3):680-689.e2. PubMed ID: 24931457
[TBL] [Abstract][Full Text] [Related]
35. A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation.
van de Vosse E; van Wengen A; van Geelen JA; de Boer M; Roos D; van Dissel JT
J Hum Genet; 2009 Jun; 54(6):313-6. PubMed ID: 19329991
[TBL] [Abstract][Full Text] [Related]
36. A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi Jews.
de Boer M; Tzur S; van Leeuwen K; Dencher PC; Skorecki K; Wolach B; Gavrieli R; Nasidze I; Stoneking M; Tanck MW; Roos D
Blood Cells Mol Dis; 2015 Dec; 55(4):320-7. PubMed ID: 26460255
[TBL] [Abstract][Full Text] [Related]
37. Regulatory T cell features in chronic granulomatous disease.
van de Geer A; Cuadrado E; Slot MC; van Bruggen R; Amsen D; Kuijpers TW
Clin Exp Immunol; 2019 Aug; 197(2):222-229. PubMed ID: 30924925
[TBL] [Abstract][Full Text] [Related]
38. Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.
Baba LA; Ailal F; El Hafidi N; Hubeau M; Jabot-Hanin F; Benajiba N; Aadam Z; Conti F; Deswarte C; Jeddane L; Aglaguel A; El Maataoui O; Tissent A; Mahraoui C; Najib J; Martinez-Barricarte R; Abel L; Habti N; Saile R; Casanova JL; Bustamante J; Salih Alj H; Bousfiha AA
J Clin Immunol; 2014 May; 34(4):452-8. PubMed ID: 24596025
[TBL] [Abstract][Full Text] [Related]
39. Independent and inter-dependent immunoregulatory effects of NCF1 and NOS2 in experimental autoimmune encephalomyelitis.
Zhong J; Yau ACY; Holmdahl R
J Neuroinflammation; 2020 Apr; 17(1):113. PubMed ID: 32276661
[TBL] [Abstract][Full Text] [Related]
40. Association of NOX2 subunits genetic variants with autoimmune diseases.
Zhong J; Olsson LM; Urbonaviciute V; Yang M; Bäckdahl L; Holmdahl R
Free Radic Biol Med; 2018 Sep; 125():72-80. PubMed ID: 29526808
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
