170 related articles for article (PubMed ID: 11698128)
1. Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease.
Dekker J; de Boer M; Roos D
Exp Hematol; 2001 Nov; 29(11):1319-25. PubMed ID: 11698128
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease.
Roesler J; Curnutte JT; Rae J; Barrett D; Patino P; Chanock SJ; Goerlach A
Blood; 2000 Mar; 95(6):2150-6. PubMed ID: 10706888
[TBL] [Abstract][Full Text] [Related]
4.
Kuhns DB; Hsu AP; Sun D; Lau K; Fink D; Griffith P; Huang DW; Priel DAL; Mendez L; Kreuzburg S; Zerbe CS; De Ravin SS; Malech HL; Holland SM; Wu X; Gallin JI
Blood Adv; 2019 Jan; 3(2):136-147. PubMed ID: 30651282
[TBL] [Abstract][Full Text] [Related]
5. A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease.
Görlach A; Lee PL; Roesler J; Hopkins PJ; Christensen B; Green ED; Chanock SJ; Curnutte JT
J Clin Invest; 1997 Oct; 100(8):1907-18. PubMed ID: 9329953
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1.
de Boer M; Singh V; Dekker J; Di Rocco M; Goldblatt D; Roos D
Prenat Diagn; 2002 Mar; 22(3):235-40. PubMed ID: 11920901
[TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive chronic granulomatous disease caused by defects in NCF-1, the gene encoding the phagocyte p47-phox: mutations not arising in the NCF-1 pseudogenes.
Noack D; Rae J; Cross AR; Ellis BA; Newburger PE; Curnutte JT; Heyworth PG
Blood; 2001 Jan; 97(1):305-11. PubMed ID: 11133775
[TBL] [Abstract][Full Text] [Related]
9. Novel Diagnostic Tool for p47
Wrona D; Siler U; Reichenbach J
Mol Ther Methods Clin Dev; 2019 Jun; 13():274-278. PubMed ID: 30859112
[TBL] [Abstract][Full Text] [Related]
10. Genomic structure of the human p47-phox (NCF1) gene.
Chanock SJ; Roesler J; Zhan S; Hopkins P; Lee P; Barrett DT; Christensen BL; Curnutte JT; Görlach A
Blood Cells Mol Dis; 2000 Feb; 26(1):37-46. PubMed ID: 10772875
[TBL] [Abstract][Full Text] [Related]
11. Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion: significance for A47 degrees chronic granulomatous disease carrier detection.
Heyworth PG; Noack D; Cross AR
Blood; 2002 Sep; 100(5):1845-51. PubMed ID: 12176908
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Diagnostic paradigm for evaluation of male patients with chronic granulomatous disease, based on the dihydrorhodamine 123 assay.
Jirapongsananuruk O; Malech HL; Kuhns DB; Niemela JE; Brown MR; Anderson-Cohen M; Fleisher TA
J Allergy Clin Immunol; 2003 Feb; 111(2):374-9. PubMed ID: 12589359
[TBL] [Abstract][Full Text] [Related]
15. Defining p47-phox deficient Chronic Granulomatous Disease in a Malay family.
Gill HK; Kumar HC; Dhaliwal JS; Zabidi F; Sendut IH; Noah RM; Noh LM; Latiff AH; Murad S
Asian Pac J Allergy Immunol; 2012 Dec; 30(4):313-20. PubMed ID: 23393912
[TBL] [Abstract][Full Text] [Related]
16. A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi Jews.
De Boer M; Gavrieli R; van Leeuwen K; Wolf HR; Dushnitzki M; Bar-Yosef Y; Bar-Ziv A; Behar D; Lipitz S; Miller TE; Tool ATJ; Kuijpers TW; van den Berg TK; Wolach B; Roos D; Pras E
J Med Genet; 2018 Mar; 55(3):166-172. PubMed ID: 29331982
[TBL] [Abstract][Full Text] [Related]
17. [A case of Williams syndrome with p47-phox-deficient chronic granulomatous disease].
Kabuki T; Kawai T; Kin Y; Joh K; Ohashi H; Kosho T; Yachie A; Kanegane H; Miyawaki T; Oh-ishi T
Nihon Rinsho Meneki Gakkai Kaishi; 2003 Oct; 26(5):299-303. PubMed ID: 14635404
[TBL] [Abstract][Full Text] [Related]
18. Molecular characterization of the mouse p47-phox (Ncf1) gene and comparative analysis of the mouse p47-phox (Ncf1) gene to the human NCF1 gene.
DeSilva U; Miller E; Görlach A; Foster CB; Green ED; Chanock SJ
Mol Cell Biol Res Commun; 2000 Apr; 3(4):224-30. PubMed ID: 10891396
[TBL] [Abstract][Full Text] [Related]
19. Gene-edited pseudogene resurrection corrects p47
Merling RK; Kuhns DB; Sweeney CL; Wu X; Burkett S; Chu J; Lee J; Koontz S; Di Pasquale G; Afione SA; Chiorini JA; Kang EM; Choi U; De Ravin SS; Malech HL
Blood Adv; 2017 Jan; 1(4):270-278. PubMed ID: 29296942
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of autosomal recessive chronic granulomatous disease caused by a defect of the nicotinamide adenine dinucleotide phosphate (reduced form) oxidase component p67-phox.
Patiño PJ; Rae J; Noack D; Erickson R; Ding J; de Olarte DG; Curnutte JT
Blood; 1999 Oct; 94(7):2505-14. PubMed ID: 10498624
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]