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Journal Abstract Search
258 related items for PubMed ID: 24999735
1. Genetic analysis of CYBB gene in 26 korean families with X-linked chronic granulomatous disease. Ko SH, Rhim JW, Shin KS, Hahn YS, Lee SY, Kim JG. Immunol Invest; 2014; 43(6):585-94. PubMed ID: 24999735 [Abstract] [Full Text] [Related]
2. Characterization of 17 new cases of X-linked chronic granulomatous disease with seven novel mutations in the CYBB gene. von Goessel H, Hossle JP, Seger R, Gungor T. Exp Hematol; 2006 Apr; 34(4):528-35. PubMed ID: 16569599 [Abstract] [Full Text] [Related]
3. Characterization of 11 novel mutations in the X-linked chronic granulomatous disease (CYBB gene). Gérard B, El Benna J, Alcain F, Gougerot-Pocidalo MA, Grandchamp B, Chollet-Martin S. Hum Mutat; 2001 Aug; 18(2):163. PubMed ID: 11462241 [Abstract] [Full Text] [Related]
4. Molecular characterization of a novel splice site mutation within the CYBB gene leading to X-linked chronic granulomatous disease. Barese CN, Copelli SB, De Matteo E, Zandomeni R, Salgueiro F, Di Giovanni D, Heyworth P, Rivas EM. Pediatr Blood Cancer; 2005 Apr; 44(4):420-2. PubMed ID: 15468310 [Abstract] [Full Text] [Related]
7. Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells. Bionda C, Li XJ, van Bruggen R, Eppink M, Roos D, Morel F, Stasia MJ. Hum Genet; 2004 Oct; 115(5):418-27. PubMed ID: 15338276 [Abstract] [Full Text] [Related]
10. Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. Köker MY, Camcıoğlu Y, van Leeuwen K, Kılıç SŞ, Barlan I, Yılmaz M, Metin A, de Boer M, Avcılar H, Patıroğlu T, Yıldıran A, Yeğin O, Tezcan I, Sanal Ö, Roos D. J Allergy Clin Immunol; 2013 Nov; 132(5):1156-1163.e5. PubMed ID: 23910690 [Abstract] [Full Text] [Related]
11. The search for a genetic defect in Polish patients with chronic granulomatous disease. Jurkowska M, Kurenko-Deptuch M, Bal J, Roos D. Arch Immunol Ther Exp (Warsz); 2004 Nov; 52(6):441-6. PubMed ID: 15577746 [Abstract] [Full Text] [Related]
12. A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran. Tajik S, Badalzadeh M, Fazlollahi MR, Houshmand M, Zandieh F, Khandan S, Pourpak Z. Iran J Allergy Asthma Immunol; 2016 Oct; 15(5):426-429. PubMed ID: 27917630 [Abstract] [Full Text] [Related]
13. Genetic analysis of 13 families with X-linked chronic granulomatous disease reveals a low proportion of sporadic patients and a high proportion of sporadic carriers. Ariga T, Furuta H, Cho K, Sakiyama Y. Pediatr Res; 1998 Jul; 44(1):85-92. PubMed ID: 9667376 [Abstract] [Full Text] [Related]
14. Identification and functional characterization of two novel mutations in the α-helical loop (residues 484-503) of CYBB/gp91(phox) resulting in the rare X91(+) variant of chronic granulomatous disease. Boog B, Quach A, Costabile M, Smart J, Quinn P, Singh H, Gold M, Booker G, Choo S, Hii CS, Ferrante A. Hum Mutat; 2012 Mar; 33(3):471-5. PubMed ID: 22125116 [Abstract] [Full Text] [Related]
17. Genetic and biochemical background of chronic granulomatous disease. Jurkowska M, Bernatowska E, Bal J. Arch Immunol Ther Exp (Warsz); 2004 Mar; 52(2):113-20. PubMed ID: 15179325 [Abstract] [Full Text] [Related]