BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 18402298)

  • 1. Nonsense mutations of the CYBB gene in two Thai families with X-linked chronic granulomatous disease.
    Vilaiphan P; Chatchatee P; Ngamphaiboon J; Tongkobpetch S; Suphapeetiporn K; Shotelersuk V
    Asian Pac J Allergy Immunol; 2007 Dec; 25(4):243-7. PubMed ID: 18402298
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked chronic granulomatous disease: first report of mutations in patients of Argentina.
    Barese C; Copelli S; Zandomeni R; Oleastro M; Zelazko M; Rivas EM
    J Pediatr Hematol Oncol; 2004 Oct; 26(10):656-60. PubMed ID: 15454837
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long polymerase chain reaction-based fluorescence in situ hybridization analysis of female carriers of X-linked chronic granulomatous disease deletions.
    Simon KC; Noack D; Rae J; Curnutte J; Sarraf S; Kolev V; Blancato JK
    J Mol Diagn; 2005 May; 7(2):183-6. PubMed ID: 15858141
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of deletion carriers in X-linked chronic granulomatous disease by real-time PCR.
    Chiriaco M; Di Matteo G; Sinibaldi C; Giardina E; Nardone AM; Folgori L; D'Argenio P; Rossi P; Finocchi A
    Genet Test Mol Biomarkers; 2009 Dec; 13(6):785-9. PubMed ID: 19839755
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chronic granulomatous disease in Latin American patients: clinical spectrum and molecular genetics.
    Agudelo-Flórez P; Prando-Andrade CC; López JA; Costa-Carvalho BT; Quezada A; Espinosa FJ; de Souza Paiva MA; Roxo P; Grumach A; Jacob CA; Carneiro-Sampaio MM; Newburger PE; Condino-Neto A
    Pediatr Blood Cancer; 2006 Feb; 46(2):243-52. PubMed ID: 16123991
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of six novel mutations in the CYBB gene leading to different sub-types of X-linked chronic granulomatous disease.
    Stasia MJ; Bordigoni P; Floret D; Brion JP; Bost-Bru C; Michel G; Gatel P; Durant-Vital D; Voelckel MA; Li XJ; Guillot M; Maquet E; Martel C; Morel F
    Hum Genet; 2005 Jan; 116(1-2):72-82. PubMed ID: 15538631
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked chronic granulomatous disease in a male child with an X-CGD carrier, Klinefelter brother.
    Gill HK; Kumar HC; Cheng CK; Ming CC; Nallusamy R; Yusoff NM; Mohamad SB; Ripen AM; Dhaliwal JS; Murad S
    Asian Pac J Allergy Immunol; 2013 Jun; 31(2):167-72. PubMed ID: 23859418
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one family.
    Köker MY; Sanal O; de Boer M; Tezcan I; Metin A; Tan C; Ersoy F; Roos D
    Eur J Clin Invest; 2006 Apr; 36(4):257-64. PubMed ID: 16620288
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel missense mutation in the NADPH binding domain of CYBB abolishes the NADPH oxidase activity in a male patient with increased susceptibility to infections.
    Khan TA; Kalsoom K; Iqbal A; Asif H; Rahman H; Farooq SO; Naveed H; Nasir U; Amin MU; Hussain M; Tipu HN; Florea A
    Microb Pathog; 2016 Nov; 100():163-169. PubMed ID: 27666509
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular analysis of chronic granulomatous disease caused by defects in gp91-phox.
    Patiño PJ; Perez JE; Lopez JA; Condino-Neto A; Grumach AS; Botero JH; Curnutte JT; García de Olarte D
    Hum Mutat; 1999; 13(1):29-37. PubMed ID: 9888386
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked chronic granulomatous disease (CGD) caused by an intra-exonic splice mutation (CYBB exon 3, c.262G->A) is mimicking juvenile sarcoidosis.
    Brunner J; Dockter G; Rösen-Wolff A; Roesler J
    Clin Exp Rheumatol; 2007; 25(2):336-8. PubMed ID: 17543165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations of chronic granulomatous disease in Turkish families.
    Köker MY; Sanal O; De Boer M; Tezcan I; Metin A; Ersoy F; Roos D
    Eur J Clin Invest; 2007 Jul; 37(7):589-95. PubMed ID: 17576211
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of chronic granulomatous disease in a male fetus.
    Yavuz Köker M; Metin A; Ozgür TT; de Boer M; Roos D
    Iran J Allergy Asthma Immunol; 2009 Mar; 8(1):57-61. PubMed ID: 19279361
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation of the CYBB gene resulting in severe form of X-linked chronic granulomatous disease.
    Jirapongsananuruk O; Noack D; Boonchoo S; Thepthai C; Chokephaibulkit K; Visitsunthorn N; Vichyanond P; Luangwedchakarn V; Likasitwattanakul S; Piboonpocanun S
    Asian Pac J Allergy Immunol; 2007 Dec; 25(4):249-52. PubMed ID: 18402299
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of X-linked chronic granulomatous disease by percutaneous umbilical blood sampling.
    Sun J; Wang Y; Liu D; Yu Y; Wang J; Ying W; Wang X
    Scand J Immunol; 2012 Nov; 76(5):512-8. PubMed ID: 22924737
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular analysis of four cases of chronic granulomatous disease caused by defects in NCF-2: the gene encoding the p67-phox.
    Badalzadeh M; Fattahi F; Fazlollahi MR; Tajik S; Bemanian MH; Behmanesh F; Movahedi M; Houshmand M; Pourpak Z
    Iran J Allergy Asthma Immunol; 2012 Dec; 11(4):340-4. PubMed ID: 23264412
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.