376 related articles for article (PubMed ID: 16569599)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease.
Köker MY; van Leeuwen K; de Boer M; Celmeli F; Metin A; Ozgür TT; Tezcan I; Sanal O; Roos D
Eur J Clin Invest; 2009 Apr; 39(4):311-9. PubMed ID: 19292887
[TBL] [Abstract][Full Text] [Related]
10. 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; 52(6):441-6. PubMed ID: 15577746
[TBL] [Abstract][Full Text] [Related]
11. Genetic and biochemical background of chronic granulomatous disease.
Jurkowska M; Bernatowska E; Bal J
Arch Immunol Ther Exp (Warsz); 2004; 52(2):113-20. PubMed ID: 15179325
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations.
Köker MY; Sanal O; van Leeuwen K; de Boer M; Metin A; Patiroğlu T; Ozgür TT; Tezcan I; Roos D
Eur J Clin Invest; 2009 Oct; 39(10):942-51. PubMed ID: 19624736
[TBL] [Abstract][Full Text] [Related]
14. Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease.
Teimourian S; Zomorodian E; Badalzadeh M; Pouya A; Kannengiesser C; Mansouri D; Cheraghi T; Parvaneh N
Br J Haematol; 2008 Jun; 141(6):848-51. PubMed ID: 18422995
[TBL] [Abstract][Full Text] [Related]
15. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. A splice-supporting intronic mutation in the last bp position of a cryptic exon within intron 6 of the CYBB gene induces its incorporation into the mRNA causing chronic granulomatous disease (CGD).
Rump A; Rösen-Wolff A; Gahr M; Seidenberg J; Roos C; Walter L; Günther V; Roesler J
Gene; 2006 Apr; 371(2):174-81. PubMed ID: 16516412
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
