These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

70 related articles for article (PubMed ID: 9070911)

  • 1. Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient.
    Bonizzato A; Russo MP; Donini M; Dusi S
    Biochem Biophys Res Commun; 1997 Feb; 231(3):861-3. PubMed ID: 9070911
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A mutation located at the 5' splice junction sequence of intron 3 in the p67phox gene causes the lack of p67phox mRNA in a patient with chronic granulomatous disease.
    Tanugi-Cholley LC; Issartel JP; Lunardi J; Freycon F; Morel F; Vignais PV
    Blood; 1995 Jan; 85(1):242-9. PubMed ID: 7803798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A novel and unusual case of chronic granulomatous disease in a child with a homozygous 36-bp deletion in the CYBA gene (A22(0)) leading to the activation of a cryptic splice site in intron 4.
    Stasia MJ; Bordigoni P; Martel C; Morel F
    Hum Genet; 2002 May; 110(5):444-50. PubMed ID: 12073015
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A donor splice site mutation in intron 1 of CYBA, leading to chronic granulomatous disease.
    de Boer M; Hartl D; Wintergerst U; Belohradsky BH; Roos D
    Blood Cells Mol Dis; 2005; 35(3):365-9. PubMed ID: 16157492
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of the p67phox gene: genomic organization and restriction fragment length polymorphism analysis for prenatal diagnosis in chronic granulomatous disease.
    Kenney RT; Malech HL; Epstein ND; Roberts RL; Leto TL
    Blood; 1993 Dec; 82(12):3739-44. PubMed ID: 7903171
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis.
    Hossle JP; de Boer M; Seger RA; Roos D
    Hum Genet; 1994 Apr; 93(4):437-42. PubMed ID: 8168815
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections.
    Agudelo-Flórez P; Costa-Carvalho BT; López JA; Redher J; Newburger PE; Olalla-Saad ST; Condino-Neto A
    Am J Hematol; 2004 Mar; 75(3):151-6. PubMed ID: 14978696
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Two-exon skipping due to a point mutation in p67-phox--deficient chronic granulomatous disease.
    Aoshima M; Nunoi H; Shimazu M; Shimizu S; Tatsuzawa O; Kenney RT; Kanegasaki S
    Blood; 1996 Sep; 88(5):1841-5. PubMed ID: 8781442
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Severe clinical forms of cytochrome b-negative chronic granulomatous disease (X91-) in 3 brothers with a point mutation in the promoter region of CYBB.
    Stasia MJ; Brion JP; Boutonnat J; Morel F
    J Infect Dis; 2003 Nov; 188(10):1593-604. PubMed ID: 14624387
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mutations of fragile histidine triad gene in Peutz-Jeghers syndrome and canceration].
    Zhao XR; Kang LC; Zhou YS; Jia YX; Chen Z; Kang SH; Li WM; Zhao M; Cui JT; Sun AL; Lu YY
    Ai Zheng; 2003 Jan; 22(1):50-4. PubMed ID: 12561436
    [TBL] [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; 52(2):113-20. PubMed ID: 15179325
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Incidence of p53 and ras gene mutations in DMBA-induced rat leukemias.
    Wei S; Kito K; Miyoshi A; Matsumoto S; Kauzi A; Aramoto T; Abe Y; Ueda N
    J Exp Clin Cancer Res; 2002 Sep; 21(3):389-96. PubMed ID: 12385583
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in MYOC gene of Indian primary open angle glaucoma patients.
    Mukhopadhyay A; Acharya M; Mukherjee S; Ray J; Choudhury S; Khan M; Ray K
    Mol Vis; 2002 Nov; 8():442-8. PubMed ID: 12447164
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Focus on FOCIS: the continuing diagnostic challenge of autosomal recessive chronic granulomatous disease.
    Yu G; Hong DK; Dionis KY; Rae J; Heyworth PG; Curnutte JT; Lewis DB
    Clin Immunol; 2008 Aug; 128(2):117-26. PubMed ID: 18625437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.