BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

64 related articles for article (PubMed ID: 20362046)

  • 1. A polymorphism in a staphylococcal enterotoxin receptor gene (T cell receptor BV3 recombination signal sequence) is not associated with unexplained sudden unexpected death in infancy in an Australian cohort.
    Highet AR; Gibson CS; Goldwater PN
    Microb Pathog; 2010; 49(1-2):51-3. PubMed ID: 20362046
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distribution of interleukin-1 receptor antagonist genotypes in sudden unexpected death in infancy (SUDI); unexplained SUDI have a higher frequency of allele 2.
    Highet AR; Berry AM; Goldwater PN
    Ann Med; 2010; 42(1):64-9. PubMed ID: 20092400
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CD14 (C-260T) polymorphism is not associated with sudden infant death syndrome (SIDS) in a large South Australian cohort.
    Highet AR; Gibson CS; Goldwater PN
    Innate Immun; 2011 Feb; 17(3):321-6. PubMed ID: 20472613
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interleukin-10 and sudden infant death syndrome.
    Moscovis SM; Gordon AE; Al Madani OM; Gleeson M; Scott RJ; Roberts-Thomson J; Hall ST; Weir DM; Busuttil A; Blackwell CC
    FEMS Immunol Med Microbiol; 2004 Sep; 42(1):130-8. PubMed ID: 15325406
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interleukin 1-beta responses to bacterial toxins and sudden infant death syndrome.
    Moscovis SM; Gordon AE; Hall ST; Gleeson M; Scott RJ; Roberts-Thomsom J; Weir DM; Busuttil A; Blackwell CC
    FEMS Immunol Med Microbiol; 2004 Sep; 42(1):139-45. PubMed ID: 15325407
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Apolipoprotein E e4 and its prevalence in early childhood death due to sudden infant death syndrome or to recognised causes.
    Becher JC; Keeling JW; Bell J; Wyatt B; McIntosh N
    Early Hum Dev; 2008 Aug; 84(8):549-54. PubMed ID: 18280677
    [TBL] [Abstract][Full Text] [Related]  

  • 7. IL-1 gene cluster polymorphisms and sudden infant death syndrome.
    Ferrante L; Opdal SH; Vege A; Rognum TO
    Hum Immunol; 2010 Apr; 71(4):402-6. PubMed ID: 20080142
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The IL6 -174G/C polymorphism and sudden infant death syndrome.
    Opdal SH; Rognum TO
    Hum Immunol; 2007 Jun; 68(6):541-3. PubMed ID: 17509454
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of sudden infant death syndrome with VEGF and IL-6 gene polymorphisms.
    Dashash M; Pravica V; Hutchinson IV; Barson AJ; Drucker DB
    Hum Immunol; 2006 Aug; 67(8):627-33. PubMed ID: 16916659
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The G protein beta3 subunit 825C allele is associated with sudden infant death due to infection.
    Hauge Opdal S; Melien Ø; Rootwelt H; Vege A; Arnestad M; Ole Rognum T
    Acta Paediatr; 2006 Sep; 95(9):1129-32. PubMed ID: 16938762
    [TBL] [Abstract][Full Text] [Related]  

  • 11. TNF-alpha and IL-10 gene polymorphisms versus cardioimmunological responses in sudden infant death.
    Perskvist N; Skoglund K; Edston E; Bäckström G; Lodestad I; Palm U
    Fetal Pediatr Pathol; 2008; 27(3):149-65. PubMed ID: 18633768
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic variation in hepatic glucose-6-phosphatase system genes in cases of sudden infant death syndrome.
    Forsyth L; Scott HM; Howatson A; Busuttil A; Hume R; Burchell A
    J Pathol; 2007 May; 212(1):112-20. PubMed ID: 17354259
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TNF-alpha promoter polymorphisms in sudden infant death.
    Ferrante L; Opdal SH; Vege A; Rognum TO
    Hum Immunol; 2008 Jun; 69(6):368-73. PubMed ID: 18571009
    [TBL] [Abstract][Full Text] [Related]  

  • 14. IL-10 gene polymorphisms in infectious disease and SIDS.
    Opdal SH
    FEMS Immunol Med Microbiol; 2004 Sep; 42(1):48-52. PubMed ID: 15325397
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cytokine gene polymorphisms and sudden infant death syndrome.
    Ferrante L; Opdal SH; Vege A; Rognum T
    Acta Paediatr; 2010 Mar; 99(3):384-8. PubMed ID: 19958302
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Serotonin transporter gene variation in sudden infant death syndrome.
    Opdal SH; Vege A; Rognum TO
    Acta Paediatr; 2008 Jul; 97(7):861-5. PubMed ID: 18477062
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Aquaporin-4 gene variation and sudden infant death syndrome.
    Opdal SH; Vege A; Stray-Pedersen A; Rognum TO
    Pediatr Res; 2010 Jul; 68(1):48-51. PubMed ID: 20351659
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome.
    Klintschar M; Reichenpfader B; Saternus KS
    J Pediatr; 2008 Aug; 153(2):190-3. PubMed ID: 18534229
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Staphylococcal enterotoxin genes are common in Staphylococcus aureus intestinal flora in Sudden Infant Death Syndrome (SIDS) and live comparison infants.
    Highet AR; Goldwater PN
    FEMS Immunol Med Microbiol; 2009 Nov; 57(2):151-5. PubMed ID: 19702876
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sterile site infection at autopsy in sudden unexpected deaths in infancy.
    Goldwater PN
    Arch Dis Child; 2009 Apr; 94(4):303-7. PubMed ID: 18794179
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.