BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 17429907)

  • 1. Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome.
    Opdal SH; Vege A; Arnestad M; Musse MA; Rognum TO
    Acta Paediatr; 2007 Feb; 96(2):211-4. PubMed ID: 17429907
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The sudden infant death syndrome gene: does it exist?
    Opdal SH; Rognum TO
    Pediatrics; 2004 Oct; 114(4):e506-12. PubMed ID: 15466077
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A mitochondrial DNA polymorphism associated with cardiac arrhythmia investigated in sudden infant death syndrome.
    Arnestad M; Opdal SH; Vege A; Rognum TO
    Acta Paediatr; 2007 Feb; 96(2):206-10. PubMed ID: 17429906
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Possible role of mtDNA mutations in sudden infant death.
    Opdal SH; Vege A; Egeland T; Musse MA; Rognum TO
    Pediatr Neurol; 2002 Jul; 27(1):23-9. PubMed ID: 12160969
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial deoxyribonucleic acid may play a role in a subset of sudden infant death syndrome cases.
    Läer K; Vennemann M; Rothämel T; Klintschar M
    Acta Paediatr; 2014 Jul; 103(7):775-9. PubMed ID: 25025098
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome.
    Opdal SH; Rognum TO; Torgersen H; Vege A
    Acta Paediatr; 1999 Sep; 88(9):957-60. PubMed ID: 10519336
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of the mitochondrial genome in sudden infant death syndrome.
    Divne AM; Råsten-Almqvist P; Rajs J; Gyllensten U; Allen M
    Acta Paediatr; 2003; 92(3):386-8. PubMed ID: 12725556
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Increased number of substitutions in the D-loop of mitochondrial DNA in the sudden infant death syndrome.
    Opdal SH; Rognum TO; Vege A; Stave AK; Dupuy BM; Egeland T
    Acta Paediatr; 1998 Oct; 87(10):1039-44. PubMed ID: 9825969
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transcriptional interactions between yeast tRNA genes, flanking genes and Ty elements: a genomic point of view.
    Bolton EC; Boeke JD
    Genome Res; 2003 Feb; 13(2):254-63. PubMed ID: 12566403
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Noncardiac genetic predisposition in sudden infant death syndrome.
    Gray B; Tester DJ; Wong LC; Chanana P; Jaye A; Evans JM; Baruteau AE; Evans M; Fleming P; Jeffrey I; Cohen M; Tfelt-Hansen J; Simpson MA; Ackerman MJ; Behr ER
    Genet Med; 2019 Mar; 21(3):641-649. PubMed ID: 30139991
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Post-mortem genetic investigation of cardiac disease-associated genes in sudden infant death syndrome (SIDS) cases.
    Köffer J; Scheiper-Welling S; Verhoff MA; Bajanowski T; Kauferstein S
    Int J Legal Med; 2021 Jan; 135(1):207-212. PubMed ID: 32789579
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease.
    Hofmann S; Jaksch M; Bezold R; Mertens S; Aholt S; Paprotta A; Gerbitz KD
    Hum Mol Genet; 1997 Oct; 6(11):1835-46. PubMed ID: 9302261
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Are substitutions in the first hypervariable region of the mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance?
    Arnestad M; Opdal SH; Musse MA; Vege A; Rognum TO
    Acta Paediatr; 2002; 91(10):1060-4. PubMed ID: 12434891
    [TBL] [Abstract][Full Text] [Related]  

  • 16. That's not it, either-neither polymorphisms in PHOX2B nor in MIF are involved in sudden infant death syndrome (SIDS).
    Poetsch M; Todt R; Vennemann M; Bajanowski T
    Int J Legal Med; 2015 Sep; 129(5):985-9. PubMed ID: 26104808
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.
    Wedekind H; Bajanowski T; Friederich P; Breithardt G; Wülfing T; Siebrands C; Engeland B; Mönnig G; Haverkamp W; Brinkmann B; Schulze-Bahr E
    Int J Legal Med; 2006 May; 120(3):129-37. PubMed ID: 16012827
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heat stress and sudden infant death syndrome--stress gene expression after exposure to moderate heat stress.
    Rohde MC; Corydon TJ; Hansen J; Pedersen CB; Schmidt SP; Gregersen N; Banner J
    Forensic Sci Int; 2013 Oct; 232(1-3):16-24. PubMed ID: 24053860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Sudden infant death syndrome (SIDS) and polymorphisms in Monoamine oxidase A gene (MAOA): a revisit.
    Groß M; Bajanowski T; Vennemann M; Poetsch M
    Int J Legal Med; 2014 Jan; 128(1):43-9. PubMed ID: 24173666
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.