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 *

100 related articles for article (PubMed ID: 30550627)

  • 1. Polymorphisms in the myeloid differentiation primary response 88 pathway do not explain low expression levels in sudden infant death syndrome.
    Bjørnvall CD; Opdal SH; Rognum TO; Ferrante L
    Acta Paediatr; 2019 Jul; 108(7):1262-1266. PubMed ID: 30550627
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The gene encoding the inwardly rectifying potassium channel Kir4.1 may be involved in sudden infant death syndrome.
    Opdal SH; Vege Å; Stray-Pedersen A; Rognum TO
    Acta Paediatr; 2017 Sep; 106(9):1474-1480. PubMed ID: 28520217
    [TBL] [Abstract][Full Text] [Related]  

  • 3. No association to sudden infant death syndrome detected by targeted amplicon sequencing of 24 genes.
    Ferrante L; Opdal SH; Nygaard V
    Acta Paediatr; 2020 Dec; 109(12):2636-2640. PubMed ID: 32271962
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Aquaporin-1 and aquaporin-9 gene variations in sudden infant death syndrome.
    Opdal SH; Ferrante L; Rognum TO; Stray-Pedersen A
    Int J Legal Med; 2021 May; 135(3):719-725. PubMed ID: 33462668
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Altered gene expression and possible immunodeficiency in cases of sudden infant death syndrome.
    Ferrante L; Rognum TO; Vege Å; Nygård S; Opdal SH
    Pediatr Res; 2016 Jul; 80(1):77-84. PubMed ID: 26959483
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. No association of IL-10 promoter SNP -592 and -1082 and SIDS.
    Courts C; Madea B
    Forensic Sci Int; 2011 Jan; 204(1-3):179-81. PubMed ID: 20591588
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review.
    Evans A; Bagnall RD; Duflou J; Semsarian C
    Hum Pathol; 2013 Sep; 44(9):1730-6. PubMed ID: 23623143
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A controlled study of the relationship between Bordetella pertussis infections and sudden unexpected deaths among German infants.
    Heininger U; Kleemann WJ; Cherry JD;
    Pediatrics; 2004 Jul; 114(1):e9-15. PubMed ID: 15231967
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Candidate gene variants of the immune system and sudden infant death syndrome.
    Fard D; Läer K; Rothämel T; Schürmann P; Arnold M; Cohen M; Vennemann M; Pfeiffer H; Bajanowski T; Pfeufer A; Dörk T; Klintschar M
    Int J Legal Med; 2016 Jul; 130(4):1025-1033. PubMed ID: 26975745
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic variation in the monoamine oxidase A and serotonin transporter genes in sudden infant death syndrome.
    Opdal SH; Vege Å; Rognum TO
    Acta Paediatr; 2014 Apr; 103(4):393-7. PubMed ID: 24286237
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
    Tester DJ; Wong LCH; Chanana P; Gray B; Jaye A; Evans JM; Evans M; Fleming P; Jeffrey I; Cohen M; Tfelt-Hansen J; Simpson MA; Behr ER; Ackerman MJ
    J Pediatr; 2018 Dec; 203():423-428.e11. PubMed ID: 30268395
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS).
    Studer J; Bartsch C; Haas C
    Pediatr Res; 2014 Jul; 76(1):41-5. PubMed ID: 24727946
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association between polymorphisms in the P2RY1 and SSTR2 genes and sudden infant death syndrome.
    Läer K; Vennemann M; Rothämel T; Klintschar M
    Int J Legal Med; 2013 Nov; 127(6):1087-91. PubMed ID: 23828624
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Investigating genetic variants in microRNA regulators of Neurokinin-1 receptor in sudden infant death syndrome.
    Shaukat Z; Byard RW; Vink R; Hussain R; Ricos MG; Dibbens LM
    Acta Paediatr; 2023 Feb; 112(2):273-276. PubMed ID: 36271909
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.