234 related articles for article (PubMed ID: 17509454)
21. 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]
22. 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]
23. 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]
24. Interleukin 10 genotype as a risk factor for sudden infant death syndrome: determination of IL-10 genotype from wax-embedded postmortem samples.
Korachi M; Pravica V; Barson AJ; Hutchinson IV; Drucker DB
FEMS Immunol Med Microbiol; 2004 Sep; 42(1):125-9. PubMed ID: 15325405
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. SNP association and sequence analysis of the NOS1AP gene in SIDS.
Osawa M; Kimura R; Hasegawa I; Mukasa N; Satoh F
Leg Med (Tokyo); 2009 Apr; 11 Suppl 1():S307-8. PubMed ID: 19289301
[TBL] [Abstract][Full Text] [Related]
27. IL6 G-174C associated with sudden infant death syndrome in a Caucasian Australian cohort.
Moscovis SM; Gordon AE; Al Madani OM; Gleeson M; Scott RJ; Roberts-Thomson J; Hall ST; Weir DM; Busuttil A; Blackwell CC
Hum Immunol; 2006 Oct; 67(10):819-25. PubMed ID: 17055359
[TBL] [Abstract][Full Text] [Related]
28. Molecular screening of interleukin-6 gene promoter and influence of -174G/C polymorphism on breast cancer.
Chérel M; Campion L; Bézieau S; Campone M; Charrier J; Gaschet J; Ricolleau G; Gouraud W; Charbonnel C; Jézéquel P
Cytokine; 2009 Sep; 47(3):214-23. PubMed ID: 19640729
[TBL] [Abstract][Full Text] [Related]
29. Genetic variants of IL6 gene promoter influence on C-reactive protein levels but are not associated with susceptibility to invasive pulmonary aspergillosis in haematological patients.
Sainz J; Pérez E; Gómez-Lopera S; López-Fernández E; Moratalla L; Oyonarte S; Jurado M
Cytokine; 2008 Mar; 41(3):268-78. PubMed ID: 18191407
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. 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]
33. Genetic polymorphisms in immunoresponse genes TNFA, IL6, IL10, and TLR4 are associated with recurrent acute otitis media.
Emonts M; Veenhoven RH; Wiertsema SP; Houwing-Duistermaat JJ; Walraven V; de Groot R; Hermans PW; Sanders EA
Pediatrics; 2007 Oct; 120(4):814-23. PubMed ID: 17908769
[TBL] [Abstract][Full Text] [Related]
34. Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development.
Weese-Mayer DE; Berry-Kravis EM; Zhou L; Maher BS; Curran ME; Silvestri JM; Marazita ML
Pediatr Res; 2004 Sep; 56(3):391-5. PubMed ID: 15240857
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. An infectious aetiology of sudden infant death syndrome.
Highet AR
J Appl Microbiol; 2008 Sep; 105(3):625-35. PubMed ID: 18266695
[TBL] [Abstract][Full Text] [Related]
37. Cerebral c-jun expression mapping in sudden infant death syndrome.
Rickert CH; Zahiragić L; Nolte KW; Bajanowski T; Brinkmann B; Paulus W
Acta Neuropathol; 2004 Feb; 107(2):119-26. PubMed ID: 14605833
[TBL] [Abstract][Full Text] [Related]
38. Fatty acids, IL6, and TNFalpha polymorphisms: an example of nutrigenetics in Crohn's disease.
Guerreiro CS; Ferreira P; Tavares L; Santos PM; Neves M; Brito M; Cravo M
Am J Gastroenterol; 2009 Sep; 104(9):2241-9. PubMed ID: 19550417
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Polymorphisms at the osteoprotegerin and interleukin-6 genes in relation to first-ever stroke.
Strand M; Soderstrom I; Wiklund PG; Hallmans G; Weinehall L; Soderberg S; Olsson T
Cerebrovasc Dis; 2007; 24(5):418-25. PubMed ID: 17878722
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
