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Items: 1 to 20 of 83

1.

Optimisation of postmortem tissue preservation and alternative protocol for serotonin transporter gene polymorphisms amplification in SIDS and SIUD cases.

Casale V, Oneda R, Lavezzi AM, Matturri L.

Exp Mol Pathol. 2010 Feb;88(1):202-5. doi: 10.1016/j.yexmp.2009.10.003. Epub 2009 Oct 23.

PMID:
19837061
2.

Sudden infant death syndrome and sudden intrauterine unexplained death: correlation between hypoplasia of raphé nuclei and serotonin transporter gene promoter polymorphism.

Lavezzi AM, Casale V, Oneda R, Weese-Mayer DE, Matturri L.

Pediatr Res. 2009 Jul;66(1):22-7. doi: 10.1203/PDR.0b013e3181a7bb73.

PMID:
19342987
3.

Serotonin transporter gene variation in sudden infant death syndrome.

Opdal SH, Vege A, Rognum TO.

Acta Paediatr. 2008 Jul;97(7):861-5. doi: 10.1111/j.1651-2227.2008.00813.x. Epub 2008 May 12.

PMID:
18477062
4.

Serotonin transporter gene variation is a risk factor for sudden infant death syndrome in the Japanese population.

Narita N, Narita M, Takashima S, Nakayama M, Nagai T, Okado N.

Pediatrics. 2001 Apr;107(4):690-2.

PMID:
11335745
5.

Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene.

Weese-Mayer DE, Berry-Kravis EM, Maher BS, Silvestri JM, Curran ME, Marazita ML.

Am J Med Genet A. 2003 Mar 15;117A(3):268-74.

PMID:
12599191
6.

No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians.

Haas C, Braun J, Bär W, Bartsch C.

Leg Med (Tokyo). 2009 Apr;11 Suppl 1:S210-2. doi: 10.1016/j.legalmed.2009.01.051. Epub 2009 Mar 3.

PMID:
19261524
7.

Comparative epidemiology of sudden infant death syndrome and sudden intrauterine unexplained death.

Frøen JF, Arnestad M, Vege A, Irgens LM, Rognum TO, Saugstad OD, Stray-Pedersen B.

Arch Dis Child Fetal Neonatal Ed. 2002 Sep;87(2):F118-21.

8.

Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome.

Nonnis Marzano F, Maldini M, Filonzi L, Lavezzi AM, Parmigiani S, Magnani C, Bevilacqua G, Matturri L.

Genomics. 2008 Jun;91(6):485-91. doi: 10.1016/j.ygeno.2008.01.010. Epub 2008 Apr 2.

9.

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.

Weese-Mayer DE, Zhou L, Berry-Kravis EM, Maher BS, Silvestri JM, Marazita ML.

Am J Med Genet A. 2003 Oct 15;122A(3):238-45.

PMID:
12966525
10.

Investigation of 5-HTT expression using quantitative real-time PCR in the human brain in SIDS Italian cases.

Casale V, Oneda R, Matturri L, Lavezzi AM.

Exp Mol Pathol. 2013 Feb;94(1):239-42. doi: 10.1016/j.yexmp.2012.06.009. Epub 2012 Jul 4.

PMID:
22771822
11.

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. doi: 10.1111/apa.12526. Epub 2013 Dec 27.

PMID:
24286237
12.

Sudden Infant Death Syndrome: review of implicated genetic factors.

Weese-Mayer DE, Ackerman MJ, Marazita ML, Berry-Kravis EM.

Am J Med Genet A. 2007 Apr 15;143A(8):771-88. Review.

PMID:
17340630
13.

Preservation of RNA for functional genomic studies: a multidisciplinary tumor bank protocol.

Florell SR, Coffin CM, Holden JA, Zimmermann JW, Gerwels JW, Summers BK, Jones DA, Leachman SA.

Mod Pathol. 2001 Feb;14(2):116-28.

14.

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 1;42(1):125-9.

15.

Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis.

Filonzi L, Magnani C, Lavezzi AM, Rindi G, Parmigiani S, Bevilacqua G, Matturri L, Marzano FN.

Neurogenetics. 2009 Feb;10(1):65-72. doi: 10.1007/s10048-008-0149-x. Epub 2008 Sep 23.

PMID:
18810510
16.

A controlled study of the relationship between Bordetella pertussis infections and sudden unexpected deaths among German infants.

Heininger U, Kleemann WJ, Cherry JD; Sudden Infant Death Syndrome Study Group.

Pediatrics. 2004 Jul;114(1):e9-15.

PMID:
15231967
17.

3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis.

Maher BS, Marazita ML, Rand C, Zhou L, Berry-Kravis EM, Weese-Mayer DE.

Am J Med Genet A. 2006 Jul 1;140(13):1453-7. No abstract available.

PMID:
16691588
18.

Cervical tissue collection methods for RNA preservation: comparison of snap-frozen, ethanol-fixed, and RNAlater-fixation.

Wang SS, Sherman ME, Rader JS, Carreon J, Schiffman M, Baker CC.

Diagn Mol Pathol. 2006 Sep;15(3):144-8.

PMID:
16932069
19.

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. doi: 10.1016/j.earlhumdev.2008.01.002. Epub 2008 Feb 20.

PMID:
18280677
20.

Detection of human herpesvirus-6, Epstein-Barr virus and cytomegalovirus in formalin-fixed tissues from sudden infant death: a study with quantitative real-time PCR.

Alvarez-Lafuente R, Aguilera B, Suárez-Mier MA, Morentin B, Vallejo G, Gómez J, Fernández-Rodríguez A.

Forensic Sci Int. 2008 Jul 4;178(2-3):106-11. doi: 10.1016/j.forsciint.2008.02.007.

PMID:
18424026

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