(Q46352144)

English

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

scientific article published on 23 September 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

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

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

0 references

0 references

sudden infant death syndrome

1 reference

based on heuristic

inferred from title

Anna Maria Lavezzi

3

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

Stefano Parmigiani

object named as

Stefano Parmigiani

5

0 references

object named as

Guido Rindi

4

0 references

7

object named as

Luigi Matturri

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

author name string

Laura Filonzi

1

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

Cinzia Magnani

2

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

Giulio Bevilacqua

6

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

Francesco Nonnis Marzano

8

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

publication date

23 September 2008

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

10

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

1

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

65-72

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

https://scigraph.springernature.com/pub.10.1007/s10048-008-0149-x

0 references

The changing concept of sudden infant death syndrome: diagnostic coding shifts, controversies regarding the sleeping environment, and new variables to consider in reducing risk

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Thermal insulation and SIDS-an investigation of selected 'Eastern' and 'Western' infant bedding combinations.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Recent trend of the incidence of sudden infant death syndrome in Japan

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Hypoplasia of the arcuate nucleus and maternal smoking during pregnancy in sudden unexplained perinatal and infant death

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

A serotonin malfunction hypothesis by finding clear mutual relationships between several risk factors and symptoms associated with sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

DRD2 allele frequencies and linkage disequilibria, including the -141CIns/Del promoter polymorphism, in European-American, African-American, and Japanese subjects

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Expression of the dopamine transporter gene is regulated by the 3' UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Genotype influences in vivo dopamine transporter availability in human striatum.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

A functional polymorphism in the monoamine oxidase A gene promoter

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

A promoter polymorphism in the monoamine oxidase A gene is associated with the pineal MAOA activity in Alzheimer's disease patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Allelic association of a dopamine transporter gene polymorphism with antisocial behaviour in heroin-dependent patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

DNA extraction from archival formalin-fixed, paraffin-embedded tissue sections based on the antigen retrieval principle: heating under the influence of pH.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Association of autism severity with a monoamine oxidase A functional polymorphism.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

ADHD and Disruptive Behavior scores - associations with MAO-A and 5-HTT genes and with platelet MAO-B activity in adolescents

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Role of genotype in the cycle of violence in maltreated children

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Serotonin transporter gene variation in sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

D2 dopamine receptor gene TaqI A1 and B1 restriction fragment length polymorphisms: enhanced frequencies in psychostimulant-preferring polysubstance abusers.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0149-X

21 January 2018

Techniques and criteria in pathologic and forensic-medical diagnostics in sudden unexpected infant and perinatal death

1 reference

https://pubmed.ncbi.nlm.nih.gov/18810510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children

1 reference

https://pubmed.ncbi.nlm.nih.gov/18810510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18810510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased dopamine transporter availability associated with the 9-repeat allele of the SLC6A3 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18810510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human genetics and pharmacology of neurotransmitter transporters

1 reference

https://pubmed.ncbi.nlm.nih.gov/18810510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden Infant Death Syndrome: review of implicated genetic factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/18810510

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-008-0149-X

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/18810510

ResearchGate publication ID

0 references

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