Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population (Q33575658)

28 July 2017

Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population (English)

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sudden infant death syndrome

28 July 2017

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Kyriacos Markianos

8

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Ingrid A Holm

object named as

Ingrid A Holm

4

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Alan H. Beggs

object named as

Alan H Beggs

9

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Hannah C Kinney

7

object named as

Hannah C Kinney

1 reference

28 July 2017

Kevin G Broadbelt

1

1 reference

28 July 2017

Melissa A Barger

2

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28 July 2017

David S Paterson

3

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28 July 2017

Elisabeth A Haas

5

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28 July 2017

Henry F Krous

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28 July 2017

language of work or name

English

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publication date

1 December 2009

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28 July 2017

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28 July 2017

66

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28 July 2017

6

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28 July 2017

631-635

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https://scigraph.springernature.com/pub.10.1203/pdr.0b013e3181bd5a31

28 July 2017

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cites work

Effects of cis and trans genetic ancestry on gene expression in African Americans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Serotonergic transcription of human FEV reveals direct GATA factor interactions and fate of Pet-1-deficient serotonin neuron precursors

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Smoking and the sudden infant death syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Sudden infant death syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Infant mortality statistics from the 2003 period linked birth/infant death data set.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

A genetic approach to access serotonin neurons for in vivo and in vitro studies.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Subtle autonomic and respiratory dysfunction in sudden infant death syndrome associated with serotonergic brainstem abnormalities: a case report

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

A note on exact tests of Hardy-Weinberg equilibrium

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Sudden infant death syndrome, infection and inflammatory responses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

The Ets transcription factor Fev is specifically expressed in the human central serotonergic neurons.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Gata2 specifies serotonergic neurons downstream of sonic hedgehog

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Lmx1b is essential for the development of serotonergic neurons

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Pet-1 ETS gene plays a critical role in 5-HT neuron development and is required for normal anxiety-like and aggressive behavior.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Risk factors for sudden infant death syndrome among northern plains Indians

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Developmental neurotransmitter pathology in the brainstem of sudden infant death syndrome: a review and sleep position

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

mPet-1, a mouse ETS-domain transcription factor, is expressed in central serotonergic neurons

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Sudden infant death syndrome and other causes of infant mortality: diagnosis, mechanisms, and risk for recurrence in siblings

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Medullary serotonergic network deficiency in the sudden infant death syndrome: review of a 15-year study of a single dataset

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Infant sleep position and risk for sudden infant death syndrome: report of meeting held January 13 and 14, 1994, National Institutes of Health, Bethesda, MD.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Interaction between bedding and sleeping position in the sudden infant death syndrome: a population based case-control study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Choice of sleeping position for infants: possible association with cot death

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Defining the sudden infant death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of Child Health and Human Development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Mortality among infants of black as compared with white college-educated parents

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

21 June 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

A perspective on neuropathologic findings in victims of the sudden infant death syndrome: the triple-risk model.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

Population-based recurrence risk of sudden infant death syndrome compared with other infant and fetal deaths.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

Sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

A differentially autoregulated Pet-1 enhancer region is a critical target of the transcriptional cascade that governs serotonin neuron development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

Decreased serotonergic receptor binding in rhombic lip-derived regions of the medulla oblongata in the sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

The development of the medullary serotonergic system in early human life.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

Serotoninergic receptor 1A in the sudden infant death syndrome brainstem medulla and associations with clinical risk factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

Alteration of serotonergic receptors in the brain stems of human patients with respiratory disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3181BD5A31

Lmx1b, Pet-1, andNkx2.2Coordinately Specify Serotonergic Neurotransmitter Phenotype

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2802663

10.1203/PDR.0B013E3181BD5A31

31 October 2018

Identifiers

DOI

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Dimensions Publication ID

28 July 2017

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1 reference

28 July 2017

1 reference