(Q38180042)

English

PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population

scientific article published on 18 January 2014

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

sudden infant death syndrome

1 reference

based on heuristic

inferred from title

object named as

Fan Liu

2

0 references

object named as

Oscar Lao

3

0 references

8

object named as

Albert Hofman

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Vincent W Jaddoe

7

object named as

Vincent W Jaddoe

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

author name string

Germaine Liebrechts-Akkerman

1

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Ariadne H A G Ooms

4

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Kate van Duijn

5

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Mark Vermeulen

6

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Adèle C Engelberts

9

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

Manfred Kayser

10

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

publication date

18 January 2014

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

International Journal of Legal Medicine

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

128

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

621-629

1 reference

Europe PubMed Central

PubMed publication ID

30 August 2017

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

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

SIDS and other sleep-related infant deaths: expansion of recommendations for a safe infant sleeping environment

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Postnatal parental smoking: an important risk factor for SIDS.

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

The sudden infant death syndrome gene: does it exist?

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Congenital central hypoventilation syndrome and sudden infant death syndrome: disorders of autonomic regulation

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS): kindred disorders of autonomic regulation

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Genetics and early disturbances of breathing control

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Mutations of the RET-GDNF signaling pathway in Ondine's curse

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

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%2FS00414-013-0962-0

21 January 2018

Serotonin transporter gene variation in sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

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%2FS00414-013-0962-0

21 January 2018

Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Histological findings in unclassified sudden infant death, including sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

The Generation R Study: design and cohort update 2012.

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea, and specific loss of parafacial neurons.

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Developmental alterations of the respiratory human retrotrapezoid nucleus in sudden unexplained fetal and infant death

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Sudden infant death syndrome is not associated with the mutation of PHOX2B gene, a major causative gene of congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Variable human phenotype associated with novel deletions of the PHOX2B gene

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Phox2b controls the development of peripheral chemoreceptors and afferent visceral pathways.

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

Sleep-disordered breathing in newborn mice heterozygous for the transcription factor Phox2b.

1 reference

https://api.crossref.org/works/10.1007%2FS00414-013-0962-0

21 January 2018

AutoDimer: a screening tool for primer-dimer and hairpin structures

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Excavation of a buried treasure--DNA, mRNA, miRNA and protein analysis in formalin fixed, paraffin embedded tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

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/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid and quantitative DNA sex test: fluorescence-based PCR analysis of X-Y homologous gene amelogenin

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple correlations and Bonferroni's correction

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sleeping position and cot death

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/24442913

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00414-013-0962-0

1 reference

https://api.fatcat.wiki/v0/release/tuxjlwk7vfaizam6l5ac3izxai

30 July 2022

based on heuristic

mapped directly with Wikidata item

Dimensions Publication ID

0 references

release_tuxjlwk7vfaizam6l5ac3izxai

1 reference

https://api.fatcat.wiki/v0/release/tuxjlwk7vfaizam6l5ac3izxai

30 July 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

https://api.fatcat.wiki/v0/release/tuxjlwk7vfaizam6l5ac3izxai

30 July 2022

based on heuristic

mapped directly with Wikidata item

ResearchGate publication ID

0 references

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