Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23. (Q36719156)

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scientific article published on 28 February 2008

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English	Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23.	scientific article published on 28 February 2008

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scholarly article

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3 January 2020

Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23 (English)

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hypertrophic pyloric stenosis

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based on heuristic

inferred from title

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based on heuristic

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2

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Francesca Capon

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Kate V Everett

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Christina Georgoula

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Ashley Reece

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Keith A Parker

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Cathy Cord-Udy

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Paul McKeigue

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Sally Mitton

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Agostino Pierro

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Prem Puri

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Hannah M Mitchison

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Eddie M K Chung

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R Mark Gardiner

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28 February 2008

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American Journal of Human Genetics

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756-762

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3 January 2020

A common mechanism underlies stretch activation and receptor activation of TRPC6 channels

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Canonical transient receptor potential channels promote cardiomyocyte hypertrophy through activation of calcineurin signaling

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Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16p12-p13 and evidence for genetic heterogeneity

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Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps

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Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites

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Single-nucleotide promoter polymorphism alters transcription of neuronal nitric oxide synthase exon 1c in infantile hypertrophic pyloric stenosis

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Finding genes that underlie complex traits

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TRPC6 is a candidate channel involved in receptor-stimulated cation currents in A7r5 smooth muscle cells

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Maternal and infant use of erythromycin and other macrolide antibiotics as risk factors for infantile hypertrophic pyloric stenosis

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The transient receptor potential protein homologue TRP6 is the essential component of vascular alpha(1)-adrenoceptor-activated Ca(2+)-permeable cation channel

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Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review

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Infantile hypertrophic pyloric stenosis after pertussis prophylaxis with erythromcyin: a case review and cohort study

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Genetic evidence for the neuronal nitric oxide synthase gene (NOS1) as a susceptibility locus for infantile pyloric stenosis

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Probable autosomal dominant infantile pyloric stenosis in a large kindred

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Infantile hypertrophic pyloric stenosis related to ingestion of erythromycine estolate: A report of five cases

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Neuronal nitric oxide synthase, nNOS, is not linked to infantile hypertrophic pyloric stenosis in three families.

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The epidemiology of infantile hypertrophic pyloric stenosis in a Danish population, 1950-84.

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Very early exposure to erythromycin and infantile hypertrophic pyloric stenosis

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Some epidemiological aspects of pyloric stenosis in British Columbia

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile hypertrophic pyloric stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18308288

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The epidemiology of infantile hypertrophic pyloric stenosis in New York State, 1983 to 1990

1 reference

https://pubmed.ncbi.nlm.nih.gov/18308288

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The epidemiology of infantile hypertrophic pyloric stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18308288

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two-generation pyloric stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18308288

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inheritance of congenital pyloric stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18308288

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJHG.2007.12.023

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3 January 2020

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3 January 2020

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3 January 2020

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