(Q34462847)

2 August 2017

title

Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses (English)

1 reference

2 August 2017

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Santschi EM

1

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2 August 2017

Purdy AK

2

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2 August 2017

Valberg SJ

3

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2 August 2017

Vrotsos PD

4

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2 August 2017

Kaese H

5

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2 August 2017

Mickelson JR

6

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2 August 2017

publication date

1 April 1998

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2 August 2017

number of pages

4

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inferred from page(s)

published in

Mammalian Genome

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2 August 2017

volume

9

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2 August 2017

issue

4

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2 August 2017

page(s)

306-309

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https://scigraph.springernature.com/pub.10.1007/s003359900754

2 August 2017

exact match

0 references

cites work

Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease

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Cellular and molecular biology of neural crest cell lineage determination

21 January 2018

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Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900754

Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900754

Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900754

Dominant inheritance of overo spotting in paint horses

21 January 2018

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Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) rat.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900754

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900754

Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900754

Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900754

An Epidemiological Study of Hirschsprung's Disease

21 January 2018

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A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

21 January 2018

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https://api.crossref.org/works/10.1007%2FS003359900754

Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice

21 January 2018

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Molecular and developmental genetics of mouse coat color

21 January 2018

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Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease

21 January 2018

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A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses

21 January 2018

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Overo lethal white foal syndrome: equine model of aganglionic megacolon (Hirschsprung disease).

21 January 2018

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The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families.

21 January 2018

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Quantitative trait loci that modify the severity of spotting in piebald mice.

21 January 2018

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A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

21 January 2018

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Congenital intestinal aganglionosis in white foals

21 January 2018

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A genetic study of Hirschsprung disease

21 January 2018

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12 December 2020

Wither polygenic inheritance: mapping Hirschsprung disease

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Molecular characterization and regulation of the human endothelin receptors

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Migration of ganglion cell precursors in the ileoceca of normal and lethal spotted embryos, a murine model for Hirschsprung disease

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Ileocolonic aganglionosis in white progeny of overo spotted horses

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12 December 2020

Identifiers

DOI

10.1007/S003359900754

1 reference

2 August 2017

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