A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease
about
Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horsesA high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studiesCoat color and coat color pattern-related neurologic and neuro-ophthalmic diseasesDifferential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus)Exclusion of EDNRB and KIT as the basis for white spotting in Border ColliesMapping of panda plumage color locus on the microsatellite linkage map of the Japanese quail.EndothelinThe Genetics of Deafness in Domestic AnimalsNonruminant Nutrition Symposium: Involvement of gut neural and endocrine systems in pathological disorders of the digestive tractBrainstem auditory evoked responses in an equine patient population: part I--adult horsesBrainstem auditory evoked responses in an equine patient population. Part II: foals.Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations.Next generation sequencing gives an insight into the characteristics of highly selected breeds versus non-breed horses in the course of domestication.Adaptations to climate-mediated selective pressures in sheep.Endothelin signalling in iridophore development and stripe pattern formation of zebrafishChaperoning G protein-coupled receptors: from cell biology to therapeuticsThe convergent evolution of blue iris pigmentation in primates took distinct molecular paths.Familiar hypopigmentation syndrome in sheep associated with homozygous deletion of the entire endothelin type-B receptor gene.Not just black and white: pigment pattern development and evolution in vertebratesGenetic diversity, linkage disequilibrium and selection signatures in chinese and Western pigs revealed by genome-wide SNP markers.Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb.Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses.Increased smooth muscle contractility of intestine in the genetic null of the endothelin ETB receptor: a rat model for long segment Hirschsprung's diseaseEquine clinical genomics: A clinician's primer.A deletion in the intergenic region upstream of Ednrb causes head spot in the rat strain KFRS4/Kyo.Genomic amplification of the caprine EDNRA locus might lead to a dose dependent loss of pigmentation.Endothelin receptor B2 (EDNRB2) is responsible for the tyrosinase-independent recessive white (mo(w) ) and mottled (mo) plumage phenotypes in the chicken.A gene expression study of dorso-ventrally restricted pigment pattern in adult fins of Neolamprologus meeli, an African cichlid species.Colours of domestication.A de novo mutation in KIT causes white spotting in a subpopulation of German Shepherd dogs.Extrinsic innervation of ileum and pelvic flexure of foals with ileocolonic aganglionosis.Strain-specific white-spotting patterns in laboratory mice.Novel insights into Sabino1 and splashed white coat color patterns in horses.A potential regulatory region near the EDN3 gene may control both harness racing performance and coat color variation in horses.
P2860
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P2860
A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
A missense mutation in the end ...... ersion of Hirschsprung disease
@ast
A missense mutation in the end ...... ersion of Hirschsprung disease
@en
A missense mutation in the end ...... ersion of Hirschsprung disease
@nl
type
label
A missense mutation in the end ...... ersion of Hirschsprung disease
@ast
A missense mutation in the end ...... ersion of Hirschsprung disease
@en
A missense mutation in the end ...... ersion of Hirschsprung disease
@nl
prefLabel
A missense mutation in the end ...... ersion of Hirschsprung disease
@ast
A missense mutation in the end ...... ersion of Hirschsprung disease
@en
A missense mutation in the end ...... ersion of Hirschsprung disease
@nl
P2093
P3181
P356
P1433
P1476
A missense mutation in the end ...... ersion of Hirschsprung disease
@en
P2093
A T Bowling
D L Metallinos
P2888
P304
P3181
P356
10.1007/S003359900790
P407
P577
1998-06-01T00:00:00Z