Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color
about
Novel mutations of the endothelin B receptor gene in patients with Hirschsprung's disease and their characterizationSerum response factor-GATA ternary complex required for nuclear signaling by a G-protein-coupled receptorTransplanting the enteric nervous system: a step closer to treatment for aganglionosisMapping of panda plumage color locus on the microsatellite linkage map of the Japanese quail.White paper on guidelines concerning enteric nervous system stem cell therapy for enteric neuropathiesEndothelinNonruminant Nutrition Symposium: Involvement of gut neural and endocrine systems in pathological disorders of the digestive tractPartial requirement of endothelin receptor B in spiral ganglion neurons for postnatal development of hearingEndothelin-1 impairs alveolar epithelial function via endothelial ETB receptorET(B) receptor-deficient rats exhibit reduced contraction to ET-1 despite an increase in ET(A) receptorsA whole genome Bayesian scan for adaptive genetic divergence in West African cattle.Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations.Transgenic expression of the endothelin-B receptor prevents congenital intestinal aganglionosis in a rat model of Hirschsprung disease.Hirschsprung disease and other enteric dysganglionoses.Endothelin signalling in iridophore development and stripe pattern formation of zebrafishQTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations.Intestinal motility disorders and development of the enteric nervous system.Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses.Familiar hypopigmentation syndrome in sheep associated with homozygous deletion of the entire endothelin type-B receptor gene.Role of endothelin-1 in acute lung injury.Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb.A novel bidirectional interaction between endothelin-3 and retinoic acid in rat enteric nervous system precursorsPostnatal intestinal engraftment of prospectively selected enteric neural crest stem cells in a rat model of Hirschsprung disease.The KIT gene is associated with the english spotting coat color locus and congenital megacolon in Checkered Giant rabbits (Oryctolagus cuniculus).High salt diet increases the pressor response to stress in female, but not male ETB-receptor-deficient ratsRegulation of blood pressure and salt homeostasis by endothelin.A chicken model of pharmacologically-induced Hirschsprung disease reveals an unexpected role of glucocorticoids in enteric aganglionosisHirschsprung's associated enterocolitisIntrinsic differences among spatially distinct neural crest stem cells in terms of migratory properties, fate determination, and ability to colonize the enteric nervous system.Development of occlusive neointimal lesions in distal pulmonary arteries of endothelin B receptor-deficient rats: a new model of severe pulmonary arterial hypertensionGene Expression Variations of Red-White Skin Coloration in Common Carp (Cyprinus carpio).Surgical Intervention to Rescue Hirschsprung Disease in a Rat Model.A deletion in the intergenic region upstream of Ednrb causes head spot in the rat strain KFRS4/Kyo.QTL analysis of modifiers for pigmentary disorder in rats carrying Ednrb sl mutations.Neurotransmitter receptor expression and activity during neuronal differentiation of embryonal carcinoma and stem cells: from basic research towards clinical applications.Deriving human ENS lineages for cell therapy and drug discovery in Hirschsprung disease.Pharmacological endothelin receptor interaction does not occur in veins from ET(B) receptor deficient rats.Regulation of the epithelial Na+ channel by endothelin-1 in rat collecting duct.Genetic variations associated with six-white-point coat pigmentation in Diannan small-ear pigs.Hirschsprung disease is associated with an L286P mutation in the fifth transmembrane domain of the endothelin-B receptor in the N-ethyl-N-nitrosourea-induced mutant line.
P2860
Q24309445-DE94B9B5-1F25-446B-B79B-E044F14750F4Q24548383-CC7C505A-FA4F-4AB6-9990-3B3DC0CD4893Q24679657-ADD8C2F4-6578-4C06-8780-47687D417CD0Q25257617-5C53802E-6BC1-4607-AAD0-B168D4FE6652Q26750556-51116BED-0770-4D20-A565-0A643F46FB1BQ26767156-8E38D4C7-D898-422E-8F70-86162A0A1AFDQ26823057-0AAD0DC3-71CD-4F7C-B364-2FB43265CA4EQ28392573-B098927E-4BF3-4276-907F-86E1D2A91AC7Q28575676-4CD791B5-E6D6-4522-A0B9-3B0990C20F27Q28582070-DD3F9C9C-53A2-4831-A644-F00503225C89Q28749712-4934B3DB-4785-4745-8FE0-EEB8D64650A0Q30474153-FCE2D7A8-4C44-4721-A553-C4F2F31EB886Q30500671-7FA9B6AA-4AE2-4448-8855-B6DC171AD57FQ33688226-8C612DE2-BA52-44F0-8727-4D605F139959Q33757260-FE095816-D901-4761-BF1A-54926AF3076BQ34087982-5FE1E24B-75FB-4222-A2B5-58D7786F3B2FQ34236122-2E13AC88-6470-4C9A-9002-8203F2A451C1Q34462847-5B411B70-CCF7-4CC0-9BA9-1B6F94D3AB27Q34541549-B2C63AF5-ACDD-4836-B39F-0C627D3A8027Q34615080-15658FCB-DB07-42FB-B8D3-E9D6C2F86DC9Q34762174-874A4550-6A4A-4530-A349-35F506595F32Q34989950-7EA2C70F-2ACC-4990-9003-4CCFB79ED34EQ35017167-D9D65991-FEA2-48CA-A3E0-C3299AF92657Q35149142-130E5F9A-89E8-4F72-94BB-1EC65B3F66A0Q35363150-CB4DDF60-3112-40DC-A8DD-6796C4A4C503Q35609851-20A69876-5E93-4677-8F73-73469F3259B2Q35616610-109FEC14-DEED-436C-A345-C7B85980BB4AQ35673166-B52CAE77-228B-43A3-B750-12780FF6784BQ35874911-38C6DFD8-D264-47E9-9B47-9CE0EE52D811Q35916976-3EEBEF56-26FF-48B8-9723-56496A702ABBQ36184092-C23C5AC2-F78C-4999-B113-15DDF556877CQ36211753-52DF5623-1C28-4569-A068-6ABADBFD8B3AQ36327236-F3D2874E-ED31-42A8-A096-20AFFA23E490Q36500613-9465D8D4-EA7F-47C0-8BD7-DFDDBB6490EAQ36548773-CA99C9A2-AA99-4844-9805-9DCB32B6CF3BQ36839772-8E4E2693-0826-4AE2-BFF5-576D38951D82Q36862976-26B52E25-2474-42E4-A221-5C6819CB6BE0Q36956714-795D35CC-E626-4BC8-8F18-9FF1370C98F8Q36980250-8B1192BE-2C2B-4D50-B6FA-0F4C3C4265B6Q37157112-C6972875-A855-43D1-A56C-22B464CC4AB8
P2860
Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color
description
1996 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հունվարին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 1996
@ast
im Januar 1996 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1996/01/23)
@sk
vědecký článek publikovaný v roce 1996
@cs
wetenschappelijk artikel (gepubliceerd op 1996/01/23)
@nl
наукова стаття, опублікована в січні 1996
@uk
name
Null mutation of endothelin re ...... megacolon and white coat color
@ast
Null mutation of endothelin re ...... megacolon and white coat color
@en
Null mutation of endothelin re ...... megacolon and white coat color
@nl
type
label
Null mutation of endothelin re ...... megacolon and white coat color
@ast
Null mutation of endothelin re ...... megacolon and white coat color
@en
Null mutation of endothelin re ...... megacolon and white coat color
@nl
prefLabel
Null mutation of endothelin re ...... megacolon and white coat color
@ast
Null mutation of endothelin re ...... megacolon and white coat color
@en
Null mutation of endothelin re ...... megacolon and white coat color
@nl
P2093
P2860
P3181
P356
P1476
Null mutation of endothelin re ...... megacolon and white coat color
@en
P2093
C. E. Gariepy
D. T. Cass
M. Yanagisawa
P2860
P304
P3181
P356
10.1073/PNAS.93.2.867
P407
P577
1996-01-23T00:00:00Z