Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene.
about
Organization and chromosomal localization of the human ECEL1 (XCE) gene encoding a zinc metallopeptidase involved in the nervous control of respirationDownregulation of Dlx5 and Dlx6 expression by Hand2 is essential for initiation of tongue morphogenesisRole of Dlx6 in regulation of an endothelin-1-dependent, dHAND branchial arch enhancer.mef2ca is required in cranial neural crest to effect Endothelin1 signaling in zebrafishThe transcription factor MEF2C is required for craniofacial developmentEndothelin1p36 deletion syndrome: an updateEnteric nervous system development: migration, differentiation, and diseaseMechanical regulation of cardiac developmentNuclear compartmentalization of α1-adrenergic receptor signaling in adult cardiac myocytesCompetition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Faceedn1 and hand2 Interact in early regulation of pharyngeal arch outgrowth during zebrafish developmentEndothelin@25 - new agonists, antagonists, inhibitors and emerging research frontiers: IUPHAR Review 12Src-family tyrosine kinases, phosphoinositide 3-kinase and Gab1 regulate extracellular signal-regulated kinase 1 activation induced by the type A endothelin-1 G-protein-coupled receptorVasoconstrictor activity of novel endothelin peptide, ET-1(1 - 31), in human mammary and coronary arteries in vitroDisruption of ECE-1 and ECE-2 reveals a role for endothelin-converting enzyme-2 in murine cardiac developmentHand transcription factors cooperatively regulate development of the distal midline mesenchymeEndothelin-converting enzyme-1 regulates trafficking and signalling of the neurokinin 1 receptor in endosomes of myenteric neuronesEmbryonic cardiomyocyte hypoplasia and craniofacial defects in G alpha q/G alpha 11-mutant mice.Endothelin-A receptor-dependent and -independent signaling pathways in establishing mandibular identityViable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutationA human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.Can you hear me now? Understanding vertebrate middle ear development.Transgenic expression of the endothelin-B receptor prevents congenital intestinal aganglionosis in a rat model of Hirschsprung disease.Reciprocal myocardial-endocardial interactions pattern the delay in atrioventricular junction conduction.Cyclic expression of endothelin-converting enzyme-1 mediates the functional regulation of seminiferous tubule contraction.Secretory pathways in endothelin synthesis.Elucidating timing and function of endothelin-A receptor signaling during craniofacial development using neural crest cell-specific gene deletion and receptor antagonism.Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies.Genetic model system studies of the development of the enteric nervous system, gut motility and Hirschsprung's diseaseEndothelin signalling in iridophore development and stripe pattern formation of zebrafishRole of endothelin 1 in the pathogenesis of chronic chagasic heart disease.Venous endothelin guides sympathetic innervation of the developing mouse heart.QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations.Experimental control of pancreatic development and maintenance.Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1Prevention of inflammation-associated preterm birth by knockdown of the endothelin-1-matrix metalloproteinase-1 pathway.Reduced fertility in male mice deficient in the zinc metallopeptidase NL1Hirschsprung disease, associated syndromes, and genetics: a review.Amyloid beta-degrading cryptidases: insulin degrading enzyme, presequence peptidase, and neprilysin.
P2860
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P2860
Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
Dual genetic pathways of endot ...... elin converting enzyme-1 gene.
@en
Dual genetic pathways of endot ...... elin converting enzyme-1 gene.
@nl
type
label
Dual genetic pathways of endot ...... elin converting enzyme-1 gene.
@en
Dual genetic pathways of endot ...... elin converting enzyme-1 gene.
@nl
prefLabel
Dual genetic pathways of endot ...... elin converting enzyme-1 gene.
@en
Dual genetic pathways of endot ...... elin converting enzyme-1 gene.
@nl
P2093
P1433
P1476
Dual genetic pathways of endot ...... elin converting enzyme-1 gene.
@en
P2093
D E Clouthier
H Yanagisawa
J A Richardson
M Yanagisawa
R E Hammer
S C Williams
P304
P407
P577
1998-03-01T00:00:00Z