Pages that link to "Q28593256"
Jump to navigation
Jump to search
The following pages link to Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1 (Q28593256):
Displaying 50 items.
- Molecular dynamics of retinoic acid-induced craniofacial malformations: implications for the origin of gnathostome jaws (Q21092249) (← links)
- A zebrafish screen for craniofacial mutants identifies wdr68 as a highly conserved gene required for endothelin-1 expression (Q21284144) (← links)
- Endothelin 1 (Q21981779) (← links)
- A loss-of-function mutation in the endothelin-converting enzyme 1 (ECE-1) associated with Hirschsprung disease, cardiac defects, and autonomic dysfunction (Q22008702) (← links)
- Human endothelin converting enzyme-2 (ECE2): characterization of mRNA species and chromosomal localization (Q24291925) (← links)
- Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome) (Q24311237) (← links)
- ECE-1: a membrane-bound metalloprotease that catalyzes the proteolytic activation of big endothelin-1 (Q24317184) (← links)
- Krüppel-like factor 15 regulates BMPER in endothelial cells (Q24317601) (← links)
- The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development (Q24320819) (← links)
- Molecular characterization of human and bovine endothelin converting enzyme (ECE-1) (Q24336315) (← links)
- Calpain 6 is involved in microtubule stabilization and cytoskeletal organization (Q24338909) (← links)
- Role of Dlx6 in regulation of an endothelin-1-dependent, dHAND branchial arch enhancer (Q24600201) (← links)
- A candidate gene study of obstructive sleep apnea in European Americans and African Americans (Q24616899) (← links)
- The zebrafish dyrk1b gene is important for endoderm formation (Q24646790) (← links)
- mef2ca is required in cranial neural crest to effect Endothelin1 signaling in zebrafish (Q24670788) (← links)
- The transcription factor MEF2C is required for craniofacial development (Q24672010) (← links)
- Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment (Q24803518) (← links)
- Safety, efficacy, and clinical utility of macitentan in the treatment of pulmonary arterial hypertension (Q26747812) (← links)
- Endothelin (Q26767156) (← links)
- Interplay between cardiac function and heart development (Q26767303) (← links)
- Molecular basis of cleft palates in mice (Q26795762) (← links)
- New perspectives on pharyngeal dorsoventral patterning in development and evolution of the vertebrate jaw (Q26851854) (← links)
- The role of transforming growth factor β1 in the regulation of blood pressure (Q26998564) (← links)
- Nuclear compartmentalization of α1-adrenergic receptor signaling in adult cardiac myocytes (Q27015977) (← links)
- The neural crest in cardiac congenital anomalies (Q27024385) (← links)
- Zebrafish Bone and General Physiology Are Differently Affected by Hormones or Changes in Gravity (Q27307063) (← links)
- Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face (Q27308985) (← links)
- edn1 and hand2 Interact in early regulation of pharyngeal arch outgrowth during zebrafish development (Q27312040) (← links)
- Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1 (Q27316913) (← links)
- A fourth isoform of endothelin-converting enzyme (ECE-1) is generated from an additional promoter molecular cloning and characterization (Q28144641) (← links)
- Tip60 and HDAC7 interact with the endothelin receptor a and may be involved in downstream signaling (Q28206016) (← links)
- Heterodimerization of endothelin-converting enzyme-1 isoforms regulates the subcellular distribution of this metalloprotease (Q28209988) (← links)
- Fgf and Bmp signals repress the expression of Bapx1 in the mandibular mesenchyme and control the position of the developing jaw joint (Q28239307) (← links)
- The endothelin system and endothelin-converting enzyme in the brain: molecular and cellular studies (Q28244844) (← links)
- Endothelin@25 - new agonists, antagonists, inhibitors and emerging research frontiers: IUPHAR Review 12 (Q28246158) (← links)
- Air Pollution-Induced Vascular Dysfunction: Potential Role of Endothelin-1 (ET-1) System (Q28383288) (← links)
- Endothelin in the central control of cardiovascular and respiratory functions (Q28504612) (← links)
- Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1 (Q28504748) (← links)
- Dosage-dependent requirement for mouse Vezf1 in vascular system development (Q28506356) (← links)
- Embryonic lethality in Dear gene-deficient mice: new player in angiogenesis (Q28506779) (← links)
- Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis (Q28507003) (← links)
- Neonatal lethality in mice deficient in XCE, a novel member of the endothelin-converting enzyme and neutral endopeptidase family (Q28507128) (← links)
- Disruption of ECE-1 and ECE-2 reveals a role for endothelin-converting enzyme-2 in murine cardiac development (Q28507286) (← links)
- Pancreatic beta-cell-specific targeted disruption of glucokinase gene. Diabetes mellitus due to defective insulin secretion to glucose (Q28507345) (← links)
- Collecting duct-specific knockout of endothelin-1 alters vasopressin regulation of urine osmolality (Q28508192) (← links)
- Collecting duct-specific knockout of endothelin-1 causes hypertension and sodium retention (Q28508497) (← links)
- G protein-coupled cholecystokinin-B/gastrin receptors are responsible for physiological cell growth of the stomach mucosa in vivo (Q28512542) (← links)
- Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen (Q28513404) (← links)
- Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color (Q28583252) (← links)
- Endothelin-2 deficiency causes growth retardation, hypothermia, and emphysema in mice (Q28587616) (← links)