ERK1/2-dependent vascular endothelial growth factor signaling sustains cyst growth in polycystin-2 defective mice.
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Polycystic liver diseases: advanced insights into the molecular mechanismsExperimental therapies and ongoing clinical trials to slow down progression of ADPKDThe role of hypoxia-inducible factor-1α in zinc oxide nanoparticle-induced nephrotoxicity in vitro and in vivoA genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formationA mathematical model for mechanotransduction at the early steps of suture formationPPAR-gamma agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney diseaseProtein kinase A-dependent pSer(675) -β-catenin, a novel signaling defect in a mouse model of congenital hepatic fibrosisPolycystic liver diseases.Mammalian target of rapamycin regulates vascular endothelial growth factor-dependent liver cyst growth in polycystin-2-defective mice.Aquaporin-1 promotes angiogenesis, fibrosis, and portal hypertension through mechanisms dependent on osmotically sensitive microRNAsInhibiting heat shock protein 90 (HSP90) limits the formation of liver cysts induced by conditional deletion of Pkd1 in mice.Hypoxia-inducible factor-1α (HIF-1α) and autophagy in polycystic kidney disease (PKD).Screening analysis of candidate gene mutations in a kindred with polycystic liver disease.Loss of CFTR affects biliary epithelium innate immunity and causes TLR4-NF-κB-mediated inflammatory response in miceVascular factors, angiogenesis and biliary tract diseaseEpithelial-mesenchymal interactions in biliary diseasesPolycystic liver diseases: congenital disorders of cholangiocyte signalingDevelopment of the bile ducts: essentials for the clinical hepatologist.Vascular biology of the biliary epitheliumStrategies targeting cAMP signaling in the treatment of polycystic kidney disease.Novel therapeutic approaches to autosomal dominant polycystic kidney disease.Therapeutic Targets in Polycystic Liver Disease.An overview of experimental and early investigational therapies for the treatment of polycystic kidney disease.Recent Trends in ADPKD Research.Platelet-derived growth factor-D and Rho GTPases regulate recruitment of cancer-associated fibroblasts in cholangiocarcinoma.Animal models of biliary injury and altered bile acid metabolism.Biliary infection may exacerbate biliary cystogenesis through the induction of VEGF in cholangiocytes of the polycystic kidney (PCK) ratAltered store operated calcium entry increases cyclic 3',5'-adenosine monophosphate production and extracellular signal-regulated kinases 1 and 2 phosphorylation in polycystin-2-defective cholangiocytes.Posttranslational regulation of polycystin-2 protein expression as a novel mechanism of cholangiocyte reaction and repair from biliary damage.Vascular endothelial growth factors in progenitor cells mediated liver repair.Cyclic AMP/PKA-dependent paradoxical activation of Raf/MEK/ERK signaling in polycystin-2 defective mice treated with sorafenib.The role of endothelial nitric oxide in the anti-restenotic effects of liraglutide in a mouse model of restenosis.Bile acids initiate cholestatic liver injury by triggering a hepatocyte-specific inflammatory response.Profiling of miRNAs and target genes related to cystogenesis in ADPKD mouse models.Multiple postnatal craniofacial anomalies are characterized by conditional loss of polycystic kidney disease 2 (Pkd2).β-catenin and IL-1β dependent CXCL10 production drives progression of disease in a mouse model of Congenital Hepatic Fibrosis.Possible Role of Raf-1 Kinase in the Development of Cerebral Vasospasm and Early Brain Injury After Experimental Subarachnoid Hemorrhage in Rats.The combination of an HDAC6 inhibitor and a somatostatin receptor agonist synergistically reduces hepato-renal cystogenesis in an animal model of polycystic liver disease.Graphene Oxide-Copper Nanocomposite-Coated Porous CaP Scaffold for Vascularized Bone Regeneration via Activation of Hif-1α.Primary cilia disruption differentially affects the infiltrating and resident macrophage compartment in the liver.
P2860
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P2860
ERK1/2-dependent vascular endothelial growth factor signaling sustains cyst growth in polycystin-2 defective mice.
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@ast
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@en
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@nl
type
label
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@ast
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@en
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@nl
prefLabel
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@ast
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@en
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@nl
P2093
P2860
P1433
P1476
ERK1/2-dependent vascular endo ...... n polycystin-2 defective mice.
@en
P2093
Carlo Spirli
Luca Fabris
Mario Strazzabosco
Massimiliano Cadamuro
Romina Fiorotto
Silvia Lecchi
Stefan Somlo
Stefano Okolicsanyi
P2860
P304
360-371.e7
P356
10.1053/J.GASTRO.2009.09.005
P407
P577
2009-09-18T00:00:00Z