Polycystic kidney rat is a novel animal model of Caroli's disease associated with congenital hepatic fibrosis.
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Tumor necrosis factor-alpha induces the aberrant expression of mucus core protein-2 in non-neoplastic biliary epithelial cells via the upregulation of CDX2 in chronic cholangitisHepatic cystogenesis is associated with abnormal expression and location of ion transporters and water channels in an animal model of autosomal recessive polycystic kidney diseaseInteraction of Toll-like receptors with bacterial components induces expression of CDX2 and MUC2 in rat biliary epithelium in vivo and in cultureActivation of the PI3K/mTOR pathway is involved in cystic proliferation of cholangiocytes of the PCK ratActivation of the MEK5/ERK5 cascade is responsible for biliary dysgenesis in a rat model of Caroli's diseaseWhat are the precursor and early lesions of peripheral intrahepatic cholangiocarcinoma?Hepato-renal pathology in pkd2ws25/- mice, an animal model of autosomal dominant polycystic kidney diseasePolycystic liver diseases.Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene.An incredible decade for the primary cilium: a look at a once-forgotten organelle.Renin-angiotensin system activation in congenital hepatic fibrosis in the PCK rat model of autosomal recessive polycystic kidney disease.The cAMP effectors Epac and protein kinase a (PKA) are involved in the hepatic cystogenesis of an animal model of autosomal recessive polycystic kidney disease (ARPKD).Disease stage characterization of hepatorenal fibrocystic pathology in the PCK rat model of ARPKDBiliary dysgenesis in the PCK rat, an orthologous model of autosomal recessive polycystic kidney diseaseMolecular pathology and genetics of congenital hepatorenal fibrocystic syndromesCongenital hepatic fibrosis in autosomal recessive polycystic kidney disease.Proliferation-Independent Initiation of Biliary Cysts in Polycystic Liver Diseases.Cholangiocytes with mesenchymal features contribute to progressive hepatic fibrosis of the polycystic kidney ratLiver disease in autosomal recessive polycystic kidney disease.Beneficial effect of combined treatment with octreotide and pasireotide in PCK rats, an orthologous model of human autosomal recessive polycystic kidney diseaseSrc inhibition ameliorates polycystic kidney diseaseLaparoscopic findings of congenital hepatic fibrosis: A case report and review of the published work.Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model.α1- and α5-containing laminins regulate the development of bile ducts via β1 integrin signals.Animal models of biliary injury and altered bile acid metabolism.Is congenital hepatic fibrosis a pure liver disease?Development and characterization of a cholangiocyte cell line from the PCK rat, an animal model of Autosomal Recessive Polycystic Kidney Disease.Biliary infection may exacerbate biliary cystogenesis through the induction of VEGF in cholangiocytes of the polycystic kidney (PCK) ratInhibition of intrahepatic bile duct dilation of the polycystic kidney rat with a novel tyrosine kinase inhibitor gefitinib.Establishment of a standardized liver fibrosis model with different pathological stages in rats.Initial evaluation of hepatic T1 relaxation time as an imaging marker of liver disease associated with autosomal recessive polycystic kidney disease (ARPKD).Matrix proteins of basement membrane of intrahepatic bile ducts are degraded in congenital hepatic fibrosis and Caroli's disease.Reply to 'What are ductal plate and ductal plate malformations of human livers?'.Diffuse expression of heparan sulfate proteoglycan and connective tissue growth factor in fibrous septa with many mast cells relate to unresolving hepatic fibrosis of congenital hepatic fibrosis.Bile duct dysplasia and congenital hepatic fibrosis associated with polycystic kidney (Caroli syndrome) in a rat.Roles of myofibroblasts and notch and hedgehog signaling pathways in the formation of intrahepatic bile duct lesions in polycystic kidney rats.
P2860
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P2860
Polycystic kidney rat is a novel animal model of Caroli's disease associated with congenital hepatic fibrosis.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Polycystic kidney rat is a nov ...... h congenital hepatic fibrosis.
@ast
Polycystic kidney rat is a nov ...... h congenital hepatic fibrosis.
@en
type
label
Polycystic kidney rat is a nov ...... h congenital hepatic fibrosis.
@ast
Polycystic kidney rat is a nov ...... h congenital hepatic fibrosis.
@en
prefLabel
Polycystic kidney rat is a nov ...... h congenital hepatic fibrosis.
@ast
Polycystic kidney rat is a nov ...... h congenital hepatic fibrosis.
@en
P2093
P2860
P1476
Polycystic kidney rat is a nov ...... h congenital hepatic fibrosis.
@en
P2093
P2860
P304
P356
10.1016/S0002-9440(10)64116-8
P407
P577
2001-05-01T00:00:00Z