Pages that link to "Q36559697"

The following pages link to Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1. (Q36559697):

Displaying 41 items.

• Polycystin-1: a master regulator of intersecting cystic pathways (Q26826955) (← links)
• Renal cystic disease proteins play critical roles in the organization of the olfactory epithelium (Q27342510) (← links)
• Evidence for a "Pathogenic Triumvirate" in Congenital Hepatic Fibrosis in Autosomal Recessive Polycystic Kidney Disease (Q28079756) (← links)
• A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation (Q28590393) (← links)
• Loss of oriented cell division does not initiate cyst formation (Q30493527) (← links)
• Protein kinase A-dependent pSer(675) -β-catenin, a novel signaling defect in a mouse model of congenital hepatic fibrosis (Q30552040) (← links)
• Murine Models of Polycystic Kidney Disease. (Q33856965) (← links)
• Tissue-specific regulation of the mouse Pkhd1 (ARPKD) gene promoter (Q34001299) (← links)
• Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects (Q34086721) (← links)
• Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene (Q34308868) (← links)
• Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1. (Q34339024) (← links)
• Primary cilia in pancreatic development and disease (Q34421859) (← links)
• Disease Stage Characterization of Hepatorenal Fibrocystic Pathology in the PCK Rat Model of ARPKD (Q34846108) (← links)
• Recent advances in primary ciliary dyskinesia genetics. (Q34852544) (← links)
• Effects of hydration in rats and mice with polycystic kidney disease (Q35035244) (← links)
• Epitope-tagged Pkhd1 tracks the processing, secretion, and localization of fibrocystin. (Q35647871) (← links)
• Congenital hepatic fibrosis in autosomal recessive polycystic kidney disease (Q35655072) (← links)
• Polycystic diseases in visceral organs (Q35660081) (← links)
• Proliferation-Independent Initiation of Biliary Cysts in Polycystic Liver Diseases (Q35678557) (← links)
• Cholangiociliopathies: genetics, molecular mechanisms and potential therapies (Q37317821) (← links)
• Transient receptor proteins illuminated: current views on TRPs and disease (Q37720127) (← links)
• Polycystic kidney disease, cilia, and planar polarity. (Q37723498) (← links)
• The extracellular matrix and ciliary signaling (Q38028167) (← links)
• Translational research in ADPKD: lessons from animal models (Q38241290) (← links)
• Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model (Q38348634) (← links)
• Macrophage recruitment by fibrocystin-defective biliary epithelial cells promotes portal fibrosis in congenital hepatic fibrosis. (Q38603748) (← links)
• Primary Cilia in Cystic Kidney Disease (Q39242476) (← links)
• Animal models of biliary injury and altered bile acid metabolism (Q39436033) (← links)
• Cystogenesis in ARPKD results from increased apoptosis in collecting duct epithelial cells of Pkhd1 mutant kidneys (Q39650947) (← links)
• A Novel Pkhd1 Mutation Interacts with the Nonobese Diabetic Genetic Background To Cause Autoimmune Cholangitis (Q46249993) (← links)
• β-catenin and IL-1β dependent CXCL10 production drives progression of disease in a mouse model of Congenital Hepatic Fibrosis. (Q47400159) (← links)
• Disruption of Core Planar Cell Polarity Signaling Regulates Renal Tubule Morphogenesis but Is Not Cystogenic (Q47650903) (← links)
• Recent advances in the molecular diagnosis of polycystic kidney disease (Q47737330) (← links)
• Doxycycline accelerates renal cyst growth and fibrosis in the pcy/pcy mouse model of type 3 nephronophthisis, a form of recessive polycystic kidney disease (Q47973716) (← links)
• A novel model of autosomal recessive polycystic kidney questions the role of the fibrocystin C-terminus in disease mechanism. (Q48542741) (← links)
• Genetics of Autosomal Recessive Polycystic Kidney Disease and Its Differential Diagnoses (Q50301021) (← links)
• Primary cilia disruption differentially affects the infiltrating and resident macrophage compartment in the liver (Q51739818) (← links)
• Compound heterozygous PKHD1 variants cause a wide spectrum of ductal plate malformations. (Q53339830) (← links)
• Cholangiopathies - Towards a molecular understanding (Q57109524) (← links)
• Polycystic kidney and hepatic disease 1 gene mutations in von Meyenburg complexes: Case report (Q58761572) (← links)
• Fibroinflammatory Liver Injuries as Preneoplastic Condition in Cholangiopathies (Q60919574) (← links)