| scholarly article | Q13442814 |
| P2093 | author name string | Nicholas F. LaRusso | |
| Patrick L. Splinter | |||
| Anatoliy I. Masyuk | |||
| Angela J. Stroope | |||
| Bing Q. Huang | |||
| Tatyana V. Masyuk | |||
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| News focus: Betting on cilia. | Q54304196 | ||
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| Perfused rat intrahepatic bile ducts secrete and absorb water, solute, and ions | Q73288688 | ||
| Laminar shear stress: mechanisms by which endothelial cells transduce an atheroprotective force | Q74582573 | ||
| Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm | Q24305942 | ||
| Polycystic disease of the liver | Q28283470 | ||
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| Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease | Q28585961 | ||
| The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia | Q29615732 | ||
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| Primary cilia of human endothelial cells disassemble under laminar shear stress | Q36322273 | ||
| Polycystic liver and kidney diseases | Q36336546 | ||
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| Mechanoregulation of intracellular Ca2+ concentration is attenuated in collecting duct of monocilium-impaired orpk mice | Q39721139 | ||
| Glucose reabsorption from bile. Evidence for a biliohepatic circulation | Q40368003 | ||
| Removal of the MDCK cell primary cilium abolishes flow sensing | Q40676837 | ||
| Bending the MDCK cell primary cilium increases intracellular calcium | Q40771361 | ||
| Bile duct epithelium: frontiers in transport physiology | Q41083798 | ||
| Primary cilia in normal and pathological tissues | Q41160293 | ||
| Intrahepatic bile ducts transport water in response to absorbed glucose | Q44101872 | ||
| Regulation of cholangiocyte secretion | Q44165090 | ||
| Specific inhibition of AQP1 water channels in isolated rat intrahepatic bile duct units by small interfering RNAs | Q44240350 | ||
| Effect of flow and stretch on the [Ca2+]i response of principal and intercalated cells in cortical collecting duct | Q44499345 | ||
| Sugar absorption by the biliary ductular epithelium of the rat: Evidence for two transport systems | Q46032077 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | fluid flow | Q12142910 |
| P304 | page(s) | 911–920 | |
| P577 | publication date | 2006-09-01 | |
| P1433 | published in | Gastroenterology | Q4039279 |
| P1476 | title | Cholangiocyte cilia detect changes in luminal fluid flow and transmit them into intracellular Ca2+ and cAMP signaling | |
| P478 | volume | 131 |
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| Q38255292 | An approach to cystic kidney diseases: the clinician's view |
| Q38962914 | An experimental and computational analysis of primary cilia deflection under fluid flow. |
| Q36817088 | An unexpected journey: conceptual evolution of mechanoregulated potassium transport in the distal nephron |
| Q37216909 | Attenuated, flow-induced ATP release contributes to absence of flow-sensitive, purinergic Cai2+ signaling in human ADPKD cyst epithelial cells |
| Q24656249 | Autosomal dominant polycystic kidney disease: the last 3 years |
| Q34212071 | Biliary exosomes influence cholangiocyte regulatory mechanisms and proliferation through interaction with primary cilia. |
| Q57115313 | Calcium Signaling in Liver Injury and Regeneration |
| Q38876014 | Calcium channels in primary cilia |
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| Q41960056 | Calcium signaling in cilia and ciliary-mediated intracellular calcium signaling: are they independent or coordinated molecular events? |
| Q38110517 | Calcium signaling in the liver |
| Q37798910 | Calcium-mediated mechanisms of cystic expansion |
| Q36497518 | Centrosome positioning in vertebrate development |
| Q37317821 | Cholangiociliopathies: genetics, molecular mechanisms and potential therapies |
| Q30513913 | Cholangiocyte cilia are abnormal in syndromic and non-syndromic biliary atresia |
| Q36277264 | Cholangiocyte cilia express TRPV4 and detect changes in luminal tonicity inducing bicarbonate secretion. |
| Q64913364 | Cholangiocyte pathobiology. |
| Q28577465 | Cholangiocyte primary cilia are chemosensory organelles that detect biliary nucleotides via P2Y12 purinergic receptors |
| Q36953076 | Cholangiocyte primary cilia in liver health and disease |
| Q36923647 | Ciliary subcellular localization of TGR5 determines the cholangiocyte functional response to bile acid signaling |
| Q30575795 | Cilioplasm is a cellular compartment for calcium signaling in response to mechanical and chemical stimuli |
| Q38264623 | Computational models of the primary cilium and endothelial mechanotransmission. |
| Q35655072 | Congenital hepatic fibrosis in autosomal recessive polycystic kidney disease |
| Q28566509 | Differentially expressed adenylyl cyclase isoforms mediate secretory functions in cholangiocyte subpopulation |
| Q34305511 | Direct demonstration of tubular fluid flow sensing by macula densa cells |
| Q36238180 | Dynamics of the primary cilium in shear flow |
| Q34399971 | ERK1/2-dependent vascular endothelial growth factor signaling sustains cyst growth in polycystin-2 defective mice |
| Q38064200 | Emerging role of primary cilia as mechanosensors in osteocytes |
| Q33866800 | Estrogens and the pathophysiology of the biliary tree |
| Q39990068 | Flow modulates centriole movements in tubular epithelial cells |
| Q54400236 | Fluid Shear Stress Induces Renal Epithelial Gene Expression through Polycystin-2-Dependent Trafficking of Extracellular Regulated Kinase |
| Q39995163 | Fluid flow induces mechanosensitive ATP release, calcium signalling and Cl- transport in biliary epithelial cells through a PKCzeta-dependent pathway |
| Q46565214 | Fluid flow sensing and triggered nucleotide release in epithelia. |
| Q35906117 | Force-response considerations in ciliary mechanosensation |
| Q30450537 | From central to rudimentary to primary: the history of an underappreciated organelle whose time has come. The primary cilium |
| Q34779022 | Functional anatomy of normal bile ducts |
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| Q34035361 | HDAC6 inhibition restores ciliary expression and decreases tumor growth |
| Q56931604 | HNF1B deficiency causes ciliary defects in human cholangiocytes |
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| Q34431996 | Hypertension in Autosomal Dominant Polycystic Kidney Disease: A Clinical and Basic Science Perspective |
| Q35919332 | Identification of drugs that restore primary cilium expression in cancer cells |
| Q41579424 | Identification of signaling pathways regulating primary cilium length and flow-mediated adaptation |
| Q64996451 | Inhibition of Mast Cell Degranulation With Cromolyn Sodium Exhibits Organ-Specific Effects in Polycystic Kidney (PCK) Rats. |
| Q24633724 | Liver and kidney disease in ciliopathies |
| Q41819809 | Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant. |
| Q34091331 | Mammalian target of rapamycin regulates vascular endothelial growth factor-dependent liver cyst growth in polycystin-2-defective mice. |
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| Q36527934 | Mechanosensitive Cl- secretion in biliary epithelium mediated through TMEM16A. |
| Q50182542 | MiR-433 and miR-22 dysregulations induce HDAC6 overexpression and ciliary loss in cholangiocarcinoma. |
| Q36410357 | MicroRNAs in biliary diseases. |
| Q26783579 | MicroRNAs in the Cholangiopathies: Pathogenesis, Diagnosis, and Treatment |
| Q37809245 | Molecular Mechanisms of Biliary Development |
| Q37769923 | Molecular mechanisms of bile duct development |
| Q36559639 | Morphological and functional features of hepatic cyst epithelium in autosomal dominant polycystic kidney disease |
| Q35952274 | Neuronal ciliary signaling in homeostasis and disease |
| Q38092296 | Non-motile primary cilia as fluid shear stress mechanosensors |
| Q41898964 | Non-random distribution and sensory functions of primary cilia in vascular smooth muscle cells. |
| Q92157976 | Novel functions of the primary cilium in bone disease and cancer |
| Q38273327 | Novel therapeutic approaches to autosomal dominant polycystic kidney disease |
| Q37730964 | Osteocyte primary cilium and its role in bone mechanotransduction |
| Q39440062 | Pathobiology of biliary epithelia. |
| Q92532305 | Pathobiology of inherited biliary diseases: a roadmap to understand acquired liver diseases |
| Q34623557 | Pathogenesis of Cholestatic Liver Disease and Therapeutic Approaches |
| Q34860483 | Patients, cells, and organelles: the intersection of science and serendipity |
| Q36585455 | Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins |
| Q37145917 | Physiology and pathophysiology of the vasopressin-regulated renal water reabsorption |
| Q27008523 | Physiology of cholangiocytes |
| Q35660081 | Polycystic diseases in visceral organs |
| Q33949172 | Polycystic liver diseases. |
| Q27001174 | Polycystic liver diseases: advanced insights into the molecular mechanisms |
| Q37868328 | Polycystic liver diseases: congenital disorders of cholangiocyte signaling |
| Q28591325 | Polycystin-2 and phosphodiesterase 4C are components of a ciliary A-kinase anchoring protein complex that is disrupted in cystic kidney diseases |
| Q33894574 | Primary Cilia in Tumor Biology: The Primary Cilium as a Therapeutic Target in Cholangiocarcinoma |
| Q45932817 | Primary Cilium-Dependent Signaling Mechanisms. |
| Q30479846 | Primary cilia mediate mechanosensing in bone cells by a calcium-independent mechanism. |
| Q34245120 | Primary cilia mediate mechanotransduction through control of ATP-induced Ca2+ signaling in compressed chondrocytes. |
| Q40003783 | Primary cilia modulate Ihh signal transduction in response to hydrostatic loading of growth plate chondrocytes |
| Q38832224 | Primary cilia regulates the directional migration and barrier integrity of endothelial cells through the modulation of hsp27 dependent actin cytoskeletal organization |
| Q30530971 | Primary cilia-mediated mechanotransduction in human mesenchymal stem cells |
| Q47750425 | Primary cilia: Cell and molecular mechanosensors directing whole tissue function |
| Q37252102 | Primary cilia: cellular sensors for the skeleton |
| Q37994180 | Primary cilia: highly sophisticated biological sensors |
| Q34017092 | Primary cilium-dependent mechanosensing is mediated by adenylyl cyclase 6 and cyclic AMP in bone cells |
| Q53096259 | Primary-cilium-dependent autophagy controls epithelial cell volume in response to fluid flow. |
| Q95822241 | Proceedings of the 21st International Bile Acid Meeting. October 7-14, 2010, Freiburg, Germany |
| Q35854986 | Protein composition and movements of membrane swellings associated with primary cilia |
| Q94363723 | RAPAMYCIN INCREASES LENGTH AND MECHANOSENSORY FUNCTION OF PRIMARY CILIA IN RENAL EPITHELIAL AND VASCULAR ENDOTHELIAL CELLS |
| Q30638114 | Real-time vascular mechanosensation through ex vivo artery perfusion |
| Q85887537 | Safety study of somatostatin analogue octreotide for autosomal dominant polycystic kidney disease in Japan |
| Q33606240 | Sensing a sensor: identifying the mechanosensory function of primary cilia |
| Q39426442 | Shear stress reverses dome formation in confluent renal tubular cells. |
| Q37347565 | Somatostatin signaling in neuronal cilia is critical for object recognition memory. |
| Q33809680 | Structural and functional analyses of liver cysts from the BALB/c-cpk mouse model of polycystic kidney disease |
| Q40867711 | TGR5 in the Cholangiociliopathies |
| Q37892281 | TGR5 in the biliary tree |
| Q37369328 | Targeting proteins to the ciliary membrane. |
| Q26852534 | The Liver and Polycystic Kidney Disease |
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| Q37781024 | The biliary HCO(3)(-) umbrella: a unifying hypothesis on pathogenetic and therapeutic aspects of fibrosing cholangiopathies |
| Q34717186 | 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). |
| Q39381392 | The cholangiocyte primary cilium in health and disease. |
| Q28000091 | The emerging role of Arf/Arl small GTPases in cilia and ciliopathies |
| Q37928761 | The mechanics of the primary cilium: an intricate structure with complex function |
| Q38019498 | The primary cilium as a novel extracellular sensor in bone |
| Q47681227 | The primary cilium as a signaling nexus for growth plate function and subsequent skeletal development. |
| Q38271916 | The primary cilium as sensor of fluid flow: new building blocks to the model. A review in the theme: cell signaling: proteins, pathways and mechanisms |
| Q37690035 | The primary cilium at a glance |
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| Q36529245 | The primary cilium is a self-adaptable, integrating nexus for mechanical stimuli and cellular signaling |
| Q90312189 | The primary cilium: Its role as a tumor suppressor organelle |
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| Q35082225 | The role of cilia in the regulation of bile flow |
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| Q34024396 | Treatment strategies and clinical trial design in ADPKD |
| Q29547198 | When cilia go bad: cilia defects and ciliopathies |
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