| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1097/00041552-200309000-00006 |
| P698 | PubMed publication ID | 12920399 |
| P2093 | author name string | Kenneth R Spring | |
| Helle A Praetorius | |||
| P433 | issue | 5 | |
| P304 | page(s) | 517-520 | |
| P577 | publication date | 2003-09-01 | |
| P1433 | published in | Current Opinion in Nephrology and Hypertension | Q15756282 |
| P1476 | title | The renal cell primary cilium functions as a flow sensor | |
| P478 | volume | 12 |
| Q39021418 | 5-HT6 receptor blockade regulates primary cilia morphology in striatal neurons. |
| Q36047287 | A mechanistic approach to inherited polycystic kidney disease. |
| Q37146423 | A mouse model for Meckel syndrome type 3. |
| Q35148415 | Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia. |
| Q37345965 | Advances in management of polycystic liver disease |
| Q37816944 | Alström syndrome: insights into the pathogenesis of metabolic disorders |
| Q62393730 | Alterations in renal cilium length during transient complete ureteral obstruction in the mouse |
| Q35145360 | Altered trafficking and stability of polycystins underlie polycystic kidney disease |
| Q29994736 | An ovine hepatorenal fibrocystic model of a Meckel-like syndrome associated with dysmorphic primary cilia and TMEM67 mutations |
| Q46126251 | Articular chondrocytes express connexin 43 hemichannels and P2 receptors - a putative mechanoreceptor complex involving the primary cilium? |
| Q49161658 | Artificial CSF motion ensures rhythmic activity in the developing CNS ex vivo: a mechanical source of rhythmogenesis? |
| Q34658371 | Autosomal recessive Bardet-Biedl syndrome: first-degree relatives have no predisposition to metabolic and renal disorders. |
| Q40540421 | Beta1-integrins in the primary cilium of MDCK cells potentiate fibronectin-induced Ca2+ signaling |
| Q36667037 | Biological and Chemical Removal of Primary Cilia Affects Mechanical Activation of Chondrogenesis Markers in Chondroprogenitors and Hypertrophic Chondrocytes |
| Q55191663 | Can Tissue Cilia Lengths and Urine Cilia Proteins Be Markers of Kidney Diseases? |
| Q34116745 | Canonical TRP channels and mechanotransduction: from physiology to disease states. |
| Q36644604 | Cell biology of polycystin-2. |
| Q39961011 | Characterization of primary cilia and Hedgehog signaling during development of the human pancreas and in human pancreatic duct cancer cell lines |
| Q38256488 | Chemical and Physical Sensors in the Regulation of Renal Function |
| Q36337939 | Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease? |
| Q35022641 | Cilia involvement in patterning and maintenance of the skeleton |
| Q34979672 | Cilia movement regulates expression of the Raf-1 kinase inhibitor protein |
| Q89151686 | Cilia protein IFT88 regulates extracellular protease activity by optimizing LRP-1-mediated endocytosis |
| Q37372591 | Ciliar functions in the nephron |
| Q35537057 | Ciliary ectosomes: transmissions from the cell's antenna |
| Q36050308 | Cilium-generated signaling and cilia-related disorders |
| Q42434330 | Development of the post-natal growth plate requires intraflagellar transport proteins |
| Q36505469 | Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease |
| Q34305511 | Direct demonstration of tubular fluid flow sensing by macula densa cells |
| Q36363340 | Discerning the role of mechanosensors in regulating proximal tubule function |
| Q36156370 | Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney disease |
| Q28483801 | Dynamic compression of chondrocyte-agarose constructs reveals new candidate mechanosensitive genes |
| Q34121928 | Effects of biomechanical forces on signaling in the cortical collecting duct (CCD). |
| Q37623301 | Endothelial primary cilia inhibit atherosclerosis. |
| Q38655764 | Evolutionary morphology of podocytes and primary urine-producing apparatus |
| Q34719208 | Flow regulation of collecting duct endothelin-1 production |
| Q35178609 | Flow regulation of endothelin-1 production in the inner medullary collecting duct |
| Q92145654 | Flow-activated proximal tubule function underlies glomerulotubular balance |
| Q38076051 | From bone abnormalities to mineral metabolism dysregulation in autosomal dominant polycystic kidney disease. |
| Q37264334 | Function and regulation of TRPP2 at the plasma membrane |
| Q35101099 | Function and regulation of primary cilia and intraflagellar transport proteins in the skeleton |
| Q36175595 | Gαq/11-mediated intracellular calcium responses to retrograde flow in endothelial cells |
| Q35608125 | Heterotrimeric kinesin-2 (KIF3) mediates transition zone and axoneme formation of mouse photoreceptors |
| Q44833669 | Luminal flow induces eNOS activation and translocation in the rat thick ascending limb |
| Q35652092 | Luminal flow modulates H+-ATPase activity in the cortical collecting duct (CCD). |
| Q24302034 | Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways |
| Q84088659 | Measuring cilium-induced Ca2+ increases in cultured renal epithelia |
| Q28834419 | Mechanical dynamics in live cells and fluorescence-based force/tension sensors |
| Q36066690 | Mechanical properties of a primary cilium as measured by resonant oscillation |
| Q41954733 | Mechanophysical stimulations of mucin secretion in cultures of nasal epithelial cells |
| Q42259459 | Mechanosensitive ATP release maintains proper mucus hydration of airways |
| Q30832338 | Mechanosensory function of microvilli of the kidney proximal tubule |
| Q35993959 | Na delivery and ENaC mediate flow regulation of collecting duct endothelin-1 production |
| Q35952274 | Neuronal ciliary signaling in homeostasis and disease |
| Q42549374 | Neutrophil gelatinase-associated lipocalin suppresses cyst growth by Pkd1 null cells in vitro and in vivo |
| Q36581884 | Novel insights into TRPV4 function in the kidney |
| Q38973454 | Oscillatory fluid flow influences primary cilia and microtubule mechanics |
| Q37613679 | Physiology of endothelin and the kidney |
| Q28509047 | Piezo1-dependent stretch-activated channels are inhibited by Polycystin-2 in renal tubular epithelial cells |
| Q37698284 | Planar cell polarity: keeping hairs straight is not so simple |
| Q28283470 | Polycystic disease of the liver |
| Q36917461 | Polycystic kidney disease and renal injury repair: common pathways, fluid flow, and the function of polycystin-1. |
| Q36061608 | Polycystin-2--an intracellular or plasma membrane channel? |
| Q38053059 | Polycystins and cellular Ca2+ signaling |
| Q38200953 | Polycystins and partners: proposed role in mechanosensitivity. |
| Q36124622 | Polycystins: polymodal receptor/ion-channel cellular sensors |
| Q37242240 | Potassium channels keep mobile cells on the go. |
| Q49727816 | Primary cilia exist in a small fraction of cells in trabecular bone and marrow |
| Q51328758 | Primary cilia on porcine testicular somatic cells and their role in hedgehog signaling and tubular morphogenesis in vitro. |
| Q47750425 | Primary cilia: Cell and molecular mechanosensors directing whole tissue function |
| Q39177890 | Reduction of oxidative stress during recovery accelerates normalization of primary cilia length that is altered after ischemic injury in murine kidneys |
| Q35609851 | Regulation of blood pressure and salt homeostasis by endothelin |
| Q35436920 | Regulation of glomerulotubular balance. III. Implication of cytosolic calcium in flow-dependent proximal tubule transport |
| Q39167400 | Regulation of glomerulotubular balance: flow-activated proximal tubule function |
| Q37400584 | Renal involvement in tuberous sclerosis complex and von Hippel-Lindau disease: shared disease mechanisms? |
| Q26865487 | Renal urinary shear stress: a novel actor in nephropathies |
| Q42483833 | Respiration rate in human primary renal proximal and early distal tubular cells in vitro: considerations for biohybrid renal devices |
| Q37104802 | Role of mechanical stress in regulating airway surface hydration and mucus clearance rates |
| Q85887537 | Safety study of somatostatin analogue octreotide for autosomal dominant polycystic kidney disease in Japan |
| Q35128154 | Screening analysis of candidate gene mutations in a kindred with polycystic liver disease |
| Q90010767 | Sensing of tubular flow and renal electrolyte transport |
| Q39426442 | Shear stress reverses dome formation in confluent renal tubular cells. |
| Q28505979 | Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice |
| Q37636551 | Small tubules, surprising discoveries: from efferent ductules in the turkey to the discovery that estrogen receptor alpha is essential for fertility in the male |
| Q36295665 | Soluble mediators, not cilia, determine airway surface liquid volume in normal and cystic fibrosis superficial airway epithelia |
| Q35845360 | Stem cells and fluid flow drive cyst formation in an invertebrate excretory organ |
| Q81261836 | Stress models for the study of intermediate filament function |
| Q33809680 | Structural and functional analyses of liver cysts from the BALB/c-cpk mouse model of polycystic kidney disease |
| Q36948959 | Syntaxin 5 regulates the endoplasmic reticulum channel-release properties of polycystin-2. |
| Q37053614 | TRP channels and mechanosensory transduction: insights into the arterial myogenic response. |
| Q36491758 | The Caenorhabditis elegans nephrocystins act as global modifiers of cilium structure |
| Q47833552 | The N-terminal extracellular domain is required for polycystin-1-dependent channel activity |
| Q37052472 | The cell biological basis of ciliary disease |
| Q38969488 | The growth plate's response to load is partially mediated by mechano-sensing via the chondrocytic primary cilium |
| Q49207704 | The mechanosensitive BKα/β1 channel localizes to cilia of principal cells in rabbit cortical collecting duct (CCD). |
| Q29615254 | The primary cilium as a complex signaling center |
| 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 |
| Q30480543 | The von Hippel-Lindau tumor suppressor protein controls ciliogenesis by orienting microtubule growth |
| Q38173179 | Tissue-engineered kidney disease models |
| Q30420687 | Transport and localization of signaling proteins in ciliated cells |
| Q46959770 | Type III adenylyl cyclase localizes to primary cilia throughout the adult mouse brain |
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