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Summary Anatomy Item Literature (472) Expression Attributions Wiki
XB-ANAT-3725

Papers associated with ciliated cell (and pkd2)

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Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates., Szenker-Ravi E., Nat Genet. January 1, 2022; 54 (1): 62-72.


Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5., Maerker M., Nat Commun. September 16, 2021; 12 (1): 5482.                              


A polycystin-2 protein with modified channel properties leads to an increased diameter of renal tubules and to renal cysts., Grosch M., J Cell Sci. August 15, 2021; 134 (16):                 


Aquatic models of human ciliary diseases., Corkins ME., Genesis. February 1, 2021; 59 (1-2): e23410.          


The ion channel function of polycystin-1 in the polycystin-1/polycystin-2 complex., Wang Z., EMBO Rep. November 5, 2019; 20 (11): e48336.                            


Mechanical strain, novel genes and evolutionary insights: news from the frog left-right organizer., Blum M., Curr Opin Genet Dev. June 1, 2019; 56 8-14.      


A PKD1L3 splice variant in taste buds is not cleaved at the G protein-coupled receptor proteolytic site., Kashyap P., Biochem Biophys Res Commun. May 14, 2019; 512 (4): 812-818.            


A dual function of FGF signaling in Xenopus left-right axis formation., Schneider I., Development. May 10, 2019; 146 (9):                               


Characterization of potential TRPP2 regulating proteins in early Xenopus embryos., Futel M., J Cell Biochem. December 1, 2018; 119 (12): 10338-10350.  


An Early Function of Polycystin-2 for Left-Right Organizer Induction in Xenopus., Vick P., iScience. April 27, 2018; 2 76-85.                                        


TRPP2-dependent Ca2+ signaling in dorso-lateral mesoderm is required for kidney field establishment in Xenopus., Futel M., J Cell Sci. March 1, 2015; 128 (5): 888-99.                      


The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality., Boskovski MT., Nature. December 19, 2013; 504 (7480): 456-9.    


Left-right asymmetry: lessons from Cancún., Burdine RD., Development. November 1, 2013; 140 (22): 4465-70.    


Polycystin-2 activity is controlled by transcriptional coactivator with PDZ binding motif and PALS1-associated tight junction protein., Duning K., J Biol Chem. October 29, 2010; 285 (44): 33584-8.


The RNA-binding protein bicaudal C regulates polycystin 2 in the kidney by antagonizing miR-17 activity., Tran U., Development. April 1, 2010; 137 (7): 1107-16.              


Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants., Sullivan-Brown J., Dev Biol. February 15, 2008; 314 (2): 261-75.


Cilia-driven leftward flow determines laterality in Xenopus., Schweickert A., Curr Biol. January 9, 2007; 17 (1): 60-6.        


Polycystin 2 interacts with type I inositol 1,4,5-trisphosphate receptor to modulate intracellular Ca2+ signaling., Li Y., J Biol Chem. December 16, 2005; 280 (50): 41298-306.


Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer's vesicle are required for specification of the zebrafish left-right axis., Bisgrove BW., Dev Biol. November 15, 2005; 287 (2): 274-88.


Localization and loss-of-function implicates ciliary proteins in early, cytoplasmic roles in left-right asymmetry., Qiu D., Dev Dyn. September 1, 2005; 234 (1): 176-89.      


Xenopus TRPN1 (NOMPC) localizes to microtubule-based cilia in epithelial cells, including inner-ear hair cells., Shin JB., Proc Natl Acad Sci U S A. August 30, 2005; 102 (35): 12572-7.              


A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney., Sun Z., Development. August 1, 2004; 131 (16): 4085-93.


Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization., Cano DA., Development. July 1, 2004; 131 (14): 3457-67.


Native polycystin 2 functions as a plasma membrane Ca2+-permeable cation channel in renal epithelia., Luo Y., Mol Cell Biol. April 1, 2003; 23 (7): 2600-7.

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