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Summary Anatomy Item Literature (3673) Expression Attributions Wiki
XB-ANAT-490

Papers associated with tail (and pkd1)

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The diverse effects of pathogenic point mutations on ion channel activity of a gain-of-function polycystin-2., Wang Y., J Biol Chem. May 1, 2023; 299 (5): 104674.


Regulation of PKD2 channel function by TACAN., Liu X., J Physiol. January 1, 2023; 601 (1): 83-98.


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):                 


Hydrophobic pore gates regulate ion permeation in polycystic kidney disease 2 and 2L1 channels., Zheng W., Nat Commun. June 13, 2018; 9 (1): 2302.            


Polycystin 1 loss of function is directly linked to an imbalance in G-protein signaling in the kidney., Zhang B., Development. March 22, 2018; 145 (6):                         


Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease., Stiburkova B., Am J Med Sci. October 1, 2015; 350 (4): 268-71.


Activation of ADF/cofilin by phosphorylation-regulated Slingshot phosphatase is required for the meiotic spindle assembly in Xenopus laevis oocytes., Iwase S., Mol Biol Cell. June 1, 2013; 24 (12): 1933-46.            


Identification of a polycystin-1 cleavage product, P100, that regulates store operated Ca entry through interactions with STIM1., Woodward OM., PLoS One. August 23, 2010; 5 (8): e12305.              


Polycystin-1 interacts with inositol 1,4,5-trisphosphate receptor to modulate intracellular Ca2+ signaling with implications for polycystic kidney disease., Li Y., J Biol Chem. December 25, 2009; 284 (52): 36431-36441.


Expression of the polycystin-1 C-terminal cytoplasmic tail increases Cl channel activity in Xenopus oocytes., Chernova MN., Kidney Int. August 1, 2005; 68 (2): 632-41.


Cation channel regulation by COOH-terminal cytoplasmic tail of polycystin-1: mutational and functional analysis., Vandorpe DH., Physiol Genomics. February 28, 2002; 8 (2): 87-98.


Transport function of the naturally occurring pathogenic polycystin-2 mutant, R742X., Chen XZ., Biochem Biophys Res Commun. April 20, 2001; 282 (5): 1251-6.


The cytoplasmic C-terminal fragment of polycystin-1 regulates a Ca2+-permeable cation channel., Vandorpe DH., J Biol Chem. February 9, 2001; 276 (6): 4093-101.

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