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Summary Anatomy Item Literature (1104) Expression Attributions Wiki
XB-ANAT-112

Papers associated with artery (and pkd2)

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

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.                      

TRPP2 channels regulate apoptosis through the Ca2+ concentration in the endoplasmic reticulum., Wegierski T., EMBO J. March 4, 2009; 28 (5): 490-9.

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.

Evolutionary conservation of Drosophila polycystin-2 as a calcium-activated cation channel., Venglarik CJ., J Am Soc Nephrol. May 1, 2004; 15 (5): 1168-77.

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.

Polycystin-2 interacts with troponin I, an angiogenesis inhibitor., Li Q., Biochemistry. January 21, 2003; 42 (2): 450-7.

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

Differences between the catalytic properties of recombinant human PC2 and endogenous rat PC2., Bailyes EM., Biochem J. July 15, 1995; 309 ( Pt 2) 587-94.

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