Papers associated with cell part (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.
	Comparative gene expression profiling between optic nerve and spinal cord injury in Xenopus laevis reveals a core set of genes inherent in successful regeneration of vertebrate central nervous system axons., Belrose JL., BMC Genomics. August 5, 2020; 21 (1): 540.
	Trpc1 as the Missing Link Between the Bmp and Ca2+ Signalling Pathways During Neural Specification in Amphibians., Néant I., Sci Rep. November 5, 2019; 9 (1): 16049.
	The ion channel function of polycystin-1 in the polycystin-1/polycystin-2 complex., Wang Z., EMBO Rep. November 5, 2019; 20 (11): e48336.
	Maternal pluripotency factors initiate extensive chromatin remodelling to predefine first response to inductive signals., Gentsch GE., Nat Commun. September 19, 2019; 10 (1): 4269.
	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.
	Premotor Neuron Divergence Reflects Vocal Evolution., Barkan CL., J Neurosci. June 6, 2018; 38 (23): 5325-5337.
	An Early Function of Polycystin-2 for Left-Right Organizer Induction in Xenopus., Vick P., iScience. April 27, 2018; 2 76-85.
	The Sorting Nexin 3 Retromer Pathway Regulates the Cell Surface Localization and Activity of a Wnt-Activated Polycystin Channel Complex., Feng S., J Am Soc Nephrol. October 1, 2017; 28 (10): 2973-2984.
	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.
	Hyperphosphorylation of polycystin-2 at a critical residue in disease reveals an essential role for polycystin-1-regulated dephosphorylation., Streets AJ., Hum Mol Genet. May 15, 2013; 22 (10): 1924-39.
	Molecular mechanism of the assembly of an acid-sensing receptor ion channel complex., Yu Y., Nat Commun. January 1, 2012; 3 1252.
	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.
	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.
	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.
	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.
	Structural and molecular basis of the assembly of the TRPP2/PKD1 complex., Yu Y., Proc Natl Acad Sci U S A. July 14, 2009; 106 (28): 11558-63.
	TRPP2 channels regulate apoptosis through the Ca2+ concentration in the endoplasmic reticulum., Wegierski T., EMBO J. March 4, 2009; 28 (5): 490-9.
	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.
	Polycystic kidney disease and receptor for egg jelly is a plasma membrane protein of mouse sperm head., Butscheid Y., Mol Reprod Dev. March 1, 2006; 73 (3): 350-60.
	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.
	Polycystin-2 associates with tropomyosin-1, an actin microfilament component., Li Q., J Mol Biol. January 31, 2003; 325 (5): 949-62.
	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.
	Polycystin-2 is a novel cation channel implicated in defective intracellular Ca(2+) homeostasis in polycystic kidney disease., Vassilev PM., Biochem Biophys Res Commun. March 23, 2001; 282 (1): 341-50.
	Differences in pH optima and calcium requirements for maturation of the prohormone convertases PC2 and PC3 indicates different intracellular locations for these events., Shennan KI., J Biol Chem. January 20, 1995; 270 (3): 1402-7.
	Autocatalytic maturation of the prohormone convertase PC2., Matthews G., J Biol Chem. January 7, 1994; 269 (1): 588-92.

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