Papers associated with kidney (and pkd1)

Limit to papers also referencing gene:
Show all kidney papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	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.
	Deep learning is widely applicable to phenotyping embryonic development and disease., Naert T., Development. November 1, 2021; 148 (21):
	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.
	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.
	Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
	Characterization of potential TRPP2 regulating proteins in early Xenopus embryos., Futel M., J Cell Biochem. December 1, 2018; 119 (12): 10338-10350.
	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):
	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.
	The polycystin complex mediates Wnt/Ca(2+) signalling., Kim S., Nat Cell Biol. July 1, 2016; 18 (7): 752-764.
	Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease., Stiburkova B., Am J Med Sci. October 1, 2015; 350 (4): 268-71.
	A novel PKD2L1 C-terminal domain critical for trimerization and channel function., Zheng W., Sci Rep. January 12, 2015; 5 9460.
	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.
	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.
	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.
	Cloning and expression of the amphibian homologue of the human PKD1 gene., Burtey S., Gene. August 29, 2005; 357 (1): 29-36.
	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.

???pagination.result.page??? 1