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Summary Expression Phenotypes Gene Literature (31) GO Terms (3) Nucleotides (51) Proteins (32) Interactants (180) Wiki
XB--483408

Papers associated with pkd1



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The cytoplasmic C-terminal fragment of polycystin-1 regulates a Ca2+-permeable cation channel., Vandorpe DH, Chernova MN, Jiang L, Sellin LK, Wilhelm S, Stuart-Tilley AK, Walz G, Alper SL., J Biol Chem. February 9, 2001; 276 (6): 4093-101.

Transport function of the naturally occurring pathogenic polycystin-2 mutant, R742X., Chen XZ, Segal Y, Basora N, Guo L, Peng JB, Babakhanlou H, Vassilev PM, Brown EM, Hediger MA, Zhou J., Biochem Biophys Res Commun. April 20, 2001; 282 (5): 1251-6.

Cation channel regulation by COOH-terminal cytoplasmic tail of polycystin-1: mutational and functional analysis., Vandorpe DH, Wilhelm S, Jiang L, Ibraghimov-Beskrovnaya O, Chernova MN, Stuart-Tilley AK, Alper SL., Physiol Genomics. February 28, 2002; 8 (2): 87-98.

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

Cloning and expression of the amphibian homologue of the human PKD1 gene., Burtey S, Leclerc C, Nabais E, Munch P, Gohory C, Moreau M, Fontés M., Gene. August 29, 2005; 357 (1): 29-36.          

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

Polycystic kidney disease and receptor for egg jelly is a plasma membrane protein of mouse sperm head., Butscheid Y, Chubanov V, Steger K, Meyer D, Dietrich A, Gudermann T., Mol Reprod Dev. March 1, 2006; 73 (3): 350-60.

Structural and molecular basis of the assembly of the TRPP2/PKD1 complex., Yu Y, Ulbrich MH, Li MH, Buraei Z, Chen XZ, Ong AC, Tong L, Isacoff EY, Yang J., Proc Natl Acad Sci U S A. July 14, 2009; 106 (28): 11558-63.

Polycystin-1 interacts with inositol 1,4,5-trisphosphate receptor to modulate intracellular Ca2+ signaling with implications for polycystic kidney disease., Li Y, Santoso NG, Yu S, Yu S, Woodward OM, Qian F, Guggino WB., J Biol Chem. December 25, 2009; 284 (52): 36431-36441.

The RNA-binding protein bicaudal C regulates polycystin 2 in the kidney by antagonizing miR-17 activity., Tran U, Zakin L, Schweickert A, Agrawal R, Döger R, Blum M, De Robertis EM, Wessely O., Development. April 1, 2010; 137 (7): 1107-16.              

Identification of a polycystin-1 cleavage product, P100, that regulates store operated Ca entry through interactions with STIM1., Woodward OM, Li Y, Yu S, Yu S, Greenwell P, Wodarczyk C, Boletta A, Guggino WB, Qian F., PLoS One. August 23, 2010; 5 (8): e12305.              

Hyperphosphorylation of polycystin-2 at a critical residue in disease reveals an essential role for polycystin-1-regulated dephosphorylation., Streets AJ, Wessely O, Peters DJ, Ong AC., Hum Mol Genet. May 15, 2013; 22 (10): 1924-39.

Activation of ADF/cofilin by phosphorylation-regulated Slingshot phosphatase is required for the meiotic spindle assembly in Xenopus laevis oocytes., Iwase S, Sato R, De Bock PJ, Gevaert K, Fujiki S, Tawada T, Kuchitsu M, Yamagishi Y, Ono S, Abe H., Mol Biol Cell. June 1, 2013; 24 (12): 1933-46.            

A novel PKD2L1 C-terminal domain critical for trimerization and channel function., Zheng W, Hussein S, Yang J, Huang J, Zhang F, Hernandez-Anzaldo S, Fernandez-Patron C, Cao Y, Cao Y, Zeng H, Tang J, Chen XZ., Sci Rep. January 12, 2015; 5 9460.              

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

The polycystin complex mediates Wnt/Ca(2+) signalling., Kim S, Nie H, Nesin V, Tran U, Outeda P, Bai CX, Keeling J, Maskey D, Watnick T, Wessely O, Tsiokas L., Nat Cell Biol. July 1, 2016; 18 (7): 752-764.              

The Sorting Nexin 3 Retromer Pathway Regulates the Cell Surface Localization and Activity of a Wnt-Activated Polycystin Channel Complex., Feng S, Streets AJ, Nesin V, Tran U, Nie H, Onopiuk M, Wessely O, Tsiokas L, Ong ACM., J Am Soc Nephrol. October 1, 2017; 28 (10): 2973-2984.

Direct Binding between Pre-S1 and TRP-like Domains in TRPP Channels Mediates Gating and Functional Regulation by PIP2., Zheng W, Cai R, Hofmann L, Nesin V, Hu Q, Long W, Fatehi M, Liu X, Hussein S, Kong T, Li J, Light PE, Tang J, Flockerzi V, Tsiokas L, Chen XZ., Cell Rep. February 6, 2018; 22 (6): 1560-1573.          

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

Hydrophobic pore gates regulate ion permeation in polycystic kidney disease 2 and 2L1 channels., Zheng W, Yang X, Hu R, Cai R, Hofmann L, Wang Z, Hu Q, Liu X, Bulkley D, Yu Y, Tang J, Flockerzi V, Cao Y, Cao E, Chen XZ., Nat Commun. June 13, 2018; 9 (1): 2302.            

Characterization of potential TRPP2 regulating proteins in early Xenopus embryos., Futel M, Le Bouffant R, Buisson I, Umbhauer M, Riou JF., J Cell Biochem. December 1, 2018; 119 (12): 10338-10350.  

Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM, Miller RK., Dis Model Mech. April 9, 2019; 12 (4):       

A PKD1L3 splice variant in taste buds is not cleaved at the G protein-coupled receptor proteolytic site., Kashyap P, Ng C, Wang Z, Li B, Arif Pavel M, Martin H, Yu Y., Biochem Biophys Res Commun. May 14, 2019; 512 (4): 812-818.            

The ion channel function of polycystin-1 in the polycystin-1/polycystin-2 complex., Wang Z, Ng C, Liu X, Wang Y, Li B, Kashyap P, Chaudhry HA, Castro A, Kalontar EM, Ilyayev L, Walker R, Alexander RT, Qian F, Chen XZ, Yu Y., EMBO Rep. November 5, 2019; 20 (11): e48336.                            

Maximizing CRISPR/Cas9 phenotype penetrance applying predictive modeling of editing outcomes in Xenopus and zebrafish embryos., Naert T, Tulkens D, Edwards NA, Carron M, Shaidani NI, Wlizla M, Boel A, Demuynck S, Horb ME, Coucke P, Willaert A, Zorn AM, Vleminckx K, Vleminckx K., Sci Rep. September 4, 2020; 10 (1): 14662.                      

Aquatic models of human ciliary diseases., Corkins ME, Krneta-Stankic V, Kloc M, Miller RK., Genesis. February 1, 2021; 59 (1-2): e23410.          

Protein kinase D1 variant associated with human epilepsy and peripheral nerve hypermyelination., Omer S, Jin SC, Koumangoye R, Robert SM, Duran D, Nelson-Williams C, Huttner A, DiLuna M, Kahle KT, Delpire E., Clin Genet. August 1, 2021; 100 (2): 176-186.

A polycystin-2 protein with modified channel properties leads to an increased diameter of renal tubules and to renal cysts., Grosch M, Brunner K, Ilyaskin AV, Schober M, Staudner T, Schmied D, Stumpp T, Schmidt KN, Madej MG, Pessoa TD, Othmen H, Kubitza M, Osten L, de Vries U, Mair MM, Somlo S, Moser M, Kunzelmann K, Ziegler C, Haerteis S, Korbmacher C, Witzgall R., J Cell Sci. August 15, 2021; 134 (16):                 

Deep learning is widely applicable to phenotyping embryonic development and disease., Naert T, Çiçek Ö, Ogar P, Bürgi M, Shaidani NI, Kaminski MM, Xu Y, Grand K, Vujanovic M, Prata D, Hildebrandt F, Brox T, Ronneberger O, Voigt FF, Helmchen F, Loffing J, Horb ME, Willsey HR, Lienkamp SS., Development. November 1, 2021; 148 (21):                                                                 

Regulation of PKD2 channel function by TACAN., Liu X, Zhang R, Fatehi M, Wang Y, Long W, Tian R, Deng X, Weng Z, Xu Q, Light PE, Tang J, Chen XZ., J Physiol. January 1, 2023; 601 (1): 83-98.

The diverse effects of pathogenic point mutations on ion channel activity of a gain-of-function polycystin-2., Wang Y, Wang Z, Pavel MA, Ng C, Kashyap P, Li B, Morais TDC, Ulloa GA, Yu Y., J Biol Chem. May 1, 2023; 299 (5): 104674.

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