Papers associated with pkd2Search for pkd2 morpholinos using Textpresso
Results 1 - 20 of 55 results
|Sort Newest To Oldest||Sort Oldest To Newest|
|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. January 1, 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, 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.
|Using Xenopus to study genetic kidney diseases.
Semin Cell Dev Biol. March 1, 2016; 51 117-24.
|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. January 1, 2016; 18 (7): 752-764.
|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.
|Hepatocystin is Essential for TRPM7 Function During Early Embryogenesis.
Overton JD, Komiya Y, Mezzacappa C, Nama K, Cai N, Lou L, Fedeles SV, Habas R, Runnels LW.
Sci Rep. September 21, 2015; 5 18395.
|TRPP2-dependent Ca2+ signaling in dorso-lateral mesoderm is required for kidney field establishment in Xenopus.
Futel M, Leclerc C, Le Bouffant R, Buisson I, Néant I, Umbhauer M, Moreau M, Riou JF.
J Cell Sci. March 1, 2015; 128 (5): 888-99.
|The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality.
Boskovski MT, Yuan S, Pedersen NB, Goth CK, Makova S, Clausen H, Brueckner M, Khokha MK.
Nature. December 19, 2013; 504 (7480): 456-9.
|Left-right asymmetry: lessons from Cancún.
Burdine RD, Caspary T.
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, Wessely O, Peters DJ, Ong AC.
Hum Mol Genet. May 15, 2013; 22 (10): 1924-39.
|Angiogenesis in the intermediate lobe of the pituitary gland alters its structure and function.
Tanaka S, Nakakura T, Jansen EJ, Unno K, Okada R, Suzuki M, Martens GJ, Kikuyama S.
Gen Comp Endocrinol. May 1, 2013; 185 10-8.
|Molecular mechanism of the assembly of an acid-sensing receptor ion channel complex.
Yu Y, Ulbrich MH, Li MH, Dobbins S, Zhang WK, Tong L, Isacoff EY, Yang J.
Nat Commun. March 13, 2012; 3 1252.
|α-TC1.9 cells--a model system for analyzing the endoproteolytic processing of POMC.
Chen Q, Layton K, Veo K, Angleson JK, Dores RM.
Gen Comp Endocrinol. May 15, 2011; 172 (1): 96-106.
|Polycystin-2 activity is controlled by transcriptional coactivator with PDZ binding motif and PALS1-associated tight junction protein.
Duning K, Rosenbusch D, Schlüter MA, Tian Y, Kunzelmann K, Meyer N, Schulze U, Markoff A, Pavenstädt H, Weide T.
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, Li Y, Yu S, Yu S, Greenwell P, Wodarczyk C, Boletta A, Guggino WB, Qian F.
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, Zakin L, Schweickert A, Agrawal R, Döger R, Blum M, De Robertis EM, Wessely O.
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, Santoso NG, Yu S, Yu S, Woodward OM, Qian F, Guggino WB.
J Biol Chem. December 25, 2009; 284 (52): 36431-41.
|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.
|TRPP2 channels regulate apoptosis through the Ca2+ concentration in the endoplasmic reticulum.
Wegierski T, Steffl D, Kopp C, Tauber R, Buchholz B, Nitschke R, Kuehn EW, Walz G, Köttgen M.
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, Schottenfeld J, Okabe N, Hostetter CL, Serluca FC, Thiberge SY, Burdine RD.
Dev Biol. February 15, 2008; 314 (2): 261-75.