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Summary Expression Phenotypes Gene Literature (5) GO Terms (4) Nucleotides (133) Proteins (40) Interactants (49) Wiki
XB--5910468

Papers associated with c21orf59



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In Xenopus ependymal cilia drive embryonic CSF circulation and brain development independently of cardiac pulsatile forces., Dur AH, Tang T, Viviano S, Sekuri A, Willsey HR, Tagare HD, Kahle KT, Deniz E., Fluids Barriers CNS. December 11, 2020; 17 (1): 72.                  

Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus., Date P, Ackermann P, Furey C, Fink IB, Jonas S, Khokha MK, Kahle KT, Deniz E., Sci Rep. April 17, 2019; 9 (1): 6196.                            

c21orf59/kurly Controls Both Cilia Motility and Polarization., Jaffe KM, Grimes DT, Schottenfeld-Roames J, Werner ME, Ku TS, Kim SK, Pelliccia JL, Morante NF, Mitchell BJ, Burdine RD., Cell Rep. March 1, 2016; 14 (8): 1841-9.                  

Quercetin activates human Kv1.5 channels by a residue I502 in the S6 segment., Yang L, Ma JH, Zhang PH, Zou AR, Tu DN., Clin Exp Pharmacol Physiol. February 1, 2009; 36 (2): 154-61.

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.

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