???pagination.result.count???
???pagination.result.page???
1
Cilia are required for asymmetric nodal induction in the sea urchin embryo. , Tisler M, Wetzel F, Mantino S, Kremnyov S, Thumberger T, Schweickert A, Blum M, Vick P., BMC Dev Biol. August 23, 2016; 16 (1): 28.
Oligomerization of the polycystin-2 C-terminal tail and effects on its Ca2+-binding properties. , Yang Y, Keeler C, Kuo IY, Lolis EJ, Ehrlich BE, Hodsdon ME., J Biol Chem. April 17, 2015; 290 (16): 10544-54.
The number and location of EF hand motifs dictates the calcium dependence of polycystin-2 function. , Kuo IY, Keeler C, Corbin R, Ćelić A, Petri ET, Hodsdon ME, Ehrlich BE., FASEB J. May 1, 2014; 28 (5): 2332-46.
Positive selection in the carbohydrate recognition domains of sea urchin sperm receptor for egg jelly (suREJ) proteins. , Mah SA, Swanson WJ, Vacquier VD ., Mol Biol Evol. March 1, 2005; 22 (3): 533-41.
Polycystins: what polycystic kidney disease tells us about sperm. , Kierszenbaum AL., Mol Reprod Dev. April 1, 2004; 67 (4): 385-8.
Polycystin-2 associates with the polycystin-1 homolog, suREJ3, and localizes to the acrosomal region of sea urchin spermatozoa. , Neill AT, Moy GW, Vacquier VD ., Mol Reprod Dev. April 1, 2004; 67 (4): 472-7.
The pathogenesis of autosomal dominant polycystic kidney disease: an update. , Somlo S, Markowitz GS., Curr Opin Nephrol Hypertens. July 1, 2000; 9 (4): 385-94.
Comparative analysis of the polycystic kidney disease 1 (PKD1) gene reveals an integral membrane glycoprotein with multiple evolutionary conserved domains. , Sandford R, Sgotto B, Aparicio S, Brenner S, Vaudin M, Wilson RK, Chissoe S, Pepin K, Bateman A, Chothia C, Hughes J, Harris P., Hum Mol Genet. September 1, 1997; 6 (9): 1483-9.