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Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation. , Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
Modeling congenital kidney diseases in Xenopus laevis. , Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development. , Buisson I ., Dev Biol. January 15, 2015; 397 (2): 175-90.
Specification of ion transport cells in the Xenopus larval skin. , Quigley IK ., Development. February 1, 2011; 138 (4): 705-14.
Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome. , Yu Y., Clin Genet. February 1, 2010; 77 (2): 155-62.
Organization of the pronephric kidney revealed by large-scale gene expression mapping. , Raciti D ., Genome Biol. January 1, 2008; 9 (5): R84.
Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholds. , Frey A., Hear Res. April 1, 2006; 214 (1-2): 68-75.
Activating mutation of the renal epithelial chloride channel ClC-Kb predisposing to hypertension. , Jeck N., Hypertension. June 1, 2004; 43 (6): 1175-81.
A common sequence variation of the CLCNKB gene strongly activates ClC-Kb chloride channel activity. , Jeck N., Kidney Int. January 1, 2004; 65 (1): 190-7.
Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney. , Saulnier DM., Dev Biol. August 1, 2002; 248 (1): 13-28.