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Modeling congenital kidney diseases in Xenopus laevis. , Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
Leukemia inhibitory factor signaling in Xenopus embryo: Insights from gain of function analysis and dominant negative mutant of the receptor. , Jalvy S., Dev Biol. March 15, 2019; 447 (2): 200-213.
Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development. , Yan B ., Dev Dyn. February 1, 2015; 244 (2): 181-210.
Targeting kidney CLC-K channels: pharmacological profile in a human cell line versus Xenopus oocytes. , Imbrici P., Biochim Biophys Acta. October 1, 2014; 1838 (10): 2484-91.
A cytoplasmic domain mutation in ClC-Kb affects long-distance communication across the membrane. , Martinez GQ., PLoS One. July 23, 2008; 3 (7): e2746.
Organization of the pronephric kidney revealed by large-scale gene expression mapping. , Raciti D ., Genome Biol. January 1, 2008; 9 (5): R84.
Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros. , Tran U ., Dev Biol. July 1, 2007; 307 (1): 152-64.
Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development. , Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.
Cloning and characterisation of amphibian ClC-3 and ClC-5 chloride channels. , Schmieder S., Biochim Biophys Acta. November 13, 2002; 1566 (1-2): 55-66.