Papers associated with urogenital system (and pax2)

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	no privacy, a Xenopus tropicalis mutant, is a model of human Hermansky-Pudlak Syndrome and allows visualization of internal organogenesis during tadpole development., Nakayama T., Dev Biol. June 15, 2017; 426 (2): 472-486.
	Bim gene dosage is critical in modulating nephron progenitor survival in the absence of microRNAs during kidney development., Cerqueira DM., FASEB J. August 1, 2017; 31 (8): 3540-3554.
	lrpap1 as a specific marker of proximal pronephric kidney tubuli in Xenopus laevis embryos., Neuhaus H., Int J Dev Biol. January 1, 2018; 62 (4-5): 319-324.
	Dynamin Binding Protein Is Required for Xenopus laevis Kidney Development., DeLay BD., Front Physiol. January 1, 2019; 10 143.
	Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
	Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):
	Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease., Coppenrath K., Genesis. December 1, 2021; 59 (12): e23453.
	Comparative anatomy on the development of sperm transporting pathway between the testis and mesonephros., Omotehara T., Histochem Cell Biol. March 1, 2022; 157 (3): 321-332.
	Appropriate Amounts and Activity of the Wilms' Tumor Suppressor Gene, wt1, Are Required for Normal Pronephros Development of Xenopus Embryos., Shiraki T., J Dev Biol. October 29, 2022; 10 (4):
	Hnf1b renal expression directed by a distal enhancer responsive to Pax8., Goea L., Sci Rep. November 19, 2022; 12 (1): 19921.
	Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates., Baxi AB., iScience. September 15, 2023; 26 (9): 107665.
	Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
	Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
	Prdm15 acts upstream of Wnt4 signaling in anterior neural development of Xenopus laevis., Saumweber E., Front Cell Dev Biol. January 1, 2024; 12 1316048.

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