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	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	Ca(2+)-BK channel clusters in olfactory receptor neurons and their role in odour coding., Bao G., Eur J Neurosci. December 1, 2015; 42 (11): 2985-95.
	pdzrn3 is required for pronephros morphogenesis in Xenopus laevis., Marracci S., Int J Dev Biol. January 1, 2016; 60 (1-3): 57-63.
	Proper Notch activity is necessary for the establishment of proximal cells and differentiation of intermediate, distal, and connecting tubule in Xenopus pronephros development., Katada T., Dev Dyn. April 1, 2016; 245 (4): 472-82.
	Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome., Braun DA., Nat Genet. April 1, 2016; 48 (4): 457-65.
	Technique to Target Microinjection to the Developing Xenopus Kidney., DeLay BD., J Vis Exp. May 3, 2016; (111):
	Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.
	Evolution of the hypoxia-sensitive cells involved in amniote respiratory reflexes., Hockman D., Elife. April 7, 2017; 6
	Sensing oxygen inside and out., Stupnikov MR., Elife. May 19, 2017; 6
	Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome., Braun DA., J Clin Invest. October 1, 2018; 128 (10): 4313-4328.
	Dynamin Binding Protein Is Required for Xenopus laevis Kidney Development., DeLay BD., Front Physiol. January 1, 2019; 10 143.
	Comparative Embryonic Spatio-Temporal Expression Profile Map of the Xenopus P2X Receptor Family., Blanchard C., Front Cell Neurosci. January 1, 2019; 13 340.
	Arid3a regulates nephric tubule regeneration via evolutionarily conserved regeneration signal-response enhancers., Suzuki N., Elife. January 8, 2019; 8
	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.
	Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
	DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation., Schneider R., Am J Hum Genet. December 3, 2020; 107 (6): 1113-1128.
	Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome., Mann N., J Am Soc Nephrol. March 1, 2021; 32 (3): 580-596.
	The enpp4 ectonucleotidase regulates kidney patterning signalling networks in Xenopus embryos., Massé K., Commun Biol. October 7, 2021; 4 (1): 1158.
	A comparative study of cellular diversity between the Xenopus pronephric and mouse metanephric nephron., Corkins ME., Kidney Int. January 1, 2023; 103 (1): 77-86.
	Ocular microvasculature in adult Xenopus laevis: Scanning electron microscopy of vascular casts., Lametschwandtner A., J Morphol. March 1, 2023; 284 (3): e21561.
	Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., bioRxiv. April 16, 2023;
	Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.

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