Papers associated with embryo (and mip)

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	TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):
	Polyploidization and pseudogenization in allotetraploid frog Xenopus laevis promote the evolution of aquaporin family in higher vertebrates., Jia Y., BMC Genomics. July 29, 2020; 21 (1): 525.
	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.
	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.
	In vivo analysis of aquaporin 0 function in zebrafish: permeability regulation is required for lens transparency., Clemens DM., Invest Ophthalmol Vis Sci. July 30, 2013; 54 (7): 5136-43.
	Aquaporin-11: a channel protein lacking apparent transport function expressed in brain., Gorelick DA., BMC Biochem. May 1, 2006; 7 14.
	Functional impairment of lens aquaporin in two families with dominantly inherited cataracts., Francis P., Hum Mol Genet. September 22, 2000; 9 (15): 2329-34.
	Cloning of a novel water and urea-permeable aquaporin from mouse expressed strongly in colon, placenta, liver, and heart., Ma T., Biochem Biophys Res Commun. November 17, 1997; 240 (2): 324-8.
	Incorporation of proteins into (Xenopus) oocytes by proteoliposome microinjection: functional characterization of a novel aquaporin., Le Cahérec F., J Cell Sci. June 1, 1996; 109 ( Pt 6) 1285-95.

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