Papers associated with distal (and mip)

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	Specialized stellate cells offer a privileged route for rapid water flux in Drosophila renal tubule., Cabrero P., Proc Natl Acad Sci U S A. January 21, 2020; 117 (3): 1779-1787.
	Vasotocin/V2-type receptor/aquaporin axis exists in African lungfish kidney but is functional only in terrestrial condition., Konno N., Endocrinology. March 1, 2010; 151 (3): 1089-96.
	Functional characterization of a human aquaporin 0 mutation that leads to a congenital dominant lens cataract., Varadaraj K., Exp Eye Res. July 1, 2008; 87 (1): 9-21.
	Aquaporin-11: a channel protein lacking apparent transport function expressed in brain., Gorelick DA., BMC Biochem. May 1, 2006; 7 14.
	Role of C-terminal domain and transmembrane helices 5 and 6 in function and quaternary structure of major intrinsic proteins: analysis of aquaporin/glycerol facilitator chimeric proteins., Duchesne L., J Biol Chem. June 7, 2002; 277 (23): 20598-604.
	A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice., Sidjanin DJ., Genomics. June 15, 2001; 74 (3): 313-9.
	Identification of a new water channel (Rp-MIP) in the Malpighian tubules of the insect Rhodnius prolixus., Echevarría M., Pflugers Arch. April 1, 2001; 442 (1): 27-34.
	Transmembrane helix 5 is critical for the high water permeability of aquaporin., Kuwahara M., Biochemistry. December 7, 1999; 38 (49): 16340-6.
	The human Aquaporin-5 gene. Molecular characterization and chromosomal localization., Lee MD., J Biol Chem. April 12, 1996; 271 (15): 8599-604.

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