Papers associated with embryonic structure (and mip)

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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.
	The pH sensitivity of Aqp0 channels in tetraploid and diploid teleosts., Chauvigné F., FASEB J. May 1, 2015; 29 (5): 2172-84.
	Bi-functionality of Opisthorchis viverrini aquaporins., Geadkaew A., Biochimie. January 1, 2015; 108 149-59.
	Intact and N- or C-terminal end truncated AQP0 function as open water channels and cell-to-cell adhesion proteins: end truncation could be a prelude for adjusting the refractive index of the lens to prevent spherical aberration., Sindhu Kumari S., Biochim Biophys Acta. September 1, 2014; 1840 (9): 2862-77.
	Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion., Kumari SS., Exp Eye Res. November 1, 2013; 116 371-85.
	The water permeability of lens aquaporin-0 depends on its lipid bilayer environment., Tong J., Exp Eye Res. August 1, 2013; 113 32-40.
	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.
	An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract., Senthil Kumar G., Exp Eye Res. May 1, 2013; 110 136-41.
	Regulation of AQP0 water permeability is enhanced by cooperativity., Németh-Cahalan KL., J Gen Physiol. March 1, 2013; 141 (3): 287-95.
	Quantitative analysis of ascorbic acid permeability of aquaporin 0 in the lens., Nakazawa Y., Biochem Biophys Res Commun. November 11, 2011; 415 (1): 125-30.
	The effect of the interaction between aquaporin 0 (AQP0) and the filensin tail region on AQP0 water permeability., Nakazawa Y., Mol Vis. March 23, 2011; 17 3191-9.
	Two distinct aquaporin 0s required for development and transparency of the zebrafish lens., Froger A., Invest Ophthalmol Vis Sci. December 1, 2010; 51 (12): 6582-92.
	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.
	Zinc modulation of water permeability reveals that aquaporin 0 functions as a cooperative tetramer., Németh-Cahalan KL., J Gen Physiol. November 1, 2007; 130 (5): 457-64.
	Transgenic overexpression of connexin50 induces cataracts., Chung J., Exp Eye Res. March 1, 2007; 84 (3): 513-28.
	The structure of aquaporins., Gonen T., Q Rev Biophys. November 1, 2006; 39 (4): 361-96.
	AQP0-LTR of the Cat Fr mouse alters water permeability and calcium regulation of wild type AQP0., Kalman K., Biochim Biophys Acta. August 1, 2006; 1758 (8): 1094-9.
	Aquaporin-11: a channel protein lacking apparent transport function expressed in brain., Gorelick DA., BMC Biochem. May 1, 2006; 7 14.
	Regulation of aquaporin water permeability in the lens., Varadaraj K., Invest Ophthalmol Vis Sci. April 1, 2005; 46 (4): 1393-402.
	Water permeability of C-terminally truncated aquaporin 0 (AQP0 1-243) observed in the aging human lens., Ball LE., Invest Ophthalmol Vis Sci. November 1, 2003; 44 (11): 4820-8.
	Cloning and functional expression of an MIP (AQP0) homolog from killifish (Fundulus heteroclitus) lens., Virkki LV., Am J Physiol Regul Integr Comp Physiol. December 1, 2001; 281 (6): R1994-2003.
	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.
	Functional impairment of lens aquaporin in two families with dominantly inherited cataracts., Francis P., Hum Mol Genet. September 22, 2000; 9 (15): 2329-34.
	pH and calcium regulate the water permeability of aquaporin 0., Németh-Cahalan KL., J Biol Chem. March 10, 2000; 275 (10): 6777-82.
	Transmembrane helix 5 is critical for the high water permeability of aquaporin., Kuwahara M., Biochemistry. December 7, 1999; 38 (49): 16340-6.
	Effects of lens major intrinsic protein on glycerol permeability and metabolism., Kushmerick C., J Membr Biol. January 1, 1998; 161 (1): 9-19.
	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.
	Comparison of the water transporting properties of MIP and AQP1., Chandy G., J Membr Biol. September 1, 1997; 159 (1): 29-39.
	Cloning and functional expression of a second new aquaporin abundantly expressed in testis., Ishibashi K., Biochem Biophys Res Commun. August 28, 1997; 237 (3): 714-8.
	Water and glycerol permeabilities of aquaporins 1-5 and MIP determined quantitatively by expression of epitope-tagged constructs in Xenopus oocytes., Yang B., J Biol Chem. June 27, 1997; 272 (26): 16140-6.
	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.
	The human Aquaporin-5 gene. Molecular characterization and chromosomal localization., Lee MD., J Biol Chem. April 12, 1996; 271 (15): 8599-604.
	Ion, water and neutral solute transport in Xenopus oocytes expressing frog lens MIP., Kushmerick C., Exp Eye Res. September 1, 1995; 61 (3): 351-62.
	Water channel properties of major intrinsic protein of lens., Mulders SM., J Biol Chem. April 14, 1995; 270 (15): 9010-16.
	A 28 kDa sarcolemmal antigen in kidney principal cell basolateral membranes: relationship to orthogonal arrays and MIP26., Verbavatz JM., J Cell Sci. April 1, 1994; 107 ( Pt 4) 1083-94.

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