Papers associated with aqp2

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	Mannan-binding lectin serine protease-2 (MASP-2) in human kidney and its relevance for proteolytic activation of the epithelial sodium channel., Zachar R, Thiel S, Hansen S, Henriksen ML, Skjoedt MO, Skjodt K, Hamzaei Z, Madsen K, Lund L, Hummler E, Svenningsen P, Jensen BL., Sci Rep. September 24, 2022; 12 (1): 15955.
	Further evidence for functional recovery of AQP2 mutations associated with nephrogenic diabetes insipidus., Bissonnette P, Lussier Y, Matar J, Leduc-Nadeau A, Da Cal S, Arthus MF, Unwin RJ, Steinke J, Rangaswamy D, Bichet DG., Physiol Rep. June 1, 2021; 9 (11): e14866.
	Molecular characterization of an aquaporin-2 mutation causing a severe form of nephrogenic diabetes insipidus., Saglar Ozer E, Moeller HB, Karaduman T, Fenton RA, Mergen H., Cell Mol Life Sci. March 1, 2020; 77 (5): 953-962.
	The regulation of heat shock proteins in response to dehydration in Xenopus laevis., Luu BE, Wijenayake S, Malik AI, Storey KB., Cell Stress Chaperones. January 1, 2018; 23 (1): 45-53.
	Expression of the aquaglyceroporin HC-9 in a freeze-tolerant amphibian that accumulates glycerol seasonally., Stogsdill B, Frisbie J, Krane CM, Goldstein DL., Physiol Rep. August 1, 2017; 5 (15):
	Activation of the metabolic sensor AMP-activated protein kinase inhibits aquaporin-2 function in kidney principal cells., Al-Bataineh MM, Li H, Ohmi K, Gong F, Marciszyn AL, Naveed S, Zhu X, Neumann D, Wu Q, Cheng L, Fenton RA, Pastor-Soler NM, Hallows KR., Am J Physiol Renal Physiol. November 1, 2016; 311 (5): F890-F900.
	Functional Recovery of AQP2 Recessive Mutations Through Hetero-Oligomerization with Wild-Type Counterpart., El Tarazi A, Lussier Y, Da Cal S, Bissonnette P, Bichet DG., Sci Rep. September 19, 2016; 6 33298.
	ROMK expression remains unaltered in a mouse model of familial hyperkalemic hypertension caused by the CUL3Δ403-459 mutation., Murthy M, Kurz T, O'Shaughnessy KM., Physiol Rep. July 1, 2016; 4 (13):
	Molecular and cellular characterization of urinary bladder-type aquaporin in Xenopus laevis., Shibata Y, Katayama I, Nakakura T, Ogushi Y, Okada R, Tanaka S, Suzuki M., Gen Comp Endocrinol. October 1, 2015; 222 11-9.
	Aquaporins Mediate Silicon Transport in Humans., Garneau AP, Carpentier GA, Marcoux AA, Frenette-Cotton R, Simard CF, Rémus-Borel W, Caron L, Jacob-Wagner M, Noël M, Powell JJ, Bélanger R, Côté F, Isenring P., PLoS One. August 13, 2015; 10 (8): e0136149.
	Molecular machinery for vasotocin-dependent transepithelial water movement in amphibians: aquaporins and evolution., Suzuki M, Shibata Y, Ogushi Y, Okada R., Biol Bull. August 1, 2015; 229 (1): 109-19.
	Increased water flux induced by an aquaporin-1/carbonic anhydrase II interaction., Vilas G, Krishnan D, Loganathan SK, Malhotra D, Liu L, Beggs MR, Gena P, Calamita G, Jung M, Zimmermann R, Tamma G, Casey JR, Alexander RT., Mol Biol Cell. March 15, 2015; 26 (6): 1106-18.
	Vasotocin and isotocin regulate aquaporin 1 function in the sea bream., Martos-Sitcha JA, Campinho MA, Mancera JM, Martínez-Rodríguez G, Fuentes J., J Exp Biol. March 1, 2015; 218 (Pt 5): 684-93.
	Relative CO(2)/NH(3) selectivities of mammalian aquaporins 0-9., Geyer RR, Musa-Aziz R, Qin X, Boron WF., Am J Physiol Cell Physiol. May 15, 2013; 304 (10): C985-94.
	Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology., Bichet DG, El Tarazi A, Matar J, Lussier Y, Arthus MF, Lonergan M, Bockenhauer D, Bissonnette P., Clin Kidney J. June 1, 2012; 5 (3): 195-202.
	Acyrthosiphon pisum AQP2: a multifunctional insect aquaglyceroporin., Wallace IS, Shakesby AJ, Hwang JH, Choi WG, Martínková N, Douglas AE, Roberts DM., Biochim Biophys Acta. March 1, 2012; 1818 (3): 627-35.
	Molecular and functional characterization of catfish (Heteropneustes fossilis) aquaporin-1b: changes in expression during ovarian development and hormone-induced follicular maturation., Chaube R, Chauvigné F, Tingaud-Sequeira A, Joy KP, Acharjee A, Singh V, Cerdà J., Gen Comp Endocrinol. January 1, 2011; 170 (1): 162-71.
	Stimulating effect of external Myo-inositol on the expression of mutant forms of aquaporin 2., Lussier Y, Bissonnette P, Bichet DG, Lapointe JY., J Membr Biol. July 1, 2010; 236 (2): 225-32.
	New autosomal recessive mutations in aquaporin-2 causing nephrogenic diabetes insipidus through deficient targeting display normal expression in Xenopus oocytes., Leduc-Nadeau A, Lussier Y, Arthus MF, Lonergan M, Martinez-Aguayo A, Riveira-Munoz E, Devuyst O, Bissonnette P, Bichet DG., J Physiol. June 15, 2010; 588 (Pt 12): 2205-18.
	Molecular diversity of vasotocin-dependent aquaporins closely associated with water adaptation strategy in anuran amphibians., Suzuki M, Tanaka S., J Neuroendocrinol. May 1, 2010; 22 (5): 407-12.
	Vasotocin/V2-type receptor/aquaporin axis exists in African lungfish kidney but is functional only in terrestrial condition., Konno N, Hyodo S, Yamaguchi Y, Matsuda K, Uchiyama M., Endocrinology. March 1, 2010; 151 (3): 1089-96.
	Characterization of D150E and G196D aquaporin-2 mutations responsible for nephrogenic diabetes insipidus: importance of a mild phenotype., Guyon C, Lussier Y, Bissonnette P, Leduc-Nadeau A, Lonergan M, Arthus MF, Perez RB, Tiulpakov A, Lapointe JY, Bichet DG., Am J Physiol Renal Physiol. August 1, 2009; 297 (2): F489-98.
	Syntaxin specificity of aquaporins in the inner medullary collecting duct., Mistry AC, Mallick R, Klein JD, Weimbs T, Sands JM, Fröhlich O., Am J Physiol Renal Physiol. August 1, 2009; 297 (2): F292-300.
	Molecular and cellular regulation of water homeostasis in anuran amphibians by aquaporins., Suzuki M, Tanaka S., Comp Biochem Physiol A Mol Integr Physiol. July 1, 2009; 153 (3): 231-41.
	Nucleotides downregulate aquaporin 2 via activation of apical P2 receptors., Wildman SS, Boone M, Peppiatt-Wildman CM, Contreras-Sanz A, King BF, Shirley DG, Deen PM, Unwin RJ., J Am Soc Nephrol. July 1, 2009; 20 (7): 1480-90.
	Role of multiple phosphorylation sites in the COOH-terminal tail of aquaporin-2 for water transport: evidence against channel gating., Moeller HB, MacAulay N, Knepper MA, Fenton RA., Am J Physiol Renal Physiol. March 1, 2009; 296 (3): F649-57.
	Novel treatment for lithium-induced nephrogenic diabetes insipidus rat model using the Sendai-virus vector carrying aquaporin 2 gene., Suga H, Nagasaki H, Kondo TA, Okajima Y, Suzuki C, Ozaki N, Arima H, Yamamoto T, Ozaki N, Akai M, Sato A, Uozumi N, Inoue M, Hasegawa M, Oiso Y., Endocrinology. November 1, 2008; 149 (11): 5803-10.
	Immunocytochemical and phylogenetic analyses of an arginine vasotocin-dependent aquaporin, AQP-h2K, specifically expressed in the kidney of the tree frog, Hyla japonica., Ogushi Y, Mochida H, Nakakura T, Suzuki M, Tanaka S., Endocrinology. December 1, 2007; 148 (12): 5891-901.
	Excretion and conservation of glycerol, and expression of aquaporins and glyceroporins, during cold acclimation in Cope's gray tree frog Hyla chrysoscelis., Zimmerman SL, Frisbie J, Goldstein DL, West J, Rivera K, Krane CM., Am J Physiol Regul Integr Comp Physiol. January 1, 2007; 292 (1): R544-55.
	Regulation of the immunoexpression of aquaporin 9 by ovarian hormones in the rat oviductal epithelium., Brañes MC, Morales B, Ríos M, Villalón MJ., Am J Physiol Cell Physiol. May 1, 2005; 288 (5): C1048-57.
	Conversion of aquaporin 6 from an anion channel to a water-selective channel by a single amino acid substitution., Liu K, Kozono D, Kato Y, Agre P, Hazama A, Yasui M., Proc Natl Acad Sci U S A. February 8, 2005; 102 (6): 2192-7.
	A novel mechanism in recessive nephrogenic diabetes insipidus: wild-type aquaporin-2 rescues the apical membrane expression of intracellularly retained AQP2-P262L., de Mattia F, Savelkoul PJ, Bichet DG, Kamsteeg EJ, Konings IB, Marr N, Arthus MF, Lonergan M, van Os CH, van der Sluijs P, Robertson G, Deen PM., Hum Mol Genet. December 15, 2004; 13 (24): 3045-56.
	Evidence for stabilization of aquaporin-2 folding mutants by N-linked glycosylation in endoplasmic reticulum., Buck TM, Eledge J, Skach WR., Am J Physiol Cell Physiol. November 1, 2004; 287 (5): C1292-9.
	Molecular and functional characterization of a vasotocin-sensitive aquaporin water channel in quail kidney., Yang Y, Cui Y, Wang W, Zhang L, Bufford L, Sasaki S, Fan Z, Nishimura H., Am J Physiol Regul Integr Comp Physiol. October 1, 2004; 287 (4): R915-24.
	Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus., Kamsteeg EJ, Bichet DG, Konings IB, Nivet H, Lonergan M, Arthus MF, van Os CH, Deen PM., J Cell Biol. December 8, 2003; 163 (5): 1099-109.
	Regulation of water absorption in the frog skins by two vasotocin-dependent water-channel aquaporins, AQP-h2 and AQP-h3., Hasegawa T, Tanii H, Suzuki M, Tanaka S., Endocrinology. September 1, 2003; 144 (9): 4087-96.
	Pathogenesis of nephrogenic diabetes insipidus by aquaporin-2 C-terminus mutations., Asai T, Kuwahara M, Kurihara H, Sakai T, Terada Y, Marumo F, Sasaki S., Kidney Int. July 1, 2003; 64 (1): 2-10.
	Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus., Marr N, Bichet DG, Hoefs S, Savelkoul PJ, Konings IB, De Mattia F, Graat MP, Arthus MF, Lonergan M, Fujiwara TM, Knoers NV, Landau D, Balfe WJ, Oksche A, Rosenthal W, Müller D, Van Os CH, Deen PM., J Am Soc Nephrol. September 1, 2002; 13 (9): 2267-77.
	Molecular and cellular characterization of a water-channel protein, AQP-h3, specifically expressed in the frog ventral skin., Tanii H, Hasegawa T, Hirakawa N, Suzuki M, Tanaka S., J Membr Biol. July 1, 2002; 188 (1): 43-53.
	Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families., Lin SH, Bichet DG, Sasaki S, Kuwahara M, Arthus MF, Lonergan M, Lin YF., J Clin Endocrinol Metab. June 1, 2002; 87 (6): 2694-700.
	Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus., Kuwahara M, Iwai K, Ooeda T, Igarashi T, Ogawa E, Katsushima Y, Shinbo I, Uchida S, Terada Y, Arthus MF, Lonergan M, Fujiwara TM, Bichet DG, Marumo F, Sasaki S., Am J Hum Genet. October 1, 2001; 69 (4): 738-48.
	Detection of aquaporin-2 in the plasma membranes of oocytes: a novel isolation method with improved yield and purity., Kamsteeg EJ, Deen PM., Biochem Biophys Res Commun. April 6, 2001; 282 (3): 683-90.
	Functionality of aquaporin-2 missense mutants in recessive nephrogenic diabetes insipidus., Marr N, Kamsteeg EJ, van Raak M, van Os CH, Deen PM., Pflugers Arch. April 1, 2001; 442 (1): 73-7.
	The subcellular localization of an aquaporin-2 tetramer depends on the stoichiometry of phosphorylated and nonphosphorylated monomers., Kamsteeg EJ, Heijnen I, van Os CH, Deen PM., J Cell Biol. November 13, 2000; 151 (4): 919-30.
	Importance of aquaporin-2 expression levels in genotype -phenotype studies in nephrogenic diabetes insipidus., Kamsteeg EJ, Deen PM., Am J Physiol Renal Physiol. October 1, 2000; 279 (4): F778-84.
	Functional impairment of lens aquaporin in two families with dominantly inherited cataracts., Francis P, Chung JJ, Yasui M, Berry V, Moore A, Wyatt MK, Wistow G, Bhattacharya SS, Agre P., Hum Mol Genet. September 22, 2000; 9 (15): 2329-34.
	Transmembrane helix 5 is critical for the high water permeability of aquaporin., Kuwahara M, Shinbo I, Sato K, Terada Y, Marumo F, Sasaki S., Biochemistry. December 7, 1999; 38 (49): 16340-6.
	Transport of water and glycerol in aquaporin 3 is gated by H(+)., Zeuthen T, Klaerke DA., J Biol Chem. July 30, 1999; 274 (31): 21631-6.
	An impaired routing of wild-type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus., Kamsteeg EJ, Wormhoudt TA, Rijss JP, van Os CH, Deen PM., EMBO J. May 4, 1999; 18 (9): 2394-400.
	cDNA and genomic cloning of mouse aquaporin-2: functional analysis of an orthologous mutant causing nephrogenic diabetes insipidus., Yang B, Ma T, Xu Z, Verkman AS., Genomics. April 1, 1999; 57 (1): 79-83.

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