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Summary Anatomy Item Literature (1949) Expression Attributions Wiki
XB-ANAT-3904

Papers associated with plasma membrane (and aqp2)

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Activation of the metabolic sensor AMP-activated protein kinase inhibits aquaporin-2 function in kidney principal cells., Al-Bataineh MM., Am J Physiol Renal Physiol. November 1, 2016; 311 (5): F890-F900.


Molecular and cellular characterization of urinary bladder-type aquaporin in Xenopus laevis., Shibata Y., Gen Comp Endocrinol. October 1, 2015; 222 11-9.                


Molecular machinery for vasotocin-dependent transepithelial water movement in amphibians: aquaporins and evolution., Suzuki M., Biol Bull. August 1, 2015; 229 (1): 109-19.


Relative CO(2)/NH(3) selectivities of mammalian aquaporins 0-9., Geyer RR., Am J Physiol Cell Physiol. May 15, 2013; 304 (10): C985-94.


Stimulating effect of external Myo-inositol on the expression of mutant forms of aquaporin 2., Lussier Y., 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., 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., 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., 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., Am J Physiol Renal Physiol. August 1, 2009; 297 (2): F489-98.


Molecular and cellular regulation of water homeostasis in anuran amphibians by aquaporins., Suzuki M., 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., 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., Am J Physiol Renal Physiol. March 1, 2009; 296 (3): F649-57.


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., Endocrinology. December 1, 2007; 148 (12): 5891-901.


Regulation of the immunoexpression of aquaporin 9 by ovarian hormones in the rat oviductal epithelium., Brañes MC., 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., 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., Hum Mol Genet. December 15, 2004; 13 (24): 3045-56.


Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus., Kamsteeg EJ., 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., Endocrinology. September 1, 2003; 144 (9): 4087-96.


Detection of aquaporin-2 in the plasma membranes of oocytes: a novel isolation method with improved yield and purity., Kamsteeg EJ., Biochem Biophys Res Commun. April 6, 2001; 282 (3): 683-90.


Functionality of aquaporin-2 missense mutants in recessive nephrogenic diabetes insipidus., Marr N., 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., J Cell Biol. November 13, 2000; 151 (4): 919-30.                


Functional impairment of lens aquaporin in two families with dominantly inherited cataracts., Francis P., Hum Mol Genet. September 22, 2000; 9 (15): 2329-34.


cDNA and genomic cloning of mouse aquaporin-2: functional analysis of an orthologous mutant causing nephrogenic diabetes insipidus., Yang B., Genomics. April 1, 1999; 57 (1): 79-83.


Novel mutations in aquaporin-2 gene in female siblings with nephrogenic diabetes insipidus: evidence of disrupted water channel function., Goji K., J Clin Endocrinol Metab. September 1, 1998; 83 (9): 3205-9.


The exchange of functional domains among aquaporins with different transport characteristics., Mulders SM., Pflugers Arch. July 1, 1998; 436 (4): 599-607.


An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex., Mulders SM., J Clin Invest. July 1, 1998; 102 (1): 57-66.


Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones., Tamarappoo BK., J Clin Invest. May 15, 1998; 101 (10): 2257-67.


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.


Identification and characterization of aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus with partial vasopressin response., Canfield MC., Hum Mol Genet. October 1, 1997; 6 (11): 1865-71.


Importance of the mercury-sensitive cysteine on function and routing of AQP1 and AQP2 in oocytes., Mulders SM., Am J Physiol. September 1, 1997; 273 (3 Pt 2): F451-6.


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.


Water channels encoded by mutant aquaporin-2 genes in nephrogenic diabetes insipidus are impaired in their cellular routing., Deen PM., J Clin Invest. May 1, 1995; 95 (5): 2291-6.

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