Papers associated with mesonephric tubule (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.
	Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology., Bichet DG., Clin Kidney J. June 1, 2012; 5 (3): 195-202.
	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.
	Syntaxin specificity of aquaporins in the inner medullary collecting duct., Mistry AC., Am J Physiol Renal Physiol. August 1, 2009; 297 (2): F292-300.
	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.
	Novel treatment for lithium-induced nephrogenic diabetes insipidus rat model using the Sendai-virus vector carrying aquaporin 2 gene., Suga H., Endocrinology. November 1, 2008; 149 (11): 5803-10.
	Evidence for stabilization of aquaporin-2 folding mutants by N-linked glycosylation in endoplasmic reticulum., Buck TM., 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., Am J Physiol Regul Integr Comp Physiol. October 1, 2004; 287 (4): R915-24.
	Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families., Lin SH., J Clin Endocrinol Metab. June 1, 2002; 87 (6): 2694-700.
	Fourfold reduction of water permeability in inner medullary collecting duct of aquaporin-4 knockout mice., Chou CL., Am J Physiol. February 1, 1998; 274 (2): C549-54.
	New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels., Mulders SM., J Am Soc Nephrol. February 1, 1997; 8 (2): 242-8.
	The aquaporin family of water channels in kidney., Agre P., Nephrologie. January 1, 1996; 17 (7): 409-15.
	The aquaporin family of water channels in kidney., Nielsen S., Kidney Int. October 1, 1995; 48 (4): 1057-68.
	cAMP-dependent phosphorylation stimulates water permeability of aquaporin-collecting duct water channel protein expressed in Xenopus oocytes., Kuwahara M., J Biol Chem. May 5, 1995; 270 (18): 10384-7.
	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.
	Discovery of aquaporins: a breakthrough in research on renal water transport., van Lieburg AF., Pediatr Nephrol. April 1, 1995; 9 (2): 228-34.
	Functional characterization and cell immunolocalization of AQP-CD water channel in kidney collecting duct., Fushimi K., Am J Physiol. October 1, 1994; 267 (4 Pt 2): F573-82.
	Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene., van Lieburg AF., Am J Hum Genet. October 1, 1994; 55 (4): 648-52.
	Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct., Sasaki S., J Clin Invest. March 1, 1994; 93 (3): 1250-6.

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