·        Moyer BD, Duhaime M, Shaw C, Denton J, Reynolds D, Karlson KH, Pfeiffer J, Wang S, Mickle JE, Milewski M, Cutting GR, Guggino WB, Li M, & Stanton BA (2000). The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane. J Biol Chem 275, 27069-27074.

·        Silva IV, Blaisdell CJ, Guggino SE, & Guggino WB (2000). PTH regulates expression of ClC-5 chloride channel in the kidney. Am J Physiol Renal Physiol 278, F238-F245.

·        Wang S, Yue H, Derin RB, Guggino WB, & Li M (2000). Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity. Cell 103, 169-179.

·        Wang SS, Devuyst O, Courtoy PJ, Wang XT, Wang H, Wang Y, Thakker RV, Guggino S, & Guggino WB (2000). Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis. Hum Mol Genet 9, 2937-2945.

·        Yue H, Devidas S, & Guggino WB (2000). The two halves of CFTR form a dual-pore ion channel. J Biol Chem 275, 10030-10034.

·        Afione SA, Wang J, Walsh S, Guggino WB, & Flotte TR (1999). Delayed expression of adeno-associated virus vector DNA. Intervirology 42, 213-220.

·        Beck SE, Jones LA, Chesnut K, Walsh SM, Reynolds TC, Carter BJ, Askin FB, Flotte TR, & Guggino WB (1999). Repeated delivery of adeno-associated virus vectors to the rabbit airway. J Virol 73, 9446-9455.

·        Guggino WB (1999). Cystic fibrosis and the salt controversy. Cell 96, 607-610.

·        Hanaoka K, Wright JM, Cheglakov IB, Morita T, & Guggino WB (1999). A 59 amino acid insertion increases Ca(2+) sensitivity of rbslo1, a Ca2+ -activated K(+) channel in renal epithelia. J Membr Biol 172, 193-201.

·        Moyer BD, Denton J, Karlson KH, Reynolds D, Wang S, Mickle JE, Milewski M, Cutting GR, Guggino WB, Li M, & Stanton BA (1999). A PDZ-interacting domain in CFTR is an apical membrane polarization signal. J Clin Invest 104, 1353-1361.

·        Schneider SW, Egan ME, Jena BP, Guggino WB, Oberleithner H, & Geibel JP (1999). Continuous detection of extracellular ATP on living cells by using atomic force microscopy. Proc Natl Acad Sci U S A 96, 12180-12185.

·        Schwiebert EM, Benos DJ, Egan ME, Stutts MJ, & Guggino WB (1999). CFTR is a conductance regulator as well as a chloride channel. Physiol Rev 79, S145-S166.

·        Truong-Le VL, Walsh SM, Schweibert E, Mao HQ, Guggino WB, August JT, & Leong KW (1999). Gene transfer by DNA-gelatin nanospheres. Arch Biochem Biophys 361, 47-56.

·        Wagner JA, Messner AH, Moran ML, Daifuku R, Kouyama K, Desch JK, Manley S, Norbash AM, Conrad CK, Friborg S, Reynolds T, Guggino WB, Moss RB, Carter BJ, Wine JJ, Flotte TR, & Gardner P (1999). Safety and biological efficacy of an adeno-associated virus vector-cystic fibrosis transmembrane regulator (AAV-CFTR) in the cystic fibrosis maxillary sinus. Laryngoscope 109, 266-274.

·        Yasui M, Hazama A, Kwon TH, Nielsen S, Guggino WB, & Agre P (1999). Rapid gating and anion permeability of an intracellular aquaporin. Nature 402, 184-187.

·        Devidas S, Yue H, & Guggino WB (1998). The second half of the cystic fibrosis transmembrane conductance regulator forms a functional chloride channel. J Biol Chem 273, 29373-29380.

·        Guggino WB (1998). Focus on "exocytosis is not involved in activation of Cl- secretion via CFTR in Calu-3 airway epithelial cells". Am J Physiol 275, C911-C912.

·        Hackam AS, Wang TL, Guggino WB, & Cutting GR (1998). Sequences in the amino termini of GABA rho and GABA(A) subunits specify their selective interaction in vitro. J Neurochem 70, 40-46.

·        Jiang Q, Mak D, Devidas S, Schwiebert EM, Bragin A, Zhang Y, Skach WR, Guggino WB, Foskett JK, & Engelhardt JF (1998). Cystic fibrosis transmembrane conductance regulator-associated ATP release is controlled by a chloride sensor. J Cell Biol 143, 645-657.

·        Mickle JE, Macek M, Jr., Fulmer-Smentek SB, Egan MM, Schwiebert E, Guggino W, Moss R, & Cutting GR (1998). A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis. Hum Mol Genet 7, 729-735.

·        Moyer BD, Loffing J, Schwiebert EM, Loffing-Cueni D, Halpin PA, Karlson KH, Ismailov II, Guggino WB, Langford GM, & Stanton BA (1998). Membrane trafficking of the cystic fibrosis gene product, cystic fibrosis transmembrane conductance regulator, tagged with green fluorescent protein in madin-darby canine kidney cells. J Biol Chem 273, 21759-21768.

·        Schwiebert EM, Cid-Soto LP, Stafford D, Carter M, Blaisdell CJ, Zeitlin PL, Guggino WB, & Cutting GR (1998). Analysis of ClC-2 channels as an alternative pathway for chloride conduction in cystic fibrosis airway cells. Proc Natl Acad Sci U S A 95, 3879-3884.

·        Schwiebert EM, Egan ME, & Guggino WB (1998). Assays of dynamics, mechanisms, and regulation of ATP transport and release: implications for study of ABC transporter function. Methods Enzymol  292, 664-675.

·        Schwiebert EM, Morales MM, Devidas S, Egan ME, & Guggino WB (1998). Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator. Proc Natl Acad Sci U S A 95, 2674-2679.

·        Taylor AL, Kudlow BA, Marrs KL, Gruenert DC, Guggino WB, & Schwiebert EM (1998). Bioluminescence detection of ATP release mechanisms in epithelia. Am J Physiol 275, C1391-C1406.