Defective lipoxin-mediated anti-inflammatory activity in the cystic fibrosis airway von Karp, Christopher L, Greer, Todd M, Uddin, Jasim, Atabani, Sowsan F, Petasis, Nicos A, Softic, Samir, Xu, Yan, Wills-Karp, Marsha, Guggino, William B, Whitsett, Jeffrey A, Accurso, Frank J, Keledjian, Raquel, Flick, Leah M, Yang, Rong, Belkaid, Yasmine, Park, Kiwon W

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Molecular structure of the water channel through aquaporin CHIP. The hourglass model von JIN SUP JUNG, PRESTON, G. M, SMITH, B. L, GUGGINO, W. B, AGRE, P

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Aquaporin CHIP: the archetypal molecular water channel von Agre, P, Preston, G. M, Smith, B. L, Jung, J. S, Raina, S, Moon, C, Guggino, W. B, Nielsen, S

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The mercury-sensitive residue at cysteine 189 in the CHIP28 water channel von PRESTON, G. M, JIN SUP JUNG, GUGGINO, W. B, AGRE, P

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Molecular Characterization of an Aquaporin cDNA from Brain: Candidate Osmoreceptor and Regulator of Water Balance von Jung, Jin Sup, Bhat, Ratan V., Preston, Gregory M., Guggino, William B., Baraban, Jay M., Agre, Peter

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Appearance of Water Channels in Xenopus Oocytes Expressing Red Cell CHIP28 Protein von Preston, Gregory M., Carroll, Tiziana Piazza, Guggino, William B., Agre, Peter

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WNK4 kinase regulates surface expression of the human sodium chloride cotransporter in mammalian cells von Cai, H., Cebotaru, V., Wang, Y-H, Zhang, X-M, Cebotaru, L., Guggino, S.E., Guggino, W.B.

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Structure and Dynamics of NBD1 from CFTR Characterized Using Crystallography and Hydrogen/Deuterium Exchange Mass Spectrometry von Lewis, H.A., Wang, C., Zhao, X., Hamuro, Y., Conners, K., Kearins, M.C., Lu, F., Sauder, J.M., Molnar, K.S., Coales, S.J., Maloney, P.C., Guggino, W.B., Wetmore, D.R., Weber, P.C., Hunt, J.F.

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Atrial natriuretic peptide modulates cystic fibrosis transmembrane conductance regulator chloride channel expression in rat proximal colon and human intestinal epithelial cells von Novaira, H J, Ornellas, D S, Ortiga-Carvalho, T M, Zhang, X M, Souza-Menezes, J, Guggino, S E, Guggino, W B, Morales, M M

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A role for CFTR in human autosomal dominant polycystic kidney disease von Hanaoka, K, Devuyst, O, Schwiebert, E. M, Wilson, P. D, Guggino, W. B

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Stable in vivo Expression of the Cystic Fibrosis Transmembrane Conductance Regulator with an Adeno-Associated Virus Vector von Flotte, Terence R., Afione, Sandra A., Conrad, Carol, McGarth, Sharon A., Solow, Rikki, Oka, Hidemi, Zeitlin, Pamela L., Guggino, William B., Carter, Barrie J.

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Immunocytochemical Localization of the Cystic Fibrosis Gene Product CFTR von Crawford, Isabelle, Maloney, Peter C., Zeitlin, Pamela L., Guggino, William B., Hyde, Stephen C., Turley, Helen, Gatter, Kevin C., Harris, Ann, Higgins, Christopher F.

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Cystic fibrosis salt/fluid controversy: In the thick of it von Guggino, William B

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Safety and Biological Efficacy of an Adeno-Associated Virus Vector-Cystic Fibrosis Transmembrane Regulator (AAV-CFTR) in the Cystic Fibrosis Maxillary Sinus von Wagner, John A., Messner, Anna H., Moran, Mary Lynn, Daifuku, Richard, Kouyama, Keisuke, Desch, Julie K., Manley, Sara, Norbash, Alexander M., Conrad, Carol K., Friborg, Sandra, Reynolds, Thomas, Guggino, William B., Moss, Richard B., Carter, Barrie J., Wine, Jeffrey J., Flotte, Terence R., Gardner, Phyllis

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Molecular Cloning and Characterization of AqpZ, a Water Channel from Escherichia coli von Calamita, G, Bishai, W R, Preston, G M, Guggino, W B, Agre, P

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Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents von Guggino, William B, Germino, Gregory G, Hanaoka, Kazushige, Qian, Feng, Boletta, Alessandra, Bhunia, Anil K, Piontek, Klaus, Tsiokas, Leonidas, Sukhatme, Vikas P

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Defective regulation of outwardly rectifying Cl − channels by protein kinase A corrected by insertion of CFTR von Egan, Marie, Flotte, Terence, Afione, Sandra, Solow, Rikki, Zeitlin, Pamela L, Carter, Barrie J, Guggino, William B

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Membrane topology of aquaporin CHIP. Analysis of functional epitope-scanning mutants by vectorial proteolysis von PRESTON, G. M, JUNG, J. S, GUGGINO, W. B, AGRE, P

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Apical and basolateral ATP stimulates tracheal epithelial chloride secretion via multiple purinergic receptors von Hwang, T. H, Schwiebert, E. M, Guggino, W. B

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Both the wild type and a functional isoform of CFTR are expressed in kidney von Morales, M. M, Carroll, T. P, Morita, T, Schwiebert, E. M, Devuyst, O, Wilson, P. D, Lopes, A. G, Stanton, B. A, Dietz, H. C, Cutting, G. R, Guggino, W. B

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