WS23.2 Characterization of the CFTR mutation c.3700A>G informs strategies for future medical intervention von Molinski, S.V, Gonska, T, Huan, L.J, Baskin, B, Janahi, I.A, Ray, P.N, Bear, C.E

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Disruption of ClC-2 expression is associated with progressive neurodegeneration in aging mice von Cortez, M.A, Li, C, Whitehead, S.N, Dhani, S.U, D'Antonio, C, Huan, L.J, Bennett, S.A.L, Snead, O.C, Bear, C.E

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WS13-6 Adenoviral vector gene therapy results in a wild type CFTR functional pattern in class I mutation cystic fibrosis cells von Cao, H., Ouyang, H., Laselva, O., Bartlett, C., Bear, C.E., Gonska, T., Moraes, T.J., Hu, J.

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P028 Antisense oligonucleotide splicing modulation as a novel cystic fibrosis (CF) therapeutic approach for the W1282X nonsense mutation von Barchad, O. Avizur, Oren, Y.S., Galai, E. Ozeri, Elgrabli, R., Schirelman, M.R., Blinder, T., Stampfer, C.D., Ordan, M., Laselvab, O., Cymberknoh, M. Cohen, Kerem, E., Bear, C.E., Kerem, B.

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ClC-2 activation modulates regulatory volume decrease von Xiong, H, Li, C, Garami, E, Wang, Y, Ramjeesingh, M, Galley, K, Bear, C E

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Novel method for evaluation of the oligomeric structure of membrane proteins von Ramjeesingh, M, Garami, E, Bear, C.E

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Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene von BEAR, C. E, DUGUAY, F, NAISMITH, A. L, KARTNER, N, HANRAHAN, J. W, RIORDAN, J. R

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Drugs Transported by P-Glycoprotein Inhibit a 40pS Outwardly Rectifying Chloride Channel von Bear, C.E.

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Evidence for a channel for the electrogenic transport of chloride ion in the rat hepatocyte von Bear, Christine E., Petrunka, Connie N., Strasberg, Steven M.

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