3Schwiebert EM, Benos DJ, Egan M E, et al. CFTR is a conductance regulator as well as a chloride channel [J]. Physiol Rev, 1999, 79 (1 Suppl):S145-S166.
4Boucher RC, Stutts MJ, Knowles MR, et al. Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation[J]. J Clin Invest, 1986, 78 (5):1245-1252.
5Willumsen N J, Boucher R C. Transcellular sodium transport in cultured cystic fibrosis human nasal epithelium[J]. Am J Physiol, 1991, 261 (2 ):C332-C341.
6Stutts MJ, Canessa CM, Olsen JC, et al. CFTR as a cAMP-dependent regulator of sodium channels[J]. Science, 1995, 269 (5225):847-850.
7Kunzelmann K. CFTR: interacting with everything?[J]. News Physiol Sci, 2001, 16:167-170.
8Bers DM,Perez-Reyes E. Ca channels in cardiac myocytes: structure and function in Ca influx and intracellular Ca release[J]. Cardiovasc Res, 1999, 42(2): 339-360.
9Hume JR, Duan D, Collier ML, et al. Anion transport in heart[J]. Physiol Rev, 2000, 80 (1):31-81.
10Minocherhomjee AM, Roufogalis BD, McNeill JH. Effect of disulfonic stilbene anion-channel blockers on the guinea-pig myocardium[J]. Can J Physiol Pharmacol, 1985, 63(8): 912-917.
