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Alternative splice isoforms of small conductance calcium-activated SK2 channels differ in molecular interactions and surface levels. , Scholl ES, Pirone A, Cox DH, Duncan RK, Jacob MH., Channels (Austin). January 1, 2014; 8 (1): 62-75.
Evolution of vertebrate central nervous system is accompanied by novel expression changes of duplicate genes. , Chen Y , Chen Y , Ding Y , Zhang Z , Wang W, Chen JY , Ueno N , Mao B ., J Genet Genomics. December 20, 2011; 38 (12): 577-84.
FHL-2 suppresses VEGF-induced phosphatidylinositol 3-kinase/Akt activation via interaction with sphingosine kinase-1. , Hayashi H, Nakagami H, Takami Y, Koriyama H, Mori M, Tamai K, Sun J, Nagao K, Morishita R, Kaneda Y., Arterioscler Thromb Vasc Biol. June 1, 2009; 29 (6): 909-14.
5-HT1A receptors modulate small-conductance Ca2+-activated K+ channels. , Grunnet M, Jespersen T, Perrier JF., J Neurosci Res. December 15, 2004; 78 (6): 845-54.
Halothane inhibits an intermediate conductance Ca2+-activated K+ channel by acting at the extracellular side of the ionic pore. , Hashiguchi-Ikeda M, Namba T, Ishii TM, Hisano T, Fukuda K., Anesthesiology. December 1, 2003; 99 (6): 1340-5.
Small conductance Ca2+-activated K+ channels formed by the expression of rat SK1 and SK2 genes in HEK 293 cells. , Benton DC, Monaghan AS, Hosseini R, Bahia PK, Haylett DG, Moss GW., J Physiol. November 15, 2003; 553 (Pt 1): 13-9.
Regional differences in distribution and functional expression of small-conductance Ca2+-activated K+ channels in rat brain. , Sailer CA, Hu H, Kaufmann WA, Trieb M, Schwarzer C, Storm JF, Knaus HG., J Neurosci. November 15, 2002; 22 (22): 9698-707.
ATP-dependent activation of the intermediate conductance, Ca2+-activated K+ channel, hIK1, is conferred by a C-terminal domain. , Gerlach AC, Syme CA, Giltinan L, Adelman JP, Devors DC., J Biol Chem. June 15, 2001; 276 (24): 10963-70.
Apamin interacts with all subtypes of cloned small-conductance Ca2+-activated K+ channels. , Grunnet M, Jensen BS, Olesen SP, Klaerke DA., Pflugers Arch. January 1, 2001; 441 (4): 544-50.
Inhibition of the human intermediate conductance Ca(2+)-activated K(+) channel, hIK1, by volatile anesthetics. , Namba T, Ishii TM, Ikeda M, Hisano T, Itoh T, Hirota K, Adelman JP, Fukuda K., Eur J Pharmacol. April 28, 2000; 395 (2): 95-101.
The pharmacology of hSK1 Ca2+-activated K+ channels expressed in mammalian cell lines. , Shah M, Haylett DG., Br J Pharmacol. February 1, 2000; 129 (4): 627-30.
Bicuculline block of small-conductance calcium-activated potassium channels. , Khawaled R, Bruening-Wright A, Adelman JP, Maylie J., Pflugers Arch. August 1, 1999; 438 (3): 314-21.
Determinants of apamin and d-tubocurarine block in SK potassium channels. , Ishii TM, Maylie J, Adelman JP., J Biol Chem. September 12, 1997; 272 (37): 23195-200.
Human and Xenopus cDNAs encoding budding yeast Cdc7-related kinases: in vitro phosphorylation of MCM subunits by a putative human homologue of Cdc7. , Sato N, Arai K, Masai H., EMBO J. July 16, 1997; 16 (14): 4340-51.