Abstract
A large number of K+ channel genes are expressed in the mammalian heart (for reviews, see Chandy and Gutman, 1995; Deal et al., 1996; Yost, 1999). The diversity of channel expression is enhanced further by coassembly of subunits encoded by different genes to form heteromeric channels, interaction of α-subunits with β-subunits, alternative splicing of K+ channel genes, posttranslational channel modifications, and factors that control insertion and clustering of channels on the cell membrane (Po et al., 1993; Morales et al., 1995; Kim et al., 1996; London et al., 1997; Zhou et al., 1998). This marked diversity leads to a complex array of K+ currents within the heart that varies among species and changes during development.
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London, B. (2001). Use of Transgenic and Gene-Targeted Mice to Study K+Channel Function in the Cardiovascular System. In: Archer, S.L., Rusch, N.J. (eds) Potassium Channels in Cardiovascular Biology. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-1303-2_11
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DOI: https://doi.org/10.1007/978-1-4615-1303-2_11
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