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1997 | 1 |
2001 | 1 |
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Mutations in the hminK gene cause long QT syndrome and suppress IKs function.
Nat Genet. 1997 Nov;17(3):338-40. doi: 10.1038/ng1197-338.
Nat Genet. 1997.
PMID: 9354802
AKAP proteins anchor cAMP-dependent protein kinase to KvLQT1/IsK channel complex.
Potet F, Scott JD, Mohammad-Panah R, Escande D, Baró I.
Potet F, et al.
Am J Physiol Heart Circ Physiol. 2001 May;280(5):H2038-45. doi: 10.1152/ajpheart.2001.280.5.H2038.
Am J Physiol Heart Circ Physiol. 2001.
PMID: 11299204
Free article.
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Phosphorylation of the A-kinase-anchoring protein Yotiao contributes to protein kinase A regulation of a heart potassium channel.
Chen L, Kurokawa J, Kass RS.
Chen L, et al.
J Biol Chem. 2005 Sep 9;280(36):31347-52. doi: 10.1074/jbc.M505191200. Epub 2005 Jul 7.
J Biol Chem. 2005.
PMID: 16002409
Free article.
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KCNQ1 assembly and function is blocked by long-QT syndrome mutations that disrupt interaction with calmodulin.
Ghosh S, Nunziato DA, Pitt GS.
Ghosh S, et al.
Circ Res. 2006 Apr 28;98(8):1048-54. doi: 10.1161/01.RES.0000218863.44140.f2. Epub 2006 Mar 23.
Circ Res. 2006.
PMID: 16556866
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