Egyszerű nézet

dc.contributor.author Enyedi, Péter
dc.contributor.author Czirják, Gábor
dc.date.accessioned 2020-12-07T08:55:48Z
dc.date.available 2020-12-07T08:55:48Z
dc.date.issued 2010
dc.identifier 77951041210
dc.identifier.citation journalVolume=90;journalIssueNumber=2;journalTitle=PHYSIOLOGICAL REVIEWS;pagerange=559-605;journalAbbreviatedTitle=PHYSIOL REV;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8205
dc.identifier.uri doi:10.1152/physrev.00029.2009
dc.description.abstract Enyedi P, Czirjak G. Molecular Background of Leak K+ Currents: Two-Pore Domain Potassium Channels. Physiol Rev 90: 559-605, 2010; doi:10.1152/physrev.00029.2009.-Two-pore domain K+ (K-2P) channels give rise to leak (also called background) K+ currents. The well-known role of background K+ currents is to stabilize the negative resting membrane potential and counterbalance depolarization. However, it has become apparent in the past decade (during the detailed examination of the cloned and corresponding native K-2P channel types) that this primary hyperpolarizing action is not performed passively. The K-2P channels are regulated by a wide variety of voltage-independent factors. Basic physicochemical parameters (e. g., pH, temperature, membrane stretch) and also several intracellular signaling pathways substantially and specifically modulate the different members of the six K-2P channel subfamilies (TWIK, TREK, TASK, TALK, THIK, and TRESK). The deep implication in diverse physiological processes, the circumscribed expression pattern of the different channels, and the interesting pharmacological profile brought the K-2P channel family into the spotlight. In this review, we focus on the physiological roles of K-2P channels in the most extensively investigated cell types, with special emphasis on the molecular mechanisms of channel regulation.
dc.format.extent 559-605
dc.relation.ispartof urn:issn:0031-9333
dc.title Molecular Background of Leak K+ Currents: Two-Pore Domain Potassium Channels
dc.type Journal Article
dc.date.updated 2020-02-24T08:45:33Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 1490693
dc.identifier.wos 000276672300005
dc.identifier.pubmed 20393194
dc.contributor.department SE/AOK/I/Élettani Intézet
dc.contributor.institution Semmelweis Egyetem


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