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dc.contributor.author Olschewski A
dc.contributor.author Veale EL
dc.contributor.author Nagy BM
dc.contributor.author Nagaraj C
dc.contributor.author Kwapiszewska G
dc.contributor.author Antigny F
dc.contributor.author Lambert M
dc.contributor.author Humbert M
dc.contributor.author Czirják, Gábor
dc.contributor.author Enyedi, Péter
dc.contributor.author Mathie A
dc.date.accessioned 2018-07-13T07:28:04Z
dc.date.available 2018-07-13T07:28:04Z
dc.date.issued 2017
dc.identifier 85034956739
dc.identifier.citation pagination=1700754, papers: 14; journalVolume=50; journalIssueNumber=5; journalTitle=EUROPEAN RESPIRATORY JOURNAL;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4806
dc.identifier.uri doi:10.1183/13993003.00754-2017
dc.description.abstract TWIK-related acid-sensitive potassium channel 1 (TASK-1 encoded by KCNK3) belongs to the family of two-pore domain potassium channels. This gene subfamily is constitutively active at physiological resting membrane potentials in excitable cells, including smooth muscle cells, and has been particularly linked to the human pulmonary circulation. TASK-1 channels are sensitive to a wide array of physiological and pharmacological mediators that affect their activity such as unsaturated fatty acids, extracellular pH, hypoxia, anaesthetics and intracellular signalling pathways. Recent studies show that modulation of TASK-1 channels, either directly or indirectly by targeting their regulatory mechanisms, has the potential to control pulmonary arterial tone in humans. Furthermore, mutations in KCNK3 have been identified as a rare cause of both familial and idiopathic pulmonary arterial hypertension. This review summarises our current state of knowledge of the functional role of TASK-1 channels in the pulmonary circulation in health and disease, with special emphasis on current advancements in the field. © Copyright ERS 2017.
dc.relation.ispartof urn:issn:0903-1936
dc.title TASK-1 (KCNK3) channels in the lung: From cell biology to clinical implications
dc.type Journal Article
dc.date.updated 2018-02-16T09:43:30Z
dc.language.rfc3066 en
dc.identifier.mtmt 3325266
dc.contributor.department SE/AOK/I/Élettani Intézet
dc.contributor.institution Semmelweis Egyetem


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