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dc.contributor.authorMarcel A.G. van der Heyden*
dc.contributor.authorBrian P. Delisle*
dc.contributor.authorHugues Abriel*
dc.contributor.authorBaoxin Li*
dc.date.accessioned2021-02-11T16:40:43Z
dc.date.available2021-02-11T16:40:43Z
dc.date.issued2018*
dc.date.submitted2019-01-23 14:53:43*
dc.identifier32040*
dc.identifier.issn16648714*
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/50657
dc.description.abstractA well-adjusted expression of cardiac ion channels at the sarcolemma is of crucial importance for normal action potential formation and thus cardiac function. The cellular processes that transport channel proteins from the endoplasmic reticulum towards specified regions on the sarcolemmal membrane, and subsequently take them from the plasma membrane to the protein degradation machinery are commonly known as trafficking. The research field recognizes that aberrant channel trafficking stands at the basis of many congenital and acquired arrhythmias. The collection of papers in this eBook provides state-of-the-art insight into the world of ion channel trafficking research.*
dc.languageEnglish*
dc.relation.ispartofseriesFrontiers Research Topics*
dc.subjectQP1-981*
dc.subjectQ1-390*
dc.subject.otherKv11.1 channels*
dc.subject.otherConnexin43 (Cx43)*
dc.subject.otherion channel*
dc.subject.otherarrhythmia*
dc.subject.otherTRPM4 channel*
dc.subject.otherGlycosylation*
dc.subject.otherNaV1.5 channels*
dc.subject.otherKir2.1 channels*
dc.subject.othertrafficking*
dc.subject.otherAutophagy*
dc.subject.otherProtein complexes*
dc.titleIon Channel Trafficking and Cardiac Arrhythmias*
dc.typebook
oapen.identifier.doi10.3389/978-2-88945-643-7*
oapen.relation.isPublishedBybf5ce210-e72e-4860-ba9b-c305640ff3ae*
oapen.relation.isbn9782889456437*
oapen.pages123*


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