Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder

Podobne zapisy

• Sodium permeable and “hypersensitive” TREK‐1 channels cause ventricular tachycardia
  od: Decher, Niels, i wsp.
  Wydane: (2017)
• Functional mutagenesis screens reveal the ‘cap structure’ formation in disulfide-bridge free TASK channels
  od: Goldstein, Matthias, i wsp.
  Wydane: (2016)
• A Leucine Zipper Motif Essential for Gating of Hyperpolarization-activated Channels
  od: Wemhöner, Konstantin, i wsp.
  Wydane: (2012)
• A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome.
  od: Sven Zumhagen, i wsp.
  Wydane: (2013-01-01)
• A Heterozygous Deletion Mutation in the Cardiac Sodium Channel Gene SCN5A with Loss- and Gain-of-Function Characteristics Manifests as Isolated Conduction Disease, without Signs of Brugada or Long QT Syndrome
  od: Zumhagen, Sven, i wsp.
  Wydane: (2013)