doc. MUDr. Markéta Bébarová, Ph.D.
Head of the research group, Markéta Bébarová Research Group: Excitability and its Disorders
Office: bldg. A20/326
Kamenice 753/5
625 00 Brno
Phone: | +420 549 49 3147 |
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E‑mail: |
social and academic networks: |
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Total number of publications: 223
2007
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K557E mutation in C-terminus of KCNQ1 gene as a cause of long QT syndrome
Year: 2007, type: Conference abstract
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Physiology Practicals
Year: 2007, type:
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Praktická cvičení z Fyziologie
Year: 2007, type:
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Subepicardial phase-0 block and discontinuous transmural conduction underlie right-precordial ST-segment elevation in Brugada syndrome by a novel C-terminal SCN5A mutation.
Year: 2007, type: Conference abstract
2006
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A model of IKto-channel function in rat ventricular cardiomyocytes
Engineering Mechanics 2006, year: 2006
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Clinical, genetic and biophysical characterization of three novel SCN5A mutations in patients with Brugada syndrome
Year: 2006, type: Conference abstract
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Effect of haloperidol on transient outward potassium current in rat ventricular myocytes
European Journal of Pharmacology, year: 2006, volume: 550, edition: 1-3
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Effects of sigma receptor ligand haloperidol on ionic currents in rat cardiomyocyte
Journal of Molecular and Cellular Cardiology, year: 2006, volume: 40, edition: 6
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Electrophysiological properties of C-terminal KCNQ1 mutation K557E detected in family with long QT syndrome
Year: 2006, type: Conference abstract
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Elektrofyziologické vlastnosti KCNQ1/KCNE1 kanálů s mutací v C konci KCNQ1podjednotky, Lys557Glu, detekovanou u rodiny se syndromem dlouhého QT
Year: 2006, type: Appeared in Conference without Proceedings