Anastasia K. Zaytseva
Saint Petersburg, SPE 197341, Russian Federation
Last Updated: 09/26/2026
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Found 13 publications
Charge Reversal of the Uppermost Arginine in Sliding Helix S4-I Affects Gating of Cardiac Sodium Channel.
Journal: International journal of molecular sciences
Published: November 23, 2024
Distinct molecular features of FLNC mutations, associated with different clinical phenotypes.
Journal: Cytoskeleton (Hoboken, N.J.)
Published: March 04, 2024
Biophysical mechanisms of myocardium sodium channelopathies.
Journal: Pflugers Archiv : European journal of physiology
Published: September 28, 2023
Modulation of Notch Signaling at Early Stages of Differentiation of Human Induced Pluripotent Stem Cells to Dopaminergic Neurons.
Journal: International journal of molecular sciences
Published: November 23, 2022
LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient.
Journal: Frontiers in cardiovascular medicine
Published: April 30, 2022
Characterization of the novel heterozygous SCN5A genetic variant Y739D associated with Brugada syndrome.
Journal: Biochemistry and biophysics reports
Published: December 01, 2021
Intersegment Contacts of Potentially Damaging Variants of Cardiac Sodium Channel.
Journal: Frontiers in pharmacology
Published: August 10, 2021
Possible Interactions of Extracellular Loop IVP2-S6 With Voltage-Sensing Domain III in Cardiac Sodium Channel.
Journal: Frontiers in pharmacology
Published: July 16, 2021
Case Report: Loss-of-Function ABCC9 Genetic Variant Associated With Ventricular Fibrillation.
Journal: Frontiers in genetics
Published: June 01, 2021
Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes.
Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
Published: July 16, 2020
Sodium current abnormalities and deregulation of Wnt/β-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring compound genetic variants in plakophilin 2 gene.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: November 20, 2019
Last Updated: 09/26/2026