Kseniya I. Perepelina
Saint Petersburg, SPE 194064, Russian Federation
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 17 publications
Generation of iPSCs line from patient with Singleton-Merten syndrome.
Journal: Human cell
Published: January 21, 2025
Distinct molecular features of FLNC mutations, associated with different clinical phenotypes.
Journal: Cytoskeleton (Hoboken, N.J.)
Published: March 04, 2024
LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient.
Journal: Frontiers in cardiovascular medicine
Published: April 30, 2022
Generation of iPSC line FAMRCi010-A from patient with restrictive cardiomyopathy carrying genetic variant FLNC p.Gly2011Arg.
Journal: Stem cell research
Published: October 02, 2021
Generation of iPSC line (FAMRCi009-A) from patient with familial progressive cardiac conduction disorder carrying genetic variant FLNC p.Val2264Met.
Journal: Stem cell research
Published: October 02, 2021
Diversity of Nuclear Lamin A/C Action as a Key to Tissue-Specific Regulation of Cellular Identity in Health and Disease.
Journal: Frontiers in cell and developmental biology
Published: August 19, 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
Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln.
Journal: Stem cell research
Published: June 04, 2020
Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p.His1684Arg.
Journal: Stem cell research
Published: December 04, 2019
Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val.
Journal: Stem cell research
Published: November 30, 2019
Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro.
Journal: Stem cell research
Published: November 30, 2019
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