Sergey V. Zhuk
Saint Petersburg, SPE 197341, Russian Federation
Last Updated: 09/26/2026
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Found 11 publications
Characterization of pathogenic genetic variants in Russian patients with primary ciliary dyskinesia using gene panel sequencing and transcript analysis.
Journal: Orphanet journal of rare diseases
Published: February 13, 2024
Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner.
Journal: Cell and tissue research
Published: September 13, 2022
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.
Journal: Orphanet journal of rare diseases
Published: March 02, 2022
Case Report: Two New Cases of Autosomal-Recessive Hypertrophic Cardiomyopathy Associated With TRIM63-Compound Heterozygous Variant.
Journal: Frontiers in genetics
Published: July 18, 2021
Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in Children.
Journal: Frontiers in cardiovascular medicine
Published: February 15, 2021
RBM20-Associated Ventricular Arrhythmias in a Patient with Structurally Normal Heart.
Journal: Genes
Published: December 16, 2020
Monocytes with Oncogenic Mutation JAK2 V617F as a Tool for Studies of the Pathogenic Mechanisms of Myelofibrosis.
Journal: Bulletin of experimental biology and medicine
Published: April 11, 2017
Murine and human hematopoietic progenitor cultures grown on stromal layers expressing Notch ligands
Journal: Molekuliarnaia biologiia
Published: November 16, 2015
Notch-dependent EMT is attenuated in patients with aortic aneurysm and bicuspid aortic valve.
Journal: Biochimica et biophysica acta
Published: October 02, 2015
Variants in the NOTCH1 gene in patients with aortic coarctation.
Journal: Congenital heart disease
Published: November 24, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026