Aleksei A. Sleptcov

Tomsk, TOM 634050, Russian Federation

Last Updated: 09/26/2026

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Found 18 publications

The paradigm of somatic mosaicism in complex diseases.

The paradigm of somatic mosaicism in complex diseases.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: February 26, 2026

DNA Methylation Status of Regulatory Regions of Apoptosis-Associated Genes in Dystropy «Huntington's Disease-Non-Small Cell Lung Cancer».

DNA Methylation Status of Regulatory Regions of Apoptosis-Associated Genes in Dystropy «Huntington's Disease-Non-Small Cell Lung Cancer».

Journal: Epigenomes

Published: May 27, 2025

Isogenic induced pluripotent stem cell line ICGi036-A-1 from a patient with familial hypercholesterolaemia, derived by correcting a pathogenic variant of the gene LDLR c.530C>T.

Isogenic induced pluripotent stem cell line ICGi036-A-1 from a patient with familial hypercholesterolaemia, derived by correcting a pathogenic variant of the gene LDLR c.530C>T.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: November 25, 2024

Identification of Variants of Uncertain Significance in the Genes Associated with Thoracic Aortic Disease in Russian Patients with Nonsyndromic Sporadic Subtypes of the Disorder.

Identification of Variants of Uncertain Significance in the Genes Associated with Thoracic Aortic Disease in Russian Patients with Nonsyndromic Sporadic Subtypes of the Disorder.

Journal: International journal of molecular sciences

Published: June 20, 2024

iPSC-Derived Endothelial Cells Reveal LDLR Dysfunction and Dysregulated Gene Expression Profiles in Familial Hypercholesterolemia.

iPSC-Derived Endothelial Cells Reveal LDLR Dysfunction and Dysregulated Gene Expression Profiles in Familial Hypercholesterolemia.

Journal: International journal of molecular sciences

Published: November 07, 2023

Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION.

Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION.

Journal: International journal of molecular sciences

Published: December 05, 2022

Application of Long-Read Nanopore Sequencing to the Search for Mutations in Hypertrophic Cardiomyopathy.

Application of Long-Read Nanopore Sequencing to the Search for Mutations in Hypertrophic Cardiomyopathy.

Journal: International journal of molecular sciences

Published: November 24, 2022

Methylation of Regulatory Regions of DNA Repair Genes in Carotid Atherosclerosis

Methylation of Regulatory Regions of DNA Repair Genes in Carotid Atherosclerosis

Journal: Molekuliarnaia biologiia

Published: November 16, 2022

Meier-Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of ORC6 Mutations and the Development of a Prenatal Test.

Meier-Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of ORC6 Mutations and the Development of a Prenatal Test.

Journal: International journal of molecular sciences

Published: August 02, 2022

Identification of Functionally Significant Polymorphic Variants in miRNA Genes in Carotid Atherosclerosis

Identification of Functionally Significant Polymorphic Variants in miRNA Genes in Carotid Atherosclerosis

Journal: Molekuliarnaia biologiia

Published: July 19, 2022

Induced pluripotent stem cell line ICGi038-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to compound heterozygous c.1246C > T/c.940 + 3_940 + 6del mutations in LDLR.

Induced pluripotent stem cell line ICGi038-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to compound heterozygous c.1246C > T/c.940 + 3_940 + 6del mutations in LDLR.

Journal: Stem cell research

Published: December 10, 2021

Induced pluripotent stem cell line ICGi037-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to heterozygous p.Trp443Arg mutations in LDLR.

Induced pluripotent stem cell line ICGi037-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to heterozygous p.Trp443Arg mutations in LDLR.

Journal: Stem cell research

Published: December 09, 2021

Showing 1-12 of 18

Last Updated: 09/26/2026