Vyacheslav Y. Tabakov

Moscow, MOW 115522, Russian Federation

Last Updated: 09/26/2026

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Found 40 publications

Identification and Targeted Correction of a Pathogenic PMP22 Deep Intronic Variant.

Identification and Targeted Correction of a Pathogenic PMP22 Deep Intronic Variant.

Journal: International journal of molecular sciences

Published: February 20, 2026

Optimized ND4 allotopic expression for gene therapy of Leber's hereditary optic neuropathy.

Optimized ND4 allotopic expression for gene therapy of Leber's hereditary optic neuropathy.

Journal: Frontiers in bioengineering and biotechnology

Published: December 11, 2025

Clinical and functional characterization of a novel homozygous non-canonical splice mutation (c.1910-15_1910-11delinsTTACA) in CEP290 causing Joubert syndrome.

Clinical and functional characterization of a novel homozygous non-canonical splice mutation (c.1910-15_1910-11delinsTTACA) in CEP290 causing Joubert syndrome.

Journal: Human genomics

Published: October 29, 2025

Somatic mosaicism in the δ-aminolevulinate dehydratase gene causing late-onset porphyria with erythroid-driven pathogenesis.

Somatic mosaicism in the δ-aminolevulinate dehydratase gene causing late-onset porphyria with erythroid-driven pathogenesis.

Journal: Molecular genetics and metabolism reports

Published: October 27, 2025

Generation of an Induced Pluripotent Stem Cell Line from a Duchenne Muscular Dystrophy Patient Carrying the DMD p.Ser429Ter (c.1286C>G) Nonsense Mutation.

Generation of an Induced Pluripotent Stem Cell Line from a Duchenne Muscular Dystrophy Patient Carrying the DMD p.Ser429Ter (c.1286C>G) Nonsense Mutation.

Journal: Bulletin of experimental biology and medicine

Published: September 04, 2025

POLR3A mutations cause nucleolus abnormalities and aberrant telomerase RNA metabolism in induced pluripotent stem cells from Wiedemann-Rautenstrauch premature aging syndrome patient.

POLR3A mutations cause nucleolus abnormalities and aberrant telomerase RNA metabolism in induced pluripotent stem cells from Wiedemann-Rautenstrauch premature aging syndrome patient.

Journal: Biogerontology

Published: August 02, 2025

Prime Editing Modification with FEN1 Improves F508del Variant Editing in the CFTR Gene in Airway Basal Cells.

Prime Editing Modification with FEN1 Improves F508del Variant Editing in the CFTR Gene in Airway Basal Cells.

Journal: International journal of molecular sciences

Published: July 07, 2025

Selection of Optimal pegRNAs to Enhance Efficiency of Prime Editing in AT-Rich Genome Regions.

Selection of Optimal pegRNAs to Enhance Efficiency of Prime Editing in AT-Rich Genome Regions.

Journal: Biochemistry. Biokhimiia

Published: July 03, 2025

Exploring the Phenotypic Heterogeneity and Bioenergetic Profile of the m.13513G>A mtDNA Substitution: A Heteroplasmy Perspective.

Exploring the Phenotypic Heterogeneity and Bioenergetic Profile of the m.13513G>A mtDNA Substitution: A Heteroplasmy Perspective.

Journal: International journal of molecular sciences

Published: March 31, 2025

Splicing variants in DEPDC5-related epilepsies: From functional characterization to correction.

Splicing variants in DEPDC5-related epilepsies: From functional characterization to correction.

Journal: Epilepsia

Published: January 12, 2025

Clinical features and functional analysis of novel SCN9A variants causing congenital insensitivity to pain.

Clinical features and functional analysis of novel SCN9A variants causing congenital insensitivity to pain.

Journal: Pain

Published: December 11, 2024

Human Induced Lung Organoids: A Promising Tool for Cystic Fibrosis Drug Screening.

Human Induced Lung Organoids: A Promising Tool for Cystic Fibrosis Drug Screening.

Journal: International journal of molecular sciences

Published: December 05, 2024

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Last Updated: 09/26/2026