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Biochemistry. Biokhimiia|July 5, 2022
Rational Design of ssODN to Correct Mutations by Gene EditingOlga V Volodina, Arina A Anuchina, Milyausha I Zainitdinova, et al.
Current Gene Therapy|April 16, 2024
Evolution of Prime Editing Systems: Move Forward to the Treatment of Hereditary DiseasesOlga V Volodina, Anastasia R Fabrichnikova, Arina A Anuchina, et al.
International Journal of Molecular Sciences|April 13, 2023
Bridging Gaps in HDR Improvement: The Role of MAD2L2, SCAI, and SCR7Arina A Anuchina, Milyausha I Zaynitdinova, Anna G Demchenko, et al.
Leukemia & Lymphoma|January 14, 2016
Whole-exome sequencing reveals potential molecular predictors of relapse after discontinuation of the targeted therapy in chronic myeloid leukemia patientsSvetlana A Smirnikhina, Alexander V Lavrov, Ekaterina Yu Chelysheva, et al.
Photochemistry and Photobiology|May 14, 2022
Spectral Photoluminescent Parameters of Barley Seeds (Hordéum vulgáre) Infected with Fusarium sspMaxim N Moskovsky, Yuri H Shogenov, Alexander V Lavrov, et al.
BMC Genetics|January 30, 2016
Frequent variations in cancer-related genes may play prognostic role in treatment of patients with chronic myeloid leukemiaAlexander V Lavrov, Ekaterina Y Chelysheva, Svetlana A Smirnikhina, et al.
Biochemistry. Biokhimiia|July 3, 2025
Selection of Optimal pegRNAs to Enhance Efficiency of Prime Editing in AT-Rich Genome RegionsOlga V Volodina, Anna G Demchenko, Arina A Anuchina, et al.
Plos One|September 14, 2017
Copy number variation analysis in cytochromes and glutathione S-transferases may predict efficacy of tyrosine kinase inhibitors in chronic myeloid leukemiaAlexander V Lavrov, Oksana A Ustaeva, Elmira P Adilgereeva, et al.
BMC Medical Genomics|March 16, 2019
Exome, transcriptome and miRNA analysis don't reveal any molecular markers of TKI efficacy in primary CML patientsAlexander V Lavrov, Ekaterina Yu Chelysheva, Elmira P Adilgereeva, et al.
Blood Cells, Molecules & Diseases|August 2, 2005
Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patientsEkaterina S Potekhina, Alexander V Lavrov, Larisa M Samokhodskaya, et al.
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