Author

D. V. Popov

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Research Focus:cell type annotation· 3 Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Assay:DNA methylation· 2 Research Focus:gene regulatory network inference· 2 Assay:proteomics· 2

Frequent Co-Authors

A. K. Larin· 2 shared A. P. Sharples· 2 shared D. C. Turner· 2 shared D. J. Owens· 2 shared E. A. Semenova· 2 shared E. V. Generozov· 2 shared I. I. Ahmetov· 2 shared N. S. Kurochkina· 2 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersPhysiology

A. K. Larin

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Age-related changes in human skeletal muscle transcriptome and proteome are moreaffected by chronic inflammation and physical inactivity than primary aging

N. S. Kurochkina, M. A. Orlova, M. A. Vigovskiy, V. G. Zgoda, T. F. Vepkhvadze, N. E. Vavilov, P. A. Makhnovskii, O. A. Grigorieva, Y. R. Boroday, V. V. Philippov, E. M. Lednev, A. Y. Efimenko, D. V. Popov

bioRxiv · Dec 1, 2023Physiology

Knockout of Hsp70 genes significantly affects locomotion speed and gene expression in leg skeletal muscles of Drosophila melanogaster

P. A. Makhnovskii, I. V. Kukushkina, N. S. Kurochkina, D. V. Popov

This study shows that knocking out six Hsp70 genes in Drosophila reduces locomotor speed and disrupts adaptation to exercise training, with changes in leg muscle gene expression.

bioRxiv · Dec 1, 2023Physiology

DNA methylation across the genome in aged human skeletal muscle tissue and stem cells: The role of HOX genes and physical activity

D. C. Turner, P. P. Gorski, M. F. Maasar, R. A. Seaborne, P. Baumert, A. D. Brown, M. O. Kitchen, R. M. Erskine, I. Dos-Remedios, S. Voisin, N. Eynon, R. I. Sultanov, O. V. Borisov, A. K. Larin, E. A. Semenova, , A. P. Sharples

This study identifies age-related hypermethylation in HOX genes in aged human skeletal muscle and stem cells, with physical activity inversely affecting methylation in some genes.

bioRxiv · Dec 27, 2019Physiology

UBR5 is a Novel E3 Ubiquitin Ligase involved in Skeletal Muscle Hypertrophy and Recovery from Atrophy

R. A. Seaborne, D. C. Hughes, D. C. Turner, D. J. Owens, L. M. Baehr, P. Gorski, E. A. Semenova, O. V. Borisov, A. K. Larin, D. V. Popov, E. V. Generozov, H. Sutherland, I. I. Ahmetov, J. C. Jarvis, S. C. Bodine, A. P. Sharples

This paper identifies UBR5 as a novel E3 ubiquitin ligase inversely regulated to MuRF1/MAFbx, epigenetically modulated during skeletal muscle recovery from atrophy and hypertrophy, and genetically associated with muscle fiber size and strength traits.

bioRxiv · Apr 29, 2019Physiology