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.

Biology Disciplines

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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

PhysiologybioRxivDec 1, 2023

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…·D. V. Popov

DOI 10.1111/acel.14098

humanbulk RNA-seq

𝕏 PostBluesky

PhysiologybioRxivDec 1, 2023

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.

DOI 10.1152/physiolgenomics.00143.2023

Drosophilabulk RNA-seq

𝕏 PostBluesky

PhysiologybioRxivDec 27, 2019

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…·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.

DOI 10.1038/s41598-020-72730-z

humanDNA methylation

𝕏 PostBluesky

PhysiologybioRxivApr 29, 2019

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…·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.

DOI 10.1113/jp278073

𝕏 PostBluesky