Author

Mayank Verma

University of MinnesotaORCID 0000-0003-0167-0842Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:cell type annotation· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

Atsushi AsakuraiD· 2 shared Yoko AsakuraiD· 2 shared Allison P KanniD· 1 shared Chiara VillaiD· 1 shared Dennis Keefe· 1 shared Eyemen KheiriD· 1 shared Francesca MurgantiiD· 1 shared Guo‐Hua FongiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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2 shared papersDevelopmental Biology

Atsushi AsakuraORCID

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3 papers

Recent·Most cited

Cell BiologyEMBO ReportsPeer-reviewedNov 4, 2026

CD90 identifies distinct fractions of muscle stem cells with different modalities of activation and quiescence maintenance

Eyemen Kheir, Michela Libergoli, Serena Di Savino…·Stefano Biressi

The paper identifies CD90 as a marker distinguishing two muscle stem cell subpopulations with different activation kinetics and quiescence maintenance mechanisms in mice and humans.

1 citation

mousehuman

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Developmental BiologyeLifePeer-reviewedJun 6, 2024

Endothelial cell signature in muscle stem cells validated by VEGFA-FLT1-AKT1 axis promoting survival of muscle stem cell

Mayank Verma, Yoko Asakura, Xuerui Wang…·Atsushi Asakura

The paper identifies the VEGFA-FLT1-AKT1 pathway as promoting muscle stem cell survival through endothelial gene expression.

38 citationstop 4%

mousebulk RNA-seq

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Developmental BiologyPLoS GeneticsPeer-reviewedDec 26, 2019

Amelioration of muscular dystrophy phenotype in mdx mice by inhibition of Flt1

Mayank Verma, Yuko Shimizu‐Motohashi, Yoko Asakura…·Atsushi Asakura

This study shows that inhibiting Flt1 improves the muscular dystrophy phenotype in mdx mice by increasing vascular density and reducing muscle pathology.

29 citations

mouseexperimental assay

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