Author

M. Hart

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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Cell Biology· 2 Animal Behavior & Cognition· 1 Bioengineering· 1 Cancer Biology· 1 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 8 Research Focus:cell signaling & trafficking· 3 Research Focus:cell type annotation· 3 Research Focus:development & morphogenesis· 3 Research Focus:host-pathogen & immune response· 3 Organism:human· 3 Research Focus:cancer & tumor microenvironment· 2 Research Focus:drug response / drug discovery· 2

Frequent Co-Authors

E. Meese· 2 shared V. M. Draviam· 2 shared A. A. Blackwell· 1 shared A. Denger· 1 shared A. Jamwal· 1 shared A. K. Yanamandra· 1 shared A. Knoerck· 1 shared B. Farrell· 1 shared

Activity by Year

2018-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 11 mutual co-author links

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2 shared papersCancer Biology

E. Meese

Mutual co-authors in cluster

Author profile →

8 papers

Recent·Most cited

Th17 cells target the metabolic miR-142-5p-SDHC/SDHD axis promoting invasiveness and progression of cervical cancers

M. Pohlers, S. Gies, T. Taenzer, R. Stroeder, L. Theobald, N. Ludwig, Y.-J. Kim, R. Bohle, E. F. Solomayer, E. Meese, M. Hart, B. Walch-Rueckheim

This study identifies a Th17 cell-driven miR-142-5p-SDHC/SDHD axis that enhances cervical cancer migration and invasion, with clinical correlations to metastasis and survival.

bioRxiv · Jun 29, 2023 · PreprintCancer Biology

Structure of the PfRCR complex which bridges the malaria parasite and erythrocyte during invasion

B. Farrell, N. Alam, M. Hart, A. Jamwal, R. Ragotte, H. Walters-Morgan, S. Draper, E. Knuepfer, M. K. Higgins

This paper determines the structure of the PfRCR complex using cryogenic-electron microscopy, revealing its modular architecture and interaction with erythrocyte receptors, which informs vaccine design.

bioRxiv · Jan 30, 2023Microbiology

String-Pulling as a Behavioral Assessment of Skilled Forelimb Motor Function in a Middle Cerebral Artery Occlusion Rat Model

M. Hart, A. A. Blackwell, I. Q. Whishaw, D. G. Wallace, J. L. Cheatwood

This study evaluates string-pulling behavior in a rat model of stroke to assess bilateral motor function and finds disruptions in coordinated hand movements following middle cerebral artery occlusion.

bioRxiv · Mar 31, 2022 · PreprintAnimal Behavior & Cognition

High glucose enhances antigen-independent CTL killing via TRAIL

W. Yang, A. Denger, C. Diener, F. Kueppers, L. Soriano-Baguet, G. Schaefer, A. K. Yanamandra, R. Zhao, A. Knoerck, E. C. Schwarz, M. Hart, F. Lammert, L. P. Roma, D. Brenner, G. Grigorios Christidis, , B. Qu

This study shows high glucose increases TRAIL expression in CTLs, promoting beta cell apoptosis, and identifies metformin and vitamin D as synergistic therapies to mitigate this effect.

bioRxiv · Aug 4, 2021Immunology

Multinucleation Associated DNA Damage causes quiescence despite compromised p53

M. Hart, S. D. Adams, V. M. Draviam

The paper investigates how multinucleation, a form of nuclear atypia, causes quiescence in p53-compromised cells through persistent DNA damage signaling, distinct from other nuclear atypias.

bioRxiv · Dec 22, 2020 · PreprintCell Biology

Altered substance P signaling underlies perivascular sensory nerve dysfunction in inflammatory bowel disease

C. E. Norton, E. A. Grunz-Borgmann, M. Hart, B. W. Jones, C. M. Franklin, E. M. Boerman

This study identifies altered substance P signaling in perivascular nerves of IBD, leading to impaired vascular function and blood flow.

bioRxiv · Apr 29, 2020 · PreprintPhysiology

Bioresponsive Microspheres for On-demand Delivery of Anti-inflammatory Cytokines for Osteoarthritis

E. Park, M. Hart, B. Rolauffs, J. P. Stegemann, R. T. Annamalai

This paper develops bioresponsive microspheres that release anti-inflammatory cytokines on-demand in osteoarthritic joints, reducing inflammation and preserving cartilage.

bioRxiv · May 15, 2019 · PreprintBioengineering

MARK2/Par1b present at retraction fibres corrects spindle off-centering induced by actin disassembly

M. Hart, I. Zulkipli, R. L. Shrestha, D. D. Dang, D. Conti, I. Kujawiak, V. M. Draviam

The paper identifies MARK2/Par1b as a component of retraction fibres that corrects spindle off-centering and regulates G1-S progression.

bioRxiv · Dec 31, 2018Cell Biology