Author

M. D. Menger

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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Biophysics· 2 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 2 Assay:imaging· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:host-pathogen & immune response· 1 Organism:mouse· 1

Frequent Co-Authors

M. W. Laschke· 3 shared C. Körbel· 2 shared A. Darras· 1 shared A. Kihm· 1 shared C. Rübe· 1 shared C. Wagner· 1 shared E. Ampofo· 1 shared E. Ebert· 1 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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3 shared papersBiophysics

M. W. Laschke

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Red blood cell lingering modulates hematocrit distribution in the microcirculation

Y. Rashidi, G. Simionato, Q. Zhou, T. John, A. Kihm, M. Bendaoud, T. Krueger, M. O. Bernabeu, L. Kaestner, M. W. Laschke, M. D. Menger, C. Wagner, A. Darras

This study quantifies how red blood cell lingering at microvascular bifurcations affects hematocrit distribution and shows its correlation with RBC membrane rigidity and bifurcation geometry.

bioRxiv · Aug 16, 2022Biophysics

Micro-CT analyses of the lung in mice: Parameters influencing the radiation dose and acquisition quality

S. Körner, C. Körbel, Y. Dzierma, K. Speicher, M. W. Laschke, C. Rübe, M. D. Menger, M. Linxweiler

The paper evaluates how different filters and resolutions affect radiation dose and image quality in micro-CT scans of mouse lungs.

bioRxiv · Apr 27, 2022 · PreprintBiophysics

Suppression of endothelial miR-22-3p mediates non-small cell lung cancer cell-induced angiogenesis

Y. Gu, G. Pais, V. Becker, C. Körbel, E. Ampofo, E. Ebert, J. Hohneck, N. Ludwig, E. Meese, R. M. Bohle, Y. Zhao, M. D. Menger, M. W. Laschke

The paper shows that reduced endothelial miR-22-3p in NSCLC tissues promotes angiogenesis by inhibiting SIRT1 and FGFR1, leading to AKT/mTOR inactivation and tumor growth.

bioRxiv · Apr 4, 2021Cancer Biology