Author

F. Gremse

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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Physiology· 2 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 3 Organism:mouse· 3 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1

Frequent Co-Authors

A. Babler· 2 shared M. Herrmann· 2 shared W. Jahnen-Dechent· 2 shared A. Buescher· 1 shared A. Fragoulis· 1 shared C. John· 1 shared C. Schmitz· 1 shared D. Moeckel· 1 shared

Activity by Year

2018-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersPhysiology

A. Babler

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Microvasculopathy, Luminal Calcification and Premature Aging in Fetuin-A Deficient Mice

M. Herrmann, A. Babler, I. Moshkova, F. Gremse, F. Kiessling, U. Kusebauch, V. Nelea, R. Kramann, R. L. Moritz, M. D. McKee, W. Jahnen-Dechent

This study shows fetuin-A deficiency leads to microvascular calcification and premature aging in mice, associated with thrombosis and fibrosis rather than osteochondrogenic differentiation.

bioRxiv · Oct 4, 2019 · PreprintPhysiology

Microvasculopathy And Soft Tissue Calcification In Mice Are Governed by Fetuin-A, Pyrophosphate And Magnesium

A. Babler, C. Schmitz, A. Buescher, M. Herrmann, F. Gremse, T. G. Gorgels, J. Floege, W. Jahnen-Dechent

The paper identifies fetuin-A, pyrophosphate, and magnesium as key regulators of calcification in fetuin-A deficient mice and shows that their combined deficiency can be mitigated by dietary or parenteral supplementation.

bioRxiv · Oct 1, 2019Physiology

Macrophages protect against loss of adipose tissue during cancer cachexia

M. Erdem, D. Moeckel, S. Jumpertz, C. John, A. Fragoulis, I. Rudolph, J. Wulfmeier, J. Springer, H. Horn, M. Koch, G. Lurje, T. Lammers, G. van der Kroft, F. Gremse, T. Cramer

This study shows that defective myeloid cell-mediated inflammation enhances cachexia in HCC mice, suggesting macrophages protect against fat loss in cancer cachexia.

bioRxiv · Sep 27, 2018Cancer Biology