Author

J. Hampe

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· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 1 Organism:human· 1 Assay:imaging· 1 Approach:microscopy & imaging analysis· 1 Assay:proteomics· 1 Research Focus:spatial domain detection· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Hendriks· 1 shared A. Herrmann· 1 shared C. Horenburg· 1 shared C. Rocken· 1 shared C. Schafmayer· 1 shared D. Luthjohann· 1 shared D. Vasiljevic· 1 shared F. Rost· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperPathology

A. Hendriks

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

UFMylation regulates translational homeostasis and cell cycle progression

I. A. Gak, D. Vasiljevic, T. Zerjatke, L. Yu, M. Brosch, T. I. Roumeliotis, C. Horenburg, N. Klemm, G. Bakos, A. Herrmann, J. Hampe, I. Glauche, J. S. Choudhary, J. Mansfeld

This study shows UFMylation regulates translation and cell cycle progression by controlling eIF4F complex assembly and ribosome recruitment, independent of stress response pathways.

bioRxiv · Feb 3, 2020 · PreprintCell Biology

3D spatially-resolved geometrical and functional models of human liver tissue reveal new aspects of NAFLD progression

F. Segovia-Miranda, H. Morales-Navarrete, M. Kucken, V. Moser, S. Seifert, U. Repnik, F. Rost, A. Hendriks, S. Hinz, C. Rocken, D. Luthjohann, Y. Kalaidzidis, C. Schafmayer, L. Brusch, J. Hampe, M. Zerial

This study creates 3D spatial models of human liver tissue to identify new morphometric parameters and topological defects linked to NAFLD progression.

bioRxiv · Mar 9, 2019Pathology