Author

J. Scheller

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 Biochemistry· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 4 Approach:experimental assay· 4 Research Focus:cell type annotation· 3 Organism:human· 3 Assay:proteomics· 2 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

M. R. Ahmadian· 3 shared R. P. Piekorz· 3 shared A. Lang· 2 shared A. Borchardt· 1 shared A. Hahn· 1 shared A. Reichert· 1 shared A. S. Reichert· 1 shared A. Schaenzer· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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3 shared papersCell Biology

M. R. Ahmadian

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

CoCl2 triggered pseudohypoxic stress induces proteasomal degradation of SIRT4 via polyubiquitination of lysines K78 and K299

N. Hampel, J. Georgy, M. Mehrabipour, A. Lang, J. Scheller, M. R. Ahmadian, D. M. Floss, R. P. Piekorz

This study shows CoCl2 induces SIRT4 degradation through proteasomal polyubiquitination at K78 and K299, and via autophagy/mitophagy.

bioRxiv · May 16, 2023 · PreprintBiochemistry

Alteration of myocardial structure and function in RAF1associated Noonan syndrome: Insights from cardiac disease modeling based on patient-derived iPSCs

S. Nakhaei-Rad, F. Bazgir, J. Dahlmann, A. V. Busley, M. Buchholzer, F. Haghighi, A. Schaenzer, A. Hahn, S. Koetter, D. Schanze, R. Anand, F. Funk, A. Borchardt, A. V. Kronenbitter, J. Scheller, , M. R. Ahmadian

This study uses patient-derived iPSCs to model RAF1-associated Noonan syndrome and identifies sarcomere structural abnormalities linked to cardiac dysfunction.

bioRxiv · Jan 22, 2022 · PreprintCell Biology

Investigation of fascin1, a marker of mature dendritic cells, reveals a New role for IL-6 signaling in chemotaxis.

F. Matsumura, R. Polz, S. Singh, J. Scheller, S. Yamashiro

This study shows that IL-6 signaling is required for chemotaxis of mature dendritic cells by facilitating CCR7 internalization and recycling.

The Journal of Immunology · Aug 1, 2021Peer-reviewedImmunology

Subcellular localization and mitotic interactome analyses identify SIRT4 as a centrosomally localized and microtubule associated protein

L. Bergmann, A. Lang, C. Bross, S. Altinoluk-Hambuechen, I. Fey, N. Overbeck, A. Stefanski, C. Wiek, P. Verhuelsdonk, C. Mielke, D. Sohn, K. Stühler, H. Hanenberg, R. U. Jänicke, J. Scheller, , R. P. Piekorz

This study identifies SIRT4 as a centrosomal and microtubule-associated protein that delays mitotic progression and reduces cell proliferation.

bioRxiv · Feb 17, 2020Cell Biology