Author

J. W. Bartsch

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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Cancer Biology· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:proteomics· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Pagenstecher· 2 shared A. Schaefer· 2 shared C. Nimsky· 2 shared O. Schilling· 2 shared A. Grote· 1 shared C.-Y. Chen· 1 shared E. Sabido· 1 shared G. Espadas· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersCancer Biology

A. Pagenstecher

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2 papers

Recent·Most cited

Proteomic profiling of IDH-wildtype Glioblastoma Tissue and Serum uncovers prognostic Subtypes and Marker Candidates

T. Werner, A. Schaefer, M. Hennes, M. Cosenza Contreras, G. Espadas, E. Sabido, L. Cook, A. Pagenstecher, N. Pinter, T. Feilen, A. Grote, C. Nimsky, J. W. Bartsch, O. Schilling

This study identifies proteomic subtypes and recurrence patterns in IDH-wildtype glioblastoma using tissue and serum samples, revealing prognostic markers and proteomic plasticity in recurrent tumors.

bioRxiv · Feb 29, 2024 · PreprintCancer Biology

Changes in calpain-2 expression during glioblastoma progression predisposes tumor cells to temozolomide resistance by minimizing DNA damage and p53-dependent apoptosis

M. N. Stillger, C.-Y. Chen, Z. W. Lai, M. Li, A. Schaefer, A. Pagenstecher, C. Nimsky, J. W. Bartsch, O. Schilling

This study shows that calpain-2 expression in glioblastoma cells reduces TMZ-induced DNA damage and p53-dependent apoptosis, leading to chemoresistance.

bioRxiv · Oct 19, 2022 · PreprintCancer Biology