Author

Rabea Hokamp

Düsseldorf University Hospital

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

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Christiane LoerchiD· 2 shared James AdjayeiD· 2 shared Nina GraffmanniD· 2 shared Wasco WruckiD· 2 shared Annika WittichiD· 1 shared Julian Reiss· 1 shared Malin FrommeiD· 1 shared Ole PleßiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

9 top collaborators · 30 mutual co-author links

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2 shared papersCell Biology

Christiane LoerchORCID

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2 papers

Recent·Most cited

SAHA increases chaperone expression and reduces Z-alpha-1-antitrypsin polymers in a patient specific iPSC-based liver model for alpha-1-antitrypsin deficiency

Nina Graffmann, Rabea Hokamp, Christiane Loerch, Malin Fromme, Wasco Wruck, Pavel Strnad, James Adjaye

The paper uses iPSC-derived liver cells to show SAHA reduces Z-alpha-1-antitrypsin polymers by increasing chaperone expression in AATD models.

Stem Cell Research & Therapy · Oct 27, 2026Peer-reviewedCell Biology

DPP4 inhibition affects metabolism and inflammation associated pathways in hiPSC-derived steatotic HLCs

Christiane Loerch, Wasco Wruck, Annika Wittich, Rabea Hokamp, Julian Reiss, Ole Pleß, James Adjaye, Nina Graffmann

This study shows DPP4 inhibition alters metabolism and inflammation pathways in steatotic hiPSC-derived HLCs, suggesting potential therapeutic benefits for MAFLD.

Frontiers in Cell and Developmental Biology · Feb 26, 2026Peer-reviewedCell Biology