Author

Mahbubur Rahman

University of OuluORCID 0000-0002-2233-4656Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Mahbubur Rahman2 papers · International Centre for Diarrhoeal Disease Research

Biology Disciplines

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Molecular Biology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Research Focus:variant calling· 1 Organism:yeast· 1

Frequent Co-Authors

Alexander J. KastaniotisiD· 2 shared J. Kalervo HiltuneniD· 2 shared Ali J. MasudiD· 1 shared Carol L. DieckmanniD· 1 shared Guangyu Jiang· 1 shared Irene M. G. M. HemeliD· 1 shared Kaija J. AutioiD· 1 shared Laura P. Pietikäinen· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 20 mutual co-author links

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2 shared papersPhysiology

Alexander J. KastaniotisORCID

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2 papers

Recent·Most cited

CBR4 is essential for mice but not for skeletal muscle function

Ali J. Masud, Guangyu Jiang, Kaija J. Autio, Mahbubur Rahman, Irene M. G. M. Hemel, J. Kalervo Hiltunen, Alexander J. Kastaniotis

This study shows that CBR4 is essential in mammals but not for skeletal muscle function, as muscle-specific Cbr4 knockout in mice did not cause measurable defects.

bioRxiv · Jul 18, 2026 · PreprintPhysiology

Genetic dissection of the mitochondrial lipoylation pathway in yeast

Laura P. Pietikäinen, Mahbubur Rahman, J. Kalervo Hiltunen, Carol L. Dieckmann, Alexander J. Kastaniotis

The paper characterizes the mitochondrial lipoylation pathway in yeast, showing it can use free lipoic acid and octanoic acid as substrates when activating enzymes are mitochondrial-targeted, and reveals conserved features in mammalian mitochondria.

BMC Biology · Jan 24, 2021Peer-reviewedMolecular Biology