Author

V. Timmerman

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Cell Biology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell signaling & trafficking· 3 Approach:experimental assay· 3 Organism:human· 3 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:electronic health records· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

B. Asselbergh· 3 shared E. Adriaenssens· 2 shared A. Baldwin· 1 shared A. Kremer· 1 shared A. Poletti· 1 shared B. Tedesco· 1 shared F. Antoniani· 1 shared F.-J. Müller· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersCell Biology

B. Asselbergh

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes

E. Adriaenssens, B. Tedesco, L. Mediani, B. Asselbergh, V. Crippa, F. Antoniani, S. Carra, A. Poletti, V. Timmerman

This study shows that BAG3 Pro209 mutants cause aggresome formation and disrupt chaperone-assisted selective autophagy, leading to protein homeostasis loss regardless of clinical phenotype.

bioRxiv · Mar 5, 2020Cell Biology

Dysregulated interactions triggered by a neuropathy-causing mutation in the IPV motif of HSP27

T. R. Alderson, E. Adriaenssens, B. Asselbergh, I. Pritisanac, H. Y. Gastall, M. A. Walti, J. M. Louis, V. Timmerman, A. Baldwin, J. L. P. Benesch

This study investigates how the P182L mutation in HSP27's IxI/V motif disrupts protein interactions, leading to aggregation and disease.

bioRxiv · Sep 10, 2019 · PreprintBiochemistry

Sensory neuropathy-causing mutations in ATL3 cause aberrant ER membrane tethering

M. Krols, S. Detry, B. Asselbergh, L. Almeida-Souza, A. Kremer, S. Lippens, R. de Rycke, V. De Winter, F.-J. Müller, I. Kurth, H. T. McMahon, S. N. Savvides, V. Timmerman, S. Janssens

This study shows that mutations in ATL3 cause aberrant ER membrane tethering, disrupting ER network organization and contributing to sensory neuropathy.

bioRxiv · Apr 5, 2018Cell Biology