Author

C. ten Brink

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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Research Focus:cell type annotation· 2 Research Focus:clustering· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Assay:fluorescence / live-cell microscopy· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1

Frequent Co-Authors

J. Klumperman· 2 shared N. Liv· 2 shared T. Veenendaal· 2 shared A. Carter· 1 shared A. Fasano· 1 shared A. M. Lozano· 1 shared C. Burns· 1 shared C. de Heus· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersCell Biology

J. Klumperman

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Bimodal Endocytic Probe for Three-Dimensional Correlative Light and Electron Microscopy

J. Fermie, L. de Jager, H. Foster, T. Veenendaal, C. de Heus, S. van Dijk, C. ten Brink, V. Oorschot, L. Yang, W. Li, W. Muller, S. Howes, A. Carter, F. Foerster, G. Posthuma, , N. Liv

This paper introduces fBSA-Au, a bimodal endocytic tracer for 2D and 3D CLEM, enabling accurate registration of fluorescence to EM data with sub-200 nm precision.

bioRxiv · May 18, 2021Cell Biology

VPS41 recessive mutation causes ataxia and dystonia with retinal dystrophy and mental retardation by inhibiting HOPS function and mTORC1 signaling

R. E. N. van der Welle, R. Jobling, C. Burns, P. Sanza, C. ten Brink, A. Fasano, L. Chen, F. J. Zwartkruis, S. Zwakenberg, E. F. Griffin, J. van der Beek, T. Veenendaal, N. Liv, S. Blaser, C. Sepulveda, , J. Klumperman

This paper identifies VPS41 mutations causing neurodegenerative disease by disrupting HOPS function and mTORC1 signaling, leading to lysosomal dysfunction and impaired autophagy.

bioRxiv · Dec 18, 2019 · PreprintCell Biology