Author

X. Heiligenstein

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· 3 Biophysics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:clustering· 2 Assay:electronic health records· 2 Approach:experimental assay· 2 Assay:imaging· 2 Approach:microscopy & imaging analysis· 2 Organism:C. elegans· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

F. Eyraud· 2 shared G. Raposo· 2 shared J. Heiligenstein· 2 shared M. Belle· 2 shared A. Akiva· 1 shared A. Somogyi· 1 shared C. Delevoye· 1 shared C. Kodera· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersCell Biology

F. Eyraud

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Vitrification by high pressure freezing of a wide variety of sample using the HPM Live μ

C. Kodera, Y. Bret, F. Eyraud, J. Heiligenstein, M. Belle, X. Heiligenstein

This study evaluates the effectiveness of high-pressure freezing using HPM Live μ for preserving diverse biological samples for electron microscopy, showing consistent vitrification and minimal artifacts.

bioRxiv · Mar 6, 2024Cell Biology

Catabolism of lysosome-related organelles in color-changing spiders supports intracellular turnover of pigments

F. Figon, I. Hurbain, X. Heiligenstein, S. Trepout, K. Medjoubi, A. Somogyi, C. Delevoye, G. Raposo, J. Casas

This study examines pigment organelle catabolism in crab spiders, showing they belong to the LRO family and undergo intracellular degradation without cell death or secretion.

bioRxiv · Feb 22, 2021Cell Biology

HPM Live μ for full CLEM workflow

X. Heiligenstein, M. de Beer, J. Heiligenstein, F. Eyraud, L. Manet, F. Schmitt, E. Lamers, J. Lindenau, M. Kea-te Lindert, J. Salamero, G. Raposo, N. sommerdijk, M. Belle, A. Akiva

This paper introduces a high-pressure freezing system for cryo-fixation and describes its integration with light microscopy for correlative light and electron microscopy workflows.

bioRxiv · Sep 3, 2020 · PreprintBiophysics

Dynamic-ultrastructural cell volume (3D) correlative microscopy facilitated by intracellular fluorescent nanodiamonds as multi-modal probes

N. Prabhakar, I. Belevich, M. Peurla, X. Heiligenstein, H.-C. Chang, C. Sahlgren, E. Jokitalo, J. Rosenholm

This paper introduces a method using fluorescent nanodiamonds for 3D correlative light and electron microscopy to align multi-modal cell imaging data.

bioRxiv · Oct 29, 2019Cell Biology