Author

V. Martinelli

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· 4 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 5 Organism:human· 5 Research Focus:cell signaling & trafficking· 3 Assay:proteomics· 3 Research Focus:cell type annotation· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1

Frequent Co-Authors

B. Fahrenkrog· 5 shared R. Juehlen· 2 shared R. Juhlen· 2 shared A. Dickmanns· 1 shared A. Filosa· 1 shared A. Mendes· 1 shared B. Vanhollebeke· 1 shared C. Rencurel· 1 shared

Activity by Year

2018-2023 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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5 shared papersCell Biology

B. Fahrenkrog

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Author profile →

5 papers

Recent·Most cited

Alteration of actin cytoskeletal organisation in fetal akinesia deformation sequence

R. Juhlen, V. Martinelli, C. Rencurel, B. Fahrenkrog

The paper investigates how silencing FADS-related proteins rapsyn and NUP88 in fetal fibroblasts alters actin cytoskeletal organisation, suggesting a link to impaired neuromuscular transmission in FADS.

bioRxiv · Jun 12, 2023Cell Biology

Mitotic checkpoint protein Mad1 is required for early Nup153 recruitment to chromatin and nuclear envelope integrity

I. Mossaid, G. Chatel, V. Martinelli, M. Vaz, B. Fahrenkrog

This study shows that Mad1 is required for Nup153 recruitment to anaphase chromatin and post-mitotic nuclear envelope reformation, but not for interphase NPC assembly.

bioRxiv · May 20, 2020Cell Biology

Targeted CRM1-inhibition perturbs leukemogenic NUP214 fusion proteins and exerts anti-cancer effects in leukemia cell lines with NUP214 rearrangements

A. Mendes, R. Juehlen, V. Martinelli, B. Fahrenkrog

This study shows that CRM1 inhibition disrupts NUP214 fusion proteins in leukemia cell lines, leading to anti-cancer effects by altering nuclear localization and cell viability.

bioRxiv · Apr 23, 2020Cancer Biology

Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblasts

R. Juhlen, V. Martinelli, C. Vinci, J. Breckpot, B. Fahrenkrog

The paper identifies ciliary defects in fibroblasts from individuals with fetal akinesia deformation sequence and shows that rapsyn and NUP88 are required for primary cilia formation.

bioRxiv · Feb 25, 2020Cell Biology

Mutations in nucleoporin NUP88 cause lethal neuromuscular disorder

E. Bonnin, P. Cabochette, A. Filosa, R. Juehlen, S. Komatsuzaki, M. Hezwani, A. Dickmanns, V. Martinelli, M. Vermeersch, L. Supply, N. Martins, L. Pirenne, G. Ravenscroft, M. Lombard, S. A. Port, , B. Fahrenkrog

This study identifies biallelic NUP88 mutations as a cause of lethal fetal akinesia deformation sequence (FADS) and shows their effects on neuromuscular development in zebrafish and human cells.

bioRxiv · Aug 14, 2018Cell Biology