Author

C. E. Malnou

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 Biochemistry· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Assay:proteomics· 3 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1

Frequent Co-Authors

H. Martin· 3 shared G. Cartron· 2 shared G. D'Angelo· 2 shared G. Raposo· 2 shared I. Hurbain· 2 shared J. Izopet· 2 shared J.-M. Mansuy· 2 shared M. Benard· 2 shared

Activity by Year

2018-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersCell Biology

H. Martin

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Human Cytomegalovirus modifies placental small extracellular vesicle secretion and composition towards a proviral phenotype to enhance infection of fetal recipient cells

M. Bergamelli, H. Martin, Y. Aubert, J.-M. Mansuy, M. Marcellin, O. Burlet-Schiltz, I. Hurbain, G. Raposo, J. Izopet, T. Fournier, A. Benchoua, M. Benard, M. Groussolles, G. Cartron, Y. Tanguy le Gac, , C. E. Malnou

This study shows hCMV infection alters placental sEVs to promote viral spread to fetal cells.

bioRxiv · Nov 18, 2021Cell Biology

Human cytomegalovirus infection changes the pattern of surface markers of small extracellular vesicles isolated from first trimester placental histocultures

M. Bergamelli, H. Martin, M. Benard, J. Ausseil, J.-M. Mansuy, I. Hurbain, M. Mouysset, M. Groussolles, G. Cartron, Y. Tanguy le Gac, N. Moinard, E. Suberbielle, J. Izopet, C. Tscherning, G. Raposo, , C. E. Malnou

This study examines how human cytomegalovirus infection alters surface markers on placental-derived small extracellular vesicles from first trimester histocultures.

Frontiers in Cell and Developmental Biology · Sep 10, 2021Peer-reviewedCell Biology

MeCP2-E1 isoform is a dynamically expressed, weakly DNA-bound protein with different protein and DNA interactions compared to MeCP2-E2

A. Martinez de Paz, L. Khajavi, H. Martin, R. Claveria-Gimeno, S. tom Dieck, M. S. Cheema, J. V. Sanchez-Mut, M. Moksa, A. Carles, N. Brodie, T. I. Sheikh, M. Freeman, E. Petrotchenko, C. Borchers, E. Schuman, , J. Ausio

This study compares MeCP2-E1 and E2 isoforms, showing differences in DNA binding, protein interactions, and dynamic behavior, with implications for their functional roles in chromatin regulation.

bioRxiv · Aug 17, 2018Biochemistry