Author

S. Lameiras

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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Immunology· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Organism:human· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Assay:CITE-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:genetic perturbation / CRISPR· 1

Frequent Co-Authors

S. Baulande· 2 shared A. Nicolas· 1 shared A. Seguin-Givelet· 1 shared A. Teissandier· 1 shared A. Vincent-Salomon· 1 shared A. Walczak· 1 shared B. Buttard· 1 shared C. Bromley· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersImmunology

S. Baulande

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Tissue-resident FOLR2+ macrophages associate with tumor-infiltrating CD8+ T cells and with increased survival of breast cancer patients.

R. N. Ramos, Y. Missolo-Koussou, Y. Gerber-Ferder, C. Bromley, M. Bugatti, N. G. Nunez, J. Boari Tosello, W. Richer, J. Denizeau, C. Sedlik, P. Caudana, F. Kotsias, L. L. Niborski, S. Viel, M. Bohec, , J. Helft

The paper identifies FOLR2+ macrophages in breast cancer that correlate with improved patient survival and co-localize with CD8+ T cells across multiple cancers.

bioRxiv · Apr 12, 2021 · PreprintImmunology

m6A RNA methylation regulates the fate of endogenous retroviruses

T. Chelmicki, E. Roger, A. Teissandier, S. Rucli, F. Dossin, M. Dura, C. Fouassier, S. Lameiras, D. Bourc'his

This study identifies m6A RNA methylation as a mechanism to restrict endogenous retroviruses by destabilizing their transcripts in mouse embryonic stem cells.

Nature · Jan 13, 2021Peer-reviewedCell Biology

Contribution of resident and circulating precursors to tumor-infiltrating CD8+ T cell populations in non-small cell lung cancer patients

C. Metoikidou, P. Gueguen, T. Dupic, M. Lawand, C. Goudot, S. Baulande, S. Lameiras, O. Lantz, N. Girard, A. Seguin-Givelet, M. Lefevre, T. Mora, A. Walczak, J. J. Waterfall, S. Amigorena

The paper identifies two CD8+ TIL subpopulations in NSCLC, one circulating and one resident, which transition into terminally differentiated cells through a unique state.

bioRxiv · Aug 14, 2020Immunology