Guillaume Voisinne
Affiliations: | 2011-2014 | Computational Biology | Memorial Sloan Kettering, Hauppauge, NY, United States |
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Ruminski K, Celis-Gutierrez J, Jarmuzynski N, et al. (2023) Mapping the SLP76 interactome in T cells lacking each of the GRB2-family adaptors reveals molecular plasticity of the TCR signaling pathway. Frontiers in Immunology. 14: 1139123 |
Voisinne G, Locard-Paulet M, Froment C, et al. (2022) Kinetic proofreading through the multi-step activation of the ZAP70 kinase underlies early T cell ligand discrimination. Nature Immunology. 23: 1355-1364 |
Nicolas P, Ollier J, Mori D, et al. (2022) Systems-level conservation of the proximal TCR signaling network of mice and humans. The Journal of Experimental Medicine. 219 |
Zhai Y, Celis-Gutierrez J, Voisinne G, et al. (2020) Opposing regulatory functions of the TIM3 (HAVCR2) signalosome in primary effector T cells as revealed by quantitative interactomics. Cellular & Molecular Immunology |
Locard-Paulet M, Voisinne G, Froment C, et al. (2020) LymphoAtlas: a dynamic and integrated phosphoproteomic resource of TCR signaling in primary T cells reveals ITSN2 as a regulator of effector functions. Molecular Systems Biology. 16: e9524 |
Voisinne G, Kersse K, Chaoui K, et al. (2019) Quantitative interactomics in primary T cells unveils TCR signal diversification extent and dynamics. Nature Immunology |
Voisinne G, Gonzalez de Peredo A, Roncagalli R. (2018) CD5, an Undercover Regulator of TCR Signaling. Frontiers in Immunology. 9: 2900 |
Le Floc'h A, Tanaka Y, Bantilan NS, et al. (2017) Correction: Annular PIP3 accumulation controls actin architecture and modulates cytotoxicity at the immunological synapse. The Journal of Experimental Medicine |
Voisinne G, García-Blesa A, Chaoui K, et al. (2016) Co-recruitment analysis of the CBL and CBLB signalosomes in primary T cells identifies CD5 as a key regulator of TCR-induced ubiquitylation. Molecular Systems Biology. 12: 876 |
Voisinne G, Nixon BG, Melbinger A, et al. (2015) T Cells Integrate Local and Global Cues to Discriminate between Structurally Similar Antigens. Cell Reports. 11: 1208-19 |