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Philippe Robert

Researcher at University of Oslo

Publications -  108
Citations -  1804

Philippe Robert is an academic researcher from University of Oslo. The author has contributed to research in topics: Biology & Computer science. The author has an hindex of 16, co-authored 95 publications receiving 1135 citations. Previous affiliations of Philippe Robert include Oslo University Hospital & Centre national de la recherche scientifique.

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Glutamine-dependent α-ketoglutarate production regulates the balance between T helper 1 cell and regulatory T cell generation

TL;DR: It is shown that exogenous nutrient availability regulated the differentiation of naïve CD4+ T cells into distinct subsets, and α-ketoglutarate (αKG), the glutamine-derived metabolite that enters into the mitochondrial citric acid cycle, acted as a metabolic regulator of CD4- T cell differentiation.
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A compact vocabulary of paratope-epitope interactions enables predictability of antibody-antigen binding.

TL;DR: In this paper, the authors identify structural interaction motifs, which together compose a commonly shared structure-based vocabulary of paratope-epitope interactions, and show that this vocabulary enables the machine learnability of antibody-antigen binding using generative machine learning.
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A Novel Leukocyte Adhesion Deficiency III Variant: Kindlin-3 Deficiency Results in Integrin and Nonintegrin-Related Defects in Different Steps of Leukocyte Adhesion

TL;DR: The results suggest looking for a possible kindlin-3 involvement in membrane dynamical event independent of integrin-mediated adhesion in a patient with a new mutation of FERMT3 and lack of kindlins-3 expression in platelets and leukocytes.
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Force Measurements of TCR/pMHC Recognition at T Cell Surface

TL;DR: The rupture forces and adhesion frequencies of single recognition complexes between an affinity selected peptide/MHC complex and a TCR at a murine hybridoma surface were measured using Atomic Force Microscopy to help the dissection of the sequential steps by which the TCR reads the peptide or MHC complex in order to control T cell activation.