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Bruno Delorme

Researcher at French Institute of Health and Medical Research

Publications -  67
Citations -  4370

Bruno Delorme is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Mesenchymal stem cell & Stem cell. The author has an hindex of 26, co-authored 64 publications receiving 4047 citations. Previous affiliations of Bruno Delorme include University of Minnesota & François Rabelais University.

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The In Vitro Migration Capacity of Human Bone Marrow Mesenchymal Stem Cells: Comparison of Chemokine and Growth Factor Chemotactic Activities

TL;DR: The in vitro migration capacity of human BM‐derived MSCs, preincubated or not with the inflammatory cytokines interleukin 1β (IL1β) and tumor necrosis factor α (TNFα), in response to 16 growth factors and chemokines is compared.
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Mesenchymal Stem Cell Features of Ewing Tumors

TL;DR: Gen expression analysis comparing ETs with a variety of normal tissues shows that the profiles of different EWS-FLI1-silenced Ewing cell lines converge toward that of mesenchymal stem cells (MSC).
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Multipotential mesenchymal stem cells are mobilized into peripheral blood by hypoxia.

TL;DR: It is shown that MSCs are regularly observed in the circulating blood of rats and that the circulating MSC pool is consistently and dramatically increased (by almost 15‐fold) when animals are exposed to chronic hypoxia.
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Specific plasma membrane protein phenotype of culture-amplified and native human bone marrow mesenchymal stem cells

TL;DR: The plasma membrane protein phenotype of human culture-amplified and native bone marrow mesenchymal stem cells is studied, and the new marker CD200, because of its specificity and immunomodulatory properties, deserves further in-depth studies.
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Expression Pattern of Connexin Gene Products at the Early Developmental Stages of the Mouse Cardiovascular System

TL;DR: During the early stages of mouse heart maturation, between 8.5 days post coitum (dpc), when the first rhythmic contractions appear, and 14.5 dpc, there is clearly a temporary and asymmetrical regionalization of the Cx40 gene expression that is superimposed on the functional regionalization.