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Julie Helft

Researcher at Curie Institute

Publications -  42
Citations -  9580

Julie Helft is an academic researcher from Curie Institute. The author has contributed to research in topics: CD8 & T cell. The author has an hindex of 23, co-authored 38 publications receiving 8264 citations. Previous affiliations of Julie Helft include Icahn School of Medicine at Mount Sinai & University of Paris.

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Journal ArticleDOI

The dendritic cell lineage: ontogeny and function of dendritic cells and their subsets in the steady state and the inflamed setting.

TL;DR: This review discusses major advances in the understanding of the regulation of DC lineage commitment, differentiation, diversification, and function in situ.
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Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages

TL;DR: It is identified how well-characterized surface markers, including MerTK and FcγR1 (CD64), along with a cluster of previously unidentified transcripts, were distinctly and universally associated with mature tissue macrophages and how these transcripts and the proteins they encode facilitated distinguishing macrophage from dendritic cells.
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Origin of the lamina propria dendritic cell network.

TL;DR: It is shown that monocytes gave rise exclusively to CD103(-)CX(3)CR1(+) lamina propria DCs under the control of macrophage-colony-stimulating factor receptor (M-CSFR) and Fms-like thyrosine kinase 3 (Flt3) ligands.
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The origin and development of nonlymphoid tissue CD103+ DCs

TL;DR: It is shown that two populations of CD11c+MHCII+ cells separated on the basis of CD103 and CD11b expression coexist in most nonlymphoid tissues with the exception of the lamina propria.
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GM-CSF Mouse Bone Marrow Cultures Comprise a Heterogeneous Population of CD11c(+)MHCII(+) Macrophages and Dendritic Cells.

TL;DR: It is demonstrated that CD11c(+)MHCII(+) BMDCs are in fact a heterogeneous group of cells that comprises conventional DCs and monocyte-derived macrophages, and have important implications for the interpretation of a vast array of data obtained with DC culture systems.