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Valentina Minieri

Researcher at Thomas Jefferson University

Publications -  13
Citations -  343

Valentina Minieri is an academic researcher from Thomas Jefferson University. The author has contributed to research in topics: Stem cell & DNA damage. The author has an hindex of 10, co-authored 13 publications receiving 298 citations. Previous affiliations of Valentina Minieri include University of Turin & University College London.

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High basal γH2AX levels sustain self-renewal of mouse embryonic and induced pluripotent stem cells.

TL;DR: It is shown that basal γH2AX levels decrease upon ESC and iPSC differentiation and increase when the cells are treated with self‐renewal‐enhancing small molecules, suggesting a novel function of H2AX that expands the knowledge of this histone variant beyond its role in DNA damage and into a new specialized biological function in mouse pluripotent stem cells.
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Persistent DNA damage-induced premature senescence alters the functional features of human bone marrow mesenchymal stem cells.

TL;DR: A multifaceted consequence of ActD treatment on hMSCs is disclosed that helps to preserve this stem cell pool and prevents damaged cells from undergoing neoplastic transformation, and on the other hand alters their functional effects on the surrounding tissue microenvironment in a way that might worsen their tumour‐promoting behaviour.
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Fluorescent silica nanoparticles improve optical imaging of stem cells allowing direct discrimination between live and early-stage apoptotic cells.

TL;DR: This is the first report that shows nonfunctionalized IRIS Dots can discriminate between live and early-stage apoptotic stem cells (both mesenchymal and embryonic) through a distinct external cell surface distribution.
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Structure of Nascent Chromatin Is Essential for Hematopoietic Lineage Specification.

TL;DR: It is shown here that CD34+ HPCs possess a post-replicative chromatin globally devoid of the repressive histone mark H3K27me3, required for recruitment of lineage-determining transcription factors (TFs) C/EBPα, PU.1, and GATA-1 to DNA just after DNA replication upon cytokine-induced myeloid or erythroid commitment.