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P A Bernabei

Researcher at University of Florence

Publications -  5
Citations -  473

P A Bernabei is an academic researcher from University of Florence. The author has contributed to research in topics: Haematopoiesis & Progenitor cell. The author has an hindex of 5, co-authored 5 publications receiving 463 citations.

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Incubation of murine bone marrow cells in hypoxia ensures the maintenance of marrow‐repopulating ability together with the expansion of committed progenitors

TL;DR: Severe hypoxia is able to ensure a full maintenance of progenitors sustaining MRA, together with a significant expansion of in vitro‐detectable clonogenic progenitor, including those endowed with replating ability, which could contribute to the improvement of current techniques for the in vitro treatment of human haematopoietic cell populations before transplantation.
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HERG K+ channels activation during beta(1) integrin-mediated adhesion to fibronectin induces an up-regulation of alpha(v)beta(3) integrin in the preosteoclastic leukemia cell line FLG 29.1.

TL;DR: It is demonstrated that the modulation of the electrical potential of the plasma membrane (VREST) is an early integrin-mediated signal, which is related to neurite emission in neuroblastoma cells and appears to be a determinant signal for the up-regulation of αvβ3 integrin, as well as for the increased expression of calcitonin receptor.
Journal Article

Severe hypoxia enhances the formation of erythroid bursts from human cord blood cells and the maintenance of BFU-E in vitro

TL;DR: Results indicate that hypoxia inversely regulates two subsequent phases of erythropoiesis, i.e., it enhances the maintenance of BFU-E and the early development of ERYthroid clones but inhibits the terminal expansion and maturation of these clones.
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A simple, one-step clonal assay allows the sequential detection of committed (CFU-GM-like) progenitors and several subsets of primitive (HPP-CFC) murine progenitors.

TL;DR: This simple, rapid, and versatile method allows the detection of a broad range of hematopoietic progenitors in murine BM, from committed progenitor to largely quiescent, primitive stem cells, as well as the evaluation of the progenites' self‐renewal and proliferative potential.