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Antonella Fidanza

Researcher at University of Edinburgh

Publications -  21
Citations -  770

Antonella Fidanza is an academic researcher from University of Edinburgh. The author has contributed to research in topics: Induced pluripotent stem cell & Haematopoiesis. The author has an hindex of 8, co-authored 17 publications receiving 434 citations. Previous affiliations of Antonella Fidanza include University of Teramo.

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Genetic programming of macrophages generates an in vitro model for the human erythroid island niche

TL;DR: An in vitro system to model the human EI niche is established using stem cell-derived macrophages to show that inducible expression of a transcription factor, KLF1, enhances RBC production, potentially through the induction of three soluble factors, ANGPTL7, IL33 and SERPINB2.
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Activation of KLF1 Enhances the Differentiation and Maturation of Red Blood Cells from Human Pluripotent Stem Cells.

TL;DR: This study demonstrates the successful use of an inducible genetic programing strategy that could be applied to the production of many other cell lineages from human induced pluripotent stem cells with the integration of programming factors into the AAVS1 locus providing a safer and more reproducible route to the clinic.
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Single-cell analyses and machine learning define hematopoietic progenitor and HSC-like cells derived from human PSCs.

TL;DR: By comparing the single cell transcriptome of in vitro-generated HSC-like cells with those generated within the fetal liver, it is identified transcription factors and molecular pathways that can be exploited in the future to improve the in vitro production of HSCs.
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A human iPSC line capable of differentiating into functional macrophages expressing ZsGreen: a tool for the study and in vivo tracking of therapeutic cells.

TL;DR: Targeting of the AAVS1 locus in iPSCs allows for the production of fully functional, fluorescently tagged human macrophages that can be used for in vivo tracking in disease models and provides a platform for the introduction of factors predicted to modulate and/or stabilize macrophage function.