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Valentina Di Gialleonardo

Researcher at Memorial Sloan Kettering Cancer Center

Publications -  18
Citations -  889

Valentina Di Gialleonardo is an academic researcher from Memorial Sloan Kettering Cancer Center. The author has contributed to research in topics: In vivo & Biodistribution. The author has an hindex of 11, co-authored 18 publications receiving 741 citations. Previous affiliations of Valentina Di Gialleonardo include University Medical Center Groningen & Sapienza University of Rome.

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ATM-ATR–dependent up-regulation of DNAM-1 and NKG2D ligands on multiple myeloma cells by therapeutic agents results in enhanced NK-cell susceptibility and is associated with a senescent phenotype

TL;DR: It is shown that myeloma cells treated with low doses of therapeutic agents commonly used in the management of patients with MM, such as doxorubicin, melphalan, and bortezomib, up-regulate DNAM-1 and NKG2D ligands and suggest that NK cells represent an immunosurveillance mechanism toward cells undergoing stress-induced senescent programs.
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N-(4-18F-Fluorobenzoyl)Interleukin-2 for PET of Human-Activated T Lymphocytes

TL;DR: 18F-FB-IL2 is stable, is biologically active, and allows in vivo detection of activated T lymphocytes, and capable of stimulating T cells to an extent similar to native IL2.
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In Vivo Imaging of Glutamine Metabolism to the Oncometabolite 2-Hydroxyglutarate in IDH1/2 Mutant Tumors.

TL;DR: It is demonstrated that in vivo HP [1-13C] glutamine can be used to non-invasively measure glutamine-derived HP 2-HG production, and that, in a context-dependent manner, glutamines can be a primary carbon source for 2- HG production in mutant IDH tumors.
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Non-invasive PET Imaging of PARP1 Expression in Glioblastoma Models

TL;DR: ParPi is a selective PARP1 imaging agent that can be used to visualize glioblastoma in xenograft and orthotopic mouse models with high precision and good signal/noise ratios and offers new opportunities to non-invasively image tumor growth and monitor interventions.
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Imaging of β-Cell Mass and Insulitis in Insulin-Dependent (Type 1) Diabetes Mellitus

TL;DR: The availability of a noninvasively quantify β-cell mass in vivo could be useful for understanding the natural history of human insulin-dependent (type 1) diabetes mellitus, to early diagnose children at risk to develop overt diabetes, and to select patients to be treated with immunotherapies aimed at blocking the insulitis.