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Roberta Visconti

Researcher at University of Naples Federico II

Publications -  68
Citations -  4451

Roberta Visconti is an academic researcher from University of Naples Federico II. The author has contributed to research in topics: Gene & Phosphorylation. The author has an hindex of 33, co-authored 61 publications receiving 4144 citations. Previous affiliations of Roberta Visconti include National Research Council & Mediterranea University of Reggio Calabria.

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Journal Article

High level expression of the HMGI (Y) gene during embryonic development.

TL;DR: It is demonstrated that the HMGI (Y) gene is expressed at very low levels in normal adult tissues, whereas in embryonic tissues it is expressed in high levels comparable to those detected in neoplastic tissues.
Journal Article

New insights on oxidative stress in cancer.

TL;DR: Recent findings that relate oxidative stress to cancer-associated conditions, such as chronic inflammation, steroid hormone signaling and altered chromosome segregation, are highlighted and how these studies may identify new targets for the development of drugs and strategies for cancer prevention and cure is discussed.
Journal Article

RET/PTC oncogene activation is an early event in thyroid carcinogenesis

TL;DR: It is demonstrated, by using a combined immunohistochemical and reverse transcriptase-polymerase chain reaction based approach, that RET/PTC activation is present in 11 out of 26 occult thyroid papillary carcinomas analysed and represents an early event in the process of thyroid cell transformation.
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Inhibition of Th1 immune response by glucocorticoids: dexamethasone selectively inhibits IL-12-induced Stat4 phosphorylation in T lymphocytes.

TL;DR: Blocking IL-12-induced Stat4 phosphorylation appears to be a new suppressive action of glucocorticoids on the Th1 cellular immune response and may help explain the glucoc Corticoid-induced shift toward the Th2 humoral immune response.
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Cell cycle checkpoint in cancer: a therapeutically targetable double-edged sword

TL;DR: Developing concepts on how targeting cell cycle checkpoints may provide substantial improvement to cancer therapy are summarized.