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Cristina Magnoni

Researcher at University of Modena and Reggio Emilia

Publications -  96
Citations -  2708

Cristina Magnoni is an academic researcher from University of Modena and Reggio Emilia. The author has contributed to research in topics: Skin cancer & Melanoma. The author has an hindex of 22, co-authored 96 publications receiving 2314 citations. Previous affiliations of Cristina Magnoni include University of Padua.

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Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells

TL;DR: Ex vivo gene therapy of JEB is feasible and leads to full functional correction of the disease, and retroviral integration site analysis indicated that the regenerated epidermis is maintained by a defined repertoire of transduced stem cells.
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Enhancement of DNA repair in human skin cells by thymidine dinucleotides: evidence for a p53-mediated mammalian SOS response.

Abstract: Thymidine dinucleotide (pTpT) stimulates melanogenesis in mammalian pigment cells and intact skin, mimicking the effects of UV irradiation and UV-mimetic DNA damage. Here it is shown that, in addition to tanning, pTpT induces a second photoprotective response, enhanced repair of UV-induced DNA damage. This enhanced repair results in a 2-fold increase in expression of a UV-damaged chloramphenicol acetyltransferase expression vector transfected into pTpT-treated skin fibroblasts and keratinocytes, compared with diluent-treated cells. Direct measurement of thymine dimers and (6–4) photoproducts by immunoassay demonstrates faster repair of both of these UV-induced photoproducts in pTpT-treated fibroblasts. This enhanced repair capacity also improves cell survival and colony-forming ability after irradiation. These effects of pTpT are accomplished, at least in part, by the up-regulation of a set of genes involved in DNA repair (ERCC3 and GADD45) and cell cycle inhibition (SDI1). At least two of these genes (GADD45 and SDI1) are known to be transcriptionally regulated by the p53 tumor suppressor protein. Here we show that pTpT activates p53, leading to nuclear accumulation of this protein, and also increases the specific binding of this transcription factor to its DNA consensus sequence.
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Thickness and echogenicity of the skin in children as assessed by 20-MHz ultrasound.

TL;DR: Whereas skin thickness shows a gradual increase from birth to adulthood, maturation of the skin leads to variations in the intensity of its echogenicity, depending on the different skin areas, which greatly varies in different phases of life.