Publications by authors named "M Tarozzi"

Hematological malignancies are a diverse group of cancers developing in the peripheral blood, the bone marrow or the lymphatic system. Due to their heterogeneity, the identification of novel and advanced molecular signatures is essential for enhancing their characterization and facilitate its translation to new pharmaceutical solutions and eventually to clinical applications. In this study, we collected publicly available microarray data for more than five thousand subjects, across thirteen hematological malignancies.

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Proton beam therapy is considered a step forward with respect to electromagnetic radiation, thanks to the reduction in the dose delivered. Among unwanted effects to healthy tissue, cardiovascular complications are a known long-term radiotherapy complication. The transcriptional response of cardiac tissue from xenografted BALB/c nude mice obtained at 3 and 10 days after proton irradiation covering both the tumor region and the underlying healthy tissue was analyzed as a function of dose and time.

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Background: Human immunodeficiency virus (HIV) infection can be associated with oral mucosal diseases, including oral candidiasis and HPV infection, which are putative indicators of the immune status.

Aim And Methods: This retrospective cross-sectional study was aimed at assessing the prevalence of HIV-related oral mucosal lesions in a cohort of Italian HIV+ patients regularly attending the Clinics of Infectious Diseases.

Results: One hundred seventy-seven (n = 177) patients were enrolled and 30 (16.

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Osteoradionecrosis (ORN) is a serious long-term complication of head and neck radiotherapy (RT), which is often triggered by dental extractions. It results from avascular aseptic necrosis due to irradiated bone damage. ORN is challenging to treat and can lead to severe complications.

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Article Synopsis
  • Creutzfeldt-Jakob disease (CJD) displays diverse symptoms and molecular characteristics, with six main clinical-pathological phenotypes recognized in its sporadic form (sCJD).
  • This study employs multi-omics analysis to explore the molecular differences between the two most common sCJD subtypes, MM1 and VV2, using DNA target sequencing and RNA sequencing on brain tissue.
  • Findings reveal distinct genetic and functional impairments for each subtype, with VV2 linked to issues in dopamine and calcium pathways plus similarities to Parkinson's disease, while MM1 shares traits with various neurodegenerative disorders but lacks a unique profile.
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