Search Results - "Livia Sertori Finoti"
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A novel iPSC model reveals selective vulnerability of neurons in multiple sulfatase deficiency
Published in Molecular genetics and metabolism (01-02-2024)“…Multiple sulfatase deficiency (MSD) is an ultra-rare, inherited lysosomal storage disease caused by mutations in the gene sulfatase modifying factor 1 (SUMF1)…”
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Exome and RNA‐Seq analyses of an incomplete penetrance variant in USP9X in female‐specific syndromic intellectual disability
Published in American journal of medical genetics. Part A (01-06-2022)“…Pathogenic variants in USP9X, on X chromosome, have been implicated in syndromic intellectual disability (ID) in both males and females with distinct…”
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Methylome-wide analysis in systemic microbial-induced experimental periodontal disease in mice with different susceptibility
Published in Frontiers in cellular and infection microbiology (16-07-2024)“…The study delved into the epigenetic factors associated with periodontal disease in two lineages of mice, namely C57bl/6 and Balb/c. Its primary objective was…”
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Functional Haplotypes in Interleukin 4 Gene Associated with Periodontitis
Published in PloS one (23-01-2017)“…Chronic periodontitis (CP) is an infectious inflammatory disease that affects tooth-supporting structures and in which dental plaque bacteria, immune…”
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Effect of long-term water immersion on the fracture toughness of denture base and reline resins
Published in Gerodontology (01-06-2012)“…doi: 10.1111/j.1741‐2358.2011.00573.x Effect of long‐term water immersion on the fracture toughness of denture base and reline resins purpose: This study…”
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Generation and characterization of multiple sulfatase deficiency iPSC-line and neurogenin-2-induced neurons
Published in Molecular genetics and metabolism (01-02-2024)Get full text
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Patient-derived NGN2-induced neurons recapitulate biochemical phenotypes of multiple sulfatase deficiency in vitro
Published in Molecular genetics and metabolism (01-02-2024)Get full text
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Patient-derived NGN2-induced neurons recapitulate biochemical phenotypes of multiple sulfatase deficiency
Published in Molecular genetics and metabolism (01-02-2024)Get full text
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Evaluation of deviation in implants placed at different depths with a prototype surgical guide: an in vitro study
Published in General dentistry (01-05-2022)“…The aim of this study was to measure the angular and linear deviations between planned and placed dental implant positions at different depths in an in vitro…”
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Long-term evaluation of oral gavage with periodontopathogens or ligature induction of experimental periodontal disease in mice
Published in Clinical oral investigations (01-07-2016)“…Objective To evaluate in long-term periods the destruction of periodontal tissues and bacterial colonization induced by oral gavage with periodontopathogens or…”
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Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome
Published in Genetics in medicine (01-10-2024)“…Hardikar syndrome (HS, MIM #301068) is a female-specific multiple congenital anomaly syndrome characterized by retinopathy, orofacial clefting, aortic…”
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Assessment of Deviations of Implants Installed with Prototyped Surgical Guide and Conventional Guide: In Vitro Study
Published in European journal of dentistry (01-02-2023)“…Abstract Objective The study aimed to assess the angular and linear deviations of implants installed in mannequins aided by surgical guides produced with the…”
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Dentinogenesis imperfecta type II: approach for dental treatment
Published in Revista de Odontologia da UNESP“…INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affects both primary and permanent dentitions. The DI…”
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