Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Andrea Bernini"'
Autor:
Andrea Bernini
Publikováno v:
Pylon, Vol 5 (2024)
Externí odkaz:
https://doaj.org/article/f4aacd209bca497386d7897047160256
Autor:
Luisa Frusciante, Michela Geminiani, Alfonso Trezza, Tommaso Olmastroni, Pierfrancesco Mastroeni, Laura Salvini, Stefania Lamponi, Andrea Bernini, Daniela Grasso, Elena Dreassi, Ottavia Spiga, Annalisa Santucci
Publikováno v:
Marine Drugs, Vol 22, Iss 5, p 226 (2024)
Utilizing plant-based resources, particularly their by-products, aligns with sustainability principles and circular bioeconomy, contributing to environmental preservation. The therapeutic potential of plant extracts is garnering increasing interest,
Externí odkaz:
https://doaj.org/article/2b341c8733dd4dcb82e29a840502a53a
Autor:
Maria Chiara Maccarone, Daniele Coraci, Andrea Bernini, Nicola Sarandria, Marta Rossella Valente, Anna Chiara Frigo, Yannis Dionyssiotis, Stefano Masiero
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionThe progressive loss of skeletal muscle mass, strength, and function that frequently occurs as people get older is referred to as sarcopenia. Elderly musculoskeletal aging, sarcopenia, and obesity are all intimately connected. Our study
Externí odkaz:
https://doaj.org/article/910b5ed5806749bbb6602bd4b360c2a2
Autor:
Andrea Bernini, Elena Petricci, Andrea Atrei, Maria Camilla Baratto, Fabrizio Manetti, Annalisa Santucci
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Alkaptonuria (AKU), a rare genetic disorder, is characterized by the accumulation of homogentisic acid (HGA) in organs due to a deficiency in functional levels of the enzyme homogentisate 1,2-dioxygenase (HGD), required for the breakdown of
Externí odkaz:
https://doaj.org/article/67404596870e443d8436200fe91b2752
Autor:
Ottavia Spiga, Vittoria Cicaloni, Cosimo Fiorini, Alfonso Trezza, Anna Visibelli, Lia Millucci, Giulia Bernardini, Andrea Bernini, Barbara Marzocchi, Daniela Braconi, Filippo Prischi, Annalisa Santucci
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Background Alkaptonuria (AKU) is an ultra-rare autosomal recessive disease caused by a mutation in the homogentisate 1,2-dioxygenase (HGD) gene. One of the main obstacles in studying AKU, and other ultra-rare diseases, is the lack of a stand
Externí odkaz:
https://doaj.org/article/7e00aa955b77490f827561462633086f
Autor:
Elisabetta Gambale, Anna Boddi, Adriano Pasqui, Domenico Andrea Campanacci, Guido Scoccianti, Ilaria Palchetti, Andrea Bernini, Lorenzo Antonuzzo, Serena Pillozzi
Publikováno v:
Cancer Treatment and Research Communications, Vol 31, Iss , Pp 100528- (2022)
Clinical responses to anticancer therapies in advanced soft tissue sarcoma (STS) are unfortunately limited to a small subset of patients. Much of the inter-individual variability in treatment efficacy and risk of toxicities is as result of polymorphi
Externí odkaz:
https://doaj.org/article/c438557b8aa444148c519093380f4d5b
Publikováno v:
Current Protein & Peptide Science. 24:380-392
Abstract: Alkaptonuria (AKU), a rare genetic disorder, is characterized by the accumulation of homogentisic acid (HGA) in organs, which occurs because the homogentisate 1,2-dioxygenase (HGD) enzyme is not functional due to gene variants. Over time, H
Autor:
Gabriella Doddato, Floriana Valentino, Annarita Giliberti, Filomena Tiziana Papa, Rossella Tita, Lucia Pia Bruno, Sara Resciniti, Chiara Fallerini, Elisa Benetti, Maria Palmieri, Maria Antonietta Mencarelli, Alessandra Fabbiani, Mirella Bruttini, Alfredo Orrico, Margherita Baldassarri, Francesca Fava, Diego Lopergolo, Caterina Lo Rizzo, Vittoria Lamacchia, Sara Mannucci, Anna Maria Pinto, Aurora Currò, Virginia Mancini, Oncologic Multidisciplinary Team, Azienda Ospedaliera Universitaria Senese, Oncologic Multidisciplinary Team, Azienda Usl Toscana Sud Est, Francesca Mari, Alessandra Renieri, Francesca Ariani, Alessandro Neri, Donato Casella, Andrea Bernini, Stefania Marsili, Roberto Petrioli, Salvatora Tindara Miano, Alessandra Pascucci, Ignazio Martellucci, Monica Crociani, Marta Vannini, Federica Fantozzi, Andrea Stella, Alessia Carmela Tripodi, Angelamaria Giusti, Alfonso Fausto, Lucia Mantovani, Francesca Belardi
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Hereditary Breast and Ovarian Cancer (HBOC) syndrome is a condition in which the risk of breast and ovarian cancer is higher than in the general population. The prevalent pathogenesis is attributable to inactivating variants of the BRCA1-2 highly pen
Externí odkaz:
https://doaj.org/article/ca4532e26c24440eb12237fb2fc7eb0a
Autor:
Claudia Patiti, Patrick Severin Sfragano, Serena Laschi, Serena Pillozzi, Anna Boddi, Olivia Crociani, Andrea Bernini, Ilaria Palchetti
Publikováno v:
Chemosensors, Vol 10, Iss 7, p 278 (2022)
The determination of nucleic acids has become an analytical diagnostic method with many applications in fields such as biomedical sciences, environmental monitoring, forensic identification, and food safety. Among the different methods for nucleic ac
Externí odkaz:
https://doaj.org/article/ae397ea4cda040038b9eb6c205afe2d3
Near-infrared quantum dots labelled with a tumor selective tetrabranched peptide for in vivo imaging
Autor:
Jlenia Brunetti, Giulia Riolo, Mariangela Gentile, Andrea Bernini, Eugenio Paccagnini, Chiara Falciani, Luisa Lozzi, Silvia Scali, Lorenzo Depau, Alessandro Pini, Pietro Lupetti, Luisa Bracci
Publikováno v:
Journal of Nanobiotechnology, Vol 16, Iss 1, Pp 1-10 (2018)
Abstract Background Near-infrared quantum dots (NIR QDs) are a new class of fluorescent labels with excellent bioimaging features, such as high fluorescence intensity, good fluorescence stability, sufficient electron density, and strong tissue-penetr
Externí odkaz:
https://doaj.org/article/3fa4334a5d7749a19cd6a5b86c810471