日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Exploring Genomic Variability in the Mediterranean Buffalo Breed: A Step Towards Custom SNP Array

探索地中海水牛品种的基因组变异性:迈向定制SNP芯片的一步

Arcuri, Chiara; Gabbianelli, Federica; Bencivenga, Francesca; Porcai, Gabriella; Pietrucci, Daniele; Picarone, Ludovica; Vignali, Giovanni; Toscano, Elvira; Di Maggio, Federica; Sepe, Leandra; Nunziato, Marcella; Manunza, Arianna; Lazzari, Barbara; Cozzi, Paolo; Rizzo, Francesca; Weisz, Alessandro; Smal, Marharyta; Biffani, Stefano; Castiglioni, Bianca; Paolella, Giovanni; Salvatore, Francesco; Rullo, Alessandro; Rubinacci, Salvatore; Cosenza, Gianfranco; Carpio, Mayra Gómez; Cimmino, Roberta; Di Vuolo, Gabriele; Iannuzzi, Leopoldo; Milanesi, Marco; Chillemi, Giovanni

Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman-Diamond Syndrome Subjects

p53 水平升高与 Shwachman-Diamond 综合征患者成骨细胞矿化能力下降有关

Annalisa Frattini, Simona Bolamperti, Roberto Valli, Marco Cipolli, Rita Maria Pinto, Elena Bergami, Maria Rita Frau, Simone Cesaro, Michela Signo, Valentino Bezzerri, Giovanni Porta, Abdul Waheed Khan, Alessandro Rubinacci, Isabella Villa

L-Carnitine Reduces Oxidative Stress and Promotes Cells Differentiation and Bone Matrix Proteins Expression in Human Osteoblast-Like Cells

L-肉碱减轻氧化应激并促进人类成骨样细胞分化和骨基质蛋白表达

Ileana Terruzzi, Anna Montesano, Pamela Senesi, Isabella Villa, Anita Ferraretto, Michela Bottani, Fernanda Vacante, Alice Spinello, Simona Bolamperti, Livio Luzi, Alessandro Rubinacci

Gene therapy augments the efficacy of hematopoietic cell transplantation and fully corrects mucopolysaccharidosis type I phenotype in the mouse model

基因治疗增强造血细胞移植的疗效并完全纠正小鼠模型中的 I 型粘多糖贮积症表型

Ilaria Visigalli, Stefania Delai, Letterio S Politi, Carmela Di Domenico, Federica Cerri, Emanuela Mrak, Raffaele D'Isa, Daniela Ungaro, Merel Stok, Francesca Sanvito, Elisabetta Mariani, Lidia Staszewsky, Claudia Godi, Ilaria Russo, Francesca Cecere, Ubaldo Del Carro, Alessandro Rubinacci, Riccardo

ADA-deficient SCID is associated with a specific microenvironment and bone phenotype characterized by RANKL/OPG imbalance and osteoblast insufficiency

ADA 缺陷型严重联合免疫缺陷症 (SCID) 与特定的微环境和骨表型有关,其特征是 RANKL/OPG 失衡和成骨细胞功能不足

Aisha V Sauer, Emanuela Mrak, Raisa Jofra Hernandez, Elena Zacchi, Francesco Cavani, Miriam Casiraghi, Eyal Grunebaum, Chaim M Roifman, Maria C Cervi, Alessandro Ambrosi, Filippo Carlucci, Maria Grazia Roncarolo, Anna Villa, Alessandro Rubinacci, Alessandro Aiuti