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

Radiofrequency ablation is an effective treatment for Bethesda III thyroid nodules without genetic alterations

射频消融术是治疗无基因改变的Bethesda III型甲状腺结节的有效方法。

Fugazzola, Laura; Deandrea, Maurilio; Borgato, Stefano; Dell'Acqua, Marco; Retta, Francesca; Mormile, Alberto; Carzaniga, Chiara; Gazzano, Giacomo; Pogliaghi, Gabriele; Muzza, Marina; Persani, Luca

Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism

随机表观遗传突变可能是先天性甲状腺功能减退症双胞胎表型不一致的可能解释

Gentilini, D; Muzza, M; de Filippis, T; Vigone, M C; Weber, G; Calzari, L; Cassio, A; Di Frenna, M; Bartolucci, M; Grassi, E S; Carbone, E; Olivieri, A; Persani, L

FAM83B is involved in thyroid cancer cell differentiation and migration

FAM83B 参与甲状腺癌细胞分化和迁移

Valentina Cirello, Elisa Stellaria Grassi, Gabriele Pogliaghi, Viola Ghiandai, Laura Ermellino, Marina Muzza, Giacomo Gazzano, Luca Persani, Carla Colombo, Laura Fugazzola

Thyroid cancer harboring PTEN and TP53 mutations: A peculiar molecular and clinical case report

携带PTEN和TP53突变的甲状腺癌:一例特殊的分子和临床病例报告

Colombo, Carla; Pogliaghi, Gabriele; Tosi, Delfina; Muzza, Marina; Bulfamante, Gaetano; Persani, Luca; Fugazzola, Laura; Cirello, Valentina

Oxidative Stress Correlates with More Aggressive Features in Thyroid Cancer

氧化应激与甲状腺癌的侵袭性特征相关

Marina Muzza, Gabriele Pogliaghi, Carla Colombo, Erika Carbone, Valentina Cirello, Sonia Palazzo, Francesco Frattini, Davide Gentilini, Giacomo Gazzano, Luca Persani, Laura Fugazzola

The molecular and gene/miRNA expression profiles of radioiodine resistant papillary thyroid cancer

放射性碘耐药性乳头状甲状腺癌的分子和基因/miRNA表达谱

Colombo, Carla; Minna, Emanuela; Gargiuli, Chiara; Muzza, Marina; Dugo, Matteo; De Cecco, Loris; Pogliaghi, Gabriele; Tosi, Delfina; Bulfamante, Gaetano; Greco, Angela; Fugazzola, Laura; Borrello, Maria Grazia

Update on Fundamental Mechanisms of Thyroid Cancer

甲状腺癌基本机制研究进展

Prete, Alessandro; Borges de Souza, Patricia; Censi, Simona; Muzza, Marina; Nucci, Nicole; Sponziello, Marialuisa

DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom

在英国,DUOX2/DUOXA2基因突变经常导致先天性甲状腺功能减退症,而这种疾病往往无法通过新生儿筛查检测出来。

Peters, Catherine; Nicholas, Adeline K; Schoenmakers, Erik; Lyons, Greta; Langham, Shirley; Serra, Eva G; Sebire, Neil J; Muzza, Marina; Fugazzola, Laura; Schoenmakers, Nadia

The BRAF-inhibitor PLX4720 inhibits CXCL8 secretion in BRAFV600E mutated and normal thyroid cells: a further anti-cancer effect of BRAF-inhibitors

BRAF 抑制剂 PLX4720 抑制 BRAFV600E 突变和正常甲状腺细胞中的 CXCL8 分泌:BRAF 抑制剂的进一步抗癌作用

Francesca Coperchini, Laura Croce, Marco Denegri, Oriana Awwad, Samuel Tata Ngnitejeu, Marina Muzza, Valentina Capelli, Francesco Latrofa, Luca Persani, Luca Chiovato, Mario Rotondi

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism

先天性甲状腺功能减退症病例中的双基因DUOX1和DUOX2突变

Aycan, Zehra; Cangul, Hakan; Muzza, Marina; Bas, Veysel N; Fugazzola, Laura; Chatterjee, V Krishna; Persani, Luca; Schoenmakers, Nadia