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

The L467F-F508del Complex Allele Hampers Pharmacological Rescue of Mutant CFTR by Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis Patients: The Value of the Ex Vivo Nasal Epithelial Model to Address Non-Responders to CFTR-Modulating Drugs

L467F-F508del 复合等位基因阻碍 Elexacaftor/Tezacaftor/Ivacaftor 对囊性纤维化患者中突变型 CFTR 的药物挽救:体外鼻上皮模型对治疗对 CFTR 调节药物无反应者的价值

Elvira Sondo, Federico Cresta, Cristina Pastorino, Valeria Tomati, Valeria Capurro, Emanuela Pesce, Mariateresa Lena, Michele Iacomino, Ave Maria Baffico, Domenico Coviello, Tiziano Bandiera, Federico Zara, Luis J V Galietta, Renata Bocciardi, Carlo Castellani, Nicoletta Pedemonte

Variants in the 5'UTR reduce SHOX expression and contribute to SHOX haploinsufficiency

5'UTR区域的变异会降低SHOX基因的表达,并导致SHOX单倍体功能不全。

Babu, Deepak; Vannelli, Silvia; Fanelli, Antonella; Mellone, Simona; Baffico, Ave Maria; Corrado, Lucia; Essa, Wael Al; Grandone, Anna; Bellone, Simonetta; Monzani, Alice; Vinci, Giulia; De Sanctis, Luisa; Stuppia, Liborio; Prodam, Flavia; Giordano, Mara

SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators

SHOX基因缺陷与生长发育障碍儿童:已知和新的生长发育学及放射学指标的评估

Vannelli, Silvia; Baffico, Maria; Buganza, Raffaele; Verna, Francesca; Vinci, Giulia; Tessaris, Daniele; Di Rosa, Gianpaolo; Borraccino, Alberto; de Sanctis, Luisa

Characterization of a disease-associated mutation affecting a putative splicing regulatory element in intron 6b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

对影响囊性纤维化跨膜传导调节因子 (CFTR) 基因内含子 6b 中假定剪接调控元件的疾病相关突变进行表征

Faà, Valeria; Incani, Federica; Meloni, Alessandra; Corda, Denise; Masala, Maddalena; Baffico, A Maria; Seia, Manuela; Cao, Antonio; Rosatelli, M Cristina