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

Personalized Medicine in Cystic Fibrosis: Characterization of Eight Rare CFTR Variants in Intestinal Organoids and Cellular Models

囊性纤维化个性化医疗:肠道类器官和细胞模型中八种罕见CFTR变异体的表征

Railean, Violeta; Rodrigues, Cláudia S; Pankonien, Ines; Ramalho, Sofia S; Silva, Iris A L; Doušová, Tereza; Castanhinha, Susana; Azevedo, Pilar; Roda, Juliana; Farinha, Carlos M; Amaral, Margarida D

CFTR ion transport deficiency primes the epithelium for partial epithelial-mesenchymal transition in cystic fibrosis.

囊性纤维化中 CFTR 离子转运缺陷使上皮细胞更容易发生部分上皮-间质转化

Rodrigues Cláudia S, Canto Matilde, Torres Raquel, Railean Violeta, Ramalho Sofia S, Farinha Carlos M, Pankonien Ines, Amaral Margarida D

Global functional genomics reveals GRK5 as a cystic fibrosis therapeutic target synergistic with current modulators.

全球功能基因组学揭示 GRK5 是囊性纤维化治疗靶点,可与现有调节剂产生协同作用

Botelho Hugo M, Lopes-Pacheco Miquéias, Pinto Madalena C, Railean Violeta, Pankonien Ines, Caleiro Mariana F, Clarke Luka A, Cachatra Vasco, Neumann Beate, Tischer Christian, Moiteiro Cristina, Ousingsawat Jiraporn, Kunzelmann Karl, Pepperkok Rainer, Amaral Margarida D

Synthesis and the In Vitro Evaluation of Antitumor Activity of Novel Thiobenzanilides

新型硫代苯甲酰化合物的合成及其体外抗肿瘤活性评价

Álvaro-Martins, Maria João; Railean, Violeta; Martins, Filomena; Machuqueiro, Miguel; Pacheco, Rita; Santos, Susana

Personalized medicine: Function of CFTR variant p.Arg334Trp is rescued by currently available CFTR modulators

个性化医疗:目前可用的CFTR调节剂可以恢复CFTR变异体p.Arg334Trp的功能

Railean, Violeta; Rodrigues, Cláudia S; Ramalho, Sofia S; Silva, Iris A L; Bartosch, Jan; Farinha, Carlos M; Pankonien, Ines; Amaral, Margarida D

Personalized Medicine Based on Nasal Epithelial Cells: Comparative Studies with Rectal Biopsies and Intestinal Organoids

基于鼻上皮细胞的个性化医疗:与直肠活检和肠道类器官的比较研究

Silva, Iris A L; Railean, Violeta; Duarte, Aires; Amaral, Margarida D

Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A>G.

类器官作为囊性纤维化中超罕见突变的个性化医疗工具:S955P 和 1717-2A>G 的案例

Silva Iris A L, Doušová Tereza, Ramalho Sofia, Centeio Raquel, Clarke Luka A, Railean Violeta, Botelho Hugo M, Holubová Andrea, Valášková Iveta, Yeh Jiunn-Tyng, Hwang Tzyh-Chang, Farinha Carlos M, Kunzelmann Karl, Amaral Margarida D