31
TITLE: Partial rescue of F508del-cystic fibrosis transmembrane conductance regulator channel gating with modest improvement of protein processing, but not stability, by a dual-acting small molecule
AUTHORS: Liu, J; Bihler, H; Farinha, CM; Awatade, NT; Romao, AM; Mercadante, D; Cheng, Y; Musisi, I; Jantarajit, W; Wang, YT; Cai, ZW; Amaral, MD; Mense, M; Sheppard, DN;
PUBLISHED: 2018, SOURCE: BRITISH JOURNAL OF PHARMACOLOGY, VOLUME: 175, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 15
IN MY: ORCID
32
TITLE: Compartmentalized crosstalk of CFTR and TMEM16A (ANO1) through EPAC1 and ADCY1
AUTHORS: Lerias, J; Pinto, M; Benedetto, R; Schreiber, R; Amaral, M; Aureli, M; Kunzelmann, K;
PUBLISHED: 2018, SOURCE: CELLULAR SIGNALLING, VOLUME: 44
INDEXED IN: WOS
IN MY: ORCID
34
TITLE: Cystic fibrosis: Beyond the airways. Report on the meeting of the basic science working group in Loutraki, Greece
AUTHORS: Amaral, MD; Boj, SF; Shaw, J; Leipziger, J; Beekman, JM;
PUBLISHED: 2018, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 17, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
35
TITLE: Proteomic interaction profiling reveals KIFC1 as a factor involved in early targeting of F508del-CFTR to degradation  Full Text
AUTHORS: Canato, S; Santos, JD; Carvalho, AS; Aloria, K; Amaral, MD; Matthiesen, R; Falcao, AO; Farinha, CM;
PUBLISHED: 2018, SOURCE: CELLULAR AND MOLECULAR LIFE SCIENCES, VOLUME: 75, ISSUE: 24
INDEXED IN: Scopus WOS CrossRef: 22
IN MY: ORCID
36
TITLE: Prolonged co-treatment with HGF sustains epithelial integrity and improves pharmacological rescue of Phe508del-CFTR
AUTHORS: Matos, AM; Gomes Duarte, A; Faria, M; Barros, P; Jordan, P; Amaral, MD; Matos, P;
PUBLISHED: 2018, SOURCE: SCIENTIFIC REPORTS, VOLUME: 8, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 20 Handle
IN MY: ORCID
37
TITLE: Cystic fibrosis newborn screening in Portugal: PAP value in populations with stringent rules for genetic studies
AUTHORS: Marcão, A; Barreto, C; Pereira, L; Vaz, LG; Cavaco, J; Casimiro, A; Félix, M; Silva, TR; Barbosa, T; Freitas, C; Nunes, S; Felício, V; Lopes, L; Amaral, M; Vilarinho, L;
PUBLISHED: 2018, SOURCE: International Journal of Neonatal Screening, VOLUME: 4, ISSUE: 3
INDEXED IN: Scopus CrossRef: 15 Handle
IN MY: ORCID
38
TITLE: CERTIFIED ROOMS FOR ELEARNING STUDENTS EVALUATION
AUTHORS: Jorge Borges; Carlos Vaz; Margarida Amaral; Elsa Justino; Joao Barroso ; Arsenio Reis ;
PUBLISHED: 2017, SOURCE: 11th International Conference on Technology, Education and Development (INTED) in INTED2017: 11TH INTERNATIONAL TECHNOLOGY, EDUCATION AND DEVELOPMENT CONFERENCE
INDEXED IN: WOS CrossRef: 1
39
TITLE: mRNA-based detection of rare CFTR mutations improves genetic diagnosis of cystic fibrosis in populations with high genetic heterogeneity
AUTHORS: Felicio, V; Ramalho, AS; Igreja, S; Amaral, MD;
PUBLISHED: 2017, SOURCE: CLINICAL GENETICS, VOLUME: 91, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 11
IN MY: ORCID
40
TITLE: CFTR3: PERSONALISED CHARACTERISATION OF RARE CYSTIC FIBROSIS GENOTYPES  Full Text
AUTHORS: Muehlbacher, V; Amaral, MD; Beekman, JM; Bronsveld, I; Castellani, C; de Jonge, HR; Dewachter, E; Naehrlich, L; Sermet Gaudelus, I; Wilschanski, M; Derichs, N;
PUBLISHED: 2017, SOURCE: PEDIATRIC PULMONOLOGY, VOLUME: 52
INDEXED IN: WOS
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