Margarida Sofia Pereira Duarte Amaral
AuthID: R-000-AER
31
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
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
WOS IN MY: 
ORCID
ORCID32
TITLE: Characterization of membrane complexes involved in CFTR stabilization by EPAC1 activation
AUTHORS: Santos, JD; Pinto, FR; Amaral, MD; Zaccolo, M; Farinha, CM;
PUBLISHED: 2018, SOURCE: FEBS OPEN BIO, VOLUME: 8
AUTHORS: Santos, JD; Pinto, FR; Amaral, MD; Zaccolo, M; Farinha, CM;
PUBLISHED: 2018, SOURCE: FEBS OPEN BIO, VOLUME: 8
INDEXED IN: WOS
WOS33
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
AUTHORS: Amaral, MD; Boj, SF; Shaw, J; Leipziger, J; Beekman, JM;
PUBLISHED: 2018, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 17, ISSUE: 4
34
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
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
35
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
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
36
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
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
37
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
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
38
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
AUTHORS: Felicio, V; Ramalho, AS; Igreja, S; Amaral, MD;
PUBLISHED: 2017, SOURCE: CLINICAL GENETICS, VOLUME: 91, ISSUE: 3
39
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
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
WOS40
TITLE: Biobanking: towards increased access of biomaterials in cystic fibrosis. Report on the pre-conference meeting to the 13th ECFS Basic Science Conference, Pisa, 30 March-2 April, 2016
AUTHORS: Beekman, JM; Wang, CM; Casati, S; Tuggle, KL; Gulmans, VAM; Amaral, M; De Boeck, K;
PUBLISHED: 2017, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 16, ISSUE: 5
AUTHORS: Beekman, JM; Wang, CM; Casati, S; Tuggle, KL; Gulmans, VAM; Amaral, M; De Boeck, K;
PUBLISHED: 2017, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 16, ISSUE: 5
