Margarida Sofia Pereira Duarte Amaral
AuthID: R-000-AER
11
TITLE: Mutant CFTR Drives TWIST1 mediated epithelial-mesenchymal transition
AUTHORS: Quaresma, MC; Pankonien, I; Clarke, LA; Sousa, LS; Silva, IAL; Railean, V; Dousova, T; Fuxe, J; Amaral, MD;
PUBLISHED: 2020, SOURCE: CELL DEATH & DISEASE, VOLUME: 11, ISSUE: 10
AUTHORS: Quaresma, MC; Pankonien, I; Clarke, LA; Sousa, LS; Silva, IAL; Railean, V; Dousova, T; Fuxe, J; Amaral, MD;
PUBLISHED: 2020, SOURCE: CELL DEATH & DISEASE, VOLUME: 11, ISSUE: 10
12
TITLE: Activating alternative chloride channels to treat CF: Friends or Foes?
AUTHORS: Margarida D Amaral; Jeffrey M Beekman;
PUBLISHED: 2020, SOURCE: Journal of Cystic Fibrosis, VOLUME: 19, ISSUE: 1
AUTHORS: Margarida D Amaral; Jeffrey M Beekman;
PUBLISHED: 2020, SOURCE: Journal of Cystic Fibrosis, VOLUME: 19, ISSUE: 1
13
TITLE: R560S: A class II CFTR mutation that is not rescued by current modulators Full Text
AUTHORS: Awatade, NT; Ramalho, S; Silva, IAL; Felicio, V; Botelho, HM; de Poel, E; Vonk, A; Beekman, JM; Farinha, CM; Amaral, MD;
PUBLISHED: 2019, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 18, ISSUE: 2
AUTHORS: Awatade, NT; Ramalho, S; Silva, IAL; Felicio, V; Botelho, HM; de Poel, E; Vonk, A; Beekman, JM; Farinha, CM; Amaral, MD;
PUBLISHED: 2019, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 18, ISSUE: 2
14
TITLE: Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV1) in cystic fibrosis patients receiving ivacaftor treatment
AUTHORS: Nagy, B; Bene, Z; Fejes, Z; Heltshe, SL; Reid, D; Ronan, NJ; McCarthy, Y; Smith, D; Nagy, A; Joseloff, E; Balla, G; Kappelmayer, J; Macek, M; Bell, SC; Plant, BJ; Amaral, MD; Balogh, I;
PUBLISHED: 2019, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 18, ISSUE: 2
AUTHORS: Nagy, B; Bene, Z; Fejes, Z; Heltshe, SL; Reid, D; Ronan, NJ; McCarthy, Y; Smith, D; Nagy, A; Joseloff, E; Balla, G; Kappelmayer, J; Macek, M; Bell, SC; Plant, BJ; Amaral, MD; Balogh, I;
PUBLISHED: 2019, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 18, ISSUE: 2
15
TITLE: The effect of premature termination codon mutations on CFTR mRNA abundance in human nasal epithelium and intestinal organoids: a basis for read-through therapies in cystic fibrosis
AUTHORS: Clarke, LA; Awatade, NT; Felicio, VM; Silva, IA; Calucho, M; Pereira, L; Azevedo, P; Cavaco, J; Barreto, C; Bertuzzo, C; Gartner, S; Beekman, J; Amaral, MD;
PUBLISHED: 2019, SOURCE: HUMAN MUTATION, VOLUME: 40, ISSUE: 3
AUTHORS: Clarke, LA; Awatade, NT; Felicio, VM; Silva, IA; Calucho, M; Pereira, L; Azevedo, P; Cavaco, J; Barreto, C; Bertuzzo, C; Gartner, S; Beekman, J; Amaral, MD;
PUBLISHED: 2019, SOURCE: HUMAN MUTATION, VOLUME: 40, ISSUE: 3
16
TITLE: Increases in cytosolic Ca2+ induce dynamin- and calcineurin-dependent internalisation of CFTR
AUTHORS: Patel, W; Moore, PJ; Sassano, MF; Lopes Pacheco, M; Aleksandrov, AA; Amaral, MD; Tarran, R; Gray, MA;
PUBLISHED: 2019, SOURCE: CELLULAR AND MOLECULAR LIFE SCIENCES, VOLUME: 76, ISSUE: 5
AUTHORS: Patel, W; Moore, PJ; Sassano, MF; Lopes Pacheco, M; Aleksandrov, AA; Amaral, MD; Tarran, R; Gray, MA;
PUBLISHED: 2019, SOURCE: CELLULAR AND MOLECULAR LIFE SCIENCES, VOLUME: 76, ISSUE: 5
17
TITLE: Research ethics in palliative care: A hallmark in Palliative Medicine
AUTHORS: Pereira, SM; Hernández Marrero, P;
PUBLISHED: 2019, SOURCE: Palliative Medicine
AUTHORS: Pereira, SM; Hernández Marrero, P;
PUBLISHED: 2019, SOURCE: Palliative Medicine
INDEXED IN: 
Scopus
Scopus18
TITLE: CFTR modulator theratyping: Current status, gaps and future directions
AUTHORS: Clancy, JP; Cotton, CU; Donaldson, SH; Solomon, GM; VanDevanter, DR; Boyle, MP; Gentzsch, M; Nick, JA; Illek, B; Wallenburg, JC; Sorscher, EJ; Amaral, MD; Beekman, JM; Naren, AP; Bridges, RJ; Thomas, PJ; Cutting, G; Rowe, S; Durmowicz, AG; Mense, M; ...More
PUBLISHED: 2019, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 18, ISSUE: 1
AUTHORS: Clancy, JP; Cotton, CU; Donaldson, SH; Solomon, GM; VanDevanter, DR; Boyle, MP; Gentzsch, M; Nick, JA; Illek, B; Wallenburg, JC; Sorscher, EJ; Amaral, MD; Beekman, JM; Naren, AP; Bridges, RJ; Thomas, PJ; Cutting, G; Rowe, S; Durmowicz, AG; Mense, M; ...More
PUBLISHED: 2019, SOURCE: JOURNAL OF CYSTIC FIBROSIS, VOLUME: 18, ISSUE: 1
19
TITLE: Extent of rescue of F508de1-CFTR function by VX-809 and VX-770 in human nasal epithelial cells correlates with SNP rs7512462 in SLC26A9 gene in F508del/F508del Cystic Fibrosis patients
AUTHORS: Kmit, A; Marson, FAL; Pereira, SVN; Vinagre, AM; Leite, GS; Servidoni, MF; Ribeiro, JD; Ribeiro, AF; Bertuzzo, CS; Amaral, MD;
PUBLISHED: 2019, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1865, ISSUE: 6
AUTHORS: Kmit, A; Marson, FAL; Pereira, SVN; Vinagre, AM; Leite, GS; Servidoni, MF; Ribeiro, JD; Ribeiro, AF; Bertuzzo, CS; Amaral, MD;
PUBLISHED: 2019, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1865, ISSUE: 6
20
TITLE: Folding Status Is Determinant over Traffic-Competence in Defining CFTR Interactors in the Endoplasmic Reticulum
AUTHORS: Santos, JD; Canato, S; Carvalho, AS; Botelho, HM; Aloria, K; Amaral, MD; Matthiesen, R; Falcao, AO; Farinha, CM;
PUBLISHED: 2019, SOURCE: CELLS, VOLUME: 8, ISSUE: 4
AUTHORS: Santos, JD; Canato, S; Carvalho, AS; Botelho, HM; Aloria, K; Amaral, MD; Matthiesen, R; Falcao, AO; Farinha, CM;
PUBLISHED: 2019, SOURCE: CELLS, VOLUME: 8, ISSUE: 4
