32
TITLE: Analysis of genomic CFTR DNA
AUTHORS: Ferec, C; Le Marechal, C; Audrezet, MP; Farinha, CM ; Amaral, MD ; Gallati, S; Sanz, J; Steiner, B; Mouchel, N; Harris, A; Schwarz, MJ;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus
33
TITLE: Antibodies for CFTR studies  Full Text
AUTHORS: Mendes, F ; Farinha, CM ; Roxo Rosa, M ; Fanen, P; Edelman, A; Dormer, R; McPherson, M; Davidson, H; Puchelle, E; De Jonge, H; Heda, GD; Gentzsch, M; Lukacs, GL; Penque, D ; Amaral, MD ;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus CrossRef
34
TITLE: Biochemical methods to assess CFTR expression and membrane localization  Full Text
AUTHORS: Farinha, CM ; Penque, D ; Roxo Rosa, M ; Lukacs, G; Dormer, R; McPherson, M; Pereira, M; Bot, AGM; Jorna, H; Willemsen, R; De Jonge, H; Heda, GD; Marino, CR; Fanen, P; Hinzpeter, A; Lipecka, J; Fritsch, J; Gentzsch, M; Edelman, A; Amaral, MD;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus CrossRef
35
TITLE: Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts  Full Text
AUTHORS: Ramalho, AS ; Beck, S; Farinha, CM ; Clarke, LA ; Heda, GD; Steiner, B; Sanz, J; Gallati, S; Amaral, MD ; Harris, A; Tzetis, M;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus CrossRef
36
TITLE: Non-PCR methods for the analysis of CFTR transcripts  Full Text
AUTHORS: Trezise, AEO; Farinha, CM ; Heda, GD; Harris, A; Amaral, MD ; Mouchel, N;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus CrossRef
37
TITLE: Unusually common cystic fibrosis mutation in Portugal encodes a misprocessed protein  Full Text
AUTHORS: Mendes, F ; Rosa, MR ; Dragomir, A; Farinha, CM ; Roomans, GM; Amaral, MD ; Penque, D ;
PUBLISHED: 2003, SOURCE: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, VOLUME: 311, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
38
TITLE: Processing and intracellular trafficking of wild-type and mutant CFTR
AUTHORS: Farinha, CM ; Amaral, MD;
PUBLISHED: 2002, SOURCE: 25th European Cystic Fibrosis Conference in PROCEEDINGS OF 25TH EUROPEAN CYSTIC FIBROSIS CONFERENCE
INDEXED IN: WOS
40
TITLE: Cystic fibrosis patients with the 3272-26A > G splicing mutation have milder disease than F508del homozygotes: a large European study
AUTHORS: Amaral, MD ; Pacheco, P; Beck, S; Farinha, CM ; Penque, D ; Nogueira, P; Barreto, C; Lopes, B; Casals, T; Dapena, J; Gartner, S; Vasquez, C; Perez Frias, J; Olveira, C; Cabanas, R; Estivill, X; Tzetis, M; Kanavakis, E; Doudounakis, S; Dork, T; Tummler, B; Girodon Boulandet, E; Cazeneuve, C; Goossens, M; Blayau, M; Verlingue, C; Vieira, I; Ferec, C; Claustres, M; des Georges, M; Clavel, C; Birembaut, P; Hubert, D; Bienvenu, T; Adoun, M; Chomel, JC; De Boeck, K; Cuppens, H; Lavinha, J; ...More
PUBLISHED: 2001, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 38, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef
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