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Catarina Correia de Araújo Brazão Farinha
AuthID:
R-000-3DT
Publications
Confirmed
To Validate
Document Source:
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Document Type:
All Document Types
Article (39)
Abstract (16)
Review (3)
Proceedings Paper (2)
Editorial Material (1)
Letter (1)
Book (1)
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Order:
Year Dsc
Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
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Results:
10
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50
Confirmed Publications: 63
51
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
52
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
53
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
54
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
IN MY:
ResearcherID
55
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
IN MY:
ResearcherID
56
TITLE:
The human DnaJ homologue (Hdj)-l/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70
AUTHORS:
Farinha, CM
;
Nogueira, P
;
Mendes, F
;
Penque, D
;
Amaral, MD
;
PUBLISHED:
2002
,
SOURCE:
BIOCHEMICAL JOURNAL,
VOLUME:
366,
ISSUE:
3
INDEXED IN:
Scopus
WOS
IN MY:
ResearcherID
57
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
IN MY:
ResearcherID
58
TITLE:
Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells
AUTHORS:
Penque, D
;
Mendes, F
; Beck, S;
Farinha, C
; Pacheco, P;
Nogueira, P
; Lavinha, J;
Malho, R
;
Amaral, MD
;
PUBLISHED:
2000
,
SOURCE:
LABORATORY INVESTIGATION,
VOLUME:
80,
ISSUE:
6
INDEXED IN:
Scopus
WOS
IN MY:
ResearcherID
59
TITLE:
Cystic fibrosis patients with the 3272-26A -> G mutation have mild disease, leaky alternative mRNA splicing, and CFTR protein at the cell membrane
Full Text
AUTHORS:
Beck, S;
Penque, D
; Garcia, S;
Gomes, A
;
Farinha, C
; Mata, L; Gulbenkian, S; Gil Ferreira, K;
Duarte, A
;
Pacheco, P
; Barreto, C;
Lopes, B
;
Cavaco, J
; Lavinha, J;
Amaral, MD
;
PUBLISHED:
1999
,
SOURCE:
HUMAN MUTATION,
VOLUME:
14,
ISSUE:
2
INDEXED IN:
WOS
CrossRef
:
1
IN MY:
ResearcherID
60
TITLE:
Cystic fibrosis patients with the 3272-26A→G mutation have mild disease, leaky alternative mRNA splicing, and CFTR protein at the cell membrane
Full Text
AUTHORS:
Beck, S;
Penque, D
; Garcia, S;
Gomes, A
;
Farinha, C
; Mata, L; Gulbenkian, S; Gil Ferreira, K; Duarte, A; Pacheco, P; Barreto, C; Lopes, B;
Cavaco, J
; Lavinha, J;
Amaral, MD
;
PUBLISHED:
1999
,
SOURCE:
Human Mutation,
VOLUME:
14,
ISSUE:
2
INDEXED IN:
Scopus
CrossRef
:
50
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