71
TITLE: Microarray analysis in cystic fibrosis  Full Text
AUTHORS: Galvin, P; Clarke, LA ; Harvey, S; Amaral, MD ;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus CrossRef
IN MY: ORCID
72
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
IN MY: ORCID
73
TITLE: Proteomics techniques for cystic fibrosis research
AUTHORS: Roxo Rosa, M ; Davezac, N; Bensalem, N; Majumder, M; Heda, GD; Simas, A; Penque, D ; Amaral, MD ; Lukacs, GL; Edelman, A;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus
IN MY: ORCID
74
TITLE: Quantitative methods for the analysis of CFTR transcripts/splicing variants  Full Text
AUTHORS: Amaral, MD ; Clarke, LA ; Ramalho, AS ; Beck, S; Broackes Carter, F; Rowntree, R; Mouchel, N; Williams, SH; Harris, A; Tzetis, M; Steiner, B; Sanz, J; Gallati, S; Nissim Rafinifa, M; Kerem, B; Hefferon, T; Cutting, GR; Goina, E; Pagani, F;
PUBLISHED: 2004, SOURCE: Journal of Cystic Fibrosis, VOLUME: 3, ISSUE: SUPPL. 2
INDEXED IN: Scopus CrossRef
IN MY: ORCID
75
TITLE: Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei
AUTHORS: Zink, D; Amaral, MD ; Englmann, A; Lang, S; Clarke, LA ; Rudolph, C; Alt, F; Luther, K; Braz, C; Sadoni, N; Rosenecker, J; Schindelhauer, D;
PUBLISHED: 2004, SOURCE: JOURNAL OF CELL BIOLOGY, VOLUME: 166, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
76
TITLE: Applicability of different antibodies for the immunohistochemical localization of CFTR in respiratory and intestinal tissues of human and murine origin
AUTHORS: Doucet, L; Mendes, F ; Montier, T; Delepine, P; Penque, D ; Ferec, C; Amaral, MD ;
PUBLISHED: 2003, SOURCE: JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, VOLUME: 51, ISSUE: 9
INDEXED IN: Scopus WOS
IN MY: ORCID
77
TITLE: Transcript analysis of the cystic fibrosis splicing mutation 1525-1G > A shows use of multiple alternative splicing sites and suggests a putative role of exonic splicing enhancers
AUTHORS: Ramalho, AS ; Beck, S; Penque, D ; Gonska, T; Seydewitz, HH; Mall, M; Amaral, MD ;
PUBLISHED: 2003, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 40, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
78
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: ORCID
79
TITLE: Five percent of normal cystic fibrosis transmembrane conductance regulator mRNA ameliorates the severity of pulmonary disease in cystic fibrosis
AUTHORS: Ramalho, AS ; Beck, S; Meyer, M; Penque, D ; Cutting, GR; Amaral, MD ;
PUBLISHED: 2002, SOURCE: AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, VOLUME: 27, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
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