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TÍTULO: Quantitative methods for the analysis of CFTR transcripts/splicing variants  Full Text
AUTORES: 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;
PUBLICAÇÃO: 2004, FONTE: Journal of Cystic Fibrosis, VOLUME: 3, NÚMERO: SUPPL. 2
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
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TÍTULO: 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
AUTORES: Ramalho, AS ; Beck, S; Penque, D ; Gonska, T; Seydewitz, HH; Mall, M; Amaral, MD ;
PUBLICAÇÃO: 2003, FONTE: JOURNAL OF MEDICAL GENETICS, VOLUME: 40, NÚMERO: 7
INDEXADO EM: Scopus WOS CrossRef
NO MEU: ORCID
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TÍTULO: Five percent of normal cystic fibrosis transmembrane conductance regulator mRNA ameliorates the severity of pulmonary disease in cystic fibrosis
AUTORES: Ramalho, AS ; Beck, S; Meyer, M; Penque, D ; Cutting, GR; Amaral, MD ;
PUBLICAÇÃO: 2002, FONTE: AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, VOLUME: 27, NÚMERO: 5
INDEXADO EM: Scopus WOS CrossRef
NO MEU: ORCID
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