[HTML][HTML] Peptide nucleic acids and biosensor technology for real-time detection of the cystic fibrosis W1282X mutation by surface plasmon resonance
In this paper we demonstrate that peptide nucleic acids (PNAs) are excellent probes able to
detect the W1282X point mutation of the cystic fibrosis (CF) gene when biospecific …
detect the W1282X point mutation of the cystic fibrosis (CF) gene when biospecific …
[HTML][HTML] Identificación de mutaciones en el gen CFTR en pacientes chilenos con fibrosis quística
Background: Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in
the CFTR gene, that codes for a chloride channel located in the apical surface of epithelial …
the CFTR gene, that codes for a chloride channel located in the apical surface of epithelial …
El aporte de la biología molecular al estudio de la fibrosis quística en Argentina
L Chertkoff, AA Visich - Med. infant, 2001 - pesquisa.bvsalud.org
El aporte de la biología molecular al estudio de la fibrosis quística en Argentina | Med. infant;8(2):
113-119, jun. 2001. graf, ilus | LILACS loading Conteúdo principal 1 Busca 2 Rodapé 3 +A …
113-119, jun. 2001. graf, ilus | LILACS loading Conteúdo principal 1 Busca 2 Rodapé 3 +A …