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dc.contributor.authorGarcía Fernández, Emilio 
dc.contributor.authorGonzález García, María del Carmen 
dc.contributor.authorPernagallo, Salvatore
dc.contributor.authorRuedas-Rama, Maria Jose 
dc.contributor.authorFara, Mario Antonio
dc.contributor.authorLópez Delgado, Francisco Javier
dc.contributor.authorW. Dear, James
dc.contributor.authorIlyine, Hugh
dc.contributor.authorRess, Cristina
dc.contributor.authorDíaz Mochón, Juan José 
dc.contributor.authorOrte Gutiérrez, Ángel 
dc.date.accessioned2024-12-12T12:39:56Z
dc.date.available2024-12-12T12:39:56Z
dc.date.issued2019-11-27
dc.identifier.citationGarcía Fernández, E. et. al. Chem. Commun., 2019, 55, 14958. [https://doi.org/10.1039/C9CC08069D]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/97955
dc.description.abstractA simple method for direct detection of microRNAs (miRs) in human serum without the use of polymerase amplification is presented, achieving low miR-122 concentrations and importantly, discerning effectively single-base sequence mutations. The method is based on the capture of target miRs with synthetic peptide nucleic acid oligomers, dynamic chemical labelling, separation with quaternary amine microplatforms and detection using time-gated fluorescence imaging.es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistryes_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titlemiR-122 direct detection in human serum by time-gated fluorescence imaginges_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1039/C9CC08069D
dc.type.hasVersionVoRes_ES


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