<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-14T09:44:55Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/179776" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/179776</identifier><datestamp>2025-12-04T21:45:24Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478917</setSpec><setSpec>col_2072_478933</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Synthesis, RNAi activity and nuclease-resistant properties of apolar carbohydrates siRNA conjugates</dc:title>
   <dc:creator>Vengut Climent, Empar</dc:creator>
   <dc:creator>Terrazas Martínez, Montserrat</dc:creator>
   <dc:creator>Lucas, Ricardo</dc:creator>
   <dc:creator>Arévalo Ruiz, Matilde</dc:creator>
   <dc:creator>Eritja i Casadellà, Ramon</dc:creator>
   <dc:creator>Morales, Juan Carlos</dc:creator>
   <dc:subject>RNA</dc:subject>
   <dc:subject>Oligonucleòtids</dc:subject>
   <dc:subject>Química orgànica</dc:subject>
   <dc:subject>RNA</dc:subject>
   <dc:subject>Oligonucleotides</dc:subject>
   <dc:subject>Organic chemistry</dc:subject>
   <dcterms:abstract>Oligoribonucleotide conjugates carrying apolar carbohydrates at the 5′-end and the corresponding siRNA duplexes have been prepared using phosphoramidite chemistry. All the carbohydrate-siRNA derivatives were compatible with RNA interference machinery if transfected with oligofectamine. In the absence of a transfection agent, some of them exerted certain reduction of gene expression. Double-tailed permethylated glucose conjugated to siRNA through a long spacer inhibited gene expression up to 26% compared to the scrambled duplex. Such modifications contribute positively to the stability of oligoribonucleotides against 5′-exonuclease degradation.</dcterms:abstract>
   <dcterms:issued>2021-08-30T12:45:07Z</dcterms:issued>
   <dcterms:issued>2021-08-30T12:45:07Z</dcterms:issued>
   <dcterms:issued>2013-07-15</dcterms:issued>
   <dcterms:issued>2021-08-30T12:45:07Z</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1016/j.bmcl.2013.05.065</dc:relation>
   <dc:relation>Bioorganic &amp; Medicinal Chemistry Letters, 2013, vol. 23, num. 14, p. 4048-4051</dc:relation>
   <dc:relation>https://doi.org/10.1016/j.bmcl.2013.05.065</dc:relation>
   <dc:rights>(c) Elsevier Ltd, 2013</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Elsevier Ltd</dc:publisher>
   <dc:source>Articles publicats en revistes (Química Inorgànica i Orgànica)</dc:source>
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