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pubmed-article:19783436pubmed:abstractTextPeptide nucleic acid (PNA) is a successful DNA/RNA mimic. A major challenge for research is to invent chemically modified PNAs that retain the favorable properties of the parent compound while improving biological recognition. Here, we test modified PNAs containing [bis-o-(aminoethoxy)phenyl]pyrrolocytosine bases designed to engage guanine with an additional hydrogen bond. We observe elevated melting temperatures, localization to cellular compartments, and allele-selective inhibition of mutant huntingtin protein expression.lld:pubmed
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pubmed-article:19783436pubmed:authorpubmed-author:HuJiaxinJlld:pubmed
pubmed-article:19783436pubmed:authorpubmed-author:HudsonRobert...lld:pubmed
pubmed-article:19783436pubmed:authorpubmed-author:DoddDavid WDWlld:pubmed
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pubmed-article:19783436pubmed:pagination6181-4lld:pubmed
pubmed-article:19783436pubmed:dateRevised2011-9-26lld:pubmed
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pubmed-article:19783436pubmed:year2009lld:pubmed
pubmed-article:19783436pubmed:articleTitleCellular localization and allele-selective inhibition of mutant huntingtin protein by peptide nucleic acid oligomers containing the fluorescent nucleobase [bis-o-(aminoethoxy)phenyl]pyrrolocytosine.lld:pubmed
pubmed-article:19783436pubmed:affiliationDepartment of Pharmacology, UT Southwestern Medical Center at Dallas, Dallas, 6001 Forest Park Road, TX 75390, USA.lld:pubmed
pubmed-article:19783436pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19783436pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
pubmed-article:19783436pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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