"Oligonucleotide conjugates carrying a single functionalized tetrathiafulvalene (TTF) unit linked through a threoninol molecule to the 3' or 5' ends were synthesized together with their complementary oligonucleotides carrying a TTF, pyrene, or pentafluorophenyl group. TTF-oligonucleotide conjugates formed duplexes with higher thermal stability than the corresponding unmodified oligonucleotides and pyrene- and pentafluorophenyl-modified oligonucleotides. TTF-modified oligonucleotides are able to bind to citrate-stabilized gold nanoparticles (AuNPs) and produce stable gold AuNPs functionalized with oligonucleotides. Finally, TTF-oligoribonucleotides have been synthesized to produce siRNA duplexes carrying TTF units. The presence of the TTF molecule is compatible with the RNA interference mechanism for gene inhibition."@en . "Janou\u0161ek, Ji\u0159\u00ED" . . "Biophysical and RNA Interference Inhibitory Properties of Oligonucleotides Carrying Tetrathiafulvalene Groups at Terminal Positions" . . "RIV/61388963:_____/13:00394921!RIV14-MSM-61388963" . "US - Spojen\u00E9 st\u00E1ty americk\u00E9" . . . . . "Star\u00E1, Irena G." . "63532" . . "Eritja, R." . . "10.1155/2013/650610" . "DNA; derivates; tetrathiafulvalene; TTF-oligonucleotide conjugates"@en . . . . . "Grijalvo, S." . "Biophysical and RNA Interference Inhibitory Properties of Oligonucleotides Carrying Tetrathiafulvalene Groups at Terminal Positions"@en . . "4"^^ . "[3A17226D3459]" . "RIV/61388963:_____/13:00394921" . . "Biophysical and RNA Interference Inhibitory Properties of Oligonucleotides Carrying Tetrathiafulvalene Groups at Terminal Positions" . "I, P(7E09054), P(GAP207/10/2214)" . "June" . . "11"^^ . "Journal of Chemistry" . "8"^^ . "http://dx.doi.org/10.1155/2013/650610" . . "P\u00E9rez-Rentero, S." . . "2013" . "Star\u00FD, Ivo" . . . "2090-9063" . . . "000322492900001" . "B\u011Blohradsk\u00FD, Martin" . . "Somoza, A." . "Oligonucleotide conjugates carrying a single functionalized tetrathiafulvalene (TTF) unit linked through a threoninol molecule to the 3' or 5' ends were synthesized together with their complementary oligonucleotides carrying a TTF, pyrene, or pentafluorophenyl group. TTF-oligonucleotide conjugates formed duplexes with higher thermal stability than the corresponding unmodified oligonucleotides and pyrene- and pentafluorophenyl-modified oligonucleotides. TTF-modified oligonucleotides are able to bind to citrate-stabilized gold nanoparticles (AuNPs) and produce stable gold AuNPs functionalized with oligonucleotides. Finally, TTF-oligoribonucleotides have been synthesized to produce siRNA duplexes carrying TTF units. The presence of the TTF molecule is compatible with the RNA interference mechanism for gene inhibition." . "Biophysical and RNA Interference Inhibitory Properties of Oligonucleotides Carrying Tetrathiafulvalene Groups at Terminal Positions"@en .