pargyline has been researched along with oligonucleotides in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 4 (80.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Brown, T; Cuenoud, B; Darby, RA; Fox, KR; Sollogoub, M | 1 |
Pujari, SS; Seela, F | 1 |
Leonard, P; Pujari, SS; Seela, F | 1 |
Hocek, M; Matyašovský, J; Pohl, R | 1 |
Meschaninova, MI; Novopashina, DS; Semikolenova, OA; Silnikov, VN; Venyaminova, AG | 1 |
5 other study(ies) available for pargyline and oligonucleotides
Article | Year |
---|---|
Stable DNA triple helix formation using oligonucleotides containing 2'-aminoethoxy,5-propargylamino-U.
Topics: Azo Compounds; Deoxyribonuclease I; Deoxyuridine; DNA; DNA Footprinting; Fluorescein; Nucleic Acid Conformation; Nucleic Acid Denaturation; Oligonucleotides; Pargyline; Propylamines; Spectrometry, Fluorescence; Ultraviolet Rays | 2002 |
Cross-linked DNA: propargylated ribonucleosides as "click" ligation sites for bifunctional azides.
Topics: Azides; Base Sequence; Cross-Linking Reagents; DNA; DNA, Single-Stranded; Ligation; Magnetic Resonance Spectroscopy; Molecular Structure; Oligonucleotides; Pargyline; Ribonucleosides | 2012 |
Oligonucleotides with "clickable" sugar residues: synthesis, duplex stability, and terminal versus central interstrand cross-linking of 2'-O-propargylated 2-aminoadenosine with a bifunctional azide.
Topics: Adenosine; Azides; Catalysis; Click Chemistry; Copper; Cross-Linking Reagents; DNA; Ligation; Magnetic Resonance Spectroscopy; Molecular Structure; Oligonucleotides; Pargyline | 2014 |
2-Allyl- and Propargylamino-dATPs for Site-Specific Enzymatic Introduction of a Single Modification in the Minor Groove of DNA.
Topics: Allyl Compounds; Deoxyadenine Nucleotides; DNA; Fluorescence Resonance Energy Transfer; Fluorescent Dyes; Nucleic Acid Conformation; Oligonucleotides; Pargyline; Propylamines | 2018 |
Novel Convenient Approach to the Solid-Phase Synthesis of Oligonucleotide Conjugates.
Topics: Boron Compounds; Diamines; Molecular Structure; Oligonucleotides; Pargyline; Propylamines; Pyrenes; Solid-Phase Synthesis Techniques | 2019 |