A Novel Approach for the Solid Phase Synthesis of DNA-Peptide Conjugates
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概要
- 論文の詳細を見る
- 2001-03-01
著者
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Fujii Masayuki
Department Of Chemistry Kyushu School Of Engineering Kinki University
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Kubo Takanori
Department Of Chemistry Kyushu School Of Engineering Kinki University
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Dubey Krishna
Department Of Chemistry Kyushu School Of Engineering Kinki University
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Fujii Masayuki
Department Of Biological & Environmental Chemistry School Of Humanity Oriented Science And Techn
関連論文
- Hybridization Properties of Nucleic Acid Analogs Bearing Peptide Backbone
- Design, Synthesis And Characterization of DNA Binding Peptides
- Specific Stabilization of Phophorothioate DNA Hybrids by Cationic α-Helical Peptides
- Thermal Stability of Double and Triple Stranded DNA in the Presence of Cationic Amphiphilic α-Helix Peptide
- Synthesis and Biological Activity of DNA-NLS Peptide Conjugate
- Specific Stabilization of Double and Triple Stranded DNA by Amphiphilic Cyclic Peptides
- NAD(P)^+-NAD(P)H Models. 87. Nonsteric Stereochemistry Controlled by a Carbonyl Dipole
- NAD(P)^+-NAD(P)H Models. 86. Nonsteric Stereochemistry in Hydride-Transfer to Sulfinylpyridinium Ion
- A New Method for the Preparation of Conjugated Nitro Olefins
- A Novel and Convenient Method for the Synthesis of DNA Conjugate
- Controlled Intracellular Delivery and Antisense Inhibition of DNA-Peptide Conjugates
- Highly Enhanced Silencing of bcr/abl Gene by siRNA-NES Peptide Conjugates
- Synthesis and Properties of Nucleic Acid Analogues with Peptide Backbone
- A Novel Approach for the Solid Phase Synthesis of DNA-Peptide Conjugates
- Stereoselective Synthesis of (±)-Isonitramine and (±)-Sibirine
- Synthesis of DNA-Peptide Conjugate by Solid Phase Fragment Condensation
- Synthesis and Biological Activity of Phosphorothioate DNA-Peptide Conjugate
- Synthesis of Oligonucleotide-Peptide Conjugates by Solid Phase Fragment Condensation
- Specific Inhibition of Human Telomerase Activity by siRNA and Phosphorothioate Oligonucleotide-Peptide Conjugates
- NAD(P)+-NAD(P)H models. 71. A convenient route to the synthesis of juvabione.