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Ipr Osaka Univ. | 論文
- Synthesis of a Molt-Inhibiting Hormone of the American Crayfish, Procambarus clarkii and Determination of Its Disulfide Linkage
- Synthesis of Phosphorylated Polypeptide Using an Expressed Peptide as a Building Block
- Changes in the Amounts of the Molt-Inhibiting Hormone in Sinus Glands during the Molt Cycle of the American Crayfish, Procambarus clarkii : Endocrinology
- Synthesis of a Molt-Inhibiting Hormone of the American Crayfish, Procambarus clarkii, and Determination of the Location of Its Disulfide Linkages^1
- Use of an Expressed Peptide Segment as a Building Block for the Preparation of Phosphorylated Polypeptide via the Thioester Method
- Synthesis of a Phosphorylated Polypeptide by a Thioester Method
- SYNTHESIS OF A MOLT - INHIBITING HORMONE IN THE AMERICAN CRAYFISH PROCAMBARUS CLARKII BY NATIVE CHEMICAL LIGATION
- Synthesis of Cysteine-Containing Polypeptide Using Peptide Thioester : Preparation of a Molt-Inhibiting Hormone from the American Crayfish, Procambarus clarkii
- 2P-049 天然変性蛋白質pKIDとKIXドメイン複合体形成における結合と折り畳みが共役した相互作用の計算科学による解析(蛋白質-物性(安定性,折れたたみなど),第47回日本生物物理学会年会)
- 3P-117 リゾチーム周辺における水分子の流れパターン(順流、渦流、Dry/Wet流れ)に関する分子動力学シミュレーションによる解析(水・水和/電解質,第46回日本生物物理学会年会)
- 1P-007 マルチカノニカル分子動力学シミュレーションによる57残基蛋白質の構造探索(蛋白質・構造(1),第46回日本生物物理学会年会)
- Sequential Peptide Ligation by the Combination of the Thioester Method and Extended Chemical Ligation
- N-S Acyl Shift Reaction on Peptide Backbone and Its Application to Preparation of Peptide Thioesters
- Peptide Ligation That Involves an Intramolecular N to S Acyl Shift Reaction
- Generation of an S-Peptide via an N-S Acyl Shift Reaction in a TFA Solution
- Preparation of Peptide Thioesters Based on an N-S Acyl Shift Reaction
- Analyses of Virus-Induced Homomeric and Heteromeric Protein Associations between IRF-3 and Coactivator CBP/p300
- Isolation of Bioactive Peptides from Wamide-Peptide Libraries Synthesized with a Multipeptide Synthesizer
- Characterization of Lipid-Binding Domains in Human Serum Amyloid A Using Its Fragment Peptides
- Peptide Purification Using The Selective Reaction Between Aminooxy Group and Isothiocyanate Group, Followed by Edman Degradation
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