Toward the Total Synthesis of Proteins
スポンサーリンク
概要
- 論文の詳細を見る
- 1995-10-01
著者
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Sakakibara Shumpei
Peptide Institute Inc. Protein Research Foundation
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Sakakibara Shumpei
Peptide Center, Institute for Protein Research, Osaka University
関連論文
- Molecular Mechanism of Action by Atrial Natriuretic Peptide in Rat Vascular Smooth Muscle Cells : SYMPOSIUM ON ATRIAL NATRIURETIC POLYPEPTIDE (ANP): Basic and Clinical Research : 51th Annual Scientific Session of the Japanese Circulation Society
- Enzyme-Linked Immunoassay for Midkine, and Its Application to Evaluation of Midkine Levels in Developing Mouse Brain and Sera from Patients with Hepatocellular Carcinomas
- Total Synthesis of Aequorea Green Fluorescent Protein
- Chemical Synthesis of Dendrotoxin I : Revision of the Reported Structure
- Solution Synthesis of Calcicludine (CaC) : A Potent Blocker of an L-subtype of Neuronal Ca^ Channels
- Smooth Muscle Relaxing and Hypotensive Activities of Synthetic Calciseptine and the Homologous Snake Venom Peptide FS_2
- Amino Acid Sequence of Sardine Calcitonin and Its Hypocalcemic Activity in Rats
- Solution Structure of α-Conotoxin SI Determined by Two-Dimensional NMR Spectroscopy
- Comparative Biochemistry of Renins and Angiotensins in the Vertebrates
- High Performance Liquid Chromatography of Bradykinin and Its Application to the Degradation Study of Bradykinin in Plasma (生体成分の高速液体クロマトグラフィ-)
- Application of N^-Cyclohexyloxycarbonyltryptophan to Peptide Synthesis
- Toward the Total Synthesis of Proteins
- SPECIFIC PRESSOR ACTIVITY OF ANGIOTENSINS I AND II
- Rathoimmunoassay of Human Calcitonin Using Labeled [Asu1, 7]-Human Calcitonin Analogue
- SPECIFIC PRESSOR ACTIVITY AND STABILITY OF SYNTHETIC ANGIOTENSINS
- The presence of substance P carboxy-terminal heptapeptide in pig brain stem.
- A New Protective Group Suitable for Masking Specific Amino Groups during Peptide Synthesis
- Studies on the Synthesis of Histidine Peptides. I. Nim-Tosylhistidine Derivatives as Starting Materials
- The Solid-phase Synthesis of Ile5-Angiotensin II to Demonstrate the Use of Nim-Tosyl-histidine
- Oxytocin Analogues Containing No Disulfide Bond. III. The Synthesis of Three Analogues of 1,6-Aminosuberic Acid-Oxytocin
- Enzyme-Linked Immunoassay for Midkine, and Its Application to Evaluation of Midkine Levels in Developing Mouse Brain and Sera from Patients with Hepatocellular Carcinomas.
- The Synthesis of a Series of N-t-Amyloxycarbonyl-oligo-L-proline