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Department of Bioresource Science, College of Agriculture, Ibaraki University | 論文
- Total Synthesis of (±) -syn-Copalol(Organic Chemistry)
- P-99 SOLID-PHASE SYNTHESIS OF DEHYDROPEPTIDES
- Biofilm in the Mouth : Dental Plaque(BIOFILM IN MICROBIAL ECOLOGY)
- Syntheses and Potato Tuber-inducing Activities of Unnatural Long-chain OPC-9 : 0 and OPC-10 : 0
- Syntheses of 3-Oxa-OPC and 2-Fluoro-OPC Homologues
- Utilization of Phenylpropanoids by Pseudomonas putida Soil Isolates and Its Probable Taxonomic Significance
- Colonization process of the root endophytic fungus Heteroconium chaetospira in roots of Chinese cabbage
- Correlation of the Standardized Uptake Value in FDG-PET with the Expression Level of Cell-Cycle-Related MolecularBiomarkers in Resected Non-Small Cell Lung Cancers
- Ground-glass opacities showing an adenoma-to-carcinoma sequence in the lung
- Addition of HCl to a Base-Stabilized Hydrido (silylene) tungsten Complex and Reactivity of the Adduct toward LiAlH_4
- Inhibitory Effect of Coronamic Acid Derivatives on Senescence in Cut Carnation Flowers
- Practical Stereoselective Syntheses of All Four Stereoisomers of Coronamic Acid (2-Ethyl-1-aminocyclopropane-1-carboxylic acid)
- Functions of Malonate Decarboxylase Subunits from Pseudomonas putida(Biochemistry & Molecular Biology)
- Identification of Diterpene. Biosynthetic Gene Clusters and Functional Analysis of Labdane-Related Diterpene Cyclases in Phomopsis amygdali
- Diterpene Phytoalexins Are Biosynthesized in and Exuded from the Roots of Rice Seedlings
- Improved Synthesis of the C_8-C_ Segment of Aplysiatoxins via Asymmetric Dihydroxylation of the Chiral Homoallylic Alcohol
- Analysis of the Molecular Species of Hydrogenase in the Cells of an Obligately Chemolithoautotrophic, Marine Hydrogen-Oxidizing Bacterium, Hydrogenovibrio marinus(Microbiology & Fermentation Technology)
- Total Synthesis of Biologically Active Compounds Related to Plant Disease and the Physiological Function
- Stereoselective Synthesis of a Promising Flower-Inducing KODA Analog, (9R,12S,13R,15Z)-9-Hydroxy-12,13-methylene-10-oxooctadec-15-enoic Acid