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36 results on '"I Kondo"'

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1. Use of legacy nitrogen as a resource: Unfertilized lotus fields contribute to water quality improvement and biodiversity conservation

2. Lipoprotein(a) and Benefit of PCSK9 Inhibition in Patients With Nominally Controlled LDL Cholesterol

3. Machine Performance and Its Effects on Experiments in JT-60U

4. Fabrication of SiC-SiC whisker composite by the polymer precursor method

5. THERMODYNAMIC PROPERTIES OF A LIQUID METAL USING A SOFT-SPHERE REFERENCE SYSTEM

6. JT-60 DIVERTOR PUMPING SYSTEM AND ITS INITIAL OPERATION IN OHMICALLY HEATED DIVERTOR DISCHARGES

7. SYSTEM DESIGN OF ZENKEI, THE CENTRAL CONTROL SYSTEM FOR JT-60

8. DESIGNING & DEVELOPMENT OF THE REAL-TIME CONTROL SYSTEM FOR JT-60 PLASMA DISCHARGE

9. SYSTEM DESIGN OF ZENKEI, THE CENTRAL CONTROL SYSTEM OF JT-60

10. SAFETY DESIGN OF THE JT-60 CONTROL SYSTEM

11. STUDIES ON TOXICITY AND IMMUNOGENICITY OF STAPHYLOCOCCAL EXFOLIATINS A AND B

13. A short form of gross motor function measure for Fukuyama congenital muscular dystrophy.

14. Validity of Total Kihon Checklist Score for Predicting the Incidence of 3-Year Dependency and Mortality in a Community-Dwelling Older Population.

15. Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndrome.

16. A novel regulatory pathway for cholesterol degradation via lactostatin.

17. A novel alternative splice variant of nicastrin and its implication in Alzheimer disease.

18. Lymphocyte-specific protein tyrosine kinase is a novel risk gene for Alzheimer disease.

19. Classic Rett syndrome in a boy with R133C mutation of MECP2.

20. Mechanisms of antinociception of spinal galanin: how does galanin inhibit spinal sensitization?

21. Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms.

22. Effect of genetic polymorphism of OATP-C (SLCO1B1) on lipid-lowering response to HMG-CoA reductase inhibitors.

23. Promoter polymorphism in fibroblast growth factor 1 gene increases risk of definite Alzheimer's disease.

24. A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1.

25. Hyperhomocysteinemia in Japanese patients with convalescent stage ischemic stroke: effect of combined therapy with folic acid and mecobalamine.

26. Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speech.

27. Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I.

29. Characteristic evoked potentials in childhood-onset dentatorubral-pallidoluysian atrophy.

30. Proton magnetic resonance spectroscopy on childhood-onset dentatorubral-pallidoluysian atrophy (DRPLA).

31. Molecular cloning and gene mapping of human basic and acidic calponins.

32. Dentatorubral-pallidoluysian atrophy (DRPLA): clinical, genetic, and neuroradiologic studies in a family.

33. A new learning paradigm: adaptive changes in interlimb coordination during perturbed locomotion in decerebrate cats.

34. Mitochondrial myopathy: tissue-specific expression of a defect in ubiquinol-cytochrome c reductase.

35. Gentamicin resistance in Japan.

36. Ultrasonography and brain pathology of periventricular hemorrhage and subependymal cyst in the preterm neonate.

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