152 results on '"Kuroda Y"'
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2. TU-AB-202-02: Deformable Image Registration Accuracy Between External Beam Radiotherapy and HDR Brachytherapy CT Images for Cervical Cancer Using a 3D-Printed Deformable Pelvis Phantom
3. ChemInform Abstract: Epoxidation Reaction Catalyzed by Cyclodextrin-Sandwiched Porphyrin in Aqueous Buffer Solution.
4. ChemInform Abstract: Catalytic Oxidation of Naphthalene on Palladium in Cooperation with Copper(I)/(II) Redox Couple.
5. ChemInform Abstract: The State of Excessively Ion-Exchanged Copper in Mordenite: Formation of Tetragonal Hydroxy-Bridged Copper Ion.
6. ChemInform Abstract: Fungal Metabolites. Part 7. Solution Structure of an Antibiotic Peptide, Trichosporin B-V, from Trichoderma polysporum.
7. ChemInform Abstract: Fungal Metabolites. Part 6. NMR Study of Antibiotic Peptides, Trichosporin Bs, from Trichoderma polysporum.
8. ChemInform Abstract: Molecular Recognition of Modified Porphyrins.
9. ChemInform Abstract: Syntheses of Pseudo-α-D-glucopyranose(VII), Pseudo-β-D- glucopyranose (VIII), and Validamine (X) from D-Glucuronolactone.
10. ChemInform Abstract: Enantiorecognition of a New Chiral Selector, β-Cyclodextrin Perphenylcarbamate as Studied by NMR Spectroscopy and Molecular Energy Calculation
11. ChemInform Abstract: Reduction of Aryl Mesylates Catalyzed by Nickel Complexes.
12. ChemInform Abstract: Stabilization of Copper Metal Clusters in Mordenite Micropores. Water Treatment of Evacuated Copper Ion-Exchanged Mordenite at 300 K.
13. ChemInform Abstract: Syntheses and Redox Behavior of Novel Cyclic Hosts Having Multiple Redox Centers of NAD+ Analogue.
14. ChemInform Abstract: Self-Organized Porphyrin Array.
15. The origin and fate of morphological intermediates between wild and cultivated soybeans in their natural habitats in Japan
16. Relationship of the Bovine Growth Hormone Gene to Carcass Traits in Japanese Black Cattle
17. Gastric mucin phenotype defines tumour progression and prognosis of intrahepatic cholangiocarcinoma: gastric foveolar type is associated with aggressive tumour behaviour
18. Population genetic structure of Japanese wild soybean (Glycine soja) based on microsatellite variation
19. Thermolabile phenotype of carnitine palmitoyltransferase II variations as a predisposing factor for influenza-associated encephalopathy
20. P0018 PP AMELIORATING SMALL BOWEL INJURY USING A CAVITARY TWO‐LAYER PRESERVATION METHOD WITH PERFLUOROCARBON AND A NUTRIENT‐RICH SOLUTION
21. Intra-apheresis recruitment of blood progenitor cells in children
22. Severe dermatomyositis with rhabdomyolysis and paralytic ileus: a case successfully treated with plasmapheresis and intravenous immunoglobulin
23. Cytokines and neurotrophic factors fail to affect Nogo-A mRNA expression in differentiated human neurones: implications for inflammation-related axonal regeneration in the central nervous system
24. Type II Citrullinaemia (Citrin Deficiency) in a Neonate with Hypergalactosaemia Detected by Mass Screening
25. A putative polymorphic Val44Ala variation in the synphilin-1 gene is undetectable in Japanese sporadic Parkinson's disease patients
26. Helix-stabilizing effects of the pentapeptide KIFMK and its related peptides on the sodium channel inactivation gate peptides
27. Solution structures of the cytoplasmic linkers between segments S4 and S5 (S4−S5) in domains III and IV of human brain sodium channels in SDS micelles
28. Ubiquitin C‐terminal hydrolase‐L1 (PGP9.5) expression in human neural cell lines following induction of neuronal differentiation and exposure to cytokines, neurotrophic factors or heat stress
29. Solution structures of the inactivation gate particle peptides of rat brain type‐IIA and human heart sodium channels in SDS micelles
30. A valine to methionine polymorphism at codon 83 in the 8-oxo-dGTPase gene MTH1 is not associated with sporadic Parkinson’s disease
31. Structural study of the sodium channel inactivation gate peptide including an isoleucine–phenylalanine–methionine motif and its analogous peptide (phenylalanine/glutamine) in trifluoroethanol solutions and SDS micelles
32. Cramping pain and prolonged elevation of serum creatine kinase levels in a patient with Guillain–Barré syndrome following Campylobacter jejuni enteritis
33. Missense mutations in phosphomannomutase 2 gene in two Japanese families with carbohydrate‐deficient glycoprotein syndrome type 1
34. Mutational analyses in four Japanese families with X-linked liver phosphorylase kinase deficiency type 1
35. The Side-to-Side Differences of Bone Mass at Proximal Femur in Female Rhythmic Sports Gymnasts
36. Pharmacological evaluation of portal venous isolation and charcoal haemoperfusion for high-dose intra-arterial chemotherapy of the pancreas
37. Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency
38. Research and extension expenditures and productivity in Japanese agriculture, 1960–1990
39. Interleukin‐2 therapy of Langerhans cell histiocytosis
40. Labor productivity measurement in Japanese agriculture, 1956–1990
41. DNA diagnosis of pyruvate dehydrogenase deficiency in female patients with congenital lactic acidaemia
42. ChemInform Abstract: Direct Synthesis of Unsymmetrical Carbonic Esters from Carbon Dioxide ( II), Alcohols (I), and Alkyl Halides (III).
43. ChemInform Abstract: Stereoselective Conversion of D‐Glucuronolactone into Pseudo‐Sugar: Synthesis of Pseudo‐α‐D‐glucopyranose, Pseudo‐β‐D‐ glucopyranose, and Validamine.
44. Post-transfusion chronic hepatitis C in children
45. Molecular genetic analysis of a female patient with pyruvate dehydrogenase deficiency: detection of a new mutation and differential expression of mutant gene product in cultured cells
46. ChemInform Abstract: Aldol Condensation Catalyzed by a Highly Electron‐Deficient Iron Porphyrin.
47. ChemInform Abstract: Recognition of Chirality and Residual Groups of Amino Acid Esters Using New Trifunctional Chiral Porphyrins with C2 Symmetry.
48. Magnetic resonance imaging of the brain structures in the posterior fossa in retarded autistic children
49. Multiple enzyme defects in mitochondria of a case with congenital lactic acidosis and hyperammonaemia
50. Mutation of E1α gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 protein
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