38 results on '"Mabuchi, Hiroshi"'
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2. ChemInform Abstract: Syntheses of Fused Heterocyclic Compounds and Their Inhibitory Activities for Squalene Synthase.
3. Impacts of Visceral Adipose Tissue and Subcutaneous Adipose Tissue on Metabolic Risk Factors in Middle-aged Japanese
4. Melt spinning and metal chloride vapor curing process on polymethylsilsesquioxane as SiOC fiber precursor
5. Accelerated ceramization of polymethylsilsesquioxane by aluminum- based filler reductant
6. Formation of Continuous Pore Structures in Si-C-O Fibers by Adjusting the Melt Spinning Condition of a Polycarbosilane-Polysiloxane Polymer Blend
7. Molecular Genetics of Cholesterol Transport and Cholesterol Reverse Transport Disorders (Familial Hypercholesterolemia and CETP Deficiency) and Coronary Heart Disease
8. Effects of Fenofibrate Therapy on Plasma Ubiquinol-10 and Ubiquinone-10 Levels in Japanese Patients with Hyperlipidemia and Type 2 Diabetes Mellitus
9. Low‐density Lipoprotein Apheresis Therapy With a Direct Hemoperfusion Column: A Japanese Multicenter Clinical Trial
10. Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes
11. TWO MALE PATIENTS WITH WILSON's DISEASE TREATED USING TRIENTINE AND IRON REDUCTION THERAPY
12. A Novel Missense Mutation in the SCN5A Gene Associated with Brugada Syndrome Bidirectionally Affecting Blocking Actions of Antiarrhythmic Drugs
13. The expression of messenger RNA for ADP-ribosyl cyclase in aldosterone-producing adenomas
14. Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-Pore Site ofSCN5A
15. Strategy for treating elderly Japanese with hypercholesterolemia*
16. Surgical stress‐induced transient nephrogenic diabetes insipidus (NDI) associated with decreased Vasopressin receptor2 (AVPR2) expression linked to nonsense‐mediated mRNA decay and incomplete skewed X‐inactivation in a female patient with a heterozygous AVPR2 mutation (c. 89–90 delAC)
17. SiC microsphere derived from phenolic resin?Ethyl silicate heterogeneous precursors with carbothermic reduction
18. Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy-like features
19. Two novel mutations of PTEN gene in Japanese patients with Cowden syndrome
20. Simultaneous, clonally identical T cell expansion in tonsil and synovium in a patient with rheumatoid arthritis and chronic tonsillitis
21. Long‐term Effect of Low‐density Lipoprotein Apheresis in Patients with Heterozygous Familial Hypercholesterolemia
22. Hemodynamic changes and prognosis in patients with hypertrophic cardiomyopathy and abnormal blood pressure responses during exercise
23. T-peak to T-end interval may be a better predictor of high-risk patients with hypertrophic cardiomyopathy associated with a cardiac troponin i mutation than qt dispersion
24. ChemInform Abstract: Novel 4,1‐Benzoxazepine Derivatives with Potent Squalene Synthase Inhibitory Activities.
25. Genetic analysis of the cytochrome P-450c17α (CYP17) and aldosterone synthase (CYP11B2) in Japanese patients with 17α-hydroxylase deficiency
26. Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy
27. Collagen remodeling and cardiac dysfunction in patients with hypertrophic cardiomyopathy: The significance of type III and VI collagens
28. Mutation Analysis of the PTEN/MMAC1 Gene in Japanese Patients with Cowden Disease
29. Cardiac sympathetic activity in the asymmetrically hypertrophied septum in patients with hypertension or hypertrophic cardiomyopathy
30. A theoretical foundation for solving ?no-solution? problems by abstraction
31. The expression of steroidogenic enzyme genes in human vascular cells
32. Absence of CD69 expression on peripheral eosinophils in episodic angioedema and eosinophilia
33. Efficacy of Endoscopic Esophageal Variceal Ligation in an Immunocompromised Host
34. Mutations in the Low Density Lipoprotein Receptor Gene in Japanese Patients with Familial Hypercholesterolemia
35. Regulation of fatty acid synthesis in isolated hepatocytes by intestinal chylomicrons and their remnants
36. Inhibition by somatostatin of insulin release from isolated pancreatic islets
37. Extreme Contrast of Postprandial Remnant-Like Particles Formed in Abetalipoproteinemia and Homozygous Familial Hypobetalipoproteinemia.
38. Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by Breastfeeding.
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