1,760 results on '"Kamatani, Naoyuki"'
Search Results
2. Febuxostat ameliorates muscle degeneration and movement disorder of the dystrophin mutant model in Caenorhabditis elegans
3. Apolipoprotein D modulates lipid mediators and osteopontin in an anti-inflammatory direction
4. Studies on safety and efficacy of particles containing a mixture of hydroxyapatite–argentum–titanium oxide (HAT) and sheets coated with HAT particles to be used in masks to improve nasal allergy: II. Cellular, in vivo, and clinical studies
5. Are minor alleles more likely to be risk alleles?
6. Regulation of aging by balancing mitochondrial function and antioxidant levels
7. Polyamine Inhibitor SAM486A Augments Cytarabine Cytotoxicity in Methylthioadenosine Phosphorylase-deficient Leukemia Cells
8. Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
9. Xanthine oxidase inhibitors treatment or discontinuation effects on mortality: evidence of xanthine oxidase inhibitors withdrawal syndrome
10. Genes, the brain, and artificial intelligence in evolution
11. A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis
12. Trans-ethnic meta-analysis of white blood cell phenotypes
13. List of Contributors
14. Purine and Pyrimidine Metabolism
15. Pharmacogenomics and Patient Care: One Size Does Not Fit All
16. Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations
17. Improved Parkinsons disease motor score in a single-arm open-label trial of febuxostat and inosine
18. Treatment of two mitochondrial disease patients with a combination of febuxostat and inosine that enhances cellular ATP
19. Microdeletion at ESR1 Intron 6 (DEL_6_75504) Is a Susceptibility Factor for Cryptorchidism and Hypospadias
20. Apolipoprotein D modulates lipid mediators and osteopontin in an anti-inflammatory direction
21. Estimation of the risk of a qualitative phenotype: dependence on population risk
22. Development of a SNP set for human identification: A set with high powers of discrimination which yields high genetic information from naturally degraded DNA samples in the Thai population
23. Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
24. Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs
25. Microdeletion at ESR1Intron 6 (DEL_6_75504) Is a Susceptibility Factor for Cryptorchidism and Hypospadias
26. Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride
27. Six-layer structure for genomics and its applications
28. Polynomial Time Approximate Sampler for Discretized Dirichlet Distribution
29. Deletion in the Hypoxanthine Phosphoribosyltransferase Gene Caused by Alu-Alu Recombination in Two Japanese Patients With Lesch-Nyhan Syndrome
30. Toward the Establishment of a Prediction System for the Personalized Treatment of Chronic Hepatitis C
31. Regulation of aging by balancing mitochondrial function and antioxidant levels.
32. Genome-wide Association Study Identifies Variations in 6p21.3 Associated With Nevirapine-Induced Rash
33. IL28B But Not ITPA Polymorphism Is Predictive of Response to Pegylated Interferon, Ribavirin, and Telaprevir Triple Therapy in Patients With Genotype 1 Hepatitis C
34. A First Evidence of an Asymptomatic Germline Missense Base Substitution in the Hypoxanthine Phosphoribosyltransferase (HPRT) Gene in Humans
35. The Origin of APRT*J the Most Common Disease-Related Mutation of APRT Gene Among Japanese Goes Back to a Prehistoric Era
36. Optimal Range of Serum Urate Concentrations to Minimize Risk of Gouty Attacks During Anti-Hyperuricemic Treatment
37. Microanalysis of Pathological Crystals and Urinary Calculi
38. Intracellular IL-1α-Binding Proteins Contribute to Biological Functions of Endogenous IL-1α in Systemic Sclerosis Fibroblasts
39. Search for the Mechanisms of High Incidence of APRT Deficiency Among Japanese
40. Analysis of the Genotypes for Aldehyde Dehydrogenase 2 in Japanese Patients with Primary Gout
41. Direct Evidence for a Hot Spot of Germline Mutation at HPRT Locus
42. Molecular Analysis of Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency in Japanese Patients
43. Germline and Somatic Mutations Leading to Adenine Phosphoribosyltransferase (APRT) Deficiency
44. 6 - Purine and Pyrimidine Metabolism
45. HLA-A SNPs and amino acid variants are associated with nasopharyngeal carcinoma in Malaysian Chinese
46. A Polymorphism in MAPKAPK3 Affects Response to Interferon Therapy for Chronic Hepatitis C
47. T-cell leukemia translocation-associated gene (TCTA) protein is required for human osteoclastogenesis
48. Functional Variants in ADH1B and ALDH2 Coupled With Alcohol and Smoking Synergistically Enhance Esophageal Cancer Risk
49. Selective Killing of Human Malignant Cell Lines Deficient in Methylthioadenosine Phosphorylase, a Purine Metabolic Enzyme
50. Possible Metabolic Basis for the Different Immunodeficient States Associated with Genetic Deficiencies of Adenosine Deaminase and Purine Nucleoside Phosphorylase
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