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1. A genome-wide association analysis reveals new pathogenic pathways in gout

5. Publisher Correction: A genome-wide association analysis reveals new pathogenic pathways in gout

6. Quantification of escape from X chromosome inactivation with single-cell omics data reveals heterogeneity across cell types and tissues

7. DOCK2 is involved in the host genetics and biology of severe COVID-19

8. A meta-analysis of genome-wide association studies using Japanese and Taiwanese has revealed novel loci associated with gout susceptibility

10. Increase of serum uric acid levels associated with APOE ε2 haplotype: a clinico-genetic investigation and in vivo approach

13. Regulation of Urate Homeostasis by Membrane Transporters.

16. A common variant of LDL receptor related protein 2 (LRP2) gene is associated with gout susceptibility: a meta-analysis in a Japanese population

17. Dysuricemia

19. Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers

22. Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers

24. Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals

25. Urate Transporter ABCG2 Function and Asymptomatic Hyperuricemia: A Retrospective Cohort Study of CKD Progression

29. Genome-wide meta-analysis between renal overload type and renal underexcretion type of clinically defined gout in Japanese populations

30. Nanaomycin E inhibits NLRP3 inflammasome activation by preventing mitochondrial dysfunction

34. The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited

37. OAT10/SLC22A13 Acts as a Renal Urate Re-Absorber: Clinico-Genetic and Functional Analyses With Pharmacological Impacts

38. DOCK2 is involved in the host genetics and biology of severe COVID-19

40. A common variant of leucine-rich repeat-containing 16A (LRRC16A) gene is associated with gout susceptibility

41. Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes

42. A common missense variant of monocarboxylate transporter 9 (MCT9/SLC16A9) gene is associated with renal overload gout, but not with all gout susceptibility

46. NPT1/SLC17A1 Is a Renal Urate Exporter in Humans and Its Common Gain-of-Function Variant Decreases the Risk of Renal Underexcretion Gout

47. A Proposal for Practical Diagnosis of Renal Hypouricemia: Evidenced from Genetic Studies of Nonfunctional Variants of URAT1/SLC22A12 among 30,685 Japanese Individuals

49. Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene

50. A Proposal for Practical Diagnosis of Renal Hypouricemia : Evidenced from Genetic Studies of Nonfunctional Variants of URAT1/SLC22A12 among 30,685 Japanese Individuals

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