Works by Shimizu, Seiko
Results: 31
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals.
- Published in:
- Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0339-0
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- Publication type:
- Article
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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- Biomedicines, 2021, v. 9, n. 8, p. 1012, doi. 10.3390/biomedicines9081012
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- Article
Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population.
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- Journal of Human Genetics, 2015, v. 60, n. 10, p. 613, doi. 10.1038/jhg.2015.82
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- Article
Visualization of pancreatic juice movement using unenhanced MR imaging with spin labeling: Preliminary results in normal and pathophysiologic conditions.
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- Journal of Magnetic Resonance Imaging, 2012, v. 35, n. 5, p. 1119, doi. 10.1002/jmri.23533
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- Article
Common dysfunctional variants of ABCG2 have stronger impact on hyperuricemia progression than typical environmental risk factors.
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- Scientific Reports, 2014, p. 1, doi. 10.1038/srep05227
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- Publication type:
- Article
ABCG2 dysfunction causes hyperuricemia due to both renal urate underexcretion and renal urate overload.
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- Scientific Reports, 2014, p. 1, doi. 10.1038/srep03755
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- Article
Common dysfunctional variants in ABCG2 are a major cause of early-onset gout.
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- Scientific Reports, 2013, p. 1, doi. 10.1038/srep02014
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- Article
Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene.
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- Rheumatology, 2022, v. 61, n. 3, p. 1276, doi. 10.1093/rheumatology/keab545
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- Article
Substantial anti-gout effect conferred by common and rare dysfunctional variants of URAT1/SLC22A12.
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- Rheumatology, 2021, v. 60, n. 11, p. 5224, doi. 10.1093/rheumatology/keab327
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- Article
Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families.
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- Rheumatology, 2020, v. 59, n. 12, p. 3988, doi. 10.1093/rheumatology/keaa461
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- Article
Common variants of a urate-associated gene LRP2 are not associated with gout susceptibility.
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- Rheumatology International, 2014, v. 34, n. 4, p. 473, doi. 10.1007/s00296-013-2924-8
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- Article
Effects of filtration through bleaching media on thiobarbituric acid and carbonyl values of autoxidized soybean oil.
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- Journal of the American Oil Chemists' Society (JAOCS), 1990, v. 67, n. 6, p. 373, doi. 10.1007/BF02539693
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- Article
ABCG2 Dysfunction Increases the Risk of Renal Overload Hyperuricemia.
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- Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 266, doi. 10.1080/15257770.2013.866679
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- Article
Identification of a Hypouricemia Patient with SLC2A9 R380W, A Pathogenic Mutation for Renal Hypouricemia Type 2.
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- Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 261, doi. 10.1080/15257770.2013.857781
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- Publication type:
- Article
The effects of URAT1/SLC22A12 nonfunctional variants,R90H and W258X, on serum uric acid levels and gout/hyperuricemia progression.
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- Scientific Reports, 2016, p. 20148, doi. 10.1038/srep20148
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- Publication type:
- Article
The Spatial Distribution of Water Components with Similar T<sub>2</sub> May Provide Insight into Pathways for Large Molecule Transportation in the Brain.
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- Magnetic Resonance in Medical Sciences, 2021, v. 20, n. 1, p. 34, doi. 10.2463/mrms.mp.2019-0138
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- Article
Strong genetic effect on gout revealed by genetic risk score from meta-analysis of two genome-wide association studies.
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- 2025
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- Publication type:
- Letter
Identification of novel gout loci from trans-ethnic meta-analysis of serum urate level.
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- 2025
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- Publication type:
- Letter
A meta-analysis of genome-wide association studies using Japanese and Taiwanese has revealed novel loci associated with gout susceptibility.
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- 2022
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- Publication type:
- Literature Review
Increase of serum uric acid levels associated with APOE ε2 haplotype: a clinico-genetic investigation and in vivo approach.
- Published in:
- Human Cell, 2021, v. 34, n. 6, p. 1727, doi. 10.1007/s13577-021-00609-w
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- Article
Both variants of A1CF and BAZ1B genes are associated with gout susceptibility: a replication study and meta-analysis in a Japanese population.
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- Human Cell, 2021, v. 34, n. 2, p. 293, doi. 10.1007/s13577-021-00485-4
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- Publication type:
- Article
A common variant of LDL receptor related protein 2 (LRP2) gene is associated with gout susceptibility: a meta-analysis in a Japanese population.
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- 2020
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- Publication type:
- Literature Review
A common variant of MAF/c- MAF, transcriptional factor gene in the kidney, is associated with gout susceptibility.
- Published in:
- Human Cell, 2018, v. 31, n. 1, p. 10, doi. 10.1007/s13577-017-0186-6
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- Publication type:
- Article
Common variant of ALPK1 is not associated with gout: a replication study.
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- Human Cell, 2015, v. 28, n. 1, p. 1, doi. 10.1007/s13577-014-0103-1
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- Publication type:
- Article
A common variant of leucine-rich repeat-containing 16A (LRRC16A) gene is associated with gout susceptibility.
- Published in:
- Human Cell, 2014, v. 27, n. 2, p. 1, doi. 10.1007/s13577-013-0081-8
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- Publication type:
- Article
A common missense variant of monocarboxylate transporter 9 (<i>MCT9/SLC16A9</i>) gene is associated with renal overload gout, but not with all gout susceptibility.
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- Human Cell, 2013, v. 26, n. 4, p. 133, doi. 10.1007/s13577-013-0073-8
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- Article
Genetic mapping of the rat mutation creeping and evaluation of its positional candidate gene reelin.
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- Mammalian Genome, 2000, v. 11, n. 2, p. 111, doi. 10.1007/s003350010022
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- Article
Coffee Consumption Reduces Gout Risk Independently of Serum Uric Acid Levels: Mendelian Randomization Analyses Across Ancestry Populations.
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- ACR Open Rheumatology, 2022, v. 4, n. 6, p. 534, doi. 10.1002/acr2.11425
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- Publication type:
- Article
Influence of respiration on cerebrospinal fluid movement using magnetic resonance spin labeling.
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- Fluids & Barriers of the CNS, 2013, v. 10, n. 1, p. 1, doi. 10.1186/2045-8118-10-36
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- Article
ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout.
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- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 3, p. 302, doi. 10.1002/acn3.167
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- Publication type:
- Article
OAT10/SLC22A13 Acts as a Renal Urate Re-Absorber: Clinico-Genetic and Functional Analyses With Pharmacological Impacts.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.842717
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- Publication type:
- Article