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1.
Identification of GLUT12/SLC2A12 as a urate transporter that regulates the blood urate level in hyperuricemia model mice.
Proc Natl Acad Sci U S A
; 117(31): 18175-18177, 2020 08 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-32690690
2.
Genome-wide meta-analysis between renal overload type and renal underexcretion type of clinically defined gout in Japanese populations.
Mol Genet Metab
; 136(3): 186-189, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35148957
3.
Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene.
Rheumatology (Oxford)
; 61(3): 1276-1281, 2022 03 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34255816
4.
Substantial anti-gout effect conferred by common and rare dysfunctional variants of URAT1/SLC22A12.
Rheumatology (Oxford)
; 60(11): 5224-5232, 2021 11 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33821957
5.
Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients.
Ann Rheum Dis
; 79(5): 657-665, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-32238385
6.
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout.
Ann Rheum Dis
; 78(10): 1430-1437, 2019 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-31289104
7.
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes.
Ann Rheum Dis
; 76(5): 869-877, 2017 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-27899376
8.
Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes.
Ann Rheum Dis
; 75(4): 652-9, 2016 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-25646370
9.
Dysfunctional missense variant of OAT10/SLC22A13 decreases gout risk and serum uric acid levels.
Ann Rheum Dis
; 79(1): 164-166, 2020 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31780526
10.
Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population.
J Hum Genet
; 60(10): 613-7, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26178431
11.
Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families.
Rheumatology (Oxford)
; 59(12): 3988-3990, 2020 12 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33011794
12.
Common variants of a urate-associated gene LRP2 are not associated with gout susceptibility.
Rheumatol Int
; 34(4): 473-6, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24366390
13.
The biological effects and thermal degradation of NPB-22, a synthetic cannabinoid.
Forensic Toxicol
; 2024 Jan 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-38294576
14.
Visualization of pancreatic juice movement using unenhanced MR imaging with spin labeling: preliminary results in normal and pathophysiologic conditions.
J Magn Reson Imaging
; 35(5): 1119-24, 2012 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-22180260
15.
Coffee Consumption Reduces Gout Risk Independently of Serum Uric Acid Levels: Mendelian Randomization Analyses Across Ancestry Populations.
ACR Open Rheumatol
; 4(6): 534-539, 2022 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-35348303
16.
OAT10/SLC22A13 Acts as a Renal Urate Re-Absorber: Clinico-Genetic and Functional Analyses With Pharmacological Impacts.
Front Pharmacol
; 13: 842717, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35462902
17.
The Spatial Distribution of Water Components with Similar T2 May Provide Insight into Pathways for Large Molecule Transportation in the Brain.
Magn Reson Med Sci
; 20(1): 34-39, 2021 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32074590
18.
Both variants of A1CF and BAZ1B genes are associated with gout susceptibility: a replication study and meta-analysis in a Japanese population.
Hum Cell
; 34(2): 293-299, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-33517564
19.
Increase of serum uric acid levels associated with APOE ε2 haplotype: a clinico-genetic investigation and in vivo approach.
Hum Cell
; 34(6): 1727-1733, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-34532841
20.
A Proposal for Practical Diagnosis of Renal Hypouricemia: Evidenced from Genetic Studies of Nonfunctional Variants of URAT1/SLC22A12 among 30,685 Japanese Individuals.
Biomedicines
; 9(8)2021 Aug 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-34440216