Detalhe da pesquisa
1.
Substantial anti-gout effect conferred by common and rare dysfunctional variants of URAT1/SLC22A12.
Rheumatology (Oxford)
; 60(11): 5224-5232, 2021 11 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33821957
2.
Thromboxane A2 receptor antagonist (ONO-8809) attenuates renal disorders caused by salt overload in stroke-prone spontaneously hypertensive rats.
Clin Exp Pharmacol Physiol
; 48(10): 1391-1401, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34152603
3.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-32238385
4.
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout.
Ann Rheum Dis
; 78(10): 1430-1437, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31289104
5.
Common variant of BCAS3 is associated with gout risk in Japanese population: the first replication study after gout GWAS in Han Chinese.
BMC Med Genet
; 19(1): 96, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29879923
6.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-27899376
7.
Dysfunctional missense variant of OAT10/SLC22A13 decreases gout risk and serum uric acid levels.
Ann Rheum Dis
; 79(1): 164-166, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31780526
8.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-33011794
9.
Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient.
Front Med (Lausanne)
; 11: 1374222, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38818404
10.
Meta-analysis confirms an association between gout and a common variant of LRRC16A locus.
Mod Rheumatol
; 27(3): 553-555, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27585540
11.
Hypertension-Associated Genes in the Mesenteric Artery of Three Spontaneously Hypertensive Rat Substrains Identified Using a DNA Array Method.
Front Biosci (Landmark Ed)
; 27(6): 191, 2022 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35748267
12.
Practical forensic use of kinship determination using high-density SNP profiling based on a microarray platform, focusing on low-quantity DNA.
Forensic Sci Int Genet
; 61: 102752, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35987117
13.
Assessment of Delayed Large Local Reactions After the First Dose of the SARS-CoV-2 mRNA-1273 Vaccine in Japan.
JAMA Dermatol
; 158(8): 923-927, 2022 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35649530
14.
Porphyrin accumulation in humans with common dysfunctional variants of ABCG2, a porphyrin transporter: potential association with acquired photosensitivity.
Hum Cell
; 34(4): 1082-1086, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34009629
15.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-34532841
16.
A common variant of LDL receptor related protein 2 (LRP2) gene is associated with gout susceptibility: a meta-analysis in a Japanese population.
Hum Cell
; 33(2): 303-307, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31975031
17.
A case of Hailey-Hailey disease with novel ATP2C1 gene variant (c.G925C) showing unusual phenotype.
J Dermatol
; 2024 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38711270
18.
A new approach to identifying hypertension-associated genes in the mesenteric artery of spontaneously hypertensive rats and stroke-prone spontaneously hypertensive rats.
J Hypertens
; 37(8): 1644-1656, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30882592
19.
A common variant of MAF/c-MAF, transcriptional factor gene in the kidney, is associated with gout susceptibility.
Hum Cell
; 31(1): 10-13, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29080939
20.
Independent effects of ADH1B and ALDH2 common dysfunctional variants on gout risk.
Sci Rep
; 7(1): 2500, 2017 05 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-28566767