ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study ; volume:8 ; number:1 ; day:16 ; month:2 ; year:2018 ; pages:1-9 ; date:12.2018
Scientific reports ; 8, Heft 1 (16.2.2018), 1-9, 12.2018
- Creator
-
Chen, Chung-Jen
- Contributor
-
Tseng, Chia-Chun
Yen, Jeng-Hsien
Chang, Jan-Gowth
Chou, Wen-Cheng
Chu, Hou-Wei
Chang, Shun-Jen
Liao, Wei-Ting
SpringerLink (Online service)
- DOI
-
10.1038/s41598-018-21425-7
- URN
-
urn:nbn:de:1111-201804048494
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:45 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Chen, Chung-Jen
- Tseng, Chia-Chun
- Yen, Jeng-Hsien
- Chang, Jan-Gowth
- Chou, Wen-Cheng
- Chu, Hou-Wei
- Chang, Shun-Jen
- Liao, Wei-Ting
- SpringerLink (Online service)
Other Objects (12)
Epistatic interaction between PKD2 and ABCG2 influences the pathogenesis of hyperuricemia and gout
Pleiotropic effect of the ABCG2 gene in gout: involvement in serum urate levels and progression from hyperuricemia to gout
The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients
Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2
Susceptibility genes of hyperuricemia and gout
Genetic polymorphisms and decreased protein expression of ABCG2 urate transporters are associated with susceptibility to gout, disease severity and renal-overload hyperuricemia
Circulating microRNA alternations in primary hyperuricemia and gout
NUMB dysfunction defines a novel mechanism underlying hyperuricemia and gout
Cichorium intybus L. promotes intestinal uric acid excretion by modulating ABCG2 in experimental hyperuricemia
Differential gene expression of ABCG2, SLC22A12, IL-1β, and ALPK1 in peripheral blood leukocytes of primary gout patients with hyperuricemia and their comorbidities: a case–control study
Population-specific association between ABCG2 variants and tophaceous disease in people with gout
A comprehensive analysis of the association of common variants of ABCG2 with gout
Epistatic interaction between PKD2 and ABCG2 influences the pathogenesis of hyperuricemia and gout
Pleiotropic effect of the ABCG2 gene in gout: involvement in serum urate levels and progression from hyperuricemia to gout
The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients
Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2
Susceptibility genes of hyperuricemia and gout
Genetic polymorphisms and decreased protein expression of ABCG2 urate transporters are associated with susceptibility to gout, disease severity and renal-overload hyperuricemia
Circulating microRNA alternations in primary hyperuricemia and gout
NUMB dysfunction defines a novel mechanism underlying hyperuricemia and gout
Cichorium intybus L. promotes intestinal uric acid excretion by modulating ABCG2 in experimental hyperuricemia
Differential gene expression of ABCG2, SLC22A12, IL-1β, and ALPK1 in peripheral blood leukocytes of primary gout patients with hyperuricemia and their comorbidities: a case–control study
Population-specific association between ABCG2 variants and tophaceous disease in people with gout
A comprehensive analysis of the association of common variants of ABCG2 with gout
Epistatic interaction between PKD2 and ABCG2 influences the pathogenesis of hyperuricemia and gout
Pleiotropic effect of the ABCG2 gene in gout: involvement in serum urate levels and progression from hyperuricemia to gout
The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients
Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2
Susceptibility genes of hyperuricemia and gout
Genetic polymorphisms and decreased protein expression of ABCG2 urate transporters are associated with susceptibility to gout, disease severity and renal-overload hyperuricemia
Circulating microRNA alternations in primary hyperuricemia and gout
NUMB dysfunction defines a novel mechanism underlying hyperuricemia and gout
Cichorium intybus L. promotes intestinal uric acid excretion by modulating ABCG2 in experimental hyperuricemia
Differential gene expression of ABCG2, SLC22A12, IL-1β, and ALPK1 in peripheral blood leukocytes of primary gout patients with hyperuricemia and their comorbidities: a case–control study
Population-specific association between ABCG2 variants and tophaceous disease in people with gout