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Pathophysiological impact of dysfunctional common and rare variants of urate transporter ABCG2 on urate-related diseases
Electrophoresis Letters
◽
10.2198/electroph.65.1
◽
2021
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Vol 65
(1)
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pp. 1-5
Author(s):
Yu Toyoda
◽
Tappei Takada
◽
Hirotaka Matsuo
◽
Kimiyoshi Ichida
◽
Blanka Stiburkova
◽
...
Keyword(s):
Rare Variants
◽
Urate Transporter
Download Full-text
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10.3410/f.1122807.579894
◽
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◽
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◽
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Faculty Opinions recommendation of SLC2A9 is a high-capacity urate transporter in humans.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.1124191.618718
◽
2009
◽
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Jeff Kraut
Keyword(s):
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◽
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Faculty Opinions recommendation of Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.1161406.621933
◽
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◽
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Richard J Naftalin
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◽
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Faculty Opinions recommendation of Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.1160058.620718
◽
2009
◽
Author(s):
Andrew Wilkie
Keyword(s):
Type 1 Diabetes
◽
Rare Variants
◽
Antiviral Responses
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Faculty Opinions recommendation of Serotonin transporter gene-linked polymorphic region: possible pharmacogenetic implications of rare variants.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.14731.472247
◽
2006
◽
Author(s):
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Keyword(s):
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◽
Rare Variants
◽
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◽
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◽
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Faculty Opinions recommendation of Synthetic associations created by rare variants do not explain most GWAS results.
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◽
10.3410/f.715898103.791502804
◽
2012
◽
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Keyword(s):
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Faculty Opinions recommendation of Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.717952610.793458111
◽
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Author(s):
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◽
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Faculty Opinions recommendation of Effect of rare variants in ADRB2 on risk of severe exacerbations and symptom control during longacting β agonist treatment in a multiethnic asthma population: a genetic study.
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◽
10.3410/f.718310565.793494424
◽
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Author(s):
Harold Nelson
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◽
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Faculty Opinions recommendation of Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data.
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◽
10.3410/f.718882382.793500875
◽
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◽
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◽
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◽
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◽
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Faculty Opinions recommendation of Methods for association analysis and meta-analysis of rare variants in families.
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◽
10.3410/f.725726003.793510833
◽
2015
◽
Author(s):
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Keyword(s):
Association Analysis
◽
Rare Variants
◽
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