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SLC22A12
Results: 5

#	Item
1	An update on the genetic architecture of hyperuricemia and gout Add to Reading List Source URL: arthritis-research.com Language: English Inborn errors of purine-pyrimidine metabolism Genetics Molecular biology Hyperuricemia SLC2A9 SLC22A12 Urate oxidase Gout Genome-wide association study Biology Uric acid Solute carrier family
2	PHYSIOLOGY IN MEDICINE: A SERIES OF ARTICLES LINKING MEDICINE WITH SCIENCE Physiology in Medicine: Dennis A. Ausiello, MD, Editor; Dale J. Benos, PhD, Deputy Editor; Francois Abboud, MD, Associate Editor; William J. Koop Add to Reading List Source URL: www.the-aps.org Language: English Medicine Solute carrier family Inborn errors of purine-pyrimidine metabolism Rheumatology SLC22A12 Hypouricemia Transport proteins Hyperuricemia Febuxostat Uric acid Chemistry Biology
3	Human Molecular Genetics, 2011, Vol. 20, No. 20 doi:[removed]hmg/ddr307 Advance Access published on July 18, [removed]–4068 Add to Reading List Source URL: handls.nih.gov Language: English - Date: 2012-01-28 08:19:54 Inborn errors of purine-pyrimidine metabolism Solute carrier family Genetic genealogy Population genetics Genome-wide association study SLC22A12 Single-nucleotide polymorphism International HapMap Project Gout Biology Genetics Uric acid
4	An upper limit for macromolecular crowding effects Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Medicine Organ failure Nephrology Kidney diseases Hypouricemia Solute carrier family SLC22A12 Acute uric acid nephropathy Acute kidney injury Biology Anatomy Uric acid
5	The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Anatomy Genetics Renal physiology Hypouricemia SLC22A12 Compound heterozygosity Renal function Sickle-cell disease Acute kidney injury Biology Uric acid Medicine

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