Discovery of URAT1 SNPs and association between serum uric acid levels and URAT1

por Cho, Sung Kweon, Kim, Soriul, Chung, Jae-Yong, Jee, Sun Ha
Publicado 2015

The Prevalence of Hyperuricemia Sharply Increases from the Late Menopausal Transition Stage in Middle-Aged Women

por Cho, Sung Kweon, Winkler, Cheryl A., Lee, Soo-Jin, Chang, Yoosoo, Ryu, Seungho
Publicado 2019

Review of Urate-Lowering Therapeutics: From the Past to the Future

por Jenkins, Christopher, Hwang, Jennifer H., Kopp, Jeffrey B., Winkler, Cheryl A., Cho, Sung Kweon
Publicado 2022

Preclinical pharmacokinetics, interspecies scaling, and pharmacokinetics of a Phase I clinical trial of TTAC-0001, a fully human monoclonal antibody against vascular endothelial gr...

por Lee, Weon Sup, Shim, Sang Ryeol, Lee, Seon Young, Yoo, Jin San, Cho, Sung Kweon
Publicado 2018

Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population

por Stiburkova, Blanka, Bohatá, Jana, Pavelcová, Kateřina, Tasic, Velibor, Plaseska-Karanfilska, Dijana, Cho, Sung-Kweon, Potočnaková, Ludmila, Šaligová, Jana
Publicado 2021

Efficacy of Xanthine Oxidase Inhibitors in Lowering Serum Uric Acid in Chronic Kidney Disease: A Systematic Review and Meta-Analysis

por Lee, Yoojin, Hwang, Jennifer, Desai, Shaan H., Li, Xiaobai, Jenkins, Christopher, Kopp, Jeffrey B., Winkler, Cheryl A., Cho, Sung Kweon
Publicado 2022

Antihyperglycemic mechanism of metformin occurs via the AMPK/LXRα/POMC pathway

por Cho, Kumsun, Chung, Jae Yong, Cho, Sung Kweon, Shin, Hyun-Woo, Jang, In-Jin, Park, Jong-Wan, Yu, Kyung-Sang, Cho, Joo-Youn
Publicado 2015

Shared Genetic Background between Parkinson’s Disease and Schizophrenia: A Two-Sample Mendelian Randomization Study

por Kim, Kiwon, Kim, Soyeon, Myung, Woojae, Shim, Injeong, Lee, Hyewon, Kim, Beomsu, Cho, Sung Kweon, Yoon, Joohyun, Kim, Doh Kwan, Won, Hong-Hee
Publicado 2021

Characterization of a Compound Heterozygous SLC2A9 Mutation That Causes Hypouricemia

por Yoon, Jaeho, Cachau, Raul, David, Victor A., Thompson, Mary, Jung, Wooram, Jee, Sun-Ha, Daar, Ira O., Winkler, Cheryl A., Cho, Sung-Kweon
Publicado 2021

Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals

por Cho, Sung Kweon, Kim, Beomsu, Myung, Woojae, Chang, Yoosoo, Ryu, Seungho, Kim, Han-Na, Kim, Hyung-Lae, Kuo, Po-Hsiu, Winkler, Cheryl A., Won, Hong-Hee
Publicado 2020

Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2

por Toyoda, Yu, Cho, Sung Kweon, Tasic, Velibor, Pavelcová, Kateřina, Bohatá, Jana, Suzuki, Hiroshi, David, Victor A., Yoon, Jaeho, Pallaiova, Anna, Šaligová, Jana, Nousome, Darryl, Cachau, Raul, Winkler, Cheryl A., Takada, Tappei, Stibůrková, Blanka
Publicado 2023

Contribution of SLC22A12 on hypouricemia and its clinical significance for screening purposes

por Cha, Do Hyeon, Gee, Heon Yung, Cachau, Raul, Choi, Jong Mun, Park, Daeui, Jee, Sun Ha, Ryu, Seungho, Kim, Kyeong Kyu, Won, Hong-Hee, Limou, Sophie, Myung, Woojae, Winkler, Cheryl A., Cho, Sung Kweon
Publicado 2019