PMC Links for GEO Profiles (Select 23503485) - PMC

Ana Perdomo-Ramirez, Elizabeth Cordoba-Lanus, Carmen Jane Trujillo-Frias, Carolina Gonzalez-Navasa, Elena Ramos-Trujillo, Maria Isabel Luis-Yanes, Victor Garcia-Nieto, Felix Claverie-Martin

Int J Mol Sci. 2023 May; 24(9): 8455. Published online 2023 May 8. doi: 10.3390/ijms24098455

PMCID:: PMC10179447

Abstract Article PDF–1.3M

Select item 88892755.

Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene

Akiyoshi Nakayama, Yusuke Kawamura, Yu Toyoda, Seiko Shimizu, Makoto Kawaguchi, Yuka Aoki, Kenji Takeuchi, Rieko Okada, Yoko Kubo, Toshihiko Imakiire, Satoko Iwasawa, Hiroshi Nakashima, Masashi Tsunoda, Keiichi Ito, Hiroo Kumagai, Tappei Takada, Kimiyoshi Ichida, Nariyoshi Shinomiya, Hirotaka Matsuo

Rheumatology (Oxford) 2022 Mar; 61(3): 1276–1281. Published online 2021 Jul 13. doi: 10.1093/rheumatology/keab545

PMCID:: PMC8889275

Abstract Article PDF–513K

Select item 85662566.

Substantial anti-gout effect conferred by common and rare dysfunctional variants of URAT1/SLC22A12

Yu Toyoda, Yusuke Kawamura, Akiyoshi Nakayama, Hirofumi Nakaoka, Toshihide Higashino, Seiko Shimizu, Hiroshi Ooyama, Keito Morimoto, Naohiro Uchida, Ryuichiro Shigesawa, Kenji Takeuchi, Ituro Inoue, Kimiyoshi Ichida, Hiroshi Suzuki, Nariyoshi Shinomiya, Tappei Takada, Hirotaka Matsuo

Rheumatology (Oxford) 2021 Nov; 60(11): 5224–5232. Published online 2021 Apr 2. doi: 10.1093/rheumatology/keab327

PMCID:: PMC8566256

Abstract Article PDF–436K

Select item 85291337.

The impact of an URAT1 polymorphism on the losartan treatment of hypertension and hyperuricemia

Liting Wu, Yingchao Fan, Yuan Wang, Zhumeng Li, Delong Mao, Wenfang Zhuang

J Clin Lab Anal. 2021 Oct; 35(10): e23949. Published online 2021 Sep 8. doi: 10.1002/jcla.23949

PMCID:: PMC8529133

Abstract Article PDF–336K

Select item 84741038.

Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults

Juan Manuel Vargas-Morales, Martha Guevara-Cruz, Celia Aradillas-García, Lilia G. Noriega, Armando Tovar, Jorge Alejandro Alegría-Torres

Version 2. F1000Res. 2021; 10: 217. Published online 2021 Sep 24. doi: 10.12688/f1000research.46399.2

PMCID:: PMC8474103

Abstract Article PDF–900K

Select item 81650309.

Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome

Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi

Cell. Author manuscript; available in PMC 2022 May 27.

Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011

PMCID:: PMC8165030

Abstract Article PDF–2.2M

Select item 777164310.

27‐Hydroxycholesterol regulates human SLC22A12 gene expression through estrogen receptor action

Masaya Matsubayashi, Yoshihiko M. Sakaguchi, Yoshiki Sahara, Hitoki Nanaura, Sotaro Kikuchi, Arvand Asghari, Linh Bui, Shinko Kobashigawa, Mari Nakanishi, Riko Nagata, Takeshi K. Matsui, Genro Kashino, Masatoshi Hasegawa, Shin Takasawa, Masahiro Eriguchi, Kazuhiko Tsuruya, Shushi Nagamori, Kazuma Sugie, Takahiko Nakagawa, Minoru Takasato, Michihisa Umetani, Eiichiro Mori

FASEB J. 2021 Jan; 35(1): e21262. Published online 2020 Dec 23. doi: 10.1096/fj.202002077R

PMCID:: PMC7771643

Abstract Article PDF–1.1M

Select item 773372311.

Identification of a dysfunctional splicing mutation in the SLC22A12/URAT1 gene causing renal hypouricaemia type 1: a report on two families

Yusuke Kawamura, Yu Toyoda, Takuma Ohnishi, Ryutaro Hisatomi, Toshihide Higashino, Akiyoshi Nakayama, Seiko Shimizu, Masato Yanagi, Isamu Kamimaki, Rika Fujimaru, Hiroshi Suzuki, Nariyoshi Shinomiya, Tappei Takada, Hirotaka Matsuo

Rheumatology (Oxford) 2020 Dec; 59(12): 3988–3990. Published online 2020 Oct 4. doi: 10.1093/rheumatology/keaa461

PMCID:: PMC7733723

Article PDF–223K

Select item 758246112.

Glucose, Fructose, and Urate Transporters in the Choroid Plexus Epithelium

Yoichi Chiba, Ryuta Murakami, Koichi Matsumoto, Keiji Wakamatsu, Wakako Nonaka, Naoya Uemura, Ken Yanase, Masaki Kamada, Masaki Ueno

Int J Mol Sci. 2020 Oct; 21(19): 7230. Published online 2020 Sep 30. doi: 10.3390/ijms21197230

PMCID:: PMC7582461

Abstract Article PDF–2.1M

Select item 722598313.

Uric Acid Has Direct Proinflammatory Effects on Human Macrophages by Increasing Proinflammatory Mediators and Bacterial Phagocytosis Probably via URAT1

Camilo P. Martínez-Reyes, Aarón N. Manjarrez-Reyna, Lucia A. Méndez-García, José A. Aguayo-Guerrero, Beatriz Aguirre-Sierra, Rafael Villalobos-Molina, Yolanda López-Vidal, Karen Bobadilla, Galileo Escobedo

Biomolecules. 2020 Apr; 10(4): 576. Published online 2020 Apr 9. doi: 10.3390/biom10040576

PMCID:: PMC7225983

Abstract Article PDF–7.0M

Select item 720197814.

Deciphering genetic signatures by whole exome sequencing in a case of co-prevalence of severe renal hypouricemia and diabetes with impaired insulin secretion

Motohiro Sekiya, Takaaki Matsuda, Yuki Yamamoto, Yasuhisa Furuta, Mariko Ohyama, Yuki Murayama, Yoko Sugano, Yoshinori Ohsaki, Hitoshi Iwasaki, Naoya Yahagi, Shigeru Yatoh, Hiroaki Suzuki, Hitoshi Shimano

BMC Med Genet. 2020; 21: 91. Published online 2020 May 6. doi: 10.1186/s12881-020-01031-z

PMCID:: PMC7201978

Abstract Article PDF–2.5M

Select item 715393215.

Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels

Kazuharu Misawa, Takanori Hasegawa, Eikan Mishima, Promsuk Jutabha, Motoshi Ouchi, Kaname Kojima, Yosuke Kawai, Masafumi Matsuo, Naohiko Anzai, Masao Nagasaki

Genetics. 2020 Apr; 214(4): 1079–1090. Published online 2020 Jan 31. doi: 10.1534/genetics.119.303006

PMCID:: PMC7153932

Abstract Article PDF–1.2M

Select item 714514516.

A population-specific low-frequency variant of SLC22A12 (p.W258*) explains nearby genome-wide association signals for serum uric acid concentrations among Koreans

Sun-Wha Im, Jeesoo Chae, Ho-Young Son, Belong Cho, Jong-Il Kim, Jin-Ho Park

PLoS One. 2020; 15(4): e0231336. Published online 2020 Apr 9. doi: 10.1371/journal.pone.0231336

PMCID:: PMC7145145

Abstract Article PDF–1.0M

Select item 707700117.

ABCG2 rs2231142 variant in hyperuricemia is modified by SLC2A9 and SLC22A12 polymorphisms and cardiovascular risk factors in an elderly community-dwelling population

Jia Liu, Wei Yang, Yun Li, Zhanyun Wei, Xiaojuan Dan

BMC Med Genet. 2020; 21: 54. Published online 2020 Mar 17. doi: 10.1186/s12881-020-0987-4

PMCID:: PMC7077001

Abstract Article PDF–612K

Select item 701584618.

Refining genome-wide associated loci for serum uric acid in individuals with African ancestry

Guanjie Chen, Daniel Shriner, Ayo P Doumatey, Jie Zhou, Amy R Bentley, Lin Lei, Adebowale Adeyemo, Charles N Rotimi

Hum Mol Genet. 2020 Feb 1; 29(3): 506–514. Published online 2019 Dec 16. doi: 10.1093/hmg/ddz272

PMCID:: PMC7015846

Abstract Article PDF–652K

Select item 677987819.

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

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

Sci Rep. 2019; 9: 14360. Published online 2019 Oct 7. doi: 10.1038/s41598-019-50798-6

PMCID:: PMC6779878

Abstract Article PDF–1.7M

Select item 662539920.

Urate transport capacity of glucose transporter 9 and urate transporter 1 in cartilage chondrocytes

Bingqing Zhang, Mengyuan Duan, Bo Long, Baozhong Zhang, Dongmei Wang, Yun Zhang, Jialin Chen, Xiaoming Huang, Yang Jiao, Lei Zhu, Xuejun Zeng

Mol Med Rep. 2019 Aug; 20(2): 1645–1654. Published online 2019 Jun 25. doi: 10.3892/mmr.2019.10426

PMCID:: PMC6625399

Abstract Article PDF–866K

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