Works matching AU Kimiyoshi Ichida

Results: 78

Altered d-methionine kinetics in rats with renal impairment.

Published in:

Amino Acids, 2011, v. 40, n. 4, p. 1205, doi. 10.1007/s00726-010-0746-5

By:

Hasegawa, Hiroshi;
Shinohara, Yoshihiko;
Akahane, Kenji;
Hashimoto, Takao;
Ichida, Kimiyoshi

Publication type:

Article

Production and Characterization of Transgenic Mice Harboring Mutant Human UMOD Gene.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2008, v. 27, n. 6/7, p. 596, doi. 10.1080/15257770802136065

By:

Takiue, Yuichi;
Hosoyamada, Makoto;
Yokoo, Takuya;
Kimura, Masaki;
Ochiai, Manami;
Kaneko, Kiyoko;
Ichida, Kimiyoshi;
Hosoya, Tatsuo;
Shibasaki, Toshiaki

Publication type:

Article

Identification of Febuxostat as a New Strong ABCG2 Inhibitor: Potential Applications and Risks in Clinical Situations.

Published in:

Frontiers in Pharmacology, 2016, v. 7, p. 1, doi. 10.3389/fphar.2016.00518

By:

Hiroshi Miyata;
Tappei Takada;
Yu Toyoda;
Hirotaka Matsuo;
Kimiyoshi Ichida;
Hiroshi Suzuki;
Michaelis, Martin;
Peng Hsiao

Publication type:

Article

Prenatal Brain Disruption in Molybdenum Cofactor Deficiency.

Published in:

Journal of Child Neurology, 2011, v. 26, n. 4, p. 460, doi. 10.1177/0883073810383017

By:

Carmi-Nawi, Nirit;
Malinger, Gustavo;
Mandel, Hanna;
Ichida, Kimiyoshi;
Lerman-Sagie, Tally;
Lev, Dorit

Publication type:

Article

Possible Use of Non-purine Selective Xanthine Oxidoreductase Inhibitors for Prevention of Exercise-induced Acute Kidney Injury Associated with Renal Hypouricemia.

Published in:

Internal Medicine, 2023, v. 62, n. 18, p. 2725, doi. 10.2169/internalmedicine.0678-22

By:

Chiharu Aizawa;
Masahiro Okabe;
Daisuke Takahashi;
Makoto Sagasaki;
Mao Watanabe;
Toshinari Fujimoto;
Yuuki Yoshioka;
Ai Katsuma;
Ai Kimura;
Daisuke Miyamoto;
Nana Sato;
Ken Okamoto;
Kimiyoshi Ichida;
Yoichi Miyazaki;
Takashi Yokoo

Publication type:

Article

Characterization of Urate Metabolism and Complications of Patients with Renal Hypouricemia.

Published in:

Internal Medicine, 2023, v. 62, n. 13, p. 1915, doi. 10.2169/internalmedicine.0457-22

By:

Satoshi Miyazaki;
Toshihiro Hamada;
Tadahiro Isoyama;
Shinichi Okada;
Katsuyuki Tomita;
Yusuke Endo;
Masanari Kuwabara;
Shinobu Sugihara;
Kazuhide Ogino;
Haruaki Ninomiya;
Kimiyoshi Ichida;
Kazuhiro Yamamoto;
Atsushi Takenaka;
Ichiro Hisatome

Publication type:

Article

A Novel PRPS1 Mutation in a Japanese Patient with CMTX5 .

Published in:

Internal Medicine, 2022, v. 61, n. 11, p. 1749, doi. 10.2169/internalmedicine.8029-21

By:

Shunichi Shirakawa;
Tatsufumi Murakami;
Akihiro Hashiguchi;
Hiroshi Takashima;
Hiroshi Hasegawa;
Kimiyoshi Ichida;
Yoshihide Sunada

Publication type:

Article

Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function.

Published in:

Internal Medicine, 2022, v. 61, n. 9, p. 1383, doi. 10.2169/internalmedicine.7897-21

By:

Satoshi Miyazaki;
Toshihiro Hamada;
Shinobu Sugihara;
Einosuke Mizuta;
Yusuke Endo;
Akira Ohtahara;
Koji Komatsu;
Masanari Kuwabara;
Tomoko Fukuuchi;
Kiyoko Kaneko;
Kimiyoshi Ichida;
Kazuhide Ogino;
Haruaki Ninomiya;
Kazuhiro Yamamoto;
Takashi Nakamura;
Ichiro Hisatome

Publication type:

Article

Association between polymorphism at IGF-1 rs35767 gene locus and long-term decline in renal function: a Japanese retrospective longitudinal cohort study.

Published in:

2021

By:

Honda, Kosuke;
Kuriyama, Satoru;
Ichida, Kimiyoshi;
Nakano, Tomoko;
Sugano, Naoki;
Yokoo, Takashi

Publication type:

journal article

Plasma and Urinary Metabolomic Analysis of Gout and Asymptomatic Hyperuricemia and Profiling of Potential Biomarkers: A Pilot Study.

Published in:

Biomedicines, 2024, v. 12, n. 2, p. 300, doi. 10.3390/biomedicines12020300

By:

Ohashi, Yuki;
Ooyama, Hiroshi;
Makinoshima, Hideki;
Takada, Tappei;
Matsuo, Hirotaka;
Ichida, Kimiyoshi

Publication type:

Article

Dysuricemia.

Published in:

Biomedicines, 2023, v. 11, n. 12, p. 3169, doi. 10.3390/biomedicines11123169

By:

Nakayama, Akiyoshi;
Kurajoh, Masafumi;
Toyoda, Yu;
Takada, Tappei;
Ichida, Kimiyoshi;
Matsuo, Hirotaka

Publication type:

Article

Genetic Basis of the Epidemiological Features and Clinical Significance of Renal Hypouricemia.

Published in:

Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071696

By:

Hakoda, Masayuki;
Ichida, Kimiyoshi

Publication type:

Article

Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal Hypouricemia.

Published in:

Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071584

By:

Miyamoto, Daisuke;
Sato, Nana;
Nagata, Koji;
Sakai, Yukinao;
Sugihara, Hitoshi;
Ohashi, Yuki;
Stiburkova, Blanka;
Sebesta, Ivan;
Ichida, Kimiyoshi;
Okamoto, Ken

Publication type:

Article

Association of Mutations Identified in Xanthinuria with the Function and Inhibition Mechanism of Xanthine Oxidoreductase.

Published in:

Biomedicines, 2021, v. 9, n. 11, p. 1723, doi. 10.3390/biomedicines9111723

By:

Sekine, Mai;
Okamoto, Ken;
Ichida, Kimiyoshi

Publication type:

Article

Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure.

Published in:

Pediatrics International, 2007, v. 49, n. 2, p. 235, doi. 10.1111/j.1442-200X.2007.02337.x

By:

Ohtsuka, Yasufumi;
Zaitsu, Masafumi;
Ichida, Kimiyoshi;
Isomura, Naoko;
Tsuji, Kosuke;
Sato, Tadashi;
Hamasaki, Yuhei

Publication type:

Article

Renaturation of Lyophilized Concanavalin a Treated in Water Content Controlled Hydrated Ionic Liquids.

Published in:

Applied Sciences (2076-3417), 2021, v. 11, n. 1, p. 57, doi. 10.3390/app11010057

By:

Fujita, Kyoko;
Fujii, Ryota;
Ichida, Kimiyoshi

Publication type:

Article

Renal stone and chronic kidney failure associated with hypouricemia: Answers.

Published in:

Pediatric Nephrology, 2019, v. 34, n. 7, p. 1225, doi. 10.1007/s00467-018-4170-5

By:

Aksoy, Gulsah Kaya;
Koyun, Mustafa;
Ichida, Kimiyoshi;
Comak, Elif;
Akman, Sema

Publication type:

Article

Renal stone and chronic kidney failure associated with hypouricemia: Questions.

Published in:

2019

By:

Aksoy, Gulsah Kaya;
Koyun, Mustafa;
Ichida, Kimiyoshi;
Comak, Elif;
Akman, Sema

Publication type:

Case Study

Common Defects of ABCG2, a High-Capacity Urate Exporter, Cause Gout: A Function-Based Genetic Analysis in a Japanese Population.

Published in:

Science Translational Medicine, 2009, v. 1, n. 5, p. 1, doi. 10.1126/scitranslmed.3000237

By:

Matsuo, Hirotaka;
Takada, Tappei;
Ichida, Kimiyoshi;
Nakamura, Takahiro;
Nakayama, Akiyoshi;
Ikebuchi, Yuki;
Ito, Kousei;
Kusanagi, Yasuyoshi;
Chiba, Toshinori;
Tadokoro, Shin;
Takada, Yuzo;
Oikawa, Yuji;
Inoue, Hiroki;
Suzuki, Koji;
Okada, Riek;
Nishiyama, Junichiro;
Domoto, Hideharu;
Watanabe, Satoru;
Fujita, Masanori;
Morimoto, Yuji

Publication type:

Article

A case of renal hypouricemia due to T217M mutation in SLC22A12 incidentally associated with IgA nephropathy.

Published in:

2024

By:

Sakurabu, Yoshimasa;
Uchida, Haruhito A.;
Tahara, Toshihisa;
Asakawa, Tomohiko;
Yamasaki, Haruka;
Katayama, Katsuyoshi;
Okamoto, Shugo;
Onishi, Yasuhiro;
Matsuoka‐Uchiyama, Natsumi;
Tanaka, Keiko;
Takeuchi, Hidemi;
Tsuji, Kenji;
Umebayashi, Ryoko;
Ohashi, Yuki;
Ichida, Kimiyoshi;
Wada, Jun

Publication type:

Case Study

Paracellular route is the major urate transport pathway across the blood-placental barrier.

Published in:

Physiological Reports, 2014, v. 2, n. 5, p. n/a, doi. 10.14814/phy2.12013

By:

Uehara, Ichiro;
Kimura, Toru;
Tanigaki, Shinji;
Fukutomi, Toshiyuki;
Sakai, Keiji;
Shinohara, Yoshihiko;
Ichida, Kimiyoshi;
Iwashita, Mitsutoshi;
Sakurai, Hiroyuki

Publication type:

Article

Common dysfunctional variants in ABCG2 are a major cause of early-onset gout.

Published in:

Scientific Reports, 2013, p. 1, doi. 10.1038/srep02014

By:

Hirotaka Matsuo;
Kimiyoshi Ichida;
Tappei Takada;
Akiyoshi Nakayama;
Hiroshi Nakashima;
Takahiro Nakamura;
Yusuke Kawamura;
Yuzo Takada;
Ken Yamamoto;
Hiroki Inoue;
Yuji Oikawa;
Mariko Naito;
Asahi Hishida;
Kenji Wakai;
Chisa Okada;
Seiko Shimizu;
Masayuki Sakiyama;
Toshinori Chiba;
Hiraku Ogata;
Kazuki Niwa

Publication type:

Article

OAT10/SLC22A13 Acts as a Renal Urate Re-Absorber: Clinico-Genetic and Functional Analyses With Pharmacological Impacts.

Published in:

Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.842717

By:

Toyoda, Yu;
Kawamura, Yusuke;
Nakayama, Akiyoshi;
Morimoto, Keito;
Shimizu, Seiko;
Tanahashi, Yuki;
Tamura, Takashi;
Kondo, Takaaki;
Kato, Yasufumi;
Ichida, Kimiyoshi;
Suzuki, Hiroshi;
Shinomiya, Nariyoshi;
Kobayashi, Yasushi;
Takada, Tappei;
Matsuo, Hirotaka

Publication type:

Article

Annual change in eGFR in renal hypouricemia: a retrospective pilot study.

Published in:

Clinical & Experimental Nephrology, 2025, v. 29, n. 2, p. 173, doi. 10.1007/s10157-024-02558-8

By:

Sugihara, Shinobu;
Yamamoto, Yasutaka;
Teramoto, Kei;
Hamada, Toshiro;
Miyazaki, Satoshi;
Ogino, Kazuhide;
Kuwabara, Masanari;
Ohtahara, Akira;
Mizuta, Einosuke;
Ichida, Kimiyoshi;
Endo, Yusuke;
Minato, Hiroyuki;
Ninomiya, Haruaki;
Kato, Masahiko;
Yamamoto, Kazuhiro;
Hisatome, Ichiro

Publication type:

Article

Vitamin C transporter SVCT1 serves a physiological role as a urate importer: functional analyses and in vivo investigations.

Published in:

Pflügers Archiv: European Journal of Physiology, 2023, v. 475, n. 4, p. 489, doi. 10.1007/s00424-023-02792-1

By:

Toyoda, Yu;
Miyata, Hiroshi;
Uchida, Naohiro;
Morimoto, Keito;
Shigesawa, Ryuichiro;
Kassai, Hidetoshi;
Nakao, Kazuki;
Tomioka, Naoko H.;
Matsuo, Hirotaka;
Ichida, Kimiyoshi;
Hosoyamada, Makoto;
Aiba, Atsu;
Suzuki, Hiroshi;
Takada, Tappei

Publication type:

Article

Successful living-related kidney transplantation in hereditary renal hypouricaemia.

Published in:

Nephrology Dialysis Transplantation, 2006, v. 21, n. 7, p. 2041, doi. 10.1093/ndt/gfk103

By:

Izumi Yamamoto;
Hiroyasu Yamamoto;
Kimiyoshi Ichida;
Jun Mitome;
Yudo Tanno;
Naohiko Katoh;
Keitaro Yokoyama;
Tatsuo Hosoya

Publication type:

Article

Effect of uric acid-lowering therapy on renal function in patients with chronic kidney disease: a systematic review and meta-analysis.

Published in:

Renal Replacement Therapy, 2021, v. 7, n. 1, p. 1, doi. 10.1186/s41100-021-00363-7

By:

Maruyama, Yukio;
Kumagai, Takanori;
Sugano, Naoki;
Yoshida, Shigetaka;
Ichida, Kimiyoshi;
Uchida, Shunya

Publication type:

Article

Single-nephron assessment of urate excretion in patients with IgA nephropathy.

Published in:

Clinical Kidney Journal, 2024, v. 17, n. 3, p. 1, doi. 10.1093/ckj/sfae036

By:

Marumoto, Hirokazu;
Tsuboi, Nobuo;
Sasaki, Takaya;
Okabayashi, Yusuke;
Haruhara, Kotaro;
Kanzaki, Go;
Ichida, Kimiyoshi;
Yokoo, Takashi

Publication type:

Article

Human Xanthine Oxidase Changes its Substrate Specificity to Aldehyde Oxidase Type upon Mutation of Amino Acid Residues in the Active Site: Roles of Active Site Residues in Binding and Activation of Purine Substrate.

Published in:

Journal of Biochemistry, 2007, v. 141, n. 4, p. 513, doi. 10.1093/jb/mvm053

By:

Yamaguchi, Yuichiro;
Matsumura, Tomohiro;
Ichida, Kimiyoshi;
Okamoto, Ken;
Nishino, Takeshi

Publication type:

Article

Xanthine oxidoreductase knockout mice with high HPRT activity were not rescued by NAD<sup>+</sup> replenishment.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2020, v. 39, n. 10-12, p. 1465, doi. 10.1080/15257770.2020.1725044

By:

Hosoyamada, Makoto;
Tomioka, Naoko H.;
Ohtsubo, Toshio;
Ichida, Kimiyoshi

Publication type:

Article

Modified forearm ischemic test in hypouricemic patients.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2020, v. 39, n. 10-12, p. 1432, doi. 10.1080/15257770.2020.1750636

By:

Sebesta, Ivan;
Miyamoto, Daisuke;
Stiburkova, Blanka;
Blahova, Sarka;
Sato, Nana;
Nagata, Koji;
Okamoto, Ken;
Tsuruoka, Shuichi;
Ichida, Kimiyoshi

Publication type:

Article

Expression of a human NPT1/SLC17A1 missense variant which increases urate export.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2016, v. 35, n. 10-12, p. 536, doi. 10.1080/15257770.2016.1149192

By:

Sakiyama, Masayuki;
Matsuo, Hirotaka;
Nagamori, Shushi;
Ling, Wei;
Kawamura, Yusuke;
Nakayama, Akiyoshi;
Higashino, Toshihide;
Chiba, Toshinori;
Ichida, Kimiyoshi;
Kanai, Yoshikatsu;
Shinomiya, Nariyoshi

Publication type:

Article

ABCG2 Dysfunction Increases the Risk of Renal Overload Hyperuricemia.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 266, doi. 10.1080/15257770.2013.866679

By:

Matsuo, Hirotaka;
Takada, Tappei;
Nakayama, Akiyoshi;
Shimizu, Toru;
Sakiyama, Masayuki;
Shimizu, Seiko;
Chiba, Toshinori;
Nakashima, Hiroshi;
Nakamura, Takahiro;
Takada, Yuzo;
Sakurai, Yutaka;
Hosoya, Tatsuo;
Shinomiya, Nariyoshi;
Ichida, Kimiyoshi

Publication type:

Article

Hypoxanthine Guanine Phosphoribosyltransferase (HPRT) Deficiencies: HPRT1 Mutations in New Japanese Families and PRPP Concentration.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 218, doi. 10.1080/15257770.2013.865743

By:

Yamada, Yasukazu;
Nomura, Noriko;
Yamada, Kenichiro;
Kimura, Reiko;
Fukushi, Daisuke;
Wakamatsu, Nobuaki;
Matsuda, Yasufumi;
Yamauchi, Takahiro;
Ueda, Takanori;
Hasegawa, Hiroshi;
Nakamura, Makiko;
Ichida, Kimiyoshi;
Kaneko, Kiyoko;
Fujimori, Shin

Publication type:

Article

ABCG2 Dysfunction Increases Serum Uric Acid by Decreased Intestinal Urate Excretion.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 275, doi. 10.1080/15257770.2013.854902

By:

Takada, Tappei;
Ichida, Kimiyoshi;
Matsuo, Hirotaka;
Nakayama, Akiyoshi;
Murakami, Keizo;
Yamanashi, Yoshihide;
Kasuga, Hiroshi;
Shinomiya, Nariyoshi;
Suzuki, Hiroshi

Publication type:

Article

Gout and Hyperuricemia in Japan: Perspectives for International Research on Purines and Pyrimidines in Man.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1001, doi. 10.1080/15257770.2011.633955

By:

Hosoya, Tatsuo;
Ohno, Iwao;
Ichida, Kimiyoshi;
Peters, GodefridusJ.

Publication type:

Article

ABCG2/BCRP Dysfunction as a Major Cause of Gout.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1117, doi. 10.1080/15257770.2011.633954

By:

Matsuo, Hirotaka;
Takada, Tappei;
Ichida, Kimiyoshi;
Nakamura, Takahiro;
Nakayama, Akiyoshi;
Suzuki, Hiroshi;
Hosoya, Tatsuo;
Shinomiya, Nariyoshi

Publication type:

Article

ABCG2 is a High-Capacity Urate Transporter and its Genetic Impairment Increases Serum Uric Acid Levels in Humans.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1091, doi. 10.1080/15257770.2011.633953

By:

Nakayama, Akiyoshi;
Matsuo, Hirotaka;
Takada, Tappei;
Ichida, Kimiyoshi;
Nakamura, Takahiro;
Ikebuchi, Yuki;
Ito, Kousei;
Hosoya, Tatsuo;
Kanai, Yoshikatsu;
Suzuki, Hiroshi;
Shinomiya, Nariyoshi

Publication type:

Article

Increased Expression of SLC2A9 Decreases Urate Excretion From the Kidney.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1295, doi. 10.1080/15257770.2011.628354

By:

Kimura, Toru;
Amonpatumrat, Sirirat;
Tsukada, Ai;
Fukutomi, Toshiyuki;
Jutabha, Promsuk;
Thammapratip, Thanapol;
Lee, EunJ.;
Ichida, Kimiyoshi;
Anzai, Naohiko;
Sakurai, Hiroyuki

Publication type:

Article

Diagnostic Tests for Primary Renal Hypouricemia.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2011, v. 30, n. 12, p. 1112, doi. 10.1080/15257770.2011.611483

By:

Sebesta, Ivan;
Stiburkova, Blanka;
Bartl, Josef;
Ichida, Kimiyoshi;
Hosoyamada, Makoto;
Taylor, Judy;
Marinaki, Anthony

Publication type:

Article

Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency.

Published in:

Developmental Medicine & Child Neurology, 2010, v. 52, n. 9, p. 868, doi. 10.1111/j.1469-8749.2010.03724.x

By:

GÜMÜŞ, HAKAN;
GHESQUIERE, STIJN;
PER, HÜSEYIN;
KONDOLOT, MEDA;
ICHIDA, KIMIYOSHI;
POYRAZOĞLU, GAMZE;
KUMANDAŞ, SEFER;
ENGELEN, JOHN;
DUNDAR, MUNIS;
ÇAĞLAYAN, AHMET OKAY

Publication type:

Article

Mutations Associated with Functional Disorder of Xanthine Oxidoreductase and Hereditary Xanthinuria in Humans.

Published in:

International Journal of Molecular Sciences, 2012, v. 13, n. 11, p. 15475, doi. 10.3390/ijms131115475

By:

Ichida, Kimiyoshi;
Amaya, Yoshihiro;
Okamoto, Ken;
Nishino, Takeshi

Publication type:

Article

Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.

Published in:

Clinical & Experimental Nephrology, 2016, v. 20, n. 4, p. 578, doi. 10.1007/s10157-015-1186-z

By:

Mancikova, Andrea;
Krylov, Vladimir;
Hurba, Olha;
Sebesta, Ivan;
Nakamura, Makiko;
Ichida, Kimiyoshi;
Stiburkova, Blanka

Publication type:

Article

Apoptosis induced by an uromodulin mutant C112Y and its suppression by topiroxostat.

Published in:

Clinical & Experimental Nephrology, 2015, v. 19, n. 4, p. 576, doi. 10.1007/s10157-014-1032-8

By:

Utami, Sulistiyati;
Mahati, Endang;
Li, Peili;
Maharani, Nani;
Ikeda, Nobuhito;
Bahrudin, Udin;
Munemura, Chishio;
Hosoyamada, Makoto;
Yamamoto, Yasutaka;
Yoshida, Akio;
Nakayama, Yuji;
Higaki, Katsumi;
Nanba, Eiji;
Ninomiya, Haruaki;
Shirayoshi, Yasuaki;
Ichida, Kimiyoshi;
Yamamoto, Kazuhiro;
Hosoya, Tatsuo;
Hisatome, Ichiro

Publication type:

Article

Common variants of a urate-associated gene LRP2 are not associated with gout susceptibility.

Published in:

Rheumatology International, 2014, v. 34, n. 4, p. 473, doi. 10.1007/s00296-013-2924-8

By:

Nakayama, Akiyoshi;
Matsuo, Hirotaka;
Shimizu, Toru;
Takada, Yuzo;
Nakamura, Takahiro;
Shimizu, Seiko;
Chiba, Toshinori;
Sakiyama, Masayuki;
Naito, Mariko;
Morita, Emi;
Ichida, Kimiyoshi;
Shinomiya, Nariyoshi

Publication type:

Article

Regulation of Urate Homeostasis by Membrane Transporters.

Published in:

Gout, Urate, & Crystal Deposition Disease, 2024, v. 2, n. 2, p. 206, doi. 10.3390/gucdd2020016

By:

Takada, Tappei;
Miyata, Hiroshi;
Toyoda, Yu;
Nakayama, Akiyoshi;
Ichida, Kimiyoshi;
Matsuo, Hirotaka

Publication type:

Article

Molecular identification of a renal urate-anion exchanger that regulates blood urate levels.

Published in:

Nature, 2002, v. 417, n. 6887, p. 447, doi. 10.1038/nature742

By:

Enomoto, Atsushi;
Kimura, Hiroaki;
Chairoungdua, Arthit;
Shigeta, Yasuhiro;
Jutabha, Promsuk;
Seok Ho Cha;
Hosoyamada, Makoto;
Takeda, Michio;
Sekine, Takashi;
Igarashi, Takashi;
Matsuo, Hirotaka;
Kikuchi, Yuichi;
Oda, Takashi;
Ichida, Kimiyoshi;
Hosoya, Tatsuo;
Shimokata, Kaoru;
Niwa, Toshimitsu;
Kanai, Yoshikatsu;
Endou, Hitoshi

Publication type:

Article

Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1067, doi. 10.1038/ejhg.2013.3

By:

Stiburkova, Blanka;
Sebesta, Ivan;
Ichida, Kimiyoshi;
Nakamura, Makiko;
Hulkova, Helena;
Krylov, Vladimir;
Kryspinova, Lenka;
Jahnova, Helena

Publication type:

Article

Hyperuricemia in acute gastroenteritis is caused by decreased urate excretion via ABCG2.

Published in:

Scientific Reports, 2016, p. 31003, doi. 10.1038/srep31003

By:

Matsuo, Hirotaka;
Tsunoda, Tomoyuki;
Ooyama, Keiko;
Sakiyama, Masayuki;
Sogo, Tsuyoshi;
Takada, Tappei;
Nakashima, Akio;
Nakayama, Akiyoshi;
Kawaguchi, Makoto;
Higashino, Toshihide;
Wakai, Kenji;
Ooyama, Hiroshi;
Hokari, Ryota;
Suzuki, Hiroshi;
Ichida, Kimiyoshi;
Inui, Ayano;
Fujimori, Shin;
Shinomiya, Nariyoshi

Publication type:

Article

The effects of URAT1/SLC22A12 nonfunctional variants,R90H and W258X, on serum uric acid levels and gout/hyperuricemia progression.

Published in:

Scientific Reports, 2016, p. 20148, doi. 10.1038/srep20148

By:

Sakiyama, Masayuki;
Matsuo, Hirotaka;
Shimizu, Seiko;
Nakashima, Hiroshi;
Nakamura, Takahiro;
Nakayama, Akiyoshi;
Higashino, Toshihide;
Naito, Mariko;
Suma, Shino;
Hishida, Asahi;
Satoh, Takahiro;
Sakurai, Yutaka;
Takada, Tappei;
Ichida, Kimiyoshi;
Ooyama, Hiroshi;
Shimizu, Toru;
Shinomiya, Nariyoshi

Publication type:

Article