Výsledky vyhledávání - Kimiyoshi Ichida
- Zobrazuji výsledky 1 - 20 z 25
- Přejít na další stránku
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
Clinical practice guideline for renal hypouricemia (1st edition) Autor Akiyoshi Nakayama, Hirotaka Matsuo, Akira Ohtahara, Kazuhíde Oginö, Masayuki Hakoda, Toshihiro Hamada, Makoto Hosoyamada, Satoshi Yamaguchi, Ichiro Hisatome, Kimiyoshi Ichida, Nariyoshi Shinomiya
Vydáno 2019Revisão -
9
Plasma Urate Level Is Directly Regulated by a Voltage-driven Urate Efflux Transporter URATv1 (SLC2A9) in Humans Autor Naohiko Anzai, Kimiyoshi Ichida, Promsuk Jutabha, Tōru Kimura, Ellappan Babu, Chun Ji Jin, Sunena Srivastava, Kenichiro Kitamura, Ichiro Hisatome, Hitoshi Endou, Hiroyuki Sakurai
Vydáno 2008Artigo -
10
Depletion of Uric Acid Due to SLC22A12 (URAT1) Loss-of-Function Mutation Causes Endothelial Dysfunction in Hypouricemia Autor Shinobu Sugihara, Ichiro Hisatome, Masanari Kuwabara, Koichiro Niwa, Nani Maharani, Masahiko Kato, Kazuhíde Oginö, Toshihiro Hamada, Haruaki Ninomiya, Yukihito Higashi, Kimiyoshi Ichida, Kazuhiro Yamamoto
Vydáno 2015Artigo -
11
Evaluation of ABCG2-mediated extra-renal urate excretion in hemodialysis patients Autor Yuki Ohashi, Masao Toyoda, Nobumichi Saito, Masahiro Koizumi, Genta Kanai, Hirotaka Komaba, Moritsugu Kimura, Takehiko Wada, Hiroo Takahashi, Yuichiro Takahashi, Naoto Ishida, Takatoshi Kakuta, Masafumi Fukagawa, Kimiyoshi Ichida
Vydáno 2023Artigo -
12
The effects of URAT1/SLC22A12 nonfunctional variants,R90H and W258X, on serum uric acid levels and gout/hyperuricemia progression Autor Masayuki Sakiyama, Hirotaka Matsuo, Seiko Shimizu, Hiroshi Nakashima, Takahiro Nakamura, Akiyoshi Nakayama, Toshihide Higashino, Mariko Naito, Shino Suma, Asahi Hishida, Takahiro Satoh, Yutaka Sakurai, Tappei Takada, Kimiyoshi Ichida, Hiroshi Ooyama, Toru Shimizu, Nariyoshi Shinomiya
Vydáno 2016Artigo -
13
Identification of ABCG2 as an Exporter of Uremic Toxin Indoxyl Sulfate in Mice and as a Crucial Factor Influencing CKD Progression Autor Tappei Takada, Takehito Yamamoto, Hirotaka Matsuo, Jiang Tan, Keiko Ooyama, Masayuki Sakiyama, Hiroshi Miyata, Yoshihide Yamanashi, Yu Toyoda, Toshihide Higashino, Akiyoshi Nakayama, Akio Nakashima, Nariyoshi Shinomiya, Kimiyoshi Ichida, Hiroshi Ooyama, Shin Fujimori, Hiroshi Suzuki
Vydáno 2018Artigo -
14
Hyperuricemia in acute gastroenteritis is caused by decreased urate excretion via ABCG2 Autor Hirotaka Matsuo, Tomoyuki Tsunoda, Keiko Ooyama, Masayuki Sakiyama, Tsuyoshi Sogo, Tappei Takada, Akio Nakashima, Akiyoshi Nakayama, Makoto Kawaguchi, Toshihide Higashino, Kenji Wakai, Hiroshi Ooyama, Ryota Hokari, Hiroshi Suzuki, Kimiyoshi Ichida, Inui Ayano, Shin Fujimori, Nariyoshi Shinomiya
Vydáno 2016Artigo -
15
Exploring the Multifaceted Nexus of Uric Acid and Health: A Review of Recent Studies on Diverse Diseases Autor Masanari Kuwabara, Tomoko Fukuuchi, Yuhei Aoki, Einosuke Mizuta, Motoshi Ouchi, Masafumi Kurajoh, Tatsuya Maruhashi, Atsushi Tanaka, Nagisa Morikawa, Kensuke Nishimiya, Naoyuki Akashi, Yoshihiro Tanaka, Naoyuki Otani, Mihoko Morita, Hiroshi Miyata, Tappei Takada, Hiroshi Tsutani, Kazuhíde Oginö, Kimiyoshi Ichida, Ichiro Hisatome, Kohtaro Abe
Vydáno 2023Revisão -
16
A common missense variant of monocarboxylate transporter 9 (MCT9/SLC16A9) gene is associated with renal overload gout, but not with all gout susceptibility Autor Akiyoshi Nakayama, Hirotaka Matsuo, Takuya Shimizu, Hiraku Ogata, Yuzo Takada, Hiroshi Nakashima, Takahiro Nakamura, Seiko Shimizu, Toshinori Chiba, Masayuki Sakiyama, Chisaki Ushiyama, Tappei Takada, Katsuhisa Inoue, Sayo Kawai, Asahi Hishida, Kenji Wakai, Nobuyuki Hamajima, Kimiyoshi Ichida, Yutaka Sakurai, Yukio Kato, Toru Shimizu, Nariyoshi Shinomiya
Vydáno 2013Artigo -
17
Decreased extra-renal urate excretion is a common cause of hyperuricemia Autor Kimiyoshi Ichida, Hirotaka Matsuo, Tappei Takada, Akiyoshi Nakayama, Keizo Murakami, Toru Shimizu, Yoshihide Yamanashi, Hiroshi Kasuga, Hiroshi Nakashima, Takahiro Nakamura, Yuzo Takada, Yusuke Kawamura, Hiroki Inoue, Chisa Okada, Yoshitaka Utsumi, Yuki Ikebuchi, Kousei Ito, Makiko Nakamura, Yoshihiko Shinohara, Makoto Hosoyamada, Yutaka Sakurai, Nariyoshi Shinomiya, Tatsuo Hosoya, Hiroshi Suzuki
Vydáno 2012Artigo -
18
Common dysfunctional variants of ABCG2 have stronger impact on hyperuricemia progression than typical environmental risk factors Autor Akiyoshi Nakayama, Hirotaka Matsuo, Hirofumi Nakaoka, Takahiro Nakamura, Hiroshi Nakashima, Yuzo Takada, Yuji Oikawa, Tappei Takada, Masayuki Sakiyama, Seiko Shimizu, Yusuke Kawamura, Toshinori Chiba, Junko Abe, Kenji Wakai, Sayo Kawai, Rieko Okada, Takashi Tamura, Yuka Shichijo, A Akashi, Hiroshi Suzuki, Tatsuo Hosoya, Yutaka Sakurai, Kimiyoshi Ichida, Nariyoshi Shinomiya
Vydáno 2014Artigo -
19
ABCG2 dysfunction causes hyperuricemia due to both renal urate underexcretion and renal urate overload Autor Hirotaka Matsuo, Akiyoshi Nakayama, Masayuki Sakiyama, Toshinori Chiba, Seiko Shimizu, Yusuke Kawamura, Hiroshi Nakashima, Takahiro Nakamura, Yuzo Takada, Yuji Oikawa, Tappei Takada, Hirofumi Nakaoka, Junko Abe, Hiroki Inoue, Kenji Wakai, Sayo Kawai, Guang Yin, Hiroko Nakagawa, Toshimitsu Ito, Kazuki Niwa, Ken Yamamoto, Yutaka Sakurai, Hiroshi Suzuki, Tatsuo Hosoya, Kimiyoshi Ichida, Toru Shimizu, Nariyoshi Shinomiya
Vydáno 2014Artigo -
20
Common dysfunctional variants in ABCG2 are a major cause of early-onset gout Autor 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, Makoto Hosoyamada, Atsuyoshi Mori, Nobuyuki Hamajima, Hiroshi Suzuki, Yoshikatsu Kanai, Yutaka Sakurai, Tatsuo Hosoya, Toru Shimizu, Nariyoshi Shinomiya
Vydáno 2013Artigo
Vyhledávací nástroje:
Související témata
Medicine
Gene
Internal medicine
Biology
Uric acid
Gout
Hyperuricemia
Biochemistry
Genetics
Transporter
Endocrinology
Chemistry
ATP-binding cassette transporter
Abcg2
Genome-wide association study
Genotype
Single-nucleotide polymorphism
Bioinformatics
Enzyme
Hypouricemia
Mutation
Excretion
Genetic association
Kidney
Kidney disease
Organic anion transporter 1
Pharmacology
Xanthine
Xanthine dehydrogenase
Xanthine oxidase