Works matching AU Toshihide Higashino

Results: 14

Meta-analysis confirms an association between gout and a common variant of LRRC16A locus.

Published in:

Modern Rheumatology, 2017, v. 27, n. 3, p. 553, doi. 10.1080/14397595.2016.1218413

By:

Hiraku Ogata;
Hirotaka Matsuo;
Masayuki Sakiyama;
Toshihide Higashino;
Makoto Kawaguchi;
Akiyoshi Nakayama;
Mariko Naito;
Hiroshi Ooyama;
Kimiyoshi Ichida;
Nariyoshi Shinomiya

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

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

Increase of serum uric acid levels associated with APOE ε2 haplotype: a clinico-genetic investigation and in vivo approach.

Published in:

Human Cell, 2021, v. 34, n. 6, p. 1727, doi. 10.1007/s13577-021-00609-w

By:

Ogura, Masatsune;
Toyoda, Yu;
Sakiyama, Masayuki;
Kawamura, Yusuke;
Nakayama, Akiyoshi;
Yamanashi, Yoshihide;
Takada, Tappei;
Shimizu, Seiko;
Higashino, Toshihide;
Nakajima, Mayuko;
Naito, Mariko;
Hishida, Asahi;
Kawai, Sayo;
Okada, Rieko;
Sasaki, Makoto;
Ayaori, Makoto;
Suzuki, Hiroshi;
Takata, Koki;
Ikewaki, Katsunori;
Harada-Shiba, Mariko

Publication type:

Article

Porphyrin accumulation in humans with common dysfunctional variants of ABCG2, a porphyrin transporter: potential association with acquired photosensitivity.

Published in:

Human Cell, 2021, v. 34, n. 4, p. 1082, doi. 10.1007/s13577-021-00534-y

By:

Sakiyama, Masayuki;
Matsuo, Hirotaka;
Toyoda, Yu;
Yonekura, Yuiko;
Ishikawa, Takahiro;
Nakayama, Akiyoshi;
Higashino, Toshihide;
Kawamura, Yusuke;
Fujimoto, Norihiro;
Shinomiya, Nariyoshi;
Satoh, Takahiro

Publication type:

Article

A common variant of LDL receptor related protein 2 (LRP2) gene is associated with gout susceptibility: a meta-analysis in a Japanese population.

Published in:

2020

By:

Akashi, Airi;
Nakayama, Akiyoshi;
Kamatani, Yoichiro;
Higashino, Toshihide;
Shimizu, Seiko;
Kawamura, Yusuke;
Imoto, Misaki;
Naito, Mariko;
Hishida, Asahi;
Kawaguchi, Makoto;
Takao, Mikiya;
Matsuo, Michinori;
Takada, Tappei;
Ichida, Kimiyoshi;
Ooyama, Hiroshi;
Shinomiya, Nariyoshi;
Matsuo, Hirotaka

Publication type:

Literature Review

A common variant of MAF/c- MAF, transcriptional factor gene in the kidney, is associated with gout susceptibility.

Published in:

Human Cell, 2018, v. 31, n. 1, p. 10, doi. 10.1007/s13577-017-0186-6

By:

Higashino, Toshihide;
Matsuo, Hirotaka;
Okada, Yukinori;
Nakashima, Hiroshi;
Shimizu, Seiko;
Sakiyama, Masayuki;
Tadokoro, Shin;
Nakayama, Akiyoshi;
Kawaguchi, Makoto;
Komatsu, Mako;
Hishida, Asahi;
Nakatochi, Masahiro;
Ooyama, Hiroshi;
Imaki, Junko;
Shinomiya, Nariyoshi

Publication type:

Article

Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient.

Published in:

Frontiers in Medicine, 2024, p. 1, doi. 10.3389/fmed.2024.1374222

By:

Satoko Minakawa;
Yasushi Matsuzaki;
Toshihide Higashino;
Tamio Suzuki;
Hirofumi Tomita;
Eijiro Akasaka;
Daisuke Sawamura

Publication type:

Article

Thromboxane A<sub>2</sub> receptor antagonist (ONO‐8809) attenuates renal disorders caused by salt overload in stroke‐prone spontaneously hypertensive rats.

Published in:

Clinical & Experimental Pharmacology & Physiology, 2021, v. 48, n. 10, p. 1391, doi. 10.1111/1440-1681.13543

By:

Nagatani, Yusuke;
Higashino, Toshihide;
Kinoshita, Kosho;
Higashino, Hideaki

Publication type:

Article

Common variant of <italic>BCAS3</italic> is associated with gout risk in Japanese population: the first replication study after gout GWAS in Han Chinese.

Published in:

BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0583-z

By:

Sakiyama, Masayuki;
Matsuo, Hirotaka;
Nakaoka, Hirofumi;
Kawamura, Yusuke;
Kawaguchi, Makoto;
Higashino, Toshihide;
Nakayama, Akiyoshi;
Akashi, Airi;
Ueyama, Jun;
Kondo, Takaaki;
Wakai, Kenji;
Sakurai, Yutaka;
Yamamoto, Ken;
Ooyama, Hiroshi;
Shinomiya, Nariyoshi

Publication type:

Article

Assessment of Delayed Large Local Reactions After the First Dose of the SARS-CoV-2 mRNA-1273 Vaccine in Japan.

Published in:

JAMA Dermatology, 2022, v. 158, n. 8, p. 923, doi. 10.1001/jamadermatol.2022.2088

By:

Higashino, Toshihide;
Yamazaki, Yuki;
Senda, Satoko;
Satou, Yushi;
Yonekura, Yuiko;
Imai, Kazuo;
Arakawa, Junko;
Kawano, Shuichi;
Horinosono, Hiroshi;
Miura, Yoshinori

Publication type:

Article

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

Published in:

Rheumatology, 2021, v. 60, n. 11, p. 5224, doi. 10.1093/rheumatology/keab327

By:

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

Publication type:

Article

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

Published in:

Rheumatology, 2020, v. 59, n. 12, p. 3988, doi. 10.1093/rheumatology/keaa461

By:

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

Publication type:

Article