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The Journal of Clinical Endocrinology and Metabolism|July 18, 2025
The significance of high expression of circulating miR-222-3p in patients with unilateral primary aldosteronismKentaro Okamoto, Masakatsu Sone, Daisuke Taura, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 4, 2022
Thyroid hormone economy in mice overexpressing iodothyronine deiodinasesIchiro Yamauchi, Yoriko Sakane, Takafumi Yamashita, et al.
Clinical Endocrinology|September 14, 2021
Bezafibrate induces hypothyroidism in a patient with resistance to thyroid hormone β due to a G347R variantIchiro Yamauchi, Takafumi Yamashita, Taku Sugawa, et al.
Endocrinology|May 16, 2024
Neprilysin Inhibition Promotes Skeletal Growth via the CNP/NPR-B PathwayTakuro Hakata, Yohei Ueda, Takafumi Yamashita, et al.
Endocrinology|June 13, 2022
High-throughput Screening in Combination With a Cohort Study for Iodothyronine DeiodinasesIchiro Yamauchi, Yoriko Sakane, Yukiko Okuno, et al.
Frontiers in Endocrinology|September 18, 2023
18F-labeled PEGylated exendin-4 imaging noninvasively differentiates insulinoma from an accessory spleen: the first case report of [18F]FB(ePEG12)12-exendin-4 positron emission tomography/computed tomography for insulinomaKentaro Sakaki, Takaaki Murakami, Hiroyuki Fujimoto, et al.
Iscience|January 15, 2025
Transcriptomic landscape of hyperthyroidism in mice overexpressing thyroid-stimulating hormoneIchiro Yamauchi, Taku Sugawa, Takuro Hakata, et al.
Iscience|February 18, 2025
Erratum: Transcriptomic landscape of hyperthyroidism in mice overexpressing thyroid-stimulating hormoneIchiro Yamauchi, Taku Sugawa, Takuro Hakata, et al.
Elife|March 15, 2022
C-type natriuretic peptide facilitates autonomic Ca2+ entry in growth plate chondrocytes for stimulating bone growthYuu Miyazaki, Atsuhiko Ichimura, Ryo Kitayama, et al.
Frontiers in Endocrinology|December 25, 2024
Case report: Duplication of the GCK gene is a novel cause of nesidioblastosis: evidence from a case with Silver-Russell syndrome-like phenotype related to chromosome 7Takashi Shoji, Ichiro Yamauchi, Hidenori Kawasaki, et al.
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