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Clinical Case Reports|December 28, 2020
A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformationHaruka Kishi, Teruo Jojima, Takahiko Kogai, et al.
Internal Medicine (Tokyo, Japan)|July 19, 2017
An Autopsy Case of Fulminant Hepatitis in a Patient with Multiple Sclerosis Treated by Interferon-Beta-1aYuichi Yamazaki, Aya Suzuki, Kimitoshi Hirayanagi, et al.
Endocrine Journal|April 6, 2018
Usage of continuous glucose monitoring (CGM) for detecting an unrecognized hypoglycemia and management of glucocorticoid replacement therapy in adult patients with central hypoadrenalismTakuya Watanabe, Atsushi Ozawa, Sumiyasu Ishii, et al.
Endocrine Journal|July 30, 2014
Somatic mutations of the catalytic subunit of cyclic AMP-dependent protein kinase (PRKACA) gene in Japanese patients with several adrenal adenomas secreting cortisol [Rapid Communication]Yasuyo Nakajima, Takashi Okamura, Tamae Gohko, et al.
Endocrinology|July 9, 2014
Protection against high-fat diet-induced obesity in Helz2-deficient male mice due to enhanced expression of hepatic leptin receptorSatoshi Yoshino, Tetsurou Satoh, Masanobu Yamada, et al.
Scientific Reports|June 21, 2020
Transcriptional Regulation of the Angptl8 Gene by Hepatocyte Nuclear Factor-1 in the Murine LiverTakuya Watanabe, Atsushi Ozawa, Shinnosuke Masuda, et al.
Endocrine Journal|September 30, 2016
Characteristics of Japanese aldosterone-producing adenomas with KCNJ5 mutationsTakashi Okamura, Yasuyo Nakajima, Akiko Katano-Toki, et al.
Endocrine Journal|May 26, 2018
Transducin β-like 1, X-linked and nuclear receptor co-repressor cooperatively augment the ligand-independent stimulation of TRH and TSHβ gene promoters by thyroid hormone receptorsTetsuya Takamizawa, Tetsurou Satoh, Tomoko Miyamoto, et al.
Frontiers in Microbiology|March 8, 2017
HELZ2 Is an IFN Effector Mediating Suppression of Dengue VirusDahlene N Fusco, Henry Pratt, Stephen Kandilas, et al.
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