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Journal of Diabetes Investigation|January 12, 2020
Nicotinic acetylcholine receptor signaling regulates inositol-requiring enzyme 1α activation to protect β-cells against terminal unfolded protein response under irremediable endoplasmic reticulum stressTatsuya Ishibashi, Shuhei Morita, Shohei Kishimoto, et al.
Endocrine Journal|June 12, 2020
False-positive staining of thyroglobulin distinguished from mixed medullary and follicular thyroid carcinoma by duplex in situ hybridizationKen Takeshima, Hiroyuki Ariyasu, Shinsuke Uraki, et al.
Endocrine Journal|April 28, 2020
The influence of thyroid autoimmunity on pregnancy outcome in infertile women: a prospective studyYuko Inagaki, Ken Takeshima, Masahiro Nishi, et al.
BMC Endocrine Disorders|April 9, 2020
Autoimmune polyglandular syndrome type 2 and autoimmune hepatitis with thymoma-associated myasthenia gravis: case reportHidefumi Inaba, Hiroyuki Ariyasu, Hiroshi Iwakura, et al.
The Journal of Clinical Endocrinology and Metabolism|June 14, 2018
Imbalanced Expression of IGF2 and PCSK4 Is Associated With Overproduction of Big IGF2 in SFT With NICTH: A Pilot StudyShintaro Kawai, Hiroyuki Ariyasu, Shinsuke Uraki, et al.
Clinical Genetics|January 15, 2024
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasiaShuhei Morita, Shunsuke Nomura, Kenko Azuma, et al.
International Journal of Molecular Sciences|September 4, 2020
Targeting Adaptive IRE1α Signaling and PLK2 in Multiple Myeloma: Possible Anti-Tumor Mechanisms of KIRA8 and NilotinibYusuke Yamashita, Shuhei Morita, Hiroki Hosoi, et al.
Molecular Genetics and Metabolism Reports|July 10, 2024
Familial schwannomatosis carrying LZTR1 variant p.R340X with brain tumor: A case reportMasaki Ibe, Shinobu Tamura, Hideki Kosako, et al.
Journal of Neurosurgery|September 30, 2017
Brainstem pilocytic astrocytoma with H3 K27M mutation: case reportShuhei Morita, Masayuki Nitta, Yoshihiro Muragaki, et al.
Journal of Diabetes Investigation|August 8, 2019
Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6-year clinical courseShinsuke Uraki, Hiroto Furuta, Masakazu Miyawaki, et al.
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