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Clinical Parkinsonism & Related Disorders|June 1, 2022
A cross-sectional study of Parkinson's disease and the prodromal phase in community-dwelling older adults in eastern JapanKeita Taguchi, Kazuhiro Iwaoka, Takashi Yamaguchi, et al.
Endocrinology|February 13, 2014
β-Cell proliferation after a partial pancreatectomy is independent of IRS-2 in miceYu Togashi, Jun Shirakawa, Kazuki Orime, et al.
Modern Rheumatology|July 18, 2012
Ultrasonography is a potent tool for the prediction of progressive joint destruction during clinical remission of rheumatoid arthritisRyusuke Yoshimi, Maasa Hama, Kaoru Takase, et al.
Oral and Maxillofacial Surgery|January 9, 2025
Reduction of ischemic time using the pull-through technique for scapular free flapYoshio Ohyama, Kazuki Hasegawa, Narikazu Uzawa, et al.
Cancer Research|June 3, 2005
Chemopreventive effect of peroxisome proliferator-activated receptor gamma on gastric carcinogenesis in miceJie Lu, Kazuhiro Imamura, Sachiyo Nomura, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 20, 2011
Combined microwave irradiation and intraarticular glutamine administration-induced HSP70 expression therapy prevents cartilage degradation in a rat osteoarthritis modelShinya Fujita, Yuji Arai, Shuji Nakagawa, et al.
The Journal of Clinical Investigation|April 7, 2004
PPARgamma insufficiency enhances osteogenesis through osteoblast formation from bone marrow progenitorsToru Akune, Shinsuke Ohba, Satoru Kamekura, et al.
Bioorganic & Medicinal Chemistry|October 1, 2014
Design, synthesis, and structure-activity relationships of a series of novel N-aryl-2-phenylcyclopropanecarboxamide that are potent and orally active orexin receptor antagonistsYu Yoshida, Taro Terauchi, Yoshimitsu Naoe, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 26, 2018
Conserved fungal effector suppresses PAMP-triggered immunity by targeting plant immune kinasesHiroki Irieda, Yoshihiro Inoue, Masashi Mori, et al.
Bioorganic & Medicinal Chemistry|October 16, 2012
Synthesis and structure-activity relationships of 8-substituted-2-aryl-5-alkylaminoquinolines: Potent, orally active corticotropin-releasing factor-1 receptor antagonistsKunitoshi Takeda, Taro Terauchi, Minako Hashizume, et al.
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