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Science Translational Medicine|June 14, 2023
Fusobacterium infection facilitates the development of endometriosis through the phenotypic transition of endometrial fibroblastsAyako Muraoka, Miho Suzuki, Tomonari Hamaguchi, et al.
Nature Communications|May 14, 2015
FUS regulates AMPA receptor function and FTLD/ALS-associated behaviour via GluA1 mRNA stabilizationTsuyoshi Udagawa, Yusuke Fujioka, Motoki Tanaka, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 17, 2024
Calcitriol ameliorates motor deficits and prolongs survival of Chrne-deficient mouse, a model for congenital myasthenic syndrome, by inducing Rspo2Bisei Ohkawara, Hiroyuki Tomita, Taro Inoue, et al.
European Journal of Pharmacology|May 22, 2002
Effects of ginsenosides, active components of ginseng, on nicotinic acetylcholine receptors expressed in Xenopus oocytesSeok Choi, Se Yeon Jung, Jun Ho Lee, et al.
Free Radical Biology & Medicine|October 30, 2016
Molecular hydrogen ameliorates several characteristics of preeclampsia in the Reduced Uterine Perfusion Pressure (RUPP) rat modelTakafumi Ushida, Tomomi Kotani, Hiroyuki Tsuda, et al.
Gut Microbes|February 19, 2026
Bacterial constipation: Mucin-degrading intestinal commensal bacteria cause constipationTomonari Hamaguchi, Noriaki Gibo, Misuzu Ohara, et al.
JCI Insight|January 26, 2018
Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunitXin-Ming Shen, Joan M Brengman, Shelley Shen, et al.
Frontiers in Neurology|March 31, 2018
Myopathy With SQSTM1 and TIA1 Variants: Clinical and Pathological FeaturesZhiyv Niu, Carly Sabine Pontifex, Sarah Berini, et al.
Scientific Reports|September 17, 2017
An ENU-induced splice site mutation of mouse Col1a1 causing recessive osteogenesis imperfecta and revealing a novel splicing rescueKoichi Tabeta, Xin Du, Kei Arimatsu, et al.
Neurology|February 28, 2014
A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1Yosuke Kokunai, Tomohiko Nakata, Mitsuru Furuta, et al.
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