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Circulation|July 21, 2004
Celiprolol, a vasodilatory beta-blocker, inhibits pressure overload-induced cardiac hypertrophy and prevents the transition to heart failure via nitric oxide-dependent mechanisms in miceYulin Liao, Masanori Asakura, Seiji Takashima, et al.
Journal of Neuroinflammation|August 7, 2019
Next-generation sequencing identifies contribution of both class I and II HLA genes on susceptibility of multiple sclerosis in JapaneseKotaro Ogawa, Tatsusada Okuno, Kazuyoshi Hosomichi, et al.
Biochemical and Biophysical Research Communications|November 21, 2007
Identification of a novel substrate for TNFalpha-induced kinase NUAK2Hiroyuki Yamamoto, Seiji Takashima, Yasunori Shintani, et al.
The American Journal of Cardiology|December 10, 2013
Usefulness of transient elastography for noninvasive and reliable estimation of right-sided filling pressure in heart failureTatsunori Taniguchi, Yasushi Sakata, Tomohito Ohtani, et al.
Internal Medicine (Tokyo, Japan)|March 22, 2023
End-stage Hypertrophic Cardiomyopathy with Advanced Heart Failure in Patients Carrying MYH7 R453 Variants: A Case SeriesSusumu Naito, Shuichiro Higo, Satoshi Kameda, et al.
Cardiovascular Drugs and Therapy|June 9, 2006
The antagonism of aldosterone receptor prevents the development of hypertensive heart failure induced by chronic inhibition of nitric oxide synthesis in ratsOsamu Tsukamoto, Tetsuo Minamino, Shoji Sanada, et al.
Brain & Development|May 1, 2025
Challenges in genetic counseling for RYR1-related myopathiesRina Shimomura, Yuki Kihara, Tomoe Yanagishita, et al.
EMBO Reports|February 6, 2025
HSC70 coordinates COP9 signalosome and SCF ubiquitin ligase activity to enable a prompt stress responseShunsuke Nishimura, Hidetaka Kioka, Shan Ding, et al.
Human Genome Variation|May 16, 2024
Characteristic craniofacial defects associated with a novel USP9X truncation mutationNamiki Nagata, Hiroshi Kurosaka, Kotaro Higashi, et al.
Human Molecular Genetics|September 13, 2024
Compromised actin dynamics underlie the orofacial cleft in Baraitser-Winter Cerebrofrontofacial syndrome with a variant in ACTBTakayuki Tsujimoto, Yushi Ou, Makoto Suzuki, et al.
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