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Irregular Narrow QRS Tachycardia: What Is the Mechanism?
Matsuura H, Kamakura T, Ishiwata M, Kusano K. Matsuura H, et al. Among authors: ishiwata m. J Cardiovasc Electrophysiol. 2024 Dec 30. doi: 10.1111/jce.16558. Online ahead of print. J Cardiovasc Electrophysiol. 2024. PMID: 39736081 No abstract available.
SMART Pass automatic deactivation of subcutaneous implantable cardioverter-defibrillators.
Ishiwata M, Ueda N, Ishibashi K, Nakamura T, Oka S, Miyazaki Y, Wakamiya A, Nakajima K, Kamakura T, Wada M, Inoue Y, Miyamoto K, Nagase S, Aiba T, Kitai T, Izumi C, Noguchi T, Kusano K. Ishiwata M, et al. Heart Rhythm. 2024 Aug 23:S1547-5271(24)03235-1. doi: 10.1016/j.hrthm.2024.08.037. Online ahead of print. Heart Rhythm. 2024. PMID: 39181486
Transcriptomic dysregulation and autistic-like behaviors in Kmt2c haploinsufficient mice rescued by an LSD1 inhibitor.
Nakamura T, Yoshihara T, Tanegashima C, Kadota M, Kobayashi Y, Honda K, Ishiwata M, Ueda J, Hara T, Nakanishi M, Takumi T, Itohara S, Kuraku S, Asano M, Kasahara T, Nakajima K, Tsuboi T, Takata A, Kato T. Nakamura T, et al. Among authors: ishiwata m. Mol Psychiatry. 2024 Sep;29(9):2888-2904. doi: 10.1038/s41380-024-02479-8. Epub 2024 Mar 26. Mol Psychiatry. 2024. PMID: 38528071 Free PMC article.
DAPagliflozin for the attenuation of albuminuria in Patients with hEaRt failure and type 2 diabetes (DAPPER study): a multicentre, randomised, open-label, parallel-group, standard treatment-controlled trial.
Yoshihara F, Imazu M, Sakuma I, Hiroi Y, Hara H, Okazaki O, Ishiguro C, Izumi C, Noguchi T, Shiraiwa T, Nishioka N, Fujii K, Iwakura K, Tomonaga O, Kobayashi K, Takihata M, Yumoto K, Takase H, Himi T, Shimizu I, Murakami T, Wagatsuma K, Sato K, Hiramatsu T, Akabame S, Hata S, Asakura M, Kawabata T, Omae K, Ito S, Kitakaze M; DAPPER Investigators. Yoshihara F, et al. EClinicalMedicine. 2023 Nov 27;66:102334. doi: 10.1016/j.eclinm.2023.102334. eCollection 2023 Dec. EClinicalMedicine. 2023. PMID: 38192595 Free PMC article.
Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder.
Nishioka M, Takayama J, Sakai N, Kazuno AA, Ishiwata M, Ueda J, Hayama T, Fujii K, Someya T, Kuriyama S, Tamiya G, Takata A, Kato T. Nishioka M, et al. Among authors: ishiwata m. Mol Psychiatry. 2023 Oct;28(10):4294-4306. doi: 10.1038/s41380-023-02096-x. Epub 2023 May 30. Mol Psychiatry. 2023. PMID: 37248276 Free PMC article.
Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder.
Nishioka M, Kazuno AA, Nakamura T, Sakai N, Hayama T, Fujii K, Matsuo K, Komori A, Ishiwata M, Watanabe Y, Oka T, Matoba N, Kataoka M, Alkanaq AN, Hamanaka K, Tsuboi T, Sengoku T, Ogata K, Iwata N, Ikeda M, Matsumoto N, Kato T, Takata A. Nishioka M, et al. Among authors: ishiwata m. Nat Commun. 2021 Jun 18;12(1):3750. doi: 10.1038/s41467-021-23453-w. Nat Commun. 2021. PMID: 34145229 Free PMC article.
Brain-specific heterozygous loss-of-function of ATP2A2, endoplasmic reticulum Ca2+ pump responsible for Darier's disease, causes behavioral abnormalities and a hyper-dopaminergic state.
Nakajima K, Ishiwata M, Weitemier AZ, Shoji H, Monai H, Miyamoto H, Yamakawa K, Miyakawa T, McHugh TJ, Kato T. Nakajima K, et al. Among authors: ishiwata m. Hum Mol Genet. 2021 Aug 28;30(18):1762-1772. doi: 10.1093/hmg/ddab137. Hum Mol Genet. 2021. PMID: 34104969 Free PMC article.
45 results