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Author Correction: CXCR7 ameliorates myocardial infarction as a β-arrestin-biased receptor.
Ishizuka M, Harada M, Nomura S, Ko T, Ikeda Y, Guo J, Bujo S, Yanagisawa-Murakami H, Satoh M, Yamada S, Kumagai H, Motozawa Y, Hara H, Fujiwara T, Sato T, Takeda N, Takeda N, Otsu K, Morita H, Toko H, Komuro I. Ishizuka M, et al. Among authors: nomura s. Sci Rep. 2021 Jun 7;11(1):12340. doi: 10.1038/s41598-021-91788-x. Sci Rep. 2021. PMID: 34099846 Free PMC article. No abstract available.
Complement C1q activates canonical Wnt signaling and promotes aging-related phenotypes.
Naito AT, Sumida T, Nomura S, Liu ML, Higo T, Nakagawa A, Okada K, Sakai T, Hashimoto A, Hara Y, Shimizu I, Zhu W, Toko H, Katada A, Akazawa H, Oka T, Lee JK, Minamino T, Nagai T, Walsh K, Kikuchi A, Matsumoto M, Botto M, Shiojima I, Komuro I. Naito AT, et al. Among authors: nomura s. Cell. 2012 Jun 8;149(6):1298-313. doi: 10.1016/j.cell.2012.03.047. Cell. 2012. PMID: 22682250 Free PMC article.
Complement C1q-induced activation of β-catenin signalling causes hypertensive arterial remodelling.
Sumida T, Naito AT, Nomura S, Nakagawa A, Higo T, Hashimoto A, Okada K, Sakai T, Ito M, Yamaguchi T, Oka T, Akazawa H, Lee JK, Minamino T, Offermanns S, Noda T, Botto M, Kobayashi Y, Morita H, Manabe I, Nagai T, Shiojima I, Komuro I. Sumida T, et al. Among authors: nomura s. Nat Commun. 2015 Feb 26;6:6241. doi: 10.1038/ncomms7241. Nat Commun. 2015. PMID: 25716000 Free PMC article.
Quantitative Measurement of GPCR Endocytosis via Pulse-Chase Covalent Labeling.
Kumagai H, Ikeda Y, Motozawa Y, Fujishiro M, Okamura T, Fujio K, Okazaki H, Nomura S, Takeda N, Harada M, Toko H, Takimoto E, Akazawa H, Morita H, Suzuki J, Yamazaki T, Yamamoto K, Komuro I, Yanagisawa M. Kumagai H, et al. Among authors: nomura s. PLoS One. 2015 May 28;10(5):e0129394. doi: 10.1371/journal.pone.0129394. eCollection 2015. PLoS One. 2015. PMID: 26020647 Free PMC article.
Monitoring β-arrestin recruitment via β-lactamase enzyme fragment complementation: purification of peptide E as a low-affinity ligand for mammalian bombesin receptors.
Ikeda Y, Kumagai H, Okazaki H, Fujishiro M, Motozawa Y, Nomura S, Takeda N, Toko H, Takimoto E, Akazawa H, Morita H, Suzuki J, Yamazaki T, Komuro I, Yanagisawa M. Ikeda Y, et al. Among authors: nomura s. PLoS One. 2015 Jun 1;10(6):e0127445. doi: 10.1371/journal.pone.0127445. eCollection 2015. PLoS One. 2015. PMID: 26030739 Free PMC article.
Activation of endothelial β-catenin signaling induces heart failure.
Nakagawa A, Naito AT, Sumida T, Nomura S, Shibamoto M, Higo T, Okada K, Sakai T, Hashimoto A, Kuramoto Y, Oka T, Lee JK, Harada M, Ueda K, Shiojima I, Limbourg FP, Adams RH, Noda T, Sakata Y, Akazawa H, Komuro I. Nakagawa A, et al. Among authors: nomura s. Sci Rep. 2016 May 5;6:25009. doi: 10.1038/srep25009. Sci Rep. 2016. PMID: 27146149 Free PMC article.
Dysbiosis and compositional alterations with aging in the gut microbiota of patients with heart failure.
Kamo T, Akazawa H, Suda W, Saga-Kamo A, Shimizu Y, Yagi H, Liu Q, Nomura S, Naito AT, Takeda N, Harada M, Toko H, Kumagai H, Ikeda Y, Takimoto E, Suzuki JI, Honda K, Morita H, Hattori M, Komuro I. Kamo T, et al. Among authors: nomura s. PLoS One. 2017 Mar 22;12(3):e0174099. doi: 10.1371/journal.pone.0174099. eCollection 2017. PLoS One. 2017. PMID: 28328981 Free PMC article.
Identification of MYLK3 mutations in familial dilated cardiomyopathy.
Tobita T, Nomura S, Morita H, Ko T, Fujita T, Toko H, Uto K, Hagiwara N, Aburatani H, Komuro I. Tobita T, et al. Among authors: nomura s. Sci Rep. 2017 Dec 13;7(1):17495. doi: 10.1038/s41598-017-17769-1. Sci Rep. 2017. PMID: 29235529 Free PMC article.
Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling.
Tobita T, Nomura S, Fujita T, Morita H, Asano Y, Onoue K, Ito M, Imai Y, Suzuki A, Ko T, Satoh M, Fujita K, Naito AT, Furutani Y, Toko H, Harada M, Amiya E, Hatano M, Takimoto E, Shiga T, Nakanishi T, Sakata Y, Ono M, Saito Y, Takashima S, Hagiwara N, Aburatani H, Komuro I. Tobita T, et al. Among authors: nomura s. Sci Rep. 2018 Jan 31;8(1):1998. doi: 10.1038/s41598-018-20114-9. Sci Rep. 2018. PMID: 29386531 Free PMC article.
Distinct variants affecting differential splicing of TGFBR1 exon 5 cause either Loeys-Dietz syndrome or multiple self-healing squamous epithelioma.
Fujiwara T, Takeda N, Hara H, Morita H, Kishihara J, Inuzuka R, Yagi H, Maemura S, Toko H, Harada M, Ikeda Y, Kumagai H, Nomura S, Takimoto E, Akazawa H, Ako J, Komuro I. Fujiwara T, et al. Among authors: nomura s. Eur J Hum Genet. 2018 Aug;26(8):1151-1158. doi: 10.1038/s41431-018-0127-1. Epub 2018 Apr 30. Eur J Hum Genet. 2018. PMID: 29706644 Free PMC article.
2,887 results