Yagi H - Search Results

1

Impact of Pathogenic FBN1 Variant Types on the Progression of Aortic Disease in Patients With Marfan Syndrome.

Takeda N, Inuzuka R, Maemura S, Morita H, Nawata K, Fujita D, Taniguchi Y, Yamauchi H, Yagi H, Kato M, Nishimura H, Hirata Y, Ikeda Y, Kumagai H, Amiya E, Hara H, Fujiwara T, Akazawa H, Suzuki JI, Imai Y, Nagai R, Takamoto S, Hirata Y, Ono M, Komuro I. Takeda N, et al. Among authors: yagi h. Circ Genom Precis Med. 2018 Jun;11(6):e002058. doi: 10.1161/CIRCGEN.117.002058. Circ Genom Precis Med. 2018. PMID: 29848614

2

In-stent restenosis exacerbated by drug-induced severe eosinophilia after second-generation drug-eluting stent implantation.

Yagi H, Amiya E, Ando J, Watanabe M, Yanaba K, Ikemura M, Fukayama M, Komuro I. Yagi H, et al. Am J Case Rep. 2014 Sep 17;15:397-400. doi: 10.12659/AJCR.891106. Am J Case Rep. 2014. PMID: 25227966 Free PMC article.

3

A representative case of hereditary transthyretin amyloidosis complicated by intramyocardial hemorrhage.

Yagi H, Amiya E, Shintani Y, Nitta D, Numakura S, Hosoya Y, Watanabe M, Fukayama M, Komuro I. Yagi H, et al. Amyloid. 2015 Mar;22(1):70-2. doi: 10.3109/13506129.2014.987865. Epub 2014 Nov 27. Amyloid. 2015. PMID: 25427692 No abstract available.

4

Congenital Contractural Arachnodactyly without FBN1 or FBN2 Gene Mutations Complicated by Dilated Cardiomyopathy.

Yagi H, Hatano M, Takeda N, Harada S, Suzuki Y, Taniguchi Y, Shintani Y, Morita H, Kanamori N, Aoyama T, Watanabe M, Manabe I, Akazawa H, Kinugawa K, Komuro I. Yagi H, et al. Intern Med. 2015;54(10):1237-41. doi: 10.2169/internalmedicine.54.4280. Epub 2015 May 15. Intern Med. 2015. PMID: 25986263 Free article.

5

Monocyte-derived extracellular Nampt-dependent biosynthesis of NAD(+) protects the heart against pressure overload.

Yano M, Akazawa H, Oka T, Yabumoto C, Kudo-Sakamoto Y, Kamo T, Shimizu Y, Yagi H, Naito AT, Lee JK, Suzuki J, Sakata Y, Komuro I. Yano M, et al. Among authors: yagi h. Sci Rep. 2015 Nov 2;5:15857. doi: 10.1038/srep15857. Sci Rep. 2015. PMID: 26522369 Free PMC article.

6

Angiotensin II receptor blockade promotes repair of skeletal muscle through down-regulation of aging-promoting C1q expression.

Yabumoto C, Akazawa H, Yamamoto R, Yano M, Kudo-Sakamoto Y, Sumida T, Kamo T, Yagi H, Shimizu Y, Saga-Kamo A, Naito AT, Oka T, Lee JK, Suzuki J, Sakata Y, Uejima E, Komuro I. Yabumoto C, et al. Among authors: yagi h. Sci Rep. 2015 Sep 25;5:14453. doi: 10.1038/srep14453. Sci Rep. 2015. PMID: 26571361 Free PMC article.

7

Pathophysiology and Management of Cardiovascular Manifestations in Marfan and Loeys-Dietz Syndromes.

Takeda N, Yagi H, Hara H, Fujiwara T, Fujita D, Nawata K, Inuzuka R, Taniguchi Y, Harada M, Toko H, Akazawa H, Komuro I. Takeda N, et al. Among authors: yagi h. Int Heart J. 2016 May 25;57(3):271-7. doi: 10.1536/ihj.16-094. Epub 2016 May 13. Int Heart J. 2016. PMID: 27181042 Free article. Review.

8

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: yagi h. PLoS One. 2017 Mar 22;12(3):e0174099. doi: 10.1371/journal.pone.0174099. eCollection 2017. PLoS One. 2017. PMID: 28328981 Free PMC article.

9

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: yagi h. 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.

10

Activation of TGF-β signaling in an aortic aneurysm in a patient with Loeys-Dietz syndrome caused by a novel loss-of-function variant of TGFBR1.

Hara H, Takeda N, Fujiwara T, Yagi H, Maemura S, Kanaya T, Nawata K, Morita H, Komuro I. Hara H, et al. Among authors: yagi h. Hum Genome Var. 2019 Jan 18;6:6. doi: 10.1038/s41439-019-0038-x. eCollection 2019. Hum Genome Var. 2019. PMID: 30701076 Free PMC article.

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