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Page 1
Clinical and Echocardiographic Impact of Tafazzin Variants on Dilated Cardiomyopathy Phenotype in Left Ventricular Non-Compaction Patients in Early Infancy.
Hirono K, Hata Y, Nakazawa M, Momoi N, Tsuji T, Matsuoka T, Ayusawa M, Abe Y, Hayashi T, Tsujii N, Abe T, Sakaguchi H, Wang C, Takasaki A, Takarada S, Okabe M, Miyao N, Nakaoka H, Ibuki K, Saito K, Ozawa S, Nishida N, Bowles NE, Ichida F. Hirono K, et al. Among authors: takarada s. Circ J. 2018 Sep 25;82(10):2609-2618. doi: 10.1253/circj.CJ-18-0470. Epub 2018 Aug 18. Circ J. 2018. PMID: 30122738 Free article.
TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway.
Miyao N, Hata Y, Izumi H, Nagaoka R, Oku Y, Takasaki I, Ishikawa T, Takarada S, Okabe M, Nakaoka H, Ibuki K, Ozawa S, Yoshida T, Hasegawa H, Makita N, Nishida N, Mori H, Ichida F, Hirono K. Miyao N, et al. Among authors: takarada s. PLoS One. 2020 Apr 1;15(4):e0227393. doi: 10.1371/journal.pone.0227393. eCollection 2020. PLoS One. 2020. PMID: 32236096 Free PMC article.
Increased Burden of Ion Channel Gene Variants Is Related to Distinct Phenotypes in Pediatric Patients With Left Ventricular Noncompaction.
Hirono K, Hata Y, Miyao N, Okabe M, Takarada S, Nakaoka H, Ibuki K, Ozawa S, Origasa H, Nishida N, Ichida F; LVNC study collaborates*. Hirono K, et al. Among authors: takarada s. Circ Genom Precis Med. 2020 Aug;13(4):e002940. doi: 10.1161/CIRCGEN.119.002940. Epub 2020 Jun 29. Circ Genom Precis Med. 2020. PMID: 32600061
A burden of sarcomere gene variants in fetal-onset patients with left ventricular noncompaction.
Hirono K, Hata Y, Ozawa SW, Toda T, Momoi N, Fukuda Y, Inuzuka R, Nagamine H, Sakaguchi H, Kurosaki K, Okabe M, Takarada S, Miyao N, Nakaoka H, Ibuki K, Origasa H, Bowles NE, Nishida N, Ichida F; for LVNC study collaborators. Hirono K, et al. Among authors: takarada s. Int J Cardiol. 2021 Apr 1;328:122-129. doi: 10.1016/j.ijcard.2020.12.013. Epub 2020 Dec 10. Int J Cardiol. 2021. PMID: 33309763
G0S2 regulates innate immunity in Kawasaki disease via lncRNA HSD11B1-AS1.
Okabe M, Takarada S, Miyao N, Nakaoka H, Ibuki K, Ozawa S, Watanabe K, Tsuji H, Hashimoto I, Hatasaki K, Hayakawa S, Hamaguchi Y, Hamada M, Ichida F, Hirono K. Okabe M, et al. Among authors: takarada s. Pediatr Res. 2022 Aug;92(2):378-387. doi: 10.1038/s41390-022-01999-9. Epub 2022 Mar 15. Pediatr Res. 2022. PMID: 35292727 Free PMC article.
79 results