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Functional Evaluation of Human Bioengineered Cardiac Tissue Using iPS Cells Derived from a Patient with Lamin Variant Dilated Cardiomyopathy.
Miura K, Matsuura K, Yamasaki Itoyama Y, Sasaki D, Takada T, Furutani Y, Hayama E, Ito M, Nomura S, Morita H, Toyoda M, Umezawa A, Onoue K, Saito Y, Aburatani H, Nakanishi T, Hagiwara N, Komuro I, Shimizu T. Miura K, et al. Among authors: furutani y. Int Heart J. 2022;63(2):338-346. doi: 10.1536/ihj.21-790. Int Heart J. 2022. PMID: 35354754 Free article.
Mutations of NOTCH3 in childhood pulmonary arterial hypertension.
Chida A, Shintani M, Matsushita Y, Sato H, Eitoku T, Nakayama T, Furutani Y, Hayama E, Kawamura Y, Inai K, Ohtsuki S, Saji T, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: furutani y. Mol Genet Genomic Med. 2014 May;2(3):229-39. doi: 10.1002/mgg3.58. Epub 2014 Apr 1. Mol Genet Genomic Med. 2014. PMID: 24936512 Free PMC article.
Compound Mutations Cause Increased Cardiac Events in Children with Long QT Syndrome: Can the Sequence Homology-Based Tools be Applied for Prediction of Phenotypic Severity?
Izumi G, Hayama E, Yamazawa H, Inai K, Shimada M, Furutani M, Nishizawa T, Furutani Y, Matsuoka R, Nakanishi T. Izumi G, et al. Among authors: furutani m, furutani y. Pediatr Cardiol. 2016 Jun;37(5):962-70. doi: 10.1007/s00246-016-1378-7. Epub 2016 Apr 4. Pediatr Cardiol. 2016. PMID: 27041096
ACVRL1 gene variant in a patient with vein of Galen aneurysmal malformation.
Chida A, Shintani M, Wakamatsu H, Tsutsumi Y, Iizuka Y, Kawaguchi N, Furutani Y, Inai K, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: furutani y. J Pediatr Genet. 2013 Dec;2(4):181-9. doi: 10.3233/PGE-13067. J Pediatr Genet. 2013. PMID: 27625857 Free PMC article.
Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.
Chida A, Inai K, Sato H, Shimada E, Nishizawa T, Shimada M, Furutani M, Furutani Y, Kawamura Y, Sugimoto M, Ishihara J, Fujiwara M, Soga T, Kawana M, Fuji S, Tateno S, Kuraishi K, Kogaki S, Nishimura M, Ayusawa M, Ichida F, Yamazawa H, Matsuoka R, Nonoyama S, Nakanishi T. Chida A, et al. Among authors: furutani m, furutani y. Heart Vessels. 2017 Jun;32(6):700-707. doi: 10.1007/s00380-016-0920-0. Epub 2016 Nov 24. Heart Vessels. 2017. PMID: 27885498
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: furutani y. Sci Rep. 2018 Jan 31;8(1):1998. doi: 10.1038/s41598-018-20114-9. Sci Rep. 2018. PMID: 29386531 Free PMC article.
314 results