未登录Induced Pluripotent Stem Cell-Derived Cardiomyocytes with SCN5A R1623Q Mutation Associated with Severe Long QT Syndrome in Fetuses and Neonates Recapitulates Pathophysiological Phenotypes
Hayama, Emiko; Furutani, Yoshiyuki; Kawaguchi, Nanako; Seki, Akiko; Nagashima, Yoji; Okita, Keisuke; Takeuchi, Daiji; Matsuoka, Rumiko; Inai, Kei; Hagiwara, Nobuhisa; Nakanishi, Toshio .png)
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收藏分享 收藏 RAF1 mutations in childhood-onset dilated cardiomyopathyDhandapany, Perundurai S.; Razzaque, Md Abdur; Muthusami, Uthiralingam; Kunnoth, Sreejith; Edwards, Jonathan J.; Mulero-Navarro, Sonia; Riess, Ilan; Pardo, Sherly; Sheng, Jipo; Rani, Deepa Selvi; Rani, Bindu; Govindaraj, Periyasamy; Flex, Elisabetta; Yokota, Tomohiro; Furutani, Michiko; Nishizawa, Tsutomu; Nakanishi, Toshio; Robbins, Jeffrey; Limongelli, Giuseppe; Hajjar, Roger J.; Lebeche, Djamel; Bahl, Ajay; Khullar, Madhu; Rathinavel, Andiappan; Sadler, Kirsten C.; Tartaglia, Marco; Matsuoka, Rumiko; Thangaraj, Kumarasamy; Gelb, Bruce D. 分享 收藏 Soluble ST2 and N-terminal pro-Brain Natriuretic Peptide Combination - Useful Biomarker for Predicting Outcome of Childhood Pulmonary Arterial HypertensionChida, Ayako; Sato, Hiroki; Shintani, Masaki; Nakayama, Tomotaka; Kawamura, Yoichi; Furutani, Yoshiyuki; Inai, Kei; Saji, Tsutomu; Matsuoka, Rumiko; Nonoyama, Shigeaki; Nakanishi, Toshio 分享 收藏 Brefeldin A Is an Estrogenic, Erk1/2-Activating Component in the Extract of Agaricus blazei MyceliaDong, Sijun; Furutani, Yoshiyuki; Kimura, Sadao; Zhu, Yun; Kawabata, Kazutaka; Furutani, Michiko; Nishikawa, Toshio; Tanaka, Takeshi; Masaki, Tomoh; Matsuoka, Rumiko; Kiyama, Ryoiti 分享 收藏 Estrogen-like activity and dual roles in cell signaling of an Agaricus blazei Murrill mycelia-dikaryon extractDong, Sijun; Furutani, Yoshiyuki; Suto, Yumiko; Furutani, Michiko; Zhu, Yun; Yoneyama, Makoto; Kato, Taichi; Itabe, Hiroyuki; Nishikawa, Toshio; Tomimatsu, Hirofumi; Tanaka, Takeshi; Kasanuki, Hiroshi; Masaki, Tomoh; Kiyama, Ryoiti; Matsuoka, Rumiko 分享 收藏 Genetic Analysis of Essential Cardiac Transcription Factors in 256 Patients With Non-Syndromic Congenital Heart DefectsKodo, Kazuki; Nishizawa, Tsutomu; Furutani, Michiko; Arai, Shoichi; Ishihara, Kazuaki; Oda, Mayumi; Makino, Shinji; Fukuda, Keiichi; Takahashi, Takao; Matsuoka, Rumiko; Nakanishi, Toshio; Yamagishi, Hiroyuki 分享 收藏 分享 收藏 分享 收藏 Activation of STAT5 confers imatinib resistance on leukemic cells through the transcription of TERT and MDR1Yamada, Osamu; Ozaki, Kohji; Furukawa, Thoru; Machida, Mitsuyo; Wang, Yan-Hua; Motoji, Toshiko; Mitsuishi, Tsuyoshi; Akiyama, Masaharu; Yamada, Hisashi; Kawauchi, Kiyotaka; Matsuoka, Rumiko 分享 收藏 Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden death在左心室致密化不全和猝死的家庭中鉴定新的TPM1突变Chang, Bo; Nishizawa, Tsutomu; Furutani, Michiko; Fujiki, Akira; Tani, Masanao; Kawaguchi, Makoto; Ibuki, Keijiro; Hirono, Keiichi; Taneichi, Hiromichi; Uese, Keiichiro; Onuma, Yoshiko; Bowles, Neil E.; Ichida, Fukiko; Inoue, Hiroshi; Matsuoka, Rumiko; Miyawaki, Toshio 分享 收藏 分享 收藏 分享 收藏 分享 收藏 RETRACTED: Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF) (Retracted article. See vol. 111, pg. 2398, 2014)撤回: 共有一个共同亚基的2种染色质重塑复合物的独特功能，威廉姆斯综合征转录因子 (WSTF) (撤回的文章。见111卷，2398页，2014页)Yoshimura, Kimihiro; Kitagawa, Hirochika; Fujiki, Ryoji; Tanabe, Masahiko; Takezawa, Shinichiro; Takada, Ichiro; Yamaoka, Ikuko; Yonezawa, Masayoshi; Kondo, Takeshi; Furutani, Yoshiyuki; Yagi, Hisato; Yoshinaga, Shin; Masuda, Takeyoshi; Fukuda, Toru; Yamamoto, Yoko; Ebihara, Kanae; Li, Dean Y.; Matsuoka, Rumiko; Takeuchi, Jun K.; Matsumoto, Takahiro; Kato, Shigeaki 分享 收藏 分享 收藏 分享 收藏 Implications of mutations of activin receptor-like kinase 1 gene (ALK1) in addition to bone morphogenetic protein receptor II gene (BMPR2) in children with pulmonary arterial hypertensionFujiwara, Maya; Yagi, Hisato; Matsuoka, Rumiko; Akimoto, Kaoru; Furutani, Michiko; Imamura, Shin-Ichiro; Uehara, Ritei; Nakayama, Tomotaka; Takao, Atsuyoshi; Nakazawa, Makoto; Saji, Tsutomu 分享 收藏 分享 收藏 Germline gain-of-function mutations in RAF1 cause Noonan syndromeRazzaque, M. Abdur; Nishizawa, Tsutomu; Komoike, Yuta; Yagi, Hisato; Furutani, Michiko; Amo, Ryunosuke; Kamisago, Mitsuhiro; Momma, Kazuo; Katayama, Hiroshi; Nakagawa, Masao; Fujiwara, Yuko; Matsushima, Masaki; Mizuno, Katsumi; Tokuyama, Mika; Hirota, Hamao; Muneuchi, Jun; Higashinakagawa, Toru; Matsuoka, Rumiko 分享 收藏 
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