Hiroyuki Yamagishi

Summary

Affiliation: Keio University
Country: Japan

Publications

  1. pmc Tbx1 is regulated by forkhead proteins in the secondary heart field
    Jun Maeda
    Department of Pediatrics, Division of Pediatric Cardiology, Keio University School of Medicine, Tokyo, Japan
    Dev Dyn 235:701-10. 2006
  2. ncbi request reprint Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome
    Hiroyuki Yamagishi
    Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjyuku ku, Tokyo 160 8582, Japan
    Trends Mol Med 9:383-9. 2003
  3. doi request reprint Molecular embryology for an understanding of congenital heart diseases
    Hiroyuki Yamagishi
    Department of Pediatrics, Division of Pediatric Cardiology, Keio University School of Medicine, Tokyo, Japan
    Anat Sci Int 84:88-94. 2009
  4. pmc Gene knock-outs of inositol 1,4,5-trisphosphate receptors types 1 and 2 result in perturbation of cardiogenesis
    Keiko Uchida
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan
    PLoS ONE 5:. 2010
  5. doi request reprint Inositol 1,4,5-trisphosphate receptors are essential for the development of the second heart field
    Maki Nakazawa
    Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku ku, Tokyo 160 8582, Japan
    J Mol Cell Cardiol 51:58-66. 2011
  6. ncbi request reprint Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects
    Kazuki Kodo
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan
    Circ J 76:1703-11. 2012
  7. pmc MiR-133 promotes cardiac reprogramming by directly repressing Snai1 and silencing fibroblast signatures
    Naoto Muraoka
    Department of Clinical and Molecular Cardiovascular Research, Keio University School of Medicine, Shinjuku ku Tokyo, Japan Department of Cardiology, Keio University School of Medicine, Shinjuku ku Tokyo, Japan
    EMBO J 33:1565-81. 2014
  8. ncbi request reprint Sonic hedgehog is essential for first pharyngeal arch development
    Chihiro Yamagishi
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan
    Pediatr Res 59:349-54. 2006
  9. doi request reprint Type 1 and 3 inositol trisphosphate receptors are required for extra-embryonic vascular development
    Keiko Uchida
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan Health Center, Keio University, Kanagawa, Japan
    Dev Biol 418:89-97. 2016
  10. doi request reprint Mechanisms underlying early development of pulmonary vascular obstructive disease in Down syndrome: An imbalance in biosynthesis of thromboxane A2 and prostacyclin
    Hiroyuki Fukushima
    Department of Pediatrics, Keio University School of Medicine, Shinjuku ku, Tokyo, Japan
    Am J Med Genet A 152:1919-24. 2010

Collaborators

  • Keiichi Fukuda
  • Keiko Uchida
  • Katsuhiko Mikoshiba
  • Rumiko Matsuoka
  • Deepak Srivastava
  • Kenjiro Kosaki
  • Masaki Ieda
  • Toshio Nakanishi
  • Ryo Aeba
  • Motoaki Sano
  • Shinsuke Yuasa
  • Hiroyuki Shimada
  • Takehiko Mori
  • Adriana C Gittenberger-de Groot
  • Jun Maeda
  • Kazuki Kodo
  • Takao Takahashi
  • Chihiro Yamagishi
  • Naoto Muraoka
  • Rie Wada
  • Maki Nakazawa
  • Kouichi Nakau
  • Kazutaka Miyamoto
  • Taketaro Sadahiro
  • Hiroyuki Yamakawa
  • Hiroki Kajino
  • Ruri Kaneda
  • Shugo Tohyama
  • Tomohiko Umei
  • Kohei Inagawa
  • Katsuaki Kojima
  • Masayoshi Shinjoh
  • Tonghuan Hu
  • Michiko Furutani
  • Tsutomu Nishizawa
  • Shoichi Arai
  • Hiroyuki Fukushima
  • Takatoshi Tsuchihashi
  • John McAnally
  • Junko Shiono
  • Hiroshi Azuma
  • Yoshikazu Tasaki
  • Hideharu Oka
  • Kazuki Kouno
  • Masaya Sugimoto
  • Aya Kajihama
  • Naoya Kamiyama
  • Yoshifumi Kawamura
  • Naoki Goshima
  • Shu Takeda
  • Toru Fukuda
  • Mizuha Akiyama
  • Mari Isomi
  • Hisayuki Hashimoto
  • Takahiko Nishiyama
  • Hanae Nakashima
  • Seiya Hattori
  • Tomoyuki Suzuki
  • Shuji Mikami
  • Kaichiro Kamiya
  • Midori Awazu
  • Hiroki Ide
  • Ryohei Yozu
  • Toshio Kitamura
  • Kiyokazu Kokaji
  • Naoki Hasegawa
  • Kayoko Sugita
  • Naoki Shimojima
  • Mayumi Oda
  • Kota Watanabe
  • Osamu Iketani
  • Satoshi Iwata
  • Kazuaki Ishihara
  • Mikihiko Kudo
  • Shinji Makino
  • Mitsuhiro Kamisago
  • Megumi Aramaki
  • Shinji Oana
  • Katsuhiko Mori
  • Yoshiyuki Furutani
  • Tadashi Waragai
  • Hiroyuki Matsuura
  • Yoshifumi Kojima
  • Ryohei Gatayama
  • Reiko Sato
  • Takuya Hayashi
  • Tatsuhiko Yagihashi
  • Eiji Yamamura
  • Kunitaka Joo
  • Kathryn Ivey

Detail Information

Publications23

  1. pmc Tbx1 is regulated by forkhead proteins in the secondary heart field
    Jun Maeda
    Department of Pediatrics, Division of Pediatric Cardiology, Keio University School of Medicine, Tokyo, Japan
    Dev Dyn 235:701-10. 2006
    ....
  2. ncbi request reprint Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome
    Hiroyuki Yamagishi
    Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjyuku ku, Tokyo 160 8582, Japan
    Trends Mol Med 9:383-9. 2003
    ..Armed with this knowledge, we can now begin to consider the multiple genetic "hits" that might contribute to developmental anomalies, some of which could provide targets for in utero prevention of birth defects...
  3. doi request reprint Molecular embryology for an understanding of congenital heart diseases
    Hiroyuki Yamagishi
    Department of Pediatrics, Division of Pediatric Cardiology, Keio University School of Medicine, Tokyo, Japan
    Anat Sci Int 84:88-94. 2009
    ..Discovery of the second heart field has important implications for the interpretation of cardiac outflow tract development and provides new insights into the morphogenesis of CHD...
  4. pmc Gene knock-outs of inositol 1,4,5-trisphosphate receptors types 1 and 2 result in perturbation of cardiogenesis
    Keiko Uchida
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan
    PLoS ONE 5:. 2010
    ..Although the ryanodine receptor type 2, another type of intracellular Ca2+ release channel, has been shown to play a role in embryonic cardiomyocytes, the functions of the IP3Rs in cardiogenesis remain unclear...
  5. doi request reprint Inositol 1,4,5-trisphosphate receptors are essential for the development of the second heart field
    Maki Nakazawa
    Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku ku, Tokyo 160 8582, Japan
    J Mol Cell Cardiol 51:58-66. 2011
    ..These data reveal that IP(3)R type 1 and type 3 may play a redundant role in the development of the SHF...
  6. ncbi request reprint Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects
    Kazuki Kodo
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan
    Circ J 76:1703-11. 2012
    ..The genetic basis of most congenital heart defects (CHDs), especially non-syndromic and non-familial conditions, remains largely unknown...
  7. pmc MiR-133 promotes cardiac reprogramming by directly repressing Snai1 and silencing fibroblast signatures
    Naoto Muraoka
    Department of Clinical and Molecular Cardiovascular Research, Keio University School of Medicine, Shinjuku ku Tokyo, Japan Department of Cardiology, Keio University School of Medicine, Shinjuku ku Tokyo, Japan
    EMBO J 33:1565-81. 2014
    ..Thus, silencing fibroblast signatures, mediated by miR-133/Snai1, is a key molecular roadblock during cardiac reprogramming...
  8. ncbi request reprint Sonic hedgehog is essential for first pharyngeal arch development
    Chihiro Yamagishi
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan
    Pediatr Res 59:349-54. 2006
    ..These results demonstrate that epithelial-mesenchymal signaling and transcriptional events coordinated by Shh, partly via Fgf8, is essential for cell survival and tissue outgrowth of the developing PA1...
  9. doi request reprint Type 1 and 3 inositol trisphosphate receptors are required for extra-embryonic vascular development
    Keiko Uchida
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan Health Center, Keio University, Kanagawa, Japan
    Dev Biol 418:89-97. 2016
    ..This is the first demonstration of the essential role of IP3/IP3Rs signaling in the development of the vasculature at the embryonic-maternal interface. ..
  10. doi request reprint Mechanisms underlying early development of pulmonary vascular obstructive disease in Down syndrome: An imbalance in biosynthesis of thromboxane A2 and prostacyclin
    Hiroyuki Fukushima
    Department of Pediatrics, Keio University School of Medicine, Shinjuku ku, Tokyo, Japan
    Am J Med Genet A 152:1919-24. 2010
    ..This imbalance in the biosynthesis of vasoactive eicosanoids may account for the rapid progression of PVOD in DS infants with a left-to-right shunt...
  11. pmc GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling
    Kazuki Kodo
    Department of Pediatrics, Division of Pediatric Cardiology, Keio University School of Medicine, 35 Shinanomachi, Shinjyuku ku, Tokyo 160 8582, Japan
    Proc Natl Acad Sci U S A 106:13933-8. 2009
    ..Together, our data implicate mutations in GATA6 as genetic causes of CHD involving OFT development, as a result of the disruption of the direct regulation of semaphorin-plexin signaling...
  12. ncbi request reprint A decade of advances in the molecular embryology and genetics underlying congenital heart defects
    Kazuki Kodo
    Department of Pediatrics, Division of Pediatric Cardiology, Keio University School of Medicine, Japan
    Circ J 75:2296-304. 2011
    ..This review outlines the recent discoveries of the molecular embryology of the normal heart and the genetic basis of CHD...
  13. doi request reprint Pharmacokinetics of drugs for pediatric pulmonary hypertension
    Kouichi Nakau
    Department of Pediatrics, Asahikawa Medical University, Asahikawa, Japan
    Pediatr Int 58:1112-1117. 2016
    ..The aim of this study was therefore, to measure blood drug levels and analyze the pharmacokinetics of two such drugs in children...
  14. doi request reprint Variable severity of cardiovascular phenotypes in patients with an early-onset form of Marfan syndrome harboring FBN1 mutations in exons 24-32
    Jun Maeda
    Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku ku, Tokyo, 160 8582, Japan
    Heart Vessels 31:1717-23. 2016
    ....
  15. pmc Eosinophilic cystitis presented as a manifestation of hypereosinophilic syndrome: a case report and review of the literature
    Katsuaki Kojima
    Department of Pediatrics, School of Medicine, Keio University, Tokyo, Japan
    Nephron Extra 3:30-5. 2013
    ..5 × 10(3)/μl, 60% of white blood cells). Ultrasonography and MRI of the bladder showed a bladder mass, a biopsy of which revealed eosinophilic infiltration and degranulation...
  16. doi request reprint The impact of cardiac surgery in patients with trisomy 18 and trisomy 13 in Japan
    Jun Maeda
    Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan
    Am J Med Genet A 155:2641-6. 2011
    ..Cardiac surgery was done in 6 (26%) of 23 patients. In this study, approximately a quarter of patients underwent surgery for CHD in both trisomies. Cardiac surgery may improve survival in selected patients with T18...
  17. pmc Genome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population
    Motoaki Sano
    Department of Cardiology, Keio University School of Medicine, Tokyo, Japan
    PLoS ONE 11:e0155550. 2016
    ..635 x 10-8). The transcriptional repressor, TBX3, is proposed to suppress the development of working ventricular myocardium. Our findings suggest that genetic variation of Tbx3 is associated with LV mass in a healthy Japanese population. ..
  18. pmc Induction of human cardiomyocyte-like cells from fibroblasts by defined factors
    Rie Wada
    Department of Clinical and Molecular Cardiovascular Research, School of Medicine, Keio University, Tokyo 160 8582, Japan
    Proc Natl Acad Sci U S A 110:12667-72. 2013
    ..These findings demonstrate that human fibroblasts can be directly converted to iCMs by defined factors, which may facilitate future applications in regenerative medicine. ..
  19. doi request reprint Safety and efficacy of linezolid in 16 infants and children in Japan
    Masayoshi Shinjoh
    Center for Infectious Diseases and Infection Control, Keio University School of Medicine, Tokyo, Japan
    J Infect Chemother 18:591-6. 2012
    ....
  20. ncbi request reprint Functional attenuation of UFD1l, a 22q11.2 deletion syndrome candidate gene, leads to cardiac outflow septation defects in chicken embryos
    Chihiro Yamagishi
    Department of Pediatrics, University of Texas, Southwestern Medical Center at Dallas, Dallas 75390 9148, USA
    Pediatr Res 53:546-53. 2003
    ..These data suggest that Ufd1l may play a role in cardiac NCC during conotruncal septation...
  21. pmc Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer
    Hiroyuki Yamagishi
    Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas 75390 9148, USA
    Genes Dev 17:269-81. 2003
    ..We propose that Tbx1 is a direct transcriptional target of Fox proteins and that Fox proteins may serve an intermediary role in Shh regulation of Tbx1...
  22. ncbi request reprint Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors
    Tonghuan Hu
    Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390 9148, USA
    Development 131:5491-502. 2004
    ....
  23. ncbi request reprint The 22q11.2 deletion syndrome
    Hiroyuki Yamagishi
    Department of Pediatrics and Molecular Biology, University of Texas Southwestern Medical Center, Dallas 75390 9148, USA
    Keio J Med 51:77-88. 2002
    ....