Hiroyuki Yamagishi

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Publications in SciGraph latest 50 shown

  • 2019-04 Chronotropic incompetence to exercise in anorexia nervosa patients during the body-weight recovery phase as an index of insufficient treatment in HEART AND VESSELS
  • 2019-04 Type 2 inositol 1,4,5-trisphosphate receptor inhibits the progression of pulmonary arterial hypertension via calcium signaling and apoptosis in HEART AND VESSELS
  • 2018-09-06 Living-donor lung transplantation after surgical repair of transposition of the great arteries in GENERAL THORACIC AND CARDIOVASCULAR SURGERY
  • 2018 Erratum to: Etiology and Morphogenesis of Congenital Heart Disease in ETIOLOGY AND MORPHOGENESIS OF CONGENITAL HEART DISEASE
  • 2017-12 Regulation of Sema3c and the Interaction between Cardiac Neural Crest and Second Heart Field during Outflow Tract Development in SCIENTIFIC REPORTS
  • 2016-10 Variable severity of cardiovascular phenotypes in patients with an early-onset form of Marfan syndrome harboring FBN1 mutations in exons 24–32 in HEART AND VESSELS
  • 2016 Modification of Cardiac Phenotype in Tbx1 Hypomorphic Mice in ETIOLOGY AND MORPHOGENESIS OF CONGENITAL HEART DISEASE
  • 2016 Pulmonary Arterial Hypertension in Patients with Heterotaxy/Polysplenia Syndrome in ETIOLOGY AND MORPHOGENESIS OF CONGENITAL HEART DISEASE
  • 2016 Human Genetics of Truncus Arteriosus in CONGENITAL HEART DISEASES: THE BROKEN HEART
  • 2016 The Loss of Foxc2 Expression in the Outflow Tract Links the Interrupted Arch in the Conditional Foxc2 Knockout Mouse in ETIOLOGY AND MORPHOGENESIS OF CONGENITAL HEART DISEASE
  • 2016 A History and Interaction of Outflow Progenitor Cells Implicated in “Takao Syndrome” in ETIOLOGY AND MORPHOGENESIS OF CONGENITAL HEART DISEASE
  • 2016 Inositol Trisphosphate Receptors in the Vascular Development in ETIOLOGY AND MORPHOGENESIS OF CONGENITAL HEART DISEASE
  • 2014-12 Myocardium-derived angiopoietin-1 is essential for coronary vein formation in the developing heart in NATURE COMMUNICATIONS
  • 2012-08 Safety and efficacy of linezolid in 16 infants and children in Japan in JOURNAL OF INFECTION AND CHEMOTHERAPY
  • 2010-10 GATA transcription factors in congenital heart defects: A Commentary on a novel <i>GATA6</i> mutation in patients with tetralogy of Fallot or atrial septal defect in JOURNAL OF HUMAN GENETICS
  • 2010-05 Cardiovascular surgery for congenital heart disease associated with trisomy 18 in GENERAL THORACIC AND CARDIOVASCULAR SURGERY
  • 2009-09 Molecular embryology for an understanding of congenital heart diseases in ANATOMICAL SCIENCE INTERNATIONAL
  • 2006-12 1173C>T Polymorphism in VKORC1 Modulates the Required Warfarin Dose in PEDIATRIC CARDIOLOGY
  • 2006-03 Sonic Hedgehog Is Essential for First Pharyngeal Arch Development in PEDIATRIC RESEARCH
  • 2003-04 Functional Attenuation of Ufd1l, a 22q11.2 Deletion Syndrome Candidate Gene, Leads to Cardiac Outflow Septation Defects in Chicken Embryos in PEDIATRIC RESEARCH
  • 2003-01 Congenital Long QT Syndrome and 2:1 Atrioventricular Block with a Mutation of the SCN5A Gene in PEDIATRIC CARDIOLOGY
  • 2002-05 Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis in NATURE GENETICS
  • 1998-07 Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome in HUMAN GENETICS
  • 1995-05 Behçet's disease presenting with a right atrial vegetation in PEDIATRIC CARDIOLOGY
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