Tomoki Tamakoshi

ORCID: 0000-0003-3423-0683
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About
Contact & Profiles
Research Areas
  • Congenital heart defects research
  • Muscle Physiology and Disorders
  • Skin and Cellular Biology Research
  • Lymphatic System and Diseases
  • Developmental Biology and Gene Regulation
  • Planarian Biology and Electrostimulation
  • melanin and skin pigmentation
  • Coronary Artery Anomalies
  • Neonatal Respiratory Health Research
  • Hemispheric Asymmetry in Neuroscience
  • Cleft Lip and Palate Research
  • Advanced machining processes and optimization
  • Axon Guidance and Neuronal Signaling
  • Silk-based biomaterials and applications
  • Sympathectomy and Hyperhidrosis Treatments
  • Drug Solubulity and Delivery Systems
  • Pulmonary Hypertension Research and Treatments
  • Cancer-related molecular mechanisms research
  • Epigenetics and DNA Methylation
  • Genetics, Aging, and Longevity in Model Organisms

Osaka University
2023

Hamamatsu University School of Medicine
2003-2010

Foxc2/MFH-1 is a member of the forkhead family transcription factors and Foxc2-deficient mice exhibit aortic arch anomalies (type B interruption arch). Endothelin receptor type-A (ETA) one two known endothelin receptors that belong to G-protein-coupled family. ETA-deficient show defects in great arteries, primarily type arch. Based on similar phenotypes cardiovascular system Foxc2- mice, we investigated whether Foxc2 ETA have close relationship patterning.The homozygotes were obtained by...

10.1016/j.cardiores.2004.10.017 article EN Cardiovascular Research 2004-11-09
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