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
10.1038/nm1094
article
EN
Nature Medicine
2004-08-22
10.1016/s0012-1606(03)00176-3
article
EN
publisher-specific-oa
Developmental Biology
2003-05-19
10.1016/j.bbrc.2005.11.097
article
EN
Biochemical and Biophysical Research Communications
2005-11-29
10.1016/j.lfs.2010.05.009
article
EN
Life Sciences
2010-05-28
10.1016/j.jid.2023.05.021
article
EN
publisher-specific-oa
Journal of Investigative Dermatology
2023-06-10
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
10.1016/j.bbrc.2006.03.195
article
EN
Biochemical and Biophysical Research Communications
2006-04-18
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