Projects per year
Personal profile
Education
- 2010 Phd, Department of Biology Sciences, National Sun Yat-sen University
Experience
- 2004/05~ Attending physician, Department of Anesthesiology, National Cheng Kung University Hospital
- 2008/12~2010/06 Fellow,Harvard Medical School/Brigham and Women's Hospital
- 2010/08~ Associate professor, Department of Anesthesiology, school of Medicine, National Cheng Kung University
- 2012/08~2015/01 Chairman, Department of Anesthesiology, National Cheng Kung University Hospital
Research Interests
- Nerve block
- Pain Management
- Pain Research
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Projects
Research Output
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Characterization of inhibitory effectiveness in hyperpolarization-activated cation currents by a group of ent-kaurane-type diterpenoids from croton tonkinensis
Kuo, P. C., Liu, Y. C., Lo, Y. C. & Wu, S. N., 2020 Feb, In: International journal of molecular sciences. 21, 4, 1268.Research output: Contribution to journal › Article › peer-review
Open Access3 Citations (Scopus) -
Concerted suppression of I h and activation of I K(M) by ivabradine, an HCN-channel inhibitor, in pituitary cells and hippocampal neurons
Hsiao, H. T., Liu, Y. C., Liu, P. Y. & Wu, S. N., 2019 Jul, In: Brain Research Bulletin. 149, p. 11-20 10 p.Research output: Contribution to journal › Article › peer-review
14 Citations (Scopus) -
Differential suppression of delayed-rectifier and inwardly rectifier K+ currents by a group of ent-kaurane-type diterpenoids from Croton tonkinensis, in microglial cells
Hsiao, H. T., Lee, Y. C., Liu, Y. C., Kuo, P. C. & Wu, S. N., 2019 Aug 5, In: European Journal of Pharmacology. 856, 172414.Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus) -
Effectiveness of nalbuphine, a κ-opioid receptor agonist and μ-opioid receptor antagonist, in the inhibition of INa, IK(M), and IK(erg) unlinked to interaction with opioid receptors
Liu, Y. Y., Hsiao, H. T., Wang, J. C. F., Liu, Y. C. & Wu, S. N., 2019 Sep 1, In: Drug Development Research. 80, 6, p. 846-856 11 p.Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus) -
Parecoxib, a selective blocker of cyclooxygenase-2, directly inhibits neuronal delayed-rectifier K+ current, M-type K+ current and Na+ current
Liu, Y. Y., Hsiao, H. T., Wang, J. C. F., Liu, Y. C. & Wu, S. N., 2019 Feb 5, In: European Journal of Pharmacology. 844, p. 95-101 7 p.Research output: Contribution to journal › Article › peer-review
10 Citations (Scopus)