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Byung-Chang Suh
Researcher at Daegu Gyeongbuk Institute of Science and Technology
Publications - 81
Citations - 4369
Byung-Chang Suh is an academic researcher from Daegu Gyeongbuk Institute of Science and Technology. The author has contributed to research in topics: Phospholipase C & Phosphatidylinositol. The author has an hindex of 26, co-authored 73 publications receiving 3965 citations. Previous affiliations of Byung-Chang Suh include University of Washington & Pohang University of Science and Technology.
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Journal ArticleDOI
Differential regulation of proton-sensitive ion channels by phospholipids: a comparative study between ASICs and TRPV1.
TL;DR: regulation of ASICs and TRPV1 by membrane phosphoinositides, which are general cofactors of many receptors and ion channels are compared, and it is observed that ASICs do not require membrane phosphatidylinositol 4-phosphate (PI(4)P) or phosphatids 4,5-bisph phosphate ( PI(4,5)P2) for their function.
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Dynamic phospholipid interaction of β2e subunit regulates the gating of voltage-gated Ca2+ channels.
TL;DR: Membrane targeting of the β2e subunit is dynamically regulated by M1 muscarinic receptor signaling to promote fast inactivation of CaV2.2.
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Synergistic activation of adenylyl cyclase is dependent upon phospholipase C-mediated processes in human neuroblastoma SK-N-BE(2)C cells
TL;DR: The results suggest that the increase in cytosolic Ca2+ and the coupling process between muscarinic receptor-like G-protein and phospholipase C are important for the synergistic activation of adenylyl cyclase in SK-N-BE(2)C cells.
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Allosteric modulation of alternatively spliced Ca2+-activated Cl- channels TMEM16A by PI(4,5)P2 and CaMKII.
Woori Ko,Seung-Ryoung Jung,Kwon-Woo Kim,Jun-Hee Yeon,Cheon-Gyu Park,Joo Hyun Nam,Bertil Hille,Byung-Chang Suh +7 more
TL;DR: In this article, two splice variants of TMEM16A showed different sensitivity to endogenous PI(4,5)P2 degradation, where the splice variant exhibited higher channel activity and more current inhibition.
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Syntheses of D- and L-myo-inositol 1,2,4,5-tetrakisphosphate and stereoselectivity of the I(1,4,5)P3 receptor binding.
TL;DR: D- and L-myo-Inositol 1,2,4,5-tetrakisphosphate are synthesized via resolution of the camphanate ester of a myo-inositol derivative, and the binding affinities to I(1, 4,5)P3 receptor were measured.