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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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Differential inhibition of catecholamine secretion by amitriptyline through blockage of nicotinic receptors, sodium channels, and calcium channels in bovine adrenal chromaffin cells

TL;DR: Submicromolar concentrations of amitriptyline significantly inhibited DMPP‐induced [3H]NE secretion and [Ca2+]i rise, but not veratridine‐ or 70 mM K+‐induced responses, suggesting that nicotinic acetylcholine receptors (nAChR) as well as VSCCs and VSSCs can be targeted by amitripyline.
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Dual roles of P2 purinergic receptors in Insulin-stimulated leptin production and lipolysis in differentiated rat white adipocytes

TL;DR: The data presented here suggest that white adipocytes express at least two different types of P2Y receptors and that activation of P 2Y11 receptor might be involved in inhibition of leptin production and stimulation of lipolysis, suggesting that purinergic transmission can play an important role in white adipocyte physiology.
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Induction of Cytosolic Ca2+ Elevation Mediated by Mas-7 Occurs through Membrane Pore Formation

TL;DR: The data suggest that the Mas-7-induced [Ca2+]i elevation is the combined result of Ca2+ release from stores via phosphoinositide turnover and prolonged Ca2+.
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Cholesterol modulates ion channels via down‐regulation of phosphatidylinositol 4,5‐bisphosphate

TL;DR: In this article, the effect of cholesterol on two exogenously expressed PIP2-sensitive K+ channels: human Ether-a-go-go related gene (HERG) and KCNQ was examined.
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Signal flows from two phospholipase C-linked receptors are independent in PC12 cells.

TL;DR: The data suggest that the CA secretions caused by BK or ATP may have separate secretory pathways even though they activate identical second messenger pathways.