-
1
-
-
0344549853
-
Ginseng pharmacology: Multiple constituents and multiple actions
-
Attele, A.S., Wu, J.A., and Yuan, C.S. (1999). Ginseng pharmacology: multiple constituents and multiple actions. Biochem. Pharmacol. 58, 1685-1693.
-
(1999)
Biochem. Pharmacol.
, vol.58
, pp. 1685-1693
-
-
Attele, A.S.1
Wu, J.A.2
Yuan, C.S.3
-
2
-
-
0142169482
-
Electrophysiological effects of ginseng and ginsenoside Re in guinea pig ventricular myocytes
-
Bai, C.X., Sunami, A., Namiki, T., Sawanobori, T., and Furukawa, T. (2003). Electrophysiological effects of ginseng and ginsenoside Re in guinea pig ventricular myocytes. Eur. J. Pharmacol. 476, 35-44.
-
(2003)
Eur. J. Pharmacol.
, vol.476
, pp. 35-44
-
-
Bai, C.X.1
Sunami, A.2
Namiki, T.3
Sawanobori, T.4
Furukawa, T.5
-
3
-
-
3042820953
-
2+ current by ginsenoside Re, an ingredient of Panax ginseng, in guinea-pig cardiomyocytes
-
2+ current by ginsenoside Re, an ingredient of Panax ginseng, in guinea-pig cardiomyocytes. Br. J. Pharmacol.142, 567-575.
-
(2004)
Br. J. Pharmacol.
, vol.142
, pp. 567-575
-
-
Bai, C.X.1
Takahashi, K.2
Masumiya, H.3
Sawanobori, T.4
Furukawa, T.5
-
4
-
-
0035824896
-
HERG K+ channel activity is regulated by changes in phosphatidyl inositol 4,5-bisphosphate
-
Bian, J., Cui, J., and McDonald, T.V. (2001). HERG K+ channel activity is regulated by changes in phosphatidyl inositol 4,5-bisphosphate. Circ. Res. 89, 1168-1176.
-
(2001)
Circ. Res.
, vol.89
, pp. 1168-1176
-
-
Bian, J.1
Cui, J.2
McDonald, T.V.3
-
5
-
-
65749102789
-
Protective effect of ginsenoside Re on isoproterenol-induced triggered ventricular arrhythmia in rabbits
-
Chen, C.X., and Zhang, H.Y.(2009). Protective effect of ginsenoside Re on isoproterenol-induced triggered ventricular arrhythmia in rabbits. Zhongguo Dang Dai Er Ke Za Zhi. 11, 384-388.
-
(2009)
Zhongguo Dang Dai Er Ke Za Zhi.
, vol.11
, pp. 384-388
-
-
Chen, C.X.1
Zhang, H.Y.2
-
6
-
-
67650744877
-
2+ channel current inhibitions
-
2+ channel current inhibitions. Biol. Pharm. Bull. 32, 1224-1230.
-
(2009)
Biol. Pharm. Bull.
, vol.32
, pp. 1224-1230
-
-
Choi, S.H.1
Lee, J.H.2
Pyo, M.K.3
Lee, B.H.4
Shin, T.J.5
Hwang, S.H.6
Kim, B.R.7
Lee, S.M.8
Oh, J.W.9
Kim, H.C.10
-
7
-
-
77953289251
-
+ channel currents through interacting with the K318 and V319 residues: A role of KCNE1 subunit
-
+ channel currents through interacting with the K318 and V319 residues: a role of KCNE1 subunit. Eur. J. Pharmacol. 637, 138-147.
-
(2010)
Eur. J. Pharmacol.
, vol.637
, pp. 138-147
-
-
Choi, S.H.1
Shi, T.J.2
Lee, B.H.3
Chu, D.H.4
Choe, H.5
Pyo, M.K.6
Hwang, S.H.7
Kim, B.R.8
Lee, S.M.9
Lee, J.H.10
-
8
-
-
79952989457
-
2+-activated potassium channel currents: A role of Tyr360 residue
-
2+-activated potassium channel currents: a role of Tyr360 residue. Mol. Cells 31,133-140.
-
(2011)
Mol. Cells
, vol.31
, pp. 133-140
-
-
Choi, S.H.1
Shin, T.J.2
Lee, B.H.3
Hwang, S.H.4
Lee, S.M.5
Lee, B.C.6
Park, C.S.7
Ha, T.S.8
Nah, S.Y.9
-
9
-
-
84877311452
-
2+-activated potassium channel activation by ginseng gintonin
-
2+-activated potassium channel activation by ginseng gintonin. Evid. Based Complement Alternat. Med. 2013, 323709.
-
(2013)
Evid. Based Complement Alternat. Med.
, vol.2013
, pp. 323709
-
-
Choi, S.H.1
Lee, B.H.2
Hwang, S.H.3
Kim, H.J.4
Lee, S.M.5
Kim, H.C.6
Rhim, H.W.7
Nah, S.Y.8
-
10
-
-
0034056081
-
+ current by chromanol 293B in guinea-pig ventricular cells
-
+ current by chromanol 293B in guinea-pig ventricular cells. Br. J. Pharmacol. 129, 1007-1013.
-
(2000)
Br. J. Pharmacol.
, vol.129
, pp. 1007-1013
-
-
Fujisawa, S.1
Ono, K.2
Iijima, T.3
-
11
-
-
33751119582
-
Ginsenoside Re, a main phytosterol of Panax ginseng, activates cardiac potassium channels via a nongenomic pathway of sex hormones
-
Furukawa, T., Bai, C.X., Kaihara, A., Ozaki, E., Kawano, T., Nakaya, Y., Awais, M., Sato. M., Umezawa, Y., and Kurokawa, J. (2006). Ginsenoside Re, a main phytosterol of Panax ginseng, activates cardiac potassium channels via a nongenomic pathway of sex hormones. Mol. Pharmacol. 70, 1916-1924.
-
(2006)
Mol. Pharmacol.
, vol.70
, pp. 1916-1924
-
-
Furukawa, T.1
Bai, C.X.2
Kaihara, A.3
Ozaki, E.4
Kawano, T.5
Nakaya, Y.6
Awais, M.7
Sato, M.8
Umezawa, Y.9
Kurokawa, J.10
-
12
-
-
33646814436
-
KCNQ1 assembly and function is blocked by long-QT syndrome mutations that disrupt interaction with calmodulin
-
Ghosh, S., Nunziato, D.A., and Pitt, G.S. (2006). KCNQ1 assembly and function is blocked by long-QT syndrome mutations that disrupt interaction with calmodulin. Circ. Res. 98, 1048-1054.
-
(2006)
Circ. Res.
, vol.98
, pp. 1048-1054
-
-
Ghosh, S.1
Nunziato, D.A.2
Pitt, G.S.3
-
14
-
-
84863461647
-
Gintonin, newly identified compounds from ginseng, is novel lysophosphatidic acids-protein complexes and activates G protein coupled lysophosphatidic acid receptors with high affinity
-
Hwang, S.H., Shin, T.J., Choi, S.H., Cho, H.J., Lee, B.H., Pyo, M.K.,Lee, J.H., Kang, J., Kim, H.J., Park, C.W., et al. (2012). Gintonin, newly identified compounds from ginseng, is novel lysophosphatidic acids-protein complexes and activates G protein coupled lysophosphatidic acid receptors with high affinity. Mol. Cells 33, 151-162.
-
(2012)
Mol. Cells
, vol.33
, pp. 151-162
-
-
Hwang, S.H.1
Shin, T.J.2
Choi, S.H.3
Cho, H.J.4
Lee, B.H.5
Pyo, M.K.6
Lee, J.H.7
Kang, J.8
Kim, H.J.9
Park, C.W.10
-
15
-
-
0028914837
-
Ginsenosides of the protopanaxatriol group cause endothelium-dependent relaxation in the rat aorta
-
Kang, S.Y., Schini-Kerth, V.B., and Kim, N.D. (1995). Ginsenosides of the protopanaxatriol group cause endothelium-dependent relaxation in the rat aorta. Life Sci. 56, 1577-1586.
-
(1995)
Life Sci.
, vol.56
, pp. 1577-1586
-
-
Kang, S.Y.1
Schini-Kerth, V.B.2
Kim, N.D.3
-
17
-
-
0035805542
-
Two vovelXenopus homologs of mammalian LPA1/EDG-2 function as lysophosphatidic acid receptors in Xenopus oocytes and mammalian cells
-
Kimura, Y., Schmitt, A., Fukushima, N., Ishii, I., Kimura, H., Nebreda, A.R., and Chun, J. (2001). Two vovelXenopus homologs of mammalian LPA1/EDG-2 function as lysophosphatidic acid receptors in Xenopus oocytes and mammalian cells. J. Biol. Chem. 276, 15208-15215.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 15208-15215
-
-
Kimura, Y.1
Schmitt, A.2
Fukushima, N.3
Ishii, I.4
Kimura, H.5
Nebreda, A.R.6
Chun, J.7
-
18
-
-
25144469808
-
+ current inhibition
-
+ current inhibition. Mol. Pharmacol. 68, 1114-1126.
-
(2005)
Mol. Pharmacol.
, vol.68
, pp. 1114-1126
-
-
Lee, J.H.1
Jeong, S.M.2
Kim, J.H.3
Lee, B.H.4
Yoon, I.S.5
Lee, J.H.6
Choi, S.H.7
Kim, D.H.8
Rhim, H.9
Kim, S.S.10
-
19
-
-
40849085416
-
Ginsenoside Rg3 inhibits human 1.4 channel currents by interacting with the Lys531 residue
-
Lee, J.H., Lee, B.H., Choi, S.H., Yoon, I.S., Pyo, M.K., Shin, T.J., Choi, W.S., Lim, Y., Rhim, H., Won, K.H., et al. (2008). Ginsenoside Rg3 inhibits human 1.4 channel currents by interacting with the Lys531 residue. Mol. Pharmacol. 73, 619-626.
-
(2008)
Mol. Pharmacol.
, vol.73
, pp. 619-626
-
-
Lee, J.H.1
Lee, B.H.2
Choi, S.H.3
Yoon, I.S.4
Pyo, M.K.5
Shin, T.J.6
Choi, W.S.7
Lim, Y.8
Rhim, H.9
Won, K.H.10
-
20
-
-
84880133701
-
Activation of lysophosphatidic acid receptor by gintonin inhibits Kv1.2 channel activity: Involvement of tyrosine kinase and receptor protein tyrosine phosphatase α
-
Lee, J.H., Choi, S.H., Lee, B.H., Hwang, S.H., Kim, H.J., Rhee, J., Chung, C., andNah, S.Y. (2013). Activation of lysophosphatidic acid receptor by gintonin inhibits Kv1.2 channel activity: involvement of tyrosine kinase and receptor protein tyrosine phosphatase α. Neurosci. Lett. 26, 143-148.
-
(2013)
Neurosci. Lett.
, vol.26
, pp. 143-148
-
-
Lee, J.H.1
Choi, S.H.2
Lee, B.H.3
Hwang, S.H.4
Kim, H.J.5
Rhee, J.6
Chung, C.7
Nah, S.Y.8
-
24
-
-
79959905574
-
Novel glycoproteins from ginseng, J
-
Pyo, M.K., Choi, S.H., Hwang, S.H., Shin, T.J., Lee, B.H., Lee, S.M., Lim, Y.D., and Nah, S.Y. (2011). Novel glycoproteins from ginseng, J. Gingseng Res. 35, 92-103.
-
(2011)
Gingseng Res.
, vol.35
, pp. 92-103
-
-
Pyo, M.K.1
Choi, S.H.2
Hwang, S.H.3
Shin, T.J.4
Lee, B.H.5
Lee, S.M.6
Lim, Y.D.7
Nah, S.Y.8
-
25
-
-
0034929557
-
KCNQ potassium channels: Physiology, pathophysiology, and pharmacology
-
Robbins, J. (2001). KCNQ potassium channels: physiology, pathophysiology, and pharmacology. Pharmacol. Ther. 90, 1-19.
-
(2001)
Pharmacol. Ther.
, vol.90
, pp. 1-19
-
-
Robbins, J.1
-
27
-
-
0032970148
-
Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia
-
Sanguinetti, M.C. (1999). Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia. Ann. N Y Acad. Sci. 868, 406-413.
-
(1999)
Ann. N Y Acad. Sci.
, vol.868
, pp. 406-413
-
-
Sanguinetti, M.C.1
-
28
-
-
0029854263
-
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel
-
Sanguinetti, M.C., Curran, M.E., Zou, A., Shen, J., Spector, P.S., Atkinson, D.L., and Keating, M.T. (1996). Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel. Nature 384, 80-83.
-
(1996)
Nature
, vol.384
, pp. 80-83
-
-
Sanguinetti, M.C.1
Curran, M.E.2
Zou, A.3
Shen, J.4
Spector, P.S.5
Atkinson, D.L.6
Keating, M.T.7
-
29
-
-
33646810883
-
Calmodulin is essential for cardiac IKS channel gating and assembly: Impaired function in long-QT mutations
-
Shamgar, L., Ma, L., Schmitt, N., Haitin, Y., Peretz, A., Wiener, R., Hirsch, J., Pongs, O., and Attali, B. (2006). Calmodulin is essential for cardiac IKS channel gating and assembly: impaired function in long-QT mutations. Circ. Res. 98, 1055-1063.
-
(2006)
Circ. Res.
, vol.98
, pp. 1055-1063
-
-
Shamgar, L.1
Ma, L.2
Schmitt, N.3
Haitin, Y.4
Peretz, A.5
Wiener, R.6
Hirsch, J.7
Pongs, O.8
Attali, B.9
-
30
-
-
0025210005
-
Calcium-sensitive delayed rectifier potassium current in guinea pig ventricular cells
-
Tohse, N. (1990). Calcium-sensitive delayed rectifier potassium current in guinea pig ventricular cells. Am. J. Physiol. 258, H1200-1207.
-
(1990)
Am. J. Physiol.
, vol.258
, pp. 1200-1207
-
-
Tohse, N.1
-
31
-
-
0037047394
-
The identification and characterization of a noncontinuouscalmodulinbinding site in noninactivating voltage-dependent KCNQ potassium channels
-
Yus-Najera, E., Santana-Castro, I., andVillarroel, A. (2002). The identification and characterization of a noncontinuouscalmodulinbinding site in noninactivating voltage-dependent KCNQ potassium channels. J. Biol. Chem. 277, 28545-28553.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 28545-28553
-
-
Yus-Najera, E.1
Santana-Castro, I.2
Villarroel, A.3
|