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T-type calcium channels blockers inhibit HSV-2 infection at the late stage of genome replication

European journal of pharmacology, 2021-02, Vol.892, p.173782-173782, Article 173782

2021

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Calcium overload-induced arrhythmia is suppressed by farnesol in rat heart

European journal of pharmacology, 2019-09, Vol.859, p.172488-172488, Article 172488

2019

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Pregabalin is a potent and selective ligand for α 2δ-1 and α 2δ-2 calcium channel subunits

European journal of pharmacology, 2011-09, Vol.667 (1), p.80-90

2011

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ML218 modulates calcium binding protein, oxidative stress, and inflammation during ischemia-reperfusion brain injury in mice

European journal of pharmacology, 2024-11, Vol.982, p.176919, Article 176919

2024

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Essential role of Cav3.2 T-type calcium channels in butyrate-induced colonic pain and nociceptor hypersensitivity in mice

European journal of pharmacology, 2020-11, Vol.887, p.173576-173576, Article 173576

2020

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Effect of ABT-639 on Cav3.2 channel activity and its analgesic actions in mouse models of inflammatory and neuropathic pain

European journal of pharmacology, 2024-03, Vol.967, p.176416-176416, Article 176416

2024

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Synthetic Aβ oligomers (Aβ1–42 globulomer) modulate presynaptic calcium currents: Prevention of Aβ-induced synaptic deficits by calcium channel blockers

European journal of pharmacology, 2013-02, Vol.702 (1-3), p.44-55

2013

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Isradipine, an L-type calcium channel blocker, attenuates cocaine effects in mice by reducing central glutamate release

European journal of pharmacology, 2024-05, Vol.971, p.176489-176489, Article 176489

2024

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Cav3.2 overexpression in L4 dorsal root ganglion neurons after L5 spinal nerve cutting involves Egr-1, USP5 and HMGB1 in rats: An emerging signaling pathway for neuropathic pain

European journal of pharmacology, 2020-12, Vol.888, p.173587-173587, Article 173587

2020

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L-type calcium channels contribute to 5-HT3-receptor-evoked CaMKIIα and ERK activation and induction of emesis in the least shrew (Cryptotis parva)

European journal of pharmacology, 2015-05, Vol.755, p.110-118

2015

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Functional, electrophysiology, and molecular dynamics analysis of quercetin-induced contraction of rat vascular musculature

European journal of pharmacology, 2022-03, Vol.918, p.174778-174778, Article 174778

2022

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L-type calcium channel blockers decrease the iron overload-mediated oxidative stress in renal epithelial cells by reducing iron accumulation

European journal of pharmacology, 2020-11, Vol.886, p.173513-173513, Article 173513

2020

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Relaxation effect of a novel Danshensu/tetramethylpyrazine derivative on rat mesenteric arteries

European journal of pharmacology, 2015-08, Vol.761, p.153-160

2015

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N- and L-type calcium channels blocker cilnidipine ameliorates neuropathic pain

European journal of pharmacology, 2016-12, Vol.793, p.66-75

2016

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Vasorelaxation to capsaicin and its effects on calcium influx in arteries

European journal of pharmacology, 2012-04, Vol.681 (1-3), p.88-93

2012

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Hydrogen sulfide inhibited L-type calcium channels (CaV1.2) via up-regulation of the channel sulfhydration in vascular smooth muscle cells

European journal of pharmacology, 2019-09, Vol.858, p.172455-172455, Article 172455

2019

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The L-, N-, and T-type triple calcium channel blocker benidipine acts as an antagonist of mineralocorticoid receptor, a member of nuclear receptor family

European journal of pharmacology, 2010-06, Vol.635 (1), p.49-55

2010

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Tonic arterial contraction mediated by L-type Ca2+ channels requires sustained Ca2+ influx, G protein-associated Ca2+ release, and RhoA/ROCK activation

European journal of pharmacology, 2012-12, Vol.697 (1-3), p.88-96

2012

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Effects of intermediate-conductance Ca2+-activated K+ channel modulators on human prostate cancer cell proliferation

European journal of pharmacology, 2003-06, Vol.471 (3), p.157-164

2003

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Distinct properties of amlodipine and nicardipine block of the voltage-dependent Ca2+ channels Cav1.2 and Cav2.1 and the mutant channels Cav1.2/Dihydropyridine insensitive and Cav2.1/Dihydropyridine sensitive

European journal of pharmacology, 2011-11, Vol.670 (1), p.105-113

2011

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Effects of iron overload, an iron chelator and a T-Type calcium channel blocker on cardiac mitochondrial biogenesis and mitochondrial dynamics in thalassemic mice

European journal of pharmacology, 2017-03, Vol.799, p.118-127

2017

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T1143 essential for Ca V 1.2 inhibition by diltiazem

European journal of pharmacology, 2021-03, Vol.895, p.173889

Shabbir, Waheed

2021

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Calcium channels and their blockers in intraocular pressure and glaucoma

European journal of pharmacology, 2014-09, Vol.739, p.96-105

Mayama, Chihiro

2014

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Interactions between calcium channels and SK channels in midbrain dopamine neurons and their impact on pacemaker regularity: Contrasting roles of N- and L-type channels

European journal of pharmacology, 2016-10, Vol.788, p.274-279

2016

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Effects of menthol on circular smooth muscle of human colon: Analysis of the mechanism of action

European journal of pharmacology, 2014-10, Vol.740, p.295-301

2014

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T-type calcium channels blockers inhibit HSV-2 infection at the late stage of genome replication

Calcium overload-induced arrhythmia is suppressed by farnesol in rat heart

Pregabalin is a potent and selective ligand for α 2δ-1 and α 2δ-2 calcium channel subunits

ML218 modulates calcium binding protein, oxidative stress, and inflammation during ischemia-reperfusion brain injury in mice

Essential role of Cav3.2 T-type calcium channels in butyrate-induced colonic pain and nociceptor hypersensitivity in mice

Effect of ABT-639 on Cav3.2 channel activity and its analgesic actions in mouse models of inflammatory and neuropathic pain

Synthetic Aβ oligomers (Aβ1–42 globulomer) modulate presynaptic calcium currents: Prevention of Aβ-induced synaptic deficits by calcium channel blockers

Isradipine, an L-type calcium channel blocker, attenuates cocaine effects in mice by reducing central glutamate release

Cav3.2 overexpression in L4 dorsal root ganglion neurons after L5 spinal nerve cutting involves Egr-1, USP5 and HMGB1 in rats: An emerging signaling pathway for neuropathic pain

L-type calcium channels contribute to 5-HT3-receptor-evoked CaMKIIα and ERK activation and induction of emesis in the least shrew (Cryptotis parva)

Functional, electrophysiology, and molecular dynamics analysis of quercetin-induced contraction of rat vascular musculature

L-type calcium channel blockers decrease the iron overload-mediated oxidative stress in renal epithelial cells by reducing iron accumulation

Relaxation effect of a novel Danshensu/tetramethylpyrazine derivative on rat mesenteric arteries

N- and L-type calcium channels blocker cilnidipine ameliorates neuropathic pain

Vasorelaxation to capsaicin and its effects on calcium influx in arteries

Hydrogen sulfide inhibited L-type calcium channels (CaV1.2) via up-regulation of the channel sulfhydration in vascular smooth muscle cells

The L-, N-, and T-type triple calcium channel blocker benidipine acts as an antagonist of mineralocorticoid receptor, a member of nuclear receptor family

Tonic arterial contraction mediated by L-type Ca2+ channels requires sustained Ca2+ influx, G protein-associated Ca2+ release, and RhoA/ROCK activation

Effects of intermediate-conductance Ca2+-activated K+ channel modulators on human prostate cancer cell proliferation

Distinct properties of amlodipine and nicardipine block of the voltage-dependent Ca2+ channels Cav1.2 and Cav2.1 and the mutant channels Cav1.2/Dihydropyridine insensitive and Cav2.1/Dihydropyridine sensitive

Effects of iron overload, an iron chelator and a T-Type calcium channel blocker on cardiac mitochondrial biogenesis and mitochondrial dynamics in thalassemic mice

T1143 essential for Ca V 1.2 inhibition by diltiazem

Calcium channels and their blockers in intraocular pressure and glaucoma

Interactions between calcium channels and SK channels in midbrain dopamine neurons and their impact on pacemaker regularity: Contrasting roles of N- and L-type channels

Effects of menthol on circular smooth muscle of human colon: Analysis of the mechanism of action

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