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Enhanced inactivation increases the sensitivity of pathogenic Cav1.3 L-type Ca2+channel variants to dihydropyridine Ca2+channel blockers
被引:0
|
作者
:
Toeroek, F.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Innsbruck, Dept Pharmacol & Toxicol, Inst Pharm, Innsbruck, Austria
Ctr Mol Biosci Innsbruck, Innsbruck, Austria
Univ Innsbruck, Dept Pharmacol & Toxicol, Inst Pharm, Innsbruck, Austria
Toeroek, F.
[
1
,
2
]
Ortner, N. J.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Innsbruck, Dept Pharmacol & Toxicol, Inst Pharm, Innsbruck, Austria
Ctr Mol Biosci Innsbruck, Innsbruck, Austria
Univ Innsbruck, Dept Pharmacol & Toxicol, Inst Pharm, Innsbruck, Austria
Ortner, N. J.
[
1
,
2
]
Striessnig, J.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Innsbruck, Dept Pharmacol & Toxicol, Inst Pharm, Innsbruck, Austria
Ctr Mol Biosci Innsbruck, Innsbruck, Austria
Univ Innsbruck, Dept Pharmacol & Toxicol, Inst Pharm, Innsbruck, Austria
Striessnig, J.
[
1
,
2
]
机构
:
[1]
Univ Innsbruck, Dept Pharmacol & Toxicol, Inst Pharm, Innsbruck, Austria
[2]
Ctr Mol Biosci Innsbruck, Innsbruck, Austria
来源
:
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY
|
2023年
/ 396卷
基金
:
奥地利科学基金会;
关键词
:
D O I
:
暂无
中图分类号
:
R9 [药学];
学科分类号
:
1007 ;
摘要
:
66
引用
收藏
页码:S18 / S18
页数:1
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