Suppr超能文献

相似文献

3
Ca2+ entry channels in rat thoracic aortic smooth muscle cells activated by endothelin-1.
Jpn J Pharmacol. 1999 Aug;80(4):281-8. doi: 10.1254/jjp.80.281.
4
[Characterization of voltage-independent Ca2+ channels activated by endothelin-1].
Nihon Yakurigaku Zasshi. 1999 Oct;114 Suppl 1:96P-102P. doi: 10.1254/fpj.114.supplement_96.
5
Pharmacological properties of calcium entry channels in A7r5 cells activated by endothelin-1.
J Cardiovasc Pharmacol. 2000 Nov;36(5 Suppl 1):S107-9. doi: 10.1097/00005344-200036051-00035.
6
[Analysis of Ca2+ entry channels in endothelin-1-induced contraction of rat aorta using new blockers].
Nihon Yakurigaku Zasshi. 1999 Oct;114 Suppl 1:103P-109P. doi: 10.1254/fpj.114.supplement_103.
9
Endothelin-1-induced contraction of rat thoracic aorta depends on calcium entry through three types of calcium channel.
J Cardiovasc Pharmacol. 2000 Nov;36(5 Suppl 1):S105-6. doi: 10.1097/00005344-200036051-00034.
10
Activation of two types of Ca2+-permeable nonselective cation channel by endothelin-1 in A7r5 cells.
Br J Pharmacol. 1998 Aug;124(7):1541-9. doi: 10.1038/sj.bjp.0701984.

引用本文的文献

1
Development of Store-Operated Calcium Entry-Targeted Compounds in Cancer.
Front Pharmacol. 2021 May 28;12:688244. doi: 10.3389/fphar.2021.688244. eCollection 2021.
3
Non-selective cation channels, transient receptor potential channels and ischemic stroke.
Biochim Biophys Acta. 2007 Aug;1772(8):947-57. doi: 10.1016/j.bbadis.2007.03.004. Epub 2007 Mar 19.
4
Mechanisms of the prostaglandin F2alpha-induced rise in [Ca2+]i in rat intrapulmonary arteries.
J Physiol. 2006 Feb 15;571(Pt 1):147-63. doi: 10.1113/jphysiol.2005.101394. Epub 2005 Dec 15.
7
Non-selective cationic channels of smooth muscle and the mammalian homologues of Drosophila TRP.
J Physiol. 2004 Sep 15;559(Pt 3):685-706. doi: 10.1113/jphysiol.2004.068734. Epub 2004 Jul 22.
8
Pharmacological profile of store-operated channels in cerebral arteriolar smooth muscle cells.
Br J Pharmacol. 2003 Jul;139(5):955-65. doi: 10.1038/sj.bjp.0705327.

本文引用的文献

1
Activation of two types of Ca2+-permeable nonselective cation channel by endothelin-1 in A7r5 cells.
Br J Pharmacol. 1998 Aug;124(7):1541-9. doi: 10.1038/sj.bjp.0701984.
3
Physiological role of Ca2+-permeable nonselective cation channel in endothelin-1-induced contraction of rabbit aorta.
J Cardiovasc Pharmacol. 1997 Oct;30(4):504-9. doi: 10.1097/00005344-199710000-00015.
5
Pharmacological and functional properties of voltage-independent Ca2+ channels.
Cell Calcium. 1996 Apr;19(4):269-79. doi: 10.1016/s0143-4160(96)90068-8.
6
Inhibition of a store-operated Ca2+ entry pathway in human endothelial cells by the isoquinoline derivative LOE 908.
Br J Pharmacol. 1996 Oct;119(4):702-6. doi: 10.1111/j.1476-5381.1996.tb15729.x.
7
Endothelin receptor subtypes and their role in transmembrane signaling mechanisms.
Pharmacol Ther. 1995;68(3):435-71. doi: 10.1016/0163-7258(95)02015-2.
8
Inhibition of Ca2+ transport pathways in thymic lymphocytes by econazole, miconazole, and SKF 96365.
Am J Physiol. 1993 Mar;264(3 Pt 1):C654-62. doi: 10.1152/ajpcell.1993.264.3.C654.
9
Inositol trisphosphate and calcium signalling.
Nature. 1993 Jan 28;361(6410):315-25. doi: 10.1038/361315a0.
10
Receptor-activated Ca2+ influx: how many mechanisms for how many channels?
Trends Pharmacol Sci. 1994 Mar;15(3):77-83. doi: 10.1016/0165-6147(94)90282-8.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验