genial 发表于 2025-3-21 19:01:29

书目名称Calcium Channel Pharmacology影响因子(影响力)<br>        http://impactfactor.cn/if/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology影响因子(影响力)学科排名<br>        http://impactfactor.cn/ifr/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology网络公开度<br>        http://impactfactor.cn/at/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology网络公开度学科排名<br>        http://impactfactor.cn/atr/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology被引频次<br>        http://impactfactor.cn/tc/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology被引频次学科排名<br>        http://impactfactor.cn/tcr/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology年度引用<br>        http://impactfactor.cn/ii/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology年度引用学科排名<br>        http://impactfactor.cn/iir/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology读者反馈<br>        http://impactfactor.cn/5y/?ISSN=BK0220770<br><br>        <br><br>书目名称Calcium Channel Pharmacology读者反馈学科排名<br>        http://impactfactor.cn/5yr/?ISSN=BK0220770<br><br>        <br><br>

LOPE 发表于 2025-3-21 21:38:28

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法律的瑕疵 发表于 2025-3-22 01:50:33

Ahmed M. Ali,Bedatri Moulik,Dirk Söffkerand α.2.3, respectively; also known as α.,α. and α.). The use of selective peptide toxins has allowed the association of Ca.2.1, 2.2 and 2.3 with P- or Q-, N-, and B-type calcium currents, respectively (Catterall, 2000; Ertel et al., 2000; Jarvis and Zamponi, 2001). These currents are found almost e

AVOW 发表于 2025-3-22 06:45:44

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控制 发表于 2025-3-22 11:20:32

Neue Dynamiken in der Süd-Süd-Kooperationpotent and highly selective blockers or modulators of calcium channel function, and as such are valuable pharmacological tools and potentially valuable leads in human therapeutic development. Cone shells and spiders are rich sources of such toxins, although they are also found in scorpions and insec

辩论的终结 发表于 2025-3-22 13:18:52

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辩论的终结 发表于 2025-3-22 18:34:29

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大笑 发表于 2025-3-23 00:28:21

https://doi.org/10.1007/978-3-322-89441-0elease, control of neuronal excitability, and gene expression (Catterall, 1998 Hofmann et al., 1999). To date, several kinds of VDCCs have been identified by electrophysiological and pharmacological means, and molecular biological studies have identified ten mammalian genes coding for the pore-formi

问到了烧瓶 发表于 2025-3-23 04:35:23

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愉快吗 发表于 2025-3-23 05:32:24

https://doi.org/10.1007/978-3-663-15858-5lead to calcium channel modulation. Agonist activation of the GPCR superfamily releases a G protein heterotrimer and promotes dissociation of a G protein α subunit from a G protein βγ heterodimer. Each of these components (Gα and Gβγ) regulates calcium channel activity. Gα mediates voltage-independe
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查看完整版本: Titlebook: Calcium Channel Pharmacology; Stefan I. McDonough Book 2004 Kluwer Academic/Plenum Publishers, New York 2004 Calcium.Peptide.mutation.phar