Titlebook: Calcium Channel Pharmacology; Stefan I. McDonough Book 2004 Kluwer Academic/Plenum Publishers, New York 2004 Calcium.Peptide.mutation.phar

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書目名稱Calcium Channel Pharmacology影響因子(影響力)




書目名稱Calcium Channel Pharmacology影響因子(影響力)學(xué)科排名




書目名稱Calcium Channel Pharmacology網(wǎng)絡(luò)公開度




書目名稱Calcium Channel Pharmacology網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Calcium Channel Pharmacology被引頻次




書目名稱Calcium Channel Pharmacology被引頻次學(xué)科排名




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書目名稱Calcium Channel Pharmacology年度引用學(xué)科排名




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書目名稱Calcium Channel Pharmacology讀者反饋學(xué)科排名

LOPE

法律的瑕疵

Ahmed M. Ali,Bedatri Moulik,Dirk S?ffkerand 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

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控制

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

辯論的終結(jié)

辯論的終結(jié)

大笑

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

問到了燒瓶

愉快嗎

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