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Titlebook: Dihydropyridines; Progress in Pharmaco Wolf-Dieter Busse (Professor),Bernward Garthoff,Fr Conference proceedings 1993 Springer-Verlag Berli

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書目名稱Dihydropyridines
副標(biāo)題Progress in Pharmaco
編輯Wolf-Dieter Busse (Professor),Bernward Garthoff,Fr
視頻videohttp://file.papertrans.cn/281/280437/280437.mp4
圖書封面Titlebook: Dihydropyridines; Progress in Pharmaco Wolf-Dieter Busse (Professor),Bernward Garthoff,Fr Conference proceedings 1993 Springer-Verlag Berli
出版日期Conference proceedings 1993
關(guān)鍵詞calcium antagonist; calcium channel; cardiovascular; coronary heart disease; hypertension
版次1
doihttps://doi.org/10.1007/978-3-642-95716-1
isbn_softcover978-3-540-57308-1
isbn_ebook978-3-642-95716-1
copyrightSpringer-Verlag Berlin Heidelberg 1993
The information of publication is updating

書目名稱Dihydropyridines影響因子(影響力)




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Pharmacological Classification of High-Threshold Calcium Channels in Rat Neurons,zed by an action potential. One important function of calcium channels in neurons is to mediate release of neurotransmitter from presynaptic nerve terminals. In addition, calcium channels help initiate electrical action potentials in various cell bodies and dendrites. It is very likely that calcium
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Effects of Dihydropyridine Calcium Antagonists upon Microvascular Function Following Ischemia and Oion before the induction of ischemia (Nayler 1988). The components of protection probably involve a combination of several factors occurring during the ischemic period. These factors include energy preservation (Watts et al. 1980), decreased accumulation of cytosolic calcium and lactic acid (Watts e
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Nimodipine and Learning in Aging Rabbits,e aging brain may be impaired in their ability to produce such changes. In our approach we have utilized eyeblink conditioning and the in vivo and in vitro rabbit hippocampus for behavioral, neurophysiological, and biophysical studies of associative learning. We have also investigated the potential
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,From the Cardiovascular to the Central Nervous System — An Adventure in the Pharmacology of Dihydroagement of a pharmaceutical company, which employed me at that time, a research project involving a search for novel Ca. antagonists. In the opinion of the research management, however, the blockade of Ca. entry into the cells was most likely to be associated with severe side effects, so that Ca. an
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