Titlebook: Voltammetry in the Neurosciences; Principles, Methods, Joseph B. Justice Book 1987 Springer Science+Business Media New York 1987 brain.cate

欺騙某人

書目名稱Voltammetry in the Neurosciences影響因子(影響力)




書目名稱Voltammetry in the Neurosciences影響因子(影響力)學(xué)科排名




書目名稱Voltammetry in the Neurosciences網(wǎng)絡(luò)公開(kāi)度




書目名稱Voltammetry in the Neurosciences網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書目名稱Voltammetry in the Neurosciences被引頻次




書目名稱Voltammetry in the Neurosciences被引頻次學(xué)科排名




書目名稱Voltammetry in the Neurosciences年度引用




書目名稱Voltammetry in the Neurosciences年度引用學(xué)科排名




書目名稱Voltammetry in the Neurosciences讀者反饋




書目名稱Voltammetry in the Neurosciences讀者反饋學(xué)科排名

率直

Introduction to In Vivo Voltammetryular, the easily oxidizable catecholamine and indoleamine neurotransmitters, metabolites, and related compounds can be studied with this technique. Since the original report from the laboratory of R. N. Adams (Kissinger et al., 1973), more than 150 papers have been published on in vivo voltammetry a

帶子

音樂(lè)會(huì)

Quantitative Interpretations of In Vivo Chronoamperometry5-HT), as well as ascorbic and uric acid. There are many different groups working on various aspects of the function of these substances (. Adams and Marsden, 1979; and Marsden, 1984). To date the electrochemical signals that have been measured have largely been interpreted only as evidence for a st

SEVER

In Vivo Electrochemical Monitoring of Dopamine Releasen et al., 1984). Moreover, at least nine chapters of this volume will be entirely or partly devoted to this subject. Therefore this problem does not require further introduction. For the same reason the present chapter may not be an objective review on this subject since I plan to concentrate on our

不妥協(xié)

Monitoring Extracellular DOPAC Following Stimulated Release of Dopamineimals are needed to complement studies using lesions of dopaminergic systems. Monitoring DA release directly is relatively difficult, particularly in behaving animals. One approach to the problem of monitoring DA release has been to use metabolite levels, either total tissue levels or extracellular

CORD

In Vivo Voltammetryincipally ligand binding methods. It is essential, however, that a correlation is demonstrated between the ligand binding data and a functional response. The latter should preferably be in vivo, such as a behavioral or physiological response. This can prove difficult especially with regard to recept

Ethics

FID

較早