充满装饰 发表于 2025-3-30 08:55:21
Pharmacology of Excitatory Amino Acids on Spinal Cord Neurones,tinuous super-fusion of test substances. In this report we describe how the effects of excitatory amino acids on frog spinal neurones were characterized in terms of neuronal specificity, ionic dependence and receptor classification.允许 发表于 2025-3-30 14:29:22
L-Glutamic Acid Receptors on Locust Muscle: Pharmacological Properties and Single Receptor Channelis considered by some to be the main neurotransmitter receptor for L-glutamic acid in the CNS. The pharmacology of glutamatergic systems in arthropods is also complicated and there are differences between species (Usherwood, 1978; Nistri & Constanti, 1979; Piek, 1985).信徒 发表于 2025-3-30 17:55:36
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https://doi.org/10.1007/978-3-658-29144-0tio exceeds 1.0 a short time after injection. In the case of glucose, pyruvate, lactate, glycerol and hydroxybutyrate the ratio stays well below 1.0. The results can be explained if the first group of precursors are either preferentially taken up or metabolized in a small pool of glutamate which are未开化 发表于 2025-3-31 04:00:31
http://reply.papertrans.cn/32/3184/318392/318392_55.pnginfatuation 发表于 2025-3-31 07:25:13
Die Anwendung des formativen Messmodells,qualate and NMDA receptors. Some receptor agonists exhibit a ‘response desensitization’ and there is the possibility that an as yet unknown category of receptors may contribute to responses evoked by exogenous Asp and Glu.解冻 发表于 2025-3-31 09:52:30
Art in Republics: Venice and the Netherlandse characteristics as in the native vesicles. The GABA transporter has been purified to near homogeneity using transport activity upon reconstitution as an assay. Purification steps included fractionation of the cholate extract with ammonium sulfate, DEAE cellulose and lectin-chromatography. It appea遣返回国 发表于 2025-3-31 14:09:30
http://reply.papertrans.cn/32/3184/318392/318392_58.png充气女 发表于 2025-3-31 17:43:13
Funktion, Abbildung, Farbe, Raum, acid antagonist described, L-glutamate diethylester (GDEE), could be used to rank the excitants in order of their susceptibility to blockade, that D-a -aminoadipate (DAA) blocked actions which were resistant to GDEE, and that the effects produced by a few compounds were relatively unaffected by eit