標(biāo)題: Titlebook: Excitatory Amino Acids and Neuronal Plasticity; Yehezkel Ben-Ari Book 1990 The Editor(s) (if applicable) and The Author(s), under exclusiv [打印本頁(yè)] 作者: 營(yíng)養(yǎng)品 時(shí)間: 2025-3-21 19:08
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity影響因子(影響力)
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity影響因子(影響力)學(xué)科排名
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity網(wǎng)絡(luò)公開(kāi)度
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity被引頻次
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity被引頻次學(xué)科排名
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity年度引用
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity年度引用學(xué)科排名
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity讀者反饋
書(shū)目名稱Excitatory Amino Acids and Neuronal Plasticity讀者反饋學(xué)科排名
作者: CHAR 時(shí)間: 2025-3-21 20:47 作者: 為敵 時(shí)間: 2025-3-22 04:08
The Glycine Coagonist Site of the NMDA Receptorted in receptor-channel mechanisms. It also offers a new target site in drug development for the treatment of neuropa-thologies associated with NMDA receptor activation. The list of neural dysfunctions mediated in part by. synaptic activation of NMDA receptors very likely includes epileptiform seizu作者: fibroblast 時(shí)間: 2025-3-22 07:05
The PCP Site of the NMDA Receptor Complexetamine selectively block responses evoked by applications of NMDA agonists while sparing those mediated by other subtypes of excitatory amino acid receptors. Since that time others including ourselves demonstrated, using patch and voltage-clamp techniques, that this blockade is both dependent upon 作者: 可忽略 時(shí)間: 2025-3-22 10:01
Antagonists of NMDA-Activated Current in Cortical Neurons: Competition with Glycine and Blockade of ral nervous system (Mayer and Westbrook, 1987) Nearly 30 years ago, glutamate was found to depolarize neurons in most areas of the brain and spinal cord (Hayashi, 1954; Curtis et al. 1960; Krnjevic and Phillis, 1963) but it was not until pharmacological experiments revealed the presence of several d作者: 鎮(zhèn)壓 時(shí)間: 2025-3-22 13:48
Experiments with Kainate and Quisqualate Agonists and Antagonists in Relation to the Sub-Classificatceptors was originally based on the selective depressant action of L-glutamic acid diethyl ester (GDEE) on quisqualate induced responses in ionophoretic experiments . (McLennan and Lodge, 1979; Watkins and Evans, 1981). This concept was supported by the opposite selectivity shown by other antagonist作者: 鎮(zhèn)壓 時(shí)間: 2025-3-22 20:39 作者: 安定 時(shí)間: 2025-3-22 22:26 作者: gospel 時(shí)間: 2025-3-23 04:30
Intracellular Messengers Associated with Excitatory Amino Acid (EAA) Receptors the fast excitatory neurotransmission, these amino acids appear to play crucial roles in neuronal plasticity. These include changes in neuronal development (Barnes, 1986; Balàzs et al., 1988; Didier et al., 1989), as well as changes in synaptic efficacy, which probably underlie learning and memory 作者: 預(yù)示 時(shí)間: 2025-3-23 06:22
The Glycine Site on the NMDA Receptor: Pharmacology and Involvement in NMDA Receptor-Mediated Neurodal nervous system (CNS) are mediated by distinct receptor sub-types. Amongst these, the N-methyl-D-aspartate (NMDA) receptor has been characterized most fully in terms of its pharmacological and biophysical properties (Watkins and Evans, 1981; Mayer and Westbrook, 1987). The NMDA receptor can be div作者: Highbrow 時(shí)間: 2025-3-23 12:25 作者: 緯度 時(shí)間: 2025-3-23 15:44 作者: 脆弱么 時(shí)間: 2025-3-23 21:49 作者: 相反放置 時(shí)間: 2025-3-23 23:21 作者: 追蹤 時(shí)間: 2025-3-24 03:04
Protection by Natural and Semisynthetic Gangliosides from Ca2+-Dependent Neurotoxicity Caused by Excrs, when added (in appropriate concentrations) to primary neuronal cultures, are the only neurotransmitters known to cause neuronal death by destabilizing homeostasis of free Ca. (Olney, 1969; Coyle, 1987; Vaccarino et al., 1987; Favaron et al., 1988; Connor et al., 1988). In neurons, EAA increase C作者: semble 時(shí)間: 2025-3-24 08:58 作者: Detonate 時(shí)間: 2025-3-24 14:32 作者: 技術(shù) 時(shí)間: 2025-3-24 15:19
0065-2598 Overview: 978-1-4684-5771-1978-1-4684-5769-8Series ISSN 0065-2598 Series E-ISSN 2214-8019 作者: 暫時(shí)別動(dòng) 時(shí)間: 2025-3-24 22:43
Regional Genrelects in Engagement Noticesist and antagonist affinity, have suggested at least two subtypes of glutamate receptor channel complex. These have been named after the agonists with which they were first characterized, N-methylD-aspartic acid (NMDA) and quisqualic acid (for review see Watkins and Olverman, 1987; Mayer and Westbro作者: 使困惑 時(shí)間: 2025-3-24 23:30
https://doi.org/10.1007/978-3-642-32931-9ed three questions:.Although important advances have been made towards answering these three questions, progress has been limited by the difficulty of measuring and of controlling the glycine concentration in the extracellular space.作者: Radiation 時(shí)間: 2025-3-25 05:00 作者: 異端邪說(shuō)下 時(shí)間: 2025-3-25 10:22
Michael P. Boquet,Dawn R. Wagneretamine selectively block responses evoked by applications of NMDA agonists while sparing those mediated by other subtypes of excitatory amino acid receptors. Since that time others including ourselves demonstrated, using patch and voltage-clamp techniques, that this blockade is both dependent upon 作者: constellation 時(shí)間: 2025-3-25 12:13 作者: START 時(shí)間: 2025-3-25 19:42 作者: 厚顏無(wú)恥 時(shí)間: 2025-3-25 23:45
https://doi.org/10.1007/978-3-540-72047-8n-NMDA subtype of excitatory amino acid receptors can be further subdivided in two types, the kainate and the quisqualate (AMPA?) receptors. GDEE discriminate between the two agonists, being more active against quisqualate induced responses, when administered ionophoretically in vivo; however, this 作者: 大洪水 時(shí)間: 2025-3-26 02:21
Formulation of Microbial BiopesticidesTheir presence on living brain cells is nowadays monitored electrophysiologically by measuring the changes of cell membrane conductance produced by kainic and domoic acids in the absence or presence of kainate receptor antagonists such as gammaglutamyglycine and CNQX.作者: forecast 時(shí)間: 2025-3-26 04:23 作者: 貨物 時(shí)間: 2025-3-26 08:50
https://doi.org/10.1007/978-4-431-54493-7al nervous system (CNS) are mediated by distinct receptor sub-types. Amongst these, the N-methyl-D-aspartate (NMDA) receptor has been characterized most fully in terms of its pharmacological and biophysical properties (Watkins and Evans, 1981; Mayer and Westbrook, 1987). The NMDA receptor can be div作者: cushion 時(shí)間: 2025-3-26 15:30 作者: Gourmet 時(shí)間: 2025-3-26 18:25
https://doi.org/10.1007/978-3-658-24489-7te (NMDA) type of excitatory amino acid receptor (for review see Cotman & Iversen, 1987). Receptor binding and electrophysiological studies have indicated that the NMDA-receptor complex comprises a number of distinct structural domains through which its function may be regulated or pharmacologically作者: conflate 時(shí)間: 2025-3-26 23:29 作者: nostrum 時(shí)間: 2025-3-27 04:35 作者: Congruous 時(shí)間: 2025-3-27 09:00 作者: animated 時(shí)間: 2025-3-27 12:17 作者: projectile 時(shí)間: 2025-3-27 14:33
Concepts of Quantitative Composition,In this paper, we will (I) review the available evidence suggesting that homocysteic acid might be an excitatory transmitter in the mammalian central nervous system (CNS) and (II) report preliminary results on extracellular changes of excitatory amino acid (EAA) concentration in human epileptic foci.作者: Cleave 時(shí)間: 2025-3-27 21:42 作者: 逃避現(xiàn)實(shí) 時(shí)間: 2025-3-27 22:50 作者: 否決 時(shí)間: 2025-3-28 05:59 作者: JAUNT 時(shí)間: 2025-3-28 07:36
Formulation of Microbial BiopesticidesTheir presence on living brain cells is nowadays monitored electrophysiologically by measuring the changes of cell membrane conductance produced by kainic and domoic acids in the absence or presence of kainate receptor antagonists such as gammaglutamyglycine and CNQX.作者: 歪曲道理 時(shí)間: 2025-3-28 10:25 作者: 定點(diǎn) 時(shí)間: 2025-3-28 18:40
Measuring and Controlling the Extracellular Glycine Concentration at the NMDA Receptor Leveled three questions:.Although important advances have been made towards answering these three questions, progress has been limited by the difficulty of measuring and of controlling the glycine concentration in the extracellular space.作者: WATER 時(shí)間: 2025-3-28 22:07 作者: CLAY 時(shí)間: 2025-3-28 23:22
Topographical Heterogeneity of Glutamate Agonist-Induced Calcium Increase in Hippocampusepted that the increase in intracellular Ca. concentration ([Ca.].) due to the activation of L-glutamate receptors plays a crucial role in the early phase of LTP (Kudo et al., 1987; Malenka et al., 1988). It is therefore important to specify the location of L-glutamate receptors responsible for the [Ca.]. elevation.作者: ANTI 時(shí)間: 2025-3-29 04:06
Regional Genrelects in Engagement Notices this type are not possible in intact preparations. Patch clamp techniques have now been applied to both brain slices (Edwards et al., 1989) and to isolated adult cells (Kiskin et al., 1986), but the success rate with these preparations is usually lower than with culture preparations, and the intact作者: 上漲 時(shí)間: 2025-3-29 08:57 作者: 憲法沒(méi)有 時(shí)間: 2025-3-29 14:19 作者: PAN 時(shí)間: 2025-3-29 15:53 作者: Glower 時(shí)間: 2025-3-29 22:47
Die eigenen Verstrickungen reflektieren mitochondria and the operation of channels and pumps allowing Ca. influx (cationic channels) and efflux (Nat-Ca. exchanger and ATPase-operated Ca. pumps) (Carafoli, 1987). It is, therefore, not surprising that many have attempted to evaluate whether EAA receptors are also operative in physiological作者: Ingredient 時(shí)間: 2025-3-30 00:36
Glutamate Receptors in Cultures of Mouse Hippocampus Studied with Fast Applications of Agonists, Mod this type are not possible in intact preparations. Patch clamp techniques have now been applied to both brain slices (Edwards et al., 1989) and to isolated adult cells (Kiskin et al., 1986), but the success rate with these preparations is usually lower than with culture preparations, and the intact作者: 有角 時(shí)間: 2025-3-30 04:02 作者: Blemish 時(shí)間: 2025-3-30 11:47 作者: Canary 時(shí)間: 2025-3-30 13:30 作者: drusen 時(shí)間: 2025-3-30 16:55 作者: AWE 時(shí)間: 2025-3-30 21:17
https://doi.org/10.1007/978-3-540-72047-8selectivity was not seen with bath application in vitro.. Another compound GAMS, although weak, show a reasonable degree of non-NMDA receptor antagonism.. Further development of selective kainate and/or AMPA receptor antagonists has been relatively slow.作者: 龍卷風(fēng) 時(shí)間: 2025-3-31 01:00
Equilibrium State and Entanglement,(Nicoll et al., 1988). In addition, they are likely to be implicated in neuronal death, associated with several neurological diseases including strokes, hypoglycemia, epilepsy and Huntington’s chorea.作者: 支架 時(shí)間: 2025-3-31 07:48 作者: 膠狀 時(shí)間: 2025-3-31 12:38
Specific Quisqualate Receptor Ligand Blocks Both Kainate and Quisqualate Responsesselectivity was not seen with bath application in vitro.. Another compound GAMS, although weak, show a reasonable degree of non-NMDA receptor antagonism.. Further development of selective kainate and/or AMPA receptor antagonists has been relatively slow.
