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Titlebook: Current Aspects of the Neurosciences; Volume 3 Neville N. Osborne Textbook 1991Latest edition Macmillan Publishers Limited 1991 amino acid.

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樓主: metabolism
21#
發(fā)表于 2025-3-25 03:23:25 | 只看該作者
22#
發(fā)表于 2025-3-25 10:03:23 | 只看該作者
Weather Shocks and Women Empowerment era. As was the case with mAbs raised against many other antigens, some of these mAbs have been used extensively, thus significantly contributing to the advancement of AChR and MG research, whereas others proved much less valuable tools.
23#
發(fā)表于 2025-3-25 11:43:24 | 只看該作者
Tigist M. Melesse,Yesuf M. Awelnd intracellular calcium. Finally, the missing link (inositol trisphosphate) between membrane receptor-coupled phosphoinositide metabolism and the changes in intracellular calcium originating from internal stores was discovered by Berridge and Irvine in 1984.
24#
發(fā)表于 2025-3-25 16:23:44 | 只看該作者
Excitatory Amino Acid Receptors and Phosphoinositide Breakdown: Facts and Perspectives,nd intracellular calcium. Finally, the missing link (inositol trisphosphate) between membrane receptor-coupled phosphoinositide metabolism and the changes in intracellular calcium originating from internal stores was discovered by Berridge and Irvine in 1984.
25#
發(fā)表于 2025-3-25 22:55:26 | 只看該作者
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發(fā)表于 2025-3-26 07:01:39 | 只看該作者
Weather Shocks and Women Empowermentd anatomically precise. Serotonin (5-hydroxytryptamine; 5-HT) is a neuro-transmitter widely distributed in the brain. It has been implicated in many brain functions (e.g. sleep cycle: Jouvet, 1967; food intake: Blundell and Hill, 1987) and in disorders ranging from migraine (e.g. Andersen and Dafny,
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發(fā)表于 2025-3-26 10:41:40 | 只看該作者
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發(fā)表于 2025-3-26 15:46:38 | 只看該作者
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發(fā)表于 2025-3-26 20:17:50 | 只看該作者
Tigist M. Melesse,Yesuf M. Awelter in the mammalian central nervous system, where the GABA receptors are ubiquitous, playing an important role in the control of neuronal excitability. There are two pharmacological subclasses of GABA receptors. These are the GABA. receptor, a ligand-gated chloride ion channel, whose pharmacology i
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