WordNet
- a cellular structure that is postulated to exist in order to mediate between a chemical agent that acts on nervous tissue and the physiological response
- the 13th letter of the Roman alphabet (同)m
- the imperial dynasty of China from 1368 to 1644 (同)Ming dynasty
- a measure of the money supply; includes currency in circulation plus demand deposits or checking account balances
PrepTutorEJDIC
- =sense organ / 受信装置
- Mach number / mark[s] / Monsieur
- (中国の)明,明朝(1368‐1644)
UpToDate Contents
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English Journal
- An original pharmacoepidemiological-pharmacodynamic method: application to antipsychotic-induced movement disorders.
- Nguyen TT1,2,3, Pariente A4, Montastruc JL1,2,4,5,6, Lapeyre-Mestre M1,2,5,6, Rousseau V1,2,7,5, Rascol O1,5,6, Bégaud B4, Montastruc F1,4,7,5,6.
- British journal of clinical pharmacology.Br J Clin Pharmacol.2017 Mar;83(3):612-622. doi: 10.1111/bcp.13145. Epub 2016 Nov 6.
- AIMS: Pharmacovigilance databases are usually used to detect new potential signals that are relevant for drug safety. They are seldom used for explanatory purposes, e.g. to understand the mechanisms of adverse drug reactions (ADRs). The aim of the present study was to combine pharmacovigilance and p
- PMID 27687785
- Acetylcholine release in prefrontal cortex promotes gamma oscillations and theta-gamma coupling during cue detection.
- Howe WM1,2,3, Gritton HJ4,2, Lusk N4, Roberts EA2, Hetrick VL4, Berke JD4,5, Sarter M1.
- The Journal of neuroscience : the official journal of the Society for Neuroscience.J Neurosci.2017 Feb 17. pii: 2737-16. doi: 10.1523/JNEUROSCI.2737-16.2017. [Epub ahead of print]
- The capacity for using external cues to guide behavior ("cue detection") constitutes an essential aspect of attention and goal-directed behavior. The cortical cholinergic input system, via phasic increases in prefrontal acetylcholine release, plays an essential role in attention by mediating such cu
- PMID 28213446
- FRET Studies of Quinolone-Based Bitopic Ligands and Their Structural Analogues at the Muscarinic M1 Receptor.
- Messerer R1, Kauk M2,3, Volpato D1, Alonso Canizal MC2,3, Klöckner J1, Zabel U2,3, Nuber S2,3, Hoffmann C2,3, Holzgrabe U1.
- ACS chemical biology.ACS Chem Biol.2017 Feb 6. doi: 10.1021/acschembio.6b00828. [Epub ahead of print]
- Aiming to design partial agonists as well as allosteric modulators for the M1 muscarinic acetylcholine (M1AChR) receptor, two different series of bipharmacophoric ligands and their structural analogues were designed and synthesized. The hybrids were composed of the benzyl quinolone carboxylic acid (
- PMID 28117571
Japanese Journal
- Expression of Adrenergic and Cholinergic Receptors in Murine Renal Intercalated Cells
- M1 is a major subtype of muscarinic acetylcholine receptors on mouse colonic epithelial cells
- Intracellular calcium level is an important factor influencing ion channel modulations by PLC-coupled metabotropic receptors in hippocampal neurons
Related Links
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- Muscarinic receptor agonists and antagonists could prove useful in the research and treatment of a wide range of central nervous system diseases including Alzheimer's disease and Parkinson's disease. The table below summarizes ...
★リンクテーブル★
[★]
- 英
- muscarinic M1 receptor
- 関
- ムスカリンM1レセプター
[★]
- 英
- muscarinic M1 receptor
- 関
- ムスカリンM1受容体
[★]
- 関
- cholinergic、cholinergic agent、cholinergic drug、cholinomimetic、muscarine、muscarinic agent、muscarinic agonist
[★]
メチオニン methionine
[★]
M1受容体、M1レセプター