「nicotinic」の共起表現一覧(1語右で並び替え)
該当件数 : 90件
elieves the inhibition of both α2β2 and α4β2 | Nicotinic Acetylcholine Receptors by β-Amyloid (1-42) |
c modulator for the α2β2 subtype of neuronal | nicotinic acetylcholine receptor. |
Structure of the | nicotinic acetylcholine receptor (nAchR: PDB 2BG9) whi |
nds to, activates, and desensitizes neuronal | nicotinic acetylcholine receptors, though at much lowe |
is which acts as a partial agonist at neural | nicotinic acetylcholine receptors. |
of the ligand-gated ionic channel family and | nicotinic acetylcholine receptor gene superfamily. |
is a drug which acts as an agonist at neural | nicotinic acetylcholine receptors with high selectivit |
The | nicotinic acetylcholine receptors (nAChRs) are members |
lective agonist for the α7 subtype of neural | nicotinic acetylcholine receptors. |
Furthermore selective block of α9α10 | nicotinic acetylcholine receptors by the conotoxin RgI |
partial agonist for the α7 subtype of neural | nicotinic acetylcholine receptors. |
α-Bungarotoxin blocks | nicotinic acetylcholine receptors and has been used to |
ve full agonist for the α7 subtype of neural | nicotinic acetylcholine receptors. |
s glycine receptors with similar potency and | nicotinic acetylcholine receptors to a much lesser ext |
partial agonist for the α7 subtype of neural | nicotinic acetylcholine receptors. |
xin is also a selective antagonist of the α7 | nicotinic acetylcholine receptor in the brain, and as |
nds were also found to act as selective α3β4 | nicotinic acetylcholine antagonists, with little or no |
choline and acts as a partial agonist of the | nicotinic acetylcholine receptor. |
nd which acts as a partial agonist at neural | nicotinic acetylcholine receptors, binding to both the |
and has been identified as an antagonist of | nicotinic acetylcholine receptors (nAChrs) in the musc |
drinking alcohol because alcohol potentiates | nicotinic acetylcholine receptors, leading to re-sensi |
n, and acts as a mixed agonist-antagonist at | nicotinic acetylcholine receptors and an antagonist at |
Selective block of α9α10 | nicotinic acetylcholine receptors by the conotoxin RgI |
y Abbott, which acts as an agonist at neural | nicotinic acetylcholine receptors selective for the α4 |
lective agonist for the α7 subtype of neural | nicotinic acetylcholine receptors, with a high level o |
camylamine, and 18-methoxycoronaridine block | nicotinic acetylcholine receptors in the brain and can |
t is expected that development of new neural | nicotinic acetylcholine receptor agonists will be like |
which acts as a partial agonist at neuronal | nicotinic acetylcholine receptors, binding to both the |
n confirmed as selective potentiator of α4β2 | nicotinic acetylcholine receptor responses by using tw |
el positive allosteric modulator of neuronal | nicotinic acetylcholine receptor with sub-type specifi |
superfamily that also includes the neuronal | nicotinic acetylcholine receptors (nAChRs), and the in |
hain acting as an antagonist towards various | nicotinic acetylcholine receptors. |
y Abbott, which acts as an agonist at neural | nicotinic acetylcholine receptors and has been researc |
le: 'Synthesis of a radiotracer for studying | nicotinic acetylcholine receptors: (+/-)-Exo-2-(2-[F-1 |
t with GABA receptors, opioid receptors, and | nicotinic acetylcholine receptors, but not benzodiazep |
sms of action including antagonist action at | nicotinic acetylcholine receptors, and it has also bee |
ropane is a potent and selective agonist for | nicotinic acetylcholine receptors, with twice the pote |
Ligand-gated ion channels such as the | nicotinic acetylcholine receptor and GABAA receptor ar |
f, 18-MAC acts primarily as a selective α3β4 | nicotinic acetylcholine antagonist, and is even more s |
ype selective partial agonist at α4β2 neural | nicotinic acetylcholine receptors, acting as an agonis |
nervous system but acts as antagonist at the | nicotinic acetylcholine receptors at the neuromuscular |
muscular blocking drugs in a long lineage of | nicotinic acetylcholine receptor anatagonists synthesi |
It is a | nicotinic acetylcholine receptor antagonist. |
It also acts as a | nicotinic acetylcholine receptor antagonist. |
CHRNA7, coding the neuronal | nicotinic acetylcholine receptor alpha7 subunit. |
ein encoded by this gene is a subunit of the | nicotinic acetylcholine receptor (nAchR). |
Dimethylphenylpiperazinium (DMPP) is a | nicotinic acetylcholine receptor agonist which is sele |
r is most closely related by homology to the | nicotinic acetylcholine receptor. |
ts as a potent, noncompetitive α3β4 neuronal | nicotinic acetylcholine receptor antagonist. |
ine; however, nicotine acts primarily on the | nicotinic acetylcholine receptor. |
renia, likely through dopamine modulation by | nicotinic acetylcholine receptors. |
of the insect's nervous system by inhibiting | nicotinic acetylcholine receptors. |
nicotinic acetylcholine receptors (nAChR, also known a | |
Its mode of action is through the | nicotinic acetylcholine receptor where it acts as an a |
ug which acts as a partial agonist at neural | nicotinic acetylcholine receptors. |
Cytisine is a | nicotinic acetylcholine receptor agonist, and as a pha |
gated ion channel superfamily is composed of | nicotinic acetylcholine, GABAA, GABAA-ρ, glycine and 5 |
the work of Joseph Goldberger, he found that | nicotinic acid cured black tongue in dogs, an analogou |
tudies have cited the phospholipase A2 beta, | nicotinic acid adenine dinucleotide phosphate (NAADP), |
Nicotinic acid adenine dinucleotide phosphate, also kn | |
ose is as effective as are standard doses of | nicotinic acid . |
common use include niacin ribonucleotidase, | nicotinic acid mononucleotide glycohydrolase, nicotini |
It contains acids like ascorbic acid, | nicotinic acid and riboflavin. |
He was the first to isolate | nicotinic acid (also called niacin or vitamin B3). |
Other names in common use include | nicotinic acid hydroxylase, and nicotinate hydroxylase |
Another example is that both niacinamide and | nicotinic acid (niacin) have vitamin B3 activity. |
broken down into the metabolites Niacin (aka | Nicotinic acid) and Inositol at a slower rate. |
Niacin ( | nicotinic acid) and aspirin are two relatively safe, e |
is most often used as the salt with niacin ( | nicotinic acid), known as xantinol nicotinate. |
terminal 3H domain may bind to nicotinamide, | nicotinic acid, or other substrate/products. |
, estrogens, oral contraceptives, phenytoin, | nicotinic acid, sympathomimetics, calcium channel bloc |
It is an isomer of | nicotinic acid, which has the carboxyl side chain at t |
Owing to its muscarinic and | nicotinic agonist properties, arecoline has shown impr |
Examples include the | nicotinic agonists suxamethonium and decamethonium. |
alpha-10 also known as cholinergic receptor | nicotinic alpha 10 is a protein that in humans is enco |
shown to interact with Cholinergic receptor, | nicotinic, alpha 1. |
Nicotinic and muscarinic are two main kinds of "cholin | |
Molecular biology has shown that the | nicotinic and muscarinic receptors belong to distinct |
18-MC is a selective α3β4 | nicotinic antagonist and, in contrast to ibogaine, has |
A | nicotinic antagonist is a type of anticholinergic that |
nervous systems, which are both regulated by | nicotinic ligand-gated ionotropic acetylcholine recept |
rom only one type of subunit, such as the α7 | nicotinic receptor which is made up from five α7 subun |
The ganglion type | nicotinic receptor is a type of nicotinic acetylcholin |
The muscle type | nicotinic receptor is a type of nicotinic acetylcholin |
The alpha-3 beta-4 | nicotinic receptor, also known as the α3β4 receptor, i |
lcium ions and is a major component of brain | nicotinic receptors that are blocked by, and highly se |
lobeline, an agonist on Ganglion type | nicotinic receptors and also affects sensory nerve ter |
s muscarinic receptors without any effect on | nicotinic receptors. |
tively terminates an NMBA ability to bind to | nicotinic receptors. |
antagonism to acetylcholine receptors of the | nicotinic type. |
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