「receptors」の共起表現(1語右で並び替え)5ページ目

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「receptors」の共起表現一覧(1語右で並び替え)5ページ目

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rons may interact with alpha-2A and alpha-2C	receptors to inhibit neurally released norepinephrine.
been proposed to play a role in movement of	receptors to the plasma membrane.
vator that can interact with nuclear hormone	receptors to enhance their transcriptional activator f
s its effects through ionotropic [GABA(A/C)]	receptors, to produce fast synaptic inhibition, and me
ubunit alters the sensitivity of recombinant	receptors to modulatory agents such as pregnanolone.
at bridges the Fas-receptor, and other death	receptors, to caspase-8 through its death domain to fo
The renal effects allow the	receptors to change the mean pressure in the system in
in is involved in the transportation of AMPA	receptors to the synaptic membrane, and the regulation
The sensitivity of P2X	receptors to ATP is strongly modulated by changes in e
The Activin type I	receptors transduce signals for a variety of members o
ligands for heterotrimeric G protein-coupled	receptors, transforming agents, and carcinogens, activ
chemoeffector gradients involves chemotaxis	receptors, transmembrane (TM) proteins that detect sti
Activated I1-imidazoline	receptors trigger the hydrolysis of phosphatidylcholin
of TGFβ superfamily ligands to extracellular	receptors triggers phosphorylation of Smad2 at a Serin
Activation of central 5-HT1A	receptors triggers the release or inhibition of norepi
Chemokine	receptors, two of which acting as binding proteins for
different types of serine (threonine) kinase	receptors: type I receptors of about 50-55 kD and type
central nervous system effects on muscarinic	receptors, type 4 and 5.
tegory of organic molecules that includes Fc	receptors, Ulks, Calcineurins, K chips, and urocortins
ctin ligands and fibrin, but not fibrinogen,	receptors under hemodynamic flow conditions pertinent
with preferential actions over α2-adrenergic	receptors, underlying its hypotensive rather than hype
c effects apparently mediated through opioid	receptors, unlike the inactive natural enantiomer (-)-
over, itopride has no affinity for the 5-HT4	receptors unlike other benzamides such as cisapride an
d efficacious agonist at the M1 and δ-opioid	receptors, unlike clozapine as well.
Interaction of this protein with the	receptors unmasks the N-terminal effector domain(see s
By activating 5-HT2C	receptors, vabicaserin inhibits dopamine release in th
nates are innervated by pain and temperature	receptors, via the trigeminal nerve (or, the fifth cra
aptor protein that forms a complex with many	receptors via its PTB domain.
Quazepam modulates specific GABAA	receptors via the benzodiazepine site on the GABAA rec
lly indirectly affected by G protein-coupled	receptors via effector proteins (such as phospholipase
omodimers or heterodimers with retinoic acid	receptors, vitamin D receptors, thyroid receptors or p
ribed as 100-fold selective for GluN1/GluN2A	receptors vs. GluN1/GluN2B receptors, more detailed st
New terminology for NOD-like	receptors was adopted by the Human Genome Organization
uroleptic because it does not block dopamine	receptors well.
tint in a detox program, in which his opiate	receptors were cleaned.
Historically,	receptors were discovered by using ligands to "fish" f
concentration indicating that the COX enzyme	receptors were already saturated and blocked by the br
c drugs, which do not act on the D2 dopamine	receptors were thought to have reduced the incidence o
Hence by definition, these	receptors were not orphans.
Moreover, 5-HT2B	receptors were recently shown to be overexpressed in h
agonist, and has been used to identify these	receptors when labeled with tritium.
Like other type II nuclear	receptors, when activated, it forms a heterodimer with
es (also known as immunoglobulins) or T cell	receptors where these proteins complement an antigen's
with the exception of the 5-HT2A and 5-HT2C	receptors where it acts as a partial agonist.
y norepinephrine (noradrenaline) (adrenergic	receptors), whereas parasympathetic systems are acetyl
M1, M2, M3, M4 and M5 subtypes of muscarinic	receptors whereas modern antimuscarinic treatments for
A single antibody molecule has two antigen	receptors, wherefore it contains twelve CDRs.
ked seven-transmembrane spanning leukotriene	receptors which are highly expressed in inflammation a
Its inhibition of beta-2	receptors, which are mainly located in the bronchial s
has also been shown to colocalize with GABAA	receptors, which serve as ligand-gated ion channels to
rent types of bacterial 60 kDa transmembrane	receptors, which share similar topology and signalling
selective, mixed agonist-antagonist at GABAA	receptors, which acts as a partial agonist at the α2 a
through a site separate from the CB1 and CB2	receptors, which responds to abnormal cannabidiol, O-1
n the mammalian brain where it acts at GABAA	receptors, which are ligand-gated chloride channels.
the mammalian brain where it acts at GABA-A	receptors, which are ligand-gated chloride channels.
It has a preference for beta-1	receptors, which are predominantly located in the hear
retinoid X receptor (RXR) family of nuclear	receptors which are involved in mediating the antiprol
d with the indirect function of metabotropic	receptors, which use second messengers.
I result in unopposed stimulation of the AT2	receptors, which are, in addition, upregulated.
through the stimulation of cell surface ACTH	receptors, which are located primarily on adrenocortic
The	receptors, which are located on liver cells, remove th
SB-269,970 is used to study the 5-HT7	receptors which are thought to be involved in the func
in the mammalian brain where it acts at GABA	receptors, which are ligand-gated chloride channels.
eceptor antagonist of the OX1 and OX2 orexin	receptors, which was being developed by the pharmaceut
the mammalian brain where it acts at GABA-A	receptors, which are ligand-gated chloride channels.
duced through the agonization of cannabinoid	receptors which prevents microglial activation that el
n is relatively selective for α1a-adrenergic	receptors, which are mainly present in the prostate.
bits the dimerization of HER2 with other HER	receptors, which is hypothesized to result in slowed t
novel family of C-type lectin transmembrane	receptors which play a role not only in cell-cell adhe
e, potent and selective agonist for androgen	receptors which was shown to have anabolic effects in
CD93 is a C-type lectin transmembrane	receptors which play a role not only in cell-cell adhe
a much longer-lasting effect than ionotropic	receptors, which open quickly but only remain open for
isoning by blocking muscarinic acetylcholine	receptors, which would otherwise be overstimulated by
t role in this kindling phenomenon with AMPA	receptors which are a subtype of glutamate receptors b
gene is a member of the family of serotonin	receptors, which are G protein coupled receptors that
Unlike the H1 and H2	receptors which have primarily peripheral actions, but
ugs selectively targets type1 benzodiazepine	receptors which results reduced sleep latency in promo
tein belongs to the subfamily B class of LIR	receptors which contain two or four extracellular immu
a subunit of the N-methyl-D-aspartate (NMDA)	receptors, which belong to the superfamily of glutamat
ent focus because glutamate blocks some NMDA	receptors which, on their own, induce schizophrenic be
are produced through activation of melatonin	receptors, while others are due to its role as a perva
t studies in mice suggest that the different	receptors, while having certain extent of redundancy,
RANTES) are working on long-term chemotaxis	receptors, while vasoactive peptides (e.g.
blocking glutamatergic N-methyl-D-aspartate	receptors, while gamma-aminobutyric acid (GABA) type A
eptor family is a group of G-protein coupled	receptors whose principal ligand is the protein bradyk
ns in the TLR family are pattern recognition	receptors whose task is to alert the immune system of
Type I cytokine	receptors, whose members have certain conserved motifs
Respectively, these	receptors will increase somatostatin output and decrea
of deep burn there will be no pain as these	receptors will be burned off.
It has high affinity for both CB1 and CB2	receptors, with Ki values of 1.5nM at CB1 and 0.32nM a
α7 subtype of neural nicotinic acetylcholine	receptors, with a high level of brain penetration and
MG-3 is a potent agonist at both CB1 and CB2	receptors with a Ki of 0.32nM at CB1 and 0.52nM at CB2
as fairly high affinity for both CB1 and CB2	receptors, with Ki values of 2.91nM at CB1 and 4.24nM
BN acts as a weak agonist of the CB1 and CB2	receptors, with lower affinity in comparison to THC.
tagonist for the 5-HT2B and 5-HT2C serotonin	receptors, with good selectivity over other serotonin
is a potent agonist at both the CB1 and CB2	receptors, with a binding affinity of 0.1nM at CB1 and
lgesia involves blocking activation of these	receptors with NMDAR antagonists such as ketamine, dex
ered the first family of mammalian pheromone	receptors with Nobel laureate Richard Axel.
antagonism at dopamine and serotonin type 2	receptors, with greater activity at serotonin 5-HT2 re
laced radiolabelled ketanserin from 5-HT2A/C	receptors with a Ki of 74.5, as compared to a Ki of 80
a subtype-selective partial agonist at GABAA	receptors, with highest affinity for the α3 subtype, b
t has moderate affinity for both CB1 and CB2	receptors, with Ki values of 8.36nM at CB1 and 7.95nM
ve agonist for the 5-HT2 family of serotonin	receptors, with highest binding affinity for the 5-HT2
It is a partial agonist at CB1	receptors, with a Ki of 87nM, making it roughly half t
an agonist at neural nicotinic acetylcholine	receptors with high selectivity for the α4β2 subtype.
elective agonist for nicotinic acetylcholine	receptors, with twice the potency of nicotine.
and has modest affinity for both CB1 and CB2	receptors, with Ki values of 48.3nM at CB1 and 45.5nM
showed potent antagonism of human muscarinic	receptors, with a long residence time at M3 receptors
cannabinoid agonist at both the CB1 and CB2	receptors, with Ki values of 0.46nM at CB1 and 0.69nM
in belongs to a subfamily of tyrosine kinase	receptors with a homology region to the Dictyostelium
eptor, since either subunit alone results in	receptors with very low conductance and response ampli
and kainate families of ionotropic glutamate	receptors, with selectivity for the GluR5 subtype of t
eceptor antagonist and also inhibits glycine	receptors with similar potency and nicotinic acetylcho
ghly potent full agonist for the cannabinoid	receptors, with a Ki of 1.8nM at CB1 and 2.2nM at CB2
denosine receptor group of G protein-coupled	receptors with adenosine as endogenous ligand.
agonist of both the CB1 and CB2 cannabinoid	receptors, with a reported binding affinity of 9.00+/-
oderately potent agonist for the cannabinoid	receptors, with a Ki of 13.5nM at CB1 and 49.5nM at CB
211, is a mixed agonist-antagonist at opioid	receptors with a similar pharmacological profile to pe
It has high affinity for these	receptors with dissociation constants of 2.8 nM and 3.
oximately equal affinity for the CB1 and CB2	receptors, with a Ki of 6.6nM at CB1 and 6.9nM at CB2.
It forms one subunit of type I cytokine	receptors within the IL-6 receptor family.
ester that selectively stimulates muscarinic	receptors without any effect on nicotinic receptors.
(5-HT2), adrenaline (α1), and histamine (H1)	receptors, without affecting the muscarinic acetylchol

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「receptors」の共起表現一覧(1語右で並び替え)5ページ目