「receptors」の共起表現(2語右で並び替え)

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共起表現

「receptors」の共起表現一覧(2語右で並び替え)

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onist-antagonist at muscarinic acetylcholine	receptors, being a potent and selective agonist for th
α7 subtype of neural nicotinic acetylcholine	receptors, with a high level of brain penetration and
These	receptors have a critical role in regulating neurotran
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
culline, ROD-188 acts as an agonist at GABAA	receptors, being a positive allosteric modulator actin
signaling pathways, coregulators and nuclear	receptors at a promoter showing local nucleosomal cond
n region that is abundant in nuclear hormone	receptors in a sexually dimorphic manner, strongly imp
ately equal affinity at both the CB1 and CB2	receptors, having a Ki of 8.0nM at CB1 and 7.0nM at CB
N-methyl-D-aspartate (NMDA)	receptors are a class of ionotropic glutamate receptor
is a potent agonist at both the CB1 and CB2	receptors, with a binding affinity of 0.1nM at CB1 and
gerol as a high affinity agonist for alpha-2	receptors and a medium affinity antagonist at the 5-HT
Fungal pheromone mating factor	receptors form a distinct family of G-protein coupled
TonB-dependent	receptors is a family of beta-barrel proteins from the
ytic effects is by modulating benzodiazepine	receptors, in a similar manner to other drugs of this
inding domain of HNF4, as with other nuclear	receptors, adopts a canonical alpha helical sandwich f
Type I and II	receptors form a stable complex after ligand binding,
laced radiolabelled ketanserin from 5-HT2A/C	receptors with a Ki of 74.5, as compared to a Ki of 80
It acts on D1 and α	receptors as a agonist.
Cys-loop	receptors possess a characteristic loop formed by a di
TonB-dependent	receptors include a plug domain, an independently fold
It is a partial agonist at CB1	receptors, with a Ki of 87nM, making it roughly half t
CCK-B	receptors possess a complex regulation of dopamine act
These	receptors have a variety of functions, with the V1A an
These	receptors have a unique hybrid structure in which an e
Warm and cold	receptors play a part in sensing innocuous environment
ditionally binds to a cell that expresses Fc	receptors, like a macrophage, a natural killer cell or
showed potent antagonism of human muscarinic	receptors, with a long residence time at M3 receptors
in belongs to a subfamily of tyrosine kinase	receptors with a homology region to the Dictyostelium
The bone morphogenetic protein (BMP)	receptors are a family of transmembrane serine/threoni
Olfactory	receptors share a 7-transmembrane domain structure wit
cross a synaptic cleft to be detected by the	receptors on a postsynaptic neuron.
The D1 and D5	receptors have a high degree of structural homology an
ghly potent full agonist for the cannabinoid	receptors, with a Ki of 1.8nM at CB1 and 2.2nM at CB2
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
ine Beecham Compound Bank using cloned 5-HT6	receptors as a target, with an initial lead compound b
211, is a mixed agonist-antagonist at opioid	receptors with a similar pharmacological profile to pe
The other	receptors elicit a variety of responses in the body an
is series showed much lower affinity at both	receptors, reflecting a generally reduced affinity for
oximately equal affinity for the CB1 and CB2	receptors, with a Ki of 6.6nM at CB1 and 6.9nM at CB2.
otracer for studying nicotinic acetylcholine	receptors: (+/-)-Exo-2-(2-[F-18]fluoro-5-pyridyl)-7-az
For example, 5-HT1E	receptors are abundant in the hippocampus but are not
olecule, with activation of some of the same	receptors as acetylcholine.
ffects of interleukin-1 (IL-1) while type II	receptors may act as a suppressor of IL-1 activity by
ative drug which acts as an agonist at GABAA	receptors, specifically acting as a positive allosteri
s the theory that estrogen inhibits dopamine	receptors, therefore acting as a protectorate against
Since vascular beds widely express α1	receptors, the action of oxymetazoline results in vaso
GPRs are cell surface	receptors that activate guanine-nucleotide binding pro
Like other type II nuclear	receptors, when activated, it forms a heterodimer with
Since opening channels by metabotropic	receptors involves activating a number of molecules in
Note that only the α1-adrenergic	receptors in active muscle will be blocked.
selective, mixed agonist-antagonist at GABAA	receptors, which acts as a partial agonist at the α2 a
th either GRIK4 or GRIK5 to form heteromeric	receptors and acts as an excitatory neurotransmitter a
it possesses intrinsic activity at the D2/D3	receptors, and acts as a weak partial agonist at these
There are three type I Activin	receptors: ACVR1, ACVR1B, and ACVR1C.
denosine receptor group of G protein-coupled	receptors with adenosine as endogenous ligand.
Circulating fibrinogen binds these	receptors on adjacent platelets, further strengthening
New terminology for NOD-like	receptors was adopted by the Human Genome Organization
exerts its effects by blocking a variety of	receptors, including adrenergic receptors, dopamine re
Sigma	receptors are affected by cocaine, as cocaine function
(5-HT2), adrenaline (α1), and histamine (H1)	receptors, without affecting the muscarinic acetylchol
ligands for heterotrimeric G protein-coupled	receptors, transforming agents, and carcinogens, activ
The cyclic AMP	receptors coordinate aggregation of individual cells i
These	receptors are all transmembrane proteins, composed of
a song, aimed at the same brainial pleasure	receptors as almost everything Calvin Harris has relea
concentration indicating that the COX enzyme	receptors were already saturated and blocked by the br
elated compounds that primarily act on GABAB	receptors, but also exhibit a range of effects which w
CB2	receptors are also found throughout the gastrointestin
eline, an agonist on Ganglion type nicotinic	receptors and also affects sensory nerve terminals
These	receptors are also closely related to the activin rece
nicotinic acetylcholine	receptors (nAChR, also known as "ionotropic" acetylcho
muscarinic acetylcholine	receptors (mAChR, also known as "metabotropic" acetylc
The subset of GABAA	receptors that also bind benzodiazepines are referred
Ion-channel-linked	receptors are also called ligand-gated channels.
Merkel	receptors are also located in the mammary glands.
considered to encompass not only traditional	receptors but also ion channels and transporters in th
CCKA	receptors are also expressed in the brain to some exte
These	receptors are also known under the name hemopoietin re
although recent evidence has shown that CB1	receptors can also regulate neurotransmitter release b
her members of the P2X receptor family, P2X4	receptors are also very sensitive to modulation by the
The weak agonist activity of pergolide at D1	receptors somewhat alters its clinical and side effect
omplex molecules, and then later with T cell	receptors through amino acids that are continuous in a
of a variety of ion channels, including NMDA	receptors and AMPA receptors.
receptor, a weak agonist at both CB1 and CB2	receptors, and an inhibitor of anandamide reuptake.
The VEGF	receptors have an extracellular portion consisting of
s the neurons by activating AMPA and kainate	receptors, causing an influx of calcium.
an agonist at the P2Y2 subtype of purinergic	receptors, opening an alternative chloride channel and
The VEGF	receptors have an extracellular portion consisting of
gonist-antagonist at nicotinic acetylcholine	receptors and an antagonist at μ-opioid receptors.
n architecture common to all nuclear hormone	receptors, namely an N-terminal transcriptional activa
is a region of the peroxisomal protein that	receptors recognize and bind to.
	Receptors recognize and bind to a region of the peroxi
s as a selective antagonist at the serotonin	receptors 5-HT1B and 5-HT1D.
receptor family, particularly the activating	receptors LILRA1 and LILRA3
Retinoid X	receptors (RXRs) and retinoic acid receptors (RARs), a
Mating factor	receptors, STE2 and STE3 are integral membrane protein
CD16 has been identified as Fc	receptors FcγRIIIa and FcγRIIIb.
They function by binding their physiologic	receptors, Tie-1 and Tie-2.
s belong to the seven transmembrane class of	receptors (7TMR) and have in their extracellular regio
The number of	receptors decreases, and when the administration of th
It is a selective agonist for the melatonin	receptors MT1 and MT2 in the suprachiasmatic nucleus o
tely potent agonist for both the cannabinoid	receptors CB1 and CB2, but with some dispute between s
promotes Lyn-mediated phosphorylation of IP3	receptors 1 and 2.
anchored cytokines, cell adhesion molecules,	receptors, ligands, and enzymes.
nably selective antagonist for the adenosine	receptors A1 and A2A, having a Ki of 3.3nM at A2A and
ncludes the neuronal nicotinic acetylcholine	receptors (nAChRs), and the inhibitory neurotransmitte
lower levels of follicle stimulating hormone	receptors (FSHR) and higher levels of luteinizing horm
s form obligate heterodimers with retinoid X	receptors (RXRs) and regulate expression of target gen
the antigen receptor (TCR) and costimulatory	receptors (CD28 and ICOS) are thought to be main recep
d also as a partial agonist at the histamine	receptors H1 and H2.
ic acids are suspected ligands for toll-like	receptors 2 and 4. Teichoic acids also assist in regul
lls by diffusion, and interact with specific	receptors in another cell, triggering a response in th
imilar to other positive modulators of GABAA	receptors, including anxiolytic and anticonvulsant act
mine, muscarinic acetylcholine, or serotonin	receptors, or any of the monoamine transporters.
ester that selectively stimulates muscarinic	receptors without any effect on nicotinic receptors.
to its action on endothelial postsynaptic α2	receptors; systemic application of α2 agonists, in con
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
and is a major component of brain nicotinic	receptors that are blocked by, and highly sensitive to
Ionotropic	receptors (iGluRs) are fast-acting ligand-gated ion ch
tigens) are recognized as foreign by antigen	receptors that are expressed on the surface of lymphoc
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
The	receptors themselves are zinc-finger proteins.
Killer-cell immunoglobulin-like	receptors (KIRs) are transmembrane glycoproteins expre
through the stimulation of cell surface ACTH	receptors, which are located primarily on adrenocortic
ght to be an endogenous ligand for vanilloid	receptors (which are involved in the transduction of a
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
Several ion channels and neurotransmitters	receptors pre-mRNa are substrates for ADARs.
in the mammalian brain where it acts at GABA	receptors, which are ligand-gated chloride channels.
otrimeric G-protein signalling, cell surface	receptors (GPCRs) are coupled to membrane-associated h
gs to a family of ligand-activated glutamate	receptors that are sensitive to alpha-amino-3-hydroxy-
ylcholine, GABAA, GABAA-ρ, glycine and 5-HT3	receptors that are composed of five protein subunits w
the mammalian brain where it acts at GABA-A	receptors, which are ligand-gated chloride channels.
n is relatively selective for α1a-adrenergic	receptors, which are mainly present in the prostate.
The EGF module-containing Mucin-like hormone	Receptors (EMRs) are closely related subgroup of G pro
The nicotinic acetylcholine	receptors (nAChRs) are members of a superfamily of lig
sible cause for post-viral cough is that the	receptors that are responsible for stimulating the cou
GABAA	receptors that are made up of different combinations o
d to a discovery that there are cell-surface	receptors that are stimulated by hormones and neurotra
GABAB	receptors (GABABR) are metabotropic transmembrane rece
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
Killer cell immunoglobulin-like	receptors (KIRs) are transmembrane glycoproteins expre
I result in unopposed stimulation of the AT2	receptors, which are, in addition, upregulated.
mbers of a large family of G-protein-coupled	receptors (GPCR) arising from single coding-exon genes
Phosphacan can also bind to cell surface	receptors such as NCAM.
rimary tumor mass, and if HA associates with	receptors such as CD44, the activation of Rho GTPases
acts as an agonist at the 5-HT1A and 5-HT1B	receptors and as an antagonist at the 5-HT2C receptor.
s by interacting with cell surface chemokine	receptors such as CCR1, CCR2, CCR5 and CCR8.
specialized senses	receptors such as cutaneous receptors ( meisners and p
Molecules act on various	receptors, such as NgR1, LINGO1, p75, TROY and other u
as been also found for other steroid hormone	receptors such as estrogen receptors, androgen recepto
ion, the interaction of HAS produced HA with	receptors such as CD44 or RHAMM promote the cell chang
o mediate retrieval of various transmembrane	receptors, such as the cation-independent mannose 6-ph
Some Eph	receptors such as EPHB4 participate in both forward an
s by interacting with cell surface chemokine	receptors such as CCR4.
Glutamate	receptors function as the main excitatory neurotransmi
eceptor, but without blocking other dopamine	receptors such as D2.
1 over D5 with negligible affinity for other	receptors; acts as an antagonist at D1 but as an agoni
ective mixed agonist-antagonist for dopamine	receptors, acting as a weak partial agonist at the D3
decreased expression of fibronectin-binding	receptors, such as α5β1 integrins.
brane-bound enzyme activated through protein	receptors such as α1 adrenergic receptors.
in light and heavy chains; in several T-cell	receptors such as CD2 (Cluster of Differentiation 2),
The protein encoded by this gene binds	receptors such as the epidermal growth factor receptor
D3 heteromers) or between entirely unrelated	receptors such as CB1/A2A , glutamate mGluR5 / adenosi
HT2C), 5-HT6, 5-HT7, α1-adrenergic, and NMDA	receptors, and as agonists at the sigma receptors (σ1
, receptor tyrosine kinases (RTKs), cytokine	receptors (JAK/STATs), as well as modulation of variou
onist at α4β2 neural nicotinic acetylcholine	receptors, acting as an agonist at (α4)2(β2)3 pentamer
esensitizes neuronal nicotinic acetylcholine	receptors, though at much lower potency in comparison.
In the right atrium, the stretch	receptors occur at the junction of the venae cavae.
It acts through at least two types of	receptors termed AT1 and AT2.
The sensitivity of P2X	receptors to ATP is strongly modulated by changes in e
, the ATP sensitivity of P2X1, P2X3 and P2X4	receptors is attenuated when the extracellular pH<7, w
CC chemokine that utilizes multiple cellular	receptors to attract and activate human leukocytes.
lection) that causes them to have more OR1D2	receptors on average, both in the nose as well as in s
Professor Dan Koshland, identifying membrane	receptors for bacterial chemotaxis.
The classification of glutamate	receptors is based on their activation by different ph
of deep burn there will be no pain as these	receptors will be burned off.
Ligand-gated	receptors can be excited by neurotransmitters (ligands
Defects in these	receptors can be associated with disease.
Cytokine	receptors may be both membrane-bound and soluble.
In so-called ERKO mice different estrogens	receptors can be disabled allowing to study the role o
The work of his team indicated that N-P	receptors must be blocked for at least 2 hours to caus
of the receptor, the effects of metabotropic	receptors can be more widespread through the cell.
During exercise these α1-adrenergic	receptors can be selectively blocked by sympathetic ne
activated so that the actions of the δ and κ	receptors can be studied separately, in contrast to be
Drugs blocking the cannabinoid	receptors may be a future strategy for appetite suppre
similarity between these families: the cAMP	receptors thus bear their own unique '7TM' signature.
ions like irritable bowel syndrome (IBS) the	receptors have become faulty or oversensitive.
More recently, androgen	receptors have been shown to have a second mode of act
At least 16 distinct subunits of GABAA	receptors have been identified.
At least 16 distinct subunits of GABA-A	receptors have been identified.
Additional information on GABAB	receptors has been reviewed elsewhere.
Mannose	receptors have been researched as a target for vaccine
Given its distribution in the brain, A2a	receptors have been investigated for the treatment of

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共起表現

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「receptors」の共起表現一覧(2語右で並び替え)