「receptors」の共起表現(1語右で並び替え)4ページ目

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共起表現

「receptors」の共起表現一覧(1語右で並び替え)4ページ目

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table to stimulation through beta adrenergic	receptors of intracellular adenyl cyclase, the enzyme
-living forms, and a great number of sensory	receptors of many different types.
It is also one of the	receptors of reelin, an extracellular matrix protein w
The other nuclear	receptors of the same families (NR1D2 or Rev-erb-β; NR
Taste	receptors of the T1R family, belonging to the same cla
-adrenergic receptor agonist that stimulates	receptors of the smooth muscle in the lungs, uterus, a
g reverse genetics, the DNA of genes for the	receptors of many neurotransmitters have been cloned a
NF-κB-inducing signalling cascade common to	receptors of the tumour-necrosis/nerve-growth factor (
IL2RG), a common gamma subunit shared by the	receptors of many different cytokines.
its competitive antagonism to acetylcholine	receptors of the nicotinic type.
n to these domains which can be found in all	receptors of the gene family, LDL receptor and certain
ediated effects but also activates adenosine	receptors, often with opposing (patho-) physiological
thought to do this by stimulating the 5-HT4	receptors on the adrenal glands.
, the macrophage expresses more CD40 and TNF	receptors on its surface which helps increase the leve
and indirectly via binding onto CCK2/gastrin	receptors on ECL cells in the stomach, which then resp
sympathetic nerve terminals) to the alpha-1	receptors on the membrane of vascular smooth muscle ce
IP3 enters the cytoplasm and activates IP3	receptors on the smooth endoplasmic reticulum (ER), wh
ium, the tail section of the virion binds to	receptors on the cell surface, and delivers the DNA in
fuses across the synaptic cleft and binds to	receptors on the post synaptic membrane, causing an in
The complex set of olfactory	receptors on different olfactory neurons can distingui
most tumor cells do not have characteristic	receptors on their surface indicating that they are un
xternal stimuli, it can bind to cell-surface	receptors on the same cell that produced it.
OX40 binds to	receptors on T-cells, preventing them from dying and s
ing domains which can bind to different cell	receptors on the epithelial cell surface.
thout binding to IgE already boud by the IgE	receptors on mast cells and basophils.
rt muscle, when binding to beta-1 adrenergic	receptors on this tissue.
resent in the endplate membrane close to the	receptors on the post synaptic membrane, and quickly h
lation through hepatocyte asialoglycoprotein	receptors on Kuppfer cells.
mour production through blockage of the beta	receptors on the ciliary epithelium.
AMH works by interacting with specific	receptors on the surfaces of the cells of target tissu
the autocrine agent) that binds to autocrine	receptors on the same cell, leading to changes in the
ligands (odorant particles) bind to specific	receptors on the external surface of cilia, olfactory
lection) that causes them to have more OR1D2	receptors on average, both in the nose as well as in s
egulates expression of sialyl Lewis X homing	receptors on Th1/Th2 lymphocytes".
between activating versus inhibitory IgG Fc	receptors on leukocytes, thereby enhancing autoimmune
The action of norfenfluramine on 5HT2B	receptors on heart valves leads to a characteristic pa
Circulating fibrinogen binds these	receptors on adjacent platelets, further strengthening
tant for neutrophils acting at BLT1 and BLT2	receptors on the plasma membrane of these cells.
the autocrine agent) that binds to autocrine	receptors on the same cell, leading to changes in the
nically activating alpha 6-containing GABA-A	receptors on the granule cell.
Glutamate opens NMDA	receptors on other neurons which allows calcium ions i
Stimulation of these	receptors on central nervous system neurons causes an
acetylcholine on cholinergic (or muscarinic)	receptors on the surface of muscle cells.
These protrusions will only bind to certain	receptors on the host cell: they are essential for bot
cross a synaptic cleft to be detected by the	receptors on a postsynaptic neuron.
cludes 6 tail fibers which initially bind to	receptors on the bacterial cell wall and a tail spike
Different STs recognize distinct	receptors on the surface of animal cells and thereby a
f opioid analgesia can be mediated by opioid	receptors on peripheral sensory neurons, particularly
ction of PGF2α is dependent on the number of	receptors on the corpus luteum membrane.
There are currently ten known prostaglandin	receptors on various cell types.
They bind to G protein-coupled	receptors on the cell surface to elicit their effects.
and nebracetam show affinity for muscarinic	receptors, only nefiracetam shows it at the nanomolar
an agonist at the P2Y2 subtype of purinergic	receptors, opening an alternative chloride channel and
It has been shown to interact with GABA	receptors, opioid receptors, and nicotinic acetylcholi
idered the total set of genes giving rise to	receptors or receptor molecules.
s initiated either by stimulation of stretch	receptors or stimulation of proprioceptors activated b
osphorylated tyrosine-containing peptides on	receptors or scaffold proteins with a preference for p
rse agonists) at either the GABAA or glycine	receptors, or ionotropic glutamate receptor agonists.
mine, muscarinic acetylcholine, or serotonin	receptors, or any of the monoamine transporters.
es can act in numerous ways, often acting as	receptors or ligands (the molecule that activates a re
is drug does not have any effect on dopamine	receptors or muscarinic receptors.
ently to bind the C-termini of transmembrane	receptors or ion channels.
the effect on kappa and delta opioid, sigma	receptors, or the NMDA system are not well understood.
Cholecystokinin	receptors or CCK receptors are a group of G-protein co
by mouth and senses, or by other apertures,	receptors, or behaviours.
A slow response to GABA is mediated by GABAB	receptors, originally defined on the basis of pharmaco
imilar to those described for B cell antigen	receptors, otherwise known as immunoglobulins.
radrenaline) in particular), on β-adrenergic	receptors, part of the sympathetic nervous system whic
diffuses through the cytosol to bind to IP3	receptors, particular calcium channels in the endoplas
nder normal conditions, the opening of GABAA	receptors permits the hyperpolarizing influx of chlori
ministered small molecule antagonist of VEGF	receptors, platelet-derived growth factor receptors, a
Warm and cold	receptors play a part in sensing innocuous environment
Cys-loop	receptors possess a characteristic loop formed by a di
CCK-B	receptors possess a complex regulation of dopamine act
ptide receptor (FPR) belongs to the class of	receptors possessing seven hydrophobic transmembrane d
s an agonist for the D2, D3, and D4 dopamine	receptors, pramipexole may directly stimulate the unde
Several ion channels and neurotransmitters	receptors pre-mRNa are substrates for ADARs.
nce suggested that flibanserin targets these	receptors preferentially in selective brain areas and
Pulmonary stretch	receptors present in the smooth muscle of the airways
Amtolmetin guacil stimulates capsaicin	receptors present on gastro intestinal walls, because
utocrines, or paracrines by binding to their	receptors present on the cell surface.
ng agonist activity at a number of serotonin	receptors, primarily 5-HT2A, 5-HT2C and 5-HT1A.
this polymorphism this reduces the number of	receptors produced by the brain, making brain cells mo
As with other type II nuclear	receptors, RAR heterodimerizes with RXR and in the abs
is a region of the peroxisomal protein that	receptors recognize and bind to.
	Receptors recognize and bind to a region of the peroxi
is series showed much lower affinity at both	receptors, reflecting a generally reduced affinity for
equence of the ligand-binding domain between	receptors reflects the different ligand specificities.
D1	receptors regulate neuronal growth and development, me
These	receptors respond to changes in the wall tension, whic
Electromagnetic	receptors respond to electromagnetic waves
he cloning and dissection of nuclear hormone	receptors, revealing their structure and showing how t
At D2 and possibly D3	receptors roxindole is a partial agonist with preferen
y at one of the five sphingosine-1-phosphate	receptors, S1PR1.
sense organs are a simpler types of sensory	receptors seen in skin.
an agonist at neural nicotinic acetylcholine	receptors selective for the α4β2 subtype, and has been
They are also called G-protein-coupled	receptors, sensory receptors or ionotropic receptors.
an antagonist at types 1, 2, and 4 dopamine	receptors, serotonin (5-HT) receptor types 2A and 2C,
Olfactory	receptors share a 7-transmembrane domain structure wit
The translated	receptors show less variability.
ical effects at both the mu and delta opioid	receptors, showing selectivity for the delta receptor.
as antimicrobial peptides, leukocyte surface	receptors, signal transduction pathways, and transcrip
CCK	receptors significantly influence neurotransmission in
iety and do not antagonize these cholinergic	receptors significantly.
and Lymphomas malignant cells express these	receptors, so denileukin diftitox can target these.
rivatives, but is a partial agonist at GABAA	receptors, so the sedative effects are relatively mild
The weak agonist activity of pergolide at D1	receptors somewhat alters its clinical and side effect
ative drug which acts as an agonist at GABAA	receptors, specifically acting as a positive allosteri
t acts as an inverse agonist at melanocortin	receptors, specifically, MC1.
NMDA	receptors start to become unresponsive, slowing areas
Mating factor	receptors, STE2 and STE3 are integral membrane protein
Increasing stretch of the	receptors stimulates both an increase in heart rate an
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
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.
eceptor, but without blocking other dopamine	receptors such as D2.
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
superfamily far exceeds the number of known	receptors, suggesting the promiscuity that exists betw
idence for receptor overexpression and spare	receptors suggests that the calculation of the net cha
to its action on endothelial postsynaptic α2	receptors; systemic application of α2 agonists, in con
There are three known mammalian tachykinin	receptors termed NK1, NK2 and NK3.
It acts through at least two types of	receptors termed AT1 and AT2.
M, and no significant affinity for any other	receptors tested.
nts elicit activity from greater a number of	receptors than do lower concentrations.
t has a much higher selectivity for δ opioid	receptors than μ receptors, and has little to no effec
mes more binding affinity for benzodiazepine	receptors than diazepam.
4 is 10-40 times more potent in blocking AT1	receptors than losartan.
turally more closely related to CC chemokine	receptors than to other CXC chemokine receptors
ar, is a member of a family of transmembrane	receptors that mediate chemotactic response in certain
and is a major component of brain nicotinic	receptors that are blocked by, and highly sensitive to
tigens) are recognized as foreign by antigen	receptors that are expressed on the surface of lymphoc
man cells have low-density lipoprotein (LDL)	receptors that extract cholesterol from the bloodstrea
The	receptors that have been identified at the molecular l
re originally identified in Xenopus frogs as	receptors that induce the proliferation of peroxisomes
So far, cell	receptors that have been identified for HA fall into t
ember of the large family of 7-transmembrane	receptors that couple to guanosine-nucleotide-binding
There are numerous	receptors that now known to use intracellular kinases
of structurally closely related cell surface	receptors that fulfill diverse biological functions in
The subset of GABAA	receptors that also bind benzodiazepines are referred
PPARs are nuclear hormone	receptors that bind peroxisome proliferators and contr
immune	receptors that bind carbohydrates: CD1, T cell recepto
gs to a family of ligand-activated glutamate	receptors that are sensitive to alpha-amino-3-hydroxy-
These proteins are type-I transmembrane	receptors that share an intracellular 200 residue doma
ylcholine, GABAA, GABAA-ρ, glycine and 5-HT3	receptors that are composed of five protein subunits w
The PPARs are a class of intracellular	receptors that modulate carbohydrate and fat metabolis
Other neurokinin subtypes and neurokinin	receptors that interact with SP have also been reporte
alpha, "TNFR" is often used to describe the	receptors that bind to TNF alpha - namely, CD120.
n that human and animal tongues have special	receptors that respond to umami, the fifth taste.
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
nd gp130 are members of a family of cytokine	receptors that includes components of the receptors fo
A cell may have several different	receptors that recognize the same hormone and activate
d to a discovery that there are cell-surface	receptors that are stimulated by hormones and neurotra
receptor is one of two of G protein-coupled	receptors that have been found which bind bradykinin a
Although they stimulate the same	receptors that GnRH does, since they are present conti
GPRs are cell surface	receptors that activate guanine-nucleotide binding pro
As is commonly seen in G protein-coupled	receptors, the CB2 receptor has seven transmembrane sp
unit common to all members of that family of	receptors, the GP130 signal transducing subunit.
As with other type II nuclear	receptors, the RXR heterodimer in the absence of ligan
In such	receptors, the signaling molecule (the ligand) binds t
n complementary DNA strands hybridize to the	receptors, the charge distribution near the surface ch
in medicine: in addition to acting on sigma	receptors, the O-methyl derivative of its dextrorotary
Since vascular beds widely express α1	receptors, the action of oxymetazoline results in vaso
nous cannabinoid system includes cannabinoid	receptors, their endogenous ligands (endocannabinoids)
The	receptors themselves are zinc-finger proteins.
If a cell does not express these	receptors then the virus cannot normally infect it.
CB1	receptors then reduce the amount of neurotransmitter r
t on the nematode via binding to Latrophilin	receptors, there is also recent evidence that indicate
However, rT3 binds to these	receptors, thereby blocking the action of T3.
e reassociation of the G proteins with their	receptors, thereby preventing reactivation of the sign
s the theory that estrogen inhibits dopamine	receptors, therefore acting as a protectorate against
and (+)-naltrexone lack affinity for opioid	receptors, they do not block the effects of opioid ana
Like other cytokine	receptors, this receptor likely has a multimeric struc
t tissues and are associated with particular	receptors, this makes it possible for selective inhibi
Just as in A1	receptors, this normally serves as a protective mechan
esensitizes neuronal nicotinic acetylcholine	receptors, though at much lower potency in comparison.
has some affinity for the 5-HT2A and 5-HT2C	receptors, though it is unlikely that these properties
inding competitively to rat uterine estrogen	receptors, though with a very low binding affinity of
is in contrast to cortisol, which binds both	receptors, though it binds Type II with greater affini
omplex molecules, and then later with T cell	receptors through amino acids that are continuous in a
similarity between these families: the cAMP	receptors thus bear their own unique '7TM' signature.
They function by binding their physiologic	receptors, Tie-1 and Tie-2.
example, must bind to specific cell surface	receptors to enter a cell.
-screening" substances towards a huge set of	receptors to study effect and interaction.
Lipid signaling involves G-protein coupled	receptors to which lysophosphatidic acid (LPA) binds,
CC chemokine that utilizes multiple cellular	receptors to attract and activate human leukocytes.
lular inhibitors of signal transference from	receptors to G proteins.
interact with muscarinic-2 and muscarinic-4	receptors to inhibit neurally released acetylcholine.

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共起表現

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「receptors」の共起表現一覧(1語右で並び替え)4ページ目