「receptors」の共起表現(1語右で並び替え)2ページ目

Weblio 辞書 > 英和辞典・和英辞典 > receptorsの意味・解説 > receptorsに関連した共起表現

意味

例文

共起表現

「receptors」の共起表現一覧(1語右で並び替え)2ページ目

該当件数 : 923件

＜前へ 1 2 3 4 5 次へ＞

Beta adrenergic	receptors are involved in the epinephrine- and norepin
n Aplysia long-term potentiation, since NMDA	receptors are required for both.
Both	receptors are Gi-coupled (inhibit adenylate cyclase ac
The bone morphogenetic protein (BMP)	receptors are a family of transmembrane serine/threoni
These	receptors are not present in early B cell precursors o
, and cytoskeletal organization and syndecan	receptors are required for internalization of the HIV-
CCKA	receptors are also expressed in the brain to some exte
These	receptors are linked to the G protein Gs, which activa
Insect ecdysone	receptors are currently better characterized than thos
In the cornea cold	receptors are thought to respond with an increase in f
Adenosine A3	receptors are G protein-coupled receptors that are inv
Glutamate	receptors are the predominant excitatory neurotransmit
as those produced by binding to cell surface	receptors are called endocrine, autocrine, or paracrin
These	receptors are also known under the name hemopoietin re
Type I cytokine	receptors are transmembrane receptors expressed on the
Integrin	receptors are involved in the attachment of adherent c
Muscles and associated sensory	receptors are innvervated by type I and II sensory fib
GABAС	receptors are exclusively composed of ρ (rho) subunits
fferences in brain expression patters, these	receptors are unlikely to mediate similar functions in
her members of the P2X receptor family, P2X4	receptors are also very sensitive to modulation by the
The tie	receptors are tyrosine kinases, so named because they
In this region the cone	receptors are found to be longer, slimmer and more den
tamine, both of which block glutamate (NMDA)	receptors, are known to cause psychosis closely resemb
These high-affinity	receptors are located both synaptically and extrasynap
a song, aimed at the same brainial pleasure	receptors as almost everything Calvin Harris has relea
he NMDA receptor, some aquaporins, some AMPA	receptors, as well as some enzymes.
albicans as virulence factors and toll-like	receptors as relevant mediators of the inflammatory ho
It acts on D1 and α	receptors as a agonist.
olecule, with activation of some of the same	receptors as acetylcholine.
pine, trazodone, and nefazodone block 5-HT2C	receptors as well, they also antagonize other receptor
It does not block dopamine	receptors as with most antipsychotic drugs, but does i
FMN stands out from the 'conventional' photo	receptors as the signaling state and not an E/Z isomer
This causes downregulation of these	receptors, as well as an up-regulation in the producti
tinoid specifically selective for retinoid X	receptors, as opposed to the retinoic acid receptors.
high affinity for the dopamine D2, D3 and D4	receptors, as well as serotonin 5-HT1A and 5-HT2A/C re
selective for Y4 over the related Y1 and Y5	receptors, as the first non-peptide Y4 antagonist deve
ity for antagonising the H1 and H2 histamine	receptors, as well as the muscarinic acetylcholine rec
ine Beecham Compound Bank using cloned 5-HT6	receptors as a target, with an initial lead compound b
d by slow genomic mechanisms through nuclear	receptors as well as by fast nongenomic mechanisms thr
signaling pathways, coregulators and nuclear	receptors at a promoter showing local nucleosomal cond
g beta2-agonist, which also stimulates beta1	receptors at doses above the recommended therapeutic d
) and pravadoline did not bind to the opioid	receptors at concentrations up to 10μM.
s and Feet add two hand targets to the arrow	receptors at the top of the screen during normal game
It can act on	receptors at pre-ganglionic sites in both the sympathe
ies, it becomes possible to identify related	receptors based on sequence similarity to known recept
idal molecules can interact with the steroid	receptors because of a similarity of shape.
no direct contact to the macrophage surface	receptors, because they can not see the parasite insid
It has also very weak affinity to μ-opioid	receptors because the 3-hydroxy group which is essenti
onist-antagonist at muscarinic acetylcholine	receptors, being a potent and selective agonist for th
culline, ROD-188 acts as an agonist at GABAA	receptors, being a positive allosteric modulator actin
has shown that the nicotinic and muscarinic	receptors belong to distinct protein superfamilies.
Muscarinic acetylcholine	receptors belong to a class of metabotropic receptors
The G-CSF	receptors belongs to a family of cytokine receptors kn
B receptor, and most older ligands for these	receptors bind to both subtypes with approximately equ
In the absence of TonB, these	receptors bind their substrates but do not carry out a
Type II	receptors bind ligands in the absence of type I recept
These	receptors bind to the Fc portion of IgG antibodies.
agonist at neuronal nicotinic acetylcholine	receptors, binding to both the α3β4 and the α4β2 subty
al agonist at neural nicotinic acetylcholine	receptors, binding to both the α3β4 and the α4β2 subty
that some patients had over 90% of their D2	receptors blocked by antipsychotic drugs, but showed l
glucagon or epinephrine bind to cell surface	receptors, but the main cause of phosphorylation is du
selective agonist for the 5-HT2A and 5-HT2C	receptors, but unlike the corresponding benzocyclobute
vorphanol has affinity to μ, κ, and δ opioid	receptors, but lacks complete cross-tolerance with mor
r binding affinity for the 5-HT1A and 5-HT2A	receptors, but is less potent in producing drug-approp
oxone has no significant affinity for opioid	receptors, but instead has been discovered to act as a
elated compounds that primarily act on GABAB	receptors, but also exhibit a range of effects which w
cannabinoid agonist at both the CB1 and CB2	receptors, but with moderate selectivity for CB2, havi
The signal is transduced by GPCR	receptors, but the intracellular pathway is not yet kn
he structure and function of the cannabinoid	receptors, but has been made illegal in some countries
omers usually show elements from both parent	receptors, but may also produce quite unexpected pharm
considered to encompass not only traditional	receptors but also ion channels and transporters in th
have been demonstrated to bind to nociceptin	receptors, but this binding is relatively insignifican
ychotic aripiprazole occupies over 90% of D2	receptors, but this drug is both an agonist and an ant
erve endings and activation of the olfactory	receptors, but science has yet to fully explain this i
f both α2β2 and α4β2 Nicotinic Acetylcholine	Receptors by β-Amyloid (1-42) Peptide .
e antagonist is a drug which blocks dopamine	receptors by receptor antagonism.
potentiates ATP-gated currents through P2X4	receptors by increasing the open probability of the ch
Blockade of androgens	receptors by bicalutamide in the brain will eliminate
ceptor models preceded accurate knowledge of	receptors by many years.
ctive block of α9α10 nicotinic acetylcholine	receptors by the conotoxin RgIA has been shown to be a
ctive block of α9α10 nicotinic acetylcholine	receptors by the conotoxin RgIA has been shown to be a
The allosteric modulation of P2X	receptors by pH and metals appears to be conferred by
ion of three high-affinity G-protein-coupled	receptors called LPA1, LPA2, and LPA3 (also known as E
by binding to several different cell surface	receptors called chemokine receptors.
lso binds a second-receptor type besides Trk	receptors, called the LNGFR (for "low affinity nerve g
binding and signaling through a TrkC-related	receptors called TrkB.
Dysregulation of autotaxin or the LPA	receptors can lead to hyperproliferation, which may co
Ligand-gated	receptors can be excited by neurotransmitters (ligands
Antagonists for the CCK	receptors can thus have multiple functions in both the
Defects in these	receptors can be associated with disease.
Metabotropic	receptors can both open and close channels.
In so-called ERKO mice different estrogens	receptors can be disabled allowing to study the role o
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
although recent evidence has shown that CB1	receptors can also regulate neurotransmitter release b
Androgen binding to cytoplasmic androgen	receptors can cause rapid changes in cell function ind
ransduction pathways by cytoplasmic androgen	receptors can indirectly lead to changes in gene trans
xicity, in which overactivation of glutamate	receptors causes excessive calcium entry into the cell
leases IL-2, which binds to its own new IL-2	receptors, causing self-stimulation and ultimately a m
s the neurons by activating AMPA and kainate	receptors, causing an influx of calcium.
tely potent agonist for both the cannabinoid	receptors CB1 and CB2, but with some dispute between s
Unlike many of the antibody	receptors, CD23 is a C-type lectin.
entified to bind to potential membrane bound	receptors complex containing proteins 25 kDa and 120 k
The amino acid sequences of both	receptors contain high proportions of hydrophobic resi
The amino acid sequences of the	receptors contain high proportions of hydrophobic resi
G protein-coupled	receptors contain 7 transmembrane domains and transduc
nds which are moderately selective for GABAA	receptors containing the α5 subunit.
receptor subtypes, being selective for GABAA	receptors containing α1 and β3 subunits, but exhibitin
, benzodiazepines show no affinity for GABAA	receptors containing α4 and α6 subunits with an argini
Concanavalin A interacts with diverse	receptors containing mannose carbohydrates, notably rh
The "C" sub-family of chemokine	receptors contains only one member: XCR1, the receptor
The species-specificity between these	receptors contributes to prevention of breeding betwee
These	receptors control development in Dictyostelium discoid
The cyclic AMP	receptors coordinate aggregation of individual cells i
t mice, it was found that absence of the GIP	receptors correlates with resistance to obesity.
r of the class B G-protein coupled family of	receptors, coupled to G alpha i, Gs and to a lesser ex
ne coupling and activating G protein coupled	receptors coupled to the Gq alpha subunit, activating
Since all types of G-protein	receptors currently known are activated through bindin
There are at least five subtypes of dopamine	receptors, D1, D2, D3, D4, and D5.
gligible affinity for blocking the following	receptors: D2 receptor (2,300 nM) > H1 receptor (3,100
In biochemistry, there are decoy	receptors, decoy substrates and decoy RNA.
The number of	receptors decreases, and when the administration of th
The speculation is that lingual cold	receptors deliver information that modulates the sense
rogen either increased or decreased dopamine	receptors, depending on the time allotted for the expe
For example, P2X1 and P2X3	receptors desensitize rapidly (a few hundred milliseco
e, CCK mediates satiety by acting on the CCK	receptors distributed widely throughout the central ne
phic factor (BDNF), glutamate acting at NMDA	receptors, dopamine through activation of the D1 recep
olvement in the aggregation of acetylcholine	receptors during synaptogenesis.
e basis of its high selectivity over related	receptors, ease of synthesis, and good in vivo propert
ergens, and it does not bind to β-adrenergic	receptors either.
The other	receptors elicit a variety of responses in the body an
The	receptors encoded by this gene mediate agonist-depende
Molecular neuroscience studies ion channels,	receptors, enzymes to understand neural function.
α1, α2, α3, and α5-subunit containing GABAA	receptors equally.
rch into the function of the 5-HT2 family of	receptors, especially to study the role of 5-HT2B rece
vate PPAR (peroxisome proliferator-activated	receptors), especially PPARα.
These	receptors exert their action by binding, as homodimers
regulated proteins, such as many enzymes and	receptors, exist in different interconvertible states
oids in a retrograde fashion, binding to CB1	receptors expressed on nerve terminals of an input neu
CD16 has been identified as Fc	receptors FcγRIIIa and FcγRIIIb.
Although stimulating estrogen	receptors, Femarelle does not appear to change the hor
ignal transducing beta subunit shared by the	receptors for interleukin 3 (IL3), colony stimulating
Various domains of and	receptors for TSP1 have been shown to have pro-adhesiv
okines, an increase in the number of surface	receptors for other molecules, or the suppression of t
n potential formation, there are not as many	receptors for GABA to bind to - meaning that sympathet
ts like osteoprotegerin as both act as decoy	receptors for osteoblastic RANKL.
eceptor on the platelets, it may occupy some	receptors for weeks.
Both have	receptors for testosterone.
It is one of the several	receptors for thyroid hormone, and has been shown to m
ous voles (that did not pair bond) had brain	receptors for oxytocin and vasopressin in different br
nt which acts to increase the stimulation of	receptors for excitatory amino acids (primarily glutam
eins that appear to function as cell-surface	receptors for Wnts.
PKC family members also serve as major	receptors for phorbol esters, a class of tumor promote
, and a β chain which is also present in the	receptors for IL-3 and IL-5.
Chemokine	receptors for which CCL11 is a ligand include CCR2,CCR
Some of these might encode	receptors for water-soluble attractants, repellents an
Professor Dan Koshland, identifying membrane	receptors for bacterial chemotaxis.
egral proteins that function as cell-surface	receptors for Wnts called serpentine receptors.
seven-transmembrane domain proteins that are	receptors for the Wingless type MMTV integration site
sunitinib, an inhibitor of the	receptors for FGF, PDGF and VEGF is also based on earl
In the central nervous system, CB1	receptors, for the most part, influence neuronal excit
inguish a receptor from the other ionotropic	receptors for glutamate such as NMDA and AMPA.
be a large number of these G-protein-coupled	receptors for neurotransmitters, hormones, and other s
ode 7-transmembrane domain proteins that are	receptors for Wnt signaling proteins.
Fungal pheromone mating factor	receptors form a distinct family of G-protein coupled
Type I and II	receptors form a stable complex after ligand binding,
Hormone-activated estrogen	receptors form dimers, and, since the two forms are co
n to be important in recycling transmembrane	receptors from endosomes to the trans-Golgi network (T
Cyclic AMP	receptors from slime molds are a distinct family of G-
that regulate activity of G-protein coupled	receptors from secretin receptor family.
Such heteromers may be between	receptors from the same family (e.g.
ptor conformation), functional decoupling of	receptors from G-proteins (leading to receptor desensi
Glutamate	receptors function as the main excitatory neurotransmi
ular domain of the protein which is also the	receptors G protein coupling domain.Therefore editing
b-family of cell surface seven-transmembrane	receptors, G-protein-coupled receptors.
a heterodimer of two related 7-transmembrane	receptors, GABA(B) receptor 1 and GABA(B) receptor 2.
elective, non-peptide agonist at the galanin	receptors GALR.
elective, non-peptide agonist at the galanin	receptors GALR.
The regulation of gene expression by nuclear	receptors generally only happens when a ligand - a mol
These	receptors generally function via intracellular second
y within their DNA binding domains, androgen	receptors, glucocorticoid receptors, mineralocorticoid
d also as a partial agonist at the histamine	receptors H1 and H2.
olterodine, although it acts on all types of	receptors, has fewer side effects than oxybutynin (M3
Additional information on GABAB	receptors has been reviewed elsewhere.
These	receptors have a critical role in regulating neurotran
More recently, androgen	receptors have been shown to have a second mode of act
As IP3	receptors have sparse or little distribution throughou
The VEGF	receptors have an extracellular portion consisting of
At least 16 distinct subunits of GABAA	receptors have been identified.
At least 16 distinct subunits of GABA-A	receptors have been identified.
ions like irritable bowel syndrome (IBS) the	receptors have become faulty or oversensitive.
These	receptors have a variety of functions, with the V1A an
Mannose	receptors have been researched as a target for vaccine
These	receptors have a unique hybrid structure in which an e
Given its distribution in the brain, A2a	receptors have been investigated for the treatment of
nin, histamine, and muscarinic acetylcholine	receptors have not been assayed, but uniquely among mo
The VEGF	receptors have an extracellular portion consisting of
The D1 and D5	receptors have a high degree of structural homology an

＜前へ 1 2 3 4 5 次へ＞

共起表現

「receptors」の共起表現(1語右で並び替え)2ページ目 - Weblio英語共起表現検索

「receptors」の共起表現一覧(1語右で並び替え)2ページ目