「binding」の共起表現一覧(1語右で並び替え)
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T3, through | binding a nuclear thyroid hormone receptor, influence |
It was used for | binding, a palimpsest. |
r ligands, piquindone displays Na2+-dependent | binding, a property it shares with tropapride, zetido |
hich activates transcription of the ncRNAs by | binding a conserved upstream activating sequence (UAS |
, as a base for the gold leaf and to give the | binding a greater depth and luster. |
such threats as would justify a magistrate in | binding a man to keep the peace; or by persistently f |
d maple top with hand scraped edges and cream | binding, a set-neck maple neck (bolt-on on some model |
Following receptor-ligand | binding, a conformational change induced in the recep |
ty to change the protein's surface charge and | binding ability. |
But there's nothing | binding about it. |
equence, there is a widespread shutdown in T3 | binding across the body. |
erens-type junctions, where it is involved in | binding actin to the membrane. |
nce with the synthesis, secretion, transport, | binding, action, or elimination of natural hormones i |
Glutamine | binding active site with Cys269 and His353 residues s |
The publisher and a part of the book | binding activity continue to exist. |
en receptor modulator (SERM) with competitive | binding activity against estradiol for estrogen recep |
is gene encodes a protein that lacks the zinc | binding activity and may be an expressed pseudogene. |
sphorylated eIF2, though, due to its stronger | binding acts as an inhibitor of its own GEF (eIF2B). |
ia bacteria-binding proteins that have strong | binding affinities to specific protein or carbohydrat |
h from the TCR of the T-cell, because of weak | binding affinities (monomeric MHC-epitope complexes c |
lication to the calculation of protein-ligand | binding affinities, which have pharmaceutical applica |
MDV3100 has approximately fivefold higher | binding affinity for the androgen receptor (AR) compa |
Its | binding affinity at the CB1 receptor is only 51.0nM, |
onformational change necessary to confer high | binding affinity for the endothelial adhesion molecul |
le the (R)-2-pentylamide shows similar 5-HT2A | binding affinity to LSD in vitro but has only around |
II, which has unique ability to increase its | binding affinity to CaM by autophosphorylation, makin |
δ antagonist naltrindole, but with different | binding affinity for the δ1 and δ2 subtypes, which ma |
allucinogens, DOBU has an even stronger 5-HT2 | binding affinity but fails to substitute for hallucin |
nd CB2 cannabinoid receptors, with a reported | binding affinity of 9.00+/-5.00 |
icant linear correlation was observed between | binding affinity and lipophilicity. |
DAA-1106 has a sub-nanomolar | binding affinity (Ki) of 0.28nM, and has been used ex |
the serotonin 5-HT2B receptor, with a 5-HT2B | binding affinity (Ki) of 3.4nM, and high selectivity |
Two agonists with similar | binding affinity |
known 5-HT2A agonist DOI, indicating similar | binding affinity at the receptor. |
Coumestol has about the same | binding affinity for the ER-β estrogen receptor as 17 |
humans, such as buprenorphine, for which the | binding affinity is so high that naloxone does not re |
effects of very strong opioids for which the | binding affinity is so high that naloxone does not ef |
and 0.52nM at CB2, and its particularly high | binding affinity has led to it being used as a templa |
2 family of serotonin receptors, with highest | binding affinity for the 5-HT2C subtype and around 4x |
Trenbolone compounds have a | binding affinity for the androgen receptor five times |
ts appearing at higher doses, despite its low | binding affinity for CB1. |
e brain, however this drug has slightly lower | binding affinity than the N-methyl analogue and so is |
e resulting compound exhibits slightly better | binding affinity for the CB1 receptor (with a Ki valu |
The comparatively higher | binding affinity of CTLA4 has made it a potential the |
ng a conformational change that increases the | binding affinity of CB1 agonists such as CP 55,940, w |
A5 is a naturally-occurring protein with avid | binding affinity for PS. |
Binding affinity is most commonly determined using a | |
Fludiazepam has 4 times more | binding affinity for benzodiazepine receptors than di |
n analysis performed are the determination of | binding affinity and kinetic parameters, and to ident |
l analog of Phencyclidine with slightly lower | binding affinity than the parent compound. |
It has similar | binding affinity to LSD itself as both a 5-HT1A and 5 |
ative of JWH-007, JWH-018 has slightly higher | binding affinity for CB1. |
ules that possess a desired property, such as | binding affinity for a particular ligand or an activi |
orresponding (R)-2-pentyl analogue has higher | binding affinity for the 5-HT1A and 5-HT2A receptors, |
otonin receptor, but 2C-B-FLY also has a high | binding affinity for the 5-HT2B and 5-HT2C serotonin |
Despite very low | binding affinity with the androgen receptor, oxymetho |
n the naphthoylindole series, having a higher | binding affinity (i.e. |
JWH-193 has a | binding affinity at the CB1 receptor of 6nM, binding |
the concentrations increase and the proteins | binding affinity can then be estimated. |
The | binding affinity for 5-HT2A receptor is 13 +/- 2 nM ( |
It is less potent by weight due to reduced | binding affinity to its target site, yet longer actin |
ist at both the CB1 and CB2 receptors, with a | binding affinity of 0.1nM at CB1 and 0.2nM at CB2. |
t blocking dopamine reuptake despite its high | binding affinity, which led to its investigation as a |
n a quantitative study of the ligand-receptor | binding affinity, see the comprehensive article on th |
also result in increased cannabinoid receptor | binding affinity. |
region led to substantial decreases in DTX-I | binding affinity. |
vorable and therefore contribute favorably to | binding affinity. |
.) of the drug candidate which will influence | binding affinity. |
to him and argued that their marriage is not | binding after 11 years of separate living. |
Binding agent in food pastes and pastas | |
te (Na2C4H4O6) is used as an emulsifier and a | binding agent in food products such as jellies, marga |
It is the first selective relaxant | binding agent (SRBA) and was discovered at the Newhou |
ith many recipes including eggs or flour as a | binding agent, and additional flavoring such as ginge |
Selective Relaxant | Binding Agents (SRBAs) are a new class of drugs that |
Special | binding agents for demanding applications such as noi |
rangement (FTVA), in the United Kingdom, is a | binding agreement with a debtors creditors to pay all |
The Concession Agreement is a | binding agreement between the British and French gove |
There is no legally | binding agreement as to where the boundaries lie betw |
ember broke up in acrimony, without a legally | binding agreement on how to cut carbon emissions. |
The | binding agreements were made a year later, and in spr |
ass of complexing agents that were capable of | binding alkali metal cations. |
Binding alleged that he then met Knowles in Spain and | |
This decreased | binding allows chromatin expansion, permitting geneti |
For example, in prothrombin, calcium | binding allows the protein to associate with the plas |
Binding also requires that alpha subunits contain a h | |
, for example, is emerging as a powerful data | binding alternative to XML. |
Sm proteins and contributes to substrate (U6) | binding and not the catalytic rate of splicing. |
Uptake, | binding and clearance of divalent cadmium in Glycera |
Structure, O2 | binding, and reduction of globins appear optimized fo |
The beta subunit is activated by the ligand | binding, and is required for the biological activitie |
consist of separable regions that mediate DNA | binding and interaction with transcriptional activato |
op 3 changes the topological status of DNA by | binding and cleaving single stranded DNA and passing |
tes that reasonably high-affinity cannabinoid | binding and agonist effects can be produced by compou |
s model has been customized with checkerboard | binding and a half inched spaced classic reissue toas |
IPTG induces production of β-galactosidase by | binding and inhibiting the lac repressor. |
divorce and remarry, he strongly opposed foot | binding and concubinage that were widely practiced in |
gaard LignoTech is a supplier of lignin-based | binding and dispersing agents (lignosulphonates). |
The direct link between ligand | binding and opening or closing of the ion channel, wh |
less than a 60% majority would not have been | binding, and would have permitted the Common Council |
s, it was held that a separation agreement is | binding and a party can only apply for spousal suppor |
ement of mRNA structure is mediated by ligand | binding, and this results in modulation of gene expre |
C termini are required for activity: receptor | binding and activation functions may reside in the N |
5 amino acid was shown to be critical for RNA | binding and re-localisation to SGs. |
r divorce from Joseph Simpson was not legally | binding and she still is married to him, only to lear |
ially act similarly to an IgA - inhibiting by | binding and blocking. |
ylation of key tyrosines, thus initiating the | binding and activation of downstream, intracellular e |
of Christ" as being the ones who exercise the | binding and loosing of absolution and excommunication |
The protein encoded by this gene is a DNA | binding and apoptosis-inducing protein and is localiz |
A role in bacterial | binding and sequestration is suggested by studies sho |
Lothar | Binding and Frank-Walter Steinmeier |
d featuring 20 medium-jumbo frets, black neck | binding and block-shaped position markers. |
It employs perfect | binding and always features a work of outdoor art on |
ds such as β-CIT, and so has less nonspecific | binding and produces "cleaner" images. |
eta-sheet central domain involved in receptor | binding; and a C-terminal beta-sandwich domain (IPR00 |
ement of mRNA structure is mediated by ligand | binding, and this results in modulation of gene expre |
vered the RNA sequence necessary for ribosome | binding and the initiation of protein synthesis in ba |
craftsmanship in its design, typography, and | binding, and its excellent illustrations. |
It works by | binding and activating the prostaglandin E2 receptor. |
up on the indole ring is not required for CB1 | binding, and tends to increase affinity for CB2 inste |
t its own temporary court orders were legally | binding and that the rights contained in the conventi |
Examples, include amputation, foot | binding, and genital cutting. |
That decision became | binding and enforceable on 19 December 2000. |
shi appears on the inside column (next to the | binding) and that of the Tosafists on the outside col |
ion-compliant and furthermore allow both late | binding and traditional, compile-time early binding. |
the people, although the election was not yet | binding and the President-elect could have been repla |
20 elicits its effects on its target cells by | binding and activating the chemokine receptor CCR6. |
eceptor proteins that carry out high-affinity | binding and energy-dependent uptake of specific subst |
l dimers that prevent G protein gamma subunit | binding and G protein alpha subunit association, ther |
aid semiannually, which indebtedness shall be | binding and obligatory on the independent school dist |
s) class, as well CREB (cAMP response element | binding) and its subtypes. |
The beta subunit is activated by the ligand | binding, and is required for the biological activitie |
of residues thought to be involved in agonist | binding and in G protein-coupling. |
of office products including paper shredders, | binding and laminating equipment, desktop accessories |
ures formed in shallow water by the trapping, | binding, and cementation of sedimentary grains by bio |
n bass, featured all black body, checkerboard | binding, and black dot "S" type neck with binding, an |
o-acid C-terminal of CFP-10, is essential for | binding and attaching to the surface of host white bl |
s a radiused, carved Basswood body with cream | binding and flamed maple top, P/J pickups, Jazz Bass |
f the protein: a basic region involved in DNA | binding and a leucine zipper motif involved in dimeri |
and vitamin D receptors, increasing both DNA | binding and transcriptional function on their respect |
The | binding and regulatory activities of this protein hav |
Since General Assembly resolutions are not | binding, and only serve as advisory statements, there |
mall subunit contains one active site for the | binding and deamination of glutamine to make ammonia |
However, NT-3 is capable of | binding and signaling through a TrkC-related receptor |
This flat surface facilitates | binding and cleavage of precursor tRNA substrates. |
eceptor in a conformation receptive to ligand | binding and preventing the premature binding of ARNT. |
at the amine nitrogen is not required for DAT | binding and reuptake inhibition. |
inhibits estrogen biosynthesis by permanently | binding and inactivating aromatase in adipose and per |
ulate the expression levels of other genes by | binding and cleaving mRNAs or inhibiting translation. |
be involved in calcium-dependent phospholipid | binding and in membrane targeting processes such as s |
dissociation of the auxochrome group helps in | binding and it is due to this reason a basic substanc |
component of egg white responsible for biotin | binding, and, in collaboration with Paul Gyorgy, conf |
d in the object representation created by the | binding application. |
ebruary 12, voted 96-13 in favour of entering | binding arbitration with the players in a bid to save |
004, Barbados elected to force the issue into | binding arbitration under the United Nations Conventi |
rty in a labour dispute the right to call for | binding arbitration after sixty days. |
lower the Oklahoma income tax, and to reform | binding arbitration, the process by which Oklahoma mu |
Charter in favor of collective bargaining and | binding arbitration, and modify rules regarding bindi |
e terms and conditions of their employment to | binding arbitration. |
important residues for ATP hydrolysis and/or | binding are located in the P-loop. |
(The only antibodies capable of | binding are two units of IgG or one IgM. |
ses recruited to a receptor following hormone | binding are receptor-associated tyrosine kinases and |
Bandhu, Sanskrit for relation or | binding, are the connections that, according to the V |
This large | binding area explains why previous studies could only |
Hoche talks about euthanasia as proposed by | Binding, arguing that if killing a person would lead |
Binding array Interface | |
These receptors exert their action by | binding, as homodimers or heterodimers, to specific s |
Resolution 731 was not legally | binding, as it was passed under Chapter VI of the Uni |
o its own past decisions (which are generally | binding), as well as those of the Grievance Settlemen |
This channel is also sensitive to drug | binding, as well as decreased extracellular potassium |
reham and Catherine, which was effectively as | binding as marriage itself, especially if the couple |
ce 5'-TGACGTCA-3' as recognition sequence and | binding as a dimer. |
complicated bonding modes are known including | binding as unidentate ligand and a bridging ligand us |
ey General of Canada, he holds that it is not | binding as a matter of stare decisis. |
Filter | binding assay |
Selection and amplification | binding assay (SAAB) is a molecular biology technique |
In medicine, a ligand | binding assay is technique to identify the presence o |
The AFP-L3% assay, a liquid-phase | binding assay, will help to identify at-risk subjects |
Cloned SK2 are most sensitive for Apamin in | binding assays and physiological recordings. |
analysis, for example by enzymatic or ligand | binding assays or mass spectrometry. |
an salvinorin A, but human tests and receptor | binding assays could not confirm this. |
are not available in purified form, in vitro | binding assays cannot be performed. |
In receptor | binding assays, amitripylinoxide was found to have ge |
Amino groups are available for | binding at the N-terminals and at side-chains of argi |
X-ray crystallography studies have confirmed | binding at the ATP-binding site located on the gyrB s |
RLI has two C-terminal ABC domains; upon | binding ATP they form a characteristic “ATP-sandwich, |
re thought to be specifically involved in ATP | binding, ATP hydrolysis and translocation on the nucl |
eter for the validation of immune and protein | binding based assays such as ELISA and RIA. |
k of support from farmers for the use of wire | binding because small bits of wire often got into fee |
rom some of the Ministers present too legally | binding, before the official endorsement from the G8 |
riage is for Life, a holy institution that is | binding before God, giving neither partner liberty to |
al loops that are essential for high-affinity | binding between members of the EGF-family and their c |
The | binding between a ligand immobilized on the biosensor |
Actual irreversible covalent | binding between a ligand and its target molecule is r |
s the first scientist to demonstrate specific | binding between protein and DNA, and his lifelong wor |
f histone tails and encouraging high-affinity | binding between the histones and DNA backbone. |
ious two-hybrid system, where a high affinity | binding between two proteins (i.e., higher expression |
Binding between 5S rRNA and TFIIIA serves to both rep | |
teins including hnRNPs, cAMP response element | binding binding protein (CBP), proteasome, and Drosop |
ight, Fire Emblem Gaiden and Fire Emblem: The | Binding Blade. |
Binding both not to "occupy" any part of Central Amer | |
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