「Subtypes」の共起表現一覧(1語右で並び替え)
該当件数 : 59件
| energic receptors include 3 highly homologous | subtypes: alpha2A, alpha2B, and alpha2C. |
| Other neurokinin | subtypes and neurokinin receptors that interact with S |
| he behavioural effects of the different 5-HT2 | subtypes, and how they influence the effects of other |
| GABAA agonist acting mainly at α1β2 and α1β3 | subtypes, and also a 5HT5A partial agonist. |
| ood selectivity over other serotonin receptor | subtypes and slight preference for 5-HT2C over 5-HT2B. |
| 00x selectivity over other serotonin receptor | subtypes and other targets. |
| 2, selective over other glutamate transporter | subtypes and highly selective over metabotropic and io |
| Because the different ion channel | subtypes are expressed to different extents in differe |
| Since different RGS | subtypes are expressed in different tissues and are as |
| s agonist activity at other dopamine receptor | subtypes as well, similar to cabergoline. |
| agonist with no specificity for any receptor | subtypes as it is the precursor for dopamine is rarily |
| t, likely at the 5-HT2A, 5-HT2C, and/or 5-HT3 | subtypes, as well as an H1 receptor inverse agonist/an |
| The complex numbers and all its | subtypes behave exactly like the types of numbers know |
| losteric modulation of several GABAA receptor | subtypes, being selective for GABAA receptors containi |
| ch acts as a partial agonist at the α2 and α3 | subtypes, but as a silent antagonist at α1 and α5 subt |
| It binds to the α1, α2, α3 and α5 | subtypes, but shows much higher efficacy at the α5 sub |
| blocks the Cav2.1 and Cav2.3 calcium channel | subtypes, but it has the great advantage of being oral |
| igands for the other three adenosine receptor | subtypes, but a number of A2B-selective compounds have |
| There are two different | subtypes CCKA and CCKB which are ~50% homologous: Vari |
| Dopamine receptor agonist, selective for | subtypes D2 and D3. |
| selective antagonist at the dopamine receptor | subtypes D2 and D3, and the serotonin receptor 5-HT3. |
| For each subunit, many | subtypes exist (α1-6, β1-3, and γ1-3). |
| ADAR2 and ADAR3, although only the first two | subtypes have been shown to have RNA editing activity. |
| made up of different combinations of subunit | subtypes have different properties, different distribu |
| inhibitor of carbonic anhydrase, particularly | subtypes II and IV. |
| Subtypes include Gower 1, Gower 2, and Portland 2. | |
| It consists of three highly homologous | subtypes, including α1A-, α1B-, and α1D-adrenergic. |
| breaks down physical affection into multiple | subtypes, including backrubs/massages, caressing/strok |
| vity over 5-HT2A and other serotonin receptor | subtypes, it has only around 3x selectivity for 2B ove |
| But they do have types and can be | subtypes of normal classes. |
| There are at least five | subtypes of dopamine receptors, D1, D2, D3, D4, and D5 |
| There are two | subtypes of this receptor known at present, defined as |
| Genette provided five | subtypes of transtextuality, namely: intertextuality, |
| There are two | subtypes of the receptor, GABAB1 and GABAB2, and these |
| The language | subtypes of frontotemporal lobar degeneration (semanti |
| ide variety of combinations to form different | subtypes of the ion channel. |
| r affinity than β1 or β3, the two other known | subtypes of the beta adrenoceptor. |
| Tolterodine acts on M1, M2, M3, M4 and M5 | subtypes of muscarinic receptors whereas modern antimu |
| operativity with an orthosteric ligand at all | subtypes of a given receptor except the subtype of int |
| ctive drug which binds primarily to the α2/α3 | subtypes of the GABAA receptor which are responsible f |
| The main | subtypes of this disease are: mild cognitive impairmen |
| Several other common | subtypes of uranium glass have their own nicknames: cu |
| hosphodiesterase inhibitor, selective for the | subtypes PDE5, PDE6, PDE9 and PDE11. |
| t the same time differentiating it into three | subtypes: pedophilic type (attracted to children young |
| For example, the blocking of certain | subtypes results in a decrease in pain sensitivity, wh |
| There are four | subtypes: sieberi (Crete), atticus (Attica area around |
| t was one of between four and seven primitive | subtypes that preceded the domestication of the horse, |
| It has two main | subtypes, the M-type, the most powerful, (M-BWO) and t |
| with reasonable selectivity for the M1 and M4 | subtypes, though it is also known to act as a M5 recep |
| ce revealed that both the alpha2A and alpha2C | subtypes were required for normal presynaptic control |
| different binding affinity for the δ1 and δ2 | subtypes, which makes it useful for distinguishing the |
| There are a number of other | subtypes with evolving nomenclature and definitions ba |
| r both the 5-HT6 and 5-HT7 serotonin receptor | subtypes, with good selectivity over other receptors. |
| Abstract types, generic modules, subsorts ( | subtypes with multiple inheritance), pattern-matching |
| both the 5-HT2B and 5-HT2C serotonin receptor | subtypes, with good selectivity over the closely relat |
| both the 5-HT2B and 5-HT2C serotonin receptor | subtypes, with moderate selectivity for 5-HT2C, but re |
| lder ligands for these receptors bind to both | subtypes with approximately equal affinity, so develop |
| otent and selective agonist for the M1 and M4 | subtypes, yet an antagonist at the M2, M3 and M5 subty |
こんにちは ゲスト さん
|
ログイン |
Weblio会員(無料)になると
|
こんにちは ゲスト さん
|
ログイン |
Weblio会員(無料)になると
|