ஆங்கிலம் Receptor ஐப் பயன்படுத்துவதற்கான எடுத்துக்காட்டுகள் மற்றும் அவற்றின் மொழிபெயர்ப்புகள் தமிழ்
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Growth factor receptor.
Selective androgen receptor modulators for frailty and osteoporosis.
Prostaglandin E2 receptor.
Mu-opiod receptor agonist.
Lorcaserin is a selective serotonin 2c receptor agonist.
It is a type of serotonin receptor antagonist and a type of antiemetic.
Raw Unifiram powder is a positive allosteric AMPA receptor modulator.
Glucocorticoid receptor binding could be form of negative feedback that decreases circulating cortisol.
Drug Class 5-HT2C receptor inhibitor.
Secondly, it has been hypothesised that Hydrafinil(Fluorenol) acts as a serotonin 5-HT6 receptor antagonist.
It is angiotensin II receptor antagonists.
Selective androgen receptor modulator, YK11, regulates myogenic differentiation of C2C12 myoblasts by follistatin expression.
Drug Class serotonin receptor agonists.
Orange juice neutralizes the proinflammatory effect of a high-fat,high-carbohydrate meal and prevents endotoxin increase and Toll-like receptor expression.
Tocilizumab(Anti-IL-6 receptor): Approved by China.
YK-11 is classified under(SARMs) Selective Androgen Receptor Modulators.
Lorcaserin HCL powder is a selective 5-HT2C receptor agonist that is thought to decrease food intake through the central POMC system.
This makes 4-DHEA lessestrogenic by not acting directly upon the estrogen receptor like DHEA has been found to do.
Melanin-concentrating hormone receptor 1 Identifiers Symbol MCHR1 Alt. symbols GPR24 Entrez 2847 HUGO 4479 OMIM 601751 RefSeq NM_005297 UniProt Q99705 Other data Locus Chr.
Teveten is an angiotensin II receptor antagonist.
Melanin-concentrating hormone receptor 2 Identifiers Symbol MCHR2 Alt. symbols GPR145 Entrez 84539 HUGO 20867 OMIM 606111 RefSeq NM_032503 UniProt Q969V1 Other data Locus Chr.
It refers to angiotensin II receptor antagonists.
One of themost popular options for PCT is selective estrogen receptor modulators(SERMs).
Ganglioside GT1b is a putative host cell receptor for the Merkel cell polyomavirus.
Mathematical model of human growth hormone(hGH)-stimulated cellproliferation explains the efficacy of hGH variants as receptor agonists or antagonists(Basic Model).
ER-modulating compounds are typically selective estrogen receptor modulators(SERMs) or selective estrogen receptor degraders(SERDs).
Raw 17-Methyltestosterone powderis also a methylated synthetic androgen receptor agonist with anabolic effects.
Small structural changes result in large differences in adrenergic receptor binding and subsequently the ability to produce cardiovascular effects.
Mathematical model of human growth hormone(hGH)-stimulated cellproliferation explains the efficacy of hGH variants as receptor agonists or antagonists(Steady State Model).
One study has proposed that elevatedlevels of soluble urokinase-type plasminogen activator receptor(SuPAR) in seminal plasma might be useful as a marker for MAGI.