「GnRH」の共起表現一覧(2語左で並び替え)
該当件数 : 28件
The drug works by blocking the action of | GnRH upon the pituitary, thus rapidly suppressing th |
red a gonadotropin-releasing hormone agonist or | GnRH agonist. |
Normally administered are analogues of | GnRH, such as leuprolide or goserelin. |
Leuprolide acts as an agonist at pituitary | GnRH receptors. |
nd follicle-stimulating hormone (FSH) caused by | GnRH. |
Agonists do not quickly dissociate from the | GnRH receptor. |
gonadotropin-releasing hormone ( | GnRH) |
Gonadotropin-releasing hormone ( | GnRH), |
ion, binding to gonadotropin-releasing hormone ( | GnRH) receptors in the pituitary gland and blocking |
ptide analog of gonadotropin-releasing hormone ( | GnRH) with added potency. |
Either Gonadotropin-releasing hormone ( | GnRH) or any Gonadotropin-releasing hormone agonist |
Gonadotropin-releasing hormone ( | GnRH) is released by the hypothalamus in a pulsatile |
able gonadotropin-releasing hormone antagonist ( | GnRH antagonist). |
in is a Gonadotropin-releasing hormone agonist ( | GnRH agonist). |
in is a gonadotropin-releasing hormone agonist ( | GnRH agonist). |
able gonadotropin-releasing hormone antagonist ( | GnRH antagonist). |
e gonadotropin releasing hormone super-agonist ( | GnRH agonist), also known as a luteinizing hormone r |
xpressing neurons and is involved in regulating | GnRH neurons. |
Like other | GnRH agonists, buserelin may be used in the treatmen |
sterone produced from the corpus luteum inhibit | GnRH, FSH and LH at the hypothalamus and anterior pi |
tile stimulation and the desensitization of the | GnRH receptors; it indirectly down regulates the sec |
Although they stimulate the same receptors that | GnRH does, since they are present continuously and n |
Gonadotropin releasing hormone ( | GnRH) is a well known decapeptide that participate i |
re synthetic peptide derivatives of the natural | GnRH decapeptide - a hormone that is made by neurons |
r, GPR54 (21-23), which is believed to regulate | GnRH and gonadotropin hormone secretion. |
idating the structures of neurohormones TRH and | GnRH) |
e release of prolactin, which in turn decreases | GnRH. |
Unlike other | GnRH agonists, which are mainly used to inhibit lute |
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