Examples of 'gonadotropin-releasing' in a sentence
Meaning of "gonadotropin-releasing"
gonadotropin-releasing (verb) - Referring to the action of releasing a hormone that stimulates the gonads (reproductive organs) in the body
How to use "gonadotropin-releasing" in a sentence
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gonadotropin-releasing
It is the receptor of gonadotropin-releasing hormone GnRH.
Gonadotropin-releasing hormone has been isolated and characterized as a decapeptide.
Role in the release of gonadotropin-releasing hormone.
Gonadotropin-releasing hormone receptor antagonists and methods relating thereto.
Social regulation of gonadotropin-releasing hormone.
When gonadotropin-releasing hormone agonists are administered testosterone concentrations are ultimately reduced.
Testosterone replacement or medications containing gonadotropin-releasing hormone.
Thus it is considered a gonadotropin-releasing hormone agonist or GnRH agonist.
Deslorelin is a synthetic analogue of naturally occurring gonadotropin-releasing hormone GnRH.
There are differences in gonadotropin-releasing hormone secretion between females and males.
Goserelin is a synthetic analogue of a naturally occurring gonadotropin-releasing hormone GnRH.
Gonadotropin-releasing hormone analogues for women with ovarian cancer undergoing chemotherapy.
There is something unique about the gonadotropin-releasing hormone.
Gonadotropin-releasing hormone agonists are used on a short-term basis to reduce blood flow.
This secretion is regulated by gonadotropin-releasing hormone produced in the hypothalamus.
See also
In the hypothalamus, activins are thought to stimulate the release of gonadotropin-releasing hormone.
Gonadotropin-releasing hormone agonist may improve the ability of those who are infertile to get pregnant.
For example, goserelin is a superagonist of the gonadotropin-releasing hormone receptor.
A gonadotropin-releasing hormone agonist ( GnRH agonist ) is a type of medication which affects gonadotropins and sex hormones.
In men, estrogen gives a negative feedback to block secretion of gonadotropin-releasing hormone.
Insulin also has stimulatory effects on gonadotropin-releasing hormone from the hypothalamus, thus favoring fertility.
Melatonin is thought to act by regulating the hypothalamic pulse activity of the gonadotropin-releasing hormone.
Gonadotropin-releasing hormone Gonadotropin-releasing hormone antagonist Progonadotropin.
A drug that belongs to a family of drugs called gonadotropin-releasing hormone analogs.
Gonadotropin-releasing hormone receptor Gonadotropin receptor Steroid hormone receptor.
This in turn causes your body to release the gonadotropin-releasing hormone GnRH.
Gonadotropin-releasing hormone ( GnRH ) secretes from the hypothalamus.
In a preferred embodiment, the present method does not employ a gonadotropin-releasing hormone analogue.
Gonadotropin-releasing hormone family.
This gene lies adjacent to and downstream of the gonadotropin-releasing hormone precursor gene.
Gonadotropin-releasing hormone analog.
This invention relates to conjugate compounds and in particular to gonadotropin-releasing hormone conjugate compounds.
Leuprorelin is in the gonadotropin-releasing hormone ( GnRH ) analogue family of medications.
Gonadotropins are secreted by the pituitary gland under the control of hypothalamic gonadotropin-releasing hormone ( GnRH ).
These may also be called gonadotropin-releasing hormone blockers ( GnRH blockers ).
Another treatment, typically used when other options have failed, is injection of a gonadotropin-releasing hormone agonist.
Leuprorelin is a gonadotropin-releasing hormone ( GnRH ) analogue acting as an agonist at pituitary GnRH receptors.
The compound of the present invention possesses excellent gonadotropin-releasing hormone antagonizing activity.
Key words, gonadotropin-releasing hormone receptor, transcriptional regulation, desensitization, signal transduction.
The results of small studies involving the use of gonadotropin-releasing hormone agonists have been controversial.
Gonadotropin-releasing hormone (GnRH) is a long-acting hormone used to cause temporary menopause.
In one embodiment, the agent treating the endocrine system is a gonadotropin-releasing hormone agonist or antagonist.
The gonadotropin-releasing hormone ( GnRH ) pump is used to release doses of GnRH in a pulsatile fashion.
Pharmacoperones have been identified that restore function of Gonadotropin-releasing hormone receptor.
Patients on gonadotropin-releasing hormone agonist therapy had the highest risk of these problems . ”.
Leuprolide acetate is a synthetic nonapeptide analog of naturally-occurring gonadotropin-releasing hormone GnRH or LHRH.
The hhi 's main causes deficiency of gonadotropin-releasing hormone ( gnrh ), with significant genetic heterogeneity.
First, low blood levels of DHT stimulate the hypothalamus to produce gonadotropin-releasing hormone GnRH.
The gonadotropin-releasing hormones ( GnRH ) ( gonadoliberin ) are a family of peptides that play a pivotal role in reproduction.
Gonadotropin insensitivity includes, Luteinizing hormone insensitivity Follicle-stimulating hormone insensitivity Gonadotropin-releasing hormone insensitivity.
