Health / Medical Topics

    OXT wt Allele

    Human OXT wild-type allele is located in the vicinity of 20p13 and is approximately 1 kb in length. This allele, which encodes oxytocin-neurophysin 1 protein, is involved in the regulation of smooth muscle contraction during both childbirth and lactation, cardiovascular homeostasis and complex neural processes such as cognition, adaptation and maternal behavior. (NCI Thesaurus)




    YOU MAY ALSO LIKE

    This gene plays a regulatory role in smooth muscle contraction during processes such as parturition and lactation.
    The hydrochloride salt form of oxprenolol, a lipophilic, nonselective beta-adrenergic receptor antagonist with anti-arrhythmic, anti-anginal and antihypertensive activities. Oxprenolol competitively binds to…
    A lipophilic, nonselective beta-adrenergic receptor antagonist with anti-arrhythmic, anti-anginal and antihypertensive activities. Oxprenolol competitively binds to and blocks beta-1 adrenergic receptors in…
    A spironolactone derivative and a potent aldosterone antagonist on mineralocorticoid biosynthesis with diuretic activity. As an aldosterone antagonist, oxprenoate may inhibit sodium…
    An aromatic amino acid with antidepressant activity. In vivo, oxitriptan (or 5-hydroxytryptophan) is converted into 5-hydroxytryptamine (5-HT or serotonin) as well as…
    A nicotinic acid derivative.

    © 1991-2023 The Titi Tudorancea Bulletin | Titi Tudorancea® is a Registered Trademark | Terms of use and privacy policy
    Contact