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1 in birds and mammals by inhibiting GnRH and gonadotropin secretion.
2 NKB neurons play a role in the regulation of gonadotropin secretion.
3 between these two peptides in the control of gonadotropin secretion.
4 cycle via negative and positive feedback on gonadotropin secretion.
5 H) neurons generating a pulsatile pattern of gonadotropin secretion.
6 ain circuits, mediating hormonal feedback on gonadotropin secretion.
7 rtility, at least in part, via inhibition of gonadotropin secretion.
8 ssociation with the pubertal reactivation of gonadotropin secretion.
9 egions critical for kisspeptin regulation of gonadotropin secretion.
10 nally, it causes a complete shutdown of both gonadotropins secretion.
12 othesis that a NKB antagonist would decrease gonadotropin secretion and inhibit folliculogenesis in h
13 t leptin might play a role in the control of gonadotropin secretion and initiated studies on its poss
14 inhibited by 57 %, and both human chorionic gonadotropin secretion and L-leucine influx through syst
16 nterior olfactory nucleus markedly increases gonadotropin secretion and prevents the testicular regre
18 halamus, areas involved in the regulation of gonadotropin secretion and sex behavior, GABAergic neuro
20 low oxygen leads to reduced human chorionic gonadotropin secretion and STB-associated gene expressio
22 n mice induced anovulation, reduced GnRH and gonadotropin secretion, and diminished kisspeptin expres
23 ural pathways mediating hormonal feedback on gonadotropin secretion, and it appears to provide direct
24 tive feedback effects of ovarian steroids on gonadotropin secretion, and the preoptic region of the h
25 n duration oscillations that drive pulsatile gonadotropin secretion, and, in females, a gradual and v
26 ications because of their ability to inhibit gonadotropin secretion as long as an adequate concentrat
27 G did not effect a pregnancy-like pattern of gonadotropin secretion, but the functional life span of
28 he negative and positive feedback control of gonadotropin secretion by sex steroids, timing of pubert
29 eptin plays an important role in controlling gonadotropin secretion by stimulatory hypothalamic and p
30 ls and, through its age-dependent effects on gonadotropin secretion, facilitated appropriately timed
31 hysiology of birds and mammals by inhibiting gonadotropin secretion from the anterior pituitary gland
33 l hypothalamus that is capable of inhibiting gonadotropin secretion in cultured quail pituitary cells
34 estosterone may somehow stimulate endogenous gonadotropin secretion in gonadotropin-deficient subject
36 and triptorelin on the LHRH-R mRNA level and gonadotropin secretion in ovariectomized (OVX) and norma
37 inhibitory effect of the olfactory bulbs on gonadotropin secretion is mediated by fibers that exit t
39 owever, only GATAD1 abundance increases when gonadotropin secretion is suppressed during late infancy
41 neural tracts involved in this influence on gonadotropin secretion, lesions were placed in several p
42 es associated with these structures, such as gonadotropin secretion, reproductive behaviors, seizure
44 b/ob mouse is infertile and has a pattern of gonadotropin secretion similar to that of prepubertal an
45 We have shown recently that Mn2+ stimulates gonadotropin secretion via an action at the hypothalamic
47 G (hCG), cynomolgus monkeys whose endogenous gonadotropin secretion was blocked during the luteal pha
48 ly-Leu-Arg-Pro-Gly-NH2) stimulates pituitary gonadotropin secretion, which in turn stimulates the gon