1 ning were found in aneurysms of the superior hypophyseal artery (seven of 18 [38.9%] studies), superi

2 esting that sex hormones act via the gonadal-hypophyseal axis.

3 dal insufficiency with a normal hypothalamic-hypophyseal axis.

4  hypothalamic neurohormones into a plexus of hypophyseal capillaries.

5 tuberohypophyseal (THDA) and periventricular hypophyseal DAergic (PHDA) neurons regulate PRL secretio

6 seal dopaminergic (THDA) and periventricular-hypophyseal dopaminergic (PHDA) neurons.

7 ion of tuberohypophyseal and periventricular-hypophyseal dopaminergic neurons to the regulation of th

8 ons of tuberohypophyseal and periventricular-hypophyseal dopaminergic neurons, while leaving tuberoin

9 ed anterolaterally in the braincase, and the hypophyseal duct opens anteriorly towards the oral cavit

10 ee structures (the paired nasal sacs and the hypophyseal duct) were thus already independent of each

11 pment and alters cell type patterning of the hypophyseal lineage in the root, leading to a displaceme

12 ssociated with either chondrichthyans (large hypophyseal opening accommodating the internal carotid a

13 aovarian environment (e.g., the hypothalamic-hypophyseal ovarian axis).

14  (SCN) but exhibits robust expression in the hypophyseal pars tuberalis (PT).

15 tuberohypophyseal (THDA) and periventricular-hypophyseal (PHDA)] was determined.

16         In each sheep, time series from both hypophyseal portal blood (HPB) and peripheral blood were

17 tems prior to maturation of the hypothalamic-hypophyseal portal system.

18 perturbing GnRH release into the hypothalamo-hypophyseal portal system.

19 ergic pathways are defined: 1) the preoptico-hypophyseal tract runs in close association with the lat

20                 Simultaneously, they promote hypophyseal vascularisation, exerting early direct effec