ライフサイエンスコーパス: supraoptic nuclei

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1 lease of oxytocin from dendrites in isolated supraoptic nuclei.

2 thalamus, dorsolateral to the borders of the supraoptic nuclei.

3 oid receptors in the rat paraventricular and supraoptic nuclei.

4 ry system, including the paraventricular and supraoptic nuclei.

5 y expressed in the mouse paraventricular and supraoptic nuclei after 10 days of drinking 2% saline, o

6 and vasopressin release from intact isolated supraoptic nuclei and from the neurophypophyses in rats

7 ific subdivisions of the paraventricular and supraoptic nuclei, and in the arcuate and ventromedial n

8 edian and anteroventral preoptic nuclei, and supraoptic nuclei as well as the magnocellular portion o

9 e (VP-ir) neurons in the paraventricular and supraoptic nuclei, as well as an unusually extensive dis

10 ber of CFLI cells in the Paraventricular and Supraoptic nuclei, but preloads of mineral oil did not.

11 tary tract, hypothalamic paraventricular and supraoptic nuclei, central nucleus of amygdala, lateral

12 nt variation in PAC1 mRNA within the SCN and supraoptic nuclei during the light-dark cycle and in con

13 By contrast, in supraoptic nuclei from adult rats allopregnanolone-induc

14 In supraoptic nuclei from rats of 3-4 weeks old or less, al

15 , neuroendocrine system (paraventricular and supraoptic nuclei, hypothalamic visceromotor pattern gen

16 Using supraoptic nuclei in brain slices from lactating rats, w

17 muscimol also induced oxytocin release from supraoptic nuclei in young rats, but had no effect in ad

18 raventricular, accessory magnocellulary, and supraoptic nuclei, in the retrochiasmatic part of the su

19 al (EW), lateral superior olivary (LSO), and supraoptic nuclei; lower levels of expression are seen i

20 S binding was significantly increased in the supraoptic nuclei of both morphine-dependent and salt-lo

21 ls within the dorsal (oxytocin neurone-rich) supraoptic nuclei of rats given an intracerebroventricul

22 s, most prominently, the paraventricular and supraoptic nuclei of the hypothalamus (13-fold and 80-fo

23 the inferior olive, the paraventricular and supraoptic nuclei of the hypothalamus, and in the ventra

24 a, the zona incerta, the paraventricular and supraoptic nuclei of the hypothalamus, the substantia ni

25 he surviving vasopressinergic neurons in the supraoptic nuclei of the ST + CISL group was significant

26 ampal, periventricular, suprachiasmatic, and supraoptic nuclei; Purkinje cells in the cerebellum; and

27 cid (mRNA) levels in the paraventricular and supraoptic nuclei (PVN and SON) of the ovariectomized ra

28 Studies of the paraventricular and supraoptic nuclei revealed induction of the chaperone pr

29 were found in the paraventricular (PVN) and supraoptic nuclei (SON) and VP-ir projections from these

30 Injection of AdAVP into the supraoptic nuclei (SON) of the hypothalamus resulted in

31 organum vasculosum lamina terminalis (OVLT), supraoptic nuclei (SON), and magnocellular region of the

32 ng the LT and hypothalamic areas such as the supraoptic nuclei (SON), is unclear.

33 cells that have anatomic projections to the supraoptic nuclei (SON).

34 n the hypothalamic paraventricular (PVN) and supraoptic nuclei (SON).

35 Fos in the paraventricular nuclei (PVN) and supraoptic nuclei (SON).

36 xpression in parallel with AVP expression in supraoptic nuclei (SONs) and paraventicular nuclei (PVNs

37 diagonal band of Broca, paraventricular and supraoptic nuclei, suprachiasmatic nucleus, and dorsomed

38 s IR in the hypothalamic paraventricular and supraoptic nuclei, the subfornical organ (SFO), and the

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