ライフサイエンスコーパス: neurohypophysis

1 nts of a cantilever positioned on top of the neurohypophysis.

2 of vasopressin (VP) and oxytocin (OT) by the neurohypophysis.

3 rent modulation of calcium transients in the neurohypophysis.

4 tion of peptide hormone release from the rat neurohypophysis.

5 tation of stimulus-secretion coupling at the neurohypophysis.

6 gma receptors modulate K+ channels in rodent neurohypophysis.

7 cretion of oxytocin and vasopressin from the neurohypophysis.

8 promote release of vasopressin (VP) from the neurohypophysis.

9 ntrolling only oxytocin release from the rat neurohypophysis.

10 at single, isolated nerve endings of the rat neurohypophysis.

11 deregulation of vasopressin excretion by the neurohypophysis.

12 degeneration of AVP and OT terminals in the neurohypophysis.

13 ereas the neural ectoderm contributes to the neurohypophysis.

14 esence of IGIF mRNA was also detected in the neurohypophysis although induction by stress was not sig

15 yp26b1-positive astroglial pituicytes of the neurohypophysis and prop1-positive adenohypophyseal prog

16 such as the subfornical organ, pineal gland, neurohypophysis, and hypothalamus.

17 ouse cardiomyocytes and as well as in intact neurohypophysis, and in glucose-stimulated murine islets

18 n (OT) and vasopressin (VP) release from the neurohypophysis are correlated with the electrical activ

19 Ca2+ channels in other preparations, in the neurohypophysis Ba2+ substitution or intracellular BAPTA

20 of oxytocin and vasopressin release from the neurohypophysis by isoflurane and propofol.

21 hat Fgf10 and Fgf3 secreted from the forming neurohypophysis exert direct guidance effects on hypotha

22 halamic axons and capillaries to the forming neurohypophysis in embryogenesis is therefore crucial to

23 The neurohypophysis is a crucial component of the hypothalam

24 opeptide arginine vasopressin (AVP) from the neurohypophysis is optimized by short phasic bursts of a

25 At any given release site in the neurohypophysis, it seems that several hundred spikes ar

26 Peptidergic nerve terminals of the neurohypophysis (NH) secrete both oxytocin and vasopress

27 channels in isolated terminals from the rat neurohypophysis (NH).

28 ion techniques in nerve terminals of the rat neurohypophysis (NHP) and bovine chromaffin cells.

29 A normal neurohypophysis occurred in 67 of 73 children with norma

30 in nerve terminals acutely dissociated from neurohypophysis of adult rats to investigate modulation

31 a, and alpha-synuclein deposits in the adeno/neurohypophysis of patients with ND and control patients

32 -mediated modulation of K(+) channels in the neurohypophysis (posterior pituitary).

33 retion from nerve terminals of the mammalian neurohypophysis (posterior pituitary).

34 Acute application of alcohol to the rat neurohypophysis potentiates large-conductance calcium-se

35 , TRH-immunoreactive fibers were seen in the neurohypophysis, proximal pars distalis, and pars interm

36 ly distinct structure by 24 hpf, whereas the neurohypophysis remains indistinct until 72 hpf.

37 omologues to the vertebrate hypothalamus and neurohypophysis, rooting the evolutionary origin of thes

38 In rat neurohypophysis the sigma receptor ligands SKF10047, pen

39 In the nerve terminals of the neurohypophysis, the roles of L-, N-, and P/Q-type Ca(2+

40 e spike modulation is uniform throughout the neurohypophysis, thereby excluding propagation failure a

41 s (INa) in nerve terminals isolated from rat neurohypophysis using patch-clamp electrophysiological a

42 e present study, taurine distribution in the neurohypophysis was determined by using a well-character

43 The lamprey neurohypophysis was not innervated by Galphat-S-ir fiber

44 meabilized isolated nerve endings of the rat neurohypophysis were studied.

45 producing cells and the posterior pituitary/neurohypophysis, which relays the passage of hormones fr

46 Voltage imaging in intact neurohypophysis with a voltage sensitive absorbance dye