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1 of vasopressin (VP) and oxytocin (OT) by the neurohypophysis.
2 nts of a cantilever positioned on top of the neurohypophysis.
3 promote release of vasopressin (VP) from the neurohypophysis.
4 rent modulation of calcium transients in the neurohypophysis.
5 tion of peptide hormone release from the rat neurohypophysis.
6 tation of stimulus-secretion coupling at the neurohypophysis.
7 gma receptors modulate K+ channels in rodent neurohypophysis.
8 cretion of oxytocin and vasopressin from the neurohypophysis.
9 ntrolling only oxytocin release from the rat neurohypophysis.
10 deregulation of vasopressin excretion by the neurohypophysis.
11 at single, isolated nerve endings of the rat neurohypophysis.
12  degeneration of AVP and OT terminals in the neurohypophysis.
13 esence of IGIF mRNA was also detected in the neurohypophysis although induction by stress was not sig
14 such as the subfornical organ, pineal gland, neurohypophysis, and hypothalamus.
15 n (OT) and vasopressin (VP) release from the neurohypophysis are correlated with the electrical activ
16  Ca2+ channels in other preparations, in the neurohypophysis Ba2+ substitution or intracellular BAPTA
17 of oxytocin and vasopressin release from the neurohypophysis by isoflurane and propofol.
18 hat Fgf10 and Fgf3 secreted from the forming neurohypophysis exert direct guidance effects on hypotha
19 halamic axons and capillaries to the forming neurohypophysis in embryogenesis is therefore crucial to
20                                          The neurohypophysis is a crucial component of the hypothalam
21 opeptide arginine vasopressin (AVP) from the neurohypophysis is optimized by short phasic bursts of a
22             At any given release site in the neurohypophysis, it seems that several hundred spikes ar
23           Peptidergic nerve terminals of the neurohypophysis (NH) secrete both oxytocin and vasopress
24  channels in isolated terminals from the rat neurohypophysis (NH).
25 ion techniques in nerve terminals of the rat neurohypophysis (NHP) and bovine chromaffin cells.
26                                     A normal neurohypophysis occurred in 67 of 73 children with norma
27  in nerve terminals acutely dissociated from neurohypophysis of adult rats to investigate modulation
28 a, and alpha-synuclein deposits in the adeno/neurohypophysis of patients with ND and control patients
29 -mediated modulation of K(+) channels in the neurohypophysis (posterior pituitary).
30 retion from nerve terminals of the mammalian neurohypophysis (posterior pituitary).
31      Acute application of alcohol to the rat neurohypophysis potentiates large-conductance calcium-se
32 ly distinct structure by 24 hpf, whereas the neurohypophysis remains indistinct until 72 hpf.
33                                       In rat neurohypophysis the sigma receptor ligands SKF10047, pen
34                In the nerve terminals of the neurohypophysis, the roles of L-, N-, and P/Q-type Ca(2+
35 e spike modulation is uniform throughout the neurohypophysis, thereby excluding propagation failure a
36 s (INa) in nerve terminals isolated from rat neurohypophysis using patch-clamp electrophysiological a
37 e present study, taurine distribution in the neurohypophysis was determined by using a well-character
38                                  The lamprey neurohypophysis was not innervated by Galphat-S-ir fiber
39 meabilized isolated nerve endings of the rat neurohypophysis were studied.
40                    Voltage imaging in intact neurohypophysis with a voltage sensitive absorbance dye

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