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