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1         Magnetic resonance imaging disclosed neurohypophyseal abnormalities in 27 of the 28 children
2 his study is to determine the reliability of neurohypophyseal abnormalities on magnetic resonance ima
3                                              Neurohypophyseal abnormalities on MRI are sensitive and
4                                              Neurohypophyseal abnormalities, including absent pituita
5 er4.3+) and mouse (Sox1+) contribute to both neurohypophyseal and a subset of adenohypophyseal cells.
6                        Glucopenia stimulates neurohypophyseal arginine vasopressin (AVP) secretion an
7 egrated neurohemal wiring of the hypothalamo-neurohypophyseal axis.
8                  Here we show that the Ciona neurohypophyseal canal is present from the end of neurul
9                               This so-called neurohypophyseal canal was previously thought to be a se
10                  Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is a progre
11 essin (VP) cause autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a rare inh
12                                     Familial neurohypophyseal diabetes insipidus (FNDI) in humans is
13                                     Familial neurohypophyseal diabetes insipidus (FNDI) is an autosom
14 (AVP) gene cause autosomal dominant familial neurohypophyseal diabetes insipidus (FNDI).
15                                     Familial neurohypophyseal diabetes insipidus is an autosomal domi
16                  Autosomal dominant familial neurohypophyseal diabetes insipidus is caused by mutatio
17 sin parents and three children affected with neurohypophyseal diabetes insipidus, suggesting autosoma
18 o contribute to the pathogenesis of familial neurohypophyseal diabetes insipidus.
19 m both in the cardiovascular response to the neurohypophyseal hormone arginine vasopressin (AVP) and
20                                          The neurohypophyseal hormone oxytocin (OT) regulates biologi
21 ized that combine into a single molecule the neurohypophyseal hormone oxytocin and the potent vasopre
22                                  Oxytocin, a neurohypophyseal hormone, has been traditionally conside
23 es that are required for biosynthesis of the neurohypophyseal hormones vasopressin and oxytocin.
24 tive resistant or R-type Ca2+ current in rat neurohypophyseal nerve terminals, but concentrations of
25                          Using as models the neurohypophyseal nonapeptide hormone oxytocin and its an
26  excretion by the kidney is regulated by the neurohypophyseal peptide hormone vasopressin through act
27                 Arginine8 vasotocin (AVT), a neurohypophyseal peptide in nonmammalian vertebrates, pl
28  that the phylogenetic plasticity of central neurohypophyseal peptide receptor expression may contrib
29      A number of studies have implicated the neurohypophyseal peptides oxytocin and vasopressin in th
30 ing throughout the striatum and hypothalamic-neurohypophyseal region.
31  Physiological activation of the hypothalamo-neurohypophyseal system (HNS) by dehydration results is
32 VP) release from explants of the hypothalamo-neurohypophyseal system (HNS), but the response is not s
33 cin release from explants of the hypothalamo-neurohypophyseal system (HNS), two hypotheses were teste
34  we show expression in the brain hypothalamo-neurohypophyseal system (HNS), wherein upregulation foll
35 reactive fibers, were located throughout the neurohypophyseal tract and within the posterior pituitar
36 ers were evident outside of the hypothalamic-neurohypophyseal tract, a plexus of fibers in the latera