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   2 ors with two radioligands, [(125)I]ornithine vasotocin analog ([(125)I]OVTA) and [(125)I]linear VP an
     3 duction pathways underlying acute effects of vasotocin and corticosterone, presumably mediated via "n
     4 ians, the hypothalamic neuropeptide arginine vasotocin and the adrenal steroid corticosterone interac
     5 es with synthetic oligonucleotide probes for vasotocin and the related neuropeptide mesotocin, as wel
     6  with an emerging pattern of distribution of vasotocin- and vasopressin-like peptides in vertebrates.
     7 ations are compared with previous studies of vasotocin- and vasopressin-like systems in vertebrates. 
  
  
    10 ra and interspecific comparisons of arginine vasotocin (AVT) and its mammalian homolog arginine vasop
  
    12 he neuroanatomical distributions of arginine vasotocin (AVT) and mesotocin (MST), non-mammalian homol
    13 trometry, we identified the peptide arginine vasotocin (AVT) in brain and pituitary extracts from the
    14 demonstrated that isotocin (IT) and arginine vasotocin (AVT) modulate fictive vocalizations divergent
  
    16 mals (i.e., distributions of met-enkephalin, vasotocin, galanin, calcitonin gene-related peptide, tyr
    17  in situ hybridization, we conclude that the vasotocin immunohistochemical procedures used identify v
    18 typical group sizes, we now demonstrate that vasotocin-immunoreactive (VT-ir) neurons of the BSTm exh
    19 he highest sensitivity is attained with arg8-vasotocin, in which a total of 300 amol is detected in a
  
    21 ural vocalizations was modulated by arginine-vasotocin, isotocin and their antagonists delivered to t
    22 nt of whole brain minces with vasopressin or vasotocin led to increases in PKCalpha in membrane fract
  
    24 the neuroanatomical distribution of arginine vasotocin-like systems in the roughskin newt (Taricha gr
    25 immunohistochemical procedures used identify vasotocin-like, but not mesotocin-like, elements in the 
  
  
  
    29 es were immunofluorescently multilabeled for vasotocin, mesotocin (MT), corticotropin-releasing hormo
    30 als) and its evolutionary precursor arginine-vasotocin (non-mammals) modulate reproductive physiology
    31 eceptor antagonist ([d(CH2)5-Tyr (Me)2-Orn8]-Vasotocin [OTA]; 25 microg i.t. in 5 microl saline) sign
  
    33 xamine the effects of corticosterone and the vasotocin receptor agonist arginine vasopressin, alone a
    34 ithin the brain, while calcitonin, SIFamide, vasotocin, RGWamide, DLamide, FLamide, FVamide, MIP, and
    35 es that acoustically court females (arginine-vasotocin-sensitive) than in females and sneak-spawning 
    36  urodele amphibians possess a well-developed vasotocin system, perhaps more extensive than other vert
  
    38 V1 vasopressin receptor agonist, [Phe2,Orn8]-vasotocin, (V1 agonist) induced a significant accumulati
  
  
  
  
  
  
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