These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 19341739)

  • 21. Neuropeptide regulation of social behavior in a monogamous cichlid fish.
    Oldfield RG; Hofmann HA
    Physiol Behav; 2011 Mar; 102(3-4):296-303. PubMed ID: 21112347
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An essential role of the arginine vasotocin system in mate-guarding behaviors in triadic relationships of medaka fish (Oryzias latipes).
    Yokoi S; Okuyama T; Kamei Y; Naruse K; Taniguchi Y; Ansai S; Kinoshita M; Young LJ; Takemori N; Kubo T; Takeuchi H
    PLoS Genet; 2015; 11(2):e1005009. PubMed ID: 25719383
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Effect of septal lesions on male song and aggression in the colonial zebra finch (Taeniopygia guttata) and the territorial field sparrow (Spizella pusilla).
    Goodson JL; Eibach R; Sakata J; Adkins-Regan E
    Behav Brain Res; 1999 Jan; 98(1):167-80. PubMed ID: 10210532
    [TBL] [Abstract][Full Text] [Related]  

  • 24. DSP-4, a noradrenergic neurotoxin, produces sex-specific effects on pairing and courtship behavior in zebra finches.
    Vahaba DM; Lacey WH; Tomaszycki ML
    Behav Brain Res; 2013 Sep; 252():164-75. PubMed ID: 23747610
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Aggression- and sex-induced neural activity across vasotocin populations in the brown anole.
    Kabelik D; Alix VC; Burford ER; Singh LJ
    Horm Behav; 2013 Mar; 63(3):437-46. PubMed ID: 23201179
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Housing conditions and sacrifice protocol affect neural activity and vocal behavior in a songbird species, the zebra finch (Taeniopygia guttata).
    Elie JE; Soula HA; Trouvé C; Mathevon N; Vignal C
    C R Biol; 2015 Dec; 338(12):825-37. PubMed ID: 26599152
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Behavioral relevance of species-specific vasotocin anatomy in gregarious finches.
    Kelly AM; Goodson JL
    Front Neurosci; 2013; 7():242. PubMed ID: 24381536
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Sexual dimorphism in numbers of vasotocin-immunoreactive neurons in brain areas associated with reproductive behaviors in the roughskin newt.
    Moore FL; Richardson C; Lowry CA
    Gen Comp Endocrinol; 2000 Feb; 117(2):281-98. PubMed ID: 10642450
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Manipulations of the AVT system shift social status and related courtship and aggressive behavior in the bluehead wrasse.
    Semsar K; Kandel FL; Godwin J
    Horm Behav; 2001 Aug; 40(1):21-31. PubMed ID: 11467881
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Neural distribution of nonapeptide binding sites in two species of songbird.
    Leung CH; Goode CT; Young LJ; Maney DL
    J Comp Neurol; 2009 Mar; 513(2):197-208. PubMed ID: 19132730
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Developmental effects of vasotocin and nonapeptide receptors on early social attachment and affiliative behavior in the zebra finch.
    Baran NM; Sklar NC; Adkins-Regan E
    Horm Behav; 2016 Feb; 78():20-31. PubMed ID: 26476409
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Arginine vasotocin, steroid hormones and social behavior in the green anole lizard (Anolis carolinensis).
    Dunham LA; Wilczynski W
    J Exp Biol; 2014 Oct; 217(Pt 20):3670-6. PubMed ID: 25147242
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Effect of septal lesions on male song and aggression in the colonial zebra finch (Taeniopygia guttata) and the territorial field sparrow (Spizella pusilla).
    Goodson JL; Eibach R; Sakata J; Adkins-Regan E
    Behav Brain Res; 1999 May; 101(1):167-80. PubMed ID: 10342406
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Juvenile social experience affects pairing success at adulthood: congruence with the loser effect?
    Mariette MM; Cathaud C; Chambon R; Vignal C
    Proc Biol Sci; 2013 Sep; 280(1767):20131514. PubMed ID: 23902911
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Arginine vasotocin, isotocin and nonapeptide receptor gene expression link to social status and aggression in sex-dependent patterns.
    Lema SC; Sanders KE; Walti KA
    J Neuroendocrinol; 2015 Feb; 27(2):142-57. PubMed ID: 25425529
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Effects of social conditions during adolescence on courtship and aggressive behavior are not abolished by adult social experience.
    Ruploh T; Henning M; Bischof HJ; von Engelhardt N
    Dev Psychobiol; 2015 Jan; 57(1):73-82. PubMed ID: 25545997
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Acute exogenous corticosterone treatments have few effects on courtship and pair bonding in zebra finches.
    Scalera A; Tomaszycki ML
    Gen Comp Endocrinol; 2018 Nov; 268():121-127. PubMed ID: 30102882
    [TBL] [Abstract][Full Text] [Related]  

  • 38. An aggression-specific cell type in the anterior hypothalamus of finches.
    Goodson JL; Kelly AM; Kingsbury MA; Thompson RR
    Proc Natl Acad Sci U S A; 2012 Aug; 109(34):13847-52. PubMed ID: 22872869
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Vasotocin treatment inhibits courtship in male zebra finches; concomitant androgen treatment inhibits this effect.
    Harding CF; Rowe SA
    Horm Behav; 2003 Dec; 44(5):413-8. PubMed ID: 14644635
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Committed for the long haul: Do nonapeptides regulate long-term pair maintenance in zebra finches?
    Kelly EM
    Gen Comp Endocrinol; 2019 May; 276():86-92. PubMed ID: 30690035
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.