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 *

128 related articles for article (PubMed ID: 15794997)

  • 1. Inhibitors of carbohydrate metabolism reduce undirected song production at doses that do not alter food intake in singly housed male zebra finches.
    Cappendijk SL; Johnson F
    Behav Brain Res; 2005 Apr; 159(1):51-4. PubMed ID: 15794997
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Food availability but not cold ambient temperature affects undirected singing in adult male zebra finches.
    Johnson F; Rashotte M
    Physiol Behav; 2002 May; 76(1):9-20. PubMed ID: 12175584
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Influence of food and water availability on undirected singing and energetic status in adult male zebra finches (Taeniopygia guttata).
    Rashotte ME; Sedunova EV; Johnson F; Pastukhov IF
    Physiol Behav; 2001; 74(4-5):533-41. PubMed ID: 11790413
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Opioid modulation of song in male zebra finches (Taenopygia guttata).
    Khurshid N; Jayaprakash N; Hameed LS; Mohanasundaram S; Iyengar S
    Behav Brain Res; 2010 Apr; 208(2):359-70. PubMed ID: 20015456
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Physiological insights into the social-context-dependent changes in the rhythm of the song motor program.
    Cooper BG; Goller F
    J Neurophysiol; 2006 Jun; 95(6):3798-809. PubMed ID: 16554509
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The effect of social environment on singing behavior in the zebra finch (Taeniopygia guttata) and its implication for neuronal recruitment.
    Adar E; Lotem A; Barnea A
    Behav Brain Res; 2008 Feb; 187(1):178-84. PubMed ID: 17950475
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cue hierarchies and testicular development: is food a more potent stimulus than day length in an opportunistic breeder (Taeniopygia g. guttata)?
    Perfito N; Kwong JM; Bentley GE; Hau M
    Horm Behav; 2008 Apr; 53(4):567-72. PubMed ID: 18295766
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Effects of intake rate on energy expenditure, somatic repair and reproduction of zebra finches.
    Wiersma P; Verhulst S
    J Exp Biol; 2005 Nov; 208(Pt 21):4091-8. PubMed ID: 16244168
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cross-fostering diminishes song discrimination in zebra finches (Taeniopygia guttata).
    Campbell DL; Hauber ME
    Anim Cogn; 2009 May; 12(3):481-90. PubMed ID: 19130101
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Song perception during the sensitive period of song learning in zebra finches (Taeniopygia guttata).
    Braaten RF; Petzoldt M; Colbath A
    J Comp Psychol; 2006 May; 120(2):79-88. PubMed ID: 16719585
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Immediate early gene (ZENK) responses to song in juvenile female and male zebra finches: effects of rearing environment.
    Tomaszycki ML; Sluzas EM; Sundberg KA; Newman SW; DeVoogd TJ
    J Neurobiol; 2006 Sep; 66(11):1175-82. PubMed ID: 16858693
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Differential responsiveness in brain and behavior to sexually dimorphic long calls in male and female zebra finches.
    Gobes SM; Ter Haar SM; Vignal C; Vergne AL; Mathevon N; Bolhuis JJ
    J Comp Neurol; 2009 Oct; 516(4):312-20. PubMed ID: 19637285
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expression of mu- and delta-opioid receptors in song control regions of adult male zebra finches (Taenopygia guttata).
    Khurshid N; Agarwal V; Iyengar S
    J Chem Neuroanat; 2009 May; 37(3):158-69. PubMed ID: 19118622
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FnTm2, a novel brain-specific transcript, is dynamically expressed in the song learning circuit of the zebra finch.
    Agate RJ; Hertel M; Nottebohm F
    J Comp Neurol; 2007 Sep; 504(2):127-48. PubMed ID: 17626267
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Is there an energetic-based trade-off between thermoregulation and the acute phase response in zebra finches?
    Burness G; Armstrong C; Fee T; Tilman-Schindel E
    J Exp Biol; 2010 Apr; 213(Pt 8):1386-94. PubMed ID: 20348351
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acoustic characteristics, early experience, and endocrine status interact to modulate female zebra finches' behavioral responses to songs.
    Vyas A; Harding C; Borg L; Bogdan D
    Horm Behav; 2009 Jan; 55(1):50-9. PubMed ID: 18804474
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Food intake, locomotor activity, and egg laying in zebra finches: contributions to reproductive energy demand?
    Williams TD; Ternan SP
    Physiol Biochem Zool; 1999; 72(1):19-27. PubMed ID: 9882599
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Noradrenergic neurotoxin, N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine hydrochloride (DSP-4), treatment eliminates estrogenic effects on song responsiveness in female zebra finches (Taeniopygia guttata).
    Vyas A; Harding C; McGowan J; Snare R; Bogdan D
    Behav Neurosci; 2008 Oct; 122(5):1148-57. PubMed ID: 18823170
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Adult female and male zebra finches show distinct patterns of spine deficits in an auditory area and in the song system when reared without exposure to normal adult song.
    Lauay C; Komorowski RW; Beaudin AE; Devoogd TJ
    J Comp Neurol; 2005 Jun; 487(2):119-26. PubMed ID: 15880474
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Post-natal exposure to corticosterone affects standard metabolic rate in the zebra finch (Taeniopygia guttata).
    Spencer KA; Verhulst S
    Gen Comp Endocrinol; 2008; 159(2-3):250-6. PubMed ID: 18854187
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.