347 related articles for article (PubMed ID: 24492024)
21. Developmental modulation and predictability of age-dependent vocal plasticity in adult zebra finches.
James LS; Sakata JT
Brain Res; 2019 Oct; 1721():146336. PubMed ID: 31310739
[TBL] [Abstract][Full Text] [Related]
22. Silent synapses in a thalamo-cortical circuit necessary for song learning in zebra finches.
Bottjer SW
J Neurophysiol; 2005 Dec; 94(6):3698-707. PubMed ID: 16107531
[TBL] [Abstract][Full Text] [Related]
23. Does sex matter? Differential responses to corticosterone administration in the zebra finch.
Khan N; Robert K
Zoology (Jena); 2013 Oct; 116(5):293-9. PubMed ID: 24035000
[TBL] [Abstract][Full Text] [Related]
24. Behavioral and neural trade-offs between song complexity and stress reaction in a wild and a domesticated finch strain.
Suzuki K; Ikebuchi M; Bischof HJ; Okanoya K
Neurosci Biobehav Rev; 2014 Oct; 46 Pt 4():547-56. PubMed ID: 25092250
[TBL] [Abstract][Full Text] [Related]
25. Long memory in song learning by zebra finches.
Funabiki Y; Konishi M
J Neurosci; 2003 Jul; 23(17):6928-35. PubMed ID: 12890787
[TBL] [Abstract][Full Text] [Related]
26. Delayed behavioral effects of postnatal exposure to corticosterone in the zebra finch (Taeniopygia guttata).
Spencer KA; Verhulst S
Horm Behav; 2007 Feb; 51(2):273-80. PubMed ID: 17196201
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. Regulation of learned vocal behavior by an auditory motor cortical nucleus in juvenile zebra finches.
Naie K; Hahnloser RH
J Neurophysiol; 2011 Jul; 106(1):291-300. PubMed ID: 21525374
[TBL] [Abstract][Full Text] [Related]
30. Relative salience of syllable structure and syllable order in zebra finch song.
Lawson SL; Fishbein AR; Prior NH; Ball GF; Dooling RJ
Anim Cogn; 2018 Jul; 21(4):467-480. PubMed ID: 29766379
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. 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]
34. Mitochondria as the powerhouses of sexual selection: Testing mechanistic links between development, cellular respiration, and bird song.
Crino OL; Falk S; Katsis AC; Kraft FOH; Buchanan KL
Horm Behav; 2022 Jun; 142():105184. PubMed ID: 35596967
[TBL] [Abstract][Full Text] [Related]
35. Beeswax corticosterone implants produce long-term elevation of plasma corticosterone and influence condition.
Beck ML; Davies S; Moore IT; Schoenle LA; Kerman K; Vernasco BJ; Sewall KB
Gen Comp Endocrinol; 2016 Jul; 233():109-114. PubMed ID: 27222349
[TBL] [Abstract][Full Text] [Related]
36. Changes in ultra-structures and electrophysiological properties in HVC of untutored and deafened Bengalese finches relation to normally reared birds: implications for song learning.
Peng Z; Zhang X; Xi C; Zeng S; Liu N; Zuo M; Zhang X
Brain Res Bull; 2012 Dec; 89(5-6):211-22. PubMed ID: 22982255
[TBL] [Abstract][Full Text] [Related]
37. Adrenocortical responses in zebra finches (Taeniopygia guttata): individual variation, repeatability, and relationship to phenotypic quality.
Wada H; Salvante KG; Stables C; Wagner E; Williams TD; Breuner CW
Horm Behav; 2008 Mar; 53(3):472-80. PubMed ID: 18221739
[TBL] [Abstract][Full Text] [Related]
38. Dissociation between extension of the sensitive period for avian vocal learning and dendritic spine loss in the song nucleus lMAN.
Heinrich JE; Nordeen KW; Nordeen EJ
Neurobiol Learn Mem; 2005 Mar; 83(2):143-50. PubMed ID: 15721798
[TBL] [Abstract][Full Text] [Related]
39. Physiological, morphological and behavioural effects of selecting zebra finches for divergent levels of corticosterone.
Roberts ML; Buchanan KL; Hasselquist D; Bennett AT; Evans MR
J Exp Biol; 2007 Dec; 210(Pt 24):4368-78. PubMed ID: 18055626
[TBL] [Abstract][Full Text] [Related]
40. Spatial ability is impaired and hippocampal mineralocorticoid receptor mRNA expression reduced in zebra finches (Taeniopygia guttata) selected for acute high corticosterone response to stress.
Hodgson ZG; Meddle SL; Roberts ML; Buchanan KL; Evans MR; Metzdorf R; Gahr M; Healy SD
Proc Biol Sci; 2007 Jan; 274(1607):239-45. PubMed ID: 17148253
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]