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1  an analysis to a songbird, the zebra finch (Taeniopygia guttata).
2 e learned songs of adult male zebra finches (Taeniopygia guttata).
3  the pigeon (Columba livia) and zebra finch (Taeniopygia guttata).
4 cture of learned song in male zebra finches (Taeniopygia guttata).
5 ngs of HVC neurons in singing zebra finches (Taeniopygia guttata).
6  song control system of adult zebra finches (Taeniopygia guttata).
7 s of the nidopallium) of male zebra finches (Taeniopygia guttata).
8 anaries (Serinus canaria) and zebra finches (Taeniopygia guttata).
9 he regulation of immunity, in zebra finches (Taeniopygia guttata).
10 sexual attractiveness in male zebra finches (Taeniopygia guttata).
11  in the brain of an oscine, the zebra finch (Taeniopygia guttata).
12         Here, we show that in zebra finches (Taeniopygia guttata), a colonial-breeding songbird speci
13 n acoustic communication in the zebra finch (Taeniopygia guttata), a songbird species in which the ma
14  in the brain of the adult male zebra finch (Taeniopygia guttata), a songbird species.
15 rd species) with results from zebra finches (Taeniopygia guttata, a songbird species) and humans (Hom
16             Here we show, in the zebra finch Taeniopygia guttata, an extraordinary degree of inter-ma
17 to investigate the ability of zebra finches (Taeniopygia guttata) and Bengalese finches (Lonchura str
18 monic sounds were measured in zebra finches (Taeniopygia guttata) and budgerigars (Melopsittacus undu
19 ctions from the brain of male zebra finches (Taeniopygia guttata) and make them publicly available th
20  (Trachemys scripta elegans), zebra finches (Taeniopygia guttata), and mice (Mus musculus) utilizing
21  hummingbirds (Calypte anna), zebra finches (Taeniopygia guttata), and pigeons (Columba livia).
22 ed song in juvenile and adult zebra finches (Taeniopygia guttata), and to test for possible developme
23 eeding causes early death in the zebra finch Taeniopygia guttata, and among inbred individuals of the
24  data for two bird species: the zebra finch, Taeniopygia guttata, and the long-tailed finch, Poephila
25        Here we show that Zebra Finch chicks (Taeniopygia guttata) are capable of identifying parental
26                               Zebra finches (Taeniopygia guttata) are regarded as opportunistic breed
27                          Male zebra finches (Taeniopygia guttata) are vocal learners that acquire a s
28  an R2 retrotransposon from the zebra finch, Taeniopygia guttata, as an orthologue that can be retarg
29 ified partial sequence from the zebra finch, Taeniopygia guttata, as well as the previously identifie
30 ory forebrain of anesthetized zebra finches (Taeniopygia guttata) at 32 sites simultaneously, to cont
31 e vocalisations of individual zebra finches (Taeniopygia guttata) behaving freely in social groups, w
32  highly gregarious zebra finch (Estrildidae: Taeniopygia guttata), blockade of nonapeptide receptors
33 medial nidopallium (NCM) of the zebra finch (Taeniopygia guttata) brain.
34     We made cDNA libraries from zebra finch (Taeniopygia guttata) brains at different developmental s
35 mmingbirds (Calypte anna) and zebra finches (Taeniopygia guttata) by using in vivo extracellular elec
36  We report that juvenile male zebra finches, Taeniopygia guttata, can master their imitation of the s
37             Earlier work on the zebra finch (Taeniopygia guttata castanotis) showed that the GRC is i
38 species of estrildid finches (zebra finches, Taeniopygia guttata castanotis; long-tailed finches, Poe
39                A comparison with zebra finch Taeniopygia guttata, chicken Gallus gallus and the green
40      We show that pair-bonded zebra finches (Taeniopygia guttata) communicating through the virtual e
41  collected a large corpus of zebra finches' (Taeniopygia guttata) decisions about song syllable simil
42 al neostriatum (NCM) of adult zebra finches (Taeniopygia guttata) decreased upon repeated, unreinforc
43 HVC (proper name) in juvenile zebra finches (Taeniopygia guttata) during auditory learning of a tutor
44 m vocal effectors of juvenile zebra finches (Taeniopygia guttata) during the stage of sensorimotor in
45 ircuit of juvenile songbirds (zebra finches, Taeniopygia guttata) during vocal learning: (1) one in w
46 ally section oviduct tissue from zebra finch Taeniopygia guttata females label free by harnessing tis
47 We examined neural responses in zebra finch (Taeniopygia guttata) field L (homologous to primary audi
48 medial neostriatum (NCM) of the zebra finch (Taeniopygia guttata) forebrain habituate to repeated pre
49 how that in male zebra finches (Estrildidae: Taeniopygia guttata), Fos activity within a subpopulatio
50 evelopment in the brains of the zebra finch (Taeniopygia guttata) from chick at posthatch day (d) 8 t
51    The recent sequencing of the zebra finch (Taeniopygia guttata) genome allowed an assessment of the
52 the chicken (Gallus gallus) and zebra finch (Taeniopygia guttata) genomes places the Ppu020 and Faede
53 outs of singing in adult male zebra finches (Taeniopygia guttata) induce persistent increases in firi
54                             The zebra finch (Taeniopygia guttata) is an important model organism for
55  Song development in juvenile zebra finches (Taeniopygia guttata) is characterized by sleep-dependent
56 song responsiveness in female zebra finches (Taeniopygia guttata) is strongly modulated by circulatin
57 mmunoreactivity in the brain of zebra finch, Taeniopygia guttata, its interaction with NPY, and their
58                 A juvenile male zebra finch, Taeniopygia guttata, kept singly with its father develop
59                          A male zebra finch, Taeniopygia guttata, kept with its father until adulthoo
60                               Zebra finches (Taeniopygia guttata) learn a specific song pattern durin
61                               Zebra finches (Taeniopygia guttata) learn to produce songs in a manner
62                    A young male zebra finch (Taeniopygia guttata) learns to sing by copying the vocal
63                          Male zebra finches (Taeniopygia guttata) master the imitation of a song mode
64            We PIT-tagged wild zebra finches (Taeniopygia guttata), monitoring their reproduction and
65                 Juvenile male zebra finches (Taeniopygia guttata) must be exposed to an adult tutor d
66   Sexual differentiation of the zebra finch (Taeniopygia guttata) neural song circuit is thought to b
67 oximately 7%) of captive male zebra finches (Taeniopygia guttata) produce variant acoustic birdsong p
68       The songs of adult male zebra finches (Taeniopygia guttata), produced as rapid sequences of voc
69 rally and biochemically characterize R2 from Taeniopygia guttata (R2Tg).
70              Song learning in zebra finches (Taeniopygia guttata) requires exposure to the song of a
71 tral examination of song of the zebra finch (Taeniopygia guttata) reveals a class of rapid song modul
72 anaries (Serinus canaria) and zebra finches (taeniopygia guttata) sends an ipsilateral projection to
73 are added, too, to the HVC of zebra finches (Taeniopygia guttata) that do not learn new songs in adul
74 migrating songbird, we fasted zebra finches (Taeniopygia guttata) that had been dosed with 0.0, 0.1,
75 n the vocal control system of zebra finches (Taeniopygia guttata) the pre-motor mechanisms of vocal v
76 dence that song learning in the zebra finch (Taeniopygia guttata), the most common model species of v
77                      In adult zebra finches (Taeniopygia guttata), the telencephalon occupies 64% of
78 imaging in anesthetized adult zebra finches (Taeniopygia guttata) to examine how learned birdsong and
79  the yellowbeak mutation in the zebra finch (Taeniopygia guttata) to investigate the genetic basis of
80  MRI method in mildly sedated zebra finches (Taeniopygia guttata) to localize and characterize song d
81  in the gregarious zebra finch (Estrildidae: Taeniopygia guttata) underscore this functional specific
82 nome-wide analysis of LD in the zebra finch (Taeniopygia guttata) using 838 single nucleotide polymor
83 hole-genome linkage map for the zebra finch (Taeniopygia guttata) using a 354-bird pedigree.
84 ow (Zonotrichia albicollis) and zebra finch (Taeniopygia guttata), we labeled putative VT receptors w
85 s to the singing behaviour of zebra finches (Taeniopygia guttata), we show that syllable spread in lo
86 ourting a mate change as male zebra finches (Taeniopygia guttata) were provided with opportunities to
87 anaries, Serinus canaria, and zebra finches, Taeniopygia guttata, whenever these songbirds sing or he
88    Here, we used a species, the zebra finch, Taeniopygia guttata, where males have been shown to decr
89                  Adult female zebra finches (Taeniopygia guttata), which do not produce learned songs
90 s of the genome sequence of the zebra finch (Taeniopygia guttata), which is a songbird belonging to t
91  male-only singing behavior: the zebra finch Taeniopygia guttata, which sings a single, stereotyped s
92 uestion, we use a songbird, the zebra finch (Taeniopygia guttata), whose learned song and underlying
93 g an experimental approach in zebra finches (Taeniopygia guttata) with an analysis of natural develop
94     We raised male and female zebra finches (Taeniopygia guttata) with differing amounts of exposure
95 gated a passerine songbird, the zebra finch (Taeniopygia guttata), with a biparental caring system.