ライフサイエンスコーパス: Taeniopygia guttata

1 cture of learned song in male zebra finches (Taeniopygia guttata).

2 an analysis to a songbird, the zebra finch (Taeniopygia guttata).

3 ngs of HVC neurons in singing zebra finches (Taeniopygia guttata).

4 e learned songs of adult male zebra finches (Taeniopygia guttata).

5 song control system of adult zebra finches (Taeniopygia guttata).

6 s of the nidopallium) of male zebra finches (Taeniopygia guttata).

7 anaries (Serinus canaria) and zebra finches (Taeniopygia guttata).

8 the pigeon (Columba livia) and zebra finch (Taeniopygia guttata).

9 sexual attractiveness in male zebra finches (Taeniopygia guttata).

10 in the brain of an oscine, the zebra finch (Taeniopygia guttata).

11 in the brain of the adult male zebra finch (Taeniopygia guttata), a songbird species.

12 rd species) with results from zebra finches (Taeniopygia guttata, a songbird species) and humans (Hom

13 Here we show, in the zebra finch Taeniopygia guttata, an extraordinary degree of inter-ma

14 to investigate the ability of zebra finches (Taeniopygia guttata) and Bengalese finches (Lonchura str

15 monic sounds were measured in zebra finches (Taeniopygia guttata) and budgerigars (Melopsittacus undu

16 ctions from the brain of male zebra finches (Taeniopygia guttata) and make them publicly available th

17 (Trachemys scripta elegans), zebra finches (Taeniopygia guttata), and mice (Mus musculus) utilizing

18 ed song in juvenile and adult zebra finches (Taeniopygia guttata), and to test for possible developme

19 eeding causes early death in the zebra finch Taeniopygia guttata, and among inbred individuals of the

20 data for two bird species: the zebra finch, Taeniopygia guttata, and the long-tailed finch, Poephila

21 Here we show that Zebra Finch chicks (Taeniopygia guttata) are capable of identifying parental

22 Zebra finches (Taeniopygia guttata) are regarded as opportunistic breed

23 Male zebra finches (Taeniopygia guttata) are vocal learners that acquire a s

24 ified partial sequence from the zebra finch, Taeniopygia guttata, as well as the previously identifie

25 ory forebrain of anesthetized zebra finches (Taeniopygia guttata) at 32 sites simultaneously, to cont

26 e vocalisations of individual zebra finches (Taeniopygia guttata) behaving freely in social groups, w

27 highly gregarious zebra finch (Estrildidae: Taeniopygia guttata), blockade of nonapeptide receptors

28 medial nidopallium (NCM) of the zebra finch (Taeniopygia guttata) brain.

29 We made cDNA libraries from zebra finch (Taeniopygia guttata) brains at different developmental s

30 We report that juvenile male zebra finches, Taeniopygia guttata, can master their imitation of the s

31 A comparison with zebra finch Taeniopygia guttata, chicken Gallus gallus and the green

32 al neostriatum (NCM) of adult zebra finches (Taeniopygia guttata) decreased upon repeated, unreinforc

33 m vocal effectors of juvenile zebra finches (Taeniopygia guttata) during the stage of sensorimotor in

34 ircuit of juvenile songbirds (zebra finches, Taeniopygia guttata) during vocal learning: (1) one in w

35 We examined neural responses in zebra finch (Taeniopygia guttata) field L (homologous to primary audi

36 medial neostriatum (NCM) of the zebra finch (Taeniopygia guttata) forebrain habituate to repeated pre

37 how that in male zebra finches (Estrildidae: Taeniopygia guttata), Fos activity within a subpopulatio

38 The recent sequencing of the zebra finch (Taeniopygia guttata) genome allowed an assessment of the

39 the chicken (Gallus gallus) and zebra finch (Taeniopygia guttata) genomes places the Ppu020 and Faede

40 outs of singing in adult male zebra finches (Taeniopygia guttata) induce persistent increases in firi

41 The zebra finch (Taeniopygia guttata) is an important model organism for

42 Song development in juvenile zebra finches (Taeniopygia guttata) is characterized by sleep-dependent

43 song responsiveness in female zebra finches (Taeniopygia guttata) is strongly modulated by circulatin

44 mmunoreactivity in the brain of zebra finch, Taeniopygia guttata, its interaction with NPY, and their

45 A juvenile male zebra finch, Taeniopygia guttata, kept singly with its father develop

46 A male zebra finch, Taeniopygia guttata, kept with its father until adulthoo

47 Zebra finches (Taeniopygia guttata) learn a specific song pattern durin

48 Zebra finches (Taeniopygia guttata) learn to produce songs in a manner

49 A young male zebra finch (Taeniopygia guttata) learns to sing by copying the vocal

50 Male zebra finches (Taeniopygia guttata) master the imitation of a song mode

51 Sexual differentiation of the zebra finch (Taeniopygia guttata) neural song circuit is thought to b

52 oximately 7%) of captive male zebra finches (Taeniopygia guttata) produce variant acoustic birdsong p

53 The songs of adult male zebra finches (Taeniopygia guttata), produced as rapid sequences of voc

54 tral examination of song of the zebra finch (Taeniopygia guttata) reveals a class of rapid song modul

55 anaries (Serinus canaria) and zebra finches (taeniopygia guttata) sends an ipsilateral projection to

56 are added, too, to the HVC of zebra finches (Taeniopygia guttata) that do not learn new songs in adul

57 migrating songbird, we fasted zebra finches (Taeniopygia guttata) that had been dosed with 0.0, 0.1,

58 n the vocal control system of zebra finches (Taeniopygia guttata) the pre-motor mechanisms of vocal v

59 In adult zebra finches (Taeniopygia guttata), the telencephalon occupies 64% of

60 imaging in anesthetized adult zebra finches (Taeniopygia guttata) to examine how learned birdsong and

61 the yellowbeak mutation in the zebra finch (Taeniopygia guttata) to investigate the genetic basis of

62 MRI method in mildly sedated zebra finches (Taeniopygia guttata) to localize and characterize song d

63 in the gregarious zebra finch (Estrildidae: Taeniopygia guttata) underscore this functional specific

64 nome-wide analysis of LD in the zebra finch (Taeniopygia guttata) using 838 single nucleotide polymor

65 hole-genome linkage map for the zebra finch (Taeniopygia guttata) using a 354-bird pedigree.

66 ow (Zonotrichia albicollis) and zebra finch (Taeniopygia guttata), we labeled putative VT receptors w

67 anaries, Serinus canaria, and zebra finches, Taeniopygia guttata, whenever these songbirds sing or he

68 s of the genome sequence of the zebra finch (Taeniopygia guttata), which is a songbird belonging to t

69 male-only singing behavior: the zebra finch Taeniopygia guttata, which sings a single, stereotyped s

70 uestion, we use a songbird, the zebra finch (Taeniopygia guttata), whose learned song and underlying

71 g an experimental approach in zebra finches (Taeniopygia guttata) with an analysis of natural develop

72 We raised male and female zebra finches (Taeniopygia guttata) with differing amounts of exposure