ライフサイエンスコーパス: Gallus gallus

1 lymphopoiesis, such as that of the chicken (Gallus gallus).

2 low-frequency cochlear regions of the chick (Gallus gallus).

3 auditory telencephalon of an avian species (Gallus gallus).

4 on the well-studied model organism chicken (Gallus gallus).

5 SON neurons in NL was examined in chickens (Gallus gallus).

6 e typical avian model, the domestic chicken (Gallus gallus).

7 barn owl (Tyto alba) and the domestic chick (Gallus gallus).

8 of sexual size dimorphism in red junglefowl (Gallus gallus).

9 connections of Imc were examined in chicks (Gallus gallus).

10 ed partial cDNA clone for SSDP from chicken (Gallus gallus).

11 o dissect the function of TIM4 in the chick (Gallus gallus).

12 tures and a stressful condition in chickens (Gallus gallus).

13 ion of UCN3 mRNA in a sauropsid-the chicken, Gallus gallus.

14 bulbs to the caudal end of the brainstem in Gallus gallus.

15 mic and other information about the chicken, Gallus gallus.

16 and expression of DNase II from the chicken, Gallus gallus.

17 ated RNase A ribonucleases from the chicken, Gallus gallus.

18 raft genome sequence of the red jungle fowl, Gallus gallus.

19 of unprecedented sophistication in the fowl Gallus gallus.

20 Here, we show that in male red junglefowl, Gallus gallus, along with changes in sperm numbers and S

21 Bos taurus, Rattus norvegicus, Danio rerio, Gallus gallus and Arabidopsis thaliana).

22 ith zebra finch Taeniopygia guttata, chicken Gallus gallus and the green anole lizard Anolis caroline

23 to those of the inner centromere proteins of Gallus gallus and Xenopus laevis, which are mitotic phos

24 rom two non-migratory bird species, chicken (Gallus gallus) and pigeon (Columba livia).

25 ociated with a stress condition in chickens (Gallus gallus) and to unravel their interactions by impl

26 d, epithelial beta-defensins of the chicken (Gallus gallus) and turkey (Meleagris gallopavo), respect

27 microsatellite markers against the chicken (Gallus gallus) and zebra finch (Taeniopygia guttata) gen

28 alis), zebrafish (Danio rerio), and chicken (Gallus gallus) and, using phylogenetic analysis, identif

29 We investigated LD in chickens (Gallus gallus) at the highest resolution to date for bro

30 animals (Canis lupus familiaris, Ovis aries, Gallus gallus, Bos taurus, Felis catus, and Capra hircus

31 ress in a poultry animal model, the chicken (Gallus gallus), by reusing and combining data previously

32 fasciatus), frog (Xenopus laevis), chicken (Gallus gallus), chameleon (Anolis carolinensis), goat (C

33 idopsis, Oryza sativa (rice), Drosophila and Gallus gallus (chicken).

34 Chicks (Gallus gallus, Cornell K Strain) were raised either unde

35 Chicken (Gallus gallus) Cx26 gap junction channels lack Lys108 an

36 nce in sensitivity between domestic chicken (Gallus gallus domesticus) and common tern (Sterna hirund

37 one such behavior, the crowing of chickens (Gallus gallus domesticus) and Japanese quail (Coturnix c

38 Though chickens (Gallus gallus domesticus) are globally ubiquitous today,

39 anxiety) in fast- and slow-growing broilers (Gallus gallus domesticus) as they gain weight.

40 Chicken (Gallus gallus domesticus) is today one of the most wides

41 In domestic leghorn chickens (Gallus gallus domesticus) sexual maturation brings about

42 n of a specific neuronal circuit in chicken (Gallus gallus domesticus) with that of the GFP quail.

43 gg albumin, extracted from fresh egg whites (Gallus gallus domesticus), was quantified using the Brad

44 tica, Equus caballus, Oryctolagus cuniculus, Gallus gallus domesticus, Meleagris gallopavo and Coturn

45 male reproductive senescence in feral fowl, Gallus gallus domesticus, where socially dominant males

46 on under native regulatory control in chick (Gallus gallus) embryos, our findings show that SHH is un

47 multi-photon time-lapse microscopy of chick (Gallus gallus) embryos, we reveal a medio-lateral cell i

48 cine site ligands with tubulin isolated from Gallus gallus erythrocytes (CeTb), which is approximatel

49 o sex determination of the domestic chicken (Gallus gallus f. dom.) already at day 3.5 of egg incubat

50 tify the BST-2 sequence in domestic chicken (Gallus gallus) for the first time and demonstrate its ac

51 he 14 avian beta-defensins identified in the Gallus gallus genome, only 3 are present in the chicken

52 Here, a detailed analysis of the chicken (Gallus gallus) genome identified 10 clade B serpin genes

53 l rearrangements between it and the chicken (Gallus gallus) genome, revealing a surprisingly high num

54 Gallus gallus (Gg) laforin is more stable in vitro than

55 us leucas), toadfish (Opsanus tau), chicken (Gallus gallus), hagfish (Myxine glutinosa), horseshoe cr

56 er and a partial cDNA for DNA POL gamma from Gallus gallus have been cloned.

57 is orthologous to the human and the chicken (Gallus gallus) HDAC3 genes.

58 ver, the eagle regularly preyed on chickens (Gallus gallus) (i.e., domestic Galliformes) which were c

59 ma3F, Nrp1, Nrp2, and PlxnA1 in the chicken (Gallus gallus) inner ear from embryonic day (E)5-E10.

60 Chicken, Gallus gallus, is a valuable species both as a food sour

61 e its wild progenitor - the red jungle fowl (Gallus gallus) - lives in tropical ecosystems and does n

62 Chicken (Gallus gallus) MHCY class I molecules are highly polymor

63 Here we utilized the chicken (Gallus gallus) model to investigate impacts of NA-chelat

64 thaliana ubiquitin-conjugating enzyme, and a Gallus gallus mRNA zipcode-binding protein.

65 ncluding Caenorhabditis elegans, Drosophila, Gallus gallus, Mus musculus, and Homo sapiens.

66 In chickens (Gallus gallus), NL is a well-studied model system for ac

67 We trained 3-day-old chicks (Gallus gallus) on a given numerical magnitude (5).

68 croscopic structural characterization of the Gallus gallus PCFT was obtained, which shares significan

69 in a single generation of a broiler breeder (Gallus gallus) pedigree dam line.

70 specifically expressed in distinct chicken (Gallus gallus) photoreceptor subtypes, we developed fluo

71 ree important agricultural species: chicken (Gallus gallus), pig (Sus scrofa), and cattle (Bos taurus

72 licate seminatural groups of red junglefowl, Gallus gallus, polyandry eroded variance in male mating

73 Third, using data from a red junglefowl (Gallus gallus) population, we show that declines in prec

74 hus mykiss), frog (Xenopus laevis), chicken (Gallus gallus), rat (Rattus norvegicus), mouse (Mus musc

75 model organisms: Homo sapiens, Mus musculus, Gallus gallus, Rattus norvegicus, Arabidopsis thaliana,

76 peptides (QCAT protein) from several chick (Gallus gallus) skeletal muscle proteins and features for

77 the use of bovine (Bos taurus) and poultry (Gallus gallus) specific primers that amplify small fragm

78 dius alimentum), and the non-native chicken (Gallus gallus) suggests that anthropogenic loss of the f

79 ution to cardiomyocytes of the ventricles in Gallus gallus, supported by Wnt1-Cre lineage analysis in

80 ical MHC class I genes found in the chicken (Gallus gallus) that have sequence homology to the mammal

81 be the draft genome sequence of the chicken, Gallus gallus, the first species sequenced that is both

82 proteome of the polyandrous Red junglefowl, Gallus gallus, the wild species that gave rise to the do

83 In chickens (Gallus gallus), three pathways arise from nucleus lamina

84 Here we trained 4-day-old domestic chicks (Gallus gallus) to respond to stimuli depicting multiple

85 tory sexual selection in male red junglefowl Gallus gallus, using replicate groups across three exper

86 aring significant homology with the chicken (Gallus gallus) VgR and particularly the Drosophila melan

87 This indicator is based on the Gallus gallus voltage-sensitive phosphatase with the pho

88 velopment and function, transgenic chickens (Gallus gallus) were designed to produce H chain-only Abs

89 Chicks (Gallus gallus) were raised in either a 12-hour light-dar

90 tsynaptic targets in the tectum of chickens (Gallus gallus) with neural tracers and performed an ultr

91 The Gallus gallus Z chromosome provides a useful opportunity