ライフサイエンスコーパス: Gallus

1 al neuroanatomical data of model archosaurs (Gallus, Alligator), crown birds exhibit a distinct allom

2 conservation of the seven Cbfa sites in the Gallus and human BSP promoters, suggest that suppressor

3 es for two species of Perdix, two species of Gallus, and Lagopus lagopus and L. mutus also indicate a

4 volvement of Cbfa sites in expression of the Gallus BSP gene.

5 Responsiveness of the 1.2-kb Gallus BSP promoter to Cbfa factors Cbfa1, Cbfa2, and Cb

6 entified as myosin light chain 1, designated Gallus domesticus 7 (Gal d 7).

7 the developing optic tectum of the chicken (Gallus domesticus) and performed in ovo retroviral trans

8 The chick embryo (Gallus domesticus) is one of the most important model sy

9 estigated in soil and chicken feed, chicken (Gallus domesticus) tissues, eggs on 0, 7, and 14 days af

10 nical nociceptors of monoarthritic chickens (Gallus domesticus) were studied by recording the electri

11 Chickens (Gallus domesticus) were trained on a multiple alternativ

12 y hepatocyte cultures prepared from chicken (Gallus domesticus), Pekin duck (Anas platyrhynchos domes

13 rods in cone dominant retinas from chicken (Gallus domesticus), turkey (Meleagris gallopavo), and pi

14 GEISHA (Gallus Expression In Situ Hybridization Analysis) is an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

37 The Gallus gallus Z chromosome provides a useful opportunity

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 of unprecedented sophistication in the fowl Gallus gallus.

106 Gallus GBrowse provides online access to genomic and oth

107 These tools make the Gallus GBrowse server a valuable resource for researcher

108 the avian ciliary ganglion, we identified 6 Gallus genes by their homology in structure to mouse lyn

109 abditis elegans, Drosophila melanogaster, G. gallus, Homo sapiens, Mus musculus or Rattus norvegicus

110 genes and Gene Ontology (GO) terms, links to Gallus In Situ Hybridization Analysis (GEISHA), Unigene

111 R2 variants onto the crystal structure of G. gallus KDELR2 indicated that these lead to an inactive r

112 Expression of the endogenous BSP gene in Gallus osteoblasts was similarly downregulated by forced

113 melanogaster, and the C-terminal half of G. gallus, respectively.

114 based proteomic analysis further revealed 6 Gallus sequences annotated as 'uncharacterized' because

115 after the three genera diverged but prior to Gallus speciation.