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

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

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

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

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

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

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

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

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

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

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

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

16 of unprecedented sophistication in the fowl Gallus gallus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 The Gallus gallus Z chromosome provides a useful opportunity