ライフサイエンスコーパス: crane

1 nd life stage on gut microbiota of red-crown cranes.

2 icrobiota from captive and artificially bred cranes.

3 These effects are likely not unique to cranes.

4 e a working prototype of a conjugated proton crane, a reversible tautomeric switching molecule in whi

5 established to determine the key factors and crane accident chain by combining text mining, complex n

6 dentify key causative factors and create the crane accident chain due to large amounts of accident da

7 Furthermore, the crane accident chain was established using ISM.

8 Finally, a practical tower crane accident was used to verify the rationality of the

9 Causative factors of crane accidents were firstly identified using text minin

10 , there has been more frequent occurrence of crane accidents, which makes it difficult to identify ke

11 atans is a main food source for the Siberian Crane, an indicator species for migratory birds in Poyan

12 Lastly, bobbing of the head as the animal cranes and explores is phase-locked to sniffing and to m

13 g performance in previously described proton cranes and provides an unprecedented switching efficienc

14 s with pigeons, mesites, and sandgrouse; (3) cranes and their relatives; (4) a comprehensive waterbir

15 common crane (Grus grus, n = 20), demoiselle crane (Anthropoides virgo, n = 66), black-necked crane (

16 return, duration and staging use of sandhill crane Antigone canadensis migration; and estimation of t

17 genicity of RCPV is unknown, the red-crowned cranes are among the rarest crane species.

18 Cranes are widely used in the construction industry for

19 ices in avian prion proteins (chicken, duck, crane) are better accommodated in a helical state, which

20 Finally, cranes arrived early at the breeding grounds when ambien

21 represent a form of disturbance to foraging cranes but is habitat dependent.

22 serves primarily as a visual obstruction for cranes, causing them to increase the frequency of vigila

23 e annual cycle for four species of migratory crane: common crane (Grus grus, n = 20), demoiselle cran

24 d provide abundant food sources for Siberian Crane during winter.

25 Writing in Nature, Crane et al. (2015) show that a specialized condensin co

26 Furthermore, we found that cranes' experiences of the environment emerge from time-

27 ounding zone sediment system at the front of Crane Fjord.

28 Basal-branching crane flies (Nephrotoma) also enrich maternal pangolin t

29 anin is present in the facet walls of living crane-flies, in which it forms the outermost ommatidial

30 roanatomy of the eyes of 54-million-year-old crane-flies, which together provide a proxy for the inte

31 X and Y sex chromosomes in crane fly (Nephrotoma suturalis) spermatocytes exhibit a

32 eiotic chromosomes in spermatocytes from the crane fly Nephrotoma suturalis.

33 forces on chromosome arms during meiosis in crane fly spermatocytes and strongly suggest that the me

34 Cold arrest induced a fraction of meiosis II crane fly spermatocytes to form (n + 1) and (n - 1) daug

35 hat act on chromosome arms during meiosis in crane fly spermatocytes.

36 in the snow fly (Chionea spp.), a flightless crane fly that is active throughout the winter in boreal

37 o stop chromosome movements in Mesostoma and crane-fly spermatocytes and inward movements of spindle

38 ome movements in Mesostoma spermatocytes and crane-fly spermatocytes as 2-3 and 6-10 pN, respectively

39 In crane-fly spermatocytes trap powers of 56-85 mW stopped

40 of single kinetochore (K-) fibers in living crane-fly spermatocytes, from their origins as nascent K

41 must be involved in metaphase positioning in crane-fly spermatocytes.

42 In time-lapse movies of crane-fly spermtocytes, fluorescent speckles generated w

43 ourists influence the vigilance behaviour of cranes foraging in Suaeda salsa salt marshes and S. sals

44 ologic mapping of the fjord suggest that the Crane Glacier grounding zone was well within the fjord b

45 ve model for juvenile (<1 year old) sandhill crane Grus canadensis recruitment of the Rocky Mountain

46 ty and energy expenditure of birds, Eurasian cranes Grus grus, during the winter of 2013-14, which sa

47 for four species of migratory crane: common crane (Grus grus, n = 20), demoiselle crane (Anthropoide

48 The Endangered Red-crowned Crane (Grus japonensis) is one of the most culturally ic

49 The black-necked crane (Grus nigricollis) is the only alpine crane specie

50 e (Anthropoides virgo, n = 66), black-necked crane (Grus nigricollis, n = 9), and white-naped crane (

51 ance, and annual survival of the White-naped Crane (Grus vipio) population in eastern Mongolia were s

52 e (Grus nigricollis, n = 9), and white-naped crane (Grus vipio, n = 9).

53 ator population (the endangered, red-crowned crane, Grus japonensis).

54 Especially, wild cranes had distinct compositions of gut microbiota from

55 sity was found in captive cranes, while wild cranes had the least.

56 Reintroduction of the threatened red-crowned crane has been unsuccessful.

57 of INDOLE-3-ACETIC ACID INDUCIBLE28 (IAA28), CRANE (IAA18), WOODEN LEG, and ARABIDOPSIS RESPONSE REGU

58 nce triggering a high degree of vigilance by cranes identified at 300 m.

59 ne European tree species at the Swiss Canopy Crane II site.

60 neral decline observed in this population of cranes in recent decades.

61 ting factor on population growth of sandhill cranes in the RMP, which could become more limiting with

62 velopment of China to secure this endangered crane lineage and other wildlife on the Tibetan Plateau.

63 ter data in the Nino 4 region and Demoiselle Crane migration data.

64 mponents known to be important to aspects of crane natural history: enhanced vegetation index (resour

65 er site increased migration speed during the cranes' northbound migration to their breeding grounds.

66 erence for the targeted safety management of crane operation and improve crane operation safety in th

67 Meanwhile, an indicator system for crane operation causative factors was established by cal

68 ty management of crane operation and improve crane operation safety in the construction.

69 management" were found to play a key role of crane operation.

70 e of the snakes and artificial structures in Crane Park to document their space use, activity, and th

71 d an adjacent tourist bird park (Red-crowned Crane Park).

72 ructures of two aveparvoviruses, red-crowned crane parvovirus (RCPV) and turkey parvovirus (TuPV), ex

73 two bird viruses of this genus: red-crowned crane parvovirus (RCPV) and turkey parvovirus (TuPV).

74 dge of the mechanisms underlying White-naped Crane population decline in eastern Mongolia identified

75 he conservation of the migratory red-crowned crane population that winters in the Yellow River Delta

76 Additionally, our model suggested that the crane prefers to breed in alpine meadows at an elevation

77 ial feeding areas decreased dramatically and cranes restricted their activity to a small partially un

78 tion model (SDM) to analyze the black-necked crane's breeding habitats.

79 crane (Grus nigricollis) is the only alpine crane species and is endemic to the Tibetan Plateau.

80 the red-crowned cranes are among the rarest crane species.

81 With the increased use of cranes, there has been more frequent occurrence of crane

82 e is little information on gut microbiota of cranes under different conservation strategies.

83 Crane vigilance declined with increasing distance from w

84 Increased frequency in crane vigilance only occurred in the much taller S. sals

85 ound that both the frequency and duration of crane vigilance significantly increased in the presence

86 tracking data from 105 reintroduced whooping cranes, we reveal an interplay between social and experi

87 Using 8 years of data on migrating whooping cranes, we were able to partition genetic and socially l

88 bred adolescent and artificially bred adult cranes were characterized by next-generation sequencing

89 reatest alpha diversity was found in captive cranes, while wild cranes had the least.

90 We fitted 23 cranes with telemetry devices and used remote sensing da