ライフサイエンスコーパス: goose

1 ouse, canvasback duck, tundra swan, and snow goose.

2 d to naive birds, and turkey infections with goose 15a/01 induced production of aMPV-specific antibod

3 V) recently isolated from wild Canada geese (goose 15a/01) in the United States, together with its re

4 However, increased snow goose abundance appeared to buffer this effect through p

5 d or 2-week-old turkeys vaccinated with live goose aMPV resulted in lower clinical scores in 33% of t

6 equence identity, and genome organization of goose aMPV were similar to those of turkey aMPV subtype

7 he promoters of the FAS genes in rat, human, goose and chicken is conserved regarding CBF-binding sit

8 onserved in the FAS promoters of rat, human, goose and chicken.

9 plant green-up, and this 'mismatch' between goose and plant phenologies could in turn affect gosling

10 cies (cattle, pig, chicken, turkey, duck and goose) and relatively stable during the meat aging and o

11 t as previously reported for the heron, Ross goose, and stork hepatitis B viruses, an AUG codon was f

12 Goose arrival at stopovers was more closely tied to the

13 ng-distance migrant, the light-bellied Brent goose (Branta bernicla hrota).

14 etically within a living species, the Canada goose (Branta canadensis) and is related most closely to

15 The barnacle goose (Branta leucopsis) is also nested within the Canad

16 of a trophic cascade, driven by Lesser Snow Goose (Chen caerulescens caerulescens) overgrazing on th

17 report that commercially available duck- or goose-derived foie gras contains birefringent congophili

18 h are homologous to a lytic transglycosylase goose egg white lysozyme domain and an NLPC_P60 domain (

19 d bacteriophage lytic transglycosylases, and goose egg white lysozyme.

20 The chicken and goose egg white lysozymes (ChEWL and GoEWL) are homologu

21 Snow goose family groups eventually responded to their own de

22 erse chemicals in fish oil, linseed oil, and goose fat at 37 degrees C.

23 affecting muscle integrity were examined in goose (GG) and duck (DG) gizzard smooth muscle stored at

24 90% of asymptotic size compared with Canada goose goslings fed 18% protein.

25 Canada goose goslings fed low-protein (10%) diets were on avera

26 Canada and snow goose goslings fed low-protein diets had reduced growth

27 rowth trajectories of Canada and lesser snow goose goslings raised on grass-based diets that differed

28 In contrast, snow goose goslings were unable to survive on the low-protein

29 n top chambers (OTCs) and to three levels of goose grazing pressure were assessed over two summer gro

30 showed that the virus clustered with the H5 Goose/Guandong/1/96 lineage and 1997 Hong Kong human iso

31 ons caused by a new clade (clade 2.2.1.1) of goose/Guangdong (gs/GD) lineage H5N1 viruses were report

32 Since the isolation of A/goose/Guangdong/1/1996 (H5N1) in farmed geese in souther

33 enic avian influenza (HPAI) viruses of the A/goose/Guangdong/1/96 (Gs/GD) lineage during 2005, 2010,

34 magglutinin and neuraminidase genes of the A/goose/Guangdong/1/96 (Gs/Gd) lineage.

35 elicited by immunization with viral HA of A/Goose/Guangdong/1/96 (H5N1), the immediate precursor of

36 A genes similar to those of the H5N1 virus A/goose/Guangdong/1/96 and five different combinations of

37 xes with H5 HAs of A/Vietnam/1203/2004 and A/Goose/Guangdong/1/96 reveal a conserved epitope in the H

38 Because A/goose/Guangdong/1/96-like (H5N1; Go/Gd) viruses are the

39 A/Goose/Guangdong/1/96-like H5N1 influenza viruses now cir

40 Shedding of A/Goose/Guangdong/1/96-like H5N1 virus by immunized chicke

41 enetically and are most closely related to A/Goose/Guangdong/1/96.

42 bird polyomaviruses (avian polyomavirus and goose hemorrhagic polyomavirus) from the mammalian polyo

43 Snow goose hepatitis B virus (SGHBV) is the only known hepadn

44 ck virus clones were closely related to Ross goose hepatitis B virus.

45 /duck/Hubei/49/05) or a weakly pathogenic (A/goose/Hubei/65/05) H5N1 virus.

46 y related to a WN virus isolated from a dead goose in Israel in 1998.

47 The peripheral isolation of the barnacle goose in the Palearctic apparently allowed the evolution

48 Phylogenetic analyses placed goose isolates in an independent cluster, and more notab

49 t lacking in psittacine ABVs were present in goose isolates.

50 es against herbivory by flightless geese and goose-like ducks that were extirpated by Polynesians wit

51 analysis showing that GPV-QH15 evolved from goose lineage parvoviruses, rather than from Muscovy duc

52 validity of this proposal by overexpressing goose malonyl-CoA decarboxylase (MCD) in INS-1 cells, bu

53 g frame showing 70.3% amino acid identity to goose malonyl-CoA decarboxylase (MCD).

54 rminal peroxisomal targeting sequence in the goose MCD construct, raising the possibility that a sign

55 g of this region has widened the gap between goose migration timing and plant green-up, and this 'mis

56 ative remains alive (the endangered Hawaiian goose or nene, Branta sandvicensis).

57 st that GPV-QH15 represents a new variant of goose-origin parvovirus that currently circulates in duc

58 found to be closely clustered with two known goose-origin parvoviruses (GPVa2006 and GPV1995), togeth

59 ed a parvovirus with a greater similarity to goose parvovirus (GPV) (97% protein homology) than to Mu

60 Goose parvovirus (GPV) is both autonomous and pathogenic

61 The goose parvovirus (GPV) Rep 1 and Rep 2 proteins are enco

62 The RNA transcription profile of the goose parvovirus (GPV) was determined, and it is a surpr

63 om AAV Rep78 and Rep1 of the closely related goose parvovirus.

64 l require further study to help predict snow goose population dynamics and manage the trophic cascade

65 warmer climate could negatively affect snow goose populations in the long-run, but it will depend on

66 While goose presence had little effect on aphid density or hos

67 ies were increased by OTCs but unaffected by goose presence in both years.

68 oth years and there was a significant OTC by goose presence interaction in 2004.

69 The giant Hawaii goose resembles the moa-nalos, a group of massive, extin

70 leucopsis) is also nested within the Canada goose species and is related most closely to the small-b

71 fluenza virus RNA sequences from an archival goose specimen collected in 1917, can also be explained

72 ing that Tse3 possesses one open accessible, goose-type lysozyme-like domain with peptidoglycan hydro

73 However, the goose virus contained the largest attachment (G) gene of

74 In vitro, the goose virus replicated to levels (2 x 10(5) to 5 x 10(5)

75 turkeys did not indicate the presence of the goose virus-like strain.

76 peptide markers unique to chicken, duck and goose were identified, with significant scores.

77 d and among 70 other Greenland white-fronted goose wintering subpopulations.