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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 oose Anser fabalis and Greater White-fronted Goose A. albifrons, are representative examples and they
5                      However, increased snow goose abundance appeared to buffer this effect through p
6 d or 2-week-old turkeys vaccinated with live goose aMPV resulted in lower clinical scores in 33% of t
7 equence identity, and genome organization of goose aMPV were similar to those of turkey aMPV subtype
8 ide-based LC-MS methods for monitoring duck, goose and chicken in processed meat products.
9 he promoters of the FAS genes in rat, human, goose and chicken is conserved regarding CBF-binding sit
10 h allows high-confidence monitoring of duck, goose and chicken meat (ten specific peptides), simultan
11 onserved in the FAS promoters of rat, human, goose and chicken.
12  proteins, and illegal substitution of veal, goose and duck meat with cheaper pork.
13  plant green-up, and this 'mismatch' between goose and plant phenologies could in turn affect gosling
14 cies (cattle, pig, chicken, turkey, duck and goose) and relatively stable during the meat aging and o
15 t as previously reported for the heron, Ross goose, and stork hepatitis B viruses, an AUG codon was f
16 ntified from poultry samples (i.e., chicken, goose, and turkey), including viruses associated with ac
17 Russian migratory populations of Tundra Bean Goose Anser fabalis and Greater White-fronted Goose A. a
18 ort a new, genetically distinct pegivirus in goose (Anser cygnoides), the first identified in a nonma
19                                              Goose arrival at stopovers was more closely tied to the
20 es significant advancements in understanding goose-beaked whale behavior at depth over long time scal
21                                              Goose-beaked whales (Ziphius cavirostris) are a deep-div
22  (DOA) localization to track the position of goose-beaked whales from echolocation clicks recorded on
23               Overall, 2738 tracks of diving goose-beaked whales were processed from acoustic recordi
24 long-lived, long-distance migrant, the Brent goose Branta bernicla hrota over periods of months to ye
25 ng-distance migrant, the light-bellied Brent goose (Branta bernicla hrota).
26 etically within a living species, the Canada goose (Branta canadensis) and is related most closely to
27                                 The barnacle goose (Branta leucopsis) is also nested within the Canad
28                       The Greenland barnacle goose (Branta leucopsis) population has increased tenfol
29  of a trophic cascade, driven by Lesser Snow Goose (Chen caerulescens caerulescens) overgrazing on th
30 tbreak risk in remaining sites due to larger goose congregations, and 3) facilitate AIV transmission
31 atures that distinguish the genome of Canada goose coronavirus include 6 novel ORFs, a partial duplic
32                               We showed that goose decision-making varied across landcover types, eco
33  report that commercially available duck- or goose-derived foie gras contains birefringent congophili
34 h are homologous to a lytic transglycosylase goose egg white lysozyme domain and an NLPC_P60 domain (
35 d bacteriophage lytic transglycosylases, and goose egg white lysozyme.
36                              The chicken and goose egg white lysozymes (ChEWL and GoEWL) are homologu
37 ) can be propagated in goslings, embryonated goose eggs, and primary goose embryo fibroblasts, and is
38 oslings, embryonated goose eggs, and primary goose embryo fibroblasts, and is thus the first pegiviru
39                                         Snow goose family groups eventually responded to their own de
40 erse chemicals in fish oil, linseed oil, and goose fat at 37 degrees C.
41 ing a human-animal interaction-a woman and a goose-from the Late Epipaleolithic (c.
42  affecting muscle integrity were examined in goose (GG) and duck (DG) gizzard smooth muscle stored at
43  90% of asymptotic size compared with Canada goose goslings fed 18% protein.
44                                       Canada goose goslings fed low-protein (10%) diets were on avera
45                              Canada and snow goose goslings fed low-protein diets had reduced growth
46 rowth trajectories of Canada and lesser snow goose goslings raised on grass-based diets that differed
47                            In contrast, snow goose goslings were unable to survive on the low-protein
48 n top chambers (OTCs) and to three levels of goose grazing pressure were assessed over two summer gro
49  showed that the virus clustered with the H5 Goose/Guandong/1/96 lineage and 1997 Hong Kong human iso
50 ons caused by a new clade (clade 2.2.1.1) of goose/Guangdong (gs/GD) lineage H5N1 viruses were report
51 America, HPAI A(H5N1) viruses related to the goose/Guangdong 2.3.4.4b hemagglutinin phylogenetic clad
52                     Since the isolation of A/goose/Guangdong/1/1996 (H5N1) in farmed geese in souther
53 enic avian influenza (HPAI) viruses of the A/Goose/Guangdong/1/1996 lineage (GsGd), which threaten th
54                        The introduction of A/goose/Guangdong/1/1996 lineage highly pathogenic (HP) cl
55  avian influenza (HPAI) H5 viruses, of the A/goose/Guangdong/1/1996 lineage, have exhibited substanti
56 enic avian influenza (HPAI) viruses of the A/goose/Guangdong/1/96 (Gs/GD) lineage during 2005, 2010,
57 magglutinin and neuraminidase genes of the A/goose/Guangdong/1/96 (Gs/Gd) lineage.
58  elicited by immunization with viral HA of A/Goose/Guangdong/1/96 (H5N1), the immediate precursor of
59 A genes similar to those of the H5N1 virus A/goose/Guangdong/1/96 and five different combinations of
60 c avian influenza (HPAI) viruses of the H5 A/goose/Guangdong/1/96 lineage can cause severe disease in
61 enic avian influenza (HPAI) viruses of the A/goose/Guangdong/1/96 lineage continue to circulate widel
62        H5N1 avian influenza viruses of the A/goose/Guangdong/1/96 lineage have been circulating in wi
63 avian influenza (HPAI) H5Nx viruses of the A/Goose/Guangdong/1/96 lineage in birds regularly causes i
64 xes with H5 HAs of A/Vietnam/1203/2004 and A/Goose/Guangdong/1/96 reveal a conserved epitope in the H
65                                            A/goose/Guangdong/1/96-like (GsGd) highly pathogenic avian
66                                    Because A/goose/Guangdong/1/96-like (H5N1; Go/Gd) viruses are the
67                                            A/Goose/Guangdong/1/96-like H5N1 influenza viruses now cir
68                                Shedding of A/Goose/Guangdong/1/96-like H5N1 virus by immunized chicke
69 enetically and are most closely related to A/Goose/Guangdong/1/96.
70 hogenic avian influenza virus (HPAIV) H5N1 A/goose/Guangdong/1996 (Gs/GD) lineage in the agricultural
71 hogenic avian influenza virus (HPAIV) H5N1 A/goose/Guangdong/1996 lineage (Gs/GD) is endemic in poult
72 avian influenza (HPAI) viruses from the H5Nx Goose/Guangdong/96 lineage continue to cause outbreaks i
73 ANCE Outbreaks of H5Nx HPAI viruses from the goose/Guangdong/96 lineage continue to occur in many cou
74  bird polyomaviruses (avian polyomavirus and goose hemorrhagic polyomavirus) from the mammalian polyo
75                                         Snow goose hepatitis B virus (SGHBV) is the only known hepadn
76 ck virus clones were closely related to Ross goose hepatitis B virus.
77 /duck/Hubei/49/05) or a weakly pathogenic (A/goose/Hubei/65/05) H5N1 virus.
78 y related to a WN virus isolated from a dead goose in Israel in 1998.
79     The peripheral isolation of the barnacle goose in the Palearctic apparently allowed the evolution
80                               The bar-headed goose is famed for migratory flight at extreme altitude.
81                 Phylogenetic analyses placed goose isolates in an independent cluster, and more notab
82 t lacking in psittacine ABVs were present in goose isolates.
83 es against herbivory by flightless geese and goose-like ducks that were extirpated by Polynesians wit
84  analysis showing that GPV-QH15 evolved from goose lineage parvoviruses, rather than from Muscovy duc
85  validity of this proposal by overexpressing goose malonyl-CoA decarboxylase (MCD) in INS-1 cells, bu
86 g frame showing 70.3% amino acid identity to goose malonyl-CoA decarboxylase (MCD).
87 rminal peroxisomal targeting sequence in the goose MCD construct, raising the possibility that a sign
88 g of this region has widened the gap between goose migration timing and plant green-up, and this 'mis
89                         We collected data on goose numbers and weather conditions from 1975 to 2017 t
90 ative remains alive (the endangered Hawaiian goose or nene, Branta sandvicensis).
91 st that GPV-QH15 represents a new variant of goose-origin parvovirus that currently circulates in duc
92 found to be closely clustered with two known goose-origin parvoviruses (GPVa2006 and GPV1995), togeth
93 Forbidden City, Temple of Heaven, Giant Wild Goose Pagoda, Terracotta Warriors, and Mogao Grottoes),
94 ed a parvovirus with a greater similarity to goose parvovirus (GPV) (97% protein homology) than to Mu
95                                              Goose parvovirus (GPV) is both autonomous and pathogenic
96                                          The goose parvovirus (GPV) Rep 1 and Rep 2 proteins are enco
97         The RNA transcription profile of the goose parvovirus (GPV) was determined, and it is a surpr
98 eriments show GPgV lymphotropism and promote goose parvovirus clinical manifestations.
99 PgV could promote clinical manifestations of goose parvovirus infection, including reduced weight gai
100 om AAV Rep78 and Rep1 of the closely related goose parvovirus.
101                                              Goose pegivirus (GPgV) can be propagated in goslings, em
102  Here, we report a phylogenetically distinct goose pegivirus (GPgV) that should be classified as a ne
103 l require further study to help predict snow goose population dynamics and manage the trophic cascade
104                                          The goose population has doubled in size during the past 25
105  warmer climate could negatively affect snow goose populations in the long-run, but it will depend on
106 c peptide markers from meats (chicken, duck, goose, pork and beef) and common protein allergenic addi
107                                        While goose presence had little effect on aphid density or hos
108 ies were increased by OTCs but unaffected by goose presence in both years.
109 oth years and there was a significant OTC by goose presence interaction in 2004.
110                             The giant Hawaii goose resembles the moa-nalos, a group of massive, extin
111  leucopsis) is also nested within the Canada goose species and is related most closely to the small-b
112 fluenza virus RNA sequences from an archival goose specimen collected in 1917, can also be explained
113 ure and precipitation and Greenland barnacle goose survival and productivity over a 50 year period fr
114 mythological scene between the woman and the goose that is consistent with an animistic belief system
115 d directly from the cloacal swab of a Canada goose that perished in a die-off of Canada and Snow gees
116 ing that Tse3 possesses one open accessible, goose-type lysozyme-like domain with peptidoglycan hydro
117  landscapes is a likely mechanism explaining goose use of highly variable ecosystems during winter in
118                                 However, the goose virus contained the largest attachment (G) gene of
119                                In vitro, the goose virus replicated to levels (2 x 10(5) to 5 x 10(5)
120 turkeys did not indicate the presence of the goose virus-like strain.
121  peptide markers unique to chicken, duck and goose were identified, with significant scores.
122 d and among 70 other Greenland white-fronted goose wintering subpopulations.
123 uctive allocation in a long-lived species of goose, with a particular emphasis on the effect of posit

 
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