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1 into recombinant A/Vietnam/1203/04 (VN1203) H5N1 influenza virus.
2 ckens (B(2)/B(2)) protected them from lethal H5N1 influenza virus.
3 protected mice from a lethal challenge with H5N1 influenza virus.
4 ted with a lethal dose of A/Vietnam/1203/04 (H5N1) influenza virus.
5 ed with 10-100 MLD50 of H1N1, H3N1, H3N2 and H5N1 influenza viruses.
6 otential as live attenuated vaccines against H5N1 influenza viruses.
7 ogens and stimulate cross-protection against H5N1 influenza viruses.
8 1) against antigenically distinct strains of H5N1 influenza viruses.
9 duck has become the "Trojan horse" of Asian H5N1 influenza viruses.
10 uation and spread of these highly pathogenic H5N1 influenza viruses.
11 d create a situation for the perpetuation of H5N1 influenza viruses.
12 we developed two antibodies that neutralize H5N1 influenza viruses.
13 se the transmissibility of highly pathogenic H5N1 influenza viruses.
14 le in the pathogenicity of highly pathogenic H5N1 influenza viruses.
15 caused by the highly pathogenic avian (HPAI) H5N1 influenza viruses.
16 and risk assessment of currently circulating H5N1 influenza viruses.
17 ion of the lethally infected mice by H1N1 or H5N1 influenza viruses.
18 ng the pandemic potential of recent Egyptian H5N1 influenza viruses.
19 mic virus as well as heterosubtypic H3N2 and H5N1 influenza viruses.
20 ent neutralizing antibody responses to avian H5N1 influenza viruses.
21 for a few persistent host markers than avian H5N1 influenza viruses.
22 enuated vaccine strains based on recombinant H5N1 influenza virus A/Viet Nam/1203/04 was generated.
23 In this report, the natural history of the H5N1 influenza virus A/Vietnam/1203/04 influenza infecti
25 he pandemic potential of widely disseminated H5N1 influenza viruses, a ferret contact model using exp
26 e dose of an antigenically variant strain of H5N1 influenza virus and could be a useful strategy for
27 tively replicate in macrophages is unique to H5N1 influenza viruses and may contribute to their incre
28 H5 HA receptor-binding site that neutralized H5N1 influenza viruses and pseudoviruses carrying the HA
29 e immunity against the currently circulating H5N1 influenza viruses and that this protective immunity
30 eriodic outbreaks of highly pathogenic avian H5N1 influenza viruses and the current H1N1 pandemic hig
32 specificities of two highly efficacious anti-H5N1 influenza virus antibodies into a bispecific FcDART
33 results show that the PA and PB1 genes of HP H5N1 influenza viruses are associated with lethality in
36 , clinical, and laboratory data suggest that H5N1 influenza viruses are transmitted through and predo
39 ot be as effective against highly pathogenic H5N1 influenza viruses as they are against less pathogen
42 of malaria falciparum (LSA-NRC) or HA1 from H5N1 influenza virus ('avian flu'), the system selected
44 e substantial efforts to control and contain H5N1 influenza viruses, bird flu viruses continue to spr
45 earlier survived the lethal challenge of an H5N1 influenza virus, but infected birds shed H5N1 influ
46 n subject demonstrates that vaccination with H5N1 influenza virus can elicit B cells expressing stem
47 in late 2002, outbreaks of highly pathogenic H5N1 influenza virus caused deaths among wild migratory
48 tected ferrets against lethal heterosubtypic H5N1 influenza virus challenge despite the absence of de
49 otection against a lethal A/Duck/Laos/25/06 (H5N1) influenza virus challenge, with no evidence of mor
51 r of human infections with highly pathogenic H5N1 influenza viruses continues to rise, these viruses
52 ted that exposure of the digestive system to H5N1 influenza viruses could initiate infection either t
55 us to ask whether waterfowl are resistant to H5N1 influenza virus disease and whether they can still
57 on the contribution of HA acid stability to H5N1 influenza virus fitness and transmissibility in mam
58 The data suggest that adaptation of avian H5N1 influenza virus for infection in mammals is support
63 n IAVs, recent isolates of highly pathogenic H5N1 influenza viruses had a high proportion of PB1-F2 t
64 s of oseltamivir-resistant highly pathogenic H5N1 influenza viruses has important clinical implicatio
66 ction of humans with highly pathogenic avian H5N1 influenza viruses has suggested viral mutation as o
67 uch mechanisms and virulent determinants for H5N1 influenza viruses have not been fully elucidated.
69 rus-like particles (VLP) (M8-VLP) expressing H5N1 influenza virus hemagglutinin (HA) and neuraminidas
71 HA protein influence the fitness of an avian H5N1 influenza virus in a mammalian model, we infected C
75 influenza virus did not cross-react with an H5N1 influenza virus in neutralization or hemagglutinati
76 acheal inoculation of a liquid suspension of H5N1 influenza virus in nonhuman primates likely results
77 d with recent, widely circulating strains of H5N1 influenza virus in poultry, the recurring introduct
78 tation was found to enhance the growth of an H5N1 influenza virus in the mammalian upper respiratory
81 lay critical roles in the virulence of avian H5N1 influenza viruses in a mammalian host in vitro and
84 read distribution of highly pathogenic avian H5N1 influenza viruses in domesticated and wild birds co
85 otein plays a key role in the propagation of H5N1 influenza viruses in ducks and may be a novel molec
87 findings indicate that the human and poultry H5N1 influenza viruses in Hong Kong in 1997 were reassor
88 Since the reemergence of highly pathogenic H5N1 influenza viruses in humans in 2003, these viruses
91 rotected chickens from lethal infection with H5N1 influenza viruses in the Hong Kong markets in 1997
95 ntinuing evolution of highly pathogenic (HP) H5N1 influenza viruses in wild birds with transmission t
98 tes, and administration of STAg 2 days after H5N1 influenza virus infection enhanced survival, lowere
99 asma gondii prior to highly pathogenic avian H5N1 influenza virus infection led to decreased lung vir
101 enous IFN-gamma alone enhanced survival from H5N1 influenza virus infection, although not to the same
103 atory cytokines are markedly elevated during H5N1 influenza virus infection, the "cytokine storm" is
104 TNF-alpha may contribute to morbidity during H5N1 influenza virus infection, while IL-1 may be import
105 he protective immune response against severe H5N1 influenza virus infections even when a single dose
106 y differs from human highly pathogenic avian H5N1 influenza virus infections, there is a similar rapi
110 olution, from a highly pathogenic Vietnamese H5N1 influenza virus, is more related to the 1918 and ot
111 type, we cloned the human A/Vietnam/1203/04 (H5N1) influenza virus isolate that is highly pathogenic
113 report that the polymerase PB2 protein of an H5N1 influenza virus isolated from a human in Vietnam (A
114 ared to those of a highly pathogenic chicken H5N1 influenza virus isolated from Hong Kong in April 19
115 ulated mallards with antigenically different H5N1 influenza viruses isolated between 1997 and 2003.
117 ra tested, 8 (0.25%) were positive for avian H5N1 influenza viruses isolated in 2004 by virus neutral
118 oculated juvenile mallards with 23 different H5N1 influenza viruses isolated in Asia between 2003 and
126 ntification of amino-acid mutations in avian H5N1 influenza virus polymerase complexes that confer in
131 the digestive tract is not the main site of H5N1 influenza virus replication in ducks and that the f
132 The threat posed by the highly pathogenic H5N1 influenza virus requires public health authorities
134 ith the highly pathogenic A/Vietnam/1203/04 (H5N1) influenza virus strain; the vaccines encoded influ
135 y a subset of highly pathogenic avian (HPAI) H5N1 influenza virus strains could productively replicat
137 l genes of Qa/HK/G1/97 virus to those of the H5N1 influenza viruses suggests that the quail virus may
138 searchers announced that they had created an H5N1 influenza virus that was transmissible between ferr
140 recent emergence of highly pathogenic avian (H5N1) influenza viruses, their epizootic and panzootic n
141 n of DNA target sequences derived from avian H5N1 influenza virus to gold surface-attached single-str
143 onal transmission of highly pathogenic avian H5N1 influenza viruses to humans causes severe pneumonia
144 Multiple cases of transmission of avian H5N1 influenza viruses to humans illustrate the urgent n
151 oadly specific against antigenically drifted H5N1 influenza viruses, we developed two neutralizing mo
152 late the acid stability of the HA protein of H5N1 influenza viruses, we performed a mutational analys
153 or by aerosols with a human (H3N2) or avian (H5N1) influenza virus, we demonstrate that aerosol inocu
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