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1 , Crimean-Congo Hemorrhagic Fever, Nipah and Hendra viruses).
2 l as emerging viral threats (e.g., Nipah and Hendra viruses).
3 ts (Pteropus spp.), parameterized to reflect Hendra virus.
4 the zoonotic paramyxoviruses Nipah virus and Hendra virus.
5 the zoonotic paramyxoviruses Nipah virus and Hendra virus.
6 to protect them from a lethal infection with Hendra virus.
7 l emerging pathogens such as Nipah virus and Hendra virus.
8 ar to the closely related zoonotic Nipah and Hendra viruses.
9 al tropism and cellular effects of Nipah and Hendra viruses.
10 red by envelope glycoproteins of the related Hendra virus and another paramyxovirus.
11      Seropositive human sera also neutralize Hendra virus and Gh-M74a (an African HNV) pseudoparticle
12                                              Hendra virus and Nipah virus (NiV) are lethal, zoonotic
13  at plasma membrane budding sites.IMPORTANCE Hendra virus and Nipah virus are zoonotic paramyxoviruse
14 ily, which includes emerging viruses such as Hendra virus and Nipah virus as well as many important h
15 athogens as well as emerging viruses such as Hendra virus and Nipah virus.
16 za virus type 5, measles virus, mumps virus, Hendra virus, and Nipah virus.
17  family Paramxyoviridae, including Nipah and Hendra viruses, and the family Filoviridae, including Eb
18 Highly lethal pathogens (e.g., hantaviruses, hendra virus, anthrax, or plague) pose unique public-hea
19                        Nipah virus (NiV) and Hendra virus are the type species of the highly pathogen
20                              Nipah virus and Hendra virus are two paramyxoviruses associated with hig
21                                            A Hendra virus attachment (G) glycoprotein subunit vaccine
22 mergent deadly viruses Nipah virus (NiV) and Hendra virus belong to the Henipavirus genus in the Para
23                                          The Hendra virus CBF(2) Y79A and P89A mutants showed signifi
24                     For both Nipah virus and Hendra virus, contact between the V protein and the PLK1
25               We here analyse three years of Hendra virus data from nine Australian flying fox roosts
26  C-terminal proline residues was observed in Hendra virus-derived peptides presented by Ptal-N*01:01
27 activity inhibited proteolytic processing of Hendra virus F but had no effect on simian virus 5 F pro
28 e examined the intracellular distribution of Hendra virus F following endocytosis and showed that it
29 somal protease cathepsin L, but the route of Hendra virus F following internalization and the recycli
30                  To be fusogenically active, Hendra virus F must undergo endocytic recycling and clea
31 ed a nondetectable amount of cleavage of the Hendra virus F protein and significantly decreased membr
32 d to demonstrate that isolated TM domains of Hendra virus F protein associate in a monomer-trimer equ
33 that endocytosis is critically important for Hendra virus F protein cleavage, representing a new para
34 y identify the class of protease involved in Hendra virus F protein cleavage, Vero cells transfected
35                                          The Hendra virus F protein cytoplasmic tail contains a conse
36  the unique endocytic trafficking pathway of Hendra virus F protein is required for proper viral asse
37 leavage motif, cleavage of the newly emerged Hendra virus F protein occurs by a previously unidentifi
38 cessing and membrane fusion promotion of the Hendra virus F protein, mutation of tyrosine 525 to alan
39                                              Hendra virus F protein-promoted membrane fusion requires
40 of CBF1 in both the simian virus 5 (SV5) and Hendra virus F proteins.
41 created in both the simian virus 5 (SV5) and Hendra virus F proteins.
42  virus F TMDs correlated with alterations to Hendra virus F recycling, suggesting that appropriate TM
43  Y498 were found to be important for correct Hendra virus F recycling, with the hydroxyl group of S49
44 ched residues was found, and analysis of the Hendra virus F TM domain revealed a heptad repeat leucin
45 rt a model whereby the C-terminal end of the Hendra virus F TMD is an important regulator of TMD-TMD
46 addition, changes in association of isolated Hendra virus F TMDs correlated with alterations to Hendr
47                                              Hendra virus F transmembrane domain (TMD) residues S490
48  fusion peptide is an important regulator of Hendra virus F triggering.
49    The levels of surface expression for both Hendra virus F Y525A and Hendra virus F Y525F were highe
50                   The rate of endocytosis of Hendra virus F Y525A was significantly reduced compared
51 rotein, mutation of tyrosine 525 to alanine (Hendra virus F Y525A) or phenylalanine (Hendra virus F Y
52  of proteolytic processing were observed for Hendra virus F Y525A, although initial transport to the
53 expression for both Hendra virus F Y525A and Hendra virus F Y525F were higher than that of the wt pro
54 ine (Hendra virus F Y525A) or phenylalanine (Hendra virus F Y525F) was performed.
55 ediate level of endocytosis was observed for Hendra virus F Y525F.
56 d human cathepsin L processed immunopurified Hendra virus F(0) into F(1) and F(2) fragments.
57 ory pathway trafficking than is observed for Hendra virus F.
58      Further characterization reveals that a Hendra virus-F-specific nAb (mAb36) and many antibodies
59 d-use change, bat behaviour and spillover of Hendra virus from Pteropodid bats to horses in subtropic
60                                          The Hendra virus fusion (F) protein contains five potential
61                            Triggering of the Hendra virus fusion (F) protein is required to initiate
62                                          The Hendra virus fusion (F) protein is synthesized as a prec
63                  Proteolytic cleavage of the Hendra virus fusion (F) protein results in the formation
64      Results presented here demonstrate that Hendra virus G undergoes slower secretory pathway traffi
65                                     Instead, Hendra virus G was found to undergo intrinsically slow o
66 d messenger RNA vaccine encoding the soluble Hendra virus glycoprotein protected up to 70% of Syrian
67            The V proteins of Nipah virus and Hendra virus have been demonstrated to bind to cellular
68                                              Hendra virus (HeV) and Nipah virus (NiV) are bat-borne z
69                                              Hendra virus (HeV) and Nipah virus (NiV) are closely rel
70                                              Hendra virus (HeV) and Nipah virus (NiV) are closely rel
71                                              Hendra virus (HeV) and Nipah virus (NiV) are closely rel
72                                              Hendra virus (HeV) and Nipah virus (NiV) are deadly zoon
73                                              Hendra virus (HeV) and Nipah virus (NiV) are deadly zoon
74              The emerging zoonotic pathogens Hendra virus (HeV) and Nipah virus (NiV) are in the genu
75                                              Hendra virus (HeV) and Nipah virus (NiV) are reportedly
76                                              Hendra virus (HeV) and Nipah virus (NiV) belong to the g
77                                              Hendra virus (HeV) and Nipah virus (NiV) constitute the
78 n henipaviruses (HNVs) related to pathogenic Hendra virus (HeV) and Nipah virus (NiV) from Southeast
79                           The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are capable of
80                           The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are emerging z
81                           The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are paramyxovi
82               The genus Henipavirus includes Hendra virus (HeV) and Nipah virus (NiV), for which frui
83 n infants, and the emerging zoonotic viruses Hendra virus (HeV) and Nipah virus (NiV), which cause le
84  viruses carried by the Pteropid fruit bats: Hendra virus (HeV) and Nipah virus (NiV).
85 ghly pathogenic emerging zoonotic pathogens, Hendra virus (HeV) and Nipah virus (NiV).
86 sk posed by related henipaviruses, including Hendra virus (HeV) and Nipah virus Malaysia (NiVM), is l
87 ere tested for the presence of antibodies to Hendra virus (HeV) and Nipah virus, and tested for the p
88 unknown, receptor than Nipah virus (NiV) and Hendra virus (HeV) and that NiV- and HeV-elicited monocl
89                        Nipah virus (NiV) and Hendra virus (HeV) are closely related henipaviruses of
90                        Nipah virus (NiV) and Hendra virus (HeV) are closely related, recently emerged
91                        Nipah virus (NiV) and Hendra virus (HeV) are emerging zoonotic viruses and the
92                        Nipah virus (NiV) and Hendra virus (HeV) are novel paramyxoviruses from pigs a
93                        Nipah virus (NiV) and Hendra virus (HeV) are paramyxoviruses capable of causin
94                        Nipah virus (NiV) and Hendra virus (HeV) are pathogenic paramyxoviruses that c
95                        Nipah virus (NiV) and Hendra virus (HeV) are recently emergent zoonotic and hi
96                        Nipah virus (NiV) and Hendra virus (HeV) are zoonotic henipaviruses (HNVs) res
97                        Nipah virus (NiV) and Hendra virus (HeV) are zoonotic henipaviruses (HNVs) res
98                        Nipah virus (NiV) and Hendra virus (HeV) are zoonotic paramyxoviruses that cau
99 nd sequence similarities between the NiV and Hendra virus (HeV) attachment G glycoproteins, and the e
100 nal antibodies against Nipah virus (NiV) and Hendra virus (HeV) by panning a large nonimmune antibody
101  henipaviruses such as Nipah virus (NiV) and Hendra virus (HeV) cause respiratory symptoms, with seve
102  for HeV fusion.IMPORTANCE The paramyxovirus Hendra virus (HeV) causes severe respiratory illness and
103             Seven of ten antibodies bind the Hendra virus (HeV) F protein.
104    To examine the sequence dependence of the Hendra virus (HeV) fusion (F) protein FP, the first eigh
105 antibody (mAb) cross-reactive to the NiV and Hendra virus (HeV) G glycoprotein, m102.4, has been test
106 ation of structures of Nipah virus (NiV) and Hendra virus (HeV) G glycoproteins bound and unbound to
107 ative, in complex with the GP of the related Hendra Virus (HeV) has been solved, the structural inter
108                                              Hendra virus (HeV) is a member of the broadly tropic and
109                                              Hendra virus (HeV) is a recently identified paramyxoviru
110                                              Hendra virus (HeV) is a zoonotic emerging virus belongin
111                                              Hendra virus (HeV) is a zoonotic paramyxovirus that caus
112                                              Hendra virus (HeV) is a zoonotic paramyxovirus that util
113                                              Hendra virus (HeV) is an emerging paramyxovirus capable
114                                              Hendra virus (HeV) is an emerging pathogen of concern in
115                                              Hendra virus (HeV) is one of the two prototypical member
116 genome systems for the Nipah virus (NiV) and Hendra virus (HeV) that provide a convenient alternative
117 e show that the attachment glycoprotein G of Hendra virus (HeV), a deadly paramyxovirus, is N-glycosy
118                                 The zoonotic Hendra virus (HeV), a member of the family Paramyxovirid
119 nipaviruses, including Nipah virus (NiV) and Hendra virus (HeV), are biosafety level 4 (BSL-4) zoonot
120     The henipaviruses, Nipah virus (NiV) and Hendra virus (HeV), are lethal emerging paramyxoviruses.
121                        Nipah virus (NiV) and Hendra virus (HeV), members of the Henipavirus genus in
122 d apoptosis.IMPORTANCE Nipah virus (NiV) and Hendra virus (HeV), members of the Henipavirus genus, ar
123 henipavirus related to Nipah virus (NiV) and Hendra virus (HeV), zoonotic agents of fatal human disea
124 s a known reservoir of Nipah virus (NiV) and Hendra virus (HeV).
125 l cleavage site and efficient propagation of Hendra virus in a furin-deficient cell line indicate tha
126 as measles, mumps, parainfluenza, Nipah, and Hendra viruses, infect host cells by directing fusion of
127 were completely protected against subsequent Hendra virus infection and disease.
128 g species, as well as specific insights into Hendra virus infection dynamics and spillover risk in a
129                                              Hendra virus is a highly pathogenic paramyxovirus classi
130                    The fusion (F) protein of Hendra virus is critical for promoting viral entry and c
131       We found that for both Nipah virus and Hendra virus, M protein expression in the absence of any
132                                    Nipah and Hendra viruses (NiV and HeV) exhibit high lethality in h
133 nsically disordered C-terminal domain of the Hendra virus nucleoprotein (NTAIL) and compared its inte
134                                              Hendra virus outbreaks in Australia, all involving horse
135 se cathepsin L is involved in converting the Hendra virus precursor F protein (F(0)) to the active F(
136 ry and vein cells highlighted that Nipah and Hendra viruses preferentially infected arteries; arterie
137 restingly, MDC-mediated capture of Nipah and Hendra virus (recently emerged zoonotic paramyxoviruses)
138 logous to the fusion protein of the zoonotic Hendra virus reduced protein expression and fusion activ
139    Batborne henipaviruses, such as Nipah and Hendra viruses, represent a major threat to global healt
140 ing Ebola virus, Marburg virus, Nipah virus, Hendra virus, severe acute respiratory syndrome coronavi
141  disease, henipaviruses, including Nipah and Hendra viruses, use different members of one protein fam
142 Here we demonstrate that the closely related Hendra virus V protein also inhibits cellular responses
143 sidue 199 mediates the PLK1 interaction with Hendra virus V protein.
144  infection of human vasculature by Nipah and Hendra viruses, which are extraordinarily deadly (~57%-5
145  the cell entry receptor for Nipah virus and Hendra virus, zoonotic viruses that can cause respirator

 
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