戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 as identified recently as a receptor for the hepatitis A virus.
2 ths were Salmonella Typhi, Taenia solium and hepatitis A virus.
3 fectively prevented with vaccination against hepatitis A virus.
4 rent infection as the community reservoir of hepatitis A virus.
5 e genome is conserved among strains, such as hepatitis A virus.
6 solate, respectively, of the HM175 strain of hepatitis A virus.
7 the parameters for the ubiquitination of the hepatitis A virus 3C protease are K(m) = 20 +/- 5 microm
8 we amplified virtually the entire genomes of hepatitis A virus (a member of the Picornaviridae family
9 andomization, 1414 (31%) were susceptible to hepatitis A virus and 1090 were eligible for the per-pro
10                      However, recent work on hepatitis A virus and hepatitis E virus challenges this
11 multiple human maladies, yet currently, only hepatitis A virus and poliovirus can be controlled with
12 ad through the oral-fecal route (salmonella, hepatitis A virus), and organisms spread through direct
13 , Chlamydia pneumoniae, Helicobacter pylori, hepatitis A virus, and herpes simplex virus-1 were measu
14 fter vaccination were tested for antibody to hepatitis A virus (anti-HAV) by ELISA.
15 f passively transferred maternal antibody to hepatitis A virus (anti-HAV) on the duration of seroposi
16                                Antibodies to hepatitis A virus (anti-HAV) were measured in children f
17 es of the encephalomyocarditis virus and the hepatitis A virus are both type III substrates for the m
18  rhinovirus, encephalomyocarditis virus, and hepatitis A virus) are morphologically similar, comprisi
19 enteric viruses, such as Human Norovirus and Hepatitis A Virus, are readily transmitted via the fecal
20 cally linked to asthma and is a receptor for hepatitis A virus, but the endogenous ligand of TIM-1 is
21 an KIM-1 exhibits homology to a monkey gene, hepatitis A virus cell receptor 1 (HAVcr-1), which was i
22                                          The hepatitis A virus cellular receptor 1 (HAVcr-1) cDNA cod
23                                          The hepatitis A virus cellular receptor 1 (HAVcr-1) cDNA was
24 e toxin binds to protein receptors including hepatitis A virus cellular receptor 1 (HAVCR1), but the
25                                          The hepatitis A virus cellular receptor 1 (HAVCR1/TIM1), a m
26 expression of the inhibitory receptors PD-1, hepatitis A virus cellular receptor 2 (TIM3), lymphocyte
27 in-containing protein 3 (TIM3, also known as hepatitis A virus cellular receptor 2), and their respec
28 munized sequentially with tetanus toxoid and hepatitis A virus failed to develop antibody to either a
29                                 Sequences of hepatitis A virus from all 170 patients who were tested
30                                              Hepatitis A virus genotype IB was identified in 144 of 1
31                                              Hepatitis A virus genotype IB, uncommon in the Americas,
32 dministered to persons after exposure to the hepatitis A virus has not been compared directly with im
33                         Herein, we show that hepatitis A virus (HAV) 3C protease (3Cpro) cleaves NEMO
34   Vaccination provides long-term immunity to hepatitis A virus (HAV) among the general population, bu
35 lages in rural Alaska between 2 epidemics of hepatitis A virus (HAV) and after the second epidemic (1
36 ess the protective 190/4 epitope, they bound hepatitis A virus (HAV) and gained limited susceptibilit
37                                              Hepatitis A virus (HAV) and hepatitis C virus (HCV) are
38 irus B3, human rhinovirus 14, mengovirus, or hepatitis A virus (HAV) capsid proteins were supplied in
39                         To determine whether hepatitis A virus (HAV) could tolerate the insertion of
40                                              Hepatitis A virus (HAV) differs from other members of th
41                                              Hepatitis A virus (HAV) encodes a single polyprotein whi
42                                              Hepatitis A virus (HAV) has been adapted to grow efficie
43                                              Hepatitis A virus (HAV) immunoassays use cell culture-de
44                           Fecal excretion of hepatitis A virus (HAV) in 18 patients with HAV infectio
45                               Replication of hepatitis A virus (HAV) in cultured cells is inefficient
46 r highly specific and sensitive detection of hepatitis A virus (HAV) in food and water are of particu
47             The possible association between hepatitis A virus (HAV) infection and coronary artery di
48                                              Hepatitis A virus (HAV) infection can stimulate the prod
49             Acute liver failure (ALF) due to hepatitis A virus (HAV) infection is an uncommon but pot
50                We describe a murine model of hepatitis A virus (HAV) infection that recapitulates cri
51                                              Hepatitis A virus (HAV) infection typically resolves wit
52 on has dramatically reduced the incidence of hepatitis A virus (HAV) infection, but new infections co
53 n of HEV infection has broad similarities to hepatitis A virus (HAV) infection, with most cases being
54 ed prospectively in natural and experimental hepatitis A virus (HAV) infection.
55                                              Hepatitis A virus (HAV) infects African green monkey kid
56                                              Hepatitis A virus (HAV) infects African green monkey kid
57                              Remarkably, the hepatitis A virus (HAV) IRES requires eIF4E for its tran
58                                              Hepatitis A virus (HAV) is a hepatotropic picornavirus t
59                                              Hepatitis A virus (HAV) is an ancient and ubiquitous hum
60                                              Hepatitis A virus (HAV) is an hepatotropic human picorna
61                 Unlike other picornaviruses, hepatitis A virus (HAV) is cloaked in host membranes whe
62                                              Hepatitis A virus (HAV) is naturally transmitted by the
63 the high-risk groups for vaccination against hepatitis A virus (HAV) is unlikely to have a significan
64                   The genetic relatedness of hepatitis A virus (HAV) isolates was determined to ident
65                                  The current Hepatitis A virus (HAV) molecular epidemiology in Israel
66                             Coinfection with hepatitis A virus (HAV) or hepatitis B virus (HBV) in pa
67            The human homolog of TIM-1 is the hepatitis A virus (HAV) receptor, which may explain the
68                                              Hepatitis A virus (HAV) remains enigmatic, despite 1.4 m
69                 Initiation of translation of hepatitis A virus (HAV) RNA occurs by internal entry and
70 otein poly(rC) binding protein 2 (PCBP2) for hepatitis A virus (HAV) RNA translation.
71                                              Hepatitis A virus (HAV) superinfection in persons with h
72                                              Hepatitis A virus (HAV) superinfection is associated wit
73                                     However, hepatitis A virus (HAV) temporarily inhibits Treg-cell f
74 ody (MAb) 190/4, which blocks the binding of hepatitis A virus (HAV) to AGMK cells.
75 lonal antibody (MAb) 190/4 blocks binding of hepatitis A virus (HAV) to the HAV cellular receptor 1 (
76 or Disease Control and Prevention recommends hepatitis A virus (HAV) vaccination for all children at
77                                              Hepatitis A virus (HAV) vaccination is recommended in ch
78                             Universal 2-dose hepatitis A virus (HAV) vaccination of toddlers effectiv
79 h men (MSM) receiving two and three doses of hepatitis A virus (HAV) vaccine and HIV-uninfected MSM r
80  the safety and immunogenicity of 2 doses of hepatitis A virus (HAV) vaccine followed by a booster do
81 lity of virulent hepatitis E virus (HEV) and hepatitis A virus (HAV) was compared.
82                         The AGM-27 strain OF hepatitis A virus (HAV) was originally isolated from an
83 ' nontranslated region in the replication of hepatitis A virus (HAV) was studied by analyzing the tra
84 uman (HM-175) and simian (AGM-27) strains of hepatitis A virus (HAV) were constructed to evaluate the
85 tream of the internal ribosome entry site of Hepatitis A virus (HAV) were studied, a 35mer (HAV-35),
86                           Here, we show that hepatitis A virus (HAV), a hepatotropic picornavirus, ab
87 f the internal ribosome entry site (IRES) of Hepatitis A virus (HAV), a picornavirus.
88 of positive-strand RNA viruses that includes hepatitis A virus (HAV), an ancient human pathogen that
89                                              Hepatitis A virus (HAV), an atypical member of the Picor
90 s known about the mechanism of cell entry of hepatitis A virus (HAV), and the identification of cellu
91 on, all participants were vaccinated against hepatitis A virus (HAV), and the increase of antibody ti
92     IgG antibodies to cytomegalovirus (CMV), hepatitis A virus (HAV), herpes simplex virus type 1 (HS
93 'NTR) of an attenuated, cell culture-adapted hepatitis A virus (HAV), HM175/P16, enhance growth in cu
94                    During infection with the hepatitis A virus (HAV), most patients develop mild or a
95                         Human wild-type (wt) hepatitis A virus (HAV), the causative agent of acute he
96 y a stem-loop structure with cre function in hepatitis A virus (HAV), the type species of this genus,
97                                              Hepatitis A virus (HAV), unlike other picornaviruses, ha
98 ial serological studies were consistent with hepatitis A virus (HAV), with prozone phenomenon.
99  a cytopathogenic mutant (HM 175/24a) of the hepatitis A virus (HAV).
100  have had exposure and resultant immunity to hepatitis A virus (HAV).
101 se and control subjects were also tested for hepatitis A virus (HAV).
102                     These results pertain to hepatitis A virus (HAV).
103 e period were negative for IgM antibodies to hepatitis A virus (HAV).
104 udies show that some picornaviruses, notably hepatitis A virus (HAV; genus Hepatovirus) and some memb
105  respond to a recall antigen and neoantigen (hepatitis A virus [HAV] vaccine) after 3 vaccinations.
106                      Tuberculosis organisms, hepatitis A virus, hepatitis B virus, and measles virus
107  chimpanzee sera; sera from chimpanzees with hepatitis A virus, hepatitis B virus, or hepatitis C vir
108  actions can help rapidly detect and control hepatitis A virus illness caused by imported food.
109 ecovered from specimens from 117 people with hepatitis A virus illness.
110  Mutations which positively affect growth of hepatitis A virus in cell culture may negatively affect
111 uring serial passage of the HM-175 strain of hepatitis A virus in MRC-5 cell cultures in order to det
112         To better understand transmission of hepatitis A virus in such countries, the authors prospec
113 itis B virus now joins hepatitis C virus and hepatitis A virus in targeting the same innate immune re
114 der had a significantly higher prevalence of hepatitis A virus infection (37%) than children living i
115 ica, DRB1*1301 is associated with protracted hepatitis A virus infection which may enhance exposure t
116     In May, 2013, an outbreak of symptomatic hepatitis A virus infections occurred in the USA.
117 passively transferred maternal antibodies to hepatitis A virus (maternal anti-HAV) may lower the infa
118 l bacteria in the gastrointestinal tract and hepatitis A virus, may normally induce the development o
119 erved as controls, with infections by either hepatitis A virus or hepatitis B virus (HBV), or a nonin
120 tion from transcripts containing the IRES of hepatitis A virus or hepatitis C virus in BS-C-1 cells a
121 that the heterogeneous mixture of infectious hepatitis A virus particles (virions and provirions) typ
122 ore protein peptide, whereas no binding to a hepatitis A virus peptide control was observed.
123         When the growth kinetics of immature hepatitis A virus provirions and mature virions were mon
124 ing information, and did genetic analysis of hepatitis A virus recovered from patients' serum and sto
125                                              Hepatitis A virus RNA detected in clinical specimens was
126 ad elevated titers of antibody to H. pylori, hepatitis A virus, rotavirus, and malaria at the outset,
127 unoglobulins A (IgA), G (IgG), and M (IgM)], hepatitis A virus, rotavirus, tetanus toxoid (IgG), and
128 patitis A (HepA) vaccine was assessed in 133 hepatitis A virus-seronegative, human immunodeficiency v
129                                 In contrast, hepatitis A virus seroprevalence increased with age.
130 idence interval: 0.8, 2.9) of H. pylori with hepatitis A virus seroprevalence that weakened after adj
131 tion since proteins of hepatitis C virus and hepatitis A virus similarly bind IPS-1 and target it for
132 ible for the normally asynchronous nature of hepatitis A virus uncoating kinetics.
133 lace, and postexposure prophylaxis with both hepatitis A virus vaccine and immunoglobulin was provide
134  to 18 years of age) to receive MenB-FHbp or hepatitis A virus vaccine and saline and assigned 3304 y
135 ore reactions at the injection site than the hepatitis A virus vaccine and saline.
136                   Symptomatic infection with hepatitis A virus was confirmed in 25 contacts receiving
137                                           No hepatitis A virus was detected in product B.
138                                              Hepatitis A virus was sequenced from serologic specimens
139         We conclude that for species such as hepatitis A virus with high levels of sequence conservat

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top