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1 ted (4460 [2465] pg/mL) and varicella-zoster virus-associated (5386 [1778] pg/mL) uveitis.
2 fection is programmed in large part by early virus-associated Ag-nonspecific factors, and imply that
3  identical to those observed in Epstein-Barr virus-associated AIDS-related lymphoma.
4                  Thus, community respiratory virus-associated airflow decline seems to be specific to
5 ducible MHC class II expression and a direct virus-associated alteration in Janus kinase levels.
6 k squamous cell cancer, both human papilloma virus-associated and human papilloma virus-negative tumo
7 of intracellular and extracellular levels of virus-associated antigens showed an enhanced accumulatio
8 fection studies to achieve similar levels of virus-associated APO3G and (ii) we constructed stable ce
9 lly account for the Vif-induced reduction of virus-associated APOBEC3G, suggesting that Vif may funct
10 eptococcus, Moraxella, or Haemophilus marked virus-associated ARIs.
11 ent with anti-IgE antibody to blunt seasonal virus-associated asthma exacerbations in children provid
12                  Posttransplant Epstein-Barr virus-associated B-cell lymphoproliferative disease (PTL
13                It is also a leading cause of virus-associated birth defects and is associated with at
14 n immunotherapies in the treatment of select virus-associated cancers.
15  to be a useful strategy in the treatment of virus-associated cancers.
16 ved the way for using immunotherapy to treat virus-associated cancers.
17  persistent viruses, and a high incidence of virus-associated cancers.
18 ies with a catalase inhibitor indicated that virus-associated catalase can have a role in protecting
19 d GC B cells are a useful model for studying virus-associated changes contributing to the pathogenesi
20                      A model for hepatitis B virus-associated chronic liver disease has been made usi
21 BACKGROUND & AIMS: Patients with hepatitis C virus-associated cirrhosis and clinical significant port
22 ctive study of 226 patients with hepatitis C virus-associated cirrhosis and CSPH who had SVR to inter
23 ue for identifying patients with hepatitis C virus-associated cirrhosis likely to develop HCC within
24 iver biopsies from patients with hepatitis C virus-associated cirrhosis or liver tissues removed duri
25 ospective study of patients with hepatitis C virus-associated cirrhosis, an SVR to all-oral therapy s
26                   The incidence of influenza virus-associated clinic visits was highest among patient
27                                        Mumps virus-associated CNS complications in vaccinees continue
28 ents designed to reduce the risk of vaccinia virus-associated complications during pregnancy.
29 IV-1 entry depends on an interaction between virus-associated CyPA and CD147 on a target cell.
30                                              Virus-associated CyPA coimmunoprecipitated with CD147 fr
31 nslocation into the nucleus and the rates of virus-associated cytopathic effects.
32 acycline, while little viral replication and virus-associated cytotoxicity was observed in infected g
33                       Human immunodeficiency virus-associated dementia (HAD) is associated with incre
34 op Kaposi's sarcoma and various Epstein Barr virus associated disease processes.
35 pled receptor (vGPCR) has been implicated in virus-associated disease pathogenesis due principally to
36       Rather than severe virus burden, BR/08 virus-associated disease severity correlated with extens
37 importance in the context of human papilloma virus-associated disease, in which young patients will b
38 ola virus glycoprotein effectively prevented virus-associated disease.
39 humans that appears to protect the host from virus-associated disease.
40 he lungs of infected mice, thereby promoting virus-associated disease.
41 ave many potential benefits as treatment for virus-associated diseases and malignancies, due to their
42 region in HTLV-1 replication or in mediating virus-associated diseases remain to be defined.
43 n and family studies of various Epstein-Barr virus-associated diseases suggests a substantial genetic
44 e development of two sequential Epstein-Barr virus-associated disorders in an immunosuppressed patien
45                  These findings suggest that virus-associated disruption of fyn kinase-mediated signa
46 alcoholic fatty liver disease or hepatitis C virus-associated dysmetabolic syndrome, will take statin
47              The 2000-2001 outbreak of Sudan virus-associated EHF in the Gulu district of Uganda led
48  correlation between ERK/MAPK activation and virus-associated encephalitis.
49 sed in developed countries, the Epstein-Barr-virus-associated endemic subtype, and an HIV-associated
50  designs and determine which ones best mimic virus-associated Env trimers.
51                      Lesional herpes simplex virus associated erythema multiforme keratinocytes also
52 mistry studies indicated that herpes simplex virus associated erythema multiforme lesional skin from
53 ret the data to indicate that herpes simplex virus associated erythema multiforme pathology includes
54 (76%) DNA polymerase positive herpes simplex virus associated erythema multiforme patients was also p
55 onal skin from 21 of 26 (81%) herpes simplex virus associated erythema multiforme patients was positi
56 ot in herpes simplex virus or herpes simplex virus associated erythema multiforme patients, and lesio
57  virus, a syndrome designated herpes simplex virus associated erythema multiforme.
58 oracic Society Steps 2-5), with a history of virus-associated exacerbations, were randomized to 14-da
59 minants of acute HCV infection dynamics than virus-associated factors.
60                By proteotyping analysis, EKC virus-associated fiber knobs were uniquely shared.
61 uenza virus, as well as reducing chikungunya virus-associated foot swelling and viral load.
62 us (WHV) and serve as a model of hepatitis B virus-associated HCC in humans.
63          In HBV replicating cells, including virus-associated HCCs, suppressor of zeste 12 homolog (S
64 ing adoptive T cells against post-transplant virus-associated hematologic malignancies, lymphoma and
65 e a consideration in males with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis (EBV
66  was an 11-year-old white boy diagnosed with virus-associated hemophagocytic syndrome (VAHS).
67 learly show that retrovirus binds FN through virus-associated heparan sulfate (HS) and that binding i
68 ly against hepatitis B virus- or hepatitis C virus-associated hepatocellular carcinoma (HCC).
69 nflammatory disorders, including hepatitis B virus-associated hepatocellular carcinoma.
70 lated in human cancer, including hepatitis B virus-associated hepatocellular carcinomas (HCCs).
71 iotemporal profiles of virus replication and virus-associated histopathology in the central nervous s
72 onsistent detection of LMP2A in Epstein-Barr virus-associated HL, this implicates a role for LMP2A in
73 other hand, the 4 patients with Epstein-Barr virus-associated HLH typically had depressed numbers of
74  we show data suggesting that several of the virus-associated host plant proteins accumulated to high
75 be personalized to target specific viral and virus-associated host processes that are only present in
76  responsible for a substantial proportion of virus-associated human cancers, particularly in immunoco
77 cellular targets in a hypoxic environment in virus-associated human cancers.
78 zidothymidine (AZT) is used to treat several virus-associated human cancers.
79 eminiscent of the activity of the adenoviral virus-associated I (VAI) RNA, a known inhibitor of the a
80                                              Virus-associated I (VAI) RNAs of adenoviruses are requir
81  the vector index may help prevent West Nile virus-associated illness.
82          At the cellular level, we show that virus-associated immune activation by IFN-alpha blocks B
83 lutely critical for the effective control of virus-associated infectious complications in hematopoiet
84 dissemination in the brain and may constrain virus-associated injury.
85         Here we investigate the influence of virus-associated innate immune activation on lymphocyte
86 giogenic, implicating it as a contributor to virus-associated Kaposi's sarcoma, primary effusion lymp
87 orescent stainings on human immunodeficiency virus-associated Kaposi's sarcoma.
88    Five patients with human immunodeficiency virus-associated KS (4 receiving antiretroviral therapy)
89 siologic basis for human T cell lymphotropic virus-associated leukemia/lymphoma as well as past, pres
90 ructural data for DC-SIGNR in complex with a virus-associated ligand, and unique binding modes were o
91 SR-BI interaction rather than changes in the virus-associated lipoprotein-E2 interaction.
92 l a novel role of HVR1 for the properties of virus-associated lipoproteins.
93  After liver transplantation for hepatitis C virus-associated liver failure, standard immunosuppressi
94 iver cancer (aflatoxin exposure, hepatitis B virus-associated liver injury, p53 loss, p53ser249 mutat
95 failure, and the development of Epstein-Barr virus-associated LPD were each associated with 10-20% lo
96 resent a heterogeneous group of Epstein-Barr virus-associated lymphoid proliferations that arise in i
97  (NK) cell lymphoma (NNL) is an Epstein-Barr virus-associated lymphoma of cytotoxic NK cell origin.
98 t instead developed large human Epstein-Barr virus-associated lymphomas by 12 weeks.
99 creased risk reflects an increase in Epstein-virus-associated lymphomas.
100                                 Epstein-Barr virus-associated lymphoproliferative developed in two pa
101                                 Epstein-Barr virus-associated lymphoproliferative disease (EBV-LPD) i
102             Posttransplantation Epstein-Barr virus-associated lymphoproliferative disease (PTLPD) occ
103                 Among these are Epstein-Barr virus-associated lymphoproliferative diseases in immunoc
104  granulomatosis (LYG) is a rare Epstein-Barr virus-associated lymphoproliferative disorder.
105                              The influenza A virus-associated M2 ion channel is generally believed to
106 d with development of immunity against fatal virus-associated malaria without accelerating SHIV disea
107 d to bursting parasite replication and fatal virus-associated malaria.
108  treatment of opportunistic disease and some virus-associated malignancies such as Epstein-Barr virus
109 m the model include that SV40 infections and virus-associated malignancies will be restricted geograp
110 host, making the patient more susceptible to virus-associated malignancies.
111 haryngeal carcinoma (NPC) is an Epstein-Barr virus-associated malignancy most common in East Asia and
112 haryngeal carcinoma (NPC) is an Epstein-Barr virus-associated malignancy most common in East Asia, Af
113 iferative disorder (PTLD) is an Epstein-Barr virus-associated malignancy that occurs in the setting o
114 ted transcription regulates the formation of virus-associated membrane compartments.
115 virus in the presence or absence of dsRNA, a virus associated molecular pattern.
116        We conclude that dsRNA is a practical virus-associated molecular pattern that can be targeted
117 brate counterparts, can recognize dsRNA as a virus-associated molecular pattern, resulting in the act
118      TLR3 signaling is activated by dsRNA, a virus-associated molecular pattern.
119  response is initiated by the recognition of virus-associated molecular patterns such as dsRNA, a vir
120 e immune activation and could be mimicked by virus-associated molecular patterns such as the syntheti
121                           The recognition of virus-associated molecular patterns, including double- a
122 kinase in dendritic cells (DCs), which sense virus-associated molecular patterns.
123 ection is critical, when tens to hundreds of virus-associated molecules are present in the patient's
124 gerous, because pregnant women suffer higher virus-associated morbidity and mortality than do nonpreg
125                                              Virus-associated mortality (but not the number of cases)
126 and targeted apoptosis as a key mechanism of virus-associated myocardial injury in vitro and in vivo.
127  ligand MIP1alpha protects against Coxsackie virus-associated myocarditis.
128 IL-6) has been implicated as a key factor in virus-associated neoplasia because of its proproliferati
129 g glomerulosclerosis, human immunodeficiency virus associated nephropathy, Denys-Drash, diabetic neph
130 tation after losing their renal grafts to BK virus-associated nephropathy (BKAN) are described.
131                                           BK virus-associated nephropathy (BKVAN) causes renal allogr
132                                           BK virus-associated nephropathy (BKVN) is associated with a
133                       Human immunodeficiency virus-associated nephropathy (HIVAN) affects up to 10% o
134 ained hematuria), and human immunodeficiency virus-associated nephropathy (or exclusion of it in case
135                Because the course of polyoma virus-associated nephropathy (PVAN) has not been evaluat
136                                           BK virus-associated nephropathy is an increasingly recogniz
137 nships between ongoing viral replication and virus-associated neurodegeneration.
138 ations for understanding the pathogenesis of virus-associated neurodevelopmental damage.
139 S is an essential step in the development of virus-associated neuroinflammatory diseases, notably mye
140                       Human immunodeficiency virus-associated neurological disease (HAND) still cause
141 abuse opiates can have a higher incidence of virus-associated neuropathology.
142        We examined the types of Epstein-Barr virus-associated nuclear antigen-1 (EBNA-1) gene carboxy
143    This study directly correlates individual virus-associated objects observed in light microscopy wi
144 umor samples and expand our understanding of virus-associated oncogenesis.
145 host DDR factors in the MCPyV life cycle and virus-associated oncogenesis.
146 sociated with different asthma phenotypes as virus-associated or steroid-resistant asthma.
147 fect of radiation therapy in human papilloma virus-associated oropharyngeal SCC, we hypothesized that
148 fect of radiation therapy in human papilloma virus-associated oropharyngeal squamous cell carcinoma,
149 d mature p26 Gag and decreased extracellular virus-associated p26 Gag were observed by Western blot a
150  in the viral replication cycle and promotes virus-associated pathology.
151 nts that reduce or eliminate HPV and reverse virus-associated pathology.
152 vated by the specific recognition of various virus-associated patterns by several retinoic acid-induc
153 transplant (HCT) recipients with respiratory virus-associated pneumonia.
154 ng host LLOs required for N-glycosylation of virus-associated polypeptides.
155  immunosuppressed patients with Epstein-Barr virus-associated posttransplant lymphoma and in some pat
156                                 Epstein-Barr virus-associated posttransplant lymphoproliferative dise
157  histology resembled lesions of Epstein-Barr virus-associated posttransplant lymphoproliferative dise
158  suggested an increased risk of Epstein-Barr virus-associated posttransplant lymphoproliferative diso
159 transplantation with potential advantages in virus-associated posttransplant malignancies as well as
160 the S phase, which may then allow subsequent virus-associated processes, such as RNA splicing, transp
161           Significantly, this mouse model of virus-associated pulmonary B-cell lymphoma closely mimic
162                                              Virus-associated pyramids (VAPs) assemble in the host ce
163 me has strong similarities with familial and virus-associated reactive hemophagocytic lymphohistiocyt
164                    The differentiation of BK virus-associated renal allograft nephropathy (BKVAN) fro
165 th microtubules facilitates the formation of virus-associated replication complexes, which are requir
166  nuclear RNA U6 gene (U6) and the adenovirus virus-associated RNA 1 (Ad VA1) gene promoters yielded h
167 nscription by RNA polymerase III on tRNA and virus-associated RNA genes and initiates preinitiation c
168 irect recognition of promoters (for tRNA and virus-associated RNA genes) or promoter-TFIIIA complexes
169 ofiles and binding affinities for adenoviral virus-associated RNA I (VA RNAI) and HIV-1 trans-activat
170                                              Virus-associated RNA I (VA RNAI) is a short ( approximat
171                           Adenovirus encodes virus-associated RNA I (VAI), a highly structured RNA in
172           Mutants of adenovirus type 5 (Ad5) virus-associated RNA I deficient in inhibiting the activ
173                                          The virus-associated RNA, vRNA, was identified by DNase I tr
174                                   Adenovirus virus-associated RNA-I (VAI) is a short, noncoding trans
175  was prevented by the addition of adenovirus virus-associated RNA1 (VA RNAI), an inhibitor of PKR act
176 come was the incidence of clinically defined virus-associated RTI episodes confirmed from nasal swabs
177 tic supplementation would reduce the risk of virus-associated RTIs during the first year of life in a
178 ry role for IFN-gamma in the pathogenesis of virus-associated secondary HLH as opposed to its central
179 knowledge, we established an animal model of virus-associated secondary HLH by infecting immunocompet
180  hypothesized that in human immunodeficiency virus-associated sensory neuropathy (HIV-SN), damaged mt
181 (myocardial infarction and stroke), cancers (virus associated, smoking related, and other), severe ne
182 vents are believed to be key determinants of virus-associated spread, antiviral immune responses, and
183 poradic, endemic, and human immunodeficiency virus-associated subtypes.
184  >64 years) using the cumulative (12 months) virus-associated symptomatic attack rates from 12 countr
185 rus vector to specific tissues and to reduce virus-associated toxicity after systemic application.
186  viral genes, allowing for infection without virus-associated toxicity.
187      The incidence of human immunodeficiency virus-associated tuberculosis, which was virtually unrec
188 cell surveillance is often effective against virus-associated tumors because of their high immunogeni
189 ative head and neck cancers, suggesting that virus-associated tumors constitute a unique entity among
190                                  Hepatitis B virus-associated tumors seem to have a better prognosis
191 V)-encoded EBNA1 protein is expressed in all virus-associated tumors where it plays an essential role
192 ontribute to the development of Epstein-Barr virus-associated tumors.
193 s of LMP1 variants in cells and Epstein-Barr virus-associated tumors.
194 which such mutations may arise, including in virus-associated tumors.
195 of viral latency and in immune therapies for virus-associated tumors.
196 orylation and its deubiquitination by Herpes virus associated ubiquitin-specific protease (Hausp, a.k
197 equirements that are operative in adenovirus virus-associated (VA) RNA genes.
198 n of a small regulatory RNA, we examined the virus-associated (VA) RNA species of all 47 known human
199  helper functions E1a, E1b, E2a, E4Orf6, and virus-associated (VA) RNA; however, their combined net e
200           Most human adenoviruses encode two virus-associated (VA) RNAs, VA RNAI and VA RNAII, that a
201                             We conclude that virus-associated Vif inhibits processing of a subset of
202   We now demonstrate for the first time that virus-associated Vif is subject to proteolytic processin
203 y in 49 subjects with human immunodeficiency virus-associated weight loss (12.7 +/- 0.9% of body wt).
204     Epstein-Barr virus (EBV) is an oncogenic virus associated with a number of human malignancies inc
205  the stage of exponential increase in plasma virus associated with acute HIV infection (3, 7, 20, 35,
206 man T-cell leukemia virus type 1 (HTLV-1), a virus associated with adult T-cell leukemia, is signific
207             However, in contrast to T cells, virus associated with B cells was surface bound, as show
208                     The paucity of cell-free virus associated with BDV infection has hindered studies
209 ights into the conformational changes of the virus associated with cell entry or caused by changing o
210 ) has provided the latest possible candidate virus associated with cryptogenic hepatitis.
211        There are at least 14 subtypes of the virus associated with different human populations.
212                     Ad serotype 37 (Ad37), a virus associated with epidemic keratoconjunctivitis, but
213 tis G virus (GBV-C/HGV) is a newly described virus associated with hepatitis in humans, and GBV-C/HGV
214  virus (ISAV) infection, an Orthomyxoviridae virus associated with high mortalities in salmonid aquac
215            Ebolavirus is a hemorrhagic fever virus associated with high mortality.
216 y isolated North American lineage H7 subtype virus associated with human conjunctivitis is capable of
217 immunity to human herpesvirus 8 (HHV-8), the virus associated with Kaposi's sarcoma (KS).
218 sociated herpesvirus (KSHV), a B-cell-tropic virus associated with KS and B-cell lymphomas, encodes 1
219 Valley fever (RVF) virus is a mosquito-borne virus associated with large-scale epizootics/epidemics t
220 propose a novel mechanism by which HTLV-1, a virus associated with lymphoproliferative disease, dysre
221 arr virus (EBV) is an oncogenic gamma-herpes virus associated with malignancies that develop in both
222 ther they are reflected in the population of virus associated with peripheral blood mononuclear cells
223 venting the initial production of infectious virus associated with reactivation.
224 sociated herpesvirus (KSHV) is a human tumor virus associated with several cancers.
225 sociated herpesvirus (KSHV) is a human tumor virus associated with several cancers.
226              Ad type 37 (Ad37), a subgroup D virus associated with severe ocular infections, is unabl
227      Hepatitis C virus (HCV) is an oncogenic virus associated with the onset of hepatocellular carcin
228 sovirus (SSaDV) as the most likely candidate virus associated with tissues from symptomatic asteroids
229 us (EBV) is a well-established B-cell-tropic virus associated with various lymphoproliferative diseas
230  previously undetected RNA viruses and a DNA virus associated with wild D. melanogaster.
231 ntrols can provide a rapid means to identify viruses associated with a complex disease, paving the wa
232 are a diverse and rapidly expanding group of viruses associated with a variety of disease conditions
233                           Among the types of viruses associated with acute otitis media, respiratory
234 d human rhinovirus (HRV) are the most common viruses associated with acute respiratory tract infectio
235 may be useful for comprehensive diagnosis of viruses associated with ALF, or to exclude infectious et
236 ostic testing in detection of known or novel viruses associated with ALF.
237 crobial contamination, and discovering novel viruses associated with both acute and chronic illnesses
238                         In order to identify viruses associated with BRD, we used a metagenomics appr
239                                              Viruses associated with cancer can be detected by search
240        Polyomaviruses are small circular DNA viruses associated with chronic infections and tumors in
241  May, 1994, and May, 1996, by nested PCR for viruses associated with CNS infections in the UK.
242  the vertical transmission of ZIKV and other viruses associated with congenital disease.
243 bioinformatics analysis to identify putative viruses associated with Diaphorina citri, the Asian citr
244 athogenicity and transmissibility of two TRS viruses associated with disease in humans in the ferret
245 ing, is a powerful technique for discovering viruses associated with diseases with no definitive etio
246           Among these, HAdV-D includes those viruses associated with epidemic keratoconjunctivitis (E
247 apillomaviruses, members of a group of dsDNA viruses associated with epithelial growths and tumors, h
248 a, and corona-, calici- and lyssaviruses and viruses associated with hepatitis A and E.
249                                 Multiple RNA viruses associated with honeybees are widespread in symp
250                                          RNA viruses associated with honeybees represent a potential
251    To determine whether avian H5N1 influenza viruses associated with human infections in Vietnam had
252  changes in the HA of swine origin influenza viruses associated with increased transmission and decre
253 viruses (Ad) are double-stranded DNA (dsDNA) viruses associated with infectious diseases, but they ar
254              Many publications deal with RNA viruses associated with major disease emergence events,
255 blasts offers an in vitro model for studying viruses associated with prenatal infections.
256 uses 1 and 2 (HSV-1 and HSV-2) are large DNA viruses associated with recurring oral or genital erosio
257           This suggests that the majority of viruses associated with resurgence of measles in the Uni
258   Here we used viral metagenomics to examine viruses associated with sea turtle fibropapillomatosis (
259 nenveloped, positive-sense single-strand RNA viruses associated with self-limiting diarrhea.
260 he rates of viral detection and identified 3 viruses associated with severe BRD signs.
261 is short review we focus on newly identified viruses associated with severe haemorrhagic disease in h
262 s of human infections with novel influenza A viruses associated with severe human illness, or with th
263       Polydnaviruses are double-stranded DNA viruses associated with some subfamilies of ichneumonoid
264 y comprising the complete proteomes of seven viruses associated with T1D and open reading frames from
265 re reveal that STIV is strikingly similar to viruses associated with the Bacteria and Eukarya domains
266                 Over the last decade, rabies viruses associated with the silver-haired bat (SHBRV) ha
267                                        Those viruses associated with ticks were found to have a signi
268 e sent to CDC, Atlanta, Ga., for testing for viruses associated with viral HFs known to be present in
269  sites in the skin of human immunodeficiency virus-associated xerosis patients (upper arm, n = 12; up
270 dergic innervation in human immunodeficiency virus-associated xerosis.
271 ffer a wide range of opportunities to reduce virus-associated yield losses in cassava for farmers and

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