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2 fection is programmed in large part by early virus-associated Ag-nonspecific factors, and imply that
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
11 ent with anti-IgE antibody to blunt seasonal virus-associated asthma exacerbations in children provid
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
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
32 acycline, while little viral replication and virus-associated cytotoxicity was observed in infected g
35 pled receptor (vGPCR) has been implicated in virus-associated disease pathogenesis due principally to
37 importance in the context of human papilloma virus-associated disease, in which young patients will b
41 ave many potential benefits as treatment for virus-associated diseases and malignancies, due to their
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
46 alcoholic fatty liver disease or hepatitis C virus-associated dysmetabolic syndrome, will take statin
49 sed in developed countries, the Epstein-Barr-virus-associated endemic subtype, and an HIV-associated
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
58 oracic Society Steps 2-5), with a history of virus-associated exacerbations, were randomized to 14-da
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
67 learly show that retrovirus binds FN through virus-associated heparan sulfate (HS) and that binding i
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
79 eminiscent of the activity of the adenoviral virus-associated I (VAI) RNA, a known inhibitor of the a
83 lutely critical for the effective control of virus-associated infectious complications in hematopoiet
86 giogenic, implicating it as a contributor to virus-associated Kaposi's sarcoma, primary effusion lymp
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
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.
106 d with development of immunity against fatal virus-associated malaria without accelerating SHIV disea
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
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
117 brate counterparts, can recognize dsRNA as a virus-associated molecular pattern, resulting in the act
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
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
126 and targeted apoptosis as a key mechanism of virus-associated myocardial injury in vitro and in vivo.
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
134 ained hematuria), and human immunodeficiency virus-associated nephropathy (or exclusion of it in case
139 S is an essential step in the development of virus-associated neuroinflammatory diseases, notably mye
143 This study directly correlates individual virus-associated objects observed in light microscopy wi
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
152 vated by the specific recognition of various virus-associated patterns by several retinoic acid-induc
155 immunosuppressed patients with Epstein-Barr virus-associated posttransplant lymphoma and in some pat
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
163 me has strong similarities with familial and virus-associated reactive hemophagocytic lymphohistiocyt
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
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
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.
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
191 V)-encoded EBNA1 protein is expressed in all virus-associated tumors where it plays an essential role
196 orylation and its deubiquitination by Herpes virus associated ubiquitin-specific protease (Hausp, a.k
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
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
209 ights into the conformational changes of the virus associated with cell entry or caused by changing o
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
216 y isolated North American lineage H7 subtype virus associated with human conjunctivitis is capable of
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
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
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
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
237 crobial contamination, and discovering novel viruses associated with both acute and chronic illnesses
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
247 apillomaviruses, members of a group of dsDNA viruses associated with epithelial growths and tumors, h
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
256 uses 1 and 2 (HSV-1 and HSV-2) are large DNA viruses associated with recurring oral or genital erosio
258 Here we used viral metagenomics to examine viruses associated with sea turtle fibropapillomatosis (
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
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
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
271 ffer a wide range of opportunities to reduce virus-associated yield losses in cassava for farmers and
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