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1 en dexamethasone mouthwash for prevention of stomatitis).
2 atients had adverse events in the extension (stomatitis).
3 from Behcet's disease and recurrent aphthous stomatitis.
4 s are critical for the prevention of denture stomatitis.
5 ers, Behcet's disease and recurrent aphthous stomatitis.
6 d the percentage of patients without denture stomatitis.
7 mar-plantar erythrodysesthesia syndrome, and stomatitis.
9 on (55 [19%] of 283 vs 74 [27%] of 271), and stomatitis (138 [49%] of 284 vs 162 [59%] of 273); 60 (2
11 e group), diarrhoea (30 [9%] vs three [2%]), stomatitis (20 [6%] vs 13 [8%]), fatigue (18 [6%] vs fiv
12 association with everolimus monotherapy were stomatitis (26 [62%] of 42) and diarrhoea (16 [38%]); an
14 t common adverse events with everolimus were stomatitis (314 [67%] of 472 patients in the everolimus
15 febrile neutropenia (44 [16%] vs ten [4%]), stomatitis (37 [13%] vs four [1%]), and fatigue (34 [12%
18 [33%]), neutropenia (66 [19%] vs 49 [14%]), stomatitis (54 [15%] vs 10 [3%]), hypokalaemia (52 [15%]
19 up were neutropenia (117 [25%] vs 35 [15%]), stomatitis (59 [13%] vs three [1%]), anaemia (46 [10%] v
20 s with LTBI had lower odds of having candida stomatitis (adjusted odds ratio (OR) = 0.68, p = 0.0035)
21 limiting toxic effects-one developed grade 3 stomatitis and fatigue and one developed arthralgia and
22 y endpoint was incidence of grade 2 or worse stomatitis by 8 weeks assessed in the full analysis set
23 influenza A, Zika, Ebola, Sindbis, vesicular stomatitis, cowpox, and vaccinia, but not murine leukemi
24 he incidences of grade 3 or 4 neurotoxicity, stomatitis, diarrhea, and neutropenia were significantly
27 ure-wearing patients were recruited (denture stomatitis (DS) n = 8; non-denture stomatitis (NoDS) n =
28 hataemia (18 [12%]), arthralgia (nine [6%]), stomatitis (eight [5%]), hyponatraemia (eight [5%]), abd
29 hyperglycaemia (seven [17%] of 42 patients), stomatitis (four [10%]), and diarrhoea (three [7%]); tho
30 limus/bevacizumab were mucosal inflammation, stomatitis, hypophosphatemia, hyperglycemia, and hyperch
33 tially reduced the incidence and severity of stomatitis in patients receiving everolimus and exemesta
35 adverse events were infrequent and included stomatitis (in 18 [9%] of 202 patients in the everolimus
37 lovirus-based therapies.IMPORTANCE Vesicular stomatitis Indiana virus (VSIV) is a veterinary pathogen
39 te systems such as the rhabdovirus vesicular stomatitis Indiana virus (VSV), lentiviruses or gammaret
40 expression and protection against vesicular stomatitis Indiana virus infection compared with wild ty
43 tudied the cytotoxic activity of a vesicular stomatitis/measles hybrid virus (VSV-FH), which is super
44 s receiving EC-D reported significantly more stomatitis, myalgia or arthralgia, vomiting, nausea, fat
47 (denture stomatitis (DS) n = 8; non-denture stomatitis (NoDS) n = 11) and the oral bacterial microbi
48 one [2%]), pneumonitis (none vs five [9%]), stomatitis (none vs five [9%]), and hand-foot syndrome (
50 n a common spectrum, with recurrent aphthous stomatitis on the mild end, Behcet's disease on the seve
51 aronychia (26 [11%] in LUX-Lung 3 only), and stomatitis or mucositis (13 [5%] in LUX-Lung 6 only).
52 of 239 patients), diarrhoea (13 [5.4%]), and stomatitis or mucositis (13 [5.4%]), compared with neutr
53 OR=1.54, P=0.001), and no detectable denture stomatitis (OR=2.89, P<0.001) significantly increased af
54 enetic similarities among recurrent aphthous stomatitis, PFAPA, and Behcet's disease, placing these d
55 rt an adult case of periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome,
58 udotyped with different envelopes (vesicular stomatitis, Rabies, Mokola and Ross River viral envelope
63 which was persist for several days, aphthous stomatitis, tongued tonsillitis with moss, pharyngitis,
68 , we demonstrated that recombinant vesicular stomatitis virus (rVSV) expressing human NoV capsid prot
70 clinical efficacy of a recombinant vesicular stomatitis virus (rVSV) vaccine vector has stimulated th
71 iculoVax that contains recombinant vesicular stomatitis virus (rVSV) vectors expressing filovirus gly
73 ing of live attenuated recombinant vesicular stomatitis virus (rVSV)-based filovirus vaccine vectors
74 replication-competent, recombinant vesicular stomatitis virus (rVSV)-based vaccine candidate designed
75 replication-competent recombinant vesicular stomatitis virus (rVSV)-based vaccine expressing a Zaire
76 is a first-generation recombinant vesicular stomatitis virus (rVSV)-based vaccine expressing the ZEB
78 mulatory properties of recombinant vesicular stomatitis virus (rVSV)-based vaccines make them suitabl
79 plicating, attenuated, recombinant vesicular stomatitis virus (serotype Indiana) whose surface glycop
81 to induce G(2)/M arrest.IMPORTANCE Vesicular stomatitis virus (VSV) (a rhabdovirus) and its variant V
83 eplication of the (-)ssRNA viruses vesicular stomatitis virus (VSV) (Rhabdoviridae family) and Rift V
84 This study focuses on oncolytic vesicular stomatitis virus (VSV) against pancreatic ductal adenoca
85 ediate pH for two vesiculoviruses, vesicular stomatitis virus (VSV) and Chandipura virus (CHAV), whic
86 functions following infection with vesicular stomatitis virus (VSV) and lymphocytic choriomeningitis
87 proteins of rhabdoviruses, such as vesicular stomatitis virus (VSV) and rabies virus (RABV), possess
88 protein of rhabdoviruses, such as vesicular stomatitis virus (VSV) and rabies virus, catalyzes the t
89 The glycoproteins (G proteins) of vesicular stomatitis virus (VSV) and related rhabdoviruses (e.g.,
90 ns with enveloped viruses, such as Vesicular Stomatitis Virus (VSV) and Respiratory Syncytial Virus (
91 NA viruses with broad host ranges, vesicular stomatitis virus (VSV) and Sindbis virus (SINV), are com
92 e experimental data on the DMFE of Vesicular stomatitis virus (VSV) and Tobacco etch virus (TEV), we
94 have been employed here to purify vesicular stomatitis virus (VSV) as a model case, however this tec
95 specific detection of pseudotyped vesicular stomatitis virus (VSV) as a model virus on SP-IRIS platf
97 ribe such a strategy that utilizes vesicular stomatitis virus (VSV) as a vector for chimeric hemagglu
100 te a highly infectious recombinant vesicular stomatitis virus (VSV) bearing the SARS-CoV-2 spike glyc
101 release and infection by chimeric vesicular stomatitis virus (VSV) containing the envelope proteins
104 developed a replication-competent vesicular stomatitis virus (VSV) expressing a modified form of the
105 g an infectious molecular clone of vesicular stomatitis virus (VSV) expressing eGFP as a marker of in
106 opism, we asked whether a chimeric vesicular stomatitis virus (VSV) expressing the EBOV glycoprotein
108 strated that recombinant wild-type vesicular stomatitis virus (VSV) expressing the HBV middle surface
109 pressing the SARS-CoV-1 spike, and vesicular stomatitis virus (VSV) expressing the SARS-CoV-2 spike.
112 its very low human seroprevalence, vesicular stomatitis virus (VSV) has promise as a systemic oncolyt
114 tonomously replicating recombinant vesicular stomatitis virus (VSV) in which the glycoprotein was rep
115 na virus (VSIV), formerly known as vesicular stomatitis virus (VSV) Indiana (VSV(IND)), is a model vi
116 compassing the appendage region of vesicular stomatitis virus (VSV) Indiana serotype L protein with t
117 78 results in a robust decrease of vesicular stomatitis virus (VSV) infection and a corresponding enh
119 FN production in macrophages after vesicular stomatitis virus (VSV) infection, and HIPK2-deficient mi
126 s since the first structure of the vesicular stomatitis virus (VSV) L protein determined in 2015 and
128 The complex closely resembles the vesicular stomatitis virus (VSV) L-P, the one other known full-len
130 cule against infection with either vesicular stomatitis virus (VSV) or influenza was demonstrated to
136 constructs were incorporated onto vesicular stomatitis virus (VSV) pseudoparticles and transduction
137 o-cell fusion assays, and chimeric vesicular stomatitis virus (VSV) recombinants expressing the RABV
138 genes within the brain.IMPORTANCE Vesicular stomatitis virus (VSV) shows considerable promise both a
139 spread, and only minimally affects vesicular stomatitis virus (VSV) spread, to adjacent cells in a mo
140 udy, we have engineered a chimeric vesicular stomatitis virus (VSV) that is devoid of its natural neu
141 developed a recombinant strain of vesicular stomatitis virus (VSV) that specifically targets transfo
143 inhibitors in cells infected with vesicular stomatitis virus (VSV) to identify miRNAs that regulate
144 eficiency virus type 1 (HIV-1) and vesicular stomatitis virus (VSV) to measure the neutralising abili
145 osolic poly(I:C), 5'ppp-dsRNA, and vesicular stomatitis virus (VSV) triggers IFN-I expression in over
146 t utilizes a replication-defective vesicular stomatitis virus (VSV) vector backbone that lacks the na
147 accine that utilizes an attenuated vesicular stomatitis virus (VSV) vector, to deliver and express in
149 a simplified system, we generated vesicular stomatitis virus (VSV) virions pseudotyped with HSV-1 es
151 s work, we developed a pseudotyped vesicular stomatitis virus (VSV) with a glycoprotein of Maraba vir
153 ral activity of interferon against vesicular stomatitis virus (VSV), a model virus that whose genome
156 t MEFs exhibit impaired control of vesicular stomatitis virus (VSV), a virus sensed by STING that can
157 A, modified vaccinia Ankara (MVA), vesicular stomatitis virus (VSV), adenovirus type 5 (Ad5), rhesus
158 s of Ebola virus, influenza virus, vesicular stomatitis virus (VSV), and measles virus in GBA knockou
159 took a promising oncolytic virus, vesicular stomatitis virus (VSV), and tested the hypothesis that t
160 ficiency virus type-1 (HIV-1), and vesicular stomatitis virus (VSV), as well as a replication-compete
161 limited the cytopathic effect from Vesicular stomatitis virus (VSV), Encephalomyocarditis virus (EMCV
162 abies virus (RABV) and recombinant vesicular stomatitis virus (VSV), expressing either the codon-opti
163 bdoviral vectors, rabies virus and vesicular stomatitis virus (VSV), expressing wild-type or codon-op
165 ithin 2-6 hours after infection by vesicular stomatitis virus (VSV), newly assembled VSV particles ar
167 eficient MEFs, upon infection with vesicular stomatitis virus (VSV), revealed diminished IFNbeta expr
169 those of the related rhabdovirus, vesicular stomatitis virus (VSV), we demonstrate that both polymer
170 s and primary fibroblasts with the vesicular stomatitis virus (VSV), we detected DNA complementary to
171 of NNS RNA virus gene expression, vesicular stomatitis virus (VSV), we determined the importance of
173 strain of the negative-sense ssRNA vesicular stomatitis virus (VSV), we show that microinjection of V
175 crisis of 2013-2016, a recombinant vesicular stomatitis virus (VSV)-based EBOV vaccine was clinically
176 In this study, we developed a vesicular stomatitis virus (VSV)-based human NoV vaccine candidate
177 rrying large transgenes.IMPORTANCE Vesicular stomatitis virus (VSV)-based oncolytic viruses are promi
178 ss these limitations, we devised a vesicular stomatitis virus (VSV)-based probe to display membrane-e
181 repertoire after administration of vesicular stomatitis virus (VSV)-Ebola vaccine at 3 million, 20 mi
185 case (RLH) signaling contribute to vesicular stomatitis virus (VSV)-mediated triggering of type I IFN
186 d, Shen et al demonstrate that the vesicular stomatitis virus (VSV)-murine interferon beta (IFNbeta)-
196 ed mutagenesis of the L protein of vesicular stomatitis virus (VSV, a prototypic NNS RNA virus) to ex
197 which the transmembrane domain of vesicular stomatitis virus (VSV-TMD) promotes both initiation of f
199 y endosomes (SFV, SINV, CHIKV, and vesicular stomatitis virus [VSV]), while viruses that fuse in the
200 to infection with the RNA viruses vesicular stomatitis virus and Sendai virus and to transfection wi
201 iral infections with influenza and vesicular stomatitis virus can persist after resolution of infecti
202 endent RNA polymerase L protein of vesicular stomatitis virus catalyzes unconventional pre-mRNA cappi
206 nfluenza, measles, Ebola, Lassa or vesicular stomatitis virus envelope glycoproteins enabled us to st
207 glia, fibroblasts, or melanocytes, vesicular stomatitis virus evoked robust beta interferon (IFN-beta
208 ity in vitro against a recombinant vesicular stomatitis virus expressing MACV GPC (VSV-MACV) as well
209 e vaccines is based on recombinant vesicular stomatitis virus expressing the EBOV glycoprotein (VSV-E
210 asmid followed by infection with a vesicular stomatitis virus expressing the Zaire ebolavirus glycopr
211 s to protect from infection with a vesicular stomatitis virus expressing the Zaire ebolavirus glycopr
213 d secretory membrane glycoprotein, vesicular stomatitis virus G (VSVG) glycoprotein, was reduced comp
215 ion of the Jurkat T-cell line with vesicular stomatitis virus G glycoprotein (VSV-G)-pseudotyped HIV-
216 s," are designed to co-encapsulate vesicular stomatitis virus G protein (VSV-G) with bioactive macrom
217 By contrast, secretory traffic of vesicular stomatitis virus G protein, recycling of internalized tr
218 th virus-like particles displaying vesicular stomatitis virus G protein, RNAdjuvant promoted the form
219 of SAMHD1 does not rescue HIV-1 or vesicular stomatitis virus G-pseudotyped lentivectors infection in
220 havirus RNA replicon expresses the vesicular stomatitis virus glycoprotein (VSV G) as the only struct
221 rus RNA replicons that express the vesicular stomatitis virus glycoprotein (VSV G) has been described
223 nd that augmenting fusion with the vesicular stomatitis virus glycoprotein (VSVG) increased the amoun
224 A to an exosome-anchoring protein: vesicular stomatitis virus glycoprotein (VSVG), we demonstrate tha
225 ass III fusion proteins, including vesicular stomatitis virus glycoprotein G (VSV-G) or baculovirus g
227 ancement with LVs pseudotyped with vesicular stomatitis virus glycoproteins and also with modified gi
230 iral protection against Sendai and vesicular stomatitis virus in a TLR3 and type I IFN receptor-depen
232 ous work, a prototypic recombinant vesicular stomatitis virus Indiana serotype (rVSIV) vector express
233 ly after Listeria monocytogenes or vesicular stomatitis virus infection but comparable cytolytic func
234 vates the IFN pathway and inhibits vesicular stomatitis virus infection by directly targeting several
236 otic triggers such as etoposide or vesicular stomatitis virus infection, but disassemble into small a
237 inhibition during influenza A and vesicular stomatitis virus infection, but not murine hepatitis vir
240 ults were transiently positive for vesicular stomatitis virus nucleoprotein gene and Ebola virus glyc
245 red by an EBOV vaccine composed of vesicular stomatitis virus pseudovirions that lack native G glycop
246 hows reduced capability to control vesicular stomatitis virus replication and to induce apoptosis in
248 HAP2 on the surface of pseudotyped vesicular stomatitis virus results in homotypic virus-cell fusion.
249 from La Crosse orthobunyavirus and vesicular stomatitis virus reveal insights into RNA synthesis and
252 (ChAd3-EBO-Z) and the recombinant vesicular stomatitis virus vaccine (rVSVG-ZEBOV-GP) in Liberia.
253 fficacy of a bivalent, recombinant vesicular stomatitis virus vaccine expressing both the A/Hanoi/304
255 rus) and heterologous (inactivated vesicular stomatitis virus) antigens and acceptable accuracy/linea
256 s involving viral vectors (such as vesicular stomatitis virus), and antisense compounds directly targ
257 rticle, we study the polymerase of vesicular stomatitis virus, a member of the rhabdoviruses, which h
259 virus Ankara, complex adenovirus, vesicular stomatitis virus, alphavirus-based chimeras, and measles
260 luding encephalomyocarditis virus, vesicular stomatitis virus, and influenza virus, in susceptible ce
262 irus, influenza A virus, reovirus, vesicular stomatitis virus, human immunodeficiency virus type 1, o
263 pha interferon (IFN-alpha) against vesicular stomatitis virus, Indiana serotype (VSV(IND)), a prototy
264 n entry inhibitor for JUNV and for vesicular stomatitis virus, lymphocytic choriomeningitis virus, an
265 on of dsRNA in cells infected with vesicular stomatitis virus, measles virus, influenza A virus, and
266 enges with Listeria monocytogenes, vesicular stomatitis virus, or Vaccinia virus, but dispensable in
268 c viruses, including rabies virus, vesicular stomatitis virus, Semliki Forest virus, and herpes simpl
269 with poliovirus and then moving to vesicular stomatitis virus, where he discovered a virion RNA polym
270 recombinant, replication competent vesicular stomatitis virus-based candidate vaccine expressing a su
271 ing units (pfu) of the recombinant vesicular stomatitis virus-based candidate vaccine expressing the
273 recombinant, replication-competent vesicular stomatitis virus-based vaccine expressing a surface glyc
274 n phase 1 studies of a recombinant vesicular stomatitis virus-based vaccine expressing a ZEBOV glycop
277 e results highlight the ability of vesicular stomatitis virus-vectored vaccines to rapidly confer pro
279 expanded access to the recombinant vesicular stomatitis virus-Zaire Ebola virus (rVSV-ZEBOV) vaccine
280 immunogenicity of the recombinant vesicular stomatitis virus-Zaire Ebola virus envelope glycoprotein
281 valuated the safety of recombinant vesicular stomatitis virus-Zaire Ebola virus envelope glycoprotein
282 istency, and safety of recombinant vesicular stomatitis virus-Zaire Ebola virus envelope glycoprotein
283 expanded access to the recombinant vesicular stomatitis virus-Zaire Ebola virus vaccine (rVSV-ZEBOV)
284 cked up the use of the recombinant vesicular stomatitis virus-Zaire Ebola virus vaccine in the recomm
297 y 8 weeks, the incidence of grade 2 or worse stomatitis was two (2%) of 85 patients (95% CI 0.29-8.24
298 e most common were rash, hyperglycaemia, and stomatitis, which each affected two [2%] patients).
299 afatinib (39 [10%] vs nine [2%]), of grade 3 stomatitis with afatinib (16 [4%] vs none), and of grade