ライフサイエンスコーパス: virus-associated

1 ted (4460 [2465] pg/mL) and varicella-zoster virus-associated (5386 [1778] pg/mL) uveitis.

2 Respiratory syncytial virus-associated acute respiratory infection (RSV-ARI) c

3 fection is programmed in large part by early virus-associated Ag-nonspecific factors, and imply that

4 Thus, community respiratory virus-associated airflow decline seems to be specific to

5 2008, we estimated that 20 million influenza-virus-associated ALRI and 1 million influenza-virus-asso

6 nge [UR] 63.1-190.6), 10.1 million influenza-virus-associated ALRI cases (6.8-15.1); 870 000 influenz

7 We estimated the upper bound of influenza virus-associated ALRI deaths based on the number of in-h

8 to 34 800 (13 200-97 200) overall influenza-virus-associated ALRI deaths.

9 ted ALRI cases (6.8-15.1); 870 000 influenza-virus-associated ALRI hospital admissions (543 000-1 415

10 Chikungunya virus, a cytopathic RNA virus associated also with epidemics, required RelA, and

11 ducible MHC class II expression and a direct virus-associated alteration in Janus kinase levels.

12 k squamous cell cancer, both human papilloma virus-associated and human papilloma virus-negative tumo

13 Specifically, in both virus-associated and nonviral exacerbations, we demonstr

14 of intracellular and extracellular levels of virus-associated antigens showed an enhanced accumulatio

15 fection studies to achieve similar levels of virus-associated APO3G and (ii) we constructed stable ce

16 lly account for the Vif-induced reduction of virus-associated APOBEC3G, suggesting that Vif may funct

17 tive estimates of the absolute proportion of virus-associated ARI cases to which a viral cause can be

18 eptococcus, Moraxella, or Haemophilus marked virus-associated ARIs.

19 ent with anti-IgE antibody to blunt seasonal virus-associated asthma exacerbations in children provid

20 Posttransplant Epstein-Barr virus-associated B-cell lymphoproliferative disease (PTL

21 It is also a leading cause of virus-associated birth defects and is associated with at

22 In the phase I/II CheckMate 358 study of virus-associated cancer types, patients with resectable

23 persistent viruses, and a high incidence of virus-associated cancers.

24 iral latency and are etiologically linked to virus-associated cancers.

25 n immunotherapies in the treatment of select virus-associated cancers.

26 to be a useful strategy in the treatment of virus-associated cancers.

27 ved the way for using immunotherapy to treat virus-associated cancers.

28 ies with a catalase inhibitor indicated that virus-associated catalase can have a role in protecting

29 d GC B cells are a useful model for studying virus-associated changes contributing to the pathogenesi

30 A model for hepatitis B virus-associated chronic liver disease has been made usi

31 BACKGROUND & AIMS: Patients with hepatitis C virus-associated cirrhosis and clinical significant port

32 ctive study of 226 patients with hepatitis C virus-associated cirrhosis and CSPH who had SVR to inter

33 ue for identifying patients with hepatitis C virus-associated cirrhosis likely to develop HCC within

34 iver biopsies from patients with hepatitis C virus-associated cirrhosis or liver tissues removed duri

35 ospective study of patients with hepatitis C virus-associated cirrhosis, an SVR to all-oral therapy s

36 The incidence of influenza virus-associated clinic visits was highest among patient

37 Mumps virus-associated CNS complications in vaccinees continue

38 ents designed to reduce the risk of vaccinia virus-associated complications during pregnancy.

39 d fungal clearance in human immunodeficiency virus-associated cryptococcal meningitis.

40 IV-1 entry depends on an interaction between virus-associated CyPA and CD147 on a target cell.

41 Virus-associated CyPA coimmunoprecipitated with CD147 fr

42 nslocation into the nucleus and the rates of virus-associated cytopathic effects.

43 acycline, while little viral replication and virus-associated cytotoxicity was observed in infected g

44 Human immunodeficiency virus-associated dementia (HAD) is associated with incre

45 Supporting this, no Bombali virus-associated disease outbreaks have been reported, a

46 pled receptor (vGPCR) has been implicated in virus-associated disease pathogenesis due principally to

47 Rather than severe virus burden, BR/08 virus-associated disease severity correlated with extens

48 importance in the context of human papilloma virus-associated disease, in which young patients will b

49 humans that appears to protect the host from virus-associated disease.

50 ola virus glycoprotein effectively prevented virus-associated disease.

51 he lungs of infected mice, thereby promoting virus-associated disease.

52 ave many potential benefits as treatment for virus-associated diseases and malignancies, due to their

53 region in HTLV-1 replication or in mediating virus-associated diseases remain to be defined.

54 n and family studies of various Epstein-Barr virus-associated diseases suggests a substantial genetic

55 alcoholic fatty liver disease or hepatitis C virus-associated dysmetabolic syndrome, will take statin

56 The 2000-2001 outbreak of Sudan virus-associated EHF in the Gulu district of Uganda led

57 correlation between ERK/MAPK activation and virus-associated encephalitis.

58 sed in developed countries, the Epstein-Barr-virus-associated endemic subtype, and an HIV-associated

59 designs and determine which ones best mimic virus-associated Env trimers.

60 Lesional herpes simplex virus associated erythema multiforme keratinocytes also

61 mistry studies indicated that herpes simplex virus associated erythema multiforme lesional skin from

62 ret the data to indicate that herpes simplex virus associated erythema multiforme pathology includes

63 (76%) DNA polymerase positive herpes simplex virus associated erythema multiforme patients was also p

64 onal skin from 21 of 26 (81%) herpes simplex virus associated erythema multiforme patients was positi

65 ot in herpes simplex virus or herpes simplex virus associated erythema multiforme patients, and lesio

66 virus, a syndrome designated herpes simplex virus associated erythema multiforme.

67 tiple inflammatory cell pathways involved in virus-associated exacerbations, in contrast to squamous

68 oracic Society Steps 2-5), with a history of virus-associated exacerbations, were randomized to 14-da

69 minants of acute HCV infection dynamics than virus-associated factors.

70 Virus-associated febrile lower respiratory tract infecti

71 By proteotyping analysis, EKC virus-associated fiber knobs were uniquely shared.

72 uenza virus, as well as reducing chikungunya virus-associated foot swelling and viral load.

73 Hepatitis B and C virus-associated HCC became less common, and more patien

74 us (WHV) and serve as a model of hepatitis B virus-associated HCC in humans.

75 In HBV replicating cells, including virus-associated HCCs, suppressor of zeste 12 homolog (S

76 ing adoptive T cells against post-transplant virus-associated hematologic malignancies, lymphoma and

77 e a consideration in males with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis (EBV

78 was an 11-year-old white boy diagnosed with virus-associated hemophagocytic syndrome (VAHS).

79 learly show that retrovirus binds FN through virus-associated heparan sulfate (HS) and that binding i

80 ly against hepatitis B virus- or hepatitis C virus-associated hepatocellular carcinoma (HCC).

81 nflammatory disorders, including hepatitis B virus-associated hepatocellular carcinoma.

82 lated in human cancer, including hepatitis B virus-associated hepatocellular carcinomas (HCCs).

83 iotemporal profiles of virus replication and virus-associated histopathology in the central nervous s

84 onsistent detection of LMP2A in Epstein-Barr virus-associated HL, this implicates a role for LMP2A in

85 other hand, the 4 patients with Epstein-Barr virus-associated HLH typically had depressed numbers of

86 s have higher risks of respiratory syncytial virus-associated hospitalization than HIV-unexposed infa

87 we show data suggesting that several of the virus-associated host plant proteins accumulated to high

88 be personalized to target specific viral and virus-associated host processes that are only present in

89 responsible for a substantial proportion of virus-associated human cancers, particularly in immunoco

90 cellular targets in a hypoxic environment in virus-associated human cancers.

91 zidothymidine (AZT) is used to treat several virus-associated human cancers.

92 eminiscent of the activity of the adenoviral virus-associated I (VAI) RNA, a known inhibitor of the a

93 Virus-associated I (VAI) RNAs of adenoviruses are requir

94 the vector index may help prevent West Nile virus-associated illness.

95 At the cellular level, we show that virus-associated immune activation by IFN-alpha blocks B

96 lutely critical for the effective control of virus-associated infectious complications in hematopoiet

97 dissemination in the brain and may constrain virus-associated injury.

98 Here we investigate the influence of virus-associated innate immune activation on lymphocyte

99 giogenic, implicating it as a contributor to virus-associated Kaposi's sarcoma, primary effusion lymp

100 orescent stainings on human immunodeficiency virus-associated Kaposi's sarcoma.

101 Five patients with human immunodeficiency virus-associated KS (4 receiving antiretroviral therapy)

102 siologic basis for human T cell lymphotropic virus-associated leukemia/lymphoma as well as past, pres

103 ructural data for DC-SIGNR in complex with a virus-associated ligand, and unique binding modes were o

104 SR-BI interaction rather than changes in the virus-associated lipoprotein-E2 interaction.

105 l a novel role of HVR1 for the properties of virus-associated lipoproteins.

106 After liver transplantation for hepatitis C virus-associated liver failure, standard immunosuppressi

107 iver cancer (aflatoxin exposure, hepatitis B virus-associated liver injury, p53 loss, p53ser249 mutat

108 resent a heterogeneous group of Epstein-Barr virus-associated lymphoid proliferations that arise in i

109 (NK) cell lymphoma (NNL) is an Epstein-Barr virus-associated lymphoma of cytotoxic NK cell origin.

110 t instead developed large human Epstein-Barr virus-associated lymphomas by 12 weeks.

111 creased risk reflects an increase in Epstein-virus-associated lymphomas.

112 Epstein-Barr virus-associated lymphoproliferative disease (EBV-LPD) i

113 Posttransplantation Epstein-Barr virus-associated lymphoproliferative disease (PTLPD) occ

114 Among these are Epstein-Barr virus-associated lymphoproliferative diseases in immunoc

115 granulomatosis (LYG) is a rare Epstein-Barr virus-associated lymphoproliferative disorder.

116 d with development of immunity against fatal virus-associated malaria without accelerating SHIV disea

117 d to bursting parasite replication and fatal virus-associated malaria.

118 treatment of opportunistic disease and some virus-associated malignancies such as Epstein-Barr virus

119 m the model include that SV40 infections and virus-associated malignancies will be restricted geograp

120 haryngeal carcinoma (NPC) is an Epstein-Barr virus-associated malignancy most common in East Asia and

121 haryngeal carcinoma (NPC) is an Epstein-Barr virus-associated malignancy most common in East Asia, Af

122 iferative disorder (PTLD) is an Epstein-Barr virus-associated malignancy that occurs in the setting o

123 ng sphingolipid-based therapies against this virus-associated malignancy.

124 ted transcription regulates the formation of virus-associated membrane compartments.

125 virus in the presence or absence of dsRNA, a virus associated molecular pattern.

126 We conclude that dsRNA is a practical virus-associated molecular pattern that can be targeted

127 brate counterparts, can recognize dsRNA as a virus-associated molecular pattern, resulting in the act

128 TLR3 signaling is activated by dsRNA, a virus-associated molecular pattern.

129 response is initiated by the recognition of virus-associated molecular patterns such as dsRNA, a vir

130 e immune activation and could be mimicked by virus-associated molecular patterns such as the syntheti

131 The recognition of virus-associated molecular patterns, including double- a

132 kinase in dendritic cells (DCs), which sense virus-associated molecular patterns.

133 ection is critical, when tens to hundreds of virus-associated molecules are present in the patient's

134 gerous, because pregnant women suffer higher virus-associated morbidity and mortality than do nonpreg

135 Virus-associated mortality (but not the number of cases)

136 and targeted apoptosis as a key mechanism of virus-associated myocardial injury in vitro and in vivo.

137 ligand MIP1alpha protects against Coxsackie virus-associated myocarditis.

138 y, with a special focus on virus-induced and virus-associated myocarditis.

139 IL-6) has been implicated as a key factor in virus-associated neoplasia because of its proproliferati

140 g glomerulosclerosis, human immunodeficiency virus associated nephropathy, Denys-Drash, diabetic neph

141 tation after losing their renal grafts to BK virus-associated nephropathy (BKAN) are described.

142 BK virus-associated nephropathy (BKVAN) causes renal allogr

143 plant after allograft loss as a result of BK virus-associated nephropathy (BKVAN).

144 BK virus-associated nephropathy (BKVN) is associated with a

145 Human immunodeficiency virus-associated nephropathy (HIVAN) affects up to 10% o

146 ained hematuria), and human immunodeficiency virus-associated nephropathy (or exclusion of it in case

147 Because the course of polyoma virus-associated nephropathy (PVAN) has not been evaluat

148 BK virus-associated nephropathy is an increasingly recogniz

149 nships between ongoing viral replication and virus-associated neurodegeneration.

150 ations for understanding the pathogenesis of virus-associated neurodevelopmental damage.

151 S is an essential step in the development of virus-associated neuroinflammatory diseases, notably mye

152 Human immunodeficiency virus-associated neurological disease (HAND) still cause

153 abuse opiates can have a higher incidence of virus-associated neuropathology.

154 We examined the types of Epstein-Barr virus-associated nuclear antigen-1 (EBNA-1) gene carboxy

155 This study directly correlates individual virus-associated objects observed in light microscopy wi

156 host DDR factors in the MCPyV life cycle and virus-associated oncogenesis.

157 umor samples and expand our understanding of virus-associated oncogenesis.

158 sociated with different asthma phenotypes as virus-associated or steroid-resistant asthma.

159 phospholipids and fatty acids could lead to virus-associated organ damage via overactivation of inna

160 fect of radiation therapy in human papilloma virus-associated oropharyngeal SCC, we hypothesized that

161 fect of radiation therapy in human papilloma virus-associated oropharyngeal squamous cell carcinoma,

162 d mature p26 Gag and decreased extracellular virus-associated p26 Gag were observed by Western blot a

163 an important step for HSV-1 transmission and virus-associated pathologies.

164 in the viral replication cycle and promotes virus-associated pathology.

165 nts that reduce or eliminate HPV and reverse virus-associated pathology.

166 vated by the specific recognition of various virus-associated patterns by several retinoic acid-induc

167 transplant (HCT) recipients with respiratory virus-associated pneumonia.

168 ng host LLOs required for N-glycosylation of virus-associated polypeptides.

169 immunosuppressed patients with Epstein-Barr virus-associated posttransplant lymphoma and in some pat

170 Epstein-Barr virus-associated posttransplant lymphoproliferative dise

171 histology resembled lesions of Epstein-Barr virus-associated posttransplant lymphoproliferative dise

172 suggested an increased risk of Epstein-Barr virus-associated posttransplant lymphoproliferative diso

173 transplantation with potential advantages in virus-associated posttransplant malignancies as well as

174 the S phase, which may then allow subsequent virus-associated processes, such as RNA splicing, transp

175 Significantly, this mouse model of virus-associated pulmonary B-cell lymphoma closely mimic

176 Virus-associated pyramids (VAPs) assemble in the host ce

177 me has strong similarities with familial and virus-associated reactive hemophagocytic lymphohistiocyt

178 The differentiation of BK virus-associated renal allograft nephropathy (BKVAN) fro

179 th microtubules facilitates the formation of virus-associated replication complexes, which are requir

180 dence and hospitalisation rates of influenza-virus-associated respiratory infections by severity, cas

181 tal admissions, and mortality from influenza-virus-associated respiratory infections in children unde

182 nscription by RNA polymerase III on tRNA and virus-associated RNA genes and initiates preinitiation c

183 irect recognition of promoters (for tRNA and virus-associated RNA genes) or promoter-TFIIIA complexes

184 ofiles and binding affinities for adenoviral virus-associated RNA I (VA RNAI) and HIV-1 trans-activat

185 Virus-associated RNA I (VA RNAI) is a short ( approximat

186 Adenovirus encodes virus-associated RNA I (VAI), a highly structured RNA in

187 Mutants of adenovirus type 5 (Ad5) virus-associated RNA I deficient in inhibiting the activ

188 The virus-associated RNA, vRNA, was identified by DNase I tr

189 Adenovirus virus-associated RNA-I (VAI) is a short, noncoding trans

190 n Italian ringspot virus, and turnip crinkle virus-associated RNA; the insect plus-strand RNA [(+)RNA

191 come was the incidence of clinically defined virus-associated RTI episodes confirmed from nasal swabs

192 tic supplementation would reduce the risk of virus-associated RTIs during the first year of life in a

193 Virus-associated S dynamically samples at least four dis

194 ry role for IFN-gamma in the pathogenesis of virus-associated secondary HLH as opposed to its central

195 knowledge, we established an animal model of virus-associated secondary HLH by infecting immunocompet

196 hypothesized that in human immunodeficiency virus-associated sensory neuropathy (HIV-SN), damaged mt

197 irus-associated ALRI and 1 million influenza-virus-associated severe ALRI occurred in children under

198 (myocardial infarction and stroke), cancers (virus associated, smoking related, and other), severe ne

199 vents are believed to be key determinants of virus-associated spread, antiviral immune responses, and

200 poradic, endemic, and human immunodeficiency virus-associated subtypes.

201 >64 years) using the cumulative (12 months) virus-associated symptomatic attack rates from 12 countr

202 rus vector to specific tissues and to reduce virus-associated toxicity after systemic application.

203 viral genes, allowing for infection without virus-associated toxicity.

204 The incidence of human immunodeficiency virus-associated tuberculosis, which was virtually unrec

205 cell surveillance is often effective against virus-associated tumors because of their high immunogeni

206 ative head and neck cancers, suggesting that virus-associated tumors constitute a unique entity among

207 Hepatitis B virus-associated tumors seem to have a better prognosis

208 V)-encoded EBNA1 protein is expressed in all virus-associated tumors where it plays an essential role

209 of viral latency and in immune therapies for virus-associated tumors.

210 ontribute to the development of Epstein-Barr virus-associated tumors.

211 s of LMP1 variants in cells and Epstein-Barr virus-associated tumors.

212 which such mutations may arise, including in virus-associated tumors.

213 orylation and its deubiquitination by Herpes virus associated ubiquitin-specific protease (Hausp, a.k

214 equirements that are operative in adenovirus virus-associated (VA) RNA genes.

215 helper functions E1a, E1b, E2a, E4Orf6, and virus-associated (VA) RNA; however, their combined net e

216 Adenovirus Virus-Associated (VA) RNAs are the first discovered vira

217 Most human adenoviruses encode two virus-associated (VA) RNAs, VA RNAI and VA RNAII, that a

218 We conclude that virus-associated Vif inhibits processing of a subset of

219 We now demonstrate for the first time that virus-associated Vif is subject to proteolytic processin

220 y in 49 subjects with human immunodeficiency virus-associated weight loss (12.7 +/- 0.9% of body wt).

221 Epstein-Barr virus (EBV) is an oncogenic virus associated with a number of human malignancies inc

222 the stage of exponential increase in plasma virus associated with acute HIV infection (3, 7, 20, 35,

223 Human metapneumovirus is a common virus associated with acute lower respiratory infections

224 man T-cell leukemia virus type 1 (HTLV-1), a virus associated with adult T-cell leukemia, is signific

225 virus (MCPyV) is a small, nonenveloped tumor virus associated with an aggressive form of skin cancer,

226 However, in contrast to T cells, virus associated with B cells was surface bound, as show

227 The paucity of cell-free virus associated with BDV infection has hindered studies

228 ights into the conformational changes of the virus associated with cell entry or caused by changing o

229 ) has provided the latest possible candidate virus associated with cryptogenic hepatitis.

230 There are at least 14 subtypes of the virus associated with different human populations.

231 Ad serotype 37 (Ad37), a virus associated with epidemic keratoconjunctivitis, but

232 .IMPORTANCE Zika virus (ZIKV) is an emerging virus associated with Guillain-Barre syndrome, and fetal

233 tis G virus (GBV-C/HGV) is a newly described virus associated with hepatitis in humans, and GBV-C/HGV

234 virus (ISAV) infection, an Orthomyxoviridae virus associated with high mortalities in salmonid aquac

235 Ebolavirus is a hemorrhagic fever virus associated with high mortality.

236 y isolated North American lineage H7 subtype virus associated with human conjunctivitis is capable of

237 yield of Chandipura virus, a cytopathic RNA virus associated with human epidemics, by extending the

238 immunity to human herpesvirus 8 (HHV-8), the virus associated with Kaposi's sarcoma (KS).

239 sociated herpesvirus (KSHV), a B-cell-tropic virus associated with KS and B-cell lymphomas, encodes 1

240 Valley fever (RVF) virus is a mosquito-borne virus associated with large-scale epizootics/epidemics t

241 propose a novel mechanism by which HTLV-1, a virus associated with lymphoproliferative disease, dysre

242 arr virus (EBV) is an oncogenic gamma-herpes virus associated with malignancies that develop in both

243 Nipah virus (NiV) is an emerging virus associated with outbreaks of acute respiratory dis

244 ther they are reflected in the population of virus associated with peripheral blood mononuclear cells

245 venting the initial production of infectious virus associated with reactivation.

246 sociated herpesvirus (KSHV) is a human tumor virus associated with several cancers.

247 Ad type 37 (Ad37), a subgroup D virus associated with severe ocular infections, is unabl

248 Hepatitis C virus (HCV) is an oncogenic virus associated with the onset of hepatocellular carcin

249 amples was consistent with evidence that the virus associated with the Sao Paulo outbreak originated

250 ion that a densovirus is the predominant DNA virus associated with this syndrome and, thus, the most

251 sovirus (SSaDV) as the most likely candidate virus associated with tissues from symptomatic asteroids

252 us (EBV) is a well-established B-cell-tropic virus associated with various lymphoproliferative diseas

253 previously undetected RNA viruses and a DNA virus associated with wild D. melanogaster.

254 ntrols can provide a rapid means to identify viruses associated with a complex disease, paving the wa

255 are a diverse and rapidly expanding group of viruses associated with a variety of disease conditions

256 rus, and metapneumovirus are the most common viruses associated with acute lower respiratory infectio

257 i.e., chicken, goose, and turkey), including viruses associated with acute nephritis in chickens.

258 Among the types of viruses associated with acute otitis media, respiratory

259 d human rhinovirus (HRV) are the most common viruses associated with acute respiratory tract infectio

260 may be useful for comprehensive diagnosis of viruses associated with ALF, or to exclude infectious et

261 ostic testing in detection of known or novel viruses associated with ALF.

262 crobial contamination, and discovering novel viruses associated with both acute and chronic illnesses

263 In order to identify viruses associated with BRD, we used a metagenomics appr

264 to vaccination traits against four different viruses associated with BRDC: bovine viral diarrhea viru

265 Viruses associated with cancer can be detected by search

266 Polyomaviruses are small circular DNA viruses associated with chronic infections and tumors in

267 vaccine-preventable and zoonotic respiratory viruses associated with clusters of severe respiratory i

268 May, 1994, and May, 1996, by nested PCR for viruses associated with CNS infections in the UK.

269 the vertical transmission of ZIKV and other viruses associated with congenital disease.

270 bioinformatics analysis to identify putative viruses associated with Diaphorina citri, the Asian citr

271 athogenicity and transmissibility of two TRS viruses associated with disease in humans in the ferret

272 ing, is a powerful technique for discovering viruses associated with diseases with no definitive etio

273 IMPORTANCE Enteroviruses are a vast group of viruses associated with diverse human diseases, but only

274 Among these, HAdV-D includes those viruses associated with epidemic keratoconjunctivitis (E

275 apillomaviruses, members of a group of dsDNA viruses associated with epithelial growths and tumors, h

276 a, and corona-, calici- and lyssaviruses and viruses associated with hepatitis A and E.

277 Multiple RNA viruses associated with honeybees are widespread in symp

278 RNA viruses associated with honeybees represent a potential

279 To determine whether avian H5N1 influenza viruses associated with human infections in Vietnam had

280 changes in the HA of swine origin influenza viruses associated with increased transmission and decre

281 viruses (Ad) are double-stranded DNA (dsDNA) viruses associated with infectious diseases, but they ar

282 Many publications deal with RNA viruses associated with major disease emergence events,

283 blasts offers an in vitro model for studying viruses associated with prenatal infections.

284 uses 1 and 2 (HSV-1 and HSV-2) are large DNA viruses associated with recurring oral or genital erosio

285 Here we used viral metagenomics to examine viruses associated with sea turtle fibropapillomatosis (

286 nenveloped, positive-sense single-strand RNA viruses associated with self-limiting diarrhea.

287 he rates of viral detection and identified 3 viruses associated with severe BRD signs.

288 is short review we focus on newly identified viruses associated with severe haemorrhagic disease in h

289 s of human infections with novel influenza A viruses associated with severe human illness, or with th

290 Polydnaviruses are double-stranded DNA viruses associated with some subfamilies of ichneumonoid

291 y comprising the complete proteomes of seven viruses associated with T1D and open reading frames from

292 mples of the first uncultivated Caudovirales viruses associated with Thaumarchaeota, which we designa

293 re reveal that STIV is strikingly similar to viruses associated with the Bacteria and Eukarya domains

294 Over the last decade, rabies viruses associated with the silver-haired bat (SHBRV) ha

295 Those viruses associated with ticks were found to have a signi

296 e sent to CDC, Atlanta, Ga., for testing for viruses associated with viral HFs known to be present in

297 ty of microbes (eukaryotes, prokaryotes, and viruses) associated with larger 'host' organisms has led

298 sites in the skin of human immunodeficiency virus-associated xerosis patients (upper arm, n = 12; up

299 dergic innervation in human immunodeficiency virus-associated xerosis.

300 ffer a wide range of opportunities to reduce virus-associated yield losses in cassava for farmers and