ライフサイエンスコーパス: polyomavirus

1 r frequently associated with the Merkel cell polyomavirus.

2 c acid, is the major attachment receptor for polyomavirus.

3 virus (MWPyV) is a recently identified human polyomavirus.

4 uce MCC in mice using oncoproteins from this polyomavirus.

5 Merkel cell carcinoma virus, which is also a polyomavirus.

6 ent of trichodysplasia spinulosa caused by a polyomavirus.

7 screen to examine the humoral response to BK polyomavirus.

8 tralize BK virus subtypes and the related JC polyomavirus.

9 skin cancer often caused by the Merkel cell polyomavirus.

10 the rearrangements typical for reactivating polyomaviruses.

11 g a proteostatic latency mechanism common to polyomaviruses.

12 ion of Fe/S coordination in the sTs of other polyomaviruses.

13 ural history of the more recently discovered polyomaviruses.

14 uses, including two papillomaviruses and two polyomaviruses.

15 ds sialylated glycan receptors in many other polyomaviruses.

16 mic and clinical features of these cutaneous polyomaviruses.

17 Polyomavirus 5-gene set expression reliably distinguishe

18 Human polyomavirus 6 (HPyV6) is most often detected at the ski

19 rus, JC polyomavirus, WU polyomavirus, Human polyomavirus 6 [HPyV6], HPyV7, HPyV9, and Trichodysplasi

20 richodysplasia spinulosa polyomavirus, human polyomavirus 6 and 7 have been linked to specific skin d

21 richodysplasia spinulosa polyomavirus, human polyomavirus 6 and 7, and Malawi polyomavirus are shed f

22 Human polyomavirus 7 (HPyV7) is one of 11 HPyVs recently disco

23 JCPyV polyomavirus, a member of the human virome, causes progr

24 re included herpesviruses, papillomaviruses, polyomaviruses, adenoviruses and anelloviruses.

25 el cell, HPyV7 and trichodysplasia spinulosa polyomaviruses after drug treatment were determined by i

26 a novel strategy for the development of anti-polyomavirus agents.

27 teric viruses [human adenoviruses, JC and BK polyomaviruses, Aichi virus 1 (AiV-1), enteroviruses, an

28 In this Gem, we will discuss two viruses, polyomavirus and cytomegalovirus, in which cell culture

29 -is caused by the integration of Merkel cell polyomavirus and persistent expression of large T antige

30 patterns and determinants of acquisition of polyomaviruses and herpesviruses in childhood.

31 ersely associated with the seroprevalence of polyomaviruses and herpesviruses.

32 Our findings also suggest that eukaryotic polyomaviruses and papillomaviruses with dsDNA genomes h

33 This pore is conserved across polyomaviruses and suggests either that these viruses ha

34 tical evidence in favor of an association of polyomaviruses and their hosts over millions of years.

35 Merkel cell polyomavirus(+) and Merkel cell polyomavirus(-) cells ex

36 V9, and Trichodysplasia spinulosa-associated polyomavirus) and examined factors associated with MCPyV

37 almonella spp., Campylobacter jejuni, bovine polyomavirus, and bovine rotavirus A were present most f

38 irnaviruses, parvoviruses, papillomaviruses, polyomaviruses, and a gammaherpesvirus, were identified,

39 Herpesviruses, parvoviruses, polyomaviruses, and bacteriophages were also detected.

40 irus, human polyomavirus 6 and 7, and Malawi polyomavirus are shed from the skin, and Merkel cell pol

41 Mammalian polyomaviruses are characterized by establishing persist

42 Human polyomaviruses are double-stand DNA viruses with a conse

43 Polyomaviruses are opportunistic pathogens that are asso

44 However, MCPyV appears different from other polyomaviruses, as it requires sulfated polysaccharides,

45 g drug regimens for transplant patients with polyomavirus-associated diseases may reduce symptomatic

46 viruses and explain the rarity of some novel polyomavirus-associated diseases.

47 kidney transplant recipients who can develop polyomavirus-associated kidney disease.

48 nfiltrates in renal biopsy specimens with BK polyomavirus-associated nephropathy (BKPyVAN) and specim

49 BK polyomavirus-associated nephropathy (BKPyVAN) constitute

50 With current immunosuppressive regimens, BK polyomavirus-associated nephropathy (BKPyVAN) is still a

51 Polyomavirus-associated nephropathy (PVAN) after BK viru

52 Polyomavirus-associated nephropathy (PVAN) occurs in a s

53 omatic in healthy people; however, it causes polyomavirus-associated nephropathy in renal transplant

54 o a specific diagnosis), infections, such as polyomavirus-associated nephropathy, calcineurin inhibit

55 factors that underlie the pathophysiology of polyomavirus-associated nephropathy.

56 imental data on unperturbed adenoviruses and polyomaviruses, at the same time providing insight into

57 Polyomavirus binding, internalization, and infection are

58 Reactivation of the polyomavirus BK has been associated with de novo antibod

59 onstrating "decoy" cells, and/or significant polyomavirus BK viremia.

60 irus, and West Nile virus, as well the human polyomaviruses BK/JC/MCV, human adenoviruses, and human

61 Three recipients developed polyomavirus (BK) viremia near or >10,000 copies/ml that

62 BK polyomavirus (BKPyV) affects mostly kidney and bone marr

63 BK polyomavirus (BKPyV) frequently reactivates in kidney tr

64 ell epitopes that influence the course of BK polyomavirus (BKPyV) infection after kidney transplantat

65 t APOBEC3B is specifically upregulated by BK polyomavirus (BKPyV) infection in primary kidney cells a

66 Chronic BK polyomavirus (BKPyV) infection is recognized as a potent

67 BK polyomavirus (BKPyV) is a small DNA virus that establish

68 BK polyomavirus (BKPyV) is a ubiquitous human pathogen, wit

69 ly target BKPyV-infected cells.IMPORTANCE BK polyomavirus (BKPyV) is an emerging pathogen that reacti

70 BK polyomavirus (BKPyV) is associated with symptomatic hemo

71 e-size primary transcripts.IMPORTANCE The BK polyomavirus (BKPyV) miRNA plays an important role in re

72 BK polyomavirus (BKPyV) reactivation is associated with sev

73 fter kidney transplantation, uncontrolled BK polyomavirus (BKPyV) replication causes kidney graft fai

74 Here, we demonstrate the detection of BK Polyomavirus (BKPyV), an emerging indicator of microbiol

75 BK polyomavirus (BKPyV)-associated cancer after transplanta

76 d immunoglobulin G seroreactivity against 10 polyomaviruses (BKPyV, JCPyV, KIPyV, WUPyV, MCPyV, HPyV6

77 irus (CMV), Epstein-Barr virus (EBV), and BK polyomavirus (BKV) at transplant was a risk factor for p

78 uppression in kidney transplant patients, BK polyomavirus (BKV) has been shown to induce nephropathy

79 Recent case series describe detection of BK polyomavirus (BKV) in urinary tract cancers in kidney tr

80 we identified a peptide derived from the BK polyomavirus (BKV) minor structural proteins VP2/3 that

81 BK polyomavirus (BKV)-associated nephropathy is a threat to

82 nses in a sophisticated manner.IMPORTANCE BK polyomavirus can cause serious problems in immune-suppre

83 Human polyomaviruses can reactivate in transplant patients cau

84 Human polyomaviruses cause a common childhood infection worldw

85 affects the quantity and quality of the anti-polyomavirus CD8 T cell response and its differentiation

86 Merkel cell polyomavirus(+) and Merkel cell polyomavirus(-) cells express serine palmitoyl transfera

87 MCPyV differs from other known polyomaviruses concerning its cell tropism, entry recept

88 No trichodysplasia spinulosa-associated polyomavirus could be isolated from the skin lesions; ho

89 Merkel cell polyomavirus could contribute to the origin of this derm

90 fectious entry.IMPORTANCE MCPyV is the first polyomavirus directly implicated in the development of a

91 based on CRISPR-Cas13 accurately detects BK polyomavirus DNA and cytomegalovirus DNA from patient-de

92 omaviruses, Merkel cell carcinoma-associated polyomavirus, Epstein-Barr virus, and Kaposi's sarcoma-a

93 cell polyomavirus (MCPyV) is the first human polyomavirus etiologically associated with Merkel cell c

94 d 58.9% of eyebrow hair specimens) among all polyomaviruses examined.

95 y, and, ultimately, pathogenicity within the polyomavirus family and highlight the need for structure

96 hylogenetic relationships within the growing polyomavirus family and perhaps also for other viruses.

97 yV cell entry is unique among members of the polyomavirus family as it requires the engagement of two

98 This was also hypothesized for polyomaviruses (family Polyomaviridae), a group comprisi

99 These results suggest that, while intragraft polyomavirus gene expression may be useful as an ancilla

100 Five polyomavirus genes and seven immune-related genes (five

101 evidence that, consistent with this idea, BK polyomavirus genomes are depleted of APOBEC3B-preferred

102 Whereas mouse polyomavirus has been studied in a fair amount of detail

103 Murine polyomavirus has repeatedly provided insights into tumor

104 Polyomavirus-Haufen counts showed excellent correlation

105 Polyomavirus-Haufen were counted in 40 urine samples fro

106 Several new polyomaviruses have been discovered in the last decade,

107 Both the papillomaviruses and the polyomaviruses have served as tools for understanding pa

108 titative PCR to test for cytomegalovirus, BK polyomavirus, human herpesvirus 6B, HHV-6A, adenovirus,

109 avirus, KI polyomavirus, JC polyomavirus, WU polyomavirus, Human polyomavirus 6 [HPyV6], HPyV7, HPyV9

110 cell polyomavirus, trichodysplasia spinulosa polyomavirus, human polyomavirus 6 and 7 have been linke

111 cell polyomavirus, trichodysplasia spinulosa polyomavirus, human polyomavirus 6 and 7, and Malawi pol

112 hybridization confirmed the presence of the polyomavirus in endothelial cells at sites of myositis a

113 rare skin cancer associated with Merkel cell polyomavirus in most cases.

114 associated crAssphage, Bacteroides spp., and polyomavirus in sewage samples from 49 wastewater facili

115 zation of the noncoding control region of JC polyomavirus in vivo, mainly in CSF and blood.

116 n of large tumor T antigens (TAg) encoded by polyomaviruses in mammalian cells results in increased t

117 vides insight into how DDRs are activated by polyomaviruses in primary cells with intact cell cycle c

118 AB(5) bacterial toxins and polyomaviruses induce membrane curvature as a mechanism

119 ory of these viruses and the evolution of JC polyomavirus-induced progressive multifocal leukoencepha

120 BDCA-1(+) mDCs localized in proximity to the polyomavirus-infected tubular epithelial cells.

121 Although both polyomavirus infection and T cell-mediated rejection (TC

122 res unravel a potent modality for inhibiting polyomavirus infection in kidney transplant recipients a

123 of the skin, is associated with Merkel cell polyomavirus infection.

124 of herpes simplex, Epstein-Barr virus or BK polyomavirus infections.

125 Tumour oncogenesis is linked to Merkel cell polyomavirus integration and ultraviolet-radiation-induc

126 Merkel cell polyomavirus is a newly discovered human cancer virus th

127 BK polyomavirus is ubiquitous, with a seropositivity rate o

128 en, as well as large T antigens from related polyomaviruses, is alone capable of upregulating APOBEC3

129 the basis by which MCPyV, among all 12 human polyomaviruses, is the only one that causes cancer in hu

130 the presence of this pore is conserved among polyomaviruses, its functional role in infection or asse

131 document a unique DNA recombination between polyomavirus JC (JC virus [JCV]) and Epstein-Barr virus

132 ting disease caused by the human neurotropic polyomavirus JC (JCV) and is found almost exclusively in

133 Isolates of the human polyomavirus JC virus from patients with the frequently

134 the white matter of the brain caused by the polyomavirus JC virus, which typically occurs only in im

135 Classic human polyomaviruses (JC and BK viruses) become pathogenic whe

136 9 polyomaviruses (MCPyV, BK polyomavirus, KI polyomavirus, JC polyomavirus, WU polyomavirus, Human po

137 JC polyomavirus (JCPyV) establishes a persistent, lifelong,

138 The human JC polyomavirus (JCPyV) establishes an asymptomatic, persis

139 a fatal disease caused by reactivation of JC polyomavirus (JCPyV) in immunosuppressed individuals and

140 nitoring, metagenomic sequencing detected JC polyomavirus (JCPyV) in the urine of 7 donors and their

141 JC polyomavirus (JCPyV) infection of immunocompromised indi

142 JC polyomavirus (JCPyV) infects 50 to 80% of the population

143 JC polyomavirus (JCPyV) is reactivated in approximately 20%

144 nally, endocytosis-dependent infection by JC polyomavirus (JCPyV) was reduced in human cells with dec

145 rebral manifestations are associated with JC polyomavirus (JCPyV) which are diagnosed by detection of

146 JC polyomavirus (JCPyV), a human-specific virus, causes the

147 the receptor-binding properties of human JC polyomavirus (JCPyV), a virus that resides in the kidney

148 ividuals are asymptomatically infected by JC polyomavirus (JCPyV), but if the host immune system is c

149 from infection of oligodendrocytes by the JC polyomavirus (JCPyV).

150 uding models for the human-specific virus JC polyomavirus (JCPyV).

151 The human polyomavirus, JCPyV, is the causative agent of progressi

152 life-threatening infections caused by human polyomaviruses JCV and BKV.

153 tients that treatment with interleukin 7, JC polyomavirus (JCV) capsid protein VP1, and a Toll-like r

154 of the central nervous system (CNS) with JC polyomavirus (JCV) usually occur as a result of immunoco

155 d persistence of 9 polyomaviruses (MCPyV, BK polyomavirus, KI polyomavirus, JC polyomavirus, WU polyo

156 Combined, these results demonstrate that polyomaviruses lacking miRNAs can arise infrequently and

157 Induced expression of Merkel cell polyomavirus-large tumor antigen in human lung fibroblas

158 iated with clinical presentation: intrarenal polyomavirus load levels and Banff interstitial fibrosis

159 ic infection of oligodendrocytes by human JC polyomavirus may result in the development of progressiv

160 CD8 T cell responses to infections by human polyomaviruses may be influenced by VP1 mutations involv

161 rcinomas (MCCs) that contain the Merkel cell polyomavirus (MCPyV) and the clinical significance of tu

162 Infection with Merkel cell polyomavirus (MCPyV) can lead to Merkel cell carcinoma (

163 Merkel cell polyomavirus (MCPyV) causes the majority of cases of Mer

164 Merkel cell polyomavirus (MCPyV) causes the majority of MCC cases du

165 V), Influenza A Virus (IAV), and Merkel Cell Polyomavirus (MCPyV) could be targeted.

166 MCCs frequently contain Merkel cell polyomavirus (MCPyV) DNA and express viral transforming

167 Merkel cell polyomavirus (MCPyV) expressing viral T antigens is a co

168 ng evidence indicates a role for Merkel cell polyomavirus (MCPyV) in the development of Merkel cell c

169 Merkel cell polyomavirus (MCPyV) is a human double-stranded DNA tumo

170 Merkel cell polyomavirus (MCPyV) is a small, nonenveloped tumor viru

171 Merkel cell polyomavirus (MCPyV) is frequently associated with Merke

172 Merkel cell polyomavirus (MCPyV) is the first human polyomavirus eti

173 Merkel cell polyomavirus (MCPyV) is the newest member of the human o

174 yV infecting hominine hosts, the Merkel cell polyomavirus (MCPyV) lineage.

175 Merkel cell polyomavirus (MCPyV) may contribute to tumorigenesis in

176 Merkel cell polyomavirus (MCPyV) plays an important role in Merkel c

177 ns, copy number alterations, and Merkel cell polyomavirus (MCPyV) sequence were analyzed and compared

178 l integration of a polyomavirus, Merkel cell polyomavirus (MCPyV), and MCC tumor cells express putati

179 The Merkel cell polyomavirus (MCPyV), discovered in 2008, drives the dev

180 2008 to be caused by a PyV named Merkel cell polyomavirus (MCPyV), the first PyV linked to human canc

181 ectopic expression of different Merkel cell polyomavirus (MCPyV)-derived truncated large T antigens

182 ure to ultraviolet light and the Merkel-cell polyomavirus (MCPyV).

183 ed in the last decade, including Merkel cell polyomavirus (MCPyV).

184 in cancer commonly driven by the Merkel cell polyomavirus (MCPyV).

185 incidence, prevalence, and persistence of 9 polyomaviruses (MCPyV, BK polyomavirus, KI polyomavirus,

186 Similar to other polyomaviruses, MCPyV encodes early T antigen genes, vir

187 Like other polyomaviruses, MCPyV engages sialic acid as a (co)recep

188 Merkel cell polyomavirus (MCV) causes an aggressive skin cancer afte

189 Merkel cell polyomavirus (MCV) contributes to approximately 80% of a

190 hat harbor a clonally integrated Merkel cell polyomavirus (MCV) genome have low mutation burden and r

191 Merkel cell polyomavirus (MCV) infection and DNA integration into th

192 Merkel cell polyomavirus (MCV) is a newly discovered human cancer vi

193 Merkel cell polyomavirus (MCV) small T (sT) oncoprotein induces cent

194 Merkel cell polyomavirus (MCV) small T antigen (sT) is the main onco

195 Torque teno virus (TTV) and Merkel cell polyomavirus (MCV) were detected by qPCR in 49% and 19%

196 and tractable model for a novel mechanism of polyomavirus-mediated oncogenesis.

197 interfere with proliferation of Merkel cell polyomavirus(+) Merkel cell carcinoma cell lines.

198 ntly associated with clonal integration of a polyomavirus, Merkel cell polyomavirus (MCPyV), and MCC

199 aneous tumor system with mice expressing the polyomavirus middle T (PyMT) oncogene under control of t

200 The polyomavirus middle T antigen (PyMT) oncogene activates

201 RT-deficient mice displayed marked delays in polyomavirus middle T oncogene-induced (PyMT-induced) ma

202 tors in the mouse mammary tumor virus (MMTV)-polyomavirus middle T oncoprotein (PyMT) mouse model of

203 k Institute set out to determine whether the polyomavirus middle T-transforming protein had a similar

204 Mouse polyomavirus (MPyV) is a ubiquitous persistent natural m

205 Mouse polyomavirus (MuPyV) CNS infection causes encephalopatho

206 A mouse polyomavirus (MuPyV) with a sequence-equivalent JCPyV-PM

207 Malawi polyomavirus (MWPyV) is a recently identified human poly

208 Polyomavirus-negative matched patients (n = 943) were de

209 ons were mostly preserved in the Merkel cell polyomavirus-negative subgroup.

210 Polyomavirus nephropathy (PVAN) is a common cause of kid

211 Polyomavirus nephropathy (PVN) is a common viral infecti

212 alitative highly predictive urinary test for polyomavirus nephropathy (PVN) is the PV-Haufen test.

213 Polyomavirus nephropathy (PVN) remained inadequately cla

214 ated with hemorrhagic cystitis and also with polyomavirus nephropathy (PVN).

215 finitive PVN from the Banff Working Group on Polyomavirus Nephropathy, comprising nine transplant cen

216 novo or recurrent glomerular pathologies and polyomavirus nephropathy.

217 New Jersey polyomavirus (NJPyV-2013) is a novel polyomavirus that m

218 ding for middle T antigen (MT) is the murine polyomavirus oncogene most responsible for tumor formati

219 Middle T antigen (MT) is the primary polyomavirus oncogene responsible for tumor formation.

220 MCPyV), and MCC tumor cells express putative polyomavirus oncoprotein small T antigen (sTAg) and trun

221 viruses, herpesviruses, papillomaviruses and polyomaviruses) over time were observed in individuals w

222 ttempted to reveal the composition of the JC polyomavirus population (the quasispecies, i.e., the who

223 For the first time, the JC polyomavirus population contained in different body comp

224 Polyomavirus-positive patients (n = 943) were defined as

225 age was 70.5 years, and 64% had Merkel cell polyomavirus-positive tumors.

226 s reminiscent of the polymorphic assembly of polyomavirus proteins.

227 Polyomaviruses (PV) have been historically associated wi

228 BK polyomavirus (PyV) is a major source of kidney failure i

229 The nonenveloped simian polyomavirus (PyV) simian virus 40 (SV40) hijacks the en

230 The nonenveloped polyomavirus (PyV) simian virus 40 (SV40) traffics from

231 rovide some simian virus 40 (SV40) or murine polyomavirus (PyV) ST functions.

232 Polyomaviruses (PyV) are potentially tumorigenic in huma

233 It has long been hypothesized that polyomaviruses (PyV; family Polyomaviridae) codiverged w

234 Polyomavirus (PyVs) are small DNA pathogens that contain

235 Polyomaviruses (PyVs) are a group of emerging pathogens

236 Polyomaviruses (PyVs) cause devastating human diseases,

237 Several different polyomaviruses (PyVs) encode microRNAs (miRNAs) that reg

238 sing the early genes from six distinct human polyomaviruses (PyVs), including MCPyV.

239 Other tumor-associated polyomaviruses (PyVs), including simian virus 40 (SV40),

240 Recently, raccoon polyomavirus (RacPyV) was identified in neuroglial tumor

241 Seroprevalence of polyomaviruses ranged from 38.5% to 99.8% in cord blood

242 The effect of polyomavirus reactivation (BK viremia or JC viruria) on

243 study (n=40) to explore associations between polyomavirus reactivation and immune responses to the se

244 Furthermore, these results indicate that polyomavirus reactivation associates with immune respons

245 ore prevalent during year 1 in subjects with polyomavirus reactivation than in those without reactiva

246 It is unknown if they directly reactivate polyomavirus replication from latency beyond their gener

247 rs, at therapeutic levels, directly activate polyomavirus replication through a Skp2-dependent mechan

248 s-associated diseases may reduce symptomatic polyomavirus replication while maintaining allograft-spa

249 titative histologic assessment of intrarenal polyomavirus replication/load levels.

250 also found (gemycircularvirus [n = 5] and WU polyomavirus, Saffold virus, salivirus, cyclovirus-VN, a

251 The nonenveloped polyomavirus simian virus 40 (SV40) must penetrate the h

252 However, infectivity of the polyomavirus simian virus 40 (SV40) was not affected by

253 In the case of the nonenveloped polyomavirus simian virus 40 (SV40), the virus penetrate

254 revealed by a viral oncoprotein, Merkel cell polyomavirus small T (MCV sT).

255 We have utilized the murine polyomavirus small T antigen (PyST) as a tool to study U

256 We recently demonstrated that polyomavirus small T antigen (ST) binds YAP, a major eff

257 Polyomavirus small t antigen is a viral oncogene that co

258 t cell transformation induced by Merkel cell polyomavirus small T antigen viral oncoprotein.

259 xamined whether some of the functions of the polyomavirus small T antigens (ST) are shared by the E6

260 mavirus E7 has the same effect as the murine polyomavirus small T protein.

261 nd demonstrate the identification of a novel polyomavirus species from a public metagenome.

262 yomavirus, we show that brain-resident mouse polyomavirus-specific CD8 T cells, unlike memory cells i

263 Animal polyomavirus sT oncoproteins have been found to cause ex

264 not based on PD-L1 expression or Merkel cell polyomavirus status.

265 ace morphology from those of all other known polyomavirus structures.

266 for the transforming properties of nonhuman polyomaviruses, such as simian virus 40 (SV40), but is n

267 Here we probe polyomavirus SV40 endoplasmic reticulum (ER)-to-cytosol

268 on (RTN) protects ER membrane integrity when polyomavirus SV40 escapes the ER to reach the cytosol en

269 During entry, polyomavirus SV40 is sorted from the late endosome (LE)

270 Here we probe how the non-enveloped polyomavirus SV40 penetrates the endoplasmic reticulum (

271 Polyomavirus SV40 traffics to the endoplasmic reticulum

272 tosol membrane transport of the nonenveloped polyomavirus SV40, a decisive infection step, a cytosoli

273 In the case of the nonenveloped polyomavirus SV40, penetration of the ER membrane to rea

274 bserved for the beta-herpesvirus CMV and the polyomaviruses SV40 and SA12.

275 me E2F site is required for A3B induction by polyomavirus T antigen indicating a shared molecular mec

276 d LT protein expression for all 5 pathogenic polyomaviruses tested.

277 ng CNS infection caused by JC virus (JCV), a polyomavirus that commonly establishes persistent, asymp

278 Jersey polyomavirus (NJPyV-2013) is a novel polyomavirus that may have tropism for vascular endothel

279 f membrane behavior for all AB(5) toxins and polyomaviruses that bind glycosphingolipids to invade ho

280 question by focusing on a single lineage of polyomaviruses that infect both humans and their closest

281 cell carcinoma (MCC), making MCPyV the first polyomavirus to be clearly associated with human cancer.

282 Similar to other polyomaviruses, trafficking required microtubular transp

283 en (MT), the principal oncoprotein of murine polyomavirus, transforms by association with cellular pr

284 Merkel cell polyomavirus, trichodysplasia spinulosa polyomavirus, hu

285 irus are shed from the skin, and Merkel cell polyomavirus, trichodysplasia spinulosa polyomavirus, hu

286 we show that manifestations of the causative polyomavirus (TSPyV) occur during primary infection of t

287 witnessed the discovery of eleven new human polyomaviruses, two of which cause unusual and rare canc

288 ogous peptide exhibits similar binding to JC polyomavirus VP1 and inhibits infection with similar pot

289 arison with other structurally characterized polyomavirus VP1 proteins enhances our understanding of

290 Merkel cell polyomavirus was detected in 32 of 38 specimens (84%).

291 JC polyomavirus was detected in the CSF at the time of pres

292 JC polyomavirus was detected within the graft's collecting

293 In that same year a second human polyomavirus was discovered in the urine of a kidney tra

294 In 1971, the first human polyomavirus was isolated from the brain of a patient wh

295 JC polyomavirus was not detected in pretransplant serum, ho

296 Using mouse polyomavirus, we demonstrate that a single amino acid di

297 Using mouse polyomavirus, we show that brain-resident mouse polyomav

298 In pursuit of therapeutics for human polyomaviruses, we identified a peptide derived from the

299 Antibodies to polyomaviruses were evaluated as a control.

300 We review what is currently known about JC polyomavirus, what is suspected, and what remains to be

301 (MCPyV, BK polyomavirus, KI polyomavirus, JC polyomavirus, WU polyomavirus, Human polyomavirus 6 [HPy