ライフサイエンスコーパス: tailed

1 ), Spearman rho = 0.27, P < 4.75 x 10(-5), 2-tailed).

2 ion editing while guide RNAs and rRNAs are U-tailed.

3 on effect on global cognitive function (Pone-tailed=0.005).

4 emporal thickness and amygdalar volume (Pone-tailed=0.026, 0.019 and 0.003, respectively).

5 m participants followed up from ADNI-1 (Pone-tailed=0.028, n=165).

6 This tailed amplicon facilitates detection via hybridisation

7 The side arms of 21 of the new benzyl-tailed analogues were modeled by means of quantum mechan

8 oth the early phase (r = 0.363, P = 0.03 one-tailed) and the late phase (r = 0.538, P = 0.004).

9 as leakage data sets are statistically heavy-tailed, and that gas leaks are more extremely distribute

10 The probabilities were two-tailed, and the alpha level was set at P < 0.05.

11 s from complex interventions should be heavy tailed, as in other complex systems.

12 t of the widespread Russian (otherwise white-tailed) B. patagiatus Nylander (as B. patagiatus ganjsue

13 Giant tailed bacterial viruses, or phages, such as Pseudomonas

14 ar-spherical (icosahedral) and nonspherical (tailed) bacterial viruses were experimentally determined

15 tecture among viruses belonging to the three tailed bacteriophage families, strongly suggesting that

16 However, a larger-sized, tailed bacteriophage of the family Siphoviridae was remo

17 Tailed bacteriophage T4 employs one of the fastest and m

18 The genome packaging reactions of tailed bacteriophages and herpes viruses require the act

19 Tailed bacteriophages and herpes viruses use powerful mo

20 Tailed bacteriophages and herpesviruses assemble infecti

21 Tailed bacteriophages and herpesviruses consist of a str

22 to a preformed protein capsid exemplified by tailed bacteriophages and herpesviruses.IMPORTANCE Adeno

23 In addition to DNA, capsids of tailed bacteriophages and their distant relatives, herpe

24 The herpesviruses and tailed bacteriophages constitute two large families of d

25 A viruses such as the herpesviruses and many tailed bacteriophages includes a DNA packaging step wher

26 ne in vivo ejection of noncondensed DNA from tailed bacteriophages into bacteria.

27 ome ejection have been limited to a few head-tailed bacteriophages with a double-stranded DNA genome.

28 Within tailed bacteriophages, interaction of the receptor-bindi

29 In tailed bacteriophages, the portal system is connected to

30 Unlike tailed bacteriophages, which use a preformed tail for tr

31 ub to eject the genome, analogous to classic tailed bacteriophages.

32 an anatomical model: here the Brazilian free-tailed bat (Tadarida brasiliensis).

33 at, the Jamaican fruit bat, the Mexican free-tailed bat and the big brown bat.

34 innervate EI cells in the IC of Mexican free-tailed bats (Tadarida brasilensis mexicana) with in vivo

35 wn bats (Myotis lucifugus), and Mexican free-tailed bats (Tadarida brasiliensis) are the most common

36 t a large colony of migratory Brazilian free-tailed bats (Tadarida brasiliensis) in Texas.

37 We tested whether free-tailed bats (Tadarida brasiliensis) would employ such a

38 nsis Skorikov, n. comb.), whereas the orange-tailed bees in Japan are true B. hypocrita.

39 We find that the orange-tailed bumblebees in North China are actually part of th

40 d China are increasingly using reared orange-tailed bumblebees known previously as Bombus hypocrita P

41 timer-based models of size control and heavy-tailed cell-size distributions.

42 ily Parvoviridae) in the genomes of the long-tailed chinchilla (Chinchilla lanigera) and the degu (Oc

43 ish, krill, prawns, lobsters, and other long-tailed crustaceans swim by rhythmically moving limbs cal

44 es that store the inactive pro-forms of KDEL-tailed cysteine endopeptidases (KDEL-CysEP) associated w

45 unts of translation-competent, long poly(AU)-tailed cytochrome c oxidase subunit I and edited apocyto

46 ryonic developmental progression of the blue-tailed damselfly Ischnura elegans (Odonata), an ancient

47 mples collected antemortem from farmed white-tailed deer (n= 409).

48 bitat use that varied seasonally for a white-tailed deer (Odocoileus virginianus) and coyote (Canis l

49 empirical telemetry data set of three white-tailed deer (Odocoileus virginianus) dyads.

50 evalence of chronic wasting disease in white-tailed deer (Odocoileus virginianus).

51 c) We demonstrate that the presence of white-tailed deer and bovine NTDs hindered seeded conversion o

52 seasonal patterns in selection by the white-tailed deer and were able to link use of conifer forests

53 chronic wasting disease (CWD)-infected white-tailed deer brain homogenates and found that lipid extra

54 In the white-tailed deer examples, a recently developed index for qua

55 on) and genetic relatedness for female white-tailed deer in Wisconsin's area of highest CWD prevalenc

56 rized and inoculated intranasally into white-tailed deer once a week for 6 weeks.

57 inders seeded conversion of bovine and white-tailed deer PrP(c)s to the prion forms, but it facilitat

58 fficient seed for feline rPrP than for white-tailed deer rPrP; (iii) conversely, FSE more efficiently

59 from codon 96 glycine/glycine, captive white-tailed deer that were analyzed for prion infection post-

60 in early CWD pathogenesis, we exposed white-tailed deer to CWD prions by mucosal routes and performe

61 ative ungulate Odocoileus virginianus (white-tailed deer) is overabundant and Alliaria petiolata (gar

62 mule deer sampled but was absent from white-tailed deer, indicating that this virus originally integ

63 etropharyngeal lymph node samples from white-tailed deer, mule deer, and moose, collected in the fiel

64 iva and urine samples from CWD-exposed white-tailed deer.

65 WD infection in natural populations of white-tailed deer.

66 These networks showed a heavy-tailed degree distribution, suggesting the presence of r

67 large random graph with a prescribed (light-tailed) degree distribution.

68 are formed in aqueous mixtures of the single-tailed diacetylenic surfactant, 10,12-pentacosadiynoic a

69 repertoire, its cluster structure with heavy-tailed distribution of family sizes, and presence of the

70 , with characteristic features such as heavy-tailed distribution of fold occurrences, and a distinct

71 The injection dynamics reveal a power-law tailed distribution of injection event sizes and a negat

72 bed as a correlated random walk with a heavy-tailed distribution of step lengths.

73 These anomalously large values follow a fat-tailed distribution, with a universal exponent related t

74 how that well pads emissions rates had a fat-tailed distribution, with the emissions linearly correla

75 for their return, all followed a skewed, fat-tailed distribution.

76 Although a 'heavy-tailed' distribution is considered biologically more pla

77 own that financial asset returns exhibit fat-tailed distributions and long-term memory.

78 an Levy flights yet can still generate heavy-tailed distributions of movement lengths.

79 s in population genetics, often follow heavy tailed distributions.

80 ingredients, to account for the observed fat-tailed distributions.

81 n the multivariate phenotypes come from long tailed distributions.

82 Tailed DNA bacteriophages assemble empty procapsids that

83 The enormous prevalence of tailed DNA bacteriophages on this planet is enabled by h

84 onomer preferentially anchors itself to a 3'-tailed DNA junction and periodically reel in the 3' tail

85 bly scheme revealed here may be common among tailed DNA phages and herpesviruses.

86 This leads to the formation of 3'-tailed DNA, which serves as a substrate for the strand e

87 second hybridization with an oligonucleotide-tailed DNAzyme is performed to introduce the DNAzyme to

88 The tailed double-stranded DNA (dsDNA) bacteriophage 29 pack

89 for the initiation step of DNA packaging in tailed double-stranded DNA bacterial viruses.

90 Tailed double-stranded DNA bacteriophages and herpesviru

91 additional evidence that capsid proteins of tailed double-stranded DNA phages have a conserved fold.

92 inst phages from all three major families of tailed double-stranded DNA phages.

93 strate the importance of both modeling heavy-tailed downward events in populations, and developing co

94 We suggest modelers consider heavy-tailed, downward-skewed probability distributions, such

95 dividually recognizable and free-living fork-tailed drongos (Dicrurus adsimilis) in the southern Kala

96 ng Kong 97 (HK97), which represents the head-tailed dsDNA bacteriophages.

97 eport on the discovery of a novel lineage of tailed dsDNA phages belonging to the family Myoviridae a

98 f the human RECQ1 helicase in complexes with tailed-duplex DNA and ssDNA.

99 l quadruplex DNA than single-stranded DNA or tailed duplexes.

100 Western fat-tailed dwarf lemurs are known to hibernate for seven mon

101 the other hand, the relative amount of long-tailed edited RPS12 mRNA was not substantially affected,

102 nd tens of genomes from zebra finch and long-tailed finch populations in Australia.

103 bra finch, Taeniopygia guttata, and the long-tailed finch, Poephila acuticauda.

104 A 2-tailed Fisher exact test and paired Student t test were

105 A 2-tailed Fisher exact test was the statistical method used

106 A 2-tailed Fisher exact test was used to assess for differen

107 ur combined analysis (p = 2.68 x 10(-4), two-tailed Fisher's exact test), indicating that the SLC2A3

108 nd 1 subject without (p = 3.12 x 10(-3), two-tailed Fisher's exact test).

109 n subjects with CHDs (p = 3.30 x 10(-2), two-tailed Fisher's exact test).

110 t negative for enterovirus D68 using the two-tailed Fisher's exact test, two-sample unpaired t test,

111 limited water-level variability, i.e., short-tailed flood-level distributions, located mainly in the

112 ge claustrum, we hypothesized that the short-tailed fruit bat, Carollia perspicillata, can be a usefu

113 etinal projections were studied in the short-tailed fruit bat, Carollia perspicillata, using the ante

114 coloration in a cuckoo-host system: the fan-tailed gerygone Gerygone flavolateralis and its speciali

115 stance migratory bird, the continental black-tailed godwit Limosa limosa limosa, resulting from a spr

116 ological traits relevant to fitness in black-tailed godwits Limosa limosa limosa on their northward m

117 nts subclinically infecting wild African red-tailed guenons (Cercopithecus ascanius).

118 sules has been synthesized by connecting the tailed hydroxyl groups of C-propan-3-ol pyrogallol[4]are

119 ther it possesses a 5' or 3' single-stranded tailed invading strand.

120 el picornaviruses in fecal specimens of ring-tailed lemurs (Lemur catta) and black-and-white ruffed l

121 rculating in a mixed-species exhibit of ring-tailed lemurs, black-and-white ruffed lemurs, and black

122 anner (lesavirus 1 was detected only in ring-tailed lemurs, while lesavirus 2 was detected only in bl

123 al deposition, if such hiatuses have a heavy-tailed length distribution.

124 e starting oxoacids, many of which are multi-tailed lipids.

125 ei, and one of its main predators, the curly-tailed lizard Leiocephalus carinatus.

126 We compared populations of zebra-tailed lizards and western banded geckos, which are abun

127 Connection weights exhibit a heavy-tailed lognormal distribution spanning five orders of ma

128 an immunodeficiency virus (SIV)-infected pig-tailed macaque (Macaca nemestrina) model, but this is po

129 hing is known of this interaction in the pig-tailed macaque (Macaca nemestrina), which is used in pre

130 e obtained a 2.24-A crystal structure of pig-tailed macaque APOBEC3H with bound RNA.

131 evious experiments using a single female pig-tailed macaque as a model for M. genitalium infection, w

132 pesvirus Macaca nemestrina (RFHVMn), the pig-tailed macaque homolog of Kaposi's sarcoma-associated he

133 sequence characterization of MneRV2, the pig-tailed macaque homolog of rhesus rhadinovirus (RRV).

134 Together these results suggest that the pig-tailed macaque is a suitable model to study M. genitaliu

135 This detailed study of pig-tailed macaque MHC-I genetics and SIV polymorphisms will

136 To evaluate the suitability of a pig-tailed macaque model of M. genitalium infection, we inoc

137 We determined that the pig-tailed macaque RV2 rhadinovirus, MneRV2, is highly assoc

138 sooty mangabey and the non-natural host pig-tailed macaque.

139 Burmese long-tailed macaques (Macaca fascicularis aurea) are one of a

140 tool-assisted foraging on shellfish by long-tailed macaques (Macaca fascicularis) in Khao Sam Roi Yo

141 Here we evaluated DeltaGY in pig-tailed macaques (Macaca nemestrina), a species in which

142 vif-NL4-3) could infect and replicate in pig-tailed macaques (PTM), indicating that APOBEC3 proteins

143 e compared and contrasted pathogenic (in pig-tailed macaques [PTMs]) and nonpathogenic (in African gr

144 Our findings further support female pig-tailed macaques as a model of M. genitalium infection, p

145 This study supports the use of MneRV2 in pig-tailed macaques as an important model for studying rhadi

146 ed contrast to rhesus macaques, 19 of 21 pig-tailed macaques controlled DeltaGY replication with plas

147 Our earlier studies with pig-tailed macaques demonstrated various simian-human immuno

148 on these findings, we conclude that the pig-tailed macaques exhibit potential as a non-human animal

149 Among nonhuman primates, pig-tailed macaques following SIV infection are predisposed

150 mes were amplified from the plasma of 44 pig-tailed macaques infected with SIV(mac251) at 4 to 10 mon

151 Female pig-tailed macaques inoculated with Chlamydia trachomatis an

152 Two pig-tailed macaques progressed to disease with persisting vi

153 Pig-tailed macaques provide important models of human diseas

154 Pig-tailed macaques showed robust viral replication concomit

155 e glycoprotein cytoplasmic tail leads in pig-tailed macaques to a unique phenotype in which high leve

156 We studied the evolution of SIV in pig-tailed macaques with a range of MHC-I haplotypes.

157 In pig-tailed macaques, DeltaGY also replicated acutely to high

158 of iNKT cells in the peripheral blood of pig-tailed macaques.

159 Male lance-tailed manakins perform cooperative courtship displays i

160 ience on reproductive success of alpha lance-tailed manakins were analysed in a mixed model framework

161 ase relative breeding success for male lance-tailed manakins.

162 We used two-tailed Mann Whitney U exact tests, chi(2), and Fisher's

163 ompared with that in control mice with a two-tailed Mann-Whitney U test.

164 mparison of age and tumor size, and a single-tailed McNemar test for comparison of the technical succ

165 heso1-2 affects the profile of u-tailed miRNAs and siRNAs and increases the abundance of

166 cing-mediated biogenesis subclasses, with 5'-tailed mirtrons as, by far, the dominant subtype.

167 miRNAs in mammals: conventional mirtrons, 5'-tailed mirtrons, and 3'-tailed mirtrons.

168 ntional mirtrons, 5'-tailed mirtrons, and 3'-tailed mirtrons.

169 In the KRIPP1 knockdown, A/U-tailed mRNA encoding cytochrome c oxidase subunit 1 decl

170 lexes, identified by association of the long-tailed mRNAs with the mitoribosomes, was also disrupted.

171 cal estimates are inaccurate given the heavy-tailed nature of the distribution.

172 t; this unusual positive curvature for a two-tailed neutral lipid is likely associated with hydrogen

173 dfs for the large-scale fluctuations and fat-tailed non-Gaussian pdfs for the smaller-scale fluctuati

174 Comparisons were evaluated by using two-tailed nonpaired and paired t tests.

175 iently dismantling networks, including heavy-tailed ones for which the dismantling and decycling prob

176 on in eutherian mammals using the gray short-tailed opossum (Monodelphis domestica) as a model.

177 Our animal model, the gray short-tailed opossum (Monodelphis domestica), is a marsupial t

178 extra-embryonic membranes in the gray, short-tailed opossum (Monodelphis domestica).

179 tex of a South American marsupial, the short-tailed opossum (Monodelphis domestica).

180 tailed opossums and eutherian mammals, short-tailed opossum have a much lower cellular and neuronal d

181 Most neurons in short-tailed opossum S1 exhibited multiwhisker receptive field

182 erties in S1 of Monodelphis domestica (short-tailed opossum), a nocturnal, terrestrial marsupial that

183 ltiple developmental milestones in the short-tailed opossum, Monodelphis domestica.

184 uronal distribution is similar between short-tailed opossums and eutherian mammals, short-tailed opos

185 Short-tailed opossums lack barrels and septa in S1 but show ac

186 lection showed comparable latencies in short-tailed opossums.

187 The shape of the tailed organisms was incorporated into two modeling appr

188 Ds) with 95% confidence intervals (CIs) at 2-tailed P < 0.05 significance.

189 % CI: 1.001, 3.695; two-tailed P = .064, one-tailed P = .038).

190 (risk ratio, 1.92; 95% CI: 1.001, 3.695; two-tailed P = .064, one-tailed P = .038).

191 .9 x 10(-8)) was replicated among females (1-tailed P = 0.002), as well as replicated in meta-analysi

192 iled p = 0.004) and IL-10/IL-6 (U = 6.0; two-tailed p = 0.003), whereas IL-6 levels were more elevate

193 oma had higher levels of IL-10 (U = 7.0; two-tailed p = 0.004) and IL-10/IL-6 (U = 6.0; two-tailed p

194 s ( P = 2.6 x 10(6)) and replicated (i.e., 1-tailed P = 0.016) in the Brazilian cohort.

195 replicated in meta-analysis of both sexes (1-tailed P = 0.021).

196 icated among females in the meta-analysis (1-tailed P = 0.052).

197 with uveitis than in lymphoma (U = 15.0; two-tailed p = ns).

198 A 2-tailed P value <0.01 was considered to denote statistica

199 overall performance (AUC, 0.930 vs. 0.891; 2-tailed P value for difference, 0.31).

200 Because the 1-tailed P value from the Fisher exact test was <.001, whi

201 A two-tailed P value of .008 or less, which accounts for multi

202 confidence interval [CI], 0.32 to 0.95 [two-tailed P=0.04 for superiority]).

203 ohorts, were identified by using Student two-tailed paired and unpaired t test, respectively, with a

204 or comparison of CT fluoroscopy times, a two-tailed paired t test for comparison of age and tumor siz

205 al analyses were performed by using a single-tailed paired t test for comparison of CT fluoroscopy ti

206 two modalities were determined with the two-tailed paired t test.

207 Two-tailed paired t tests were used for statistical analysis

208 Two-tailed paired t tests were used to compare change in tum

209 imulation in essential tremor, P=0.0137; two-tailed paired Wilcoxon signed-rank tests).

210 Two-tailed Pearson correlation analysis was performed to det

211 software and were compared by means of a one-tailed Pearson correlation test.

212 is first reported crystal structure of a two-tailed peptidic bilayer reveals similarities in thicknes

213 ngential to the capsid surface with the head-tailed phage and herpesvirus viral lineage.

214 on of the assembly of a "simple" contractile-tailed phage baseplate, that of Escherichia coli phage M

215 st conservation of structural proteins among tailed phages and add to the growing body of evidence po

216 terminase function is widespread among long-tailed phages and is uniquely required for the activity

217 be identified in the majority of contractile-tailed phages and prophages.

218 Tailed phages are genome delivery machines exhibiting un

219 eshift is widely conserved among other dsDNA tailed phages in their corresponding "G" and "GT" tail g

220 ncluding all three morphological families of tailed phages, making these genes attractive for studies

221 ction, are likely to be conserved among long-tailed phages, the largest group of viruses in the Biosp

222 r complexity compared with other contractile-tailed phages.

223 om passenger pigeons and 2 genomes from band-tailed pigeons, which are passenger pigeons' closest liv

224 articular, from the data sets we uncover fat-tailed (possibly power-law) distributions associated wit

225 1-bound miRNAs are actively 3' truncated and tailed, possibly reflecting the activity of cofactors ac

226 challenge studies have established the black-tailed prairie dog (Cynomys ludovicianus) as a model of

227 The use of the tailed primers obviates the need for hapten labelling an

228 mbinase polymerase amplification, exploiting tailed primers, resulting in an amplicon of a duplex fla

229 ification method is modified slightly to use tailed primers, resulting in an amplicon with a duplex f

230 ssian features such as intermittency and fat-tailed probability density functions (PDFs).

231 han unexpected increases, and ignoring heavy-tailed process noise leads to an underestimate in the ma

232 ce and direction of black-swan events (heavy-tailed process noise) in 609 animal populations after ac

233 Our results suggest that aberrant CAT-tailed protein aggregation results from a defect in Cdc4

234 It also exhibits short-tailed reaction time distributions even when operating n

235 x, Saw1, Slx4, and Msh2/Msh3 complex at a 3' tailed recombination intermediate.

236 Chile from environmental vegetation and long-tailed rice rats (Oligoryzomys longicaudatus).

237 and increased annealing of non-specific or U-tailed RNA oligomers.

238 anning the first 12 nucleotides of an oligoU-tailed RNA.

239 equency distribution of outbreak size is fat-tailed, scaling approximately as a power-law.

240 Clupea harengus) from three sites, and white-tailed sea eagle (WTSE) eggs (Haliaeetus albicilla) from

241 e steam bubbles in boiling water, have a fat-tailed size distribution that is typical of self-organiz

242 ion included the identification of the large tailed spindle virion morphology, determination of the c

243 Here we describe a new virus, Acidianus tailed spindle virus (ATSV), initially identified by bio

244 characterize a new archaeal virus, Acidianus tailed spindle virus (ATSV), the approach can be general

245 wo tails can survive, expression of a single-tailed SSB is dominant lethal.

246 E. coli expressing only the two-tailed SSB recovers faster from exposure to DNA damaging

247 A single-tailed SSB shows defects in coupled leading and lagging

248 A two-tailed Student t test was used to compare the T1 and T2

249 A paired two-tailed Student t test was used to evaluate significance

250 tion at 1 month after therapy by using a two-tailed Student t test.

251 mpared with analysis of variance and the two-tailed Student t test.

252 Two-tailed Student t tests and repeated-measures analysis of

253 tatistical analyses were performed using a 2-tailed Student t-test.

254 nce between groups was assessed with the two-tailed Student's t test.

255 n different groups was evaluated using a two-tailed Student's t-test or Mann-Whitney U test.

256 (ovarian, P = 0.0004; breast P < 0.0001, two-tailed Student's t-test).

257 on, Saw1 facilitates targeting of Rad1 at 3' tailed substrates in vivo and in vitro, and enhances 3'

258 est guarding, in a single population of long-tailed sun skink (Eutropis longicaudata) living on Orchi

259 actant) results in the synthesis of a double-tailed surfactant product followed by spontaneous self-a

260 otochemistry of 2-oxooctanoic acid (a single-tailed surfactant) results in the synthesis of a double-

261 We then demonstrate a two-tailed swimmer swimming at 81 mum s(-1).

262 cally analyzed by performing an unpaired two-tailed t test for labeled versus unlabeled cells by usin

263 A one-tailed t test was performed to compare gadolinium concen

264 A 2-tailed t test with a significance level of .05 was used

265 19.3 degrees ) was significant (P < .001, 2-tailed t test) while the change in the global thickness

266 to 5.28 mum) was not significant (P > .12, 2-tailed t test).

267 The comparative study, carried using a two-tailed T test, demonstrated that virtual screening was a

268 igher than that with conventional grids (two-tailed t test, P < .05).

269 D vs 0.574 [0.26] for control individuals; 2-tailed t test; P = .005 and vs 0.465 [0.32] for AD; P =

270 (mean [SD], 6.7 [2.8] vs 11.1 [6.6] years; 2-tailed t test; P = .04) and more frequent alpha-synuclei

271 rd deviations and were compared by using two-tailed t tests and analysis of variance for selected gro

272 n procedures across training periods using 2-tailed t tests with statistical significance set at P <

273 Differences were evaluated using paired 2-tailed t tests.

274 eans were compared by use of independent two-tailed t tests.

275 tical significance was assessed by using two-tailed t tests.

276 red with analysis of variance and paired two-tailed t tests.

277 lts were averaged and evaluated by using two-tailed t tests.

278 MRI data were compared using group-level two-tailed t-tests in the BioImage Suite.

279 ysis was performed with one-way ANOVA or two-tailed t-tests.

280 ly significant evidence for association (one-tailed test P < 0.05).

281 ly significant evidence for association (one-tailed test P = 0.034) in an independent second cohort o

282 ented group (P = 0.034, Pearson chi-square 1-tailed test).

283 a facultative cooperative breeder, the long-tailed tit Aegithalos caudatus, to investigate the facto

284 Long-tailed tits exhibit redirected helping in which failed b

285 r normal tissue were assessed by using a two-tailed two-sample t test.

286 One-tailed two-sample t-test suggested that the connections

287 gnificant differences (student's t-test, two-tailed unequal variance p-value < 0.05) between spectra

288 Results were compared by using a two-tailed unpaired Student t test.

289 Univariate analyses (chi(2) test; 2-tailed, unpaired t test; and analysis of variance) as we

290 licer activity, can bind these truncated and tailed variants of miRNAs.

291 ORF145 from the temperate Acidianus two-tailed virus (ATV) forms a high-affinity complex with RN

292 wly isolated archaeal Haloarcula sinaiiensis tailed virus 1 has the canonical coat protein fold of HK

293 ed capsid protein from multiple uncultivated tailed virus families.

294 e a structural module characteristic of head-tailed viruses and, unusually for archaeal and bacterial

295 With the exception of the tailed viruses related to bacteriophages of the order Ca

296 al evidence that bacterial and archaeal head-tailed viruses share a common architectural principle.

297 However, when the tailed viruses were approximated as spheres, poor agreem

298 The Fisher exact test (2-tailed) was used to compare proportions, Student t test

299 (e.g. P=0.0002 for tremor amplification, two-tailed Wilcoxon rank sum test).

300 distribution of postural sequences is heavy-tailed with a core of frequent behaviours and a much lar