ライフサイエンスコーパス: tailed

1 ut not female monkeys (AT x sex; p = .032, 1-tailed).

2 res (mean rank=134.2), Z=-10.1, p<0.001 (two-tailed).

3 amine synthesis capacity at alpha = .05 (two tailed).

4 at 3 or 11 weeks (P < .000l, Barnard test, 2-tailed).

5 t 3 or 11 weeks (p<0.000l, Barnard's test, 2-tailed).

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

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

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

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

10 mean scores between the 2 groups of 0.06 (1-tailed 95% confidence interval [CI], -infinity to 0.27),

11 This tailed amplicon facilitates detection via hybridisation

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

13 including an independent paleognathous long-tailed ancestor.

14 Pumas in California eat primarily black-tailed and/or mule deer (Odocoileus hemionus), and THg i

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

16 For 10 groups of rhesus, long-tailed, and bonnet macaques, we collected social behavio

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

18 Here, a six-arginine-tailed anti-epidermal growth factor receptor (EGFR) affi

19 affecting species such as capybara and naked-tailed armadillo.

20 The interaction time distribution is heavy-tailed, as previously reported for human face-to-face in

21 ns with those of the order Caudovirales, the tailed bacterial viruses, have brought speculation regar

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

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

24 The mature virion of the tailed bacteriophage 29 is an ~33 MDa complex that conta

25 The portal proteins of tailed bacteriophage and Herpesvirus capsids form dodeca

26 Tailed bacteriophage T4 employs one of the fastest and m

27 Five tailed bacteriophages against K pneumoniae ST258 clade 1

28 Tailed bacteriophages and herpes viruses use powerful mo

29 Tailed bacteriophages and herpesviruses assemble infecti

30 The genome packaging motor of tailed bacteriophages and herpesviruses is a powerful na

31 Assembly of tailed bacteriophages and herpesviruses starts with form

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

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

34 Double-stranded DNA tailed bacteriophages typically code for 50-200 genes, o

35 Tailed bacteriophages use a DNA-packaging motor to encap

36 architecture very similar to those of other tailed bacteriophages, allowing us to directly compare s

37 d in numerous icosahedral viruses, including tailed bacteriophages, herpesviruses, and archaeal virus

38 In tailed bacteriophages, the portal system is connected to

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

40 served in some capsid-associated proteins in tailed bacteriophages, with which herpesviruses are beli

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

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

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

44 autumn migration phenology of Brazilian free-tailed bats (Tadarida brasiliensis) at Bracken Cave.

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

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

47 This postulate is explored here by three-tailed benzenesulfonamide CAIs (TTI) to fully exploit su

48 AD2, KDM5B, NSD2, FOXP1, MED13L, DYRK1A; one-tailed binomial test P <= 4.08E-05) contributed to the c

49 rst genetic assessment of the Australian red-tailed black-cockatoo (Calyptorhynchus banksii), a wides

50 mission of DWV in bumble bees using the buff-tailed bumble bee Bombus terrestris as a model.

51 ks, most particularly the presence of a long-tailed but monotone decline in the probability of intera

52 Here, we propose the use of a heavy-tailed Cauchy prior distribution for effect sizes, which

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

54 Myosin-1e (Myo1e) is a long-tailed class-I myosin that has not yet been studied in t

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

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

57 abnormalities have been documented in white-tailed deer (Odocoileus virginianus) in west-central Mon

58 es to identify microsatellite loci for white-tailed deer (Odocoileus virginianus) with the potential

59 The white-tailed deer (Odocoileus virginianus), a popular ruminant

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

61 in blood of pre-clinical CWD-infected white-tailed deer (WTD) with high sensitivity and specificity

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

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

64 Fisheries Captive Facility where adult white-tailed deer females and their fawns were administered aq

65 The first examination of MHC-DOB in white-tailed deer found significantly less polymorphism (11 al

66 region in ruminants, and suggests that white-tailed deer may have a recombination hotspot between the

67 amples from heterozygous (G(96)/S(96)) white-tailed deer orally dosed with CWD from homozygous (G(96)

68 on the MiSeq platform from an enclosed white-tailed deer population located in Alabama.

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

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

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

72 total number of documented alleles in white-tailed deer to 30 for MHC-DRB exon 2.

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

74 hat imidacloprid has direct effects on white-tailed deer when administered at field-relevant doses.

75 Overall, generalist mesocarnivores, white-tailed deer, and giant anteater were more likely to use

76 or many common research objectives for white-tailed deer.

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

78 population cycles over large areas in white-tailed deer.

79 nd to be under purifying selection for white-tailed deer.

80 n-classical, MHC II gene (MHC-DOB) for white-tailed deer.

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

82 The heavy-tailed distribution of gene expression violates the assu

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

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

85 scribing the transition from light- to heavy-tailed distributions along a continuum of behavior as pa

86 th highly intermittent fluctuations with fat-tailed distributions of amplitudes.

87 n the multivariate phenotypes come from long tailed distributions.

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

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

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

91 Tailed double-stranded DNA (dsDNA) bacteriophages, herpe

92 o the formation of infectious virions in the tailed double-stranded DNA (dsDNA) phages, herpesviruses

93 quired for the capsid shell assembly of many tailed double-stranded DNA bacteriophages, some archaeal

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

95 Tailed, double-stranded DNA bacteriophages provide a wel

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

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

98 nch), early postnatal marsupial mammals (fat-tailed dunnart), and eutherian mammals (mouse and human)

99 en the eutherian mouse and the marsupial fat-tailed dunnart.

100 ference has not been observed for 5'- and 3'-tailed duplexes, suggesting that it is the fork structur

101 We generate a reference genome for the fat-tailed dwarf lemur, Cheirogaleus medius, and use this re

102 The white-tailed eagle (Haliaeetus albicilla) in Scandinavia has s

103 , we examined PFAS levels in plasma of white-tailed eagle nestlings from northern Norway over the las

104 The Krapina white-tailed eagle talons represent a kind of jewelry worn by

105 (PFAS) using archived body feathers of white-tailed eagles (Haliaeetus albicilla) from the West Green

106 ear latent variable model with robust, heavy-tailed error and adaptive kernel learning to estimate lo

107 ochemical detection via hybridisation of the tailed, ferrocene labelled PCR product.

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

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

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

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

112 The 2-tailed Fisher exact test was used to compare outcomes be

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

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

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

116 n driven by a migratory drop-off in the fork-tailed flycatcher (Tyrannus savana) resulting in reprodu

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

118 RTN package, gene expression data, and a two-tailed Gene Set Enrichment Analysis.

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

120 light mortality of 53 satellite-tagged Black-tailed Godwits (Limosa limosa limosa) during 132 crossin

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

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

123 In contrast to tailed icosahedral double-stranded DNA (dsDNA) viruses i

124 secondary cases is consistent with being fat-tailed, implying that large superspreading events are ex

125 A two-tailed independent sample t test statistic was used to e

126 FM-UE recovery clusters was 0.79 (95% equal-tailed interval [ETI] = 0.78-0.80) at 1 week poststroke

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

128 glaucous gulls, rough-legged hawks and long-tailed jaegers) feeding on a pulsed resource (brown and

129 olecular data from a 17-year study of banner-tailed kangaroo rats (Dipodomys spectabilis) to quantify

130 elf-assembly of bolaamphiphiles with swallow-tailed lateral chains.

131 and show that superspreading, when it is fat-tailed, leads to pronounced transmission by increasing d

132 Studying ring-tailed lemur (Lemur catta) behavior and semiochemistry,

133 A recent study of ring-tailed lemurs offers some - disputed - candidate molecul

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

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

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

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

138 We show that curly-tailed lizards destabilized the coexistence of competing

139 whereas adding either green anoles or curly-tailed lizards lengthened food chains on the islands, ad

140 smaragdinus) and/or new top predators (curly-tailed lizards, Leiocephalus carinatus).

141 rison of fetal neocortex development in long-tailed macaque and human reveals that the onset of conse

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

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

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

145 te colobus), Macaca nemestrina (southern pig-tailed macaque), and Mandrillus leucophaeus (the drill).

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

147 sia, Plasmodium knowlesi, a parasite of long-tailed macaques (Macaca fascicularis), is an important c

148 ehaviour between neighbouring groups of long-tailed macaques (Macaca-fascicularis) could be explained

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

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

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

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

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

154 Pig-tailed macaques provide important models of human diseas

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

156 mong bonnet macaques, but not rhesus or long-tailed macaques, individuals who were more well-connecte

157 rone and social network dynamics in the wire-tailed manakin, a lekking bird species in which male-mal

158 mics of a cooperative bird species, the wire-tailed manakin, to evaluate the potential causes of temp

159 nd individual age from a population of lance-tailed manakins Chiroxiphia lanceolata, a species where

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

161 Two-tailed McNemar tests were used to test differences in se

162 Myosin-1C is a single-headed, short-tailed member of the myosin class I subfamily that suppo

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

164 broadly (1000-fold) and are larger for short-tailed mRNAs that have previously undergone more rapid d

165 Decay rate constants of short-tailed mRNAs vary broadly (1000-fold) and are larger for

166 ng proteins (PABs) uniformly bind to poly(A)-tailed mRNAs, regulating their stability and translation

167 sm they contribute to translation of poly(A)-tailed mRNAs.

168 Here, we report that long-tailed myosin-1e (Myo1e) is enriched at the ventral laye

169 In the nucleus, they help process UUU-3'OH-tailed nascent RNA polymerase III transcripts, such as p

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

171 e conducted independent samples t-tests (two-tailed) on pre-post change scores.

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

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

174 onse to spinal cord injury in the gray short-tailed opossum (Monodelphis domestica).

175 inactivation in a marsupial, the grey short-tailed opossum (Monodelphis domestica).

176 an chewing stroke, as conserved in the short-tailed opossum Monodelphis domestica: it is a simple sym

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

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

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

180 lection showed comparable latencies in short-tailed opossums.

181 t these can not deal with multi-modal, heavy-tailed, or discrete distributions.

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

183 % CI: 1.001, 3.695; two-tailed P = .064, one-tailed P = .038).

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

185 .9 x 10(-8)) was replicated among females (1-tailed P = 0.002), as well as replicated in meta-analysi

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

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

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

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

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

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

192 lgorithms by analyses of variance, and a two-tailed P value less than .05 indicated statistical signi

193 om zero were judged significant when the two-tailed P value was less than .05.

194 Two tailed p<0.05 was considered statistically significant.

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

196 -injection effects of FA were evaluated by 2-tailed paired t test comparison of mean 5-minute preinje

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

198 flow and 5D flow using a signed-rank or two-tailed paired t test.

199 the CMTESv2 (mean change 0.97 +/- 1.77; two-tailed paired t-test P = 0.003) and the CMTESv2-R (mean

200 over 1 year (mean change 2.24 +/- 3.09; two-tailed paired t-test P = 0.009) and over 2 years (mean c

201 he CMTESv2-R (mean change 1.21 +/- 2.52; two-tailed paired t-test P = 0.009) increase significantly w

202 over 2 years (mean change 4.00 +/- 3.79; two-tailed paired t-test P = 0.031) with respective standard

203 minant CMT2A (mean change 0.84 +/- 2.42; two-tailed paired t-test P = 0.039).

204 sures analysis of variance with post hoc two-tailed paired t-tests.

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

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

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

208 ative to one another, which is common within tailed phage clusters.

209 The major coat proteins of dsDNA tailed phages (order Caudovirales) and herpesviruses for

210 Double-stranded DNA (dsDNA) tailed phages and herpesviruses assemble their capsids u

211 ons and coat protein structures of the dsDNA tailed phages and herpesviruses make phages ideal models

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

213 the genome sequences of Salmonella enterica tailed phages Sasha, Sergei, and Solent.

214 ed Salmonella podoviruses, illustrating that tailed phages use common particle-opening mechanisms but

215 ction of Gram-negative bacteria by all short-tailed phages, because such virions cannot directly deli

216 r complexity compared with other contractile-tailed phages.

217 ed with the segregation of primitive and fat-tailed phenotypes.

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

219 The genosensor exploits tailed primers and ferrocene labelled dATP analogue to p

220 Tailed primers consist of a sequence specific for the ta

221 rategy relies on the use of species-specific tailed primers for duplex amplification and simple dilut

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

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

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

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

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

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

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

229 disrupts global protein homeostasis, as CAT-tailed proteins can aggregate and sequester chaperones.

230 Failure to degrade CAT-tailed proteins disrupts global protein homeostasis, as

231 nce in an alpine-obligate species, the white-tailed ptarmigan (Lagopus leucura), a species distribute

232 genome-wide dataset generated from 95 white-tailed ptarmigan distributed throughout the species' ran

233 ture and contemporary gene flow in the thorn-tailed rayadito (Aphrastura spinicauda), a passerine bir

234 ding proteome (RBPome) associated with polyA-tailed RNA species in murine ciliated epithelial cells o

235 RNA-dependent RNA polymerases, which use pUG-tailed RNAs (pUG RNAs) as templates to synthesize small

236 This finding was in contrast to short-tailed Salmonella podoviruses, illustrating that tailed

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

238 Notably, an azide-tailed sgRNA targeting the telomeric repeat served as a

239 abundant (i.e. 500,000 breeding pairs) wedge-tailed shearwater Ardenna pacifica (WTS) when breeding i

240 ic hair sheep and the later expansion of fat-tailed sheep occurred ~11,800-9,000 years BP and ~5,300-

241 body size and short or thin tails), and fat-tailed sheep, we found an overrepresentation of MSY line

242 rs and notably slower than in noncontractile-tailed siphoviruses.

243 The ancestral long-tailed spinal nerve configuration was hypothesized from

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

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

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

247 An unpaired, two-tailed Student t test was used to compare groups; Spearm

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

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

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

251 l significance was tested using a paired two-tailed Student t test.

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

253 receiver operating characteristic curve, two-tailed Student t tests, prevalence- and bias-adjusted ka

254 We model residual errors with a heavy-tailed Student's t-distribution to estimate a manifold t

255 analysis was done by employing unpaired two-tailed Student's t-test and the p-value of < 0.05 was de

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

257 oly(A) tail length and abundance of the long-tailed subpopulation.

258 The design of three dual-tailed sulfonamide series 11a-11g, 14a-14h, and 16a-16e

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

260 Specificities were compared by using a two-tailed t test (P < .05) and sensitivities were compared

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

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

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

264 ificant difference of 0.31 +/- 0.55 mm(2) (2-tailed t test, P = .65).

265 compared between trials using a paired, two-tailed t test.

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

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

268 Two-tailed t tests were used and P values less than .05 were

269 tistical analysis was performed by using one-tailed t tests, Wilcoxon rank sum tests, one-way analysi

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

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

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

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

274 post-drug CPTs separately using paired, two-tailed t tests.

275 ippocampus decreased significantly using two-tailed t-test (p = 0.03 and p = 0.01 respectively) compa

276 targets but also accelerated decay of short-tailed target molecules.

277 ated effect of miRNAs largely prevents short-tailed target mRNAs from accumulating despite accelerate

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

279 of woodland areas, accurately captures long-tailed tit home range patterns.

280 Here we show that, in long-tailed tits (Aegithalos caudatus), a cooperative breeder

281 Here, we apply MHRA to a population of long-tailed tits Aegithalos caudatus, a non-territorial passe

282 tterns observed in a wild population of long-tailed tits Aegithalos caudatus.

283 Long-tailed tits are known to discriminate between the calls

284 operative contexts, so we conclude that long-tailed tits use the same kin discrimination rule to avoi

285 Conversely, KPAF4 inhibits uridylation of A-tailed transcripts and, therefore, premature A/U-tailing

286 seq to simultaneously characterize the non-A-tailed transcripts of a segmented dsRNA virus and the tr

287 nd 2) runaway motion that produces the heavy-tailed travel distances often associated with nonlocal t

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

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

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

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

292 ed capsid protein from multiple uncultivated tailed virus families.

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

294 The identified proviruses are related to tailed viruses of the order Caudovirales and to tailless

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

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

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

298 Two-tailed Wilcoxon tests were used for comparison (>=five p

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

300 x was typically greatest through the isoform tailed with a single uridine, although changes in this f