ライフサイエンスコーパス: genera

1 cerambycids (23 genera) and 16 buprestids (4 genera).

2 of these giant bacteria into three candidate genera.

3 taxonomic revision is needed for one or both genera.

4 of 7-epi-iridoids in Antirrhinum and related genera.

5 en identified in more than 20 cyanobacterial genera.

6 differences in species richness between both genera.

7 he reproductive structures between these two genera.

8 d these in detail to sister and more distant genera.

9 tick species in Rhipicephalus and Amblyomma genera.

10 robiome and, in particular, nitrate-reducing genera.

11 tabase of 2497 marine vertebrate and mollusc genera.

12 g feeding among 20 chameleon species in nine genera.

13 nk raises this number to 107 species from 48 genera.

14 arabacteroides, Adlercreutzia and Prevotella genera.

15 nera but frequent successful transfer within genera.

16 ns from other species in Saccharum and other genera.

17 lasticity in response to drought in six tree genera.

18 distantly related species pairs of parasite genera.

19 the Baltimore classification viral groups to genera.

20 not homologous between the two extant sloth genera.

21 tors derived from three different retroviral genera.

22 rophic hydrogen oxidizers belonging to novel genera.

23 ential was associated with just 77 bacterial genera.

24 ntative retroviruses in the known retroviral genera.

25 ere present, with minor variation among CCRA genera.

26 00 congeneric annual/perennial pairs from 28 genera.

27 members of the Pseudomonas and Achromobacter genera.

28 arison of the results for the most prevalent genera.

29 group but including species of two distinct genera.

30 are unclear for the delineation of bacterial genera.

31 ere new to science, and four belonged to new genera.

32 -scale bioclimatic distributions of 115 tree genera.

33 hages represent at least three new candidate genera.

34 ing the differences observed within parasite genera.

35 m other S. aureus strains or even from other genera.

36 tion in functional pitcher morphology within genera.

37 and 486 bacterial proteins from 18 different genera.

38 , it is difficult to differentiate these two genera.

39 c biology principles, in different bacterial genera.

40 illion y ago) to more distantly related host genera (~108 million y ago).

41 zoic, when army ants diversified into modern genera [12] and rose to ecological dominance [13, 14].

42 a total of six bacterial phyla, 17 bacterial genera, 23 bacterial species, and two genera of viruses.

43 the radioles are very diverse among sabellid genera [3] and they display many characteristics atypica

44 chanisms have been described for several ant genera [5, 8], which have evolved some of the fastest kn

45 aluation of RNA regulatory element activity (GenERA), a clustered regularly interspaced short palindr

46 (ITS) sequence to five distinct Panicoideae genera, a lineage that split from the Pooideae about 60

47 thin the family Bromeliaceae and in over 400 genera across 36 families.

48 he distribution of different Thermoproteales genera across geochemically distinct geothermal habitats

49 ed in mastitis cases, were the most abundant genera across treatments and time.

50 The largest genera (Aequorivita) decreased from 21.14% to 12.65% and

51 Across the different experiments, genera affiliated to wetter climatic regimes show higher

52 ded an increase in relative abundance of the genera Akkermansia and Lachnospiraceae, taxa commonly as

53 Coronaviruses from the genera Alphacoronavirus and Betacoronavirus, such as sev

54 ) created from all representative retroviral genera: Alpharetrovirus, Betaretrovirus, Deltaretrovirus

55 e overlap in viral diversity between the two genera, although the viromes were very similar among the

56 owly diversifying lupins and all other plant genera analysed.

57 winter were recorded for 26-33% of bacterial genera and < 15% of fungal genera, but the transcript pr

58 HTT in 195 insect genomes, representing 123 genera and 13 of the 28 insect orders.

59 2015, for a total of 11,676 species in 1225 genera and 140 families.

60 During simulated attacks, 45% of 38 genera and 33% of 61 species of silk and hawkmoth caterp

61 eae (Crucifereae) clades, comprising some 48 genera and 351 species classified into seven tribes and

62 We exposed four common CCA genera and a crustose calcifying red algae, Peyssonnelia

63 ns between levels of differentially abundant genera and cerebrospinal fluid (CSF) biomarkers of AD.

64 , with the relative importance varying among genera and climate variables.

65 several strains representing novel species, genera and even one family.

66 genetic analysis of >400 plant species in 41 genera and five families revealed that average fruit siz

67 s the chaperone function of Hfq in bacterial genera and illuminates how Sm proteins may evolve new fu

68 l extinctions were broadly synchronous among genera and independent of climate aridity and variabilit

69 und by simulations and the D-statistic among genera and inside the main clades of Diplostephium indic

70 ria comprises all but three living mammalian genera and is one of the most ecologically pervasive cla

71 classification of known and novel bacterial genera and species and for detection of uncultivable bac

72 there has been an explosion in the number of genera and species of rhizobia known to nodulate legumes

73 characterized and candidate novel families, genera and species that were archived as pure cultures.

74 of the lower caniniform in both extant sloth genera and the existence of two generations for the uppe

75 es metagenomics data revealing new virophage genera and their putative ecological interactions in two

76 Some genera and tribes also experienced younger, mesopolyploi

77 lkane degradation could be shown for several genera and yet uncultured clades.

78 hich together identified 275 cerambycids (23 genera) and 16 buprestids (4 genera).

79 repetitive sequences (that differ among the genera) and germline-expressed genes (approximately 1000

80 amily (Thymus, Ocimum, Origanum, and Monarda genera), and other plants such as those belonging to the

81 ble checklist includes 124,993 species, 6227 genera, and 355 families, which correspond to 33% of the

82 Sequences obtained blasted to 9 phyla, 66 genera, and 401 human oral taxa (HOT) in the 16S rRNA Hu

83 from 138 published papers - representing 251 genera, and 414 species of angiosperms (n = 376) and gym

84 terminal accessions representing 80% of the genera, and encompassing the global geographic range of

85 nce, which is conserved in several bacterial genera, and the oligomer does not have any detectable to

86 Highly co-speciating bacterial genera are also associated with immune diseases in human

87 Two different bacterial genera are featured, Pseudonocardia and Salinispora, and

88 dependently of Polytomella Species from both genera are free-living organisms that contain nonphotosy

89 likely represent a "core microbiome." These genera are known to perform a number of services for her

90 so given and illustrations of representative genera are provided.

91 pecies from the Thaumastus and Megalobulimus genera are reliable representatives of the atmospheric c

92 one based on all modern species; values for genera are similar.

93 scular genera, but barely 5% of non-vascular genera, are conserved ex situ.

94 d Heterotrichea are confirmed; (7) ambiguous genera Askenasia, CyclotrichiumParaspathidium and Plagio

95 mycotoxin-producing fungal species from the genera Aspergillus and Fusarium using solid-state voltam

96 d Porphyromonas (15%) were the most abundant genera associated with high levels of inflammation in fo

97 Flavobacterium (17%) were the most abundant genera associated with high levels of inflammation in he

98 Furthermore, we show that about half of genera associated with individual studies are bacteria t

99 Bacteria of the genera Bacillus and Clostridium form highly resistant sp

100 ring 517 MIC values from different bacterial genera (Bacillus, Cupriavidus, Klebsiella, Ochrobactrum,

101 tinobacteria phyla and more sequences in the genera Bacteroidetes [G-3], Porphyromonas, Abiotrophia,

102 The genera Bambusiphaga, Megadelphax and Muirodelphax are fo

103 Some genera belonging to the opportunistic pathogens were det

104 mposition and abundance of certain bacterial genera between infants infected with HRV and those infec

105 elta(15) N between 20 ant conspecifics in 10 genera between two paired forests (10 pairs of 20 forest

106 ves exhibited similar microbial families and genera but different OTUs than adults, with a transition

107 sting infrequent successful transfer between genera but frequent successful transfer within genera.

108 exhibited higher diversification in certain genera but lower diversification in others.

109 netic bias ensures that over 50% of vascular genera, but barely 5% of non-vascular genera, are conser

110 romyces is one of the best-studied microbial genera, but our understanding of the global distribution

111 -33% of bacterial genera and < 15% of fungal genera, but the transcript profiles of fungi, archaea an

112 Other bacterial genera capable of pupylation such as Corynebacterium lac

113 The genera Citrobacter (log2 fold change -3.41, P=.03), Osci

114 In mattress dust, the genera Clostridium, Facklamia, an unclassified genus wit

115 ra Escherichia, Klebsiella and Enterobacter, genera commonly associated with nosocomial infections, d

116 Our data set included 762 isolates from 13 genera constituting 41 bacterial species.

117 le farming, extant species from basal attine genera continue to farm loosely domesticated fungal cult

118 nd show that high-resolution analysis of the GenERA dataset can be used to extract functional feature

119 The largest Gemmatimonas genera decreased from 21.46% to 11.68% and the Isosphaer

120 most notable increases in the dechlorinating genera Dehalococcoides and Dehalogenimonas.

121 at higher vs. lower latitudes (8% vs. 11% of genera), despite 11-fold lower abundance (1.2% vs. 12.7%

122 The most dominant genera detected on the anode of all three SAPs based on

123 a total of 30 yeast strains belonging to the genera Dipodascus, Galactomyces, Geotrichum, Magnusiomyc

124 followed by yogurt made from these bacterial genera displayed a decreased parasite burden.

125 Most genera diverged in the Cretaceous.

126 These genera document the stepwise evolution of the aculiferan

127 Marburg virus and differentiated between the genera Ebolavirus and Marburgvirus The amount of filovir

128 Further, the dominant genera encoding a pathway were generally similar among h

129 ication using a large dataset of bird sister genera endemic to the New World.

130 Spearman correlations indicated that genera enriched in WD + PDX mice inversely correlated wi

131 find that multidrug-resistant members of the genera Escherichia, Klebsiella and Enterobacter, genera

132 , we show that patterns of diversity for the genera Escherichia, Neisseria, and Borrelia are generall

133 l genetic diversity was unveiled within both genera, even for the most abundant and well-characterize

134 amples, males of Chrysopa and other lacewing genera evidently must sequester specific chemical precur

135 Identified coral taxa (21 genera) exhibited clear depth-stratification, correspond

136 aracterized by overrepresentation of the key genera Exiguobacterium, Planococcus, Propionigenium and

137 Focusing on keyhole limpets, genera Fissurella and Diodora from Cape Verde Islands, w

138 f litter breakdown varied among twelve plant genera for which Ea could be calculated.

139 Genera from Bacteroidetes were more abundant in the colo

140 onstipation, age, body mass index, and diet; genera from Firmicutes (Faecalibacterium, Lactococcus, a

141 ates on paleontological specimens of extinct genera from North and South America with the expectation

142 Cretaceous, and the rapid diversification of genera from the early Oligocene onwards occurred in cold

143 netic analysis of 87 species belonging to 43 genera from the Indo-West Pacific and the Atlantic using

144 ggests that at least 50-60% of the bacterial genera from the intestinal microbiota of a healthy indiv

145 veral high-quality genomes representing four genera from the new phylum.

146 psy and brush samples, but were enriched for genera from the oral cavity and stomach, including Fusob

147 ent in taxa of lower abundance including the genera Fusobacterium, Atopobium, Gluconacetobacter, Hydr

148 s of ten species in agar-producing red algal genera Gelidium and Pterocladiella.

149 esenting previously described members of the genera Guttulinopsis, Rosculus and Helkesimastix, as wel

150 The genera Haemophilus (log2 fold change -2.15, P=.003), Dia

151 diales, Rykenellaceae, and in species of the genera Halothermothrix and Anaerobaculum.

152 wn phylogenetic diversity of the hepacivirus genera has absolutely exploded.

153 over the past half decade five new monotypic genera have been found in the latest Cretaceous (Maastri

154 l crustaceans (including 64 families and 185 genera) have independently overcome the challenges of co

155 y monophyletic group to Hippolyte, with both genera herein synonimised.

156 ide motifs of five retroviruses of different genera: HTLV-1, HIV-1, murine leukaemia virus (MLV), avi

157 The isolates were identified within three genera, i.e., Penicillium, Talaromyces, and Rasamsonia T

158 tions in the number of background reads, the genera identified in the background, and the number of r

159 culturable bacteria in seeds was low with 8 genera identified, dominated by Erwinia and Paenibacillu

160 ing the relative abundances of two bacterial genera in adulthood, atrazine did not affect gut bacteri

161 l in the biogeography of Inga and other tree genera in Amazonian and Guianan rain forests suggests th

162 the growth predictive model of Cladosporium genera in different temperature and relative humidity co

163 esented for most fossil fruit and all extant genera in Fagales over its c. 95 million yr history.

164 , Mycoplana, Haemophilus, Blautia, and Dorea genera in MS patients, whereas control group showed incr

165 teobacteria, occurring in many, but not all, genera in the Alphaproteobacteria, Betaproteobacteria, G

166 ly abundances of Fibrobacteres phylum and 12 genera in the E. faecalis group and antibiotics group we

167 oviu virus, which belong to the heterologous genera in the filovirus family.

168 us (BCTV), which are classified in different genera in the Geminiviridae.

169 Z, but we found higher abundance of dominant genera in the gut microflora of group JD.

170 ith Prevotella and Bacteroides, the dominant genera in the modern human gut microbiome.

171 We found that 30-40% of bacteria genera in the terrestrial and intestinal biomes have no

172 that tree-climate relationships for 15 tree genera in the upper Midwestern US have significantly alt

173 Bacterial genera included Staphlyococcus, Pseudomonas, and Strepto

174 nalyzed musculoskeletal network models in 22 genera, including members of all major extant primate gr

175 from 33.03% to 7.94%, while the Akkermansia genera increased from 1.69% to 20.23% according to the a

176 ed from 21.14% to 12.65% and the Pseudomonas genera increased from 10.57% to 12.96% according to the

177 ed from 21.46% to 11.68% and the Isosphaerae genera increased from 5.8% to 11.98% according to the ab

178 156 BisI homologs are found in >60 bacterial genera, indicating that these enzymes are widespread in

179 The GH content in bacterial genera is best described by their taxonomic affiliation.

180 enic species of the Aspergillus and Fusarium genera isolated from grapes and cereals.

181 three soil horizons revealed the presence of genera known to be involved in halogenation and dehaloge

182 The yeast genera Kondoa might be protective; Cryptococcus species

183 The largest genera (Lactococcus) decreased from 33.03% to 7.94%, whi

184 auropod eusauropods, which now includes five genera (Losillasaurus, Turiasaurus, Mierasaurus, Moabosa

185 The relative abundances of the bacterial genera Mannheimia, Moraxella, and Mycoplasma were signif

186 us distinct from that of Ebola virus (EBOV) (genera Marburgvirus and Ebolavirus, respectively).

187 ten times slower than in the closely related genera Mellita and Lanthonia.

188 We focus primarily on species in the genera Metarhizium and Beauveria, traditionally recogniz

189 e bacterial genus Smithella and the archaeal genera Methanoculleus and Methanosaeta.

190 A suite of OTUs, including taxa from the genera Methylobacterium, Acinetobacter and Mycoplasma, a

191 d by Actinobacteria including members of the genera Mycobacterium, Rhodococcus, Microbacterium and Go

192 2 novel bunyaviruses (>99% complete) in the genera Nairovirus and Phlebovirus were also identified a

193 Enteric caliciviruses in the genera Norovirus and Sapovirus are important pathogens t

194 iles and gene content suggest that virophage genera occupy different ecological niches.

195 Likewise, the dominant fungal genera occurred at high phylogenetic redundancy.

196 phylotypes were taxonomically assigned to 29 genera of 19 families in 9 classes of 5 phyla.

197 an average of 93 percent prevalence in four genera of African epauletted fruit bats.

198 , DNase II has also been identified in a few genera of bacteria and is believed to have arisen via ho

199 l hygiene harbored higher proportions of the genera of bacteria compatible with gingival disease.

200 there appears to be functional redundancy in genera of CCRA providing cues to abalone, which may furt

201 esistance data from 10 bacterial species and genera of clinical interest from our institution identif

202 s showed discordant development of bacterial genera of Enterobacteriaceae and Parabacteroides species

203 The Armillaria and Lactarius genera of fungi produce the antimicrobial and cytotoxic

204 enera, representing approximately 78% of the genera of Lamiaceae).

205 esults showed that seven classes and sixteen genera of phytoplankton in the lake underwent major temp

206 Within the study area there were 437 genera of plants in flower during April and May, but onl

207 es divergence of Sphagnum from the two other genera of Sphagnopsida.

208 Three genera of stony corals had distinct patterns of molecula

209 to hundreds of species restricted to a dozen genera of the Alphaproteobacteria and Betaproteobacteria

210 roughput sequencing revealed 22 phyla and 88 genera of the bacteria.

211 ical structure that is conserved only in two genera of the beta-subfamily and absent in alpha- and ga

212 iruses constitute two closely related sister genera of the family Flaviviridae.

213 4% in plasma, 5.6% in saliva) and in several genera of the oral microbiome.

214 o and lower coverage genomes for three other genera of tribe Pachycereeae (Pachycereus, Lophocereus,

215 terial genera, 23 bacterial species, and two genera of viruses.

216 and characterized for the first time fungal genera on plastic debris.

217 filiated close to Spiroplasma and Mycoplasma genera, one to chlamydial 'Candidatus Syngnamydia', and

218 resented 553 phylogenetic concepts (species, genera or families, at the most precise taxonomic level

219 se in frequency of these traits among marine genera over geological time could explain observed secul

220 Apicomplexan parasites include those of the genera Plasmodium, Cryptosporidium, and Toxoplasma and t

221 ts were large, in particular, for coral reef genera Platygyra, Acropora and Millepora, where classifi

222 ts in long-term alterations of gut microbial genera (predominantly Lachnospiraceae and S24-7) and red

223 f gingival bleeding were associated with the genera Prevotella (22.25% x 20%), Streptococcus (19.83%

224 Marine picocyanobacteria of the genera Prochlorococcus and Synechococcus are the most nu

225 er of candidate bacterial and archaeal virus genera, providing a near-complete sampling of epipelagic

226 of Gammaproteobacteria, and specifically the genera Pseudoalteromonas, Pseudomonas, Halomonas, and Co

227 ice, with an increased representation of the genera Pseudomonas and Lactobacillus and a reduction in

228 A total of 319 mold isolates representing 43 genera recovered from clinical specimens were evaluated.

229 Though all CCRA genera reduced growth during exposure to increased pCO2,

230 With 87 genera representing all subfamilies and tribes of Rosace

231 , as well as 61 orders, 175 families and 496 genera) representing all 13 classes of largest subphylum

232 ng of the family to date (288 species in 191 genera, representing approximately 78% of the genera of

233 iptomes of numerous hard ticks, spanning the genera Rhipicephalus, Amblyomma, and Ixodes of the Ixodi

234 species favoured alphaproteobacteria in the genera Rhizobium and Ensifer: this was confirmed by nodu

235 se-positive Gram-positive rods from multiple genera routinely classified as diphtheroids.

236 were highly diverse, consisting of multiple genera, species, and genotypes.

237 Genera specific host ranges were also informative.

238 Species of the duckweed genera, Spirodela, Landoltia, Lemna, Wolffiella and Wolf

239 Elsholtzia and its allied genera such as Collinsonia and Perilla (tribe Elsholtzie

240 All core honey bee intestinal bacterial genera such as Lactobacillus, Bifidobacterium, Snodgrass

241 significant enrichment of specific bacterial genera, such as Burkholderia and Collimonas, known for t

242 epresentative species from other spirochetal genera, suggesting that this distinctive growth mode rep

243 a true gall) shows that species within crab genera tend to inhabit the same pit shape.

244 68 species from the Eucalyptus and Corymbia genera (termed eucalypts) along an aridity gradient in s

245 rences in abundances of several families and genera than in controls.

246 ty are four autotrophic beta-proteobacterial genera that are capable of oxidizing sulfur by denitrifi

247 ge fungal scaffoldins identified across four genera that bind to NCDDs.

248 ed detailed species-level data for dozens of genera that contain both dioecious and nondioecious spec

249 identify key functional attributes of major genera that correlate with environmental parameters.

250 invertebrates provided important examples of genera that do not support the hypothesis of liberated c

251 tomatal function, although there are several genera that exhibit stomata in clusters.

252 Genera that had accumulated more species tend to occupy

253 relative abundance of potentially pathogenic genera that is associated with worse ocular mucosal dise

254 Eucalyptus, Pinus, Populus and Pseudotsuga - genera that represent diverse modes of pollination and s

255 on of this account by showing across primate genera that the helplessness of infants is a particularl

256 We identified 6 individual bacterial genera that were differentially abundant between deliver

257 For all the nine host genera, the AUC is over 0.85 and for five of them, the A

258 Across all data representing 85 plant genera, the Ea was 0.34 +/- 0.04 eV, or approximately ha

259 Despite belonging to distant papillomaviral genera, these viruses lacking a canonical E6 protein may

260 itive advantage to bacteria belonging to the genera Thioalkalibacter (Halothiobacillaceae family) and

261 e combine >14,000 occurrences for 690 fossil genera through the Neogene (23-1.8 Mya) with regional es

262 rrent study measured 19 species in these two genera to determine whether variations in 12 categories

263 We use GenERA to survey the entire regulatory landscape of a 3'

264 and subspecies, 53 Nocardia species, and 13 genera (totaling 43 species) of other aerobic actinomyce

265 us (two hosts) trypanosomatid species of the genera Trypanosoma, Leishmania, and Phytomonas, but only

266 Cave shrimps from the genera Typhlatya, Stygiocaris and Typhlopatsa (Atyidae)

267 that the great majority of designated 'rare' genera (up to 60% of all phylotypes) were always rare.

268 that intasomes derived from other retroviral genera use tetrameric integrase.

269 ealed the association of multiple pathogenic genera (Vibrio, Flavobacterium, Tenacibaculum, Pseudomon

270 The plastomes of seven MH genera were analysed in a phylogenetic context with two

271 The dominant fungal genera were Aspergillus sp., Rhizopus sp., Penicillium s

272 between these groups, and 42% of identified genera were associated with >/=1 menaquinone form.

273 , Staphylococcus aureus, and predicted which genera were associated with inhibitory activity.

274 urated sequence assemblies belonging to five genera were characterized in replicate samples of 11 hig

275 Ea values converged when genera were classified into three breakdown rate categor

276 12 included families remained intact and 55 genera were confirmed, whereas 32 genera were lumped and

277 Two genera were depleted among those with high versus low CV

278 Four genera were enriched among those with high versus low CV

279 In contrast, the same 90 bacterial genera were found in both forest types, and their relati

280 Among the Ascomycota, 65 genera were identified, and the abundant operational tax

281 act and 55 genera were confirmed, whereas 32 genera were lumped and 15 genera were split.

282 during the anaerobic process, while only 71 genera were observed during the aerobic process.

283 encing of the 16 S rRNA gene showed that 108 genera were observed during the anaerobic process, while

284 ough similar and dominant hydrogen-utilizing genera were present at both.

285 Twenty-one phyla and 137 genera were shared by all pigs, whereas 12 genera were u

286 firmed, whereas 32 genera were lumped and 15 genera were split.

287 res of richness and evenness, and individual genera were tested for associations with lifetime CVD ri

288 7 genera were shared by all pigs, whereas 12 genera were uniquely identified in the E. faecalis group

289 seolus vulgaris), belonging to two different genera were used to investigate their capacity against d

290 Some diseases are associated with over 50 genera, while most show only 10-15 genus-level changes.

291 TSS) have been found in viruses of different genera, while the ribosome-binding kl-TSS that provides

292 n-infectious viruses for nine bacterial host genera with at least 45 infecting viruses.

293 Based on nine bacterial host genera with at least 45 infectious viruses, we show that

294 compare the relative abundance of bacterial genera with clinical characteristics.

295 Genera with geographic ranges that have remained more st

296 f overall microbial richness and 6 microbial genera with lifetime CVD risk.

297 We measured guard cells across the genera with stomata to assess developmental changes in s

298 r analyses suggest that - at least for these genera with the currently available data - dioecy neithe

299 All retrovirus genera, with the exception of deltaretroviruses, have ha

300 striking difference between the two mosquito genera, with viromes of mosquitoes of the Aedes genus ex

301 published data for hundreds of plant clades (genera) within a well-studied region and find major diff