ライフサイエンスコーパス: genera

1 8 wheat wild relative accessions across five genera.

2 ccur, even between plants in closely related genera.

3 at stress and nitrogen availability for both genera.

4 of adaptive radiation in many tropical tree genera.

5 mic descriptions for 22 novel species and 16 genera.

6 t that are generalists feeding on many plant genera.

7 from three obligate intracellular bacterial genera.

8 ting dataset included 302 bee species and 56 genera.

9 sferred into three different enterobacterial genera.

10 mically restricted to a handful of bacterial genera.

11 networks representing thousands of bacterial genera.

12 rational taxonomic units (OTUs) within these genera.

13 of legumes, spanning 294 diverse papilionoid genera.

14 olic metabolites, and specific gut microbial genera.

15 d abundance of Bacteroides and Lactobacillus genera.

16 tablished evolutionary relationships and sub-genera.

17 l data are limited to representatives of two genera.

18 asing the abundances of potential pathogenic genera.

19 failed to clearly distinguish species within genera.

20 ling resulted in 35 unique species across 20 genera.

21 vel strains, 283 novel species, and 42 novel genera.

22 t codivergence across six diverse anglerfish genera.

23 ter, Anaeroplasma, Petrimonas, and Moraxella genera.

24 n addition to a variety of other interesting genera.

25 taphylococcus and Streptococcus the dominant genera.

26 d clarify the relationships among Ixodes sub-genera.

27 ed the evolution of P450s in these bacterial genera.

28 have been traditionally employed to diagnose genera.

29 aphic distribution of constituent species or genera.

30 ecific antiviral for any member of these two genera.

31 id not alter relative abundances of non-oral genera.

32 ent a conserved feature across different HPV genera.

33 ct identification of differentially abundant genera.

34 ially those belonging to the Bombus and Apis genera.

35 taset including Ys from all extant great ape genera.

36 h each species specializing on different ant genera.

37 broad range of phototrophic and chemotrophic genera.

38 de regions in bacteria belonging to distinct genera.

39 was more efficient at capturing certain bee genera.

40 a novel set of relationships between thripid genera.

41 for the appearance of 18 now-extinct faunal genera.

42 the Aedes, Anopheles, Culex, and Psorophora genera.

43 tably cashew, sumac and pistachio from other genera.

44 ew to science, including members of five new genera (2 sponges and 3 cnidarians).

45 atabase for 67 fish species, representing 54 genera, 25 families, and six major Neotropical orders.

46 chin Diadema, which split from other studied genera 250 million years ago.

47 ism and safety margin) on >150 trees from 12 genera (36 species) and spanning a stem size range from

48 These findings suggest that the genera abundance continues to change with additional str

49 minococcaceae and several butyrate-producing genera abundances with APOE genotypes.

50 -resistant bacteria-including those from the genera Acinetobacter, Pseudomonas, Klebsiella, Enterobac

51 We identified 6 genera (Acinetobacter, Lactobacillus, Lactococcus, Leuco

52 bleaching response and mortality of 14 coral genera across high-latitude eastern Australia during a g

53 rida, USA, indicate that mosquitoes of three genera, Aedes, Anopheles, and Culex are able to locate a

54 ies Mogibacteriaceae and Veillonellaceae and genera Alistipes, Anaerotruncus, CC-115, Collinsella, Co

55 Many mosquito transmitted viruses of the genera Alphavirus and Flavivirus are human pathogens of

56 used a set of 4,764 records of ticks of the genera Amblyomma, Ixodes, and Haemaphysalis and their ho

57 ned variation in the distribution of various genera among microhabitat types.

58 includes 13,634 species (68% endemic), 1,742 genera and 264 families-suggesting that New Guinea is th

59 his study identified a total of 15 bacterial genera and 27 OTUs discriminating between the observed C

60 273 Lachnospiraceae isolates representing 11 genera and 27 species from human donors and performed wh

61 rrhineae (Plantaginaceae), which contains 29 genera and 300-400 species (70-80% spurred).

62 is fauna comprises 16 native species from 11 genera and 4 tribes: Anodonta, Pseudanodonta (Anodontini

63 new ebolavirus, but also three new filovirus genera and a sixth proposed genus.

64 Association between certain AGF genera and animal lifestyles, or animal host family was

65 Twenty-eight genera and candidate genera were identified, including m

66 Centruroidinae Kraus, 1955, a clade of seven genera and more than 110 species; infers the ancestral d

67 d Central America with eight subfamilies, 41 genera and more than 300 valid species.

68 dentified in nematode species spanning three genera and multiple plant species, operative across plan

69 y-level occupancy masks high variation among genera and quantify the bias of barcoding primers on the

70 The abundance of genera and species changed during fermentation and was a

71 k to create linguistically correct names for genera and species that can be used off the shelf as nee

72 icrobial community composition between coral genera and species that persisted across space and time,

73 ge differences in the abundance of bacterial genera and species were observed at each sample site, an

74 with the initial relative abundance of some genera and tend to be affected by initial taxonomic rich

75 We demonstrate that FU occurs in all six genera and that dew-derived water may therefore be used

76 creased abundance of oil-degrading bacterial genera and the activity of exoenzyme lipase.

77 ies, and uncertainty in identifying parasite genera and/or lineages may limit the understanding of ho

78 erse at both the genus (155 of 281 eukaryote genera) and family (120) levels, but comprise only 6% of

79 events affecting eight cetacean families, 21 genera, and 35 species, which represent more than 85% of

80 3 to 90% in the classification of the extant genera, and the majority of fossil identifications (86%)

81 richness than most endemic island damselfly genera, and we discuss the potential for endosymbiont-me

82 ium, Clostridium, Borrelia, and Enterobacter genera; and a major reorganization of the family Enterob

83 ral, the Cuevavirus and proposed Dianlovirus genera appear to follow the transcription and replicatio

84 seven Arabideae subclades classified as four genera: Arabis, Aubrieta, Draba, and Pseudoturritis Inte

85 mily, the Syzygium, Eugenia and Campomanesia genera are constituted by a wide variety of fruit specie

86 gnoses of Armatognathia and Paranarthrurella genera are given.

87 asthma, but the roles of specific bacterial genera are poorly understood.

88 While two of these new genera are similar to the ebola- and marburgviruses, the

89 the Prochlorococcus and marine Synechococcus genera are the most abundant photosynthetic microbes in

90 eus, Myrtillocactus, Melocactus and Pereskia genera) are often consumed as fresh fruits, processed fo

91 alyses in Taraxacum, but also in the related genera, as well as in the closely related tribes of the

92 ence D1/D2 LSU database for all cultured AGF genera, as well as the majority of candidate genera enco

93 obacterium, Paraglaciecola, and Polaribacter genera associated with low nutrients and sea ice conditi

94 with six Caribbean coral species from three genera at four reef sites over one year.

95 nary commensal microbes, which belong to the genera Bacteroides and Prevotella, were identified to pr

96 Three genera, Bacteroides, Prevotella, and Ruminococcus, were

97 We propose the recognition of 14 genera based on solid morphological delimitations.

98 Among the 121 genera belonging to this family, the Syzygium, Eugenia a

99 d a lower relative abundance of 13 commensal genera (Benjamini-Hochberg adjusted P <= .15) in the dia

100 ctate) and favoring growth of the beneficial genera Bifidobacterium (bread crust, pilsner and black b

101 the detection of symbionts belonging to the genera Breviolum, Cladocopium, and Durusdinium.

102 pathogens, including those belonging to the genera Burkholderia and Acinetobacter.

103 and introgression are common within tilapia genera but are difficult to analyse due to limited numbe

104 alysis with autosomal SNPs separated the two genera, but failed to clearly distinguish species within

105 din is structurally similar to that of other genera, but much longer (418 amino acids).

106 homoeologous chromosomes in the crown-group genera, but not in the most ancestral Pseudoturritis gen

107 erformed by prevalent phototrophic bacterial genera, but the electron transfer pathways and the physi

108 Here we constrain the diets of 17 pterosaur genera by applying dental microwear texture analysis to

109 a Malassezia species-but not species in the genera Candida, Saccharomyces or Aspergillus-accelerated

110 der Streptophyta, family Victivallaceae, and genera Cetobacterium, Clostridium, Faecalibacterium, Lac

111 versity, co-occurrence networks of bacterial genera clearly diverged between CHD+ and CHD- individual

112 tion to yeast genomes, present in only a few genera close to Saccharomyces.

113 In both genera, coalescent analyses recovered almost all nominal

114 e identified using distribution data of 1719 genera combined with a newly generated time-calibrated m

115 nd Oscillospira were among the top bacterial genera contributing to the GMB glycerophospholipid metab

116 dust samples, the relative abundances of 41 genera correlated (r > |0.4|) with one of these axes.

117 possibility that at least three Amherstieae genera (Crudia, Berlinia, and Anthonotha) may have diver

118 rly all of the non-sauropodan sauropodomorph genera currently known from China were first reported fr

119 s and periodontal disease progression, these genera decreased in co-existing diabetes and periodontal

120 nearly 1/3 of described species from diverse genera demonstrate the potential for aerial dispersal.

121 Enterococcus, Fusobacterium, and several new genera described in this study.

122 Of 658 genera detected in the dust samples, the relative abunda

123 Both genera displayed low levels of antibiotic resistance and

124 ared seven species of lady beetles-from five genera distributed across the tribe Coccinellini-on pea

125 At the tongue site, genera earlier shown to be enriched on HNSCC mucosa, Cap

126 The genera Ecchlorolestes and Chlorolestes are monophyletic,

127 genera, as well as the majority of candidate genera encountered in prior internal transcribed spacer

128 ompared with T2-low inflammation; key fungal genera enriched in patients with T2-high inflammation in

129 TG and positively correlated with bacterial genera enriched in PDX mice.

130 ridiosomatidae spider family, at least three genera (Epeirotypus, Naatlo and Theridiosoma) use their

131 ents were dominated by facultative anaerobic genera (Escherichia, Enterococcus, and Streptococcus), w

132 -DNAs in 23 out of 275 dicot species, within genera Eutrema, Arachis, Nissolia, Quillaja, Euphorbia,

133 n; only a few taxa belonging to the dominant genera exhibited relative abundance fluctuations during

134 f the Lachnospiraceae family, as well as the genera Faecalibacterium and Dialister, were associated w

135 TMAO was associated with abundance of 13 genera (false discovery rate < 0.05), including Prevotel

136 ylogenetic groups within the Myoviridae: the genera Firehammervirus and Fletchervirus Analysis of gen

137 The dominant bacterial genera found within all groups included those belonging

138 ading to a list of 29 MS microbial candidate genera from 11 different phyla.

139 d a reference library for 78 families and 96 genera from all major plant lineages - many currently la

140 Most genera from the exclusive clades of Arg-containing NrfA

141 d 24 h later and the abundances of five BHAB genera, Gambierdiscus, Ostreopsis, Coolia, Amphidinium,

142 locene boundary that might have led to those genera going extinct at that time.

143 Two other regionally-abundant genera, Goniastrea and Turbinaria, were also largely una

144 ndant, while the mortality of wet-affiliated genera has increased in those plots where the dry season

145 among newly recruited trees, dry-affiliated genera have become more abundant, while the mortality of

146 9NA-like phages that infect two bacterial genera have been identified to date, and related phages

147 We have found that while species in both genera have essentially the same number of P450s in the

148 vealed that only 229 species belonging to 37 genera have P450s; 38% of Bacilli species, followed by 1

149 s in the United States belonged to nonnative genera, he concluded that the lack of competitive exclus

150 uses that share features with members of the genera Hepacivirus and Pegivirus.

151 We encourage further exploration of the genera highlighted in our data as potential components o

152 A comparison among N4-related phage genera highlights the evolutionary diversity of SSB prot

153 arrheal fecal specimens including the same 4 genera identified in our prior study.

154 significant increase in abundance of several genera in calves with induced acidosis.

155 ), the relative abundances of most bacterial genera in children were more similar to those of their o

156 re driven by Porphyromonas and Fusobacterium genera in chimpanzees and Haemophilus and Streptococcus

157 ted with the abundance of distinct microbial genera in feces.

158 composition and relative abundances of most genera in halite-entombed communities.

159 ht to determine whether individual bacterial genera in indoor microbiota predict the development of a

160 ether FU occurs in six common Amazonian tree genera in lowland Amazonia, and make a first estimation

161 ), one of the most diverse and abundant tree genera in Neotropical biomes.

162 lowed us to compare the effects of bacterial genera in relation to those of immunomodulatory medicati

163 regrowth of Limnobacter, one of the dominant genera in the distributed drinking water, already occurr

164 eed, until recently, these were the only two genera in the filovirus family.

165 diagnostic blood culture corresponded to the genera in the gut microbiome.

166 stimate the phylogenetic relationships of 13 genera in the lichen-forming family Lobariaceae to addre

167 ng the most widespread and species-rich tree genera in the northern hemisphere.

168 lyses reveal that the abundance of microbial genera in the ocean is highly correlated to the frequenc

169 nd 5e potently inhibited different influenza genera in vitro.

170 n of separate sexes within plant families or genera, in some cases showing that the maximum possible

171 The most severely-bleached genera included species that were either endemic to the

172 ed TTX-producing bacterial strains from four genera, including Aeromonas, Pseudomonas, Shewanella, an

173 nd relative abundances of numerous bacterial genera, including Akkermansia spp., that positively corr

174 s between delta(15) N and specific microbial genera increased as coyotes ascended trophic levels.

175 HLA haplotypes are associated with bacterial genera Intestinibacter and Romboutsia.

176 In three genera it evolves under positive selection, in four unde

177 Our findings show that some plant genera known to be cultivated as ornamentals in our syst

178 gher abundances of Bacilli species including genera Lactobacillus, Streptococcus, Enterococcus, and L

179 ongst others, cyanobacteria belonging to the genera Leptolyngbya, Lyngbya, and Phormidium.

180 e communities (at both the inter- and intra- genera level) can be inherited by offspring and supports

181 At family and genera level, 16S rRNA amplicon sequencing results obtai

182 acteria at class level and by Pseudomonas at genera level.

183 Alate termites, of the genera Macrotermes and Odontotermes, showed remarkably h

184 c families and nearly 300 previously unknown genera, many potentially endemic to this submarine volca

185 Here, we describe a methanotroph of the genera Methylobacter that is performing high-rate (up to

186 es, and representative members of two sister genera, Microsynodontis cf. batesii and Mochokiella payn

187 inhabitable range and comprises some of the genera most commonly used for human and animal nutrition

188 The abundance of 12 bacterial genera (mostly from the Actinomycetales order) was assoc

189 Pathogenic bacteria of the genera Mycobacterium and Corynebacterium cause severe hu

190 ix new) and subtribes (six new), to overhaul genera (nine new) and subgenera (three new), and to disp

191 iatus, representing the two most significant genera of arbovirus vectors that infect people, were tes

192 to specific TA-mediated responses in diverse genera of bacteria.

193 errets, dogs, cats, hamsters, and at least 2 genera of bats.

194 o alter coral bleaching for the two dominant genera of branching corals in Moorea, French Polynesia.

195 Evidence indicates that the genera of Escontria, Myrtilocactus, Hylocereus, and Sten

196 the largest and most phenotypically diverse genera of flowering plants, containing species ranging f

197 4 genera of living marine animals and 19,992 genera of fossil marine animals indicates that greater e

198 Southeast Asia and describe 12 species and 4 genera of freshwater mussels new to science.

199 es in the Lymphocryptovirus and Rhadinovirus genera of gammaherpesviruses and provide evolutionary su

200 However, an analysis of 30,074 genera of living marine animals and 19,992 genera of fos

201 ne in North America saw the extinction of 38 genera of mostly large mammals.

202 Across all six genera of Pennsylvanian arborescent lycopsids that were

203 ges of sulfide spring fishes across multiple genera of Poeciliidae is correlated with the convergent

204 aining effectors encoded predominantly by 15 genera of Proteobacteria.

205 versity and structure within and between the genera of Saccharum and Erianthus, 79 accessions from fi

206 Several genera of the Cactoideae and Pereskioideae subfamilies (

207 ing motif insertions have evolved in several genera of the Cricetidae family of rodents.

208 We trained the models on the pollen of 16 genera of the legume tribe Amherstieae, and then used th

209 hemagglutinin neuraminidase RBPs from other genera of the Paramyxoviridae, SosV-RBP and other pararu

210 ulfide bonds; they are also known in several genera of the plant family Rutaceae.

211 ich have previously been identified in other genera of the Reoviridae family.

212 lly pregnant species were identified in both genera of the syngnathids: The pipefishes (Syngnathus) d

213 rene degradation is likely mediated by novel genera or families of sulfate-reducing bacteria along wi

214 Species in the genera Parasponia, Trema, Camellia, Azadirachta, Quillaj

215 s identified by microscopy included helminth genera pathogenic for humans and animals: the whipworm T

216 re 31 OTUs, including the worldwide reported genera Penicillium, Rhodotorula and Cladosporium.

217 opical family Perilestidae consisting of two genera, Perilestes and Perissolestes, be sunk within Syn

218 For both coral genera, Pocillopora and Acropora, heat stress primarily

219 tified CRESS DNA viruses are assigned to the genera Porprismacovirus and Huchismacovirus of the famil

220 Our results identified several key genera previously described in periodontal disease (e.g.

221 expansion of SCFA-producing bacteria of the genera Prevotella and Bifidobacterium, which increased f

222 valence of pathogenic soil bacteria with two genera, Providencia and Serratia, being especially commo

223 omprises more than 2000 species in about 100 genera, providing an excellent system for studying the m

224 olitan fungal taxa, including members of the genera Pseudogymnoascus, Malassezia and Rhodotorula, whi

225 Bacteria of the genera Pseudomonas and Bacillus can promote plant growth

226 wed vertebrates with teeth, belonging to the genera Radotina, Kosoraspis, and Tlamaspis (from the Ear

227 Bacterial amplicon sequence variants of the genera Ralstonia, Pseudomonas, Hyphomicrobium, and Novos

228 ification of putative new species within the genera Rb69virus and T5virus and a putative new genus wi

229 However, the Gesneriaceae include four genera, remnant of the past palaeotropical flora, which

230 ively, and MR detected 356 and 251 bacterial genera respectively.

231 Reoviridae family, Orbivirus and Coltivirus genera, respectively.

232 at the exponential growth rates of these two genera respond to future CO(2) conditions in a manner si

233 One of the major aquatic bacterial genera responsible for human infections from seafood is

234 ngeneric species from six families and eight genera restricted to floodplain, swamp, white-sand or pl

235 s in 972 Firmicutes species belonging to 158 genera revealed that only 229 species belonging to 37 ge

236 bolic potential and distribution of the MGII genera reveals distinct roles in the environment, identi

237 Daphniids of the genera Scapholeberis and Megafenestra are adapted to the

238 elded 216 isolates belonging to 12 different genera, several of which have no prior cultured-represen

239 sts increased broad-range specificity across genera, shorter amplicon sizes that are suitable for use

240 Strains belonging to genera Sporanaerobacter, Paraclostridium, Haloimpatiens,

241 rsteinia odora), and first apomicts from the genera Stipa (Stipa splendens) and Halerpestes (Halerpes

242 such an extent that species belonging to the genera Streptococcus, Listeria, Staphylococcus, Lactobac

243 Moreover, the baseline abundance of the genera Streptococcus, Ruminococcus_torques_group, Eubact

244 of bindin evolution varies across sea urchin genera studied to date.

245 Certain bacterial species from genera such as Paracoccus, Pseudomonas, and Alcaligenes

246 ted with nutrient rich conditions, including genera such as Sulfitobacter, whereas the northern Chukc

247 tly skewed, with a small percentage of plant genera supporting the majority of Lepidoptera.

248 f the Pleistocene, and that the large mammal genera survived unchanged over multiple such cycles.

249 resistance in marine cyanobacteria from the genera Synechococcus and Prochlorococcus and compared mo

250 nd Oscillospira were among the top bacterial genera that contribute to the GMB glycerophospholipid me

251 Trend 2 was driven primarily by genera that decreased in abundance in those with diabete

252 large-scale phylogenetic hypothesis for the genera that occur in these ecosystems.

253 Acinetobacter, Treponema, and Lactobacillus genera that were differentially represented across the t

254 ntories to identify the subset of cultivated genera that were visited during pollen foraging.

255 t have been elucidated in a variety of plant genera, the genes that are responsible for morphological

256 us aceratus and sperm from a male of another genera, the ocellated icefish Chionodraco rastrospinosus

257 Subsampled and transformed marine genera time series reinforce the idea that Permian-Trias

258 ed with aldafermin, with all major phyla and genera unaltered during therapy.

259 d taxonomically distant species of different genera, using Fourier transform infrared spectroscopy (F

260 rotypes, and relative abundance of bacterial genera varied by opioid agonist and antagonist exposures

261 , including bacteria (57 targets covering 30 genera), viruses (48 targets covering 40 viruses), paras

262 no chloroplast genome-wide comparison across genera was conducted.

263 rial diversity post-FMT, and the presence of genera was linked to FMT responsiveness.

264 The relative abundance of 49 other genera was significantly different between both clusters

265 lative abundance of these 12 intercorrelated genera was significantly protective and explained the ma

266 racters for distinguishing and defining both genera was supported by Principal Component Analysis.

267 2015, so that results are comparable between genera, we detected a significant 283-fold increase in A

268 and a new phylogeny including 526 angiosperm genera, we investigated the association between taxonomi

269 onary relationships among certain species or genera, we produced novel RNA-Seq data sets for nine dif

270 a, Bacteriodetes, and Actinobacteria) and 24 genera were altered in unstabilized samples stored at RT

271 ts in the relative abundance of 14 bacterial genera were apparent between diets, including an increas

272 ction with microbial diversity or individual genera were calculated by permutational analysis of vari

273 In BAL fluid samples the dominant genera were Cladosporium, Fusarium, Aspergillus, and Alt

274 Overall, 27 phyla, 171 families and 533 genera were detected, and diversity was significantly hi

275 Additionally, 14 archaeal and 14 viral genera were found to be solely associated with CM.

276 Four predominant bacterial genera were identified as associated with HIV infection,

277 Four predominant bacterial genera were identified to be associated with HIV infecti

278 Twenty-eight genera and candidate genera were identified, including multiple novel lineage

279 The most proportionally abundant microbial genera were Mycobacterium and Achromobacter at 10,000 ft

280 Ants belonging to 14 genera were observed interacting with managed honey bee

281 detes (51.2%) and Firmicutes (27.1%), and 94 genera were represented primarily by Prevotella (17.9%)

282 tified taxa, 29.51% of strains and 63.80% of genera were shared between both metagenomes.

283 undancy analysis indicated that the Fusarium genera were significantly related to the disease index.

284 y discovered hlpP are core genes in specific genera, whereas hfp and newly discovered hlpC are sporad

285 gene as compared to 38% of strains of other genera which contain rhodopsins.

286 To address novel species and genera, which are comparatively harder to predict, MetaM

287 n Akkermansia and increased Clostridium XIVa genera, whose abundance was positively correlated with f

288 rate and lytic phages and representing novel genera with a large repertoire of unknown gene functions

289 ly extended within three different bacterial genera with heterologously expressed EcLamB.

290 f the human gut microbiota revealed multiple genera with the predicted capability to produce or consu

291 an association of 32 microbial families and genera with very-low-density and high-density subfractio

292 e in the abundance of two parasitic nematode genera with zoonotic potential: Anisakis spp. and Pseudo

293 th of host identity varied across coral host genera, with species from the genus Acropora having the

294 re designed to target all known methanogenic genera within the archaeal phylum Euryarchaeota.

295 gi, after the split of Melampsora from other genera within the class of Pucciniomycetes.

296 al products found in plants from a subset of genera within the figwort family (Scrophulariaceae).

297 Genera within the order Lactobacillales dominated dairy,

298 on-redundant clones of different species and genera within the Saccharum complex.

299 es among phyla, as well as differences among genera within the same family.

300 ae fam. nov. - is erected to accommodate two genera without family classification (Paratanaoidea ince