ライフサイエンスコーパス: phylum

1 ella, and members of the inconspicuous BD7-3 phylum).

2 h an outer membrane (OM) might exist in this phylum.

3 ht to belong exclusively to the euryarchaeal phylum.

4 concomitant reduction in the Proteobacteria phylum.

5 are present throughout the entire vertebrate phylum.

6 ed nature of habenular cell types across the phylum.

7 sent, especially for the dominant Firmicutes phylum.

8 om 24 known bacterial phyla and one archaeal phylum.

9 ols skeletogenesis throughout the echinoderm phylum.

10 esenting a new family within the Nitrospirae phylum.

11 bacteria as belonging to the Actinobacteria phylum.

12 ributed in either mode depending on the host phylum.

13 d by early life history evolution within the phylum.

14 cluding members of the poorly understood TM7 phylum.

15 t in the strikingly colorful Platyhelminthes phylum.

16 related to molluscs or assigned to their own phylum.

17 bacteria, mostly within the Proteobacterium Phylum.

18 n protozoan parasites within the Apicomplexa phylum.

19 resent a diagnostic lipid biomarker for this phylum.

20 Archaea, with Euryarchaeota as the dominant phylum.

21 dely conserved throughout the cyanobacterial phylum.

22 aused by Babesia species of the apicomplexan phylum.

23 nts an evolutionary divide in the spirochete phylum.

24 utionary history of C and N pathways in this phylum.

25 enomes representing four genera from the new phylum.

26 other arthropod species spanning the entire phylum.

27 iquity of phase-variable R-M systems in this phylum.

28 egulatory network that predates the chordate phylum.

29 on multiple occasions within the Firmicutes phylum.

30 l surface in the Gram-negative Bacteroidetes phylum.

31 to environmental adaptation in a prokaryotic phylum.

32 romyces cerevisiae belongs to the ascomycota phylum.

33 ological and ecological diversity within the phylum.

34 ria as HetL homologues are spread across the phylum.

35 d and predate the emergence of the parasitic phylum.

36 ifying programs of skeletogenesis within the phylum.

37 tantly related lineages of the Cyanobacteria phylum.

38 pted for biomineralization in the echinoderm phylum.

39 covariances of taxa within the Bacteroidetes phylum.

40 this, they have failed to place them in any phylum [14-18], demonstrating weak phylogenetic associat

41 vagina, with Proteobacteria as the dominant phylum (60 %).

42 180 individual phages infecting hosts in the phylum Actinobacteria have been sequenced and grouped in

43 The ancient phylum Actinobacteria is composed of phylogenetically an

44 through increasing the relative abundance of phylum Actinobacteria, decreasing the relative abundance

45 ptomyces and Mycobacterium, belonging to the phylum Actinobacteria, were studied owing to their contr

46 e viruses that infect bacterial hosts in the phylum Actinobacteria.

47 f Chloroflexi, Actinobacteria, and candidate phylum AD3 (or Dormibacterota) co-occurred with Ca.

48 teria have been found in all members of this phylum, almost nothing is known about their identity, lo

49 Commensal bacteria from the Bacteroidetes phylum also produce sphingolipids, but the impact of the

50 mposition or structure is evident across the phylum, although symbiont communities are characterized

51 entation with a member of the Proteobacteria phylum, an enteroadherent Escherichia coli isolated from

52 roup, especially abundances of Fibrobacteres phylum and 12 genera in the E. faecalis group and antibi

53 (F/B) ratio, and increase of Verrucomicrobia phylum and Akkermansia genus.

54 Taxonomy reveals an increase of Firmicutes phylum and Corynebacteriaceae family in MCT skin surface

55 g NNET trained on datasets classified at the phylum and family taxonomic level, respectively.

56 relative abundance of specific taxa at both phylum and genus levels between WNH and BNH women cohort

57 sed gut microbial community diversity at the phylum and genus levels by 4 and 6 wk of life, as well a

58 EM fungal community composition at both the phylum and genus levels, but had no significant effect o

59 errestrial representatives of the Arthropoda phylum, and although alpha-like OctRs have been cloned f

60 Firmicutes was the most abundant phylum, and Corynebacterium, Acinetobacter, and Staphylo

61 Firmicutes were the dominant phylum, and Staphylococcus and Streptococcus the dominan

62 ammalian host-associated members across this phylum, and their association with oral mucosal infectio

63 Arthropods are the most diverse animal phylum, and their phylogenetic relationships have been d

64 Thus, as for other echinoderms, the phylum- and order-specific aspects of this species' N-gl

65 three axes of invertebrate diversity: worms (Phylum Annelida), spiders (Class Arachnida) and insects

66 The apicoplast exists in most members of the phylum Apicomplexa and has its own genome along with org

67 lasma gondii are widely studied parasites in phylum Apicomplexa and the etiological agents of severe

68 Parasites of the phylum Apicomplexa are highly successful pathogens of hu

69 The approximately 6000 species in phylum Apicomplexa are single-celled obligate intracellu

70 Parasitic protozoa of the phylum Apicomplexa cause a range of human and animal dis

71 The phylum Apicomplexa comprises human pathogens such as Pla

72 The phylum Apicomplexa has been defined by the presence of t

73 plasma gondii is a protozoan pathogen in the phylum Apicomplexa that resides within an intracellular

74 re (Family Plasmodiidae, Order Haemosporida, Phylum Apicomplexa), was detected in condors captured in

75 ganism, an intraerythrocytic parasite of the phylum Apicomplexa, causes a febrile syndrome similar to

76 intracellular parasites, which belong to the phylum Apicomplexa, have developed mechanisms to exploit

77 d pathology associated with parasites of the phylum Apicomplexa.

78 Members of this phylum are frequently motile as well.

79 Uncultured members of the Chloroflexi phylum are highly enriched in numerous subseafloor envir

80 ing bacteria affiliated with the Nitrospinae phylum are important in dark ocean chemoautotrophy.

81 that phototrophic members of the Chloroflexi phylum are not particularly ancient, having evolved well

82 Although bacteria within the Verrucomicrobia phylum are pervasive in soils around the world, they are

83 y and undertake the study of members of this phylum as strategic experimental systems with great basi

84 ional network for fungi in the basidiomycota phylum, as Saccharomyces cerevisiae belongs to the ascom

85 abundance of species within the Bacteroides phylum, as well as increases in the richness and diversi

86 The fungal phylum Ascomycota comprises three subphyla: Saccharomyco

87 Eleven orders of the phylum Ascomycota were identified: Pleosporales (the lar

88 ant groups including the candidate bacterial phylum Atribacteria and archaeal phylum Pacearchaeota.

89 ibed here function in diverse members of the phylum Bacteroidetes and should facilitate analyses of p

90 consists of various members of the bacterial phylum Bacteroidetes as demonstrated by CRISPR spacer an

91 iota members from the dominant Gram-negative phylum Bacteroidetes depends on their ability to degrade

92 d, but the fourth clade, found in members of phylum Bacteroidetes, is uncharacterized.

93 The abundance of the phylum Bacteroidetes, specifically families S24-7 and Ba

94 ivalis, like other bacteria belonging to the phylum Bacteroidetes, synthesizes sphingolipids (SLs).

95 be associated with diverse bacteria from the phylum Bacteroidetes, which includes some of the most ab

96 nally identified 152 SRP RNAs throughout the phylum Basidiomycota.

97 Members of the archaeal phylum Bathyarchaeota are widespread and abundant in the

98 divergence occurs at a stable rate within a phylum but at different rates between phyla, and is freq

99 belong to the largest exclusively parasitic phylum, but is this perception actually true?

100 There was no significant difference on phylum, but on family and genus level bacterial composit

101 demonstrate that the body plan of an animal phylum can originate by the loss of a large part of the

102 lysed genomes of an uncharacterized archaeal phylum (Candidatus Undinarchaeota), revealing that its m

103 ected globally to discover a novel bacterial phylum ('Candidatus Kryptonia') found exclusively in hig

104 Members of the dominant Bacteroidetes phylum capture diverse polysaccharides via the action of

105 Chaetognaths (arrow worms) are a separate phylum (Chaetognatha) of small carnivorous animals, domi

106 A mosaic of cross-phylum chemical interactions occurs between all metazoan

107 tion of halophilic archaea Halobacteriaceae, phylum Chloroflexi, and classes Anaerolineae, Delta- and

108 Pyrosomes are tunicates in the phylum Chordata, which also contains vertebrates.

109 ders the evolution of the sensory PNS in the phylum Chordata.

110 Two species of parasitic fungi from the phylum Chytridiomycota (chytrids) are annihilating globa

111 The phylum Ciliophora plays important roles in a wide range

112 e microbial composition and abundance at the phylum, class, order, family, genus, and species levels.

113 and Dachsous cadherins in Hydra, a member of phylum Cnidaria a sister group of bilaterian.

114 The phylum Cnidaria represents a close outgroup to Bilateria

115 model organism hydra (a member of the animal phylum Cnidaria) secrete neuropeptides with antibacteria

116 resenting the early-branching non-bilaterian phylum Cnidaria, embryos of the sea anemone Nematostella

117 he sea anemone Nematostella vectensis of the phylum Cnidaria, which is separated from bilaterians by

118 scopic parasites, recently placed within the phylum Cnidaria.

119 thesis emerged, including the Chloroflexi, a phylum common across a wide range of modern environments

120 Members of the Firmicutes phylum comprised 39% of total sequences and were in 42%

121 The Apicomplexa phylum comprises diverse parasitic organisms that have e

122 ogenetic affinities of Xenacoelomorpha - the phylum comprising Xenoturbella bocki and acoelomorph wor

123 The echinoderm phylum consists of several model species that have signi

124 dy plans were not fixed at the origin of the phylum, countering hypotheses regarding developmental pr

125 s infecting hyperthermophilic archaea of the phylum Crenarchaeota display enormous morphological and

126 ing Thaumarchaeota/"Aigarchaeota" (candidate phylum)/Crenarchaeota/Korarchaeota (TACK).

127 ic ecosystems, particularly of the enigmatic phylum Cryptomycota.

128 The phylogenetic position of the phylum Ctenophora and the nature of ctenphore nervous sy

129 r sponges (phylum Porifera) or comb jellies (phylum Ctenophora) are the sister group of all other ani

130 Most members of the phylum Cyanobacteria lack Lon (including the model cyano

131 Cyanobacteria comprise a phylum defined by the capacity for oxygenic photosynthes

132 ved, although the levels of conservation are phylum dependent.

133 Phylum distributions differed between the young/adolesce

134 ed/heritable survival strategies evolved for phylum-diverse cellular life on Earth.

135 dy showed a similar gene function diversity, phylum diversity and overall relative abundances of king

136 peptide in the starfish Patiria pectinifera (phylum Echinodermata).

137 Organisms classified to phylum, Elusimicrobia were more abundant in the feces of

138 he unicellular trypanosomatids belong to the phylum Euglenozoa and all known species are obligate par

139 hondria of Euglena gracilis, a member of the phylum Euglenozoa that also includes human parasites.

140 e dimers from two organisms belonging to the phylum euglenozoa: Trypanosoma brucei, a lethal human pa

141 The phylum Euryarchaeota includes diverse groups of methanog

142 Within the phylum Euryarchaeota, these isolates form a separate, cl

143 nown methanogenic genera within the archaeal phylum Euryarchaeota.

144 or methane metabolism in archaea outside the phylum Euryarchaeota.

145 ative reductive dehalogenases throughout the phylum expanded the phylogenetic boundary for potential

146 ative of the widespread uncultured candidate phylum Fermentibacteria (formerly candidate division Hyd

147 ubiquitous in genomes from the Gram-positive phylum Firmicutes and in some Gram-negative bacteria.

148 On day 4 the proportion of the phylum Firmicutes and Proteobacteria in stool was signif

149 ity, and IL-17/IL-22-related declines in the phylum Firmicutes, class Clostridia, and order Clostridi

150 positive halotolerant bacterial genus in the phylum Firmicutes, commonly found in various habitats in

151 forest analyses identify 12 taxa, 11 in the phylum Firmicutes, eight of which are positively associa

152 nkeys had characteristic disturbances of the phylum Firmicutes.

153 es in the bacterial species belonging to the phylum Firmicutes.

154 Bacteria from the Saccharibacteria phylum (formerly known as TM7) are ubiquitous members of

155 ized, fitness-conferring genes unique to the phylum, from which 16 were investigated, revealing essen

156 ed negatively with the relative abundance of phylum Fusobacteria in the guts of tadpoles.

157 ational taxonomic units were assigned to the phylum Gammaproteobacteria (25 +/- 15%, n = 5 electrodes

158 Macrodasyida (phylum Gastrotricha) comprises 365 species distributed a

159 This uncultivable candidate phylum has been proposed to ferment fibre for herbivores

160 everal other uncharacterized members of this phylum have been detected in various human body sites at

161 re we describe a previously unknown archaeal phylum, Helarchaeota, belonging to the Asgard superphylu

162 rsity of carbohydrate structures within this phylum, here we conducted an in-depth analysis of N-glyc

163 f taxonomic resolution (bacterial community, phylum), ignoring key ecological knowledge gained from f

164 Proteobacteria was the most dominant phylum in all samples except for XJ1.

165 owed that Ascomycota was the dominant fungal phylum in Chinese Cordyceps and its soil microhabitat fr

166 ificant increase in taxa from Proteobacteria phylum in comparison to healthy subjects.

167 d a decreased abundance of the Bacteroidetes phylum in comparisons between both Ghanaian RVV responde

168 ent-induced changes occurred at the level of phylum in Firmicutes and Bacteroidetes.

169 In diatoms, a dominant phylum in phytoplankton, NO was reported to mediate prog

170 been elusive in Mollusca, the second largest phylum in the animal kingdom.

171 The Apicomplexa phylum includes a large group of obligate intracellular

172 The former phylum includes pathogenic strains of Escherichia coli a

173 cteria and kill members of the Bacteroidetes phylum, including Bacteroides, Parabacteroides, and Prev

174 metabolic innovations expressed within this phylum, including its importance in the development of a

175 Members of the Apicomplexa phylum, including Plasmodium and Toxoplasma, have two ty

176 important changes to the systematics of the phylum, including the elevation of Artiopoda to the rank

177 nsal microbes belonging to the Bacteroidetes phylum induce expression of IFN-beta.

178 tes, and that the monoderm phenotype in this phylum is a derived character that arose multiple times

179 The Saccharibacteria phylum is a member of Candidate Phyla Radiation, a large

180 fossils are rare, the origin of the nematode phylum is believed to be very ancient, with the divergen

181 n of bacteria belonging to the Bacteroidetes phylum is correlated with resistance to the development

182 wo populations of the deeply rooted archaeal phylum Korarchaeota, which were retrieved from the metag

183 d: EMF community composition differed at the phylum level between DT and DI seedlings, and diversity

184 classified as Proteobacteria or Firmicutes (phylum level) and Haemophilus or Streptococcus (genus le

185 variable weights by frequency method at the phylum level), compared to 91.0 using the previous MetaF

186 mic composition of the gut microbiome at the phylum level, altering the relative abundance of Actinob

187 At the phylum level, flatworms, nematodes and tardigrades show

188 At the phylum level, Principle Component Analysis revealed sign

189 At the phylum level, week 7 was associated with a significant i

190 bacterial blooms is largely conserved at the phylum level, with Proteobacteria (beta-proteobateria),

191 uracies of all algorithms, except SVM at the phylum level.

192 does not produce discernable changes at the phylum level.

193 iety of animal forms from the superphylum to phylum level.

194 The diversity and phylum-level composition of kogiid microbiomes differed

195 Consistent phylum-level habitat preferences may indicate that the f

196 c bacterium Thermodesulfobium acidiphilum, a phylum-level lineage representative.

197 o deep-branching, previously uncharacterized phylum-level lineages (here named "Candidatus Delphibact

198 majority of bacterial diversity lies within phylum-level lineages called "candidate phyla," which la

199 Bacteria from two novel phylum-level lineages have the capacity for CO2 fixation

200 crobial species affiliated with 46 different phylum-level lineages.

201 cterial phyla as well as 47 newly discovered phylum-level lineages.

202 cations are assigned from the species to the phylum levels based on the lowest common ancestors of mu

203 The recent discovery of phylum Lokiarchaeota promises understanding of biologica

204 ions of the abundant "microbial dark matter" phylum Marinimicrobia along defined energy gradients.

205 -development within phyla, we propose that a phylum may be defined as a collection of species whose g

206 Members of the phylum Mollusca demonstrate the animal kingdom's tremend

207 Members of this phylum naturally lack Shine-Dalgarno (SD) sequences in t

208 intestinal (whipworm and hookworm) and 6 pan-Phylum Nematoda (intestinal and filarial species) small

209 The phylum Nematoda offers a new and innovative system for g

210 itrophus noduliformans'-is affiliated to the phylum Nitrospirae (also known as Nitrospirota), but is

211 The phylum of annelids is one of the most disparate animal p

212 in) family proteins are conserved across the phylum of apicomplexan parasites.

213 Thaumarchaeota is an abundant and ubiquitous phylum of archaea that plays a major role in the global

214 The Firmicutes are a phylum of bacteria that dominate numerous polymicrobial

215 phylogenomic analyses support ctenophores, a phylum of carnivorous, gelatinous marine organisms, as t

216 , Flavobacteriaceae (Bacteriodetes), and the phylum of cyanobacteria (such as the Phormidium genus) c

217 ation of relationships among Cnidaria, a key phylum of early-diverging animals.

218 Apicomplexa is a large phylum of intracellular parasites that are notable for t

219 Apicomplexans are a phylum of intracellular parasites that cause major disea

220 which R occurs in other organisms within the phylum of M (in this case, Proteobacteria).

221 Tardigrada, a phylum of meiofaunal organisms, have been at the center

222 Placozoa is an enigmatic phylum of simple, microscopic, marine metazoans(1,2).

223 They belong to the phylum of Stramenopiles, which are not closely related t

224 , we provide evidence that the Chlamydiae, a phylum of strictly host-associated intracellular bacteri

225 is production by Bacteroidetes, the dominant phylum of the gut microbiome.

226 hese metabolic insights into a new candidate phylum offer hints on the targeted cultivation of the ch

227 ropods comprise the largest and most diverse phylum on Earth and play vital roles in nearly every eco

228 ne with previous reports, we observed within-phylum operational taxonomic unit (OTU) habitat preferen

229 rturbation of the microbiome at the level of phylum or genus.

230 plasmid gene content of an entire bacterial phylum over a period of around one billion years.

231 e bacterial phylum Atribacteria and archaeal phylum Pacearchaeota.

232 ity of RON2 proteins within the apicomplexan phylum, particularly that of the AMA1-RON2 complex at th

233 adpoles caused by a protist belonging to the phylum Perkinsea might represent the third most common i

234 ce of intracellular bacteria in the metazoan phylum Placozoa has been reported several times, but wit

235 The enigmatic phylum Placozoa is harboring an unknown number of crypti

236 treatment exhibited higher abundances of the phylum Planctomycetes and the genus Mycobacterium.

237 Bacteria of the phylum Planctomycetes have been previously reported to p

238 axonomic clades of the conspicuous bacterial phylum Planctomycetes.

239 s of these helminths, also trematodes of the phylum Platyhelminthes and major human pathogens, are no

240 The interrelationships of the flatworms (phylum Platyhelminthes) are poorly resolved despite deca

241 the remarkable biology found throughout the phylum Platyhelminthes.

242 Sponges (Phylum Porifera) are among the oldest Metazoa and consid

243 Sponges (phylum Porifera) are early-diverging metazoa renowned fo

244 y of silicatein enzymes from marine sponges (phylum Porifera) is unique in nature for catalyzing the

245 current debate focusing on whether sponges (phylum Porifera) or comb jellies (phylum Ctenophora) are

246 based on the recovery of eDNA from sponges (phylum Porifera), the planet's most effective water-filt

247 of opportunistic pathogens belonging to the phylum Proteobacteria and Enterococcus genus have also b

248 trong pattern emerged with Bacteria from the phylum Proteobacteria being the prominent taxon among th

249 using 20 bacterial isolates belonging to the phylum Proteobacteria that were enriched from north temp

250 g 16S rRNA gene sequencing, we observed that phylum Proteobacteria was most abundant in normal (n = 8

251 A higher abundance of genus Bosea (phylum Proteobacteria) increased with stage.

252 e and Cyanobacteria) and copiotrophic (e.g., phylum Proteobacteria) taxa were apparent through substa

253 Family Enterobacteriaceae (phylum Proteobacteria), family Lactobacillaceae, and gen

254 g different classes within the Gram-negative phylum Proteobacteria: Agrobacterium tumefaciens (syn.

255 ourteen different organisms belonging to two Phylum (Proteobactericea and Furmicutes) were identified

256 Despite its prevalence, the TM7 phylum remains recalcitrant to cultivation, making it on

257 features in Basidiomycota are accompanied by phylum-specific alterations in the RNA-binding domain of

258 ls that this unusual geometry results from a phylum-specific cleavage of the alpha subunit, in which

259 The dimer interface is formed entirely by phylum-specific components, and a peripherally associate

260 Our comparative structural analysis outlines phylum-specific CYP51 features that could direct future

261 How this phylum-specific DV inversion occurs and whether it is co

262 GPCRs and classified them into conserved and phylum-specific subfamilies.

263 r, leptospirosis, and syphilis belong to the phylum Spirochaetae-a unique lineage of bacteria most kn

264 Parasites of the Apicomplexa phylum, such as Plasmodium spp. and Toxoplasma gondii, u

265 dely conserved throughout the cyanobacterial phylum, suggesting a conserved function.

266 Belonging to the proposed candidate phylum "Tectomicrobia," Candidatus Entotheonella members

267 tremely diverse subphylum of the Chordata, a phylum that also contains the vertebrates and cephalocho

268 ms (Platyhelminthes) are a basally branching phylum that harbours a wealth of fascinating biology, in

269 Actinobacteria, a large bacterial phylum that includes the pathogen Mycobacterium tubercul

270 lobus is a bacterium from the Planctomycetes phylum that synthesizes sterols, in contrast to its hopa

271 Ammonia-oxidizing archaea of the phylum Thaumarchaeota are among the most abundant marine

272 Ammonia-oxidising archaea of the phylum Thaumarchaeota are important organisms in the nit

273 of the archaeal class Nitrososphaeria of the phylum Thaumarchaeota encompassing all known AOA.

274 ficantly, an MAG basal to organisms from the phylum Thaumarchaeota that contains mcr genes, but not t

275 lements (MGE) associated with archaea of the phylum Thaumarchaeota, we exploited the property of most

276 of cultivated representatives, including the phylum Thaumarchaeota.

277 c version is only observed in archaea of the phylum Thaumarchaeota.

278 lling systems in a deuterostome invertebrate phylum - the Echinodermata.

279 tion of dsx within the largest Arthropod sub-phylum, the Hexapoda, is unknown.

280 Within this phylum, the holothuroids (sea cucumbers) are known to pr

281 neuropeptides also occur in a deuterostomian phylum-the echinoderms.

282 We identified phylum- through genus-wide differences in bacterial abun

283 structure and abundance of GM from levels of phylum to genus, and even species.

284 f ANME with members of the poorly understood phylum Verrucomicrobia This finding, together with our o

285 In XJ1, and the most abundant phylum was Cyanobacteria, which also accounted for a lar

286 d occurrence in many members of the Porifera phylum, we suggest naming the newly described taxon Cand

287 rth, whereas many bacteria of the Firmicutes phylum were acquired at later times in infancy.

288 ial developmental strategy in the Firmicutes phylum wherein a progenitor cell that faces starvation d

289 The Apicomplexa are a large phylum which contains various parasitic protists, includ

290 eveloping enteropneust from the hemichordate phylum, which together with echinoderms form a sister gr

291 led a significant increase in the Firmicutes phylum with asthma that was associated with a concomitan

292 ell is related to Lokiarchaeota, an archaeal phylum with many eukaryotic features.

293 llow for assessing character polarity in the phylum with respect to outgroups.

294 n, although not for all phyla, including the phylum with the highest average relative abundance acros

295 f ten species, each annotated to a different phylum, with a wide range of life histories and embryoni

296 symbiont communities across the entire host phylum, with convergent forces resulting in analogous co

297 symbiont belongs to the Margulisbacteria, a phylum without cultured representatives and not known to

298 Members of the bacterial candidate phylum WPS-2 (or Eremiobacterota) are abundant in severa

299 revious studies, these data suggest that the phylum WPS-2 includes bacteria with diverse metabolic ca

300 resolved, and the position of their proposed phylum Xenacoelomorpha remains debated.