ライフサイエンスコーパス: sponge

1 sister group to all other animals (including sponges).

2 elements (MREs) in lncRNAs acting as ceRNAs (sponges).

3 dically observed in the related choanocytes (sponges).

4 ona massiliana, a hypercalcified calcaronean sponge.

5 skeleton and toward the outer surface of the sponge.

6 proton sponge derivative, coined the "Janus" sponge.

7 ents were treated with an absorbable gelatin sponge.

8 porous, superhydrophobic ultra-thin graphite sponge.

9 ting that cZNF292 does not act as a microRNA sponge.

10 ing and non-wetting liquids dispersed in the sponge.

11 e superhydrophobic TiO2 NPs coated cellulose sponge.

12 bacteria that exist as symbionts in a marine sponge.

13 D scanning and x-ray evaluation for retained sponges.

14 ernative splicing, or by acting as molecular sponges.

15 tal sampling in studies of the microbiome of sponges.

16 bility necessary to sustain cell adhesion in sponges.

17 24-ipc) is synthesized today by certain sea sponges.

18 y through symbiotic microorganisms of marine sponges.

19 of new structural classes of PBDEs in marine sponges.

20 and domination by soft-bodied ascidians and sponges.

21 at deteriorated were overtaken by excavating sponges.

22 lex multicellular animals have been found in sponges.

23 l 1,8-bis(dimethylamino)naphthalene ("proton sponge") 1 and quino[7,8-h]quinoline 2a have been examin

24 ne possible shifts from corals to excavating sponges, 217 coral colonies were monitored over 10 years

25 ions [5, 6], suggesting a general pattern of sponge abundance during collapse of Phanerozoic marine e

26 Excavating sponge abundance increased in both Fort Lauderdale and S

27 Although sponge abundance is increasing on some coral reefs, we l

28 ions there have been subsequent increases in sponge abundance.

29 lly to 47% spirorbids, 23% ascidians and 29% sponges after 100 days in acidified conditions (pH 7.7).

30 to evaluate the response of coral-excavating sponges after coral bleaching events.

31 pe biotas, but the most abundant groups were sponges, algae and worms, with non-trilobite arthropods

32 razin-2-one core was derived from the marine sponge alkaloid family of hamacanthins.

33 ogically-simple, early branching animal, the sponge Amphimedonqueenslandica, we show that the regulat

34 disposables was $0.17 for a 4X18 laparotomy sponge and $0.46 for a 10 pack of 12ply, 4X8.

35 and will likely require broader sampling of sponge and ctenophore genomes, improved analytical strat

36 Before closure, the sponge and instrument count was followed by RFD scanning

37 nd sensory attributes of two types of cakes (sponge and layer).

38 number of large corals, slope angle, maximum sponge and maximum octocoral height.

39 Nasal fluid was collected using polyurethane sponges and analysed by ImmunoCAP and multiplex assays.

40 Labile tissues occur abundantly in the sponges and are also present in other groups, including

41 n is where early branching phyla, especially sponges and comb jellies (sea gooseberries), sit in the

42 ding RNAs (lncRNAs) can function as microRNA sponges and compete for microRNA binding to protein-codi

43 nships between two ancient animal lineages - sponges and ctenophores - and the remaining animal phyla

44 xpression evolved prior to the divergence of sponges and eumetazoans, and was necessary for the evolu

45 creases in spirorbid numbers, but numbers of sponges and Molgula sp. increased.

46 of all animals and were lost secondarily in sponges and placozoans (Trichoplax) or, alternatively, e

47 metazoan stem lineage and were then lost in sponges and placozoans or evolved at least twice indepen

48 ematic mucosal sampling with rectal Weck-Cel sponges and rectal biopsies were performed.

49 everal lncRNAs were shown to act as microRNA sponges and to control ischemia-reperfusion injury or ac

50 has been proposed as a molecular fossil for sponges, and could represent the oldest evidence for ani

51 Antisense oligonucleotides, miRNA sponges, and CRISPR/Cas9 genome editing systems are bein

52 Fossils of the sponge Angulosuspongia sinensis from calcareous mudstone

53 nswer that challenge because monolithic zinc sponge anodes can be cycled in nickel-zinc alkaline cell

54 We have selected the Mediterranean sponge Aplysina cavernicola as a model species for this

55 We show that sponges are a reservoir of exceptional microbial diversi

56 Sponges are benthic filter feeders that play pivotal rol

57 As the oldest extant animals, sponges are good candidates for possessing remnants of t

58 Among marine species, sponges are immobile active filter feeders and have been

59 Marine sponges are major habitat-forming organisms in coastal b

60 The sponges are often large and structurally complex and rep

61 These shifts appear counterintuitive as sponges are suspension feeders and many rely on photosym

62 Microbial symbionts in sponges are ubiquitous, forming complex and highly diver

63 Biodegradable, clinically-approved collagen sponges are used to deliver low doses of small molecule

64 Gentamicin-containing collagen sponges are widely used for prevention of SSIs, but thei

65 ery little of the variability in octocorals, sponges, arthropods, annelids or anemones.

66 ropenimine-substituted bis-protonated proton sponge as a bifunctional phase-transfer catalyst is repo

67 reticulated vitreous carbon - gold (RVC-Au) sponge as a scaffold for enzymatic fuel cells (EFC).

68 eir relatives are an unlikely alternative to sponges as a source of Neoproterozoic 24-isopropylcholes

69 logeny [16-20], our results strongly support sponges as the sister group of all other animals and pro

70 ovide strong statistical support for placing sponges as the sister-group to all other metazoans, with

71 is in vitro and also in vivo in the matrigel sponge assay in mice.

72 ting in aortic ring and in vivo subcutaneous sponge assays from clec14a(+/+) and clec14a(-/-) mice re

73 nd saliva collected in mouthwash and Merocel sponges at day 1 and month 7 were obtained from 150 men

74 hes of eggs that were laid on stalks of dead sponges attached to nodules at depths exceeding 4,000 m.

75 nt and absent) to account for differences in sponge attachment and carbonate change for both living a

76 ution/bioerosion, coral and sponge survival, sponge attachment, and sponge symbiont health were evalu

77 D interconnected porous polydimethylsiloxane sponge based on sugar cubes.

78 Simultaneously, sponge bioerosion rates have been shown to increase as s

79 iferation of MM cells in monolayer and in 3D sponges but did not affect MM cell migration, organizati

80 ely 40%) were detected from 10 to 90 m in LC sponges, but a similar shift was not identified in spong

81 , along with other aroma quality markers, in sponge cake by means of headspace trap/GC-MS.

82 tural properties of leavened wheat bread and sponge cake fortified with cow protein isolates that had

83 lose), specifically designed for mimicking a sponge cake structure.

84 le egg was replaced by 20% by GCPI (3.5%) in sponge cake without affecting the sensory acceptability,

85 Both layer and sponge cakes exhibited an enhancement of the resistant s

86 ful development of new gluten-free (GF) mini sponge cakes fortified with broccoli leaves.

87 The incorporation of BLP into GF mini sponge cakes significantly (p<0.05) increased their anti

88 The overall sensory acceptance of GF mini sponge cakes was affected by increasing BLP content.

89 On the contrary, sponge cakes were noticeable worsened with the use of ba

90 Moreover, sponge cakes yielded more polyphenols and antioxidant ca

91 unds and the antioxidant capacity of GF mini sponge cakes.

92 The fabricated sponge can be used to clean up different types of oil, o

93 Our study provides evidence that some sponges can tolerate environments that appear unsuitable

94 BY-2 cells expressing the cAMP sponge (cAS cells), showed low levels of free cAMP and e

95 e no sulfated GAGs have been found in marine sponges, chondroitin sulfate (CS) and heparan sulfate (H

96 8.1, 7.8, and 7.6), and two levels of boring sponge (Cliona varians, present and absent) to account f

97 In this work, a 3-D porous carbon nanotube sponge (CNTS) was embedded within a shape memory polymer

98 Based on bulk stable isotopic variability, sponges collected from LC were generally more enriched i

99 Here we describe a new species of fossil sponge, Conciliospongia anjiensis gen.

100 To understand possible outcomes of the sponge-coral interaction and build the descriptive model

101 ssile colonial invertebrates-animals such as sponges, corals, bryozoans, and ascidians-can distinguis

102 interaction and build the descriptive model, sponge-corals were monitored in San Andres Island, Colom

103 The sponge count was incorrect in 36.4%, not performed due t

104 ed surgical items by using data-matrix-coded sponge-counting systems (5 pertinent studies).

105 re high-risk for retained sponges, even when sponge counts are performed and found to be correct.

106 ges recorded at different locations across a sponge cross section, together with differential cell se

107 r inclusion of the cyanoenone substrate, the sponge crystal was treated with a thiol solution.

108 Ubiquitous miRNA sponge delivery and consequent systemic miRNA inhibition

109 The two major extant groups of siliceous sponges, Demospongiae and Hexactinellida, are generally

110 The success of excavating sponges depended on the intensity of coral bleaching and

111 cyclopropenimine (DAC)-functionalized proton sponge derivative, coined the "Janus" sponge.

112 monstrate that the aggregation factor of the sponge Desmapsamma anchorata has a circular supramolecul

113 Locally administered gentamicin-collagen sponges did not reduce the incidence of SSI in elderly p

114 Conspecific sponges display remarkable stability in their symbiont c

115 lified polyphosphate kinase (ppk) genes from sponge DNA and confirmed that the gene was expressed.

116 ymbionts that are phylogenetically unique to sponges do not disproportionally contribute to the core

117 climation may support further transitions to sponge dominated reefs in the future.

118 shift algae-coral dominated reefs into algae-sponge dominated.

119 ur study reveals an extraordinarily diverse, sponge-dominated community thriving immediately after th

120 communities in the Welsh Ordovician are also sponge-dominated, suggesting a regional change in benthi

121 s lost in oven-baking steps in straight- and sponge-dough processes, respectively, whereas CNCbl rema

122 o pseudo-proton sponges while 7a-e to proton sponges due to the presence in their molecules of bulky

123 nsistent with this idea, eusocial species of sponge-dwelling Synalpheus shrimps from Belize are ecolo

124 h their mRNA targets, what has been called a sponge effect.

125 somal/lysosomal escape of NPs via the proton sponge effect.

126 This miR-122 "sponge" effect was relieved and redirected to miR-15 tar

127 r level of miR-150, supporting the theory of sponging effects of FOXD3-AS1 on miR-150.

128 The nitrogen/sulphur codoped graphene sponge electrode provides enough space for a high sulphu

129 on graphene-modified poly(dimethylsiloxane) sponge electrodes and an elastic gel membrane is develop

130 imensional nitrogen/sulphur codoped graphene sponge electrodes.

131 rgical procedures are high-risk for retained sponges, even when sponge counts are performed and found

132 tanes, consistent with growing evidence that sponges evolved long before the Cambrian explosion appro

133 Stalked-sponge fauna in the Peru Basin require the presence of m

134 We conclude that SilE is a molecular sponge for absorbing metal ions.

135 s, circRNA_100338 functions as an endogenous sponge for miR-141-3p in HCC.

136 endogenous RNA (ceRNA), effectively becoming sponge for miR-26a/b and thereby modulating the expressi

137 Male humpback dolphins appear to be using sponges for signalling purposes in multi-modal sexual di

138 ospongia muta, is a high microbial abundance sponge found on Caribbean coral reefs along shallow to m

139 s, but a similar shift was not identified in sponges from 10 to 60 m at LSI (only 17% dissimilar).

140 modiolus heckerae mussels and poecilosclerid sponges from asphalt-rich, deep-sea oil seeps at Campech

141 We further identified a 'sponge' function for OIP5-AS1, as high levels of OIP5-AS

142 Neurons seeded in a donut-shaped porous silk sponge grow robust neuronal projections within a collage

143 ran diterpenoids from the New Zealand marine sponge Hamigera tarangaensis are described.

144 ompetitive inhibitor molecules such as miRNA sponges has allowed the community to address individual

145 rsity, bottlenecks and connectivity of these sponges has become urgent in order to evaluate the poten

146 volving mitochondrial genomes in calcaronean sponges has demonstrated that accurate gene expression r

147 algae, whereas only a few close relatives of sponges have been assayed for sterols.

148 [3, 4]; in particular, almost no Hirnantian sponges have been recorded.

149 f 1,8-bis(dimethylamino)naphthalene ("proton sponge") have been obtained from the corresponding iodid

150 rse array of nitrogen transformations in the sponge holobiont.

151 While the contribution of sponge holobionts to the nitrogen cycle has been recogni

152 modified peptides families reported from the sponge host, and both Ca Entotheonella phylotypes contai

153 roportion of microbial cells associated with sponge hosts contained intracellular polyP granules.

154 tion study, such as antisense inhibitors and sponges; however, the robustness, specificity, and stabi

155 We previously demonstrated that the marine sponge Hymeniacidon heliophila displayed significant com

156 ngiogenesis by using the rodent subcutaneous sponge implant model, and we found that CLEC14A protein

157 reduction of haemoglobin content (54.2%) in sponges implanted into Slco2a1 (-/-), compared to wildty

158 ations of NaBu induced neovascularization in sponge implants in mice, evidenced by increased numbers

159 significantly attenuated vascularization of sponge implants.

160 Podocyte-specific expression of the miR-30 sponge in mice increased calcium/calcineurin pathway com

161 RFD detected retained sponges in 11 (0.5%) patients (81.8%laparotomy, 18.2% st

162 Flox mice), was significantly reduced in the sponges in alpha-KO mice.

163 Sponges in general, and Theonella swinhoei in particular

164 Furthermore, the abundance of sponges in the Hirnantian sequence of South China may ha

165 gingival tissues, we used miRNA inhibitors (sponges) in loss-of-function experiments to investigate

166 In cultured podocytes, PAN or a miR-30 sponge increased TRPC6, PPP3CA, PPP3CB, PPP3R1, and NFAT

167 In a chronic model, sponges increased oligodendrocyte and decreased astrocyt

168 Our results suggest that pelagophytes and sponges independently evolved C30 sterol biosynthesis th

169 ly, from 92% spirorbids, 3% ascidians and 4% sponges initially to 47% spirorbids, 23% ascidians and 2

170 Changes in coral-sponge interactions can alter reef accretion/erosion bal

171 addition of 2 gentamicin-containing collagen sponges into the hip joint perioperatively.

172 been reported for the closely related marine sponges Ircinia fasciculata and Ircinia variabilis that

173 The sponge is applicable for targeted sorption and collectio

174 Since the carrier sponge is degraded over time, dentine replaces the degra

175 The diagnosis of a retained surgical sponge is often delayed due to its infrequent occurrence

176 us, the proportion of C. delitrix excavating sponges is a sensitive indicator for the intensity and f

177 Cell adhesion in sponges is mediated by the calcium-dependent multivalent

178 inetically inert compounds) or pseudo-proton sponges (kinetically active) are discussed.

179 ong neutral nitrogen organic bases as proton sponges (kinetically inert compounds) or pseudo-proton s

180 etoxifying organs to cope with toxic metals, sponges lack organs but harbour a symbiotic microbiome p

181 orals have declined and the photoautotrophic sponge Lamellodysidea herbacea is now abundant.

182 derived from the low dispersal abilities of sponge larvae.

183 ded over time, dentine replaces the degraded sponge leading to a complete, effective natural repair.

184 ase are exceptionally high and sufficient to sponge let-7, which reconciles the dispensability of LIN

185 Calcareous sponge (Leucosolenia sp.) numbers increased x2.5 in pH 7

186 ODN, serving as a DC activating factor, into sponge-like macroporous cryogels.

187 ts unveil a novel crystallization pathway to sponge-like porous crystal structures.

188 ssembled and densely packaged into composite sponge-like porous microstructures (Multi-RNAi-MSs) by r

189 ytoplasmic localization on the efficacy of a sponge lncRNA.

190 Sponges loaded with lentivirus encoding for Sonic hedgeh

191 ditive-free, essentially homogenous graphene sponge materials that provide a combination of both cork

192 was examined in the subcutaneously implanted sponge matrices.

193 ronal migration and inappropriate branching, sponge-mediated inhibition results in overmigration.

194 thesis of the architecturally complex marine sponge metabolite (-)-enigmazole A has been achieved.

195 We identified the marine sponge metabolite latonduine as a corrector.

196 and stereochemical elucidation of the marine sponge metabolites (4R,6R)-plakilactone C, (4R,6R,9R)-pl

197 A new asymmetric synthesis of these marine sponge metabolites is described herein, featuring an oxi

198 -state is the recently developed Crystalline Sponge Method (CSM) by Makoto Fujita.

199 e drug candidate by means of the crystalline-sponge method is reported.

200 Core sponge microbiomes are stable and characterized by gener

201 (e.g. nitrogen cycling) can be maintained in sponge microbiomes through functional redundancy.

202 lates oxidative stress-induced apoptosis via sponging microRNA-150.

203 a potential oncogene that regulates TOP2A by sponging miR-411-5p in glioma.

204 wo extant classes further confirms siliceous sponge monophyly and demosponge-hexactinellid spicule ho

205 nophores as sister to all other animals, and sponge monophyly, are strongly supported under multiple

206 presents the first such instance in a proton sponge not having an ortho-substituent and/or being in a

207 tion on how shifts from corals to bioeroding sponges occur, and how environmental factors such as ano

208 al transition (EMT) by acting as a molecular sponge of miR-566.

209 orinated marine polyketide isolated from the sponge of Phorbas sp.

210 Sponges of bioabsorbable type I collagen membrane were e

211 Ultralight cellular sponges offer a unique set of properties.

212 is to compare the effects of PRF and gelatin sponge on the healing of palatal donor sites and the pat

213 Therefore, we sought to determine whether sponges, one of the most ancient extant metazoan lineage

214 We propose that OIP5-AS1 serves as a sponge or a competing endogenous (ce)RNA for HuR, restri

215 studies indicated that FOXD3-AS1 serves as a sponge or as a competing endogenous noncoding RNA for mi

216 ropose that let-7 disruption by LIN28B, MYCN sponging, or genetic loss is a unifying mechanism of neu

217 This bacterium was detected in multiple sponge orders, according to similarities in key genes su

218 membered macrolides isolated from the marine sponge Phakellia fusca Thiele, which was collected from

219 ve been isolated from extracts of the marine sponge Phorbas sp. collected in Howe Sound British Colum

220 Sponges (phylum Porifera) are early-diverging metazoa re

221 The family of silicatein enzymes from marine sponges (phylum Porifera) is unique in nature for cataly

222 with the current debate focusing on whether sponges (phylum Porifera) or comb jellies (phylum Ctenop

223 Sponges placed caudal to the injury had reduced impact o

224 In an acute model, sponges placed directly above the injury increased oligo

225 Considering the widespread sponge population and abundant microbial cells associate

226 a substrate, and near total collapse of such sponge populations was observed following the experiment

227 ve supported the classical scenario in which sponges (Porifera) are the sister group to all other ani

228 Traditionally, sponges (Porifera) have been interpreted as the sister g

229 differential impacts of temperature, pH and sponge presence for living and dead corals.

230 al was primarily driven by pH, regardless of sponge presence or seawater temperature.

231 Here, we document marine sponge presenting associated with visual and acoustic po

232 Furthermore, these sponges provide reversible liquid absorption for hundred

233 In particular, a 3D RVC-Au sponge provides a large accessible surface area for immo

234 suggest an important role of lncRNA-mediated sponge regulation in cancer, but also underscore the cri

235 significance and targets of lncRNA-mediated sponge regulation of cancer are mostly unknown.

236 Here we identify a lncRNA-mediated sponge regulatory network that affects the expression of

237 Layers with abundant sponge remains were deposited after other mass extinctio

238 phylogenomic analyses support the view that sponges represent the sister lineage to the rest of the

239 We show here that solvent uptake by these sponges results in new gel-like materials, which we term

240 uently, child hand rinses (n = 44) and floor sponge samples (n = 44) from low-income-households in Dh

241 Our sponge sampling technique permitted the rapid and quanti

242 rimitive capillary-like assemblies in 3D sea sponge scaffolds in vitro.

243 enomes of bacterial isolates acquired from a sponge, sea slug, and coral to examine the functional la

244 The carbon nanotube sponge shape memory polymer (CNTS/SMPs) nanocomposite co

245 mprove analytical sensitivity by integrating sponge shunt into LFA to decrease the fluid flow rate.

246 thickness, length and hydrophobicity of the sponge shunt were sequentially optimized, and achieved 1

247 ns in favor of the ctenophores-sister or the sponges-sister hypothesis, we submit that research progr

248 ard biomaterials, like bone, wood, and glass sponge skeletons, as well as manmade structures, like th

249 k approach, we demonstrate that the relevant sponge SMT duplication event overlapped with the appeara

250 lyphosphate (polyP) granules in three common sponge species of the Caribbean coral reef.

251 sites preserve a total diversity of over 75 sponge species, many with preserved soft tissues, in pro

252 as 0.90 for mouthwash specimens and 0.92 for sponge specimens; for HPV-18, rho was 0.89 and 0.86, res

253 in 93.2% of mouthwash specimens and 95.7% of sponge specimens; HPV-18 was detected in 72.1% and 65.5%

254 doskeletal materials (bone, shark cartilage, sponge spicules) to attachment devices (mussel byssal th

255 asurements of these parameters in the native sponge spicules, our modeling results correlate remarkab

256 ollenynes B-E, were isolated from the marine sponge Spirastrella mollis collected from Hogsty Reef, B

257 This paper reports sponge spray-a novel sampling and direct MS analysis app

258 Sweat was collected using a gauze sponge style patch, extracted from the gauze by centrifu

259 ation, net dissolution/bioerosion, coral and sponge survival, sponge attachment, and sponge symbiont

260 Sponge swab contents were concentrated by vacuum filtrat

261 Sponge swabbing was compared to contact plate sampling t

262 otal contamination on test surfaces, whereas sponge swabs recovered 76 to 94% of the total contaminat

263 n (0/96 contact plates; 4 case wards), while sponge swabs recovered C. difficile from 29% (87/301) of

264 hile analyzing genomic data from calcaronean sponges Sycon ciliatum and Leucosolenia complicata, we w

265 and sponge survival, sponge attachment, and sponge symbiont health were evaluated.

266 We show that a single sponge symbiotic bacterium, Entotheonella sp., constitut

267 mprehensive library of 141 conditional miRNA sponges targeting well-conserved miRNAs in Drosophila.

268 ction in the skeletal elements of the marine sponge Tethya aurantia.

269 a aspergillum, is a sediment-dwelling marine sponge that is anchored into the sea floor by a flexible

270 n to extraneous material, usually a surgical sponge that was accidentally retained within the body.

271 The sponges themselves represent the scaffold of a gel that

272 ella gemina" live associated with the marine sponge Theonella swinhoei Y, the source of numerous unus

273 rganisms in arsenic and barium cycles in the sponge Theonella swinhoei, known to accumulate high leve

274 octopods we observed suggests that, like the sponges, they may also be susceptible to habitat loss fo

275 Negligible detrimental effects to sponge tissue were observed after treatments up to five

276 ome of the bioactive natural products in the sponge tissue.

277 n about the spicules' arrangement within the sponge to develop a structural mechanics model for the s

278 bition that was not proportional to the cAMP sponge transcript level.

279 nd spatiotemporal inhibition using the miRNA sponge transgenic method in combination with the yeast t

280 While sponges transplanted between habitats displayed shifts i

281 Only adult males presented marine sponges, typically doing so in the presence of sexually

282 Additionally, sponge volume is more important for explaining social tr

283 Lastly, the Janus sponge was found to have fluorescent properties both in

284 The reported sponge was isolated as a monoprotonated salt, though no

285 l hemimandibles, rhBMP-2/absorbable collagen sponge was well mixed with allografts prior to procedure

286 surgically proven cases of retained surgical sponges was undertaken.

287 Sponges were collected along a depth gradient at Little

288 ondrial genomes of at least some calcaronean sponges were found to have a highly unusual architecture

289 Lentivirus-filled sponges were inserted into the intrathecal space surroun

290 No retained sponges were missed by the RFD system.

291 ncreased temperature (+1 degrees C) and when sponges were present; acidification had no significant e

292 Cyanobacterial symbionts cultured from sponges were shown to accumulate polyP.

293 RFD sponges were used exclusively throughout the study perio

294 (BY-2) cells were transformed with the cAMP sponge, which is a genetically encoded tool that reduces

295 dentified as staying closer to pseudo-proton sponges while 7a-e to proton sponges due to the presence

296 se increase the particulate food sources for sponges, while they themselves are relatively unaffected

297 twork structure with a similar agglomeration sponge, with more homogeneous pores compared to the hydr

298 These graphene sponges, with densities similar to air, display Poisson'

299 al products isolated from the New Guinea sea sponge Xestospongia exigua.

300 The giant barrel sponge, Xestospongia muta, is a high microbial abundance