ライフサイエンスコーパス: feeder

1 udy species of bryozoans (benthic suspension feeders).

2 ntegrated with a custom-made, low-cost paper feeder.

3 tion rates than any other zooplankton filter feeder.

4 ts were displaced to a distant site from the feeder.

5 mass (CoM) [11, 12] when heading toward the feeder.

6 ichthyosauriforms, it was probably a suction feeder.

7 helps them evade predation by mucous filter feeders.

8 arteries, en-passant arteries or perforating feeders.

9 e filtration rates of other microbial filter feeders.

10 ifferentiate into RPE-like structures on PA6 feeders.

11 low-trophic-level invertebrates and plankton-feeders.

12 ) were recorded by computer-monitored pellet feeders.

13 ll path, but prioritised movements to nearby feeders.

14 fibroblast feeders, and Matrigel replated on feeders.

15 fects systemic interactions with other plant feeders.

16 mmals: large browsers and medium-sized mixed feeders.

17 ith support from tissue-specific mesenchymal feeders.

18 associated behavioral responses of the root feeders.

19 gnostic confidence index of 2.5 for arterial feeders, 3.0 for nidus, and 3.0 for venous drainage.

20 increases with cell size in microbial filter feeders, a prediction that accords very well with observ

21 increased magnitudes of effects than deposit feeders, a trait-based sensitivity likely as a consequen

22 and ecology of organisms, for example filter feeders able to gather food at rates up to 5 times highe

23 Despite some effects of AC on these deposit feeders, absolute effects of AC amendments on growth and

24 also reversible, and removal of Y-27632 and feeders allows the cells to differentiate normally.

25 offered a choice between paired sugar water feeders amended with either a xenobiotic or solvent only

26 In no-choice feeding bioassays (capillary feeder and plate assays), the analog 1728, which contain

27 Websteroprion armstrongi was a raptorial feeder and possessed the largest jaws recorded in polych

28 amiliarity with the training route between a feeder and the ants' nest to examine its effects when th

29 species, sponges are immobile active filter feeders and have been identified as hyperaccumulators of

30 r counterintuitive as sponges are suspension feeders and many rely on photosymbionts for carbon.

31 Ticks are obligate blood-feeders and serve as vectors of human and livestock path

32 m ingested a diet comparable to extant mixed feeders and specialists on 'soft' prey such as lepidopte

33 udy was limited by the requirement for mouse feeders and the lack of in vivo data.

34 ariance, described how much individuals used feeders and was also repeatable (r: 0.34-0.62).

35 er-free Matrigel, mouse embryonic fibroblast feeders, and Matrigel replated on feeders.

36 Xa hiPSC lines after several passages on SNL feeders, and supplementation with recombinant LIF caused

37 ificantly reduced numbers of the key deposit feeders, and the decreased grazing pressure is likely to

38 ed morphologies than closely related suction feeders, and this pattern reflects the weakened function

39 protocols in that it uses entirely defined, feeder- and serum-free culture conditions and produces v

40 m hESCs at various developmental stages of a feeder- and serum-free differentiation method and show t

41 Microscopic sessile suspension feeders are a critical component in aquatic ecosystems,

42 Thus, feeders are a significant factor affecting X-inactivatio

43 Microbial filter feeders are an important group of grazers, significant t

44 Phloem feeders are known to induce plant resistance via the sal

45 rienced bees reducing exploration beyond the feeder array and flights becoming straighter with experi

46 Using the capillary feeder assay, we allowed flies to choose between sources

47 r of magnitude smaller than that produced by feeders at similar Reynolds numbers.

48 However, upon reversion to the original feeder-based culture conditions, numerous transcription

49 t either flew to a nectar feeder or a pollen feeder, but did not yet collect any food.

50 e thought to be obligate gelatinous plankton feeders, but recent studies suggest a more generalist di

51 We introduce the Capillary Feeder (CAFE), a method allowing precise, real-time meas

52 mon Drosophila feeding assays: the capillary feeder (CAFE), food labeling with a radioactive tracer o

53 Thus, child cells exposed to feeder cell culture represent a novel model system in wh

54 itor cell-purification steps or support by a feeder cell layer.

55 n the absence of exogenous growth factors or feeder cell layers.

56 d) transgenic fish using a zebrafish ovarian feeder cell line (OFC3) that was engineered to express z

57 latency by long-term cultivation on the H80 feeder cell line in the absence of TCR stimulation.

58 of the cell culture system was the use of a feeder cell line that was initiated from ovaries of a tr

59 The feeder cell line was selected in G418 and engineered to

60 hematopoietic precursors in vitro use either feeder cell, serum, conditioned culture medium or embryo

61 In MS-5 feeder cell-based long-term cultures that supported the

62 Using a novel feeder cell-culture system, we observed long-term (>pass

63 th ESCs grown on feeder cells, ESCs grown in feeder cell-free conditions exhibited decreased immunosu

64 em cell-based, chemically-defined, serum and feeder cell-free culture system, we show that the AhR is

65 y human B cell progenitors, we established a feeder cell-free in vitro system allowing the developmen

66 Here we report establishment of an in vitro feeder-cell-free LSC expansion and three-dimensional cor

67 varian cancer cells with Jagged-1-expressing feeder cells activated the promoter activity of candidat

68 defined components such as mouse-derived 3T3 feeder cells and fetal bovine serum.

69 Initial derivation is on feeder cells and is followed by adaptation to a feeder-f

70 monstrated that physical contact between the feeder cells and keratinocytes is not required for induc

71 Both feeder cells and Rho kinase inhibition are required for

72 The combination of irradiated fibroblast feeder cells and Rho kinase inhibitor, Y-27632, conditio

73 3T3-J2 feeder cells and ROCK inhibition allowed rapid expansion

74 tory culture without the use of heterologous feeder cells and their viability was demonstrated in viv

75 nued cell proliferation is dependent on both feeder cells and Y-27632, and the conditionally reprogra

76 kines IL-2, IL-21 and irradiated 3T3-msCD40L feeder cells can successfully stimulate switch-memory B

77 tocol also describes how ASCs can be used as feeder cells for maintenance of other pluripotent stem c

78 nitial TCR stimulation, but neither the PBMC feeder cells in the REP or the activated TIL expressed 4

79 m cells, we investigated whether Y-27632 and feeder cells induced a stem-like phenotype.

80 d, more importantly, that irradiation of the feeder cells is required for this induction.

81 of embryoid body, sera from animals, and the feeder cells isolated from mouse.

82 ivated mouse embryonic fibroblasts (MEFs) or feeder cells of human origin.

83 ined culture conditions and the avoidance of feeder cells or embryoid bodies allowed synchronous and

84 Moreover, the use of human feeder cells reduces the risk of zoonosis.

85 us telomerase expression and co-culture with feeder cells results in efficient extension of lifespan

86 induce pluripotency, and requires the use of feeder cells that add complexity and variability to the

87 ouse and human T cells on antigen-expressing feeder cells to develop higher-affinity TCRs.

88 verrode the requirement of serum factors and feeder cells to maintain mESCs in culture.

89 are then dispersed and plated on irradiated feeder cells to propagate and isolate individual iPSC cl

90 m cell typically rely on protein matrices or feeder cells to support attachment and growth, while mec

91 ves coculture of irradiated mouse fibroblast feeder cells with normal and tumor human epithelial cell

92 crodrops seeded with mitotically inactivated feeder cells, and then connected with neighboring microd

93 cient source of autologous iPS cells and, as feeder cells, can also maintain iPS and ES cell pluripot

94 d by using various empirical combinations of feeder cells, conditioned media, cytokines, growth facto

95 Compared with ESCs grown on feeder cells, ESCs grown in feeder cell-free conditions

96 ith other methods, our protocol does not use feeder cells, has a minimum dependence on proteins (purm

97 or (Y-27632), in combination with fibroblast feeder cells, induces normal and tumor epithelial cells

98 mically defined conditions in the absence of feeder cells, serum, and leukemia inhibitory factor.

99 e MEF and human placental stromal fibroblast feeder cells, some proteins were only expressed in suppo

100 activity alone when grown in co-culture with feeder cells, suggesting that loss of the p16(INK4a)/Rb

101 ep for 1 month were transferred onto Sertoli feeder cells, they differentiated into functional sperm

102 ly immunodeficient children were cultured on feeder cells, they well supported R5, but not X4 HIV-1 r

103 ree culture system, devoid of animal-derived feeder cells, were sorted by relative cell size and char

104 lated NGFR-expressing cells were free of PA6 feeder cells.

105 le factor (or factors) released by apoptotic feeder cells.

106 ot lead to immortalization in the absence of feeder cells.

107 tin (perlecan, fibulin-2), in the absence of feeder cells.

108 ated with radiation-induced apoptosis of the feeder cells.

109 e Notch ligand Dll4 on hESC-derived vascular feeder cells.

110 B-CLL cells died after removal of macrophage feeder cells.

111 rent to human stem-cell xenoculture on mouse feeder cells.

112 nating potential variability caused by using feeder cells.

113 genitors through coculture of hESCs with OP9 feeder cells.

114 ith Jagged-1 knockdown mesothelial and tumor feeder cells.

115 liminates the requirement for animal-derived feeder cells.

116 xtension to human iPS cells cultured without feeder cells.

117 d for expanding these cells in vitro without feeder cells.

118 In contrast, in feeder channels that are wider than the cell body, cells

119 lls rely on embryoid body formation, stromal feeder co-culture or selective survival conditions.

120 itors but was toxic to this cell fraction in feeder coculture and xenotransplant experiments, indicat

121 following BMP4 treatment in the presence of feeder-conditioned media; however, this model has not be

122 nimising travel distances between individual feeders conflicted with minimising overall distance.

123 ections, linking nodes of the rich club, and feeder connections, linking non-rich club nodes to rich

124 vation on mitotically inactivated testicular feeders containing CD34+ stromal cells.

125 re than three times the number of cells than feeder-containing substrates per surface area.

126 Preparation of glial feeder cultures must begin 2 weeks in advance, and it ta

127 mentation efficiently supports adaptation of feeder-dependent hPS cells to xeno-free conditions, clon

128 feeder-free conditions and human iPSCs using feeder-dependent or feeder/xenobiotic-free processes.

129 tecture, coil-sac distance, coil number, and feeder diameter did not significantly differ between rec

130 ion: feeding guild (chewing arthropods > sap feeders), diet breadth (specialist herbivores > generali

131 ng herbivore) and a specialist aphid (phloem feeder) differentially induce resistance against Pieris

132 ntiated AFS cells expand extensively without feeders, double in 36 h and are not tumorigenic.

133 ants of lava-filled rifts and the underlying feeder dykes that served as the magma plumbing system fo

134 lever press) and consummatory (going to the feeder, eating) behaviors.

135 e or "path motif" that involved rich club or feeder edges and thus traversed a rich club node.

136 Large, actively swimming suspension feeders evolved several times in Earth's history, arisin

137 potency and differences in the metabolism of feeder-/feeder-free cultured hESCs.

138 demonstrate that large, nektonic suspension feeders first evolved during the Cambrian explosion, as

139 s that arrived at an experimentally provided feeder for the first time were compared with experienced

140 ibronectin, and vitronectin and can serve as feeders for both autologous and heterologous pluripotent

141 that chewers induced more volatiles than sap feeders, for both total volatiles and most volatile clas

142 Human iPSCs could be generated under feeder-free (Ff) and Xf culture systems from human prima

143 ESCs toward the cholangiocytic lineage using feeder-free and defined culture conditions.

144 l technique for the COMECS protocol, using a feeder-free and serum-free (FFSF) culture system.

145 can be readily derived from adult hASCs in a feeder-free condition, thereby eliminating potential var

146 f hESC and hiPSC lines onto xeno-free (XF) / feeder-free conditions and evaluated XF substrate prefer

147 of ASCs from fat tissue into mouse iPSCs in feeder-free conditions and human iPSCs using feeder-depe

148 approach uses chemically defined media under feeder-free conditions, and it uses two small-molecule c

149 human and mouse iPS cells can be obtained in feeder-free conditions.

150 ike clusters (ILCs) from the iPS cells under feeder-free conditions.

151 o primitive endoderm-like cells under normal feeder-free culture conditions.

152 ssue culture polystyrene dishes, and for the feeder-free culture of hES cells on PMEDSAH coating in d

153 Using dual SMAD signaling inhibition in a feeder-free culture system, we have been able to expand

154 , expanded myeloid cells with GM-CSF using a feeder-free culture system.

155 In addition, feeder-free culture systems can be used to support hESCs

156 s 2 h and, as it is directly compatible with feeder-free culture, the time burden of manually identif

157 and differences in the metabolism of feeder-/feeder-free cultured hESCs.

158 After adaption to conditions of feeder-free defined and/or xeno-free culture systems, ex

159 der cells and is followed by adaptation to a feeder-free environment; competent technicians can perfo

160 ation of iPSCs from 2 LCLs (LCL-iPSCs) via a feeder-free episomal method using a cocktail of transcri

161 Toward this end, an in vitro feeder-free human B cell developmental model system was

162 del for studying the molecular mechanisms of feeder-free iPS generation and maintenance.

163 s grown on three distinct culture platforms: feeder-free Matrigel, mouse embryonic fibroblast feeders

164 Reduction of glycolysis in feeder-free primed hESCs also enhances neural specificat

165 is decreases self-renewal of naive hESCs and feeder-free primed hESCs, but not primed hESCs grown in

166 stem cell-like colonies that can grow under feeder-free stem cell culture conditions.

167 lop the first chemically defined, xeno-free, feeder-free synthetic substrates to support robust self-

168 enic coculture system (ACC) and an autogenic feeder-free system (AFF).

169 leveraged these kinetic gains to establish a feeder-free, xeno-free protocol which slashes the time,

170 kemia inhibitory factor (LIF)-expressing SNL feeders, frequently had two Xas.

171 fusion, defined as persistence through small feeders from adjacent normal pulmonary arteries; or inco

172 The obligate suspension feeder, Gastrophryne carolinensis, generally diluted the

173 Although leaf feeders generally reduce the performance of root herbivo

174 dpoles of B. terrestris (an obligate benthos feeder) generally amplified infections for the other spe

175 Ingestion by indiscriminate deposit-feeders has been reported, yet physical impacts remain u

176 I provide evidence that filter feeders have been strongly selected to take advantage of

177 If transferred to STO feeders, hHpSCs give rise to hepatoblasts, which are rec

178 Unfortunately, most fluid-feeder/host nitrogen stable-isotope studies simply repor

179 to understanding nitrogen dynamics in fluid-feeder/host systems.

180 of pines in cafeteria bioassays (the phloem-feeder Hylobius abietis and the defoliator Thaumetopoea

181 The dual feeder implementation is compatible with standard GPON a

182 then those signals were used to replace the feeders in monolayer and three-dimensional cultures to e

183 The presence of nektonic suspension feeders in the Early Cambrian, together with evidence fo

184 asic fibroblast growth factor (bFGF) support feeder-independent growth of human embryonic stem (ES) c

185 Here we report feeder-independent human ES cell culture that includes p

186 The ASC-derived iPSCs can be generated in a feeder-independent manner, representing a unique model t

187 Abundant cemented suspension feeders indicate a well-developed 'reef stage' with prol

188 ding currents produced by sessile suspension feeders inhibits their ability to access fresh fluid.

189 Caenorhabditis elegans is a filter feeder: it draws bacteria suspended in liquid into its p

190 t with DSA showed kappa of 0.85 for arterial feeders, kappa of 1.00 for nidus size, and kappa of 0.82

191 ouse-derived primed hESCs on mouse embryonic feeder layer (MEF) to a naive state within 5-6 days in n

192 lips, which are suspended above an astrocyte feeder layer and maintained in serum-free medium.

193 e of the role of HA in early development and feeder layer cultures of hESCs and the controllability o

194 and obviates the requirement for serum or a feeder layer for maintenance.

195 ead angiogenesis assay experiment, FCSC cell feeder layer induced HUVECs to form significantly shorte

196 pluripotent stem cells requires the use of a feeder layer of cells.

197 cultures by using a combination of L1 and a feeder layer of human hair follicle-derived mesenchymal

198 Blastocysts were cultured individually on a feeder layer of rat embryonic fibroblasts (REFs) in fibr

199 ns cultivated in the absence of an astrocyte feeder layer showed abundant AbetaO binding to dendritic

200 Serially passaged with 3T3 feeder layer support, the keratinocytes were examined fo

201 bal specimens and clonally expanded on a 3T3 feeder layer, followed by subcultivation of holoclones o

202 in Matrigel in the absence of a mesenchymal feeder layer, individual cells divided and formed self-o

203 ed the survival of CLL cells on a macrophage feeder layer.

204 ) cell lines were derived 25 years ago using feeder-layer-based blastocyst cultures, subsequent effor

205 er different conditions were seeded onto 3T3 feeder layers and cultured for 12 days.

206 ells cultured on bone marrow-derived stromal feeder layers are more resistant to chemotherapy, increa

207 Once cell colonies were established REF feeder layers could be replaced with REF conditioned med

208 ore, mouse and human amniocytes can serve as feeder layers for iPS cells and for mouse and human embr

209 limbal stroma when seeded on 3T3 fibroblast feeder layers from P1 to P3.

210 Mitotically inactive feeder layers have been used previously to support the g

211 In vitro colony assays with rUCMS cells as feeder layers markedly reduced Mat B III colony size and

212 rmatogonial behavior similar to that seen on feeder layers of SNL fibroblasts.

213 tent cells without the need for coculture on feeder layers or cell sorting to obtain a highly enriche

214 f these iPS cells on mitotically inactivated feeder layers prepared from the same amniocytes.

215 ddition of neuregulin-1 to cultures on MSC-1 feeder layers resulted in spermatogonial behavior simila

216 ch passage, clonogenicity on 3T3 fibroblasts feeder layers was compared among progenitor cells remove

217 ioned medium from mouse embryonic fibroblast feeder layers, and (ii) direct cell differentiation.

218 gation of hESCs on mouse fibroblast or human feeder layers, enzymatic cell removal, and spontaneous d

219 oly-L-lysine-coated glass substrates without feeder layers.

220 use yolk sac-derived endothelial cell (C166) feeder layers.

221 n blot; SC clonal growth was measured on 3T3 feeder layers.

222 c cultures in the presence or absence of MSC feeder layers.

223 ed in media with or without serum and/or 3T3 feeder layers.

224 in an undifferentiated state by culturing on feeder layers.

225 ds feeding further from their territory used feeders less than those feeding closer.

226 Filter feeders, like mussels and clams, are suitable bioindicat

227 city and bioremediation potential of deposit-feeder microbial systems.

228 Cells confined in narrow feeder microchannels prefer to enter wider branches at b

229 Moreover, great tits and males used feeders more than blue tits and females respectively, wh

230 raging patterns, binge-eating less and using feeders more when they experienced greater local competi

231 y, it is unknown what force microbial filter feeders must generate to process adequate amounts of wat

232 nge, and energetic biomarkers of the deposit feeder Neanthes arenaceodentata.

233 AVM characterization consisted of arterial feeder, nidus size, and venous drainage type identificat

234 ons for bioremediation potential and deposit-feeder nutrition.

235 Feeders of angioblasts yielded self-replication, stellat

236 , whereas we observe that sessile suspension feeders often feed at an angle to these boundaries.

237 re seen in bees that either flew to a nectar feeder or a pollen feeder, but did not yet collect any f

238 and use of the Activity Recording Capillary Feeder or CAFE (ARC), a machine-vision (automated image

239 l relies on culture systems devoid of serum, feeders or complex extracellular matrices, which enable

240 iate the need for protocols based on stromal feeders or embryoid bodies.

241 iod, whereas those injected with saline, PA6 feeders, or undifferentiated ES cells showed no rescue.

242 Because filter-feeder organisms ingest MP while feeding, they are likel

243 Traditionally, glycolysis is regarded as a feeder pathway that prepares glucose for further catabol

244 We found earlier that ants trained to a feeder placed to one side of a single shape [10] and tes

245 Large-bodied suspension feeders (planktivores), which include the most massive a

246 Among shellfish, the benthic suspension feeder Rangia cuneata (wedge clam) showed seasonal avoid

247 rsity, and overwhelmingly made by generalist feeders rather than specialized herbivores.

248 has been used encompassing sediment surface feeders, sediment ingestors, and sediment reworkers.

249 across the three habitats, with sap and leaf feeders showing higher abundances in terra firme clay fo

250 ediment surface, allowing sessile suspension feeders such as brachiopods, corals, and bryozoans to re

251 ising questions about how specialized nectar feeders such as hummingbirds sense sugars.

252 L4A5 variation were associated with usage of feeders, suggesting that longer bills may have evolved i

253 primed hESCs, but not primed hESCs grown in feeder-supported conditions.

254 events the frequently found bias towards one feeder (symmetry breaking) and leads to equal distributi

255 ed protocols were established with an animal feeder system.

256 We tested these possibilities using a novel feeder test in a wild songbird community containing thre

257 are more efficient as well as more versatile feeders than both the squirrel and guinea pig.

258 tis as a semi-sessile, epibenthic suspension feeder that could use its helens to elevate its tubular

259 we studied the enchytraeid worm, a bulk soil feeder that thrives in Arctic peatlands.

260 rs that instructed them to select one of two feeders that delivered unequal amounts of liquid.

261 bats (Desmodus rotundus) are obligate blood feeders that have evolved specialized systems to suit th

262 Sponges are benthic filter feeders that play pivotal roles in coupling benthic-pela

263 intained on mouse embryonic fibroblast (STO) feeders that support rodent SSC self-renewal in vitro bu

264 Since Pantodon is an obligatory surface feeder, the ventral retina viewing the aerial environmen

265 es dominated by sessile epifaunal suspension feeders to communities with elevated diversities of mobi

266 making clear the vulnerability of capillary feeders to surface pollutants.

267 nge of species was considered, from plankton feeders to top predators, whose trophic level (TL) was a

268 displaced experimentally from a food source (feeder) to unfamiliar terrain, ants run off a portion of

269 provide the first rationale for why suction feeders typically pollinate flowers with lower sugar con

270 at T. borealis was a microphagous suspension feeder, using its appendages for sweep-net capture of fo

271 ately 75% of eyes, typically consisting of a feeder vessel and large branching vessels resistant to a

272 A feeder vessel could be identified in 1 case.

273 A large main central vessel trunk/feeder vessel could be seen in 72% of these eyes, with v

274 excellent interreader agreement for arterial feeder vessel identification (kappa = 0.97; 95% CI = 0.9

275 d intralesional cysts (0% vs 7%, P < .0001), feeder vessels (10% vs 48%, P < .0001), intrinsic vessel

276 mension (8 vs 6 mm; P = .05), and associated feeder vessels (20% vs 47%; P = .05).

277 Signs more frequent in OSSN included feeder vessels (odds ratio [OR], 5.8 [95% CI, 3.2-10.5])

278 -onset conjunctival growth with conjunctival feeder vessels and intrinsic vessels; however, there was

279 ally, OSSN lesions more frequently exhibited feeder vessels and tended to have more leukoplakia and a

280 graphy and reported the location of arterial feeder vessels and the venous drainage type and classifi

281 V appeared large even in small lesions, with feeder vessels approaching the size of the major arcade

282 %), intrinsic blood vessels in 26 (81%), and feeder vessels in 22 (69%).

283 n the iris or in the anterior chamber angle, feeder vessels, and nodule formation.

284 agreement in the identification of arterial feeder vessels, draining veins, and Cognard classificati

285 ised at similar rates, whereas the first few feeder visits became fixed early while bees continued to

286 Analysis of 933 086 feeder visits by 3134 individuals revealed that the majo

287 rather than improvements in the sequence of feeder visits.

288 calculations, we show that living suspension feeders (Vorticella) likely actively regulate the angle

289 e, the latency to obtain seed from the novel feeder was shorter the more diverse their flocks were.

290 ssage Xa/Xi hiPSC lines generated on non-SNL feeders were converted into Xa/Xa hiPSC lines after seve

291 Paracrine signals produced by the different feeders were identified by biochemical, immunohistochemi

292 tatus) and exclusion (of nonexclusive breast feeders) were examined.

293 s in the published literature (chewers > sap feeders), while challenging other commonly held notions

294 n important source of Hg for shallow benthic feeders, while deepwater sources of mercury may be impor

295 re more likely to obtain seed from the novel feeder with greater diversity of species composition in

296 Reset cells can be expanded without feeders with a doubling time of around 24 h.

297 ped for short-term cultures and were used as feeders with hHpSCs.

298 logical role of Permopsocida as early pollen feeders with relatively unspecialized mouthparts.

299 Classification of fluid feeders with respect to the mechanism of energy dissipat

300 ns and human iPSCs using feeder-dependent or feeder/xenobiotic-free processes.