ライフサイエンスコーパス: animal cell

1 UVs in the same manner as in voltage-clamped animal cells.

2 (Fzr or Cdh1) is localized at centrosomes in animal cells.

3 damental role in the spatial coordination of animal cells.

4 NA polymerase found in mitochondria for most animal cells.

5 ineation of mechanisms of their formation in animal cells.

6 which is crucial for mitotic progression in animal cells.

7 ol the shape of the endoplasmic reticulum in animal cells.

8 the major microtubule-organizing centers of animal cells.

9 ATPase is essential for ionic homeostasis in animal cells.

10 tually exclusive cortical domains in diverse animal cells.

11 he mechanism of miRNA-mediated repression in animal cells.

12 as a similar function in autophagy of higher animal cells.

13 been used to monitor Pi dynamics in cultured animal cells.

14 e-organizing center (MTOC) during mitosis in animal cells.

15 n plants but also anisotropic cell growth in animal cells.

16 and reduce the stability of target mRNAs in animal cells.

17 regulate diverse physiological processes in animal cells.

18 nding proteins that subtends the membrane of animal cells.

19 vesicles or that of previously investigated animal cells.

20 e the main microtubule-organizing centers in animal cells.

21 rve a wide variety of essential functions in animal cells.

22 les in long- and short-distance transport in animal cells.

23 biliverdin IXalpha, is naturally present in animal cells.

24 nts for Na(+) and K(+) that are critical for animal cells.

25 ratus dictates the plane of cell cleavage in animal cells.

26 urface with a property that is orthogonal to animal cells.

27 s a major checkpoint during transcription in animal cells.

28 ight-gated cation channels when expressed in animal cells.

29 y key roles in lifespan control in yeast and animal cells.

30 n the case of mechanosensitive channels from animal cells.

31 in is a critical regulator of cytokinesis in animal cells.

32 usively mediated by the Na(+)/K(+)-ATPase in animal cells.

33 roteins dynein and kinesin is commonplace in animal cells.

34 d for the equivalent extracellular matrix in animal cells.

35 aborations may be crucial in a wide range of animal cells.

36 to different degrees in bacteria, yeast, and animal cells.

37 ucleate and branch out from existing ones in animal cells.

38 erences between yeast mitosis and mitosis in animal cells.

39 , which are responsible for its transport in animal cells.

40 on channels when heterologously expressed in animal cells.

41 ed polysaccharides which are present on most animal cells.

42 he diverse phenomena of cell size control in animal cells.

43 n microtubule organising centres in dividing animal cells.

44 defends against viral infection in plant and animal cells.

45 rotubule-organizing matrix, is a hallmark of animal cells.

46 mary microtubule-organizing center (MTOC) in animal cells.

47 e nucleus and in the sialylation pathways of animal cells.

48 o secure the final cut during cytokinesis in animal cells.

49 s, caveolae, which cover the surface of many animal cells.

50 inase acts as a regulator of RNA import into animal cells.

51 ain serine/threonine-specific phosphatase in animal cells.

52 e retarded diffusion of membrane proteins in animal cells.

53 MT organization in plant cells as they do in animal cells.

54 ylate mRNAs within the cytoplasm of infected animal cells.

55 emporal regulation of protein translation in animal cells.

56 s and to promote proper mtDNA replication in animal cells.

57 II (Pol II) occurs on thousands of genes in animal cells.

58 mportant in regulating plasmalogen levels in animal cells.

59 essential for cytokinesis in most fungal and animal cells.

60 n, development or function between plant and animal cells.

61 ) ions through the plasmalemma of nearly all animal cells.

62 lator of the direct tRNA ligation pathway in animal cells.

63 ell walls and of the extracellular matrix of animal cells.

64 GFP label microtubule plus ends in plant and animal cells.

65 nuclei by different mechanisms in fungi and animal cells.

66 tituents has never been directly observed in animal cells.

67 le stresses exceed greatly those observed in animal cells.

68 ntal for the organisation of microtubules in animal cells.

69 ins, is the microtubule-organizing center of animal cells.

70 nitiate antiviral responses in bacterial and animal cells.

71 detected by pattern-recognition receptors in animal cells.

72 lt and disassembled every cell cycle in many animal cells.

73 cell surface in other cell types, including animal cells.

74 r functional centrosomes, the major MTOCs in animal cells.

75 tic form of cell death recently described in animal cells.

76 itation of a glycan found only in plant, not animal, cells.

77 ses, at the cell division site in fungal and animal cells [1-4] to carry out a wide range of function

78 VPR, SAM and SunTag, have been developed for animal cells (2-6) .

79 Animal cells acquire cholesterol from receptor-mediated

80 Animal cells actively generate contractile stress in the

81 However, unlike animal cells, actomyosin ring constriction occurs simult

82 ntrosome organizes microtubule arrays within animal cells and comprises two centrioles surrounded by

83 egulation of mitotic PPPs focusing mainly on animal cells and explore how these actions control mitos

84 is thaliana The similarity of ferroptosis in animal cells and ferroptosis-like death in plants sugges

85 interphase microtubule cytoskeleton of most animal cells and form the poles of the mitotic spindle.

86 entrioles form the core of the centrosome in animal cells and function as basal bodies that nucleate

87 proach for accessing the complex glycomes of animal cells and is a strategy for focusing structural a

88 gger innate immunity in bacterially infected animal cells and is involved in developmental cell death

89 ned > 1,000 glycans, including antigens from animal cells and microbes, we profiled the IgG and IgM A

90 Noncoding Y RNAs are abundant in animal cells and present in many bacteria.

91 drive crawling motility and phagocytosis in animal cells and slime molds.

92 yl ether bond involves an aerobic process in animal cells and thus is fundamentally different from th

93 nt cell migration, both of which are used by animal cells and unicellular eukaryotes alike.

94 between viruses and mRNA stress granules in animal cells and will discuss important questions that r

95 Many differentiated animal cells, and all higher plant cells, build interpha

96 ome, or vacuole in yeast, for cytokinesis in animal cells, and for the budding of HIV-1 from human ma

97 y and rigidity of the plasma membrane of all animal cells, and hence, it is present in concentrations

98 sion timing is necessary for size control in animal cells, and this joint mechanism leads to a target

99 analyses in the use of both male and female animals, cells, and tissues in preclinical research.

100 ctroscopy protocols are well established for animal cells, application of the method to individual ba

101 Proliferating animal cells are able to orient their mitotic spindles a

102 ch as mast cells, biosynthesize heparin, all animal cells are capable of biosynthesizing HS.

103 Liposomes and animal cells are disintegrated during electrospray, and

104 Plasma membranes of animal cells are enriched for cholesterol.

105 bution of sialic acids (SA) or hyaluronan in animal cells are indicators of pathological conditions l

106 In vitro, animal cells are mostly cultured on a gel substrate.

107 crotubules that comprise mitotic spindles in animal cells are nucleated at centrosomes and by spindle

108 We find that animal cells are poised to respond to both increases and

109 Many plant and animal cells are polyploid, but how these polyploid tiss

110 rthologs of MKS1 and MKS6, proteins that, in animal cells, are part of a complex that assembles at th

111 the mitotic spindle is tightly controlled in animal cells as it determines the plane and orientation

112 Microtubules in animal cells assemble (nucleate) from both the centrosom

113 lopment, and describe in vitro, ex vivo, and animal cell-associated transmission models that can be u

114 d, our results are consistent with the first animal cell being able to transition between multiple st

115 centrosome and emphasizes the plasticity of animal cell biology and development.

116 The extent and dynamics of animal cell biomass accumulation during mitosis are unkn

117 Animal cells bud exosomes and microvesicles (EMVs) from

118 role during plant PCD as for mitochondria in animal cells, but it is still unclear whether they parti

119 direct impact on the control of cell size in animal cells, but its mechanistic contribution to cellul

120 ies of individual microtubule (MT) arrays in animal cells, but relatively few works address the behav

121 tic spindle determines the cleavage plane in animal cells, but what controls spindle positioning?

122 as been completed, is executed in fungal and animal cells by a contractile actin- and myosin-based ri

123 fate in yeast (Saccharomyces cerevisiae) and animal cells by extracting protein substrates from membr

124 Infection of animal cells by numerous viruses is detected and counter

125 lex controls numerous cell-fate decisions in animal cells, by mediating transcription of developmenta

126 collaborative discovery that even genes from animal cells can be cloned in bacteria.

127 In yeast and animal cells, CDC25 phosphatase dephosphorylates the CDK

128 electrical impedance spectroscopy (EIS) for animal cell concentration monitoring of adherent culture

129 Most animal cells contain a centrosome, which comprises a pai

130 astructure of actin and myosin II within the animal cell CR remains an unanswered question.

131 The zoospores, akin to animal cells, crawl using actin-mediated cell migration.

132 We conclude that not all animal cells critically rely on the sodium pump as the u

133 During animal cell cytokinesis, the spindle directs contractile

134 In animal cells, cytokinesis commonly relies on an actomyos

135 However, in contrast to animal cells, cytokinesis in yeast cells also requires t

136 Both the low animal cell density of bioreactors and their ability to

137 Cytokinesis in animal cells depends on spindle-derived spatial cues tha

138 Human and other animal cells deploy three closely related dioxygenases (

139 strate that the two main cation gradients of animal cells differentially power cholesterol transport

140 Animal cells disassemble and reassemble their nuclear en

141 The hardest working complex in animal cell division has a new gig.

142 Accurate animal cell division requires precise coordination of ch

143 During animal cell division, an actin-based ring cleaves the ce

144 During animal cell division, the central spindle, an anti-paral

145 During animal cell division, the cleavage furrow is positioned

146 thought to be fundamentally similar in most animal cell divisions and driven by the constriction of

147 To divide, most animal cells drastically change shape and round up again

148 se proteins typically enable colonization of animal cells during infection, but may in the present ca

149 ures are morphologically similar to those of animal cells, emerge from tripartite ER junctions, and m

150 Thus, plant and animal cells evolved different molecular strategies to r

151 Animal cells express heparan sulfate proteoglycans that

152 In animal cells, faithful chromosome segregation depends on

153 /microtubule cytoskeletons and organelles in animal cells, focusing on three key areas: ER structure

154 y canonical membraneless compartments within animal cells form in a manner that is at least consisten

155 In animal cells, formation of the cytokinetic furrow requir

156 Our survey of animal cells found that membrane force foci all have cho

157 scribed for yeast and many types of cultured animal cells, frequently after cell cycle arrest to aid

158 permeable and conductive membrane to protect animal cells from vacuum, thus enabling high-resolution

159 rvations provide evidence that multicellular animal cells harbor similar viruses.

160 Animal cells harbour multiple innate effector mechanisms

161 e that the universal presence of NaCl around animal cells has directly influenced the evolution of th

162 Most single animal cells have an internal vector that determines whe

163 In yeast (Saccharomyces cerevisiae) and animal cells, hundreds of pre-rRNA processing factors ha

164 mediate intercellular communication between animal cells in health and disease, but the mechanisms o

165 and favors bipolar spindle formation in most animal cells in which tubulin is in limiting amounts.

166 y component of the extracellular matrices of animal cells, including the pericellular matrix around t

167 Many animal cells initiate crawling by protruding lamellipodi

168 Division of amoebas, fungi, and animal cells into two daughter cells at the end of the c

169 erns of overlaps form in central spindles of animal cells, involving the activity of orthologous prot

170 In cultured animal cells, iron chaperones poly rC-binding protein 1

171 One solution in many animal cells is a radial array of microtubules called an

172 The final step of cytokinesis in animal cells is abscission, which is a process leading t

173 The shape of animal cells is an important regulator for many essentia

174 The shape of most animal cells is controlled by the actin cortex, a thin n

175 The process of apicobasal polarization in animal cells is controlled by the evolutionarily conserv

176 Lipid homeostasis in animal cells is maintained by sterol regulatory element-

177 Cytokinesis in animal cells is mediated by a cortical actomyosin-based

178 A paradigm of cytokinesis in animal cells is that the actomyosin contractile ring pro

179 The sodium pump (Na,K-ATPase) in animal cells is vital for actively maintaining ATP hydro

180 sphingolipid found in the plasma membrane of animal cells, is the endocytic receptor of the bacterial

181 In animal cells, it also requires trafficking of endosomes

182 in ER stress resolution and, differently to animal cells, it does not temper the ribonuclease activi

183 cross-species infections pit viruses against animals, cell lines, or even single genes from foreign s

184 In mitosis, animal cells lose their adhesion to the surrounding surf

185 In animal cells, loss of PTEN leads to increased levels of

186 In animals, cell-matrix adhesions are essential for cell mi

187 novel mechanism of regulated viral entry in animal cells mediated by host factor villin.

188 Cholesterol, a necessary component of animal cell membranes, is also needed by the lethal huma

189 In animal cells, microtubule and actin tracks and their ass

190 These channels, like their counterparts in animal cells, might regulate multiple nuclear Ca(2+) res

191 Animal cell migration is a complex process characterized

192 be formed and persist in mitochondrial DNA, animal cell mitochondria lack specialized translesion DN

193 In animal cells, mitotic spindles are oriented by the dynei

194 proper cell division, and two centrosomes in animal cells naturally become two spindle poles.

195 erythrocytes and human kidney cells HEK293), animal cells (neuroblastoma N115 and sheep red blood cel

196 In animal cells, nine aminoacyl-tRNA synthetases are associ

197 In animal cells, nuclear envelope breakdown (NEBD) is requi

198 Classically, animal cells nucleate or form new microtubules off the p

199 Defects in the nuclear lamina of animal cell nuclei have dramatic effects on nuclear stru

200 In native states, animal cells of many types are supported by a fibrous ne

201 CRISPR/Cas9-based gene knockout in animal cells, particularly in teleosts, has proven to be

202 In animal cells, Partner of Inscuteable (Pins) acts at the

203 us-end-directed microtubule motor protein in animal cells, performing a wide range of motile activiti

204 In contrast to animal cells, plants use nitrate as a major source of ni

205 To better understand animal cell plasma membranes, we studied simplified mode

206 holesterol is the most abundant component of animal cell plasma membranes.

207 he primary microtubule nucleating centers of animal cells, play key roles in forming and orienting mi

208 Par-3 regulates animal cell polarity by targeting the Par complex protei

209 plexity of the U7 snRNP, and suggest that in animal cells polyadenylation factors assemble into two a

210 Significance statement: Most, if not all, animal cells possess mechanisms that allow them to detec

211 single-cell RNA-seq protocols developed for animal cells produce informative datasets in plants.

212 nsfection agents that are commonly used with animal cells produce nanocomplexes that are significantl

213 he recombinant DBAC-L DNA into complementing animal cells produced more than 1 million DBAC-L virus p

214 eminiscent of exocytotic events in secretory animal cells progressively increased in frequency, reach

215 , replicate entirely within the cytoplasm of animal cells, raising questions regarding the relative r

216 during the chronic phase between vaccinated animal cell recipients and mock-vaccinated animal cell r

217 d animal cell recipients and mock-vaccinated animal cell recipients did not reach significance (P = 0

218 In animal cells, relicensing after S phase but before mitos

219 ar, mainly because measurements on plant and animal cells relied on independent experiments and setup

220 double ring during cytokinesis in fungal and animal cells remains unknown.

221 In animal cells, replication-dependent histone pre-mRNAs ar

222 Cytokinesis of animal cells requires the assembly of a contractile ring

223 Cytokinesis in animal cells requires the constriction of an actomyosin

224 ates, which form the outermost structures of animal cells, requires CMP-sialic acid, which is a produ

225 cholesterol in the plasma membranes (PMs) of animal cells resides in three distinct pools.

226 These findings help to explain why most animal cells round up as they enter mitosis.

227 Animal cells secrete small vesicles, otherwise known as

228 emenza for discovery of the pathway by which animal cells sense and adapt to changes in oxygen availa

229 In animal cells, several proteins, including KU70, KU80, AR

230 The cortical actin network controls many animal cell shape changes by locally modulating cortical

231 Animal cell shape is controlled primarily by the actomyo

232 The cell cortex is essential to maintain animal cell shape, and contractile forces generated with

233 tion imaging methods, we show that yeast and animal cells share the key property of gradual and stoch

234 In yeast and animal cells, signaling pathways involving small guanosi

235 In animal cells, sister chromatids gradually biorient durin

236 In animal cells, size homeostasis is controlled through two

237 ith centralspindlin underlies cytokinesis in animal cells, solving a mechanistic conundrum.

238 In animal cells, spindle orientation is regulated by the co

239 In many animal cells, stimulation of cell surface receptors coup

240 Animal cells strictly control the distribution of choles

241 In most animal cells studied, chromosome segregation occurs as a

242 Cell deformations in animal cells, such as those required for cell migration,

243 Our results, together with findings in animal cells, suggest that de novo F-actin assembly at t

244 Elevated CO(2) is generally detrimental to animal cells, suggesting an interaction with core proces

245 ectodomain shedding, a well-known process in animal cell surface proteins.

246 mechanistic importance and adaptive value to animal cell systems.

247 members abundantly found in yeast, plant and animal cells that confers actin microfilaments their bun

248 Different from animal cells that divide by constriction of the cortex i

249 id (MSA) is a metabolite of selenium (Se) in animal cells that exhibits anti-oxidative and anti-cance

250 es are the microtubule-organizing centers of animal cells that organize interphase microtubules and m

251 In contrast to nonmuscle myosins from animal cells that require phosphorylation of the regulat

252 In dividing animal cells the endoplasmic reticulum (ER) concentrates

253 Despite being ubiquitous in all animal cells, the contribution of the Na(+)/K(+) pump cu

254 In most animal cells, the dominant site for MT nucleation in mit

255 In animal cells, the kinesin-5 Eg5 primarily drives this re

256 In animal cells, the protein dynamin is involved in membran

257 ells exhibit major structural differences to animal cells, the question arises whether the plant cyto

258 In many animal cells this process starts with the formation of a

259 In animal cells, this process can be triggered by depletion

260 or degradation of Neu5Gc, which would allow animal cells to adjust Neu5Gc levels to their needs.

261 The ability of animal cells to crawl, change their shape, and respond t

262 cross the basolateral plasma membrane in all animal cells to facilitate essential biological function

263 What motivates animal cells to intercalate is a longstanding question t

264 even day-to-day physiology require plant and animal cells to make decisions based on their locations.

265 those without algae and the algae inside the animal cells to those in the egg capsule.

266 require certain nucleoporins, such as Tpr in animal cells, to properly localize to kinetochores.

267 In both plants and animals, cell-to-cell signaling controls key aspects of

268 re application of this technique for mapping animal cell traction in three-dimensional nonlinear biol

269 Moreover, in DAR-treated animals, cell transplantation-induced activation of KCs,

270 asion of microbial DNA into the cytoplasm of animal cells triggers a cascade of host immune reactions

271 ts provide a framework for understanding how animal cells tune cortical flow through local control of

272 This concept is likely to apply to other animal cell types characterized by plasma membrane expre

273 Recent experiments in diverse animal cell types demonstrate that within a cell populat

274 Different animal cell types have distinctive and characteristic si

275 ing mainstream as it is recognized that many animal cell types require the biophysical and biochemica

276 For various animal cell types, growth rates in prophase are commensu

277 central role in polarizing a broad range of animal cell types.

278 operties and stabilities may form in diverse animal cell types.

279 d in various mammalian cell lines or diverse animal cell types.

280 proteins, which mediate polarization of many animal cell types.

281 We discuss two hypotheses for the origin of animal cell types: division of labor from ancient plurif

282 Animal cells undergo dramatic actin-dependent changes in

283 As they enter mitosis, animal cells undergo profound actin-dependent changes in

284 Animal cells use a wide variety of mechanisms to slow or

285 Animal cells use pattern-recognition receptors (PRRs) to

286 All animal cells use the motor cytoplasmic dynein 1 (dynein)

287 of wall-less plant cells whereas rheology of animal cells was mainly dependent on the actin network.

288 accharides that reside at the surface of all animal cells where they can interact with a multitude of

289 ids that are enriched in plasma membranes of animal cells, where they interact to regulate membrane p

290 ceptors (IP3 Rs) are expressed in nearly all animal cells, where they mediate the release of Ca(2+) f

291 The function of HOPS is well known in animal cells, while CORVET is poorly characterized.

292 and hyperpolarized the membrane of cultured animal cells with much faster kinetics at less than one-

293 e Cbl is an obligatory cofactor, taken up by animal cells with the help of a transport protein and a

294 exhibit the same weak power law rheology as animal cells, with comparable values of elastic and loss

295 ous cells including bacterial, protistan and animal cells without prior knowledge of the cells.

296 Despite reports that animal cell Y RNAs are essential for DNA replication, ce

297 r mRNA localization and local translation in animal cells, yet how mRNA granules interact with motor

298 diate many essential signalling functions in animal cells, yet how they open remains elusive.

299 o ingress the cytokinetic cleavage furrow in animal cells, yet its filament organization and the mech

300 ticulum (ER) network is extremely dynamic in animal cells, yet little is known about the mechanism an