ライフサイエンスコーパス: polarity

1 oxylate, was remarkably sensitive to solvent polarity.

2 anisms involved in regulating bacterial cell polarity.

3 small dyes, but is independent of dye charge polarity.

4 ong-term HSC frequency and loss of stem cell polarity.

5 entary and useful for all types of molecules polarity.

6 epends on the spatiotemporal control of cell polarity.

7 tially organizing actin flow and cytoplasmic polarity.

8 AR network to ensure robust establishment of polarity.

9 contact, which establishes apicobasolateral polarity.

10 c T helper cell 2 (TH2) to neutrophilic TH17 polarity.

11 reconstitution potential and loss of protein polarity.

12 rized coordinately and display a planar cell polarity.

13 o an increase both in density and in polymer polarity.

14 sive phenotype and restores apicobasolateral polarity.

15 o an increase in extraction time and solvent polarity.

16 ssary for proper establishment of epithelial polarity.

17 xy aglycon and its dependence on the solvent polarity.

18 t role in the maintenance of epithelial cell polarity.

19 -rich stress fibers, thus strengthening cell polarity.

20 5 variants with improved packing and surface polarity.

21 high polarity is higher than those with low polarity.

22 epithelial cells, is required for epithelial polarity.

23 ross the visible spectrum by varying solvent polarity.

24 anslocation, opposite the currently accepted polarity.

25 sitive to the local solution environment and polarity.

26 to CYK-4 is essential, for ZEN-4 function in polarity.

27 ntracellular complexes that couple cell-cell polarity.

28 ment and across the metazoa to regulate cell polarity.

29 ical surface, thereby generating arcade cell polarity.

30 for the analysis of small organics with low polarities.

31 fluorescence decay rates in various solvent polarities.

32 t superfamilies and unwind DNA with opposite polarities.

33 e site can hydrolyze DNA strands of opposite polarity, a mechanism that has rarely been observed with

34 How leukocytes acquire polarity after encountering chemical gradients is not we

35 plexes on opposing cell cortex to coordinate polarity among static epithelial cells.

36 tivity advantages were realized for some low polarity analytes including both estradiol and estrone.

37 lysis of nonpolar as well as medium and high polarity analytes is also demonstrated.

38 mixtures containing analytes with different polarities and volatilities in different phases at atmos

39 decreased HSC frequency, increased stem cell polarity and a restored balance of lymphoid and myeloid

40 med by alleviation of the impairment of AQP4 polarity and accumulation of p-tau in the contralateral

41 Intriguingly, the re-establishment of polarity and adhesion during each interphase is associat

42 Physicochemical properties (polarity and basicity) were considered to guide the desi

43 ing and quantitative analysis of cell shape, polarity and behavior in epithelial tissues.

44 , diisopropyl methyl phosphonate in positive polarity and carbon dioxide, sulfur dioxide, hydrochlori

45 and cancer and entail the loss of epithelial polarity and cell adhesion.

46 The remarkable polarity and compartmentalization of neurons raises ques

47 Additional Kin1 substrates for cell polarity and cytokinesis (Tea4, Mod5, Cdc15, and Cyk3) w

48 Kin1 regulates cell polarity and cytokinesis through unknown mechanisms [4-7

49 o importin-beta and is required for cortical polarity and cytokinesis.

50 stic connection with Pom1 signaling for cell polarity and cytokinesis.

51 and Cdc42 null PECs proliferated less, lost polarity and failed to form villous protrusions and floa

52 However, the polarity and function for the WRAMP structure during cel

53 ial for the establishment of epithelial cell polarity and functional maturation of alveolar cells.

54 residues containing side chains of different polarity and length (i.e. Ala, Arg, Cys, His, Glu, and L

55 We demonstrate that the polarity and magnetization are coupled in this system wi

56 From this integrated analysis of HPC polarity and mechanics, we propose that normal heart dev

57 Integrin beta3 regulates cell polarity and migration when localized appropriately to t

58 , and endoderm organization, ectodermal cell polarity and patterning along the oral-aboral axis are d

59 hown to play a role in controlling embryonic polarity and regulating the NF-kappaB signaling pathway.

60 hter identities can result from the physical polarity and size asymmetry itself, as well as the subse

61 which red shifts upon increasing the solvent polarity and stems from an excited complex (i.e., an exc

62 e seems to involve genes with a role in cell polarity and that likely function in the maintenance of

63 nt role for brachyury in morphogenesis, cell polarity and the patterning of both ectodermal and endod

64 show that two dsDNA binding sites set the 5'polarity and to reveal unexpected control of the DNA pho

65 regulation of membrane composition, cellular polarity and trafficking, and the organization of signal

66 t is critical for developmental events, cell polarity, and migration and is usually mediated by linke

67 sequent abnormalities in cell morphogenesis, polarity, and migration.

68 production and controlling neuron migration, polarity, and morphogenesis.

69 for cell signaling, cell cycle progression, polarity, and motility.

70 scopy, as a function of temperature, solvent polarity, and pressure in the solid state have been reco

71 differential effects of D6PK and PID on PIN1 polarity, and suggest that a more complex model is neede

72 erse cellular events, such as cell motility, polarity, and vesicle traffic.

73 neous modulation of efflux carrier level and polarity; and (3) multiple patterns of influx and efflux

74 l structure results in charges with opposite polarities appearing on same surface, leading to current

75 , the mechanism by which tissue cohesion and polarity are affected remains unclear.

76 hic record in which 4 magnetozones of normal polarity are found.

77 n chloride, and hydrogen cyanide in negative polarity are investigated.

78 Establishment and inversion of this polarity are regulated hierarchically by interfacing pro

79 that asymmetric divisions resulting from CE polarity are required for commitment to differentiated s

80 h-temperature route and demonstrate that its polarity arises from partial LiNbO3-type cation ordering

81 redox mechanism for propagation of membrane polarity asymmetry in axonal degeneration.

82 Our data directly confirm the existence of polarity at the twin boundaries, and demonstrate that th

83 e size, ionization state, or electronegative polarity at these positions is crucial for obligate acid

84 153 (T153) in Kir7.1 that reduce constrained polarity at this site (T153C, T153V, T153S) make wild-ty

85 near lagging cell poles, PlpA reinforces the polarity axis of MglA and thus stabilizes the direction

86 ed rearrangement of the IF network along the polarity axis.

87 study demonstrates a new feature of neuronal polarity: axons and dendrites preferentially respond to

88 e at start sites and reduced transcriptional polarity because of strongly enhanced divergent antisens

89 trate that (1) when efflux carriers maintain polarity but change levels, maintaining the same auxin p

90 However, this modification increases its polarity by approximately 1000-fold and reduces the toxi

91 Liver TJs preserve cellular polarity by delimiting functional bile-canalicular struc

92 We found that Ssp1 promotes cell polarity by phosphorylating the activation loop of Kin1.

93 mechanism gating synaptic vesicle transport polarity by promoting anterograde transport processivity

94 Pathogens can alter epithelial polarity by recruiting polarity proteins to the apical m

95 the polarity of GS or obversely decrease the polarity by stereoselective ketal formation with an alip

96 Theoretical models suggest that polarity can arise from localized feedbacks on Fat-Ds co

97 Downstream effectors of Emx2 control bundle polarity cell-autonomously via heterotrimeric G proteins

98 y of plastic categorisation based on surface polarity characteristics of identified particles.

99 This allowed us to unveil distinct polarity characteristics of the plasma membrane and the

100 at, with the suitable channel material, such polarity-controllable technology can scale down to 5 nm

101 a PAR-3-dependent assembly that responds to polarity cues and promotes efficient segregation of aPKC

102 Drosophila neural stem cells, cell intrinsic polarity cues provide spatial and temporal information t

103 MS channels are responsible for the reverse-polarity current that appears in mutants in which normal

104 eration, segmentation, patterning and planar polarity defects.

105 cells had severe cytoskeletal, adhesion and polarity defects.

106 anine product, and discover a strong solvent polarity-dependence for the relative population of the t

107 lvanic vestibular stimulation produced large polarity-dependent corrections in arm position.

108 the neural and behavioural level, which were polarity-dependent.

109 base of the infection cell, which organizes polarity determinants necessary for plant cell invasion.

110 mination not obviously linked to the primary polarity determination mechanisms it has been previously

111 change in protein localization is linked to polarity disruption is not clear.

112 contact inhibition potentially through cell polarity disruption, and results in increased tumor form

113 pulse followed by the delivery of a negative polarity ( downward arrow) back pulse of equal voltage a

114 polarity pathway coordinates epithelial cell polarity during animal development, and loss of its acti

115 echanisms that couple spindle orientation to polarity during asymmetric cell division of Drosophila n

116 in cell shape, cell interactions and planar polarity during convergent extension in the Drosophila e

117 vous system development and in hair follicle polarity during skin development.

118 Inturned (INTU), a cilia and planar polarity effector, performs prominent ciliogenic functio

119 ons such as cytokinesis (Rho1 dependent) and polarity establishment (Cdc42 dependent).

120 on cycle 42 (CDC42) plays important roles in polarity establishment and maintenance as well as cell c

121 effect lethal and cause defects in embryonic polarity establishment, meiosis, and the integrity of th

122 ecular details of the bud site selection and polarity establishment, not much is known about how diff

123 ve therefore revealed unexpected features of polarity establishment.

124 validates their separation effectiveness as polarity-extended chromatographic methods for 274 enviro

125 lled, and in turn polarizes the apical-basal polarity factor Bazooka (Par3).

126 p) to help maintain an appropriate level of polarity for timely release of vancomycin, (iii) Eudragi

127 s (promoting cell survival and altering cell polarity) for genetic alterations of CTCF in endometrial

128 e understanding of ion selectivity, reversed polarity gating, and cAMP regulation in HCN channels.

129 asolateral, recycling, implicating this cell polarity gene in assembly or maintenance of the apical e

130 matrix, epithelial cilia or the planar cell polarity genes Vangl2 and Ptk7 In wild-type mice, collag

131 b(ponli) (ponli) and crumbs2b (crb2b) apical polarity genes' restrictive transcription in the red, gr

132 d-type worms in histology, expression of key polarity genes, or neoblast distribution.

133 differential effects of D6PK and PID on PIN1 polarity had so far been attributed to their differentia

134 Negative polarity He-CTD provided a full set of structurally info

135 other remarkable characteristics of negative polarity He-CTD.

136 nse EVs preparations suggest that epithelial polarity impacts directional release.

137 racellular permeability, loss of apico-basal polarity in 3D cultures, and anchorage-independent growt

138 amphibians and zebrafish by controlling cell polarity in a cell contact-dependent manner.

139 plasticity that maintains coordinated planar polarity in actively moving populations through the cont

140 cate that NUMB is necessary for establishing polarity in CE cells, and that asymmetric divisions resu

141 al for establishing and maintaining membrane polarity in epithelia and other polarized cells.

142 One of the most obvious manifestations of polarity in epithelia is the subdivision of the cell sur

143 hondrial function by altering their membrane polarity in floral tissues.

144 leads to a significant loss of dorsoventral polarity in large body bends.

145 MARK2 regulates the establishment of polarity in Madin-Darby canine kidney (MDCK) cells in pa

146 nd cell biological mechanisms that establish polarity in newborn neurons, synthesizing information fr

147 low to control kinase activity gradients and polarity in the C. elegans zygote.

148 Establishment of anterior-posterior polarity in the Caenorhabditis elegans zygote requires t

149 lar basis of development, morphogenesis, and polarity in the lateral line of Danio rerio and the embr

150 Establishment of cell polarity in the mammalian embryo is fundamental for the

151 .The molecular trigger that establishes cell polarity in the mammalian embryo is unclear.

152 Mutant gonads showed a loss of cell polarity in the surface epithelial layers, large interio

153 ormation is an important contributor to cell polarity in uni- and multicellular systems [1-3].

154 cted 48 h after training revealed sustained, polarity-independent increases in activity in both motor

155 cortical Myosin flows: at anaphase onset, a polarity induced, basally directed Myosin flow clears My

156 We propose that polarity-induced spatiotemporal control of Rok and Pkn i

157 Additionally, solvent polarity influences the deactivation pathway, greatly af

158 s potentially through the regulation of cell polarity integrity.

159 of TENGs can generate single- or alternating-polarity ion pulses, and is ideal for inducing nanoelect

160 matic volatiles and compounds with different polarities is used as a model sample to demonstrate the

161 Apicobasolateral polarity is a fundamental property of epithelial cells,

162 Although disruption of cell polarity is a prerequisite in epithelial tumor initiatio

163 Polarity is a shared feature of most cells.

164 Establishment of apico-basal polarity is critical for the lumenal epiblast-like morph

165 mon device produces a net photocurrent whose polarity is determined by the balance in population and

166 matostella embryos, we demonstrate that cell polarity is established by the four-cell stage and then

167 For motility, a leading-lagging cell polarity is established that is inverted during cellular

168 e developed method toward analytes with high polarity is higher than those with low polarity.

169 ition of avian trunk neural crest cell (NCC) polarity is prerequisite for directional delamination an

170 The surface polarity is quantified both by its ultrahigh water vapor

171 ge-separated state is enabled by the solvent polarity: It is deactivated/switched-off in apolar tolue

172 For 1 event, opposite polarity leaders were observed to accelerate inside the

173 the largest molecules (>520 g/mol) with low polarity (logP approximately 1.9), whereas in summer, sm

174 cell/tissue-specifically to remodel the core polarity machinery.

175 has a clathrin-independent essential role in polarity maintenance and growth.

176 ling of dividing NBs, which is essential for polarity maintenance and initial establishment of cell s

177 progressive change in membrane phospholipid polarity, manifested as phosphatidylserine externalizati

178 ality is limited only by the requirement for polarity matching of the generated radical with the Dha

179 ve hydridic C-H bond abstraction (enabled by polarity matching), alkyl halide oxidative addition, and

180 iols afford lower yields presumably due to a polarity mismatch.

181 in kinases that function within complex cell polarity networks are poorly understood.

182 ediated homophilic adhesion, that coordinate polarity non-autonomously between cells [5, 6].

183 In addition, neither solvent polarity nor radical rotation affects the correlation be

184 the analysis of six fractions of increasing polarities obtained from a sequential supercritical CO2

185 To date, the polarity of alphaherpesvirus infection in the respirator

186 l regulation of morphological and functional polarity of central neurons.

187 ace density was affected by the presence and polarity of DC electric potential, being 87-90% lower on

188 The opposite strand polarity of duplex DNA necessitates that the leading str

189 role for CTCF in the regulation of cellular polarity of endometrial glandular epithelium.

190 xylated amino acids are used to increase the polarity of GS or obversely decrease the polarity by ste

191 The polarity of hair cells was established at birth along a

192 cues, and that they do so by influencing the polarity of individual MMCs.

193 Ns are essential for maintaining the correct polarity of LD budding at the nuclear envelope, restrict

194 its oleophobicity increases with decreasing polarity of organic solvents.

195 The polarity of S1 is evidenced by a solvatochromic shift of

196 tations perturb protein folding, assembly or polarity of secretion of C1QTNF5 and, importantly, all a

197 tching and receptor matching thus change the polarity of the circuit in which they take place.

198 The polarity of the N-tier ahead of the C-tier places the le

199 We demonstrate that the presence and polarity of the overhang structure is a critical determi

200 Surprisingly, the new N-tier to C-tier polarity of translocation reveals an unforeseen quality-

201 In HCN, the polarity of voltage dependence is uniquely reversed.

202 Effects of extraction time and solvent polarity on antioxidant properties of Brassica oleracea

203 er reagent for Fischer glycosidations in low-polarity organic solvents are described.

204 useful for analyzing not only small and low-polarity organics but also polar biomolecules, such as p

205 d trans-metal-trapping strategies with lower polarity organometallic reagents (Mg(CH2 SiMe3 )2 and Al

206 The core planar polarity pathway coordinates epithelial cell polarity du

207 ontrol via the non-canonical Wnt/planar cell polarity pathway, Shh/BMP signalling, and the transcript

208 The absence of planar cell polarity (PCP) core proteins Prickle1 and Prickle2 in in

209 n epithelial cell patterning and planar cell polarity (PCP) in Drosophila.

210 (Ds) have been found to underlie planar cell polarity (PCP) in many tissues.

211 to exhibit a particular form of planar cell polarity (PCP) necessary for mechanotransduction.

212 pon cell division, transmembrane planar cell polarity (PCP) proteins are removed from the cell surfac

213 The core planar cell polarity (PCP) proteins coordinate the orientations of h

214 Core planar cell polarity (PCP) signaling controls OCD and CE in other co

215 Wnt-Frizzled/planar cell polarity (PCP) signaling establishes cell orientation wi

216 regulatory link between Shh and planar cell polarity (PCP) signaling may also occur in other develop

217 Planar cell polarity (PCP) signaling orients developmental events in

218 n flies to coordinate epithelial planar cell polarity (PCP).

219 spectrometry (UHPLC-MS/MS) for low to medium polarity pesticides.

220 ed that delicate balance between entropy and polarity plays an important role in drugs' potency.

221 In turn, polarity predicts the orientation of cellular and tissue

222 boundaries since E11.5, while cell intrinsic polarity protein Galphai3 appeared at E12.5, then polari

223 tion of p120ctn, which allows binding of the polarity protein LGN.

224 al regulator and kinesin ZEN-4/MKLP1 and the polarity protein PAR-6.

225 After NEB, the conserved polarity protein Partner of Inscuteable (Pins) sequentia

226 l interfering RNA screening, we identify the polarity protein Scrib as a downstream effector of Sema4

227 Our findings reveal Moesin as a novel apical polarity protein that drives cortical remodeling of divi

228 rther targets and suppresses PKCzeta, a cell polarity protein that has a pivotal role in directing as

229 During this process, key polarity proteins and receptors are recruited to the sur

230 These findings support a link between apical polarity proteins and renal diseases, especially renal c

231 Thus, we demonstrate a mechanism by which polarity proteins can spatially regulate Rac activity an

232 or-suppressive mechanism, whereby epithelial polarity proteins dictate the cytoarchitecture and fate

233 While it is well known that cell polarity proteins govern the formation of AJCs, the exac

234 Although conserved polarity proteins have been implicated in coordinating c

235 Here, using live imaging of apical polarity proteins in Nematostella embryos, we demonstrat

236 Finally, PAR-6 is necessary to localize polarity proteins such as DLG-1 within adherens junction

237 can alter epithelial polarity by recruiting polarity proteins to the apical membrane, but how a chan

238 ctomyosin network is essential for anchoring polarity proteins to the cell cortex and maintaining cel

239 pected non-cell autonomous role of epidermal polarity proteins, molecular determinants of cytoarchite

240 the utility of this approach by studying PAR polarity proteins, which mediate polarization of many an

241 a membrane, we observed the formation of low-polarity, raft-like nanodomains upon cholesterol additio

242 the extraction of aromatic amines in a wide polarity range (log Kow values from -0.80 to 4.05) from

243 as a common HULIS surrogate shows a similar polarity range, but the sizes are clearly larger than th

244 s to the subcellular partitioning of charged polarity-regulating Rho GTPases like Rho1 or Cdc42 in a

245 ive contribution of each process to neuronal polarity remains unknown.

246 A dramatic example of polarity remodeling occurs in proliferative basal cells

247 ly, microwave conditions and certain solvent polarities result in the formation of a robust covalent

248 he inner ear, the maculae, exhibit a line of polarity reversal (LPR) across which, hair bundles are p

249 stablished at birth along a putative line of polarity reversal (LPR), lateral to the striolar region.

250 r models predicted a dipolar far field and a polarity reversal at the center of the terminal zone.

251 ere radical termination is accomplished by a polarity reversal catalyst.

252 esis of nitrogen-containing heterocycles via polarity reversal of the amide bond.

253 Umpolung (polarity reversal) strategies of aldehydes and imines ha

254 7 ky following the Matuyama-Brunhes magnetic polarity reversal.

255 Here we show that 'reverse-polarity' (RP)-ABPP using clickable, nucleophilic hydraz

256 positions of approximately 10(6) individual polarity-sensing solvatochromic molecules, we reveal com

257 We find that repair is local, polarity sensitive, and prone to template switching, cha

258 Spectral imaging with polarity-sensitive fluorescent probes enables the quanti

259 Here, we test the performance of the polarity-sensitive membrane dyes Di-4-ANEPPDHQ, Di-4-AN(

260 actin organization in determining plant cell polarity, shape and plant growth.

261 asize the regulation and roles of macrophage polarity shift within islets in the context of T2D patho

262 PID, but not D6PK, can also induce PIN1 polarity shifts, seemingly through phosphorylation at S1

263 Our results show how polarity signaling can affect the dynamic turnover of th

264 Fat2/Lar signaling is similar to planar cell polarity signaling in terms of sub-cellular protein loca

265 erstand how Scribble PDZ domains direct cell polarity signaling, we investigated here their interacti

266 echanism, and conclude that microtubules are polarity sorted in the axon by cytoplasmic dynein but th

267 rm on only one of the two MTs, produce large polarity-sorted MT clusters, whereas tetrameric motors,

268 ately restrict microtubule movements so that polarity sorting by cytoplasmic dynein can occur in a ma

269 We present a computational model to test a "polarity sorting" mechanism for microtubule (MT) organiz

270 attention has focused on a mechanism called polarity sorting, in which microtubules of opposite orie

271 synaptic activity was modulated by DCS with polarity-specific effects.

272 econcentration technique, reversed electrode polarity stacking mode (REPSM), was applied for Ag NPs a

273 e limits of detection for analytes with high polarities such as dodecyl trimethylammonium bromide and

274 colloidal stabilization in solvents with low polarity, such as hexane (dielectric constant of about 2

275 hort-term monitoring of compounds varying in polarity, such as UV blockers and biocide compounds in w

276 parison of nucleosomes of different sequence polarities suggest that the strength of the DNA-histone

277 Prospectively, acting on the GABA-polarity switch offers a potential target for 22q11.2 DS

278 smons, and demonstrate wavelength-controlled polarity-switchable photoconductivity.

279 strate, as an example, wavelength-controlled polarity-switchable photoconductivity.

280 No mood polarity switches were observed.

281 nts, and the PCM-dependent induction of cell polarity that defines the anterior-posterior body axis f

282 acellular MRSA due to the molecular size and polarity that limit its cellular uptake.

283 m the basolateral membrane to achieve apical polarity, that Stx3 plays a role in the recruitment of c

284 As a central regulator of cell polarity, the activity of CDC42 GTPase is tightly contro

285 Depending upon solvent polarity, the resulting polymeric network forms either u

286 ic signatures show that they are of negative polarity, transporting net negative charge of 17-23 C t

287 h the Indian lithosphere, forming a reversed-polarity underthrusting.

288 meters that induce BPC consist of a positive polarity ( upward arrow) front pulse followed by the del

289 nable to form an axon and, therefore, neuron polarity was absent.

290 We found here that leukocyte polarity was generated by TIPE2 (TNFAIP8L2), a transfer

291 anges in solvent temperature, viscosity, and polarity, which affect the position and intensity of spe

292 ansition (EMT) and disrupted epithelial cell polarity, which was associated with altered expression o

293 tal assays were used to track and reduce the polarity while closely monitoring the physicochemical pr

294 ns through the continual realignment of cell polarity with the tissue axes.

295 ULIS into 55 fractions of different size and polarity, with estimated ranges of molecular weight and

296 C5a was identified as a regulator of cell polarity, with inhibition of C5a receptors during embryo

297 iggering they exhibit altered morphology and polarity, with reduced effector function compared with C

298 Such a polarity within psychomorphospace, the global versus the

299 or interface and induces charges of opposite polarity within the graphene film modifying its conducti

300 lular complex, the Wnt5a-receptor-actomyosin polarity (WRAMP) structure, which coordinates the polari