ライフサイエンスコーパス: brush

1 ed oral hygiene using a 0.5 mm interproximal brush.

2 composition of the particle core and polymer brush.

3 ursts, the most common of which is the delta brush.

4 s that allow the perception of the slightest brush.

5 ciates with viral load measured in bronchial brushes.

6 local synthesis from surface-immobilized DNA brushes.

7 wo orders of magnitude thicker than standard brushes.

8 sistent field theory for end-grafted polymer brushes.

9 pontaneous hydrolysis is possible in the pCB brushes.

10 over the past years in the field of polymer brushes.

11 uptake by multivalent display of KLA peptide brushes.

12 om combinatorial polymer and block copolymer brushes.

13 ushing habits, and the types of actions post-brushing.

14 could act as absorptive sinks for TCS during brushing.

15 uivalent to 7-12.5 doses of the TCS used per brushing.

16 ectively, in addition to regular twice-daily brushing.

17 ing filled teeth (DMFT) and the frequency of brushing.

18 ofilms for 30 seconds each: (1) rotary nylon brush; (2) Ti brush; (3) water-jet on high and (4) low,

19 seconds each: (1) rotary nylon brush; (2) Ti brush; (3) water-jet on high and (4) low, and compared t

20 The brush allele exhibited quantitative behavior since overe

21 sitivity rates were close between the Cervex-Brush and Cytobrush/spatula for all age groups tested.

22 on associated with conformational changes in brush and matrix chains.

23 ultra-low-fouling molecular structure of the brush and surface charges.

24 esolved strain rate changes across the flame brush and this change is dependent on the level of turbu

25 urface-grafted with poly(acrylic acid) (PAA) brushes and a conducting polymer sensing element with co

26 aracteristics of disordered dendritic bottle brushes and can be adjusted by the walking rate/reaction

27 and microbial metagenome analysis in airway brushes and compared machine-learning classifiers betwee

28 re expression quantitative loci in bronchial brushes and cultured HBECs, but not in lung tissue.

29 w-fouling coatings including homopolymer pCB brushes and OEG-SAMs.

30 n poly(glycidyl methacrylate) (PGMA) polymer brushes and Si wafer surfaces were activated locally usi

31 OT), followed by grafting poly(acrylic acid) brushes and then electrochemically polymerizing a conduc

32 further mitigate biofouling such as bristle brushes and UV lamps.

33 Group 3 served as control with twice daily brushing and further assigned split-mouth to Group 3a-un

34 with two types of architectures, termed as "brush" and "block," were built from positively charged m

35 In one, we treat the EGL as a molecular brush, and in the other, we treat it as a thin elastic l

36 se toothpicks, dental water jet, interdental brush, and/or dental floss (OR, 3.48; 95% CI, 1.30-9.32)

37 g their stress-strain curves in solvent-free brush- and comb-like polymer networks (elastomers).

38 Using EPS analysis, the brush anode resistance ( R(An) = 10.6 +/- 0.5 mOmega m(2

39 lity and size of HA and aggrecan lead to the brush architecture and mechanical properties of this imp

40 Notably, the brush architecture is able to offer significantly greate

41 The brush architecture provides embedded DNA strands with en

42 The development of synthetic polymer brush architectures that suppress adventitious protein a

43 Polymer brushes are defined as thin polymer films in which the i

44 The brushes are easily sculpted into micropatterned landscap

45 Grafted polymer brushes are prone to damage and do not provide sufficien

46 ell as to synthesize linear, bottlebrush and brush-arm star copolymers with degradable segments.

47 emonstrate the utility of nonfouling polymer brushes as a substrate for ultrasensitive and robust dia

48 ect of oral irrigator devices or interdental brushes as adjuncts to toothbrushing associated with den

49 t associated with breastfeeding (e.g., tooth brushing), as can be guided using tools such as direct a

50 cal and physical characterization of polymer brushes, as well as an ever increasing set of computatio

51 specimen types may be used, including swabs, brush, aspirate, and wash, and specimens may be collecte

52 yme with an increase in the number of enzyme-brush attachments.

53 review is therefore to focus on what polymer brush-based solutions can offer and to show how the prac

54 anual brushing/dental flossing + interdental brushes (BDF + Ib; n = 44); 2) manual brushing/dental fl

55 t IF reporters localize below the actin-rich brush border and are highly enriched in the lumen-envelo

56 to continuous FSS also acquired an extensive brush border and basolateral membrane invaginations rese

57 istopathological assessment revealed loss of brush border and lipid vacuolation in the renal cortex o

58 IIA localized to the basal cortex and apical brush border and mediated MHCI internalization from the

59 ositioned at the interface between the stiff brush border and soft cytoplasm suggesting a mechanical

60 ointerstitial nephritis due to antibodies to brush border antigens of the proximal tubule has been de

61 to the apical domain of enterocytes to drive brush border assembly and identifies a point of function

62 tion of CALML4 within enterocytes results in brush border assembly defects that mirror the loss of ot

63 Finally, the acceleration in brush border assembly induced by Arp2/3 inhibition was a

64 Thus, brush border assembly is limited by G-actin availability

65 In a cell culture model of brush border assembly, Arp2/3 inhibition accelerated the

66 tor, to increase G-actin availability during brush border assembly.

67 uired for the scaffold to target and mediate brush border assembly.

68 ted targeting sequence coupled with in vitro brush border binding assays suggests that it functions a

69 To understand brush border formation, we used live cell imaging to vis

70 in, and knockdown of this factor compromised brush border growth in a concentration-dependent manner.

71 Effects on brush border growth were rescued by treatment with the G

72 whereas the Txp group demonstrated only mild brush border injury without apoptosis or necrosis.

73 vacuoles, nuclear count, and proximal tubule brush border integrity, which was validated with immunoh

74 Assembly of the brush border is controlled by the intermicrovillar adhes

75 ly, the treatment strategy prevented tubular brush border loss, diminished tubular iron deposition, b

76 human intestinal biopsies revealed increased brush border membrane (BBM) and decreased cytoplasmic DM

77 The apical brush border membrane (BBM) of intestinal epithelial cel

78 anion transporter 1 (PAT1)] exchange in the brush border membrane (BBM) of villus cells.

79 ed the dynamic translocation of GLUT2 to the brush border membrane of RPTCs, and reduced glucose reab

80 ue, PgCad1 protein occurred primarily on the brush border membrane only in susceptible larvae.

81 ssays of Cry1Ac, Cry2Aa and Cry1Ca to midgut brush border membrane proteins from BPH and PWS.

82 g and oligomerization by western blots using brush border membrane vesicles (BBMV) from a strain of P

83 ence of specific binding sites on the midgut brush border membrane vesicles (BBMV) of both insect spe

84 ority of ASBT (~80%) was S-acylated in ileal brush border membrane vesicles from human organ donors,

85 membranes, including in Aedes aegypti larval brush border membrane vesicles, small unilamellar vesicl

86 significantly impaired intestinal epithelium brush border membrane, junctional polarity, and maturati

87 we have investigated the susceptibility and brush border membrane-binding properties of both species

88 ytes form through invagination of the apical brush border membrane.

89 RC and TfR1 mediate hTf uptake across apical brush border membranes of PTECs and reciprocally respond

90 Brush border microvilli enable functions that are critic

91 ocadherin-based complex found at the tips of brush border microvilli that mediates adhesion between n

92 To gain insight on how CDHR2 contributes to brush border morphogenesis and enterocyte function under

93 and careful examination of tissue, cell, and brush border morphology revealed several perturbations t

94 or actin-bundling protein that assembles the brush border of intestinal and renal epithelial cells.

95 occupies a unique intracellular niche at the brush border of intestinal epithelial cells, where it un

96 lar holo-Tf (hTf) acquisition, to the apical brush border of the PT, with expression gradually declin

97 ession of ACE2 on the small bowel enterocyte brush border supports intestinal infectivity by SARS-CoV

98 e report here that ANKS4B is directed to the brush border using a noncanonical apical targeting seque

99 One defining feature is the brush border, an array of microvilli that serves to ampl

100 fR1 mediates hTf uptake across the PT apical brush border, but in conditions of decreased cellular ir

101 s by beta-MCD jettisoned the D(1) R from the brush border, decreased sodium excretion, and increased

102 ls generate arrays of microvilli, known as a brush border, to enhance functional capacity.

103 nctions and positioned below the microvillar brush border, which suggests a protective intracellular

104 e processing and transporting factors in the brush border.

105 ctin from cortical lateral networks into the brush border.

106 f microvilli, which pack tightly to form the brush border.

107 ve with normal human kidney proximal tubular brush border.

108 collection of apical microvilli known as the brush border.

109 mble their apical microvilli into an ordered brush border.

110 ther, and ultimately clustering to form the "brush border."

111 Enrichment of PLBs with WCRW midgut brush-border membrane material resulted in a 2000-fold r

112 Villin 1, a protein typically found in the brush borders of proximal tubular cells, has been detect

113 gh concentration of actin residing in mature brush borders, we sought to determine whether enterocyte

114 h-matched and assembled into tightly packed "brush borders," which are organized by ~50-nm thread-lik

115 n reminiscent of that observed at PACSIN2 KO brush borders.

116 ctron microscopy have imaged the HA-aggrecan brush but require adsorption to a surface, dramatically

117 The generation of polymer brushes by surface-initiated controlled radical polymeri

118 is more, the ultra-small space between each brush can act as the channels for Li transportation and

119 The micellar brushes can also be grown on ultrathin two-dimensional m

120 ength, and coronal chemistry of the micellar brushes can be precisely tuned, and post-growth decorati

121 strand to an internal position, much smaller brushes can be used to achieve the same level of steric

122 ramic, or metal), and by various operations (brush, cast, dip, spin, or spray).

123 However, at the mossy fiber-to-unipolar brush cell synapse in the cerebellum, AMPAR-mediated EPS

124 nces are most probably initiated by tracheal brush cells (BC).

125 Unipolar brush cells (UBCs) are excitatory granular layer interne

126 rojections to ON and OFF classes of unipolar brush cells (UBCs), which transform single mossy fiber s

127 nocytes, pulmonary neuroendocrine cells, and brush cells and identifies a related population of NREP-

128 , group 4 medulloblastoma resembles unipolar brush cells, and PFA/PFB ependymoma and cerebellar piloc

129 Tuft (or brush) cells are solitary chemosensory cells scattered t

130 magnetic dipole coupling to assemble polymer-brush coated superparamagnetic iron oxide nanoparticles,

131 The brush-coated films of molecules with D(3h) symmetry and

132 ane-modified SiO(2) substrate by the Chinese brush-coating method.

133 ed the antifouling properties of the polymer brush coatings against human blood plasma and were surpr

134 Polymer brush coatings are effective in preventing blood coagula

135 Polymer brush coatings are frequently prepared by radical polyme

136 a powerful new tool to characterize polymer brush coatings.

137 s of mitosis(8), but during mitotic exit the brushes collapse and Ki-67 promotes chromosome clusterin

138 ) was used to evaluate the impact of KM upon brushing comfort.

139 lthy volunteers without lesions and obtained brush cytology specimens and matched scalpel biopsies fr

140 Brush cytology specimens were analyzed by machine learni

141 Most of them brushed daily (82.6%) and had university education (45.7

142 gator (BDF + Oi; n = 36); and 3) only manual brushing/dental flossing (BDF; n = 62).

143 ere categorized into three groups: 1) manual brushing/dental flossing + interdental brushes (BDF + Ib

144 dental brushes (BDF + Ib; n = 44); 2) manual brushing/dental flossing + oral irrigator (BDF + Oi; n =

145 for RP included the following items: manual brushing/dental flossing alone (odds ratio [OR] = 1.94);

146 = 4.10), and the interaction between manual brushing/dental flossing alone and smoking (OR = 6.1).

147 try of the compartment and the 2D pattern of brushes dictating the yield and mode of assembly steps.

148 on monomer composition, polymer height, and brush distribution across the surface.

149 ntisense gene regulation efficiency of these brush-DNA conjugates as a function of their nuclease sta

150 The brushing duration was significantly lower in the PG grou

151 Ki-67 forms repulsive molecular brushes during the early stages of mitosis(8), but durin

152 We collected endobronchial brush (EB) and bronchoalveolar lavage (BAL) samples from

153 of aluminium-incorporated nickel coatings by brush electroplating, focusing on the electroplating set

154 lized synthesis of proteins in a single gene brush enhances their interactions, and displacement of t

155 e multivalent binding to the immobilized GAG brushes ensures firm virus attachment to the interface.

156 ous EEG-fMRI to localise the source of delta brush events in 10 preterm infants aged 32-36 postmenstr

157 It exists in distinct forms, including brush-evoked dynamic and filament-evoked punctate hypers

158 and Lbx1 (VT3(Lbx1) neurons): the mice lost brush-evoked nocifensive responses and conditional place

159 Stabilized brushes exhibit superb resistance to biofilms, yet are l

160 fibroblasts, whereas surfaces altered by Ti brushes exhibited reduced osteoconductivity versus contr

161 ssessing their age, gender, education, tooth brushing, flossing, and tobacco use with a questionnaire

162 rticle as a sensor to understand the polymer brush formation is applicable to investigating the graft

163 G), the three-regime kinetics of the polymer brush formation is confirmed.

164 nsors for unveiling the mechanism of polymer brush formation on surfaces.

165 nal analysis and characterization of polymer brush formation relies on laborious methods that use a q

166 lly been assessed qualitatively and in broad-brush frameworks that imply simplistic macroevolutionary

167 Brushing frequency and probing depths showed little vari

168 e, and Selenomonas abundances increased with brushing frequency per day.

169 istory of chronic maternal illness, maternal brushing frequency, childbearing age, and so on.

170 The resulting polymer-brush-functionalized Janus gold nanoswimmers exhibit eff

171 erial swarming, we report a swarm of polymer-brush-grafted, glucose-oxidase-powered Janus gold nanosw

172 We modeled brush growth kinetics considering bimolecular terminatio

173 olyte macroinitiators and subsequent polymer brush growth using SI-ARGET-ATRP.

174 ect, and the age by which subjects initiated brushing habits, and the types of actions post-brushing.

175 interfacial nanoarchitectonics with polymer brushes has seen growing interest due to its potential t

176 nomena of Maxwell's spot (MS) or Haidinger's brushes (HB).

177 SNPs and expression (lung tissue, bronchial brushes, HBECs) was done using regression modeling.

178 rm provides a dynamic interface with tunable brush heights that extend up to 20 microns - two orders

179 Here we report a technique termed Polymer Brush Hypersurface Photolithography, which produces poly

180 Precise modulation of polymer brush in its thickness and grafting density can cause un

181 as detected at a soft microelectrode, gently brushed in contact mode over the tape.

182 how that the rational integration of polymer brushes in hybrid nanoarchitectures greatly improves the

183 tter than covalently grafted polyelectrolyte brushes in the presence of multivalent ions.

184 quantitative gain-of-function CNGC mutation (brush) in Lotus japonicus resulting in a leaky tetrameri

185 grew a set of biomedically relevant polymer brushes, including poly(oligo(ethylene glycol) methacryl

186 CO2-philic agent, is introduced as a carrier-brush into the GO nanochannels with chemical bonding.

187 Development of the stigma brush involved in pollen capture was compromised in the

188 Tailoring interfaces with polymer brushes is a commonly used strategy to create functional

189 this study, a printing method using natural brushes is adopted as an informative tool to realize dir

190 In bronchial brush isolated AECs, 849 differentially methylated DNA r

191 tterionic amino acid l-cysteines acts like a brush layer to prevent SERS-hotspot blockages and foulin

192 and displacement of their genes in separated brushes leads to step-by-step surface assembly.

193 Ti brushes led to visible streaks on the treated surfaces,

194 The brush-like architecture expands the diameter of the poly

195 molecules (surfactants) containing flexible, brush-like chains.

196 )-based hollow fiber membranes with grafted, brush-like CO2-philic agent alternating between GO layer

197 acteristically have monostratified arrays of brush-like dendritic terminations and respond mostly to

198 The negatively charged, brush-like glycocalyx covers the surface layer of endoth

199 This approach is based on brush-like polymer networks with crystallizable side cha

200 matrix is a robust, hyaluronan-rich polymer brush-like structure that controls access to the cell su

201 of a cationic cartilage-binding domain and a brush-lubricating domain.

202 Both current density and brush material have a significant impact on the morpholo

203 luence of bath load, current density and the brush material used was investigated.

204 ork in a comparison with an existing polymer brush model and confirm the polymer brush model's predic

205 The brush model indicated a larger layer thickness (~350 nm)

206 A polymer brush model of the glycocalyx successfully predicts the

207 polymer brush model and confirm the polymer brush model's predicted linear relationship with proport

208 mined to be 3.0-6.5 kPa (1.5-2.5 kPa for the brush model), with a significant increase in modulus wit

209 The recessive mongenic brush mutation impaired root development and infection b

210 self-assembled structures of multicomponent brush nanoparticles, by using a broad range of analytica

211 polyHIPE foam columns surface-grafted with a brush of polymer containing ion-exchange functionality f

212 ckness, the ability to generate high-density brushes of biopolymers, and the potential for regenerati

213 phiphilic Au-Fe3 O4 NPs grafted with polymer brushes of different hydrophilicity on Au and Fe3 O4 sur

214 study covalently end-grafted, nanometer-thin brushes of poly(N-isopropylacrylamide), a thermoresponsi

215 orption of biomolecules present in saliva by brushes of poly[(N-(2-hydroxypropyl) methacrylamide)-co-

216 e is further combined with ultra-low-fouling brushes of random copolymer carboxybetaine methacrylamid

217 ed poly(2-hydroxyethyl methacrylate) (pHEMA) brushes of well-defined thickness with convenience and e

218 Polymer brushes offer a broad variety of resources to manipulate

219 osterior vagina was swabbed using a cytology brush on PND 0, 2 and 16 and slides were prepared.

220 lves the fabrication of cylindrical micellar brushes on a silicon wafer through seeded growth of crys

221 reagents as microarrays on nanoscale polymer brushes on glass chips, so that all reagents are "on-chi

222 o obtain N3-chain-end-functionalized polymer brushes on the surface, uniquely controlling the N3 cove

223 are prepared through the grafting of polymer brushes onto one side of gold nanoparticles, followed by

224 imens were collected using either the Cervex-Brush or Cytobrush (or Cytobrush/spatula) for comparison

225 of the method of specimen collection (Cervex-Brush or Cytobrush/spatula) for cervical cancer screenin

226 ntities of microbial DNA than did endoscopic brushes or biopsies using quantitative PCR (p<0.0001).

227 rely mostly on grafting hydrophilic polymer brushes or coating hydrogel layers, but these methods su

228 ver the millimeter-scale by simply spinning, brushing or dip coating colloidal nanoink onto a substra

229 Gene expression classifiers based on airway brushes outperformed those using transbronchial biopsies

230 metagene score was increased in CLAD airway brushes (p = .002) and improved prediction of graft fail

231 Polymer brush patterns have a central role in established and em

232 fouling carboxybetaine polymer and copolymer brushes (pCB) as well as conventional carboxy-terminated

233 even in the physisorbed state, zwitterionic brushes perform significantly better than covalently gra

234 were obtained from bronchial and bronchiolar brushing performed under radiological guidance from thes

235 nimalis for 28 days, followed by a 5-day non-brushing period.

236 us a placebo yogurt, followed by a 5-day non-brushing period.

237 luster subunits was required to suppress the brush phenotype.

238 PEGylation of an oligonucleotide using a brush polymer can improve its biopharmaceutical characte

239 We observed that brush polymer formulations utilizing cell penetrating pe

240 from which polypeptides are grown, forming a brush polymer.

241 nction of "depth" toward the backbone of the brush polymer.

242 ly placed along the backbone of the eventual brush polymer.

243 rafting density of pro-apoptotic peptides on brush polymers correlates with increased uptake efficien

244 We focus on synthetic brush polymers of oligonucleotides, oligosaccharides, an

245 ng the chain-end N3, the obtained linear and brush polymers were connected to functional molecules vi

246 The resulting structures are brush polymers wherein a biomolecular graft is positione

247 backbone for the construction of anisotropic brush polymers with monodisperse lengths via grafting-fr

248 enzyme-responsive and pro-apoptotic peptide brush polymers.

249 hrough high-density cell penetrating peptide brush polymers.

250 Additionally, polymer brushes prepared via SI-CRP have been utilized to modify

251 Higher current densities and non-abrasive brushes produce rough, particle-rich samples.

252 Seen in this light, polymer brushes provide a new perspective from which to consider

253 ion of minority-block homopolymer in the dry-brush regime, accompanied by the expected transition fro

254 c to hexagonally packed cylinders in the wet-brush regime.

255 brush resides in a cluster of redundant CNGCs encoding s

256 ydrogen bonds, elucidating their role in the brush's temperature-induced phase separation.

257 most prevalent from bronchoscopic protected brush samples and significantly associated with a low sp

258 fference in the mutational load of bronchial brush samples between former smoking COPD cases and cont

259 Nasal brush samples for RNA sequencing were taken 7 days prior

260 We collected nasal brush samples from 82 nonsmoking participants, including

261 We called somatic mutations in airway brush samples from medium-coverage whole genome sequenci

262 High polyclonality in airway brush samples renders medium-depth sequencing insufficie

263 ssion of MUC5AC mRNA in bronchial epithelial brush samples via proxy SNP rs11602802; (p=2.50 x 10(-5)

264 the majority of taxa detected in biopsy and brush samples, but were enriched for genera from the ora

265 .3% of live cells), BW (32.5%) and bronchial brushing samples (88.9%) correlated significantly (p = 0

266 Moreover, pro-apoptotic polypeptide brushes show enhanced cell uptake over individual peptid

267 ic behavior reveals that the grafted polymer brushes significantly improve the translational diffusio

268 h a published data set from human epithelial brushes (smoker vs. non-smoker) revealed a high degree o

269 a rationally designed semiconducting polymer brush (SPPF).

270 ced 20 individual 2cm x 2cm devices by using brushing, spraying, ironing, and computerized sewing, a

271 where active extrusion of loops controls the brush structure.

272 "Nonfouling" polymer brush surfaces can greatly improve the performance of in

273 stabilization of lipase upon MPCI to polymer brush surfaces resulted from the rigidification of the e

274 This brush technology provides opportunities in a range of ar

275 1.18-9.29), whereas they were less likely to brush teeth after meals.

276 hdrawal-like irritability through the bottle brush test.

277 h as superhydrophobic structures and polymer brushes, the insights tso understand the fundamental phy

278 Unlike polyelectrolyte brushes, the lubrication properties of which diminish dr

279 oral rinse, tongue base, and pharyngeal wall brushes, then tonsil tissue (tonsillectomy).

280 Existing methods are limited in brush thickness, the ability to generate high-density br

281 ltrapure water (GMQ), scaling (SC), titanium brush (TiB), and implantoplasty (IP).

282 l group equivalent, connecting complementary brushes to form well-defined, one-dimensional nanostruct

283 sensory modality extends beyond Haidinger's brushes to the recognition of quantifiable spatial polar

284 ated tick control measures, such as clearing brush, trimming branches, and having a dry barrier betwe

285 A conjugates involving linear, Y-shaped, and brush-type PEG.

286 Recent data indicate that brush-type polymers significantly enhance in vitro and i

287 controlled growth of a wide range of polymer brushes under ambient conditions utilizing either organi

288 l event occurring as the Indian subcontinent brushed up against the western side of Sumatra, and the

289 Here, we report the growth of polymeric brushes using GOx-assisted atom transfer radical polymer

290 ultra-thick regenerating hyaluronan polymer brushes using hyaluronan synthase.

291 n, a nanoscale poly(dimethylsiloxane) (PDMS) brush was employed to use as a controllable material for

292 IL1RL1 gene expression in bronchial brushes was not different between health and disease.

293 WJ and Nylon brush were most effective in reducing CFU counts (P < 0.

294 succession of DNA/chromatin loops-a polymer "brush"-where active extrusion of loops controls the brus

295 were left and right posterior-temporal delta brushes which were associated in the left hemisphere wit

296 is self-assembled from a amphiphilic polymer brush, which comprises a light-responsive photodynamic b

297 m fluoride (control), and were instructed to brush with the assigned toothpaste twice/day for 2 years

298 Li growth can be achieved on PNIPAM polymer brushes with lithiophilic functional groups modified Cu

299 After simulated 3-month brushing with a commercial best-selling TCS-TP, over one

300 accumulate substantial amounts of TCS after brushing with TCS-formulated toothpastes (TCS-TPs).