ライフサイエンスコーパス: wall

1 are surrounded by a peptidoglycan (PG) cell wall.

2 lls (SMCs) in the medial layer of the aortic wall.

3 all enzymes cooperate to build a mature cell wall.

4 esis of flavonoid, phenylpropanoids and cell wall.

5 ascular bundles, the rectum, and the bladder wall.

6 may contribute to remodelling of the airway wall.

7 s and lipopolysaccharides linked to the cell wall.

8 adhesion and controlling the porosity of the wall.

9 hile inducing an attractive force toward the wall.

10 immune cells resident in the intimal aortic wall.

11 s and guiding leukocytes across the vascular wall.

12 he accumulation of macrophages in the vessel wall.

13 a total intramural ruptur of the esophageal wall.

14 core structural motif of the bacterial cell wall.

15 the PCSK6 role in normal and diseased vessel wall.

16 ins is their outermost compartment, the cell wall.

17 en and intramural thrombus that thickens the wall.

18 rce of the measured anisotropy in the vessel wall.

19 sulfonic-acid (TNBS) solution into the ileal wall.

20 existing phenomenology of functional domain walls.

21 lulose and epicuticular wax crystals in cell walls.

22 isting of microfibrils in plant primary cell walls.

23 can play distinct roles in legume root cell walls.

24 etric scale concentrated in the papyrus cell walls.

25 n afforded the control of the number of BNNT walls.

26 us friction between the cell and the channel walls.

27 tify the determinants that define grass cell walls.

28 s and deprotonated silanol sites on the pore walls.

29 d magnetically hard [Formula: see text] cell walls.

30 th reduces analysis time while the ultrathin wall (15 mum) efficiently dissipates heat from the separ

31 ith the highest effective doses were bladder wall (2.41E-03 mSv/MBq), followed by ovaries (1.15E-03 m

32 tems to transport proteins across their cell wall, a process that plays an important role during host

33 Regional wall abnormalities were defined by experienced physiolog

34 roxynaphthalene-melanin in the conidial cell wall amplified the epithelial transmigration of neutroph

35 Cell wall analyses of inflorescence stems revealed changes in

36 These genes included cell wall-anchored adhesins (ebh, sdrD), polysaccharide and c

37 This process is facilitated by cell wall-anchored adhesins that bind to host ligands.

38 atherogenic gene expression in the arterial wall and aortic sinus induced by severe periodontitis.

39 tofluorescent particles in the pial arterial wall and in neocortical parenchyma of young, drug-resist

40 in pigments that are deposited into the cell wall and interfere with the host immune response.

41 Ultrasound can be used to evaluate the bowel wall and the elements that surround it without the need

42 , used to promote the swelling of algae cell wall and the formation of a large oil - ethanol interpha

43 bot's axisymmetric axis perpendicular to the wall and then propels it laterally at very high speeds (

44 gs only showed hyaluronan in intact alveolar walls and perivascular tissue.

45 t cellulose-xyloglucan bonding in plant cell walls and showed that CXE and MXE action was up to 15% a

46 l composition and structure of both the cell walls and the phytolith structures.

47 non-cutinized domains of the outer epidermal wall, and affects cell size.

48 o NO stress by strengthening the fungal cell wall, and by causing over-accumulation of methylglyoxal

49 calcification and ossification of the aortic wall, and inflammation, resulting in aneurysm developmen

50 ese PRPs are absent from root epidermal cell walls, and PRP accumulation is highly localized within t

51 by pathway location for right and left free wall AP.

52 ws that PrgA protrudes far out from the cell wall (approximately 40 nm), where it presents a protease

53 We propose a model of sorghum cell wall architecture which is dominated by interactions bet

54 is mutant also displayed defects of the cell wall architecture, suggesting GPI7 is required for cell

55 Cells in vascular walls are exposed to blood pressure variability (BPV)-in

56 hes where plant and/or algal cellulosic cell walls are present.

57 methane is observed coating crater rims and walls as well as mountain tops, providing spectacular re

58 Cell wall assembly requires harmonized deposition of cellulos

59 During cell wall assembly, a lipid-linked disaccharide-peptide precu

60 Ps) are a diverse group of cell surface- and wall-associated glycoproteins.

61 indsii, including disease resistance-related wall-associated kinase (WAK), Catharanthus roseus recept

62 Plant cell wall-associated polygalacturonase-inhibiting proteins (P

63 1 in yeast and Adh2 in hyphae among the cell wall-associated proteins.

64 harbors a large family of more than 20 cell wall-attached epithelial adhesins (Epas).

65 ration at the roots aided by apoplastic cell wall barriers to thrive in saline conditions.

66 e 3; size, >= 5 cm) of an extremity or trunk wall, belonging to one of the following five histologic

67 ins from anaerobic origin or those with cell wall binding profiles.

68 lopment of new antibiotics that disrupt cell wall biogenesis, a process essential to the survival of

69 ecture, suggesting GPI7 is required for cell wall biogenesis.

70 proteins, the cornerstone to bacterial cell wall biosynthesis and division.

71 ding of the pathways that contribute to cell wall biosynthesis and how these pathways are regulated b

72 The regulatory aspects of cell wall biosynthesis are largely overlapping with those of

73 entins leads to inhibition of bacterial cell wall biosynthesis by disassembly of key divisome protein

74 UT1 downstream target genes function in cell wall biosynthesis, apoptosis, and maintenance of xylem c

75 in patients with bone, lymph node, and chest wall/breast/skin metastases at baseline was observed.

76 ith bone, liver, lung, lymph node, and chest wall/breast/skin metastases.

77 common-flow configuration with gas-permeable walls, but in the absence of any installed source of gas

78 medial properties and function of the aortic wall by enhanced proteolytic and phagocytic activity; ho

79 expelled from single vesicles onto an inner-wall carbon surface, where the duration of transmitter r

80 ique for immobilizing nIR-fluorescent single-walled carbon nanotube (SWCNT) sensors on seven differen

81 article passing through a defect in a single-walled carbon nanotube one-by-one has been achieved with

82 on of laccase from white rot fungus on multi-walled carbon nanotube surface modified with a naphthale

83 Pyrene carboxylic acid-modified single-walled carbon nanotubes (PCA/SWNTs) were deposited by qu

84 low-dimensional nanocarbons including single-walled carbon nanotubes (SWCNTs) and nanographene (NG),

85 Among emerging electronic materials, single-walled carbon nanotubes (SWCNTs) are promising candidate

86 Single-walled carbon nanotubes (SWCNTs) can be doped with potas

87 Single-walled carbon nanotubes (SWCNTs) in particular have exhi

88 bdenum disulfide (MoS(2)) crystals on single-walled carbon nanotubes (SWCNTs).

89 vantages of carbon nanomaterials like single-walled carbon nanotubes (SWNTs) in a field-effect transi

90 of oxidoreductase enzymes enabled by single walled carbon nanotubes and colloidal clays, ii) the mol

91 Here, we have employed single-walled carbon nanotubes as test tubes, and an 'atomic in

92 rophage-specific nanotherapy based on single-walled carbon nanotubes loaded with a chemical inhibitor

93 This is the lowest among the single-walled carbon nanotubes reported from artefacts so far a

94 rption of laser light by a cluster of single walled carbon nanotubes, with no requirement for a treat

95 arbon and subsequently, unconventional multi-walled carbon nanotubes.

96 Primary cell wall cellulose is synthesized by the cellulose synthase

97 tic microorganisms that have structural cell wall cellulose, suggesting expansins evolved in ancient

98 sed more than 150,000 CPU hours and weeks of wall-clock time.

99 olten lithium carbonate electrolyte, thicker walled CNTs (100-160 nm diameter) are synthesized during

100 ntration of phosphates at the bacterial cell wall compared to other bacteria, revealing the great pot

101 Cellulose is an essential plant cell wall component and represents the most abundant biopolym

102 m recognizes chitin as one of the major cell-wall components of invading fungi, but C. neoformans can

103 the interactions of LL-37 and bacterial cell wall components we crystallized LL-37 in the presence of

104 siderable interest in engineering plant cell wall components, particularly lignin, to improve forage

105 rains containing deletions of genes for cell wall components, we identified that deletion of the hydr

106 Fruit firmness, cell wall composition and enzyme activity of three apricot fl

107 ical cell wall morphology and secondary cell wall composition are suggested to contribute to the obse

108 Cell wall composition was analysed by glycome profiling assay

109 ed pyelonephritis but whether bacterial cell wall constituents inhibit HCO(3) transport in the outer

110 However, cell walls contain fractions of varying solubilities, and a f

111 e sporadically presented with an obstructing wall containing a gap that varied in width.

112 Using nanoimaging, we show that the cell wall contains pectin nanofilaments that possess an intri

113 Bacteria with these non-canonical cell-wall cross-links achieve a high optical density in cultu

114 ated a bacterium where up to 31% of the cell-wall cross-links are formed by a non-enzymatic reaction

115 Shown here is that the cold-wall CVD system is capable of suppressing the gas-phase

116 However, in the conventional hot-wall CVD system, CVD-derived graphene films suffer from

117 the turnover chemistry of Pgp3 reveals cell wall D,D-endopeptidase and D,D-carboxypeptidase activiti

118 We observed cell wall damage induced by bedaquiline and moxifloxacin thro

119 es, metabolism of simple sugars, fungal cell wall deconstruction, biofilm formation, antimicrobials b

120 enes, which may reflect the substantial cell wall defects in the psd1Delta/Delta psd2Delta/Delta muta

121 ns ascribed to QseBC may originate from cell wall defects.

122 responses, including callose-associated cell wall defenses that are under control by abscisic acid (A

123 Many bacteria can form wall-deficient variants, or L-forms, that divide by a si

124 icrometric kerogenous lamellae, plastic tube-wall deformation, and tube-wall delamination.

125 lae, plastic tube-wall deformation, and tube-wall delamination.

126 GTPases that regulate polarity and patterned wall deposition in plants.

127 n organization, vesicle trafficking and cell wall deposition, bearing consequences in pollen-stigma i

128 During distinct modes of polarized cell wall deposition, such as in the tip growth that occurs d

129 transportation (e.g., PIN-FORMED1) and cell wall development (i.e., CELLULOSE SYNTHASE1) and expansi

130 diameter z-score, left ventricular posterior wall diameter z score, left atrial diameter z score, pea

131 ed in the fluorescent platelet signal at the wall due to the increase of stiffened RBCs in flow, sugg

132 The understanding of the domain wall (DW) dynamics along magnetic nanowires is crucial f

133 Here, we examine cell wall elasticity to understand how it contributes to the

134 epen our understanding of how bacterial cell wall enzymes cooperate to build a mature cell wall.

135 rtance of the other seemingly redundant cell wall enzymes.

136 owth involves a complex interplay among cell-wall expansion, biosynthesis, and, in specific tissues,

137 Grasses have numerous cell wall features that are distinct from eudicots and other

138 xes of globular starch granules-protein-cell wall fiber formed at HHP <= 450 MPa.

139 that long arabinan side-chains maintain cell wall flexibility in water deficit.

140 ynamics simulations of low-altitude and near-wall flights based on in vivo high-speed kinematic measu

141 s in the vicinity of the active hot and cold walls for all cases considered here.

142 nin biosynthesis genes during secondary cell wall formation in P. deltoides.

143 and plants resemble the reversibly swellable walls found in various algae, suggesting that they may f

144 eleterious impact on recovery of the vaginal wall from pregnancy.

145 iosynthesis is tightly coordinated with cell wall growth and turnover, and many of these control acti

146 In arthropods, the body wall has served as a repeated source of morphological no

147 Grass cell walls have hydroxycinnamic acids attached to arabinosyl

148 chicks failed to spontaneously use a striped wall in a square arena, rats showed a modest influence o

149 MMP-2 and MMP-9 expression within the aortic wall in doxycycline-treated MFS mice.

150 s an interlinked network of polarized domain walls in a non-polar background matrix.

151 of hyperinflammation induced by fungal cell walls in CGD are still incompletely defined.

152 Nacreous walls in land plants resemble the reversibly swellable w

153 overall increase in secondary versus primary walls in mutants, indicative of higher xylem production

154 Ferroelectric domain walls in single-crystal complex oxide thin films are fou

155 he inner cell walls, not the outer epidermal wall, in guiding organ flattening of organ primordia.

156 We analyze the ferroelectric domain-wall induced negative capacitance (NC) effect in Metal-F

157 ation in cDCs is necessary to control vessel wall inflammation.

158 s functions when hardened, for example, cell walls, insect scales, and diatom tests.

159 plays an important role in maintaining cell wall integrity of xylem vessels, physiological and molec

160 showed that heating disrupted the bean cell wall integrity, protein matrix and starch granules more

161 As this pathway is critical for fungal cell wall integrity, the hexosamine biosynthesis enzymes repr

162 els in aneurysm patients with altered aortic wall integrity.

163 ogical parameters examined included aneurysm wall irregularity, presence of a daughter dome, presence

164 The formation of pollen wall is a complex but well-regulated process, which invo

165 In flowering plants, pollen wall is a specialized extracellular cell-wall matrix sur

166 ade of leukocyte interaction with the vessel wall is being studied to reduce the inflammation that co

167 the nostril sulcus representing the lateral wall is funnel-like.

168 iny in vivo and ex vivo revealed that the 3V wall is not static and is amenable to cell movements.

169 The cell wall is the primary interface between plant cells and th

170 Abnormal HA accumulation within blood vessel walls is associated with tissue inflammation and is prom

171 inorganic ions, within secondary plant cell walls is central to many biomass applications.

172 ion of solutes from the brain along arterial walls is driven by low-frequency arteriolar oscillations

173 nt of arthropod exoskeletons and fungal cell walls, is endogenously produced by fishes and amphibians

174 icle but are covered with a pectin-rich cell wall layer.

175 ing through loblolly pine (Pinus taeda) cell wall layers under 70%, 75%, or 80% relative humidity (RH

176 y in turn causes the destruction of alveolar walls leading to emphysema, making it potentially a vali

177 cks for synthesis of the cellulose-rich cyst wall, leading to subversion of amoeba encystation.

178 umber and enhancement of intracranial vessel wall lesions at 7-T MRI in individuals evaluated after i

179 Contrast material-enhancing vessel wall lesions were associated only with increasing age (R

180 und between smoking and the number of vessel wall lesions.

181 communities are associated with the caldera wall, likely shaped by two different types of hydrotherm

182 iments do mitigate some effects of gas-phase wall losses after long (>2 days) experiment run times, b

183 requires the activities of a family of cell-wall lytic enzymes called resuscitation-promoting factor

184 mercial MOS is being derived from yeast cell wall mannan and is widely used as prebiotic in feed supp

185 DE(4-7) prepared by adding gum Arabic to the wall material at a ratio of 8:2.

186 dified starch (WPI:Capsul(R)) as emulsifiers/wall materials.

187 len wall is a specialized extracellular cell-wall matrix surrounding male gametophytes and acts as a

188 ion responses through modulation of its cell wall mechanical properties.

189 al localized intracellularly and at the cell wall-membrane interface, implying the presence of reduci

190 l wall metabolite measurement implicate cell wall metabolism/integrity in betaCA3-mediated basal immu

191 Global transcriptome analysis and cell wall metabolite measurement implicate cell wall metaboli

192 ys reveal that RALF4 binds LLGs and LRX cell-wall modules with drastically different binding affiniti

193 thway is the export of the lipid-linked cell wall monomer, Lipid II, by its transporter MurJ.

194 Changes in cortical cell wall morphology and secondary cell wall composition are

195 The final model recognized regional wall motion abnormalities in the cross-validation and ex

196 performance in A1 compared with A2 and less wall motion abnormalities in the jeopardized myocardium

197 orks to automate the recognition of regional wall motion abnormalities using temporal and spatial inf

198 abnormalities that included left ventricular wall motion abnormalities, global left ventricular dysfu

199 anges associated with hypokinetic myocardial wall motion and microvascular obstruction, demonstrating

200 ts map the spatial transition between domain wall motion and the dynamics of a uniform magnetic domai

201 A tag results in normal organization of body wall muscle, but approximately half the normal levels of

202 by mechanical feedback within the inner cell walls, not the outer epidermal wall, in guiding organ fl

203 cing non-canonical cross-links into the cell wall of Escherichia coli, we generated a bacterium where

204 ral virulence lipids populate the outer cell wall of pathogenic mycobacteria.

205 The RT-PCR did not detect viral RNA in the wall of small intestine, appendix, gallbladder, bile, li

206 tation, and effacement of HA from the vessel wall of small pulmonary arteries.

207 lly-polarized motile cilia along the ventral wall of the central canal.

208 nction mutation, CaM-M37Q, into the anterior wall of the left ventricle of RyR2 wild type or mutant m

209 oted by SvBAHD05 acyltransferase in the cell wall of the model grass S. viridis.

210 f the nostril sulcus representing the medial wall of the nostril is rectangular, whereas the side of

211 the feces of 3 patients and in the duodenal wall of the patient with perforated peptic ulcer, real t

212 ce of CD8+CD161+ lymphocytes in the arterial wall of two unruptured intracranial aneurysms.

213 upture and were identified in the aneurysmal wall of unruptured brain aneurysms.

214 accumulation is highly localized within the walls of root cortical and vascular tissues.

215 ple foci of ectopic calcification within the walls of the great vessels.

216 l cells that line the bottom and the lateral walls of the third ventricle.

217 ed to create monoliths bound directly to the walls of the titanium channels.

218 iopolymer found mainly in the secondary cell walls of vascular plants, where it contributes to mechan

219 No injury was found on the bladder wall or intervening tissue.

220 of domains, topological properties of domain walls or their thermal mobility.

221 Thus, the plant cell wall, outside of the cell itself, is an active participa

222 Native yeast and yeast cell wall particles (YCWPs) were used as model cell-based car

223 idges that are cross-linked between adjacent wall peptides by penicillin-binding proteins to confer r

224 AmpDh3 hydrolyzes the cell wall peptidoglycan of the prey bacterium, which leads to

225 ssess enzymes that modify the essential cell-wall polymer peptidoglycan by O-acetylation.

226 hat do not directly reflect cereal root cell wall polysaccharide structures.

227 ng plant cytokinesis, newly synthesized cell wall polysaccharides are deposited in a restricted regio

228 exudate polysaccharides, distinct from cell wall polysaccharides, are adhesive factors secreted by r

229 on the ability to synthesize and modify cell wall polysaccharides.

230 tion peg emerging from the unmelanized, thin-walled pore at the appressorial base(1-4), forcing it th

231 oliths) to silicified and nonsilicified cell walls prepared as a flat block of epoxy-embedded awns of

232 We also show that sorghum secondary cell walls present a high ratio of amorphous to crystalline c

233 surface, thrombus and lumen volumes, maximal wall pressure, and wall shear stress [WSS]) to identify

234 envisioned as models of secondary plant cell walls prior to lignification.

235 that an as-yet-unidentified nonsecreted cell wall protein is required to promote the early epithelial

236 host tissue is mediated by GPI-anchored cell wall proteins (GPI-CWPs); the corresponding genes contai

237 Secondary cell walls provide a physical barrier that protects plants fr

238 bacterial viability; the peptidoglycan cell wall provides shape and osmotic protection to the cell,

239 ribution of calcium particularly in the cell walls, providing support for the "phytase-phytate-pectin

240 The plaque-to-healthy vessel wall ratio of (68)Ga-FOL was significantly higher than t

241 ZHD14 as effective targets for reducing cell wall recalcitrance and improving the enzymatic degradati

242 saccharide and capsule synthesis genes, cell wall remodeling genes (lytN, ddh), the urease operon, ge

243 of LEA and ELIP genes, and evidence of cell wall remodeling.

244 way to regulate brain entry through vascular wall remodeling.

245 Their thick, chitin-reinforced cell walls render cell lysis difficult, complicating their an

246 ther wings are a novel structure on the body wall resulting from gene co-option, or evolved from an e

247 tion receptors TLR7 and TLR9 in the vascular wall, resulting in profound vascular dysfunction.

248 is, and, in specific tissues, secondary cell wall (SCW) deposition, yet the coordination of these pro

249 To envisage potential applications, cell wall sequential extraction performed on dry plant yielde

250 nd lumen volumes, maximal wall pressure, and wall shear stress [WSS]) to identify relevant parameters

251 lusion Combined analysis of lumen volume and wall shear stress was associated with enlargement of abd

252 ble, it is rather limited in turgid and cell wall-shielded plant cells.

253 The assay incorporates both cell wall softening and hypo-osmotic treatment to induce cell

254 ystolic excursion and right ventricular free wall strain).

255 ut climate change in The New York Times, The Wall Street Journal, and USA Today from 1985 to 2014 (n

256 : see text] Intermittent fluctuations in the wall stress, a blueprint of turbulence in the vicinity o

257 a), which variously lead to increased aortic wall stress.

258 d cTnI, suggesting improvement in myocardial wall stress.

259 ng both the inner (blood flow) lumen and the wall structure of the aortic aneurysm from CT angiograms

260 lected as potential regulators of xylem cell wall structure.

261 integration of functional devices into thin-walled structures while preserving the structural charac

262 In this study, we provide a wall-to-wall subnational map of the origin and supply chain of B

263 tible) using metabolomics profiling and cell wall sugar characterization at different developmental s

264 ogether with an accumulation of crushed cell walls suggests that the EAS is a dynamic zone from which

265 mega-electron volts, cold ions in the inner wall surface implode towards the central axis.

266 DEGs and pathways involved in secondary cell wall synthesis and regulation of the chemical compositio

267 a valuable experimental system to study cell wall synthesis in plants, but our understanding of the g

268 nal regulation of genes responsible for cell wall synthesis, which contributes to fibre length by mod

269 er at specific sites that coincide with cell wall synthesis, while the secretion of SlpA from the cel

270 from rapid cell elongation to secondary cell wall synthesis.

271 The cell-wall-synthesis machinery responsible for rod shape in Es

272 omplexes of membrane proteins including cell-wall synthetic proteins.

273 reased troponin was high basal inferolateral wall T2 (odds ratio, 18.2 [95% CI, 3.7-90.9], P<0.0001).

274 inor polysaccharide components of plant cell walls that are particularly difficult to assign by NMR c

275 conductance of the neighboring microchannel walls (the so-called surface shunt).

276 effect originating from the conjugated inner wall, the POF material (aperture size 2.4 nm) concentrat

277 r the observed diversity of pollen and spore walls, the processes involved remained obscure until the

278 Bronchial wall thickening at CT histologically corresponded with a

279 around forming pits and under secondary cell wall thickenings in metaxylem cells.

280 atal densities (SD(aba) ) and mesophyll cell wall thickness (T(CW) ).

281 Left ventricular (LV) wall thickness and LV mass were greater in men (P<0.001)

282 is, apoptosis, and maintenance of xylem cell wall thickness and strength.

283 er asthma severity and was related to airway wall thickness and ventilation defects.

284 Cell lumen diameter and cell wall thickness in the pre-scarring fossilized wood show

285 Maximum left ventricular wall thickness was 18 +/- 8 mm, and left ventricular eje

286 The maximum left ventricular wall thickness was 22.9 +/- 8.7 mm and left ventricular

287 ventricular diameter as right ventricle free wall thickness was increased and an increase in tricuspi

288 ure, lung aeration measured via CT, alveolar wall thickness, cell infiltration, and surfactant protei

289 As a result, LV end-diastolic wall thickness-to-chamber radius (h/R) ratio increased,

290 n length, 3.6 mm outer diameter, and 200 mum wall thickness.

291 alization of directional cues across venular walls, thus causing neutrophils engaged in diapedesis to

292 In this study, we provide a wall-to-wall subnational map of the origin and supply ch

293 We categorized surgeries as abdominal wall, vascular, abdominal, cardiac, chest, or orthopedic

294 e weak correlations between risk and carotid wall volume (Kendall tau = 0.29), noncalcified plaque (t

295 introduced for burst abdomen: The abdominal wall was closed using a slowly absorbable running suture

296 e patient study, the thickness of myocardium wall was reduced on average by 21%.

297 Secondary walls were affected also in the interfascicular fibers,

298 compared with the wild type (since secondary walls were thinner).

299 hout causing any apparent damage to the cell walls when viewed by microscopy.

300 s caused by the interaction with the channel wall, which slows down the permeation by several orders