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1 ar and compact components of the ventricular wall.
2 cting the rheological properties of the cell wall.
3 hereas VSMC proliferation repairs the vessel wall.
4 s how the genetic circuitry affects the cell wall.
5 can (PG), the coat woven into bacterial cell wall.
6 o the zeta potential of the particle and the wall.
7 nd regulates the inward growth of the septal wall.
8 through the entire depth of an intact aortic wall.
9 4 expression in the atherosclerotic arterial wall.
10 d from A. fumigatus conidia and mycelia cell wall.
11 reference material would reach the intestine wall.
12 tissues, and PRX17 was localized to the cell wall.
13 nation revealed laxity of the left abdominal wall.
14 the septum (decrease) and lateral (increase) wall.
15 f leukocyte-derived foam cells in the artery wall.
16  membrane that is surrounded by a thick cell wall.
17 rystalline form of sirolimus into the vessel wall.
18 (nNOS) in nerve fibers of the murine vaginal wall.
19 s one of the main constituents of plant cell walls.
20 ting states at the center or edges of domain walls.
21 f biofuels is the modification of plant cell walls.
22  absent in/on all organically preserved cell walls.
23 r cells tether, roll, and adhere to vascular walls.
24 nto odontoblast-like cells near the dentinal walls.
25 structural integrity of secondary plant cell walls.
26 ted 7 A micropores, and ever most polar pore walls.
27 ccount for organic vapor loss to the chamber walls.
28  immature permanent teeth with thin dentinal walls.
29 nt cellulose-based composites and apple cell walls.
30 he complex carbohydrates found in plant cell walls.
31 y negligible toxic effect on arterial vessel walls.
32 ve of higher elasticity) than companion cell walls.
33 or optimal attack of alginate in intact cell walls.
34 el-Bloch-like character to the bubble domain walls.
35 nerated by a network of ferroelectric domain walls.
36 ng that utilization of yeast and fungal cell wall 1,6-beta-glucans is a widespread adaptation within
37 and vascular healing profile of a novel thin-walled (115 microm) sirolimus-eluting ultrahigh molecula
38 -nicotine injection were the urinary bladder wall (14.68 +/- 8.70 muSv/MBq), kidneys (9.56 +/- 2.46 m
39 t of nonencapsulated strains: increased cell wall accessibility, increased nonspecific opsonophagocyt
40  the commonalities in the composition of the wall across the fungal kingdom, addresses how little is
41 nts with recent STEMI exhibited increased LV wall active tension when normalized by SBP.
42 tment of platelets to the inferior vena cava wall after DVT induction were reduced in MC-deficient mi
43 in well-defined train of polarization domain walls allows undistorted propagation of polarization kno
44 ortices that form cross-tie walls and vortex walls along intersecting planes.
45  the plastic and elastic compliances of cell walls along the elongation zone, but plots of growth rat
46 ation of infection structures requiring cell wall alterations.
47 d that DNMT1-specific inhibition in arterial wall ameliorates the disturbed flow-induced atherosclero
48 phylococcus aureus expresses a panel of cell wall-anchored adhesins, including proteins belonging to
49  a highly conserved sortase A-dependent cell wall-anchored C terminus, whereas the surface-exposed N
50 computed tomography (PET/CT) of the arterial wall and a migratory phenotype of monocytes.
51   Cellulose is a major component of the cell wall and cellulose synthesis is pivotal to plant cell gr
52 bundant components of the multilaminate cell wall and essential virulence factors in pathogenic speci
53           Given the small size of the vessel wall and its proximity with blood, molecular imaging of
54 ntent could be projected through the uterine wall and perceived by the fetus, dependent on how light
55  and sage polyphenols in stabilising capsule wall and protecting fish oil encapsulates from heat indu
56 actions of 3.33 Gy over 11 days to the chest wall and the draining regional lymph nodes, followed by
57 ns are small proteins that loosen plant cell walls and cellulosic materials without lytic activity.
58 antification of ions in lignocellulosic cell walls and fungal hyphae during decay is not known.
59 onstructions were also acquired of wood cell walls and hyphae with ECM.
60 aOH steeping produced micropores in the cell walls and light microscopy revealed that NaOH steeping i
61  addition, solute segregation along cellular walls and low-angle grain boundaries can enhance disloca
62 eractions between polyphenols and plant cell walls and show that although polyphenols are associated
63 ortices and antivortices that form cross-tie walls and vortex walls along intersecting planes.
64 f defects with other defects (such as domain walls) and with the lattice.
65 y provide a better understanding of the cell wall architecture but also is vital for devising optimum
66 le LNs and, to a lesser degree, the arterial wall are inflamed in HIV, inflammation in these tissues
67                       Moreover, since domain walls are generally writable, erasable and mobile, they
68 diation dose estimates indicated the bladder wall as the dose-critical tissue (185 muSv/MBq), followe
69 r SOA mass yields due to losses of vapors to walls as a function of species volatility and particle c
70 TAG or impaired of TAG hydrolysis show spore wall assembly defects, supporting a role for TAG and/or
71 nal networks and/or modifying the plant cell wall, AvrHah1 may promote water uptake to enhance tissue
72 uch biochemical wall heterogeneities precede wall bending.
73 ungal caspofungin inhibits synthesis of cell wall beta-1,3-glucan and is used for prophylactic therap
74 s deposited in the middle of anticlinal cell walls between endodermal cells and fill the gap between
75 tative reference profile for miscanthus cell wall biomass.
76  on rates of cellulose biosynthesis and cell wall biomechanics.
77 the glycans, to study processes such as cell wall biosynthesis, polysaccharide deposition, protein-ca
78 st popular candidate materials for the first wall/blanket applications in fusion reactor.
79 tilized by S. aureus to block bacterial cell wall breakdown, limits the induction of pro-inflammatory
80  of the debate surrounding the motive of the wall-builders.
81 ureus was mediated by components of its cell wall, but was not due to peptidoglycan-induced IL-10 pro
82                      In contrast, the domain wall can be pushed to move in a direction with reduced a
83 Cellulose, the major component of plant cell walls, can be converted to bioethanol and is thus highly
84 te domains for high-affinity binding to cell wall carbohydrates and cleavage activity.
85       Addressed herein, functionalized multi-walled carbon nanotube (MWCNT) supported highly monodisp
86 ife cycle inventory was developed for single walled carbon nanotube (SWCNT) PV cells, including a lab
87 ased on asymmetric chemical doping of single-walled carbon nanotube (SWNT) papers is presented.
88          Composed of a semiconducting single-walled carbon nanotube nested in a charged, impermeable
89 rbon nanotube (SENT) via the growth of multi walled carbon nanotubes (MWNTs) onto a quartz substrate.
90 plate Cu nanoclusters (CuNCs@BSA) and single-walled carbon nanotubes (SWCNT) was synthesized to fabri
91                                       Single-walled carbon nanotubes (SWCNTs) have been incorporated
92                                       Single-walled carbon nanotubes (SWNTs) offer unique electrical
93 87-117 degrees C for 1.05 and 1.06 nm single-walled carbon nanotubes, respectively.
94 allowed to bind to xyloglucan-depleted onion walls, CBM76 labelling gave positive evidence for xylogl
95 meter is central to expansive growth rate of walled cells.
96 vel approach to the identification of aortic wall cellular inflammation in patients with abdominal ao
97 is of well-defined regions of secondary cell wall CESA proteins, with the aim of defining what distin
98 gation zone, but plots of growth rate versus wall compliances were strikingly nonlinear.
99 K-1 - DAF-16 signaling pathway, and the cell wall component of BB68 contributed to longevity.
100 d lipopolysaccharide (LPS), a bacterial cell wall component that induces inflammation, exert appetite
101                                         Cell wall components are altered in transgenic plants.
102  of fibrillar cellulosic structures and cell wall composites during or after the polymerization proce
103 n of a large number of genes related to cell wall composition and metabolism, as well as those encodi
104                                     The cell wall composition and metabolome of ccr1 ProSNBE:CCR1 sti
105 nce of proper apical membrane lipid and cell wall composition is further supported by its functional
106 re changed in response to genotype, and cell wall composition was largely unaffected.
107 me relative humidity (RH = 70%) and state of wall conditioning.
108  in chip-based devices using magnetic domain wall conduits.
109 a (-/-) APC and CD4(+) T cells in the aortic wall contribute to T cells re-activation and pro-atherog
110  for example, creating and moving conducting walls could make or break electrical connections in new
111           Patients with unilateral abdominal wall deficiency, unilateral undescended testis and femal
112  fluid properties, in the life cycle of cell wall-deficient L-form bacteria.
113 ts suggest that the maize zygote starts cell wall deposition within 30 seconds after fusion with a sp
114  functions such as xylan metabolism and cell wall development.
115 tin and glucan synthase activity during cell wall differentiation and fungal hydrophobin function.
116 l epitopes and treatment of tissue with cell wall digesting enzymes, coupled with bioassay of guard c
117 main determinant of earlywood density, while wall dimensions become more influential for latewood den
118       The contributions of tracheid size and wall dimensions to density were disentangled with sensit
119 nter setting between 2009 and 2012 for chest wall disease that had recurred.
120 ygen vacancies is confined within the domain wall, displaying discrete quantum-well energy levels.
121 ng the Navier-Stokes equations in the moving wall domain with our validated flow solver.
122 winding of the helical structure at the grid walls drives the lens shape.
123                Nanoscale changes to the cell wall during unmasking were explored in live cells with a
124              We report bi-directional domain wall (DW) motion along and against current flow directio
125 esent phase co-existence separated by domain walls (DWs) above room temperature provides immense pote
126 tress-induced non-thermally activated domain wall dynamics is progressively replaced by an intense th
127 lly related to the controllability of domain wall electronic properties.The electronic states within
128 r results introduce a concept for the domain wall electronic property, the walls own internal degrees
129 ed experimental data (analysis of guard cell wall epitopes and treatment of tissue with cell wall dig
130 ut not TLR4 was critical for sensing of cell wall extracts and whole corynebacteria.
131 r how stomatal pores form and how guard cell walls facilitate dynamic stomatal responses remain poorl
132  of nanogold affinity tags in the context of wall fibrillar organization.
133 sma membrane communication, influencing cell wall formation and cellular mechanics.
134 her tissue is critical for male meiotic cell wall formation and thus plays an important role in conso
135                    LRXs are involved in cell wall formation in vegetative tissues and required for pl
136 lved in fibre metabolism regulation and cell wall formation.
137 layer of endothelial cells lining the vessel wall forms a semipermeable barrier (in all tissue except
138 h remarkable expansions of protease and cell wall gene families, while divergent infection strategies
139 he first time, variations in miscanthus cell wall glycan components were comprehensively characterize
140 E structure, especially of the pore-rich end walls, has a direct effect on translocation efficiency.
141 opy indicates that phloem sieve element cell walls have a lower indentation modulus (indicative of hi
142                         Ferroelectric domain walls have continued to attract widespread attention due
143  logical processing based on magnetic domain walls have great potential for implementation in future
144                             Such biochemical wall heterogeneities precede wall bending.
145 e cytochrome bc1 complex, disruption of cell-wall homeostasis, and DNA damage.
146 or, recalcitrant component of the plant cell wall; however, expression of clr-1 in the absence of an
147 -B1, and its abilities to down-regulate cell wall hydrolase genes and disrupt the biofilm formation o
148                                         Such wall hydrolases are modular enzymes, composed of discret
149  germ tube that emerges from the outer spore wall in a process called outgrowth.
150 d into the anterior-lateral left ventricular wall in C57BL/6J (allogeneic model, n = 17) and C3H (syn
151 operties.The electronic states within domain walls in an interacting electronic system remain elusive
152                       Moreover, while domain walls in in-plane films are generally expected to be non
153                              Magnetic domain walls in magnetic tracks produce strong localized fields
154  which is important for the assembly of cell walls in many microorganisms.
155 (i.e. pillars fabricated on the microchannel wall) in boiling of two fluids FC-72 and water with fund
156 6 epitope is widespread throughout most cell walls including those of phloem cells.
157                    The thickness of the MGNT walls increased from 98 to 126nm upon increasing the dep
158 abeling, we demonstrate that contiguous cell walls indeed exhibit hybrid mechanochemical properties.
159 ontribute to the inconsistency of FDG vessel wall inflammation.
160  VPC in plants, and corresponding changes in wall ingrowth deposition were observed when miR156 was o
161 sion, the abundance of PP TCs with extensive wall ingrowths varied across rosette development in thre
162  juvenile phase, and extensive deposition of wall ingrowths was observed in rejuvenated leaves follow
163 1,100-3,000 MBq) was injected into the heart wall insert of an anthropomorphic torso phantom.
164                  We also found that the cell wall integrity (CWI) pathway contributes to the response
165                        The A. fumigatus cell wall is a complex network of polysaccharides among them
166 ion of circulating cells within the vascular wall is a critical event in chronic inflammatory process
167 ctural feature of whole lignin in plant cell wall is of great importance for understanding lignin bio
168       Leukocyte transmigration across vessel walls is a critical step in the innate immune response.
169 of stilbenes in stomata guard cells and cell walls is induced by P. viticola infection.
170 se found in primary and secondary plant cell walls is uncertain, but their presence enables further s
171 tial mycolic acids in the mycobacterial cell wall, is the target for the frontline anti-TB drug isoni
172 ed testis and female neonates with abdominal wall laxity are classified as Pseudo Prune Belly syndrom
173 ssumption that S-layers serve only as static wall-like structures.
174 brane protein large (MmpL) proteins are cell wall lipid transporters that are important for basic myc
175 associated with the export of bacterial cell wall lipids outside of vacuole.
176 ptide thrombin and proinflammatory bacterial wall lipopolysaccharide (LPS).
177            The incremental values of RV free wall longitudinal strain and RVESRI to risk scores were
178 wever, in the limit of vanishing particle-to-wall mass ratio, the equilibration rates remain strictly
179 ein isolate-gum Arabic complex coacervate as wall material.
180 l ingredients can be encapsulated by various wall materials for controlled release in food and digest
181 l shape by patterning the deposition of cell wall materials.
182 unknown, but the primexine, a transient cell wall matrix formed on the surface of microspores at the
183 g network, thereby playing a central role in wall mechanics and growth, but this view is challenged b
184  in treatment-refractory breast cancer chest wall metastases but responses are short-lived.
185              The optimal AuNP packing in the wall, moderated by the custom ligands and verified using
186 evelopment; however, its involvement in cell wall modification during root hair formation (RHF) has n
187 ulators (e.g., CLE peptides) and pectin/cell wall modification.
188 cted to mediate lipopolysaccharides and cell wall modification.
189 role for TAG and/or its metabolites in spore wall morphogenesis.
190 provide a better understanding of the domain wall motion.
191 e the first extracellular recordings of body-wall muscle electrophysiology inside an intact roundworm
192 l localization to actin-rich I-bands in body wall muscle.
193 opy transgenes that express rde-4(+) in body-wall muscles or hypodermis, however, enable silencing se
194 ing experiments in selected Arabidopsis cell wall mutants.
195 ial DNA, and beta-glucans, found in the cell wall of fungi, both induced MMP-7.
196 charide matrix, and considers changes in the wall of plant-pathogenic fungi during on and in planta g
197 ing direct ZIKV inoculation into the uterine wall of pregnant, immunocompetent mice to evaluate trans
198 ion-binding site located on an inner chamber wall of the enzyme.
199                    More than 90% of the cell wall of the filamentous fungus Aspergillus fumigatus com
200 ion between the plasma membrane and the cell wall of the growing tip acts as a piconewton force trans
201                 Ribosomal protein S1 forms a wall of the tunnel between RNAP and the 30S subunit, con
202 ion of the gestational sac onto the anterior wall of the uterus at the site of previous LSCS scar in
203       For bacteriophage infections, the cell walls of bacteria, consisting of a single highly polymer
204 ediastinal course, diffuse thickening of the walls of numerous bronchial branches and a "ground glass
205 een the confined molecular structure and the walls of the container, clear-cut experimental evidence
206 corporation and processing of HG in the cell walls of these two tip-growing structures.
207       (125)I-pentixafor uptake in the vessel wall on autoradiographies was located in macrophage-rich
208 ozen" state with negligible motion of domain walls on atomic and mesoscopic scales occurs in the RSG.
209 wn whether this is specific to the abdominal wall or due to an improvement in overall physical fitnes
210 for the domain wall electronic property, the walls own internal degrees of freedom, which is potentia
211                                         Cell wall peptidoglycan stimulates interleukin 10 (IL-10) pro
212 hat deletion of ami1 leads to increased cell wall permeability and enhanced susceptiblity to cell wal
213                            However, few cell wall phenotyping methodologies have proven sufficiently
214  curve measurements indicate a strong domain wall pinning along the direction orthogonal to the rips,
215 t the higher coercive field is due to domain wall pinning in deeper defects and hence a higher field
216  that LRX proteins might play a role in cell wall-plasma membrane communication, influencing cell wal
217 as a Ca(2+) capacitor, pollen tube guide and wall plasticizer into a simple but widely applicable mod
218  in platelet activation in vitro, and vessel wall platelet deposition and initial hemostasis in vivo.
219 daptive autoimmune responses in the arterial wall play critical roles in the process of atheroscleros
220                                     The cell wall plays a major role during infection.
221                               The plant cell wall plays an important role in communication, defense,
222 cleavage of the bacterial peptidoglycan cell-wall polymer.
223 lised with gum arabic as it also act as a co-wall polymer.
224 abundance and the sequential release of cell wall polymers with specific combinations of enzymes led
225 on mapping to be conducted for specific cell wall polymers.
226 n of cellulose, the most abundant plant cell wall polysaccharide, requires the cooperative activity o
227 ive enzymes (CAZymes) that modify plant cell wall polysaccharides and other complex glycans.
228 oarrays containing chemically extracted cell wall polysaccharides collected from 331 genetically dive
229 s, a network of covalently linked plant cell wall polysaccharides containing galacturonic acid (GalA)
230 improve digestion of recalcitrant plant cell wall polysaccharides may offer solutions for sustainable
231 nly be performed at one cardiac phase, while wall position in the other cardiac phases is found by im
232 wo or more ergodic components for a range of wall positions.
233 regut, hepatopancreaticobiliary vs abdominal wall procedure), and complexity (eg, adhesions; relative
234                                         Cell wall profiling techniques showed that the pretreatment l
235 ed apart from that of ionic strength on cell wall properties, however.
236 aromyces cerevisiae FLO1 gene encodes a cell wall protein that imparts cell-cell adhesion.
237                        A superfamily of cell wall proteins, the hydroxyproline-rich glycoproteins (HR
238 strain obtained from the inferior myocardial wall provided incremental prognostic information for VT/
239                            Complex abdominal wall reconstruction has witnessed tremendous success in
240 is clinically studied for treatment of chest wall recurrence of breast cancer, however with various o
241 t Ca(2+) and Mg(2+) ions and the nanochannel walls reduced the native surface charge density by up to
242 hus, a highly simplified pectic primary cell wall regulates its own synthesis by a Hechtian growth os
243  root emergence are both accompanied by cell-wall remodeling, which involves the INFLORESCENCE DEFICI
244 hemotactic protein 1 (MCP1)-induced vascular wall remodeling.
245          In addition, an optimization of end wall resistance with plant height was discovered, but fo
246 e inflammatory process involving the colonic wall secondary to fecal impaction with high morbidity an
247  land plants divide by initiating a new cell-wall segment from their center.
248 is associated with the direction of the mean wall shear stress and of the gradient of harmonic phase-
249      Here, Cho et al. report that the domain wall state in a charge-density-wave insulator 1T-TaS2 de
250 und that in the presence of vancomycin, cell wall stiffness gradually decreased over time, with a 40%
251 e cell cycle dynamics with responses to cell wall stress induced by echinocandins, a front-line class
252 hape and induce expression of the WalRK cell-wall stress regulon.
253 accurately model the experimentally observed wall stress relaxation and expansive growth rate.
254 hown that a single Pi parameter controls the wall stress relaxation rate.
255  in a wide range of processes including cell wall structure, hormone signaling, and sugar allocation
256 leads to a deformation of the initial domain wall structure.
257    However, in plants, the existence of cell walls, subcellular organelles and the lack of stable cel
258 mportant for papillae deposition on the cell wall surface, we identified the GLASSY HAIR 1 (GLH1) gen
259 TP hydrolysis and guides correct septal cell wall synthesis and cell division.
260                               Bacterial cell wall synthesis is the target for some of our most powerf
261 terial cell division by directing local cell wall synthesis.
262 rences in the change from baseline in vessel wall target-to-background ratio (TBR) from the ascending
263 meability and enhanced susceptiblity to cell wall targeting antibiotics.
264 ing high and low Mg-bands within their shell walls that cannot be explained by temperature alone.
265 T1 values were a strong predictor of 6-month wall thickening compared with late gadolinium enhancemen
266 iation process mediated by the NAC SECONDARY WALL THICKENING PROMOTING FACTORs in the hypocotyl xylem
267 ostructural dynamics during left ventricular wall thickening, and apply the technique in hypertrophic
268 the alveolar ridge (P = 0.007) and in buccal wall thickness (P = 0.003).
269 diastolic volume (P<0.0001 for each) and not wall thickness (P=0.21).
270 interstitial fibrosis and increases anterior wall thickness and cardiac contractility after infarctio
271 tachycardia (nsVT), maximum left ventricular wall thickness and obstruction were significant prognost
272                   Conclusion Maximum colonic wall thickness and subjective severity of acute divertic
273  and echocardiography showed increased heart wall thickness as well as increased heart rate.
274                                          The wall thickness of the MGNT arrays also increased while t
275 be compensated by a small increase of GCS or wall thickness or reduced diameter.
276                                              Wall thickness ranged from 0.9 mm to 3.81 mm at T1 and 0
277 t study suggests that increased gall bladder wall thickness, pleural effusion, ascites, hepatomegaly,
278 eased number of plaques or abnormal arterial wall thickness.
279 , cardiac MSCs from LVD exacerbated anterior wall thinning 28 days after myocardial infarction.
280 ded endolysin can generate holes in the cell wall through which cytoplasmic membrane material protrud
281  the pattern differentiating the future body wall tissue from the wing blade tissue.
282 les the internal stress of a rapidly growing wall to the plasma membrane.
283 een hampered by the resistance of plant cell walls to enzymatic conversion, primarily owing to lignin
284  even a few percent of holmium allows domain walls to pin with consistent and well-defined magnetisat
285 stically, beyond dyads and beyond laboratory walls, to identify neural markers of group engagement du
286 scovered, but found to be independent of end wall type.
287 h polyphenols are associated with plant cell walls under hydrated conditions, they are not immobilise
288 gnition, the electronic properties of domain walls under illumination until now have been accessible
289 e possibility of controlling magnetic domain walls using voltages offers an energy efficient route to
290 stalline cellulose, was infrequent until the wall was predigested with xyloglucanase, whereupon micro
291  metal resistance, degradation of plant cell wall was significantly increased in the degraded soils.
292 promotes papillae formation on trichome cell walls was identified as a subunit of the transcriptional
293 on of Si beneath the cuticle and in the cell walls was the first proposed hypothesis to explain how t
294          Podoplanin was expressed in the IVC wall, where it was localized in the vicinity of the ablu
295 , diverticulae) due to weakness in the bowel wall, which can become infected and inflamed causing div
296                      The polysaccharide-rich wall, which envelopes the fungal cell, is pivotal to the
297                                       Domain walls, which are intrinsically two dimensional nano-obje
298         Plant cells are embedded within cell walls, which provide structural integrity, but also spat
299 y high in all subjects throughout the airway wall with marked cytoplasmic to nuclear shift in COPD (P
300 verting effect from a more conductive domain wall within the sample.

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