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1 n NADPH oxidase activity and dendritic spine morphology.
2 ynamics within foot processes controls local morphology.
3  to the nucleus and affect hyphal growth and morphology.
4 e modular synthetic ligand dictates assembly morphology.
5 ediates the activity of IL-1beta on dendrite morphology.
6 -like melanomas to understand their clinical morphology.
7 g patterns are interpreted to infer particle morphology.
8 ediates the activity of IL-1beta on dendrite morphology.
9 s rather than the ancestral avemetatarsalian morphology.
10 t was 90% and was independent of ventricular morphology.
11 llular MT orientation, cell shape, and organ morphology.
12 ibly affected the evolution of jaw and tooth morphology.
13 well-defined diameter and resulting rod-like morphology.
14 hat have rectangular channel cross-sectional morphology.
15 s of astrocyte coupling, and changes in cell morphology.
16 pattern that correlates with ultrastructural morphology.
17 ovide a pathway to a previously inaccessible morphology.
18 s that have neuropotential but lack neuronal morphology.
19  to the routine characterization of neuronal morphology.
20 ic immune markers, treatment dose, and tumor morphology.
21 that are associated with changes in synaptic morphology.
22 ules pertinent for excitability and neuronal morphology.
23 I activity and altered mitochondrial network morphology.
24 ticle growth rate and the resulting particle morphology.
25 nd marble burying as well as dendritic spine morphology.
26 topic SoxN with svb rescued diverse denticle morphologies.
27 a broad range of reconstructed and synthetic morphologies.
28 usion-limited behavior leading to core-shell morphologies.
29 bilayers and produce arrays of new organized morphologies.
30 or of at least 1.6 relative to nonconvective morphologies.
31 on have variable AP waveforms independent of morphology, (2) Na(+) channel beta2 subunits modulate AP
32  P. putida F1 as indicated by smaller colony morphology, a more rigid membrane, and higher tolerance
33  revealed region-specific changes in ciliary morphology accompanied by alteration of acetylated tubul
34 ector proteins implicated in regulating cell morphology, adhesion, and migration in various cell type
35 s, and high hole mobility from optimized BHJ morphology afford a very high power conversion efficienc
36 emale mate choice that also predicted female morphology along the benthic-limnetic trait axis.
37 tics of SO2 reactions on MnO2 with different morphologies (alpha, beta, gamma and delta) was investig
38 ssayed during reinstatement: dendritic spine morphology, alpha-amino-3-hydroxy-5-methyl-4-isoxazole p
39 driving the diversity in vomeronasal-lingual morphology among lacertid species.
40 ted HbS fibers could be applied to study the morphologies and membrane stiffening of sickle RBCs.
41 racterized by distinct, highly inhomogeneous morphologies and sizes, where LRS powder particles are h
42                         We reconstructed the morphologies and synaptic connections of all 983 neurons
43 lly retained their parental cystic and spiky morphologies and were termed CC (cystic) and SC (spiky),
44 ncompatibility also resulted in aberrant egg morphology and a maternal-effect on embryonic chromosome
45  thereby failing to support the Sertoli cell morphology and adhesion protein complexes (e.g., occludi
46  irradiation can result in severe changes in morphology and an overall degradation of mechanical prop
47 intriguing relationship between NIMS surface morphology and analyte selectivity.
48  progenitor development, and oligodendrocyte morphology and capacity for myelination.
49 erstanding and optimization of the thin-film morphology and charge-transport properties of conjugated
50 nce of Ldo proteins results in defects in LD morphology and consumption by lipophagy.
51 ss spectrometry were used to characterize EV morphology and contents.
52 ecies, mitochondrial health, as well as cell morphology and determine that the hMSCs are minimally af
53                     We report differences in morphology and diet of the termite-eating gecko Gymnodac
54                     We observed altered cell morphology and disrupted organization of F-actin in Li1
55                                 However, the morphology and distribution of ER-PM junctions are not w
56                               We studied the morphology and diversity of retinal ganglion cells in St
57 operties, but little is understood about the morphology and dynamics of these polymer layers.
58 greatly facilitate the study of in vivo full morphology and electrophysiology of single neurons in th
59                 We demonstrate that particle morphology and evaporation is dependent on whether SOA f
60 ters and to address the influence of antenna morphology and excitation wavelength on polarization con
61 ution confocal microscopy to analyze nuclear morphology and F-actin rearrangements during the initiat
62 fness optimum of U251 glioma cell migration, morphology and F-actin retrograde flow rate can be shift
63 nd samples of dogs with relatively ancestral morphology and from different time periods.
64 , Ilk(fl/+) ;Pkhd1-Cre mice had normal renal morphology and function and survived >1 year.
65     Our findings indicate that changes in LV morphology and function depend on the type of body mass
66                    The regeneration of organ morphology and function following tissue loss is critica
67 target with downstream impact on paraspeckle morphology and function.
68           SLIP yields rich data sets on cell morphology and gene expression that illustrate the funct
69 7th December 2015) on wheat kernel endosperm morphology and gluten protein structure, using SEM, ligh
70 tic mesoderm anterior border, somite chevron morphology and hypaxial myoblast migration.
71 haracterized by different GOAL chemistry and morphology and indicates that GOAL nanochannel height di
72 nce that PFN1 is important in regulating NMJ morphology and influences survival and locomotion in Dro
73                These results reveal distinct morphology and interactions for MUC5B and MUC5AC and sug
74                  This new taxon has a unique morphology and is characterized by an unexpected combina
75  to reside in dorsal root ganglia (DRG), the morphology and location of peripheral nerve endings of s
76 he methodology for investigating 3D spheroid morphology and marker expression and for in vitro safety
77 ere, we examine the connection between spine morphology and membrane-bound diffusion through a combin
78                            The abnormal axon morphology and mitochondrial retrograde transport defect
79 ential RHOA activity determines polarized NC morphology and motility, and is regulated by the asymmet
80 argely due to the scattering that depends on morphology and not absorbance that largely depends on th
81  based on the ideas of Galileo and Goethe on morphology and of Russell on functionalism, but he was f
82 -depth studies into the relationship between morphology and performance of these complex biopolymer s
83 nnovations in molecular networks influencing morphology and physiology.
84 l heterogeneity in gene expression, cellular morphology and physiology.
85 n experiments we show that leaf orientation, morphology and position are pre-patterned by HD-ZIPIII a
86 coustic signalling is a determinant of swarm morphology and present the first compelling evidence tha
87                                          The morphology and previously suggested phylogenetic affinit
88 lves elevate above the tongue, demonstrating morphology and proliferation indices indistinguishable f
89 ce-site variant displayed changes in nuclear morphology and protein localization that are consistent
90 verexpression reversed senescence-associated morphology and reduced levels of molecular markers of se
91              We further show that overall CS morphology and regions within the superior portion are s
92 ronal-subtype molecular control of dendritic morphology and related functional adaptations, which und
93  in zebrafish embryos disrupted muscle fiber morphology and resulted in abnormal eye development.
94 l cross-links recapitulates the segregation, morphology and self-interaction of the nucleolus.
95 y implanted lesions can be imaged, and tumor morphology and size can be monitored using ultrasonograp
96  spectra are highly dependent on the cluster morphology and size of particles but the origin of this
97 over such aspects as functionality location, morphology and size of the resulting assemblies.
98                        Left ventricular (LV) morphology and systolic and diastolic function were eval
99 copic and magnetic properties along with the morphology and thermal property were analyzed using FTIR
100    Cell death introduces alterations in cell morphology and tissue micro-structures that cause measur
101 l dichalcogenide (TMD) patterns with regular morphology and unique edge structure is highly desired a
102 of these behavioural traits depended on male morphology and varied with the number of rival males in
103                                 Although the morphology and wear on its anterior teeth indicate that
104 n) is the process whereby leaves alter their morphology and/or biochemistry to optimize photosyntheti
105 val in such landscapes, changes in the nasal morphology and/or function aimed to humidify and warm th
106 umbers, BP dendritic spreads, dendritic tree morphologies, and cone-bipolar connectivity patterns wer
107 ide expression, changes in axonal projection morphology, and a switch in neuronal function.
108 ing its specific expression signature, hairy morphology, and antiapoptotic behavior.
109 butions to Gag-Gag oligomerization, particle morphology, and biogenesis.
110 butions to Gag-Gag oligomerization, particle morphology, and biogenesis.
111 ding of the relationships among composition, morphology, and crystal structure for copper sulfide-bas
112                    Given that the synthesis, morphology, and device physics are inherently related in
113 rated and comprehensive approach (synthesis, morphology, and device physics) to elucidate the fundame
114 lar calcium handling, alterations in cardiac morphology, and elevated cardiomyocyte apoptosis, which
115  relationship between corneal nerve density, morphology, and function.
116 -restricted and matched the immunophenotype, morphology, and genetic mutations of the corresponding p
117 n, combined Paris classification and surface morphology, and increasing size with increased risk for
118 s Paris classification, non-granular surface morphology, and increasing size.
119 esis, nuclear/endoplasmic reticulum membrane morphology, and lipid droplet formation, but not on grow
120 n energy metabolism and cellular physiology, morphology, and symbiotic interactions.
121  and raw-material properties influenced tool morphology, and that hook geometry in turn affected crow
122  has implications for the assembly kinetics, morphology, and toxicity of all Abeta isoforms.
123 cortical neuron types defined by physiology, morphology, and transcriptome in addition to various typ
124 -tau, changes in dendritic spine density and morphology, and upregulation of the adenosine A2A recept
125 ontemporary diagnosis, building on a largely morphology- and clinical presentation-based strategy.
126  the hard sphere systems where the assembled morphologies are prescribed by the diameter ratio betwee
127 s by which SS4 determines granule number and morphology are not understood.
128 icity and the associated changes in cellular morphology are related to the putative interactions reve
129 ulky proteins, ER stress, and defective cell morphology are secondary consequences of bulky cargo ret
130 lation relationship measures based on dental morphology are significantly correlated with those based
131  that control the establishment of astrocyte morphology are unknown, and it is unclear whether impair
132            Together, these data identify MSC morphology as a predictive feature of MSC immunosuppress
133 ent in organogel and hydrogel have different morphology as was evident from scanning electron microsc
134 ugs could strongly influence their assembled morphology as well as their structural stability in aque
135  the timed generation of neurons with mature morphologies, as well as the subsequent generation of as
136 molecules end up organized in a short scroll morphology at high ionic strengths and as long helical r
137 horacic vertebrae with a transition in facet morphology at the 11th thoracic level.
138 thermogenic gene expression and multilocular morphology at the adult stage, but cold restored their b
139 electric state reset subsequent regenerative morphology back to wild-type.
140 rrow and spleen and analyzed their endosomal morphology, BCR expression, and signal transduction.
141  CSs mimic important features of human heart morphology, biochemistry and pharmacology in vitro, offe
142 perform correlated investigations of surface morphology, biological function, and chemical compositio
143 article size, polydispersity index (PDI) and morphology, but it reduced surface charge of nanogels.
144 ed on their distinct tissue localization and morphology, but their developmental origin and mode of h
145 arginal band, that flattens the overall cell morphology by pushing on the cell cortex.
146                                        Round morphology (by transmission electron microscopy), size (
147  red blood cells (RBC) exhibit heterogeneous morphology changes and decreased deformability.
148 he crystals then continue to grow to develop morphologies characteristic of these additives.
149 arge cytoplasmic volume affects spindle pole morphology, chromosome alignment, and stringency of chec
150 wed a significant improvement in erythrocyte morphology compared to untreated controls.
151 onally, low-dose RCEM islets retained better morphology (confirmed with scanning electron microscopy)
152                       Disruption of neuronal morphology contributes to the pathology of neurodegenera
153                       Diversity in aggregate morphology correlates with the differences in AD, cement
154  improved with the addition of lymph node CT morphology criteria.
155                                          The morphology, crystal structures, chemical, and optical pr
156 ) and LAZ1 HOMOLOG1 (LAZ1H1), causes vacuole morphology defects, growth inhibition, and constitutive
157 eening data sets on nuclear and mitotic cell morphologies demonstrates that CellCognition Explorer en
158  that the adhesion of C. albicans to PMMA is morphology dependent, as hyphal tubes had increased adhe
159 few to multilayer step edges) give rise to a morphology-dependent (i.e., height-dependent) enhancemen
160 ion rate of DNA complexes, and (3) electrode morphology-dependent blocking effects.
161 l decomposition pathways that are related to morphology-dependent heterogeneity in the electrochemica
162 rn neuron with initially simple spindle-like morphology develops into a DGC, consisting of a single a
163 ere we provide the first evidence that brain morphology differs meaningfully as a function of recipro
164 n certain environments, changes in C. jejuni morphology due to genetic heterogeneity may promote C. j
165 arried out to image the evolution of droplet morphology during reaction between Al and SiO2.
166 30 min and corrected QT intervals and T-wave morphology every 60 min.
167 ructures to study the mechanical properties, morphology evolution and oxidation state changes during
168  thought to be related to the uncontrollable morphology evolution of the Li anode during cycling.
169 in gaps in knowledge concerning how vascular morphology evolves during carcinogenesis.
170 r, no method currently available can predict morphologies for a novel donor-acceptor blend.
171 ld be discriminated based on somatodendritic morphology for both superficial and gigantopyramidal neu
172 itor population and tested this by examining morphology, gene expression and in vitro self-renewal an
173                       Right ventricular (RV) morphology has been associated with drivers of atrial fi
174 s phase transition occurs, and the resultant morphologies have been investigated, sometimes with ling
175 ive cells did not display the typical B cell morphology, having in general a more dendritic cell-like
176 l-crystallographic texture, micrometer-grain morphology, high crystallinity, low trap density ( appro
177 diversity of primate vocalizations and vocal morphology, highlighting the importance of vocal physiol
178 Absence of FMRP results in abnormal neuronal morphologies in a selected manner throughout the brain,
179 l ester (PCBM) mixture, and found to predict morphologies in agreement with experimental data.
180 e in the ability to assess vascular calcific morphology in all studies with complementary unenhanced
181                       Control of interfacial morphology in electrochemical processes is essential for
182 urements of size and cytoplasmic and nuclear morphology in high throughput, but only the final cell c
183 ed alterations in mitochondrial function and morphology in NSCs, these data link mitochondrial comple
184 hobic (MorphS) surfaces that transform their morphology in response to heat are developed.
185                                 The filament morphology in such an aggressively scaled memristive dev
186 t advances that have been made to understand morphology in the dimorphic Gram-negative bacterium Caul
187 hed cells, restoring the normal hollow lumen morphology in Vitamin E treated organoids.
188 ction of backscattered light to image tissue morphology in vivo.
189 abilizes leukocyte viability and erythrocyte morphology in whole blood under ambient storage.
190  growth arrest and formation of a shmoo-like morphology in yeast cells, lower pheromone doses elicit
191 ease in CEC and beneficial changes in plaque morphology including increase in fibrous cap thickness a
192 -protein phylogenomic trees and has a unique morphology, including a novel type of extrusome (ancorac
193 e also strongly influenced by the changes in morphology induced by interfacial curvature.
194                                              Morphology influences the functionality of covalent orga
195 onstrating that the heme active site in both morphologies is accessible to small molecules for cataly
196  for brain functions, because aberrant spine morphology is associated with many neuropsychiatric diso
197                              This particular morphology is driven by anisotropic epitaxial strain.
198 al dependence on sequence and supramolecular morphology is highlighted 2-fold.
199                        However, how neuronal morphology is maintained in the adult brain remains poor
200 Muller glia organization suggests that their morphology is sculpted by specific cell to cell interact
201 a hexagonal layered structure and sheet-like morphology, is synthesized.
202         LFAO-seeded fibrils possess distinct morphology made of repeating LFAO units that could be re
203 f mammographic breast density, calcification morphology, mass margins at mammography and MR imaging,
204 ogenetic stimulation based on analysis of AT morphology may be a reliable approach for defibrillation
205       The results demonstrate that agreement morphology may be computed in a series of steps, one of
206                         Aberrant melanosomal morphology may potentially have consequences on the abil
207                                          The morphology, microstructure, and chemical composition of
208 ers in serum and tissues, and improved liver morphology more effectively than single treatments.
209      Total sperm count, sperm concentration, morphology, motility, and ejaculate volume were assessed
210 xist diverse neuronal types that can vary in morphology, neural physiology, and modes of neurotransmi
211 nabled us to observe both growth and melting morphologies of the 3D quasicrystal at temperature.
212 uations strongly influence the formation and morphology of 2D h-BN.
213 enotypes described here reflect the cerebral morphology of a common ancestor of Pancrustacea or an ex
214 optera is normally based on the markings and morphology of adults, and not on the larvae which actual
215                We describe the structure and morphology of aggregates formed by the P23T human gammaD
216 at the hairpin fold dramatically changes the morphology of assembled amyloid aggregates.
217 X-ray CT is used to investigate the size and morphology of cavities at a triple point of grain bounda
218                     Brains were examined for morphology of hippocampus and cortex.
219          In plt3plt5plt7 triple mutants, the morphology of lateral root primordia (LRP), the auxin re
220                                          The morphology of microcystoid macular changes was similar b
221 ments, leading to changes in dendritic spine morphology of NAc medium spiny neurons (MSNs).
222  compartments, which may help to explain the morphology of neocortical pyramidal neurons.
223 meters behind this effect are related to the morphology of plasmonic nanoparticles and their relative
224  STAT3 inactivation also results in abnormal morphology of repair cells and regeneration tracks, and
225                    Data on the cranial nerve morphology of tadpoles are scarce, and only one other sp
226                             Control over the morphology of the active layer of bulk heterojunction (B
227                                         Cone morphology of the dogs lacking cone ERG are truncated wi
228 by altering the structural core and external morphology of the fibrils formed.
229 t formation and verify that this affects the morphology of the fusion product and regulates transport
230 a positive correlation between the elongated morphology of the invading cells and the alignment of fi
231  for this idea of concerted evolution of the morphology of the lizard sensory system merely originate
232                Our findings suggest that the morphology of the nanoheterostructures, formed upon part
233                                              Morphology of the nuclear envelope was assessed with imm
234 al core and a solid metal shell, whereby the morphology of the outer shell is determined by the conce
235  induced significant changes in the size and morphology of the particles; approximately 15 nm aggrega
236 ant mechanisms affecting the composition and morphology of the vanadium membrane.
237                                 The size and morphology of these neurons were similar to those of lar
238 codes, we provide a detailed analysis of the morphology of these species, and document it with drawin
239  global distribution and large variations of morphology of ultralow velocity zones validate a composi
240 important roles in virus assembly and in the morphology of virus particles.
241 gnificant effects on soma size and dendritic morphology of VTA neurons but significantly decreased do
242 he dynamic model tracks the evolution of the morphology of WBC subpopulations as a patient transition
243     Readers evaluated baseline and follow-up morphology on digital color images, fluorescein angiogra
244 , does not affect intraocular pressure, bleb morphology or function after one year of follow-up in ey
245 n, MGO did not induce significant changes in morphology or mechanical properties of the collagen matr
246 pathies is caused by defective primary cilia morphology or signal transduction.
247 gnificant differences in central sulcus (CS) morphology, particularly in the inferior region.
248 damage, mitochondrial DNA (mtDNA) integrity, morphology, phenotype and cytokine secretion into storag
249                                          The morphology, photoluminescence (PL) spectra and UV-vis sp
250 nhibitory neurons exhibit remarkably diverse morphology, physiological properties and connectivity.
251 s of dendritic spine density, abnormal spine morphology, reduced dendritic arborization, and extensiv
252  neuropeptide expression evolves faster than morphology, representing a possible mechanism for the ev
253 d characterized the formulations for surface morphology, respirability, in-vitro drug release, and ev
254 in the same ratio of double-headed to normal morphology, revealing a cryptic phenotype that is not ap
255 alapagos giant tortoises have two main shell morphologies - saddleback and domed - that have been pro
256                              Cross sectional morphology showed that silica particles were dispersed i
257 ons show in vitro growth kinetics and plaque morphologies similar to those of the wild-type (WT) A24
258 l nerve fiber layer (RNFL) thickness, drusen morphology, size, extent, visibility on funduscopy, ultr
259 rgan function and development, body size and morphology, skin and hair pigmentation, and keratinizati
260   The structural evolution of the Pt surface morphology strongly resembles that found in studies of P
261 ysiological membrane properties and dendrite morphology, studied in vivo, play a role in selective se
262                                   Convective morphologies (supercells, disorganized, and QLCS) enhanc
263 ial processes, including changes of cellular morphology, surface phenotype, secretory mediators, and
264 0 metres and depths of about 500 metres with morphologies that resemble penitentes have been observed
265 sial, as it already acquired the specialized morphology that characterizes modern caecilians by the J
266 at, in contrast to CAdV, has a unique capsid morphology that contains more prominent extensions of pr
267 face molecules, and determinants of neuronal morphology that is differentially expressed in specific
268 ser setup allows us to realize two different morphologies, the first being a silicon-germanium compos
269 , but it was not associated with ventricular morphology, the subject's age, or the type of Fontan con
270 ifferent aluminum salts on the phase purity, morphologies, thermal stability of anatase and photocata
271 Here, we explore the genetic basis of P-wave morphology through meta-analysis of genome-wide associat
272 ates triacylglycerol metabolism and vacuolar morphology through the long-chain fatty acyl-CoA synthet
273 cific resources, species evolve advantageous morphologies to increase the efficiency of nutrient acqu
274 o limit possible contact site assemblies and morphologies to those that promote fast Ca(2+)-triggered
275 two distinct mechanisms for coupling droplet morphology to enzyme activity (host-guest interactions w
276 n of the type of T. danica goes beyond gross morphology to include ultrastructural details and labile
277 le regolith can generate features similar in morphology to those forming on Martian dunes today.
278 y in growing bones and ultimately gross limb morphology, to generate phenotypic variation during pren
279 ng reconnaissance revealed meandering shaped morphologies underneath bio-concretionned rocky buildups
280 go simultaneous changes of surface color and morphology upon infrared (IR) actuation.
281 nal, focusing on the most common anisotropic morphologies used for SERS.
282  a major determinant of nuclear blebbing and morphology via its contribution to nuclear rigidity.
283 ODxRS for all other suspicious calcification morphologies was 19.4 (P < .03).
284                                The resulting morphology was always observed to be a core of the origi
285 s showed that abnormal retinal microvascular morphology was evident in pediatric patients with T1D af
286                                      Surface morphology was found to significantly and selectively al
287                A drastic change of the shell morphology was observed by changing the injection rate o
288 trations a pro-oxidant effect on erythrocyte morphology was observed.
289             To assess variation in hind limb morphology, we analysed how the dimensions of the major
290 Furthermore, despite the similar gross brain morphology, we found an unexpectedly high variation in t
291 rformance and its ability to analyze various morphologies were tested using desorption electrospray i
292                             GO chemistry and morphology were controlled with easy-to-implement photor
293                Renal function and histologic morphology were evaluated.
294 ound 7 displaying a major impact in neuronal morphology when inactivated in mice.
295 ta in true leaves display normal density and morphology when PGX3 expression is altered, loss of PGX3
296 nsitive to optimization conditions and blend morphologies, which are a result of the intricate interp
297 that TbSmee1 is necessary for maintaining HC morphology, which is important for the parasite's abilit
298  ultrastructural impairment of mitochondrial morphology with a loss of internal cristae.
299  loss also resulted in aberrant adult midgut morphology with dramatically enlarged enterocytes.
300  a full 3D structural dataset of the network morphology within a white beetle wing scale.

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