コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ) and inhibit signaling at the neuromuscular junction.
2 nal cord or denervation at the neuromuscular junction.
3 selectively labeled within an immunosynaptic junction.
4 al landscape of the dynamic chemistry at the junction.
5 lish the CO(2) -dependent closing of the gap junction.
6 rectional migration of electrons via the p-n junction.
7 tation, M8R, which is located at the overlap junction.
8 rystals oriented normal to the dentinoenamel junction.
9 by the nugatory carrier transport in the P-N junction.
10 enriched claudin-5 localization at the tight junction.
11 x DNA at the double-/single-stranded (ds-ss) junction.
12 of anchoring fibrils at the dermal-epidermal junction.
13 n by controlling the bias applied across the junction.
14 impulse propagation at the atrioventricular junction.
15 ohistochemical analysis of the neuromuscular junction.
16 elopathies and diseases of the neuromuscular junction.
17 maintaining optical access to the molecular junction.
18 doG structure accommodates a second arm of a junction.
19 e increase in PCO2 (55 mmHg) closes Cx26 gap junctions.
20 g the disassembly of VE-cadherin at adherens junctions.
21 eral and apical membranes separated by tight junctions.
22 oint in space to detect both lines and their junctions.
23 f DNA cleavage in modified versus unmodified junctions.
24 but had no effect on Cx26(K125R) or Cx31 gap junctions.
25 NBDG) between HeLa cells coupled by Cx26 gap junctions.
26 c regions of the glutamatergic neuromuscular junctions.
27 ability by modulation of intercellular tight junctions.
28 hnologies, based around functional molecular junctions.
29 cells, and preserved the integrity of tight junctions.
30 Crumbs and Rok are isotropically enriched at junctions.
31 n, controlled by cadherin-mediated cell-cell junctions.
32 accumulation of NF186 requires the paranodal junctions.
33 35) causes rapid internalization of Cx43 gap junctions.
34 this process creates 3D arrays of Josephson junctions.
35 be stability, and disrupted endothelial cell junctions.
36 ify pre-existing components of intercellular junctions.
37 fness at the locations of nicks and Holliday junctions.
38 he non-dissipative nonlinearity of Josephson junctions(1) converts macroscopic superconducting circui
40 c current peaks dominate the IV cycle of the junction (+/-2 V) in ACN vapor, enhancing the reversible
41 ated particles reduces the area of cell-cell junctions-a change that correlates with increased leakin
42 ulted in muscle fiber defects, neuromuscular junction abnormalities, compromised motor performance, a
46 Our results demonstrated that the four-way junction adopts an out-of-plane geometry under low ionic
48 the potential for branching at hybridization junctions, all of which were confirmed experimentally.
50 d PBI-BM5 disrupted colonic epithelial tight junction and adherens junction, increased mucosal permea
53 gnized a 12-bp sequence at the leader-repeat junction and performed leader-side insertion before proc
54 tated by a structural component (such as DNA junction and protein-protein interaction) and DNA polari
55 C) that retained the abilities to form tight junctions and cilia and to differentiate at the air-liqu
58 scaffolding or adaptor protein at cell-cell junctions and in the cytosol, supporting normal blood ve
60 E-cadherin is a major component of adherens junctions and marks Langerhans cells (LC), the only dend
61 plex that localizes to mitochondrial cristae junctions and organizes cristae positioning within the o
62 s remaining unresolved and hemi-resolved DNA junctions and other branched species at the very late st
64 fied enzyme specifically recognises ss-dsDNA junctions and possesses ssDNA-dependent ATPase, ssDNA bi
66 ically determine the morphology of capillary junctions and thereby regulate branch-specific blood flo
69 y applying a voltage signal to the molecular junction, and the information is read out by monitoring
71 sely identified features such as cells, cell junctions, and cell types within skin to enable multifac
72 fying previously unreported proteins at cell junctions, and for gene expression analysis in multiple
73 ion adjacent to but not overlapping with gap junctions, and forms puncta before the clusters of gap j
76 d fibronectin processing, increased adherens junctions, and rescued defective lumen formation induced
77 unction, reduced total Cx43, and reduced gap junctions, and they died suddenly at 2 to 4 weeks of age
79 th specified densities of nicks and Holliday junctions are synthesized and stretched by fluid flow.
82 of sarcopenia and identify the neuromuscular junction as a focal point of mTORC1-driven muscle aging.
83 s (1) does not require the rod-cone Cx36 gap junctions as has been proposed in the past; and (2) a Cx
86 s facilitate using nanomechanical, Josephson-junction based, and other mesoscopic vibrational systems
89 verexpressed, defined by an exon-exon splice junction between exons 8 and 10 (junc8.10) and that is p
90 and connexin-43 in adherens junction and gap junction between pericytes and ECs are downregulated by
92 a single-point mutation, termed R110, at the junction between the variable and constant LC regions.
93 ation of electrical coupling through the gap junctions between inferior olive neurons by inhibitory G
95 use RPE caused cell depolarization and tight junction breakdown, and led to inhibition of RPE65 expre
98 t, we prepared n-Si/Au nanoparticle Schottky junctions by electrodeposition and characterized them us
99 These findings suggest that aging of branch junctions by phosphate release from Arp2/3 complex and m
103 t for insulin secretion, cell polarity, cell junction, cilia, cytoskeleton, vesicular trafficking, an
105 esis/metabolism (ELOVL3 and FA2H), and tight junction (CLDN8) genes were primarily seen in lesional A
107 c differentiation and connexin 43 (CX43) gap junction communication in cultured pluripotent cells fro
110 ted that elevated CO(2) reduced the Cx26 gap junction conductance (median reduction 66.7%, 95% CI, 50
111 in PCO2 caused a median reduction in the gap junction conductance of 41.7% (95% CI, 26.6-53.7%).
113 Furthermore, in the right temporoparietal junction, confidence effects were enhanced for judgments
115 ize the arrangement of cones in individual Y-Junction cores as well as the spatial distribution of Y-
117 energy substrates by reducing astrocyte gap junction coupling with dominant negative connexin 43 or
118 how that Abeta(25-35) impairs functional gap junction coupling yet increases hemichannel activity.
119 hases acting afterward as a conventional p-n junction, creates an adjustable virtual p-n-p or n-p-n j
121 lueprint that is similar to that of adherens junctions, desmosomal cadherins - called desmogleins and
122 ion efficiencies above 25 per cent in single-junction devices and 28 per cent in tandem devices(1,2).
123 codon usage, codon pair usage, dinucleotide/junction dinucleotide usage, RNA structure around the fr
125 creates an adjustable virtual p-n-p or n-p-n junction due to self-polarization in the ion-conducting
126 of a CdTe photoanode having an internal p-n junction during PEC water oxidation was enhanced by appl
127 connectivity with the right temporoparietal junction during prosocial, compared with self-relevant,
129 trochemical method used for studying the p-n junction effect in the bR and p-type semiconductor combi
133 depletion of alpha-catenin perturbs adherens junctions, enhances cell proliferation and motility, and
135 s (JV) response of nitroazobenzene molecular junctions exhibits the exponential thickness dependence
137 er ciliary activity, cilium loss, less tight junction expression (ZO-1), and more detachment of epith
138 f intercellular communication, involving gap junctions, extracellular vesicles, and tunneling nanotub
139 thic separation column, a nanofluidic liquid junction for providing post-column electrical contact, a
140 heric retina, topological defects, called "Y-Junctions", form to maintain approximately constant cell
141 on of shear stress is known to enhance tight junction formation and hence improve the barrier functio
143 in a reorientation and enhancement of tight junction formation on both coverslip and permeable inser
144 actin to recruit F-actin networks at the gap junction formation plaque, and the formation of F-actin
148 f the wires in Au-SAM-Pt and Au-SAM-graphene junctions, from which the conductance per molecule was d
150 ked to the suppression of networks for tight junction, gap junctional intercellular communication, an
159 otein complexes that generate cadherin-based junctions have ancient origins, with conserved elements
160 ar, altered distribution and function of gap junctions have been associated with acute myocardial inf
162 iffusion of oxygen along the midplane and by junctions holding lipid structures in close proximity to
163 ty and intercellular channel activity of gap junctions; however, the molecular basis for these effect
164 on of [(18)F]AV1451 at the white/gray matter junction in frontal, parietal, and temporal brain region
167 temporal dynamics in contracting and growing junctions in different genotypes, and the identification
169 vered the polarization of cristae and crista junctions in mitochondria tethered to the SSC in OHCs.
170 ondrial mitofilin protein complex at cristae junctions in patient fibroblasts bearing the CHCHD10(S59
171 roteome that is enriched at astrocyte-neuron junctions in vivo, which includes neuronal cell adhesion
172 lonic epithelial tight junction and adherens junction, increased mucosal permeability, and elevated p
173 e cell surface in the form of functional gap junctions indicating that Abeta(25-35) causes rapid inte
175 incorporation of sterically demanding spiro junctions into the backbone of nanohoops, enables the ma
177 usal evidence that the right temporoparietal junction is involved specifically in the embodied compon
178 d distribution of its subunits around crista junctions is unclear because such small length scales ar
179 arcinoma of the esophagus or esophagogastric junction, is not of major importance with regard to shor
180 in), a potent regulator for intestinal tight junctions, is highly expressed in autoimmune mice and hu
181 ne, and all were associated with an IGLJ3*02 junction (J) gene, confirming the high restriction of VJ
182 ts the four-helix bundle at the head-to-tail junction, leading to weaker tropomyosin-tropomyosin bind
183 ns, while longer pulses produce irreversible junction length changes that saturate with prolonged pul
184 We identified 171 genes and eight splicing junctions located within four genes (SNX19, ARL6IP4, APO
185 or 24 h also inhibited the increase in tight junction macromolecule permeability that occurs followin
187 promoted axonal regeneration, neuromuscular junction maturation, and functional recovery of injured
188 ultiple cellular constituents, including gap junctions, mechanosensitive ion channels, energy-consumi
189 In retinal degenerations, these same gap junctions mediate oscillatory activity that contributes
190 HP) is induced at degenerating neuromuscular junctions, mediated by an evolutionarily conserved activ
191 This scaling is promoted by tricellular junctions mediating an increase in aSF nucleation rate a
193 lity, wing and eye morphology, neuromuscular junction morphology, bang sensitivity and climbing behav
194 th just two dipole-coupled magneto-tunneling junctions (MTJ), with magnetostrictive soft layers, fabr
195 ed during expiration to the atrioventricular junction (n=5) and left ventricular myocardium (n=20) of
199 crophage-mediated response for neuromuscular junction (NMJ) reinnervation following nerve injury and
200 ll activity takes place at the neuromuscular junction (NMJ), the output of motor neurons, but its imp
204 pping identified an Fdx1-binding site at the junction of HoxE and HoxF, adjacent to iron-sulfur (FeS)
206 ITD-434) induced an allosteric pocket at the junction of the fingers and palm subdomains by displacin
209 re the tension in individual epithelial cell junctions of cells in various locations and orientations
210 us-host chimera DNA (vh-DNA), generated from junctions of hepatitis B virus (HBV) integration in the
212 NAPARK proteins, LNP1 and LNP2, at three-way junctions of the ER, the sites where different ER tubule
213 switching of tunneling current in nanoscale junctions of ultrathin CrI(3) , a natural layer antiferr
214 lmonary veins draining beyond the cavoatrial junction on transesophageal echocardiography were exclud
217 estigate other RNA systems, such as multiway junctions or pseudoknots in mixed metal ion solutions.
218 in crossover-specific processing of Holliday junctions or their precursors in meiotic chromosomes(4).
220 derm precursors in the epiblast is higher in junctions oriented in the direction of intercalation tha
221 ed in the direction of intercalation than in junctions oriented perpendicular to the direction of int
224 lated these sequences into in silico Isoform Junction Peptides, and created a customized alternative
226 oteins that target muscle, the neuromuscular junction, peripheral nerves, the spinal cord or the brai
228 arrier (BBB) integrity through loss of tight junction protein claudin-5 (cldn5) in male mice, promoti
232 invading breast cancer cells express the gap junction protein connexin-43 (Cx43), yet whether Cx43 re
233 d blood-brain barrier permeability and tight junction protein expression in the offspring at pre-wean
235 GF2BP1 interacted with the mRNA of the tight-junction protein occludin (Ocln), stabilizing Ocln mRNA
237 ll morphology and the abundance of cell-cell junction proteins were evaluated by confocal microscopy.
238 ncreased expression of the endothelial tight junction proteins ZO-1 and occludin, key mechanisms unde
239 ealed that heme primarily affected the tight junction proteins zona occludens-1, claudin-1, and claud
240 ne disease in which Abs target neuromuscular junction proteins, in particular the acetylcholine recep
241 ood-brain barrier dysfunction, loss of tight junction proteins, increased endothelial stress fibers,
242 e density, increased expression of BBB tight junction proteins, reduced brain infiltration of immunog
244 ked to the molecular behavior of the dynamic junction, quantified via fluorescence and NMR spectrosco
248 events in spindle, inflammation- and apical junction-related proteins in squamous, and extracellular
249 icting publication, we also clarify that the junction-remodelling role of Mpp5a is not specific to di
253 al stress fibers (aSFs) anchored to adherens junctions scales with cell apical area to limit larger c
255 s of the BCR can be leveraged along with the junction sequence to improve the ability to identify clo
256 to three well-known challenges in molecular junctions: series resistance of the leads, poor interfac
257 Surface ectoderm cells undergo proximal junction shortening, establishing a transitory semi-rose
258 requirement for Shrub in maintaining septate junction (SJ) integrity by transporting the claudin Mega
259 rpass the Shockley-Queisser limit for single-junction solar cell efficiency through the production of
261 depleted RNA-seq data based on back-splicing junction-spanning reads, computational tools to identify
262 are adaptive epithelial-like or filamentous junctions stabilized by N-cadherin, beta-catenin and p12
264 and their assembly into larger intercellular junction structures and discuss emerging principles that
267 orm radially symmetric, stable intercellular junctions termed immunological synapses which facilitate
269 y weakly affected expression of an exon-exon junction that tags the majority of abundant transcripts.
270 telomere sequences at the virus-subtelomere junction that were previously missed using PCR-based app
271 ely modulated by JAM-A, a component of tight junctions that acts through EPAC to up-regulate the expr
273 used as the pinning layer in magnetic tunnel junctions that form building blocks for magnetic random
274 ice became polarized and formed mature tight junctions, that the permeability of the cholangiocyte mo
280 tural and functional integration of adherens junctions, tight junctions, gap junctions (GJ), and desm
281 ognition receptors are expressed below tight junctions (TJ), strongly implicating TJ disruption as a
282 stance (~50 Omega) and an exemplary Schottky junction to top transparent conducting oxide electrode.
283 oduced in the soma and delivered through gap junctions to the germline; there it is used in fatty aci
286 role in establishing and maintaining crista junctions, tubular or slit-like structures that connect
287 a an ionic capacitive effect at the Schottky junction under the direct current modifies the space-cha
288 ar to chemical synapses, Cx36-containing gap junctions undergo activity-dependent plasticity and comp
289 in the distal esophagus or gastroesophageal junction undergoing McKeown TMIE or Ivor Lewis TMIE were
291 transport through different single-stacking junctions was approximately independent of the molecular
292 Similarly, loss of desmosomes (intercellular junctions) was seen in placental tissues from women with
293 y, many neutrophils that migrated between EC junctions were able to rejoin the blood circulation.
295 ndoplasmic reticulum (ER)-lipid droplet (LD) junctions where they mediate the directional formation o
296 ds on classical cadherin-containing adherens junctions, which link actin to the plasma membrane throu
297 ontaining the single-stranded and duplex DNA junction with the allowed extension in the 5'-to-3' pola
299 ization of field effect transistors, and p-n junctions with precise sub-mum spatial control, and a re
300 dependence of conductance in single-molecule junctions with the same building blocks, and the dominan