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1 tein, Claudin 5, and reduced S100B levels in periphery).
2 sensory input from different circuits in the periphery.
3 t homozygosity increased toward the island's periphery.
4 n the task requires attending broadly in the periphery.
5 ption factors that direct B cell fate in the periphery.
6 recursors and the fate of these cells in the periphery.
7 merozoites, MyoA was located at the parasite periphery.
8 iated transcytotic route readily used in the periphery.
9 of high-traction-stress regions at the cell periphery.
10 f responding gene loci away from the nuclear periphery.
11 and accumulation of capillaries at the tumor periphery.
12 thymic selection and egress to the lymphoid periphery.
13 ng HD-ZIPIII and KAN expression in the shoot periphery.
14 le non-repetitive sites, particularly in the periphery.
15 e optic nerve head (ONH) towards the retinal periphery.
16 bution of Ft-Ds heterodimers around the cell periphery.
17 myelinating glial cell of the CNS, into the periphery.
18 le exploration of the actin-rich growth cone periphery.
19 onfocal microcopy that localized to the cell periphery.
20 or and sensory afferents is completed in the periphery.
21 ide world is inherited by the brain from the periphery.
22 d impaired donor antigen presentation in the periphery.
23 f circuits at the interface of the brain and periphery.
24 ntrations of synthesis conditions in the arc periphery.
25 ing pain by detecting painful stimuli in the periphery.
26 activities almost exclusively in the tumour periphery.
27 r SLP-76 and actin molecules localize to the periphery.
28 mulation induced NDK recruitment to the cell periphery.
29 at escape thymic selection and end up in the periphery.
30 VD with detachment at the posterior pole and periphery.
31 perinuclear fashion, cRILP moves to the cell periphery.
32 d chromatin marginalization into the nuclear periphery.
33 he CNS, although the reverse was true in the periphery.
34 movements to receive echoes at the auditory periphery.
35 r-specific CD8(+) T cells from the tumor and periphery.
36 the post-ischemic brain originates from the periphery.
37 pain with no obvious signs of injury in the periphery.
38 ork, fostering centrosome motion to the cell periphery.
39 rs, despite their similar frequencies in the periphery.
40 al soluble tubulin concentration at the cell periphery.
41 rapid and transient ruffling of the nuclear periphery.
42 hymus and were only slightly affected in the periphery.
43 sented incomplete PVD with detachment in the periphery.
44 by preventing leukocyte trafficking from the periphery.
45 ment Sequence, targeting INO1 to the nuclear periphery.
46 ulating OT release from SON neurons into the periphery.
47 mensional snapshots of the HeLa cell nuclear periphery.
48 p tissue but not the healthy nasal mucosa or periphery.
49 functional deficiencies of Treg cells in the periphery.
50 y and functionally distinct from that of the periphery.
51 ome profiles in the brain as compared to the periphery.
52 tes that have not yet been stimulated in the periphery.
53 a, with few mitochondria present at the cell periphery.
54 d to regulate gene expression at the nuclear periphery.
55 terenol-induced ATGL translocation to the LD periphery.
56 r JIP4 results in dispersion toward the cell periphery.
57 ions and needs not rely on feedback from the periphery.
58 nucleus rather than dispersed clumps at the periphery.
59 different actin structures at the aperture's periphery.
60 ted the levels of CD4(+) Treg induced in the periphery.
61 te maintains its single mitochondrion at its periphery.
62 nction of NKT cell subsets in the thymus and periphery.
63 red to areas of nonperfusion confined to the periphery.
64 ting excitability disorders of the brain and periphery.
65 Several analogues were selective for the periphery.
66 g Abeta metabolism in both the brain and the periphery.
67 unctional responses of mature T cells in the periphery.
68 t forms at localized regions of the aperture periphery.
69 uced increment in Col-1 localization at cell peripheries.
70 ly higher in the center (0-2 mm) than in the periphery (2-10 mm) for all layers at 12 and 24 months (
71 velop novel kappa agonists restricted to the periphery, a diastereo- and enantioselective synthesis o
72 enrichment of heterochromatin in the nuclear periphery accompanied by the compaction of chromatin.
73 atterning process; yet, how signals from the periphery act to control dendritic maturation is unclear
74 ity to colonize new sites beyond their range peripheries after climate had changed at sites of occurr
75 Reticulon-1 subcellular localization to the periphery after exposure to CSF-1 for 2.5 min was shown
76 The retinal vasculature grows towards the periphery ahead of differentiated astrocytes, but behind
77 ing effects were generally larger in the far periphery and appear to be stable 12 months after traini
79 used redistribution of integrin CD49d to the periphery and cell clustering, but inhibited ERK(1/2) ac
80 undling, MT penetration into the growth cone periphery and close MT apposition to actin filaments in
81 lation improved Dox penetration in the tumor periphery and core and did not impact the distribution o
84 odulus decreases from the cell center to the periphery and from the cell rear to the front along the
85 tinal lesions were located in the mid or far periphery and had well-defined borders, resembling conge
86 nal link between localization at the nuclear periphery and heterochromatin-mediated gene silencing.
90 remains unknown whether pepcans occur in the periphery and interact with peripheral CB2 cannabinoid r
91 a VOC leads to impaired oxygen supply to the periphery and ischemia reperfusion injury, inflammation,
92 localization of myosin motors to the tunnel periphery and of adhesion complexes to the edges of aper
93 le in both intestinal Cu mobilization to the periphery and prevention of Cu over-accumulation, it is
94 ne system: Ca(2+) release starts in the cell periphery and propagates towards the cell centre by Ca(2
95 that Ki-67 organizes the mitotic chromosome periphery and recruits protein phosphatase 1 (PP1) to ch
97 accompanied by relocalization to the nuclear periphery and requires Nup2, suggesting a role for nucle
98 activation and localization of SphK1 to cell periphery and Spns2-mediated extracellular transportatio
99 esults suggest that CGRP can act in both the periphery and the brain by distinct mechanisms and that
101 f organelle-sized particles between the cell periphery and the bulk can be enhanced by dynamic deform
102 e-proglucagon (GCG peptides) act in both the periphery and the CNS to change food intake, glucose hom
103 The division plane typically has a circular periphery and the growth starts from the periphery as a
104 ng roughly a 1:1 distribution in the nuclear periphery and the intermediate regions with <15% occupyi
105 tant in regulating axonal maintenance in the periphery and the overall health and survival of sensory
106 f the important cytoskeletal proteins to the periphery and their association with the cortical actin
107 igh expression limited to tumor cells at the periphery and to CD31(+) vascular endothelium in the cor
108 ntained representations of the contralateral periphery and were selectively active for scene versus f
109 ferent immune alterations occur in brain and periphery and whether analogous mechanisms operate in th
110 nd may contribute to chronic inflammation in periphery and with immune dysfunction in the gut mucosa.
112 ted hematopoiesis in bone marrow, spleen and periphery, and augments systemic levels of hematopoiesis
114 zed in a crescent or ring away from the cell periphery, and F-actin was found in podosome-like struct
115 gic of the wiring of the taste system at the periphery, and illustrate how a labelled-line sensory ci
116 cytes subsets or numbers was observed in the periphery, and importantly no significant reactivation o
117 tribution of more F-actin fibers to the cell periphery, and promoted spreading/enlargement of transfe
118 chanisms that differ in the brain versus the periphery, and targeted inhibition of neurogenic innerva
119 target synaptic mechanisms in the vestibular periphery, and that KCNQ channel modulators might offer
120 3 in the core to the donor Coumarin 2 on the periphery, and the average distance between these two la
121 >18 x 10(6) TCRbeta sequences from the CNSs, periphery, and thymi of mice at different stages of auto
122 m where tumor cells located along the vessel periphery are able to disrupt the vessel endothelium thr
126 These observations point to the nuclear periphery as a central regulator of the aging phenotype.
127 lar periphery and the growth starts from the periphery as a membrane invagination, which grows radial
129 or-asymmetric trithiols (CD2), and (iii) the periphery-asymmetric monothiols (DB2), in which B functi
131 ears of age, all showed abnormalities at the periphery (avascular area, vessel leakage, shunts, abnor
136 e than 10 DA of nonperfusion isolated in the periphery (beyond the posterior pole), only 1 (7.7%) eye
137 al transition (EMT), cells lining the tissue periphery break up their cohesion to migrate within the
138 asticity was not induced at the level of the periphery but rather at the afferent-central neuron syna
139 selective cation channel is expressed in the periphery, but there is limited knowledge of its regulat
141 anisms by which immune-related events in the periphery can influence brain processes is essential for
144 anscribing genes such as GAL1 to the nuclear periphery, contributes to the generation of export-compe
146 the Ft-Ds bond distribution around the cell periphery defines the polarization, with greater asymmet
148 ificant genome reorganization at the nuclear periphery dominated by release of loci frequently import
149 s, our data demonstrate that spontaneous and periphery-driven activity patterns are important for the
150 Whether gene repositioning to the nuclear periphery during differentiation adds another layer of r
152 ng of the mechanisms of sensitization at the periphery during inflammation, little is known about the
153 oximately 20 Hz coherence between cortex and periphery during isometric contraction builds on the pre
154 enhancer in LADs that were released from the periphery during T-cell activation became preferentially
155 ich at the same region of the chromatin disk periphery during this window of cell division and that C
156 observed light concentration effect from the periphery dye to the central dye in one polymer structur
157 find a potent but transient response in the periphery, followed by a prolonged response in the brain
158 stribution of body heat from the core to the periphery, followed by heat loss exceeding metabolic hea
160 vels of mislocalised BEST1 expression in the periphery, from an early developmental stage, could prov
161 nt an activated subset of those found in the periphery, having a resident-memory phenotype (CD69(+)CD
162 n CD34(+) cells that HSPCs transduced in the periphery home back to the BM where they stably express
166 questration of nucleoplasmic proteins to the periphery impacts cell stemness, the response to cytotox
168 ) coronal ends and a hydrophobic (H) central periphery in a selective solvent for the terminal segmen
169 Many autoreactive B cells persist in the periphery in a state of unresponsiveness called anergy.
171 ive polarization (clustering) at the nuclear periphery in early leptotene, leading to formation of th
176 To assess how these changes at the nuclear periphery influence wider genome organization, our DamID
177 revealed, located more to the mitochondrial periphery (inner boundary membrane) than inside the cris
181 erentiation of regulatory Treg (Treg) in the periphery is critical to control inflammatory processes.
183 atification at the mixed layer base, and its periphery is stable to shear instability, suggestive of
185 oximately 20 Hz coherence between cortex and periphery is tightly linked to the presence of approxima
187 ls releases genomic regions from the nuclear periphery, leading to precocious cardiac gene expression
189 The DHA molecule is bound at the channel-periphery near the M4 helix and exerts a long-range allo
192 ains linked via polyphenolate groups on four peripheries of eclipse-arranged porphyrin macrocycles, a
193 he flat regions on top of the particles, the peripheries of the particles-which contain metal atoms w
194 and other SG-associated proteins around the peripheries of virus-encoded factories, interrupting the
198 r pores, artificial tethering to the nuclear periphery of a transcribed locus suppressed R loops in m
199 that the formation of B-N Lewis pairs at the periphery of anthracene leads to buckling of the backbon
201 opose that dynamic actomyosin tension at the periphery of collectives facilitates their movement thro
202 , in which ZO-1 binding is restricted to the periphery of GJ plaques, S365A, S365E, S368A, S368E, and
203 on LDs, consequently transporting LDs to the periphery of hepatocytes where the smooth endoplasmic re
205 BM and that immature NK cells present in the periphery of NKp46-Cre-Gata3(fl/fl) mice can rapidly exp
206 membrane, although M2 is found mostly at the periphery of regions of HA, consistent with the proposed
207 d in mature schizonts and was located at the periphery of segmenting merozoites, where it remained th
208 ional model of texture homogeneity along the periphery of skin lesion borders based on LSP is an effe
209 crease in genetic differentiation toward the periphery of species' ranges due to spatial variation in
211 ganizes so that minus ends are sorted to the periphery of the array, forming multiple nascent poles t
212 from the naphthalene diimide stations at the periphery of the axle to the central halogen bonding iod
213 se most study sites have been located on the periphery of the basin, and because interpretations can
214 se domains of C1r and C1s are located at the periphery of the C1r2s2 tetramer both when alone or with
215 icrosomal P450, but CYP4G16 localizes to the periphery of the cell and lies on the cytoplasmic side o
217 w that RSCs reside in a niche at the extreme periphery of the CMZ and divide asymmetrically along a r
218 s, the class-specific region is found at the periphery of the complex, and the plant-conserved region
222 teric site in the complex as residing at the periphery of the extracellular vestibule, interposed bet
224 ving N-S bond cleavage, and reactions on the periphery of the heteroaryl ring for late-stage diversif
226 tin nucleation promotion factor WAVE2 to the periphery of the lamellipod while suppressing polymeriza
228 Natural killer (NK) cells are located at the periphery of the lymph node, predominantly in the medull
230 that CGRP can act in both the brain and the periphery of the mouse to cause migraine-like photophobi
232 on in patients with IPF seem to start at the periphery of the pulmonary lobule and progressively exte
233 sent-day short grass prairies on the western periphery of the species' range will become favored in t
234 acentric poleward segregation occurs at the periphery of the spindle in association with interpolar
236 mpressional tectonic stress regime as in the periphery of the Tarim Basin, which explains the presenc
237 that land management practices at the upland periphery of tidal marshes can facilitate or impede ecos
238 ranslational fusion protein localized to the periphery of vegetative cells in vivo, but lost this ass
240 that SG-associated proteins localized to the periphery of virus-encoded cytoplasmic structures, terme
244 G3BP1 and relocalization of G3BP1 to the VF periphery play roles in SG disruption to facilitate MRV
245 oximately 20 Hz coherence between cortex and periphery positively correlated with the "burstiness" of
246 ol into the nucleus in cells at the meristem periphery, possibly triggering their differentiation.
250 n contrast, restricting Hdac3 to the nuclear periphery rescues myogenesis in progenitors otherwise la
251 h induces myelin autoreactive T cells in the periphery, resulted in massive immune cell recruitment i
252 slow diffusing tRNA is localized to the cell periphery (showing a 30% enrichment versus a uniform dis
254 s that has acquired through evolution in the periphery sufficient adaptation for the distinct microen
255 softer and more viscous response towards the periphery, suggesting a reduced degree of crosslinking o
256 MA), a CAF marker, were located on the tumor periphery surrounding collectively invading tumor cells
258 uman IL-6 not only enhanced thymopoiesis and periphery T-cell engraftment, but also significantly inc
259 ar pigment changes were less frequent in the periphery than in the posterior pole (46% vs. 76%) and n
260 cellular substrate at the vestibular sensory periphery that is activated by electrical currents, as w
261 ) is associated with changes to the auditory periphery that raise sensory thresholds and alter coding
262 ) is associated with changes to the auditory periphery that raise sensory thresholds and alter coding
264 pathological retinal vessels in the retinal periphery that were obscured in the fluorescein angiogra
265 he densely urbanized core and the more rural periphery, that respond differentially to flooding.
268 germinal center B cells and plasmablasts in periphery, they produced significantly reduced numbers o
269 r materials between the nucleus and the cell periphery; this transport is critical for the survival a
270 hy and contraction of NK cell numbers in the periphery through a modulated expression of SOCS3, where
272 L genes in yeast are targeted to the nuclear periphery through interaction with the nuclear pore comp
273 ting metabolic and hormonal signals from the periphery to balance food consumption and energy expendi
274 stimuli, including painful stimuli, from the periphery to central sensory and pain-processing centers
276 i were briefly presented on the visual-field periphery to experimental participants whose attention w
278 s a pathway in spinal cord that ascends from periphery to mesolimbic reward circuits (spino-mesolimbi
280 tinal ganglion cell density from the retinal periphery to the center of acute vision-fovea) would acc
283 i) excited-state energy from the ZnPs at the periphery to the H2P, (ii) electrons to C60, and (iii) h
284 exosome transfer by lymphatic flow from the periphery to the lymph node could provide a mechanism fo
285 ole], zone 2 [midperiphery], and zone 3 [far periphery]) to document the presence of peripheral lesio
287 s were observed to deplete Treg cells in the periphery, upregulation of the inhibitory Fc gamma recep
288 Tr1 cells have the ability to migrate to the periphery via a variety of chemokine receptors such as C
289 nhibition from other ON parasol cells in the periphery, via the electrically coupled amacrine cell ne
290 ort of incoming viral capsids to the nuclear periphery was unaffected by the cholesterol reduction, s
291 romosome segregation takes place at the cell periphery where half of the chromosomes are expelled int
292 produced the greatest tractions at the cell periphery, where distinct types of actin-based membrane
293 re sufficient to localize to the erythrocyte periphery, where key virulence-related modifications to
294 Active Rac1 was mainly localized to the cell periphery, whereas active Rac2 was distributed throughou
295 ity of eyes with AMD in both the mid and far periphery, whereas pigment changes and features of advan
296 This may be because of the absence of the periphery, which associates with chromosomes only after
297 elial cell lipid signatures from the CNS and periphery, which underlie a suppression of caveolae vesi
298 bited similar defective phenotypes as in the periphery with abnormal exit of SGNs from the Rosenthal'
299 pa agonist (EC50 = 1.8 nM) selective for the periphery with dose-dependent anti-inflammatory activity
300 mechanics of all MTs, the PNC, and the cell periphery with each other through their hydrodynamic int
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