コーパス検索結果 (left1)
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 OEC cultures were successfully generated from a similar
2 OECs attenuated immune cell infiltration, reduced second
3 OECs demonstrate a TLR-response profile similar to that
4 OECs from T1D participants are TLR-hyper-responsive, due
5 OECs have a unique response to P. gingivalis LPS, where
6 OECs may be used for further phenotypic, genetic, and fu
7 OECs proliferated in injection sites, cell tracts, and l
8 OECs showed a dramatic ability to rapidly change shape,
9 OECs transplanted into transected peripheral nerve have
10 OECs, but not FBs, intermingled with astrocytes, facilit
11 more (NS) and nvAMD 32-times more (P < 0.05) OECs on expansion of clusters than did non-AMD/low-risk
12 peared to be expressed in GFAP(-)/RALDH 1(-) OECs as well as in unidentified structures in the LP.
14 he applied cell suspension consisted of >98% OECs, 2) that the majority of the cells expressed the tr
15 rall improvement in locomotor function after OEC transplantation, measured using the Basso, Beattie,
16 nd share many properties in common, although OECs appear to be a better candidate for transplantation
20 re can be applied to human studies, where an OEC can be analyzed in light of an individual's entire g
21 orescent protein-labeled fibroblast (FB) and OEC transplants acutely after a complete low-thoracic sp
22 pha1 was expressed in immature OSN axons and OECs of the nerve layer, as well as mitral and tufted ce
25 referentially extend into the cell tract and OECs failed to support bridging of corticospinal axons.
26 SN axon bundles were enlarged and associated OECs increased, indicating impaired migration of OECs an
27 nstrated that immune suppression can augment OEC contact-mediated protection of axons and neurons dur
28 ively links the OER activity of the Ni-based OECs with the generation of those sites on the surface o
29 tain catalytically active phases in Ni-based OECs, in addition to the key role of the Fe impurities.
30 d to a deprotonation process of the Ni-based OECs, leading to the formation of the negatively charged
31 aracterization of two Fe-containing Ni-based OECs, namely nickel borate (Ni(Fe)-B(i)) and nickel oxyh
33 reduces interface recombination at the BiVO4/OEC junction while creating a more favorable Helmholtz l
34 lvaging ischemic murine limbs, whereas bolus OEC delivery was ineffective in preventing toe necrosis
35 neration of negatively charged sites in both OECs (NiOO(-)), which can be described as adsorbed "acti
37 sorption spectroscopy results show that both OECs are chemically similar, and that the borate anions
42 While the repertoire of TLRs expressed by OECs is similar to that expressed by macrophages (M), th
44 We investigated the onset of phagocytosis by OECs in the developing mouse olfactory system by utilizi
45 modelling (reduction) of HS 6-O-sulfation by OECs, compared with SCs, to suppress boundary formation.
46 ing two different oxygen evolution catalyst (OEC) layers, FeOOH and NiOOH, which reduces interface re
47 hotoanode with an oxygen evolution catalyst (OEC) to increase the photocurrent and reduce the onset p
50 ection model and olfactory ensheathing cell (OEC) or fibroblast (FB; control) transplantation as a re
52 eficial therapy, olfactory ensheathing cell (OEC) transplantation, results in functional improvements
54 n with cultured olfactory ensheathing cells (OEC) into the lesion cavity 6 weeks after contusion inju
55 rd migration of outgrowth endothelial cells (OECs) have been delineated, and a material incorporating
56 ure of 50% p75+ olfactory ensheathing cells (OECs) and fibroblasts derived from the outer layers of t
59 Transplants of olfactory ensheathing cells (OECs) cultured from the olfactory bulb are able to induc
64 infected human olfactory ensheathing cells (OECs) in vitro and measured bacterial invasion and the c
65 nsplantation of olfactory ensheathing cells (OECs) into injured spinal cord results in improved funct
67 flux pathway in olfactory ensheathing cells (OECs) was performed using Indo-1 calcium microfluorometr
69 (SCs), but not olfactory ensheathing cells (OECs), form a boundary with astrocytes, due to a SC-spec
70 al culturing of olfactory ensheathing cells (OECs), which can be used to understand how OECs interact
72 donor rats [GFP-olfactory ensheathing cells (OECs)] into a region of spinal cord demyelination and fo
74 riodontium, including oral epithelial cells (OECs), express innate immune receptors, including TLRs.
75 atalyst found in the oxygen evolving center (OEC) in photosystem II, nanostructured manganese oxide s
80 ity is oxidized to produce the well-known Co-OEC heterogeneous cobaltate catalyst, which is an active
81 n isotopologues produced by (18)O-labeled Co-OEC in H2(16)O reveals that water splitting catalysis pr
85 orce microscopy reveal that nucleation of Co-OEC is progressive and reaches a saturation surface cove
89 em and the high-valent active site of the Co-OEC, with specific emphasis on the manifestation of a do
93 e properties of the oxygen-evolving complex (OEC) and the structure of the Mn(4)Ca cluster in Photosy
96 is the case for the oxygen evolving complex (OEC) in photosystem II (PSII), where we have studied whe
100 down turnover of the O(2)-evolving complex (OEC) is a plausible approach to gain mechanistic informa
102 water oxidation at the O2-evolving complex (OEC) of photosystem II (PSII) is a complex process invol
104 5)Ca cluster of the oxygen-evolving complex (OEC) of Photosystem II (PSII) poised in the S(2) state w
105 binding site of the oxygen evolving complex (OEC) of photosystem II (PSII) to the paramagnetic Mn clu
109 otif present in the oxygen-evolving complex (OEC) of photosystem II and in water-oxidizing Mn/Ca laye
111 etic organisms, the oxygen-evolving complex (OEC) of photosystem II generates dioxygen from water usi
112 ry synthesis of the oxygen-evolving complex (OEC) of photosystem II has been the objective of synthet
113 hough the {CaMn4O5} oxygen evolving complex (OEC) of photosystem II is a major paradigm for water oxi
114 lly relevant to the oxygen-evolving complex (OEC) of photosystem II were prepared and characterized.
115 d reactivity of the oxygen-evolving complex (OEC) of photosystem II, a low-symmetry Mn4CaOn cluster.
116 ional models of the oxygen evolving complex (OEC) of photosystem II, we report the synthesis of site-
118 n this process, the oxygen-evolving complex (OEC) of PSII cycles through five states, S0 to S4, in wh
119 ere assigned to the oxygen-evolving complex (OEC) tetramanganese cluster (Em = 0.2 V vs NHE), quinone
120 takes place in the oxygen-evolving complex (OEC) that is comprised of a tetranuclear manganese clust
121 anganese-containing oxygen evolving complex (OEC) to the oxidized primary electron-donor chlorophyll
123 occurs at the PSII oxygen-evolving complex (OEC), which contains a tetranuclear manganese (Mn) clust
124 on reactions at the oxygen-evolving complex (OEC), which is composed of four manganese ions and one c
131 tosystem II (PS II) oxygen-evolving complex (OEC): a multiprotein assembly embedded in the thylakoid
132 mbrane-protruding oxygen-evolving complexes (OECs) associated with photosystem II (PSII) on spinach (
135 e used floating liquid marbles to co-culture OECs with Schwann cells and astrocytes which formed natu
136 he injured olfactory pathway and of cultured OECs identified 102 genes that were subsequently functio
137 rous simultaneous oxygen equilibrium curves (OECs) can be obtained under truly identical conditions f
138 ate that from early in embryonic development OECs are the primary phagocytic cells of the primary olf
145 tes give optimal improvement if targeted for OEC deposition, and whether sites catalysing water oxida
148 in addition to forming myelin, engrafted GFP-OECs provide an environment that supports the developmen
149 nd accordingly suggest a reassessment in how OEC activities of different catalysts are compared and r
150 This protocol can be used to determine how OECs and other cell types associate and interact while f
153 timicrobial program to be described in human OECs and establishes the extensive transcriptional defen
154 -hyper-inflammatory phenotype, primary human OECs from individuals with T1D and diabetes-free individ
155 to play two ostensibly antagonistic roles in OEC activity: as a promulgator of catalyst activity by e
156 To interrogate the role of the IL-17R in OECs, we generated mice with conditional deletion of IL-
157 a network of signaling pathways activated in OECs following infection involving a novel group of 378
158 ess this issue, cell populations enriched in OECs were isolated from the olfactory bulbs of adult gre
159 tive siRNA-mediated knockdown of 16 genes in OECs (ADAMTS1, BM385941, FZD1, GFRA1, LEPRE1, NCAM1, NID
163 d with OECs, and siRNA reduction of Sulfs in OECs was, in itself, sufficient to induce boundary forma
165 rated significantly higher number of initial OEC clusters and expansion potential of OECs in patients
169 T lesion paradigm to examine whether mucosal OEC preparations can provide a similar repair to those f
171 strocytes, we demonstrated that SCs, but not OECs, secrete a heat labile factor(s) that inhibits olig
172 d conditions; and observed for appearance of OEC clusters and growth characteristics on expansion.
174 ogic approach, (i) to assess the efficacy of OEC transplantation on locomotor recovery after traumati
176 risk dry AMD had a 5.6-fold higher number of OEC clusters per 20 mL blood, and subjects with nvAMD ha
177 ignificant correlation between the number of OEC clusters, expanded OECs and levels of KDR was demons
179 e mucosal cell cultures contained only 5% of OECs and a conversely much larger proportion of fibrobla
180 es from mucosal samples yielded around 5% of OECs compared with the 50% obtained from samples culture
182 functionally characterized in cocultures of OECs and primary dorsal root ganglion (DRG) neurons.
183 lly, material deployment of a combination of OECs with another cell population commonly isolated from
184 ttle is known of the detailed integration of OECs at the transplantation site in peripheral nerve.
187 tial OEC clusters and expansion potential of OECs in patients at risk for or already affected by nvAM
188 These results suggest that presentation of OECs at the time of nerve injury enhances regeneration a
189 concept that the regenerative properties of OECs are profoundly influenced by the cells with which t
196 enhanced survival of OECs and FBs, but only OEC transplantation promoted scaffold formation in the l
201 3 reaction center protein (CP43) in the PSII-OEC extrinsic domains of grana membranes under condition
203 ide analysis of HS in SC-conditioned and rat OEC-conditioned media showed that SCs secrete more highl
204 Reporter TOPGAL mice demonstrated that some OECs located in the inner olfactory nerve layer can resp
208 ll tracts, and lesion sites, indicating that OECs can also accumulate through cell proliferation.
214 sis of amino acid residues in and around the OEC has identified residue 87 in the D1 subunit as the o
215 gen bonds to water form a network around the OEC; this network is predicted to involve multiple pepti
217 is study, we have used NH 2OH to destroy the OEC, which would release any tightly bound bicarbonate i
218 atory cap" model of PS II, which follows the OEC-33 kDa-23 kDa-17 kDa binding order, as these results
220 the X-ray absorption data with those for the OEC reveal 1 to possess structural parameters that make
225 ctural changes of the Mn4CaO5 cluster in the OEC during the S state transitions using x-ray absorptio
227 roposals that one function of calcium in the OEC is to modulate the reduction potential of the cluste
228 o the geometry of the Mn4CaO5 cluster in the OEC obtained from a polarized XAS model and the 1.9-A hi
238 mber of manipulations which may increase the OEC content and the effectiveness of mucosal preparation
240 ore amino acid residues that reside near the OEC active site on the D1 and CP43 intrinsic subunits of
241 ith more structurally accurate models of the OEC ([MMn3O4]) suggest a general relationship between th
245 AgO4 cluster that models the topology of the OEC by displaying both a cubane motif and a "dangler" tr
250 re elucidation of both the structures of the OEC in the different S-states and the binding of the two
251 t a range of DFT optimized structures of the OEC may all be considered consistent with experimental E
253 genome-wide transcriptomic profiling of the OEC response by RNA-Seq revealed a network of signaling
255 s study we address whether the purity of the OEC transplant affects their ability to remyelinate.
257 Q-band CW ENDOR from the S(2) state of the OEC was obtained following multihour (17)O exchange, whi
259 rly useful to establish the structure of the OEC, consistently with high-resolution spectroscopic dat
260 rt recent proposals for the mechanism of the OEC, involving oxido migration between distinct position
271 ded invaluable structural information on the OEC and show that it comprises a [Mn(3)CaO(4)] distorted
277 is consistent with the observation that the OEC is functional only with one of these two metals.
278 2 as the protonation sites, analogous to the OEC in PS-II of the natural water oxidation system; the
279 rbonate is bound sufficiently tightly to the OEC that it cannot readily exchange with bicarbonate in
280 te ion does not bind reversibly close to the OEC, but it remains possible that bicarbonate is bound s
294 ges were often present in close proximity to OECs but they contributed only a minor role to clearing
295 These results indicate that transplanted OECs extensively integrate into transected peripheral ne
300 provide evidence for the advantages of using OECs, and not mature SCs, for transplant-mediated repair
301 gnificantly lower level by SCs compared with OECs, and siRNA reduction of Sulfs in OECs was, in itsel
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。