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1 specific time of expression, tissue type and subcellular compartment.
2 ponsible for the trafficking of TLR9 to this subcellular compartment.
3  protein activation/signaling occurs in this subcellular compartment.
4 ular effectors that act to organize a unique subcellular compartment.
5 dling it must be targeted to the appropriate subcellular compartment.
6  protein-protein interaction network of this subcellular compartment.
7 Drosophila cells where they reside in the ER subcellular compartment.
8 ing protein abundance, stress condition, and subcellular compartment.
9 g developmental signaling from a specialized subcellular compartment.
10 y when both proteins are present in the same subcellular compartment.
11 te composed of vesicles bound within a novel subcellular compartment.
12  and these pathways are specialized for each subcellular compartment.
13 ut methods for mapping the transcriptomes of subcellular compartments.
14 as mainly expressed in nucleus and nucleolus subcellular compartments.
15 ss cellular and viral substrates in distinct subcellular compartments.
16 s of CARS datasets was used to visualize the subcellular compartments.
17 ecific regulation of translation in specific subcellular compartments.
18 apoptotic bodies, originating from different subcellular compartments.
19  enzyme catalyzes different reactions in two subcellular compartments.
20 rget and deliver agents to organs, cells and subcellular compartments.
21 a membrane, resulting in Gag accumulation in subcellular compartments.
22 stabilized in both nuclear and mitochondrial subcellular compartments.
23 rison with marker proteins resident to these subcellular compartments.
24 rted localization of TOR to several distinct subcellular compartments.
25 ruitment to, and function at, various muscle subcellular compartments.
26 asma membrane (PM) are unique yet ubiquitous subcellular compartments.
27 ts and aggregation-prone proteins to diverse subcellular compartments.
28 ficking to signaling microdomains in various subcellular compartments.
29 ein kinase II (CaMKII) signaling in specific subcellular compartments.
30 nate action of multiple pathways in multiple subcellular compartments.
31 oted Hsp90 migration from cytosol into other subcellular compartments.
32 production of reactive oxygen species within subcellular compartments.
33 be targeted genetically to the cytosol or to subcellular compartments.
34 er, unclear how FAK activity is regulated at subcellular compartments.
35 eproducible proteome coverage discriminating subcellular compartments.
36 stent infection within host membrane-derived subcellular compartments.
37 rganelles in redistributing proteins between subcellular compartments.
38  membrane receptors and proteins moving into subcellular compartments.
39 olling the activity of proteins in different subcellular compartments.
40 uronal signaling and may occur within single subcellular compartments.
41 ed in cells, but orchestrated in specialized subcellular compartments.
42 yed by type III effectors to target specific subcellular compartments.
43 rential regulation of calcium signals across subcellular compartments.
44 rons display patterns restricted to specific subcellular compartments.
45 ter suited for study of relatively oxidizing subcellular compartments.
46 es in the thiol/disulfide equilibrium within subcellular compartments.
47 high basal activity, is targeted to specific subcellular compartments.
48 localization of Nox isoforms within specific subcellular compartments.
49 ep-wise process that takes place in multiple subcellular compartments.
50      We engineered SPIONs targeting distinct subcellular compartments.
51  windows, either on the same or on different subcellular compartments.
52  eIF4F and concentrates them within discrete subcellular compartments.
53 depends primarily on channel distribution in subcellular compartments.
54 different subtypes are targeted to different subcellular compartments.
55  48 h, resulting in p53 and HDM2 in distinct subcellular compartments.
56 sm, but also in the nucleus as well as other subcellular compartments.
57 microsomal TG but a reduction in TG in other subcellular compartments.
58 ernal transformation controls and markers of subcellular compartments.
59 us exosome subunits are enriched in discrete subcellular compartments.
60 f any, metabolite exchange between these two subcellular compartments.
61 er and release of the products into distinct subcellular compartments.
62 prises analyses of the proteomic networks in subcellular compartments.
63 rating the S limitation response in multiple subcellular compartments.
64  the plant cell, where they target different subcellular compartments.
65 ts that targeted PTEN protein into different subcellular compartments.
66 es in finetuning CaMKII signaling in defined subcellular compartments.
67 overn the assembly and architecture of these subcellular compartments.
68 22 to direct cargo specifically to different subcellular compartments.
69 s are present, which are targeted to various subcellular compartments.
70 splaying enzyme and pathway locations within subcellular compartments.
71 , and that serve the functions of individual subcellular compartments.
72 ntents of sphingomyelin (SM) and ceramide in subcellular compartments.
73 the determinants of S-nitrosothiol levels in subcellular compartments.
74 ins are differentially distributed to unique subcellular compartments.
75 n of targeting Top3beta to critical sites in subcellular compartments.
76 tes membrane traffic to control flux through subcellular compartments.
77 found a large fraction of them localising to subcellular compartments.
78 al cells are highly organized, with numerous subcellular compartments.
79 tly monitoring free NAD(+) concentrations in subcellular compartments.
80 ades to be activated selectively in specific subcellular compartments.
81 inct, with intrinsic preference for specific subcellular compartments.
82 phenotypes in a targeted manner in different subcellular compartments.
83 ir GTP-dependent switch regions, to distinct subcellular compartments.
84 olling the activity of proteins in different subcellular compartments.
85 tes granule cell depolarization within local subcellular compartments.
86 dual astrocytes display diverse signaling in subcellular compartments.
87 y using clickable HaloTag ligands in various subcellular compartments.
88 ing within minutes of heat shock in multiple subcellular compartments.
89 intersecting pathways spread across multiple subcellular compartments.
90 h additional domains or targeted to distinct subcellular compartments.
91 s to mediate uptake or release from cells or subcellular compartments.
92 r gD (HPV-gD) constructs to target different subcellular compartments.
93 ovide information about the contributions of subcellular compartments.
94  modulation of circadian outputs in distinct subcellular compartments.
95 multaneously measure these key components in subcellular compartments.
96 de dismutases (Fe-SODs) located in different subcellular compartments.
97 intersecting pathways spread across multiple subcellular compartments.
98 sduction by several PRR families at distinct subcellular compartments.
99 -dependent modification of dendritic spines, subcellular compartments accommodating postsynaptic spec
100 r data identify the septal pore as a complex subcellular compartment and focal point for the assembly
101 st carcinomas to assess its association with subcellular compartment and prognostic factors using Fis
102                  Thus, communication between subcellular compartments and across different cells and
103  and CD151 occur dynamically within discrete subcellular compartments and act to establish local GTPa
104         gPAPP and Bpnt1 localize to distinct subcellular compartments and are members of a conserved
105 leavage products, which localize to distinct subcellular compartments and are not structurally homolo
106 xtracellular vesicles originate from diverse subcellular compartments and are released in the extrace
107 e ways to maintain proteome integrity across subcellular compartments and between tissues to ensure a
108 ion receptors (PRRs) that reside in specific subcellular compartments and can bind pathogen-associate
109 uding the redistribution of phospholipids to subcellular compartments and delivering sterols to the m
110 mechanisms that move these receptors between subcellular compartments and domains must operate on ind
111 by specific biochemical pathways in distinct subcellular compartments and execute distinct functions.
112              These are targeted to different subcellular compartments and expressed in different orga
113                                Bacteria lack subcellular compartments and harbor a single RNA polymer
114 e signaling pathways, coordinated by several subcellular compartments and interactions between these
115 ed to assess the expression of RS in various subcellular compartments and its fractionation into solu
116 rgeting of different Kv channels to specific subcellular compartments and local translation of Kv cha
117 e applied to the molecular analysis of other subcellular compartments and macromolecules.
118 tively in multiple fly tissues for different subcellular compartments and maps the mitochondrial matr
119 ibody penetration for detecting molecules at subcellular compartments and membrane microdomains.
120             Our results from purification of subcellular compartments and proteomic studies show that
121 e storage of protein/peptide hormones within subcellular compartments and subsequent release are cruc
122 at sorafenib activates GSK-3beta in multiple subcellular compartments and that this activation underm
123 are transport reactions interconnecting nine subcellular compartments and the environment.
124 uire localization to endosomal and lysosomal subcellular compartments and their acidic pHs.
125 an serve as a drug carrier in both cells and subcellular compartments and, as such, can facilitate vi
126 re is in different neuronal types, different subcellular compartments, and across different animal sp
127 rugs enter cells, are distributed to various subcellular compartments, and are exported from cells vi
128  peripheral cytoplasmic proteins to specific subcellular compartments, and as endogenous factors for
129 ll type-specific expression, localization to subcellular compartments, and association with human dis
130 ilities of individual polysomes in different subcellular compartments, and detect 3' UTR-dependent lo
131 nd quantity of hemoproteins found in several subcellular compartments, and reduction of ABCB6 functio
132                 Primary cilia are restricted subcellular compartments, and specialized mechanisms coo
133 ls or metabolites between plastids and other subcellular compartments, and that stromules are induced
134 pe while avoiding biases caused by ancillary subcellular compartments are highly desirable.
135                   The cAMP dynamics in these subcellular compartments are ill-defined.
136 and protein-nucleic acid interactions within subcellular compartments are required for viral genome r
137 omes of many additional species, tissues and subcellular compartments are sequenced, particularly in
138 ations in NAD(+) concentrations within these subcellular compartments are thought to regulate the act
139 B is searchable by keyword, protein name and subcellular compartment, as well as by identifiers from
140 at PARP12 can alternate between two distinct subcellular compartments associated to two distinct cell
141  orchestrate signaling activity in different subcellular compartments at different timescales.
142 ed to a multitude of effectors into distinct subcellular compartments because of their multidomain ar
143 nding partners for isoforms that localize to subcellular compartments beyond the NE.
144 distinctive distributions of proteins within subcellular compartments both at steady state and during
145  different functions and to act at different subcellular compartments, but in such an intertwined way
146 stin-2, and fibrocystin) localize to various subcellular compartments, but their functional site is t
147 hout the neuron, but are confined to various subcellular compartments by anchoring molecules such as
148 , and even profiling of lipids in individual subcellular compartments by direct-organelle MS.
149      Some effectors have been found to enter subcellular compartments by mimicking host targeting seq
150         SLE-ICs transiently colocalized to a subcellular compartment containing CD32 and TLR9, and CD
151  identified TGases associated with different subcellular compartments (cytosol, membranes, and cell w
152            These data suggest cell type- and subcellular compartment-dependent differences in GRK/arr
153 c acid (K1 antigen) occur within a protected subcellular compartment designated the sialisome.
154      These data demonstrate that allelic and subcellular compartment differences can regulate the pot
155 o-defense signals into the nucleus and other subcellular compartments during immunity.
156 inding proteins that relocate from different subcellular compartments during stress.
157 he flow of molecular information to distinct subcellular compartments during the induction of activit
158  and used in toto by hemoproteins in all six subcellular compartments examined.
159  highlight the plasma membrane as a critical subcellular compartment for Hippo signal transduction.
160                    The nucleus is a critical subcellular compartment for the pathogenesis of polyglut
161                              Prokaryotes use subcellular compartments for a variety of purposes.
162  cell-autonomous defense programs to monitor subcellular compartments for infection and to evoke coun
163 ggest that plastids and mitochondria are key subcellular compartments for the synthesis of ubiquitous
164 he distribution of essential metal ions over subcellular compartments for use as cofactors requires c
165 nt cells are critical for the positioning of subcellular compartments, for coordinating intercellular
166 he use of strong oxidizing denaturants or of subcellular compartments from C. elegans has, however, b
167 ed to the isolation of various organelles or subcellular compartments from transformable organisms ot
168 localization of COPS5 and RanBP9 in the same subcellular compartments further supported the interacti
169  the intervening cytoplasm between these two subcellular compartments has not been determined.
170 allow the control of protein traffic between subcellular compartments have been valuable in elucidati
171                                              Subcellular compartments have unique protein composition
172 nal delivery of intact drug into the desired subcellular compartment, however, it is critical that th
173           The dynamics of PA in cells and in subcellular compartments, however, remains an open quest
174 r (AR) was found to localize to a lipid raft subcellular compartment in LNCaP prostate cancer cells.
175                                 Because each subcellular compartment in plants contains its own set o
176 heir intended substrates regardless of which subcellular compartment in the target cell they happen t
177 Here we studied the activation mechanism and subcellular compartment in which CTSB regulates protease
178                    PfA-M1 is abundant in two subcellular compartments in asexual intraerythrocytic pa
179 We find that MtDef4 is targeted to different subcellular compartments in each fungus.
180  and oligomerization states within different subcellular compartments in live cells.
181 in the targeting of their cargos to specific subcellular compartments in neurons.
182 oxia induces redox changes that differ among subcellular compartments in pulmonary (PASMCs) and syste
183 ontribution and specificity of each of these subcellular compartments in removing N-terminal amino ac
184 s, we discovered that TXNIP shuttles between subcellular compartments in response to oxidative stress
185  channels are expressed in multiple neuronal subcellular compartments in the cortex, where they have
186 l EC-SMC model is modified to include MPs as subcellular compartments in the EC.
187 ications, as well as for the construction of subcellular compartments in the field of synthetic biolo
188 onsible for both targeting the holoenzyme to subcellular compartments in the muscle and directing PP1
189 ed by multiple pathways located in different subcellular compartments in yeast.
190 lar protoporphyria cause damage to different subcellular compartments, in a light-triggered manner.
191 l death, which include activities at diverse subcellular compartments, including death receptor regul
192 tive features of protein organization within subcellular compartments, including the existence of pro
193  APEX-RIP can isolate RNAs from a variety of subcellular compartments, including the mitochondrial ma
194                CAPN3 is localized to several subcellular compartments, including triads, where it pla
195 ng by a modified PageRank algorithm based on subcellular compartments information, with the ranking b
196 ian LAAO targeted to lysosomes, an important subcellular compartment involved in Ag processing.
197 suggesting that sequestration of RNA to this subcellular compartment is both necessary and sufficient
198         Targeting of proteins to appropriate subcellular compartments is a crucial process in all liv
199 rget-specific tracing of proteins in various subcellular compartments is demonstrated, culminating in
200 nents that regulate MPF activity in distinct subcellular compartments is essential for their function
201 rks may be spatially arranged in specialized subcellular compartments is not often considered in path
202 ence of atypical nucleic acids in particular subcellular compartments is used by the body to detect v
203 e expression within each of the thousands of subcellular compartments made by a neuron, thereby vastl
204 nes and the rAAV vector DNA in two different subcellular compartments, made possible by using cytopla
205   A suite of targeted proteomics markers for subcellular compartment markers was developed, enabling
206 olecules such as NDGA that target a specific subcellular compartment may be beneficial in the inhibit
207       Antioxidant therapies that target this subcellular compartment may prove promising.
208 drites of nRT neurones indicate that various subcellular compartments may exhibit different membrane
209 ization of ubiquitin ligases within distinct subcellular compartments may facilitate neuronal respons
210  signaling networks are targeted to specific subcellular compartments, may generate effective antican
211  of many therapeutic agents are localized in subcellular compartments, modulation of nanoparticle-cel
212                 Specific ion conductances in subcellular compartments must also be controlled to bypa
213 gh such systems have been identified in most subcellular compartments, none have been found in the nu
214                  Nol12 is found in different subcellular compartments-nucleoli, where it associates w
215                         LOCtree predicts the subcellular compartment of a protein by mimicking the me
216                        Predicting the native subcellular compartment of a protein is an important ste
217 from the lysosomal to the zymogen-containing subcellular compartment of acinar cells and activation o
218 nerates EM contrast on a specific protein or subcellular compartment of interest.
219 pproaches for Ag delivery to the appropriate subcellular compartments of APCs and the optimization of
220 cets that guides the overall organization of subcellular compartments of cells and tissues through th
221               To identify mRNAs localized in subcellular compartments of developing neurons, we took
222 easure both voltage and calcium signals from subcellular compartments of genetically defined intercon
223  is to investigate molecular interactions in subcellular compartments of living cells to overcome the
224  preclude the accurate imaging of many small subcellular compartments of neurons.
225 c integration of an H2O2 sensor expressed in subcellular compartments of P. falciparum provides the b
226 tion of major signaling proteins between the subcellular compartments of photoreceptors.
227 BP1) and ribosomes to beta-actin mRNA within subcellular compartments of primary fibroblasts and neur
228  properties and target their innervations to subcellular compartments of principal neurons.
229 cone arrestin was distributed throughout the subcellular compartments of the cone cells.
230 redistribution of Grb14 among the individual subcellular compartments of the retinal rod photorecepto
231  important for the correct organization of a subcellular compartment or organelle such as the stalk.
232 published Arabidopsis proteome datasets from subcellular compartments or organs are stored in PPDB an
233 isms that control HCN channel trafficking to subcellular compartments or that regulate their surface
234 egregation of pathway components in specific subcellular compartments, or both.
235 on patterns of KCNQ1, KCNE1, and markers for subcellular compartments/organelles using immunofluoresc
236  unique capabilities to localize to distinct subcellular compartments, organize the actin cytoskeleto
237     In particular, it is unknown within what subcellular compartment pathogenic Htt acts and whether
238 p in proteins that reside in virtually every subcellular compartment performing diverse biological fu
239 nteracting with the FUS protein in different subcellular compartments play a fundamental role in dete
240 regulation pathways are engaged in different subcellular compartments; proteasomal degradation occurs
241                 The localization of mRNAs to subcellular compartments provides a mechanism for regula
242 entify unrecognized constituents of distinct subcellular compartments refractory to biochemical isola
243 ent of nanomedicines for precise delivery to subcellular compartments remain formidable challenges.
244 that the size of the axon initial segment, a subcellular compartment responsible for initiating actio
245 localized to specific neuronal cell types or subcellular compartments, resulting in discrete patterns
246 P2 effectors, that target PIPKIs to discrete subcellular compartments, resulting in the spatial and t
247  RCC, internalize, and reach the appropriate subcellular compartment(s) for drug release and tumor ce
248 y of signaling molecules in a cell type- and subcellular compartment-specific manner.
249                               In eukaryotes, subcellular compartments such as mitochondria, the endop
250 hat some GPCRs are also localized to various subcellular compartments such as the nucleus where they
251 n more than 40 cellular processes in various subcellular compartments, such as Ca(2+) storage and pro
252 ent from the biogenesis of proteins of other subcellular compartments, such as mitochondria and chlor
253 rent TGase isoforms were present in distinct subcellular compartments, suggesting either different ro
254 d that each isoform is located in a specific subcellular compartment: TbAK1 is exclusively found in t
255  We identified cells with an autofluorescent subcellular compartment that exclusively showed CSC feat
256 to the trans-Golgi network/early endosome, a subcellular compartment that is not previously known to
257 dy, we identified additional populations and subcellular compartments that are likely to sustain high
258 ells are organized into a complex network of subcellular compartments that are specialized for variou
259 distributions of activity among the cells or subcellular compartments that comprise the tissue elemen
260 conduct sodium action potentials in distinct subcellular compartments that differ architecturally and
261 l cells, but they are localized to different subcellular compartments that do not appear to overlap w
262 interacting signalling molecules to generate subcellular compartments that may be important for effic
263 aldehyde dehydrogenase expressed in multiple subcellular compartments that protects against hyperosmo
264  globally expressed complements of the three subcellular compartments (the cell wall, membrane, and c
265 e interspersed with another regularly spaced subcellular compartment, the carboxysome.
266 ly, StoA function is required in yet another subcellular compartment: the intermembrane space that se
267  protein changes were observed mainly in two subcellular compartments: the cardiac contractile appara
268 aled that Mi-1.2 localizes at three distinct subcellular compartments: the plasma membrane, cytoplasm
269                   When used to predict seven subcellular compartments through a 5-fold cross-validati
270 h cells can scale up a specific, specialized subcellular compartment to alter function during differe
271 e appropriate amounts of Pi to each cell and subcellular compartment to sustain essential metabolic a
272 al excitability and are targeted to specific subcellular compartments to carry out their unique funct
273 piratory metabolism, and the contribution of subcellular compartments to iron storage and mobilizatio
274 ns, which interact at a systems level across subcellular compartments to modulate flux through nonfer
275 hosphorylate specific substrates in discrete subcellular compartments to modulate many cellular proce
276   Our data suggest that PDI is released from subcellular compartments to the cytosol and translocated
277 re key to much of metabolic regulation, from subcellular compartments to whole body energy control an
278                   Transcriptomic analysis of subcellular compartments uncovered a global role for Mbn
279              Multiple proteins from multiple subcellular compartments underwent microbiota-associated
280 binant histidine-tagged proteins in distinct subcellular compartments using cell-penetrating multival
281             Proteins segregate into discrete subcellular compartments via a variety of mechanisms, in
282 P)HX repair system that is directed to three subcellular compartments via the use of alternative tran
283  of p-proteins across cellular functions and subcellular compartments was determined and showed overr
284  that the distribution of TGase in different subcellular compartments was regulated by both membrane
285 metric H(2)O(2) sensor targeted to different subcellular compartments, we demonstrate specific produc
286 cally targeting the PRIME ligase to specific subcellular compartments, we were able to selectively la
287 h cytosolic targets and targets localized in subcellular compartments were investigated.
288 killed M. tuberculosis were homogenized, and subcellular compartments were separated on Percoll densi
289 ADs are retrotranslocated into extra-luminal subcellular compartments, where Nrf1 is deglycosylated t
290 or proteins, which can localize to different subcellular compartments, where they bring together key
291 o GTPases is their association with distinct subcellular compartments, which is dictated in part by t
292                                              Subcellular compartments with fast protein turnover in H
293                                       Hence, subcellular compartments with little but functionally re
294 ovides a major advancement in fingerprinting subcellular compartments, with an increased potential to
295 bes, in contrast, they reside in distinctive subcellular compartments, with MyoD within the nucleus a
296 solve at the level of neighboring neurons or subcellular compartments within a neuron.
297 tegy for the multicolor labeling of distinct subcellular compartments within live cells without the n
298      We monitored host-cell restructuring of subcellular compartments within plant mesophyll cells du
299 he amount of fluorescent signal in different subcellular compartments without hand tuning, requiring
300  transport and delivery in tumors (including subcellular compartments) would be useful tools.

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