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1 physical events in TANGO1-driven procollagen export.
2 enes use specific machinery to promote their export.
3 th both being required for IL-6-induced MSH3 export.
4 x4Deltarcy1Delta mutant substantially blocks export.
5 mporary (2012-2017) benchmark of riverine Hg export.
6  for Ubp15 in coupling transcription to mRNA export.
7 0 enhances Sub2's abundance and impairs mRNA export.
8 the rates of oceanic productivity and carbon export.
9 nd results in abnormal RNA transcription and export.
10 on, thus advancing our understanding of mRNA export.
11 ophic-level production and additional carbon export.
12 ription state and not due to altered nuclear export.
13 lation, flagellin modification and efficient export.
14 r spore coat polysaccharide biosynthesis and export.
15 ber of the Eag family of T6SS chaperones for export.
16 ing and NPC1-dependent lysosomal cholesterol export.
17 xidation of [1-(14)C]C16:0 and decreased BHB export.
18 ansporter and licenses lysosomal cholesterol export.
19  any additional functions other than nuclear export.
20 iron endowment by controlling placental iron export.
21 ress via ATP13A2-mediated lysosomal spermine export.
22 -deficient cargos is due to their slow Golgi export.
23 splicing factor mobility, and defective mRNA export.
24  1 (M1) at the chromatin, important for vRNP export.
25 ic reticulum (ER) that disassociates post ER export.
26  of a transport intermediate for procollagen export.
27 s to be used for producing dry-aged meat for export.
28 ompartment to create an exit route for their export.
29 own molecular steps of signaling-driven vRNP export.
30 transcribed RNA before Xpo1-mediated nuclear export.
31 to locals and may be a valuable resource for export.
32 nt in strategies used for their assembly and export.
33 rocessing for egress, invasion, and effector export.
34 duced the virtual water embodied in American exports.
35                                 While rivers export ~1% of the OC sequestered by terrestrial vegetati
36                      We estimate that rivers export 18 +/- 4 Tg DBC year(-1) globally and that, inclu
37 XF1 or the GANP subunit of the TRanscription-EXport-2 (TREX-2) mRNA export complex.
38 In each pump cycle, the protein sequentially exports 3Na(+) out of the cell, then imports 2K(+) into
39 ting pheromone and selected for mutants that export a non-cognate pheromone.
40 -infecting Plasmodium species, P. falciparum exports a family of 18 FIKK serine/threonine kinases int
41 ta from common file types, processes it, and exports a mass list for compositional assignments.
42 s of a conserved fungal ABC transporter that exports a mating pheromone and selected for mutants that
43  of CD81 in this interface suppress its CD19 export activity.
44 ess, both genes may be involved in vesicular export allowing allantoin translocation from roots to sh
45 luding particulate BC fluxes, total riverine export amounts to 43 +/- 15 Tg BC year(-1) (12 +/- 5% of
46 protease-containing ABC transporters (PCATs) export amphipathic and hydrophilic bacteriocin and quoru
47 e determine that the six major Arctic rivers exported an average of 20 000 kg y(-1) of total Hg (THg,
48 ein, suggesting that balanced nuclear import/export and dendritic spine localization are essential fo
49 nations for the relationship between nuclear export and disease.
50 ical function of laminarin in oceanic carbon export and energy flow to higher trophic levels.
51 smission frequently occurs: many communities export and import strains.
52 insight into the molecular mechanism of drug export and inhibition of a major multidrug efflux pump a
53 athways for tRNAPhe retrograde import and re-export and is a tool that can be used on a genome-wide l
54 ment over the mechanism of indole import and export and no clearly defined target through which its e
55           However, the flg22-induced nuclear export and phospho-mobility shift can still be observed
56 own of MEK, ERK or RSK1 caused impaired vRNP export and reduced progeny virus titers.
57 t their transcription site, preventing their export and restoring normal SRSF7 protein levels.
58 gion additively contribute to competent mRNA export and stress granule formation, both self-associati
59                               Given that RNA export and translation machineries typically utilize cap
60 ode of Gle1 regulation to ensure proper mRNA export and translation.
61  Arabidopsis p24 proteins are involved in ER export and transport to the plasma membrane of GPI-ancho
62               Features of this plan might be exported and adapted to local circumstances elsewhere to
63 plantation forests that contribute to timber exports and the domestic production of paper(7).
64     Two modes of action within the flagellar export apparatus are proposed, in which the motor perfor
65  the F(1) ATPase motor, within the flagellar export apparatus remains unclear.
66 Brazil is the world's largest beef exporter, exporting approximately one-fifth of its production, and
67     We present defective lysosomal polyamine export as a mechanism for lysosome-dependent cell death
68 mes involved in polysaccharide synthesis and export, as well as sugar modification and show that six
69                     Currently, the source of exported assemblages is poorly understood, yet this info
70 en hijack plant cellular processes for their export back out of the cell to function as external sign
71 ted migration of isolated hemocytes, whereas exported bacterial products, including peptidoglycan der
72 imate large-scale variations in ocean carbon export, but the relationship between export efficiency (
73 amyloidogenic processing of APP impairs iron export by destabilizing ferroportin on the cell surface.
74 turation marks and licenses mRNA for nuclear export by loading the export factor NXF1-NXT1.
75 II) to minimize toxic effects and facilitate export by the Cus RND transporter efflux system.
76 ETE might be an autocrine signaling molecule exported by ABC transporters that enhances chemotaxis in
77                   Furthermore, tRNAPhe is re-exported by Crm1 and Mex67, but not by the canonical tRN
78 umarate reduction yields succinate, which is exported by DcuABC in exchange for L-aspartate and L-mal
79 clic-GMP-AMP (cGAMP) is an immunotransmitter exported by diseased cells and imported into host cells
80 hence changes in management that influence P export can ultimately affect HAB severity.
81  of the TRanscription-EXport-2 (TREX-2) mRNA export complex.
82 of the Sub2 component of TREX (transcription-export) complex for proteasomal degradation in stimulati
83                                      Nuclear export complexes composed of rev response element (RRE)
84 rade membranes at ER exit sites to create an export conduit.
85 et estimates of Arctic riverine mercury (Hg) export constrained from direct Hg measurements remain sp
86 and Spectralis OCT macular volume scans were exported, data from the central 20 degrees of both OCT d
87 omplex, and its deletion reverts the nuclear export defect of E3 ligase Rsp5 mutants.
88                                              Export demand also alters the emission ratios between NM
89 iquitin chains in the nucleus may rely on an export-dependent mechanism to be degraded by the proteas
90                                        Their export depends entirely on Crm1/Xpo1, whereas re-import
91  transporters prompt multidrug resistance by exporting different therapeutics across cell membranes,
92 ceptually simple mechanism for enforcing the export directionality of transport by NaAtm1.
93 fied life cycle stage associated with carbon export due to rapid sinking.
94  carbon export, but the relationship between export efficiency (e-ratio) of sinking organic carbon ou
95 nfection, bloom termination, and mass carbon export events and highlight an unappreciated role of vir
96 rial could have resulted in molecular oxygen export exceeding local Fe(2+) oxidation sinks, thereby c
97 enses mRNA for nuclear export by loading the export factor NXF1-NXT1.
98 0 alters mRNA export via splicing defects of export factors and/or mitochondrial dynamics/function, s
99 sing and involved in the recruitment of mRNA export factors to nascent transcripts.
100 d that Mdm30 does not facilitate splicing of export factors.
101 ) gene W903_1820, encoding a small multidrug export family protein, contributes significantly to GBS
102 n uptake (transferrin receptor 1 [TFR1]) and export (ferroportin [FPN]) were strongly regulated.
103 t not by Plasmodium knowlesi, which does not export FIKK kinases.
104 d in reduced parasite growth, suggesting the exported FIKKs may instead support functions important f
105 r electron microscopy (EM) density maps, and export files for 3D printing.
106 n of MDR1, which encodes an efflux pump that exports fluconazole.
107 atio by combining particulate organic carbon export flux from in situ measurements during 1997-2013,
108 contributes to a growing body of mechanistic export flux models that offer scope to incorporate under
109        It is estimated that 19.2% of kidneys exported for candidates with >98% calculated panel react
110                  All of these results can be exported for further analysis.
111  AF recordings and electrodes locations were exported for phase analyses.
112                             Higher glutamine export from astrocytes would increase extracellular D-se
113  in water potential, which may impede carbon export from leaves during the day because the xylem is t
114 hanism and molecular components of allantoin export from root cells are still unknown.
115 s, thus substantially contributing to carbon export from surface waters.
116 in whose activities are required for proSP-B export from the endoplasmic reticulum (ER) and sorting t
117          Kinetic studies indicate that rapid export from the ER requires recognition by Erv29/Surf4.
118 ved that the degradation of Ho-endo required export from the nucleus, in agreement with a previous re
119 w (greatest from February to April) and MeHg export from the outflow (greatest from September to Dece
120 apore became the first human monkeypox cases exported from Africa, and a related nosocomial transmiss
121 an also alter the sources and quality of DOM exported from fluvial systems, and the RCC may be signif
122 o better predict the fate and quality of DOM exported from terrestrial to coastal systems.
123 how how search results can be customized and exported from the browser in a format of choice (i.e. JS
124 ow Water (ISOW) is a primary deep water mass exported from the Norwegian Sea into the North Atlantic
125 viruses, a fraction of HERV-K transcripts is exported from the nucleus in unspliced or incompletely s
126 in of Brazilian meat, offal, and live cattle exports from 2015 to 2017, a trade worth more than $5.4
127                                 The built-in export function allows downloading filtered data and gra
128 al that IkappaBalpha, via its unique nuclear export function, enables, rather than inhibits 4-1BB-ind
129 the cryo-electron microscopy structure of an export gate containing the switch protein from a Vibrio
130          Proteins are transported through an export gate containing three proteins (FliPQR in flagell
131 e reveals that FlhB/SctU extends the helical export gate with its four predicted transmembrane helice
132 ng' through the resistive environment of the export gate, or by exerting equal and opposite stall for
133 loop wrapped around the bottom of the closed export gate.
134  a number of selective inhibitors of nuclear export have been developed.
135 ent pathway for polysaccharide synthesis and export; however, key components of this pathway have rem
136  drug binding and ATP hydrolysis-driven drug export in Pgp are poorly understood.
137 n-fold in S. calendulacea but did not affect export in S. trilobata.
138 ubiquitylase Ubp15 as a regulator of nuclear export in Saccharomyces cerevisiae.
139 gnificance of trace element mobilization and export in subglacial runoff from ice sheets is poorly co
140 iral lysis alter nutrient cycling and carbon export in the oceans, although the net impacts remain un
141 ratio are key factors to quantify the carbon export in the Southern Ocean.
142 king proteins predicts an important role for export in the turnover of nuclear proteins.
143 se ideas motivate the hypothesis that carbon export in woody plants occurs predominantly at night, wi
144 l proteins transit through endosomes and are exported in a Rab8-, Rab10-, and/or Rab11-dependent mann
145 al events-up to 39% of annual SigmaF(aq) was exported in one event.
146                                  We obtained exports in April and October, 2017, August, 2018, and De
147 tic consumption, (ii) managing waste plastic exports in the EU, (iii) design-for-recycling initiative
148 exor, an oral selective inhibitor of nuclear export, in patients with relapsed or refractory DLBCL wh
149                               Production for export increases concentration of NMVOCs (including some
150 anscription-dependent manner to promote mRNA export independently of splicing or mitochondrial functi
151 elated isolates is the likely source for the exported infections.
152 erfaces for classifier training, validation, exporting inference results, and collaborative review, a
153 and challenges in the development of nuclear export inhibitors and discuss the potential of emerging
154 PHO1) transfers Pi from root to shoot via Pi export into root xylem vessels.
155 somal RNA synthesis and processing, ribosome export into the cytoplasm, and global protein synthesis.
156 cteria, PG is assembled in the cytoplasm and exported into the periplasm where it undergoes considera
157 uclearly encoded mitochondrial proteins that export iron from the mitochondria into the cytosol.
158 otein (vRNP) complexes, suggesting that vRNP export is a signaling-induced event.
159 demonstrated that O-glycan's effect on Golgi export is probably additive.
160 y binding Galphai-GDP, whereas RGS14 nuclear export is regulated by Exportin 1 (XPO1).
161 e splicing has been shown to enhance nuclear export, it has remained unclear whether mRNAs generated
162 oteasomal degradation in stimulation of mRNA export, it remains unknown whether such ubiquitin-protea
163                 Only the deletion of the non-exported kinase FIKK8 resulted in reduced parasite growt
164               Fertilized temperate croplands export large amounts of reactive nitrogen (N), which deg
165 ane helices (TMs) and three lumenal domains, exports low-density-lipoprotein (LDL)-derived cholestero
166 that are either exported or form part of the export machinery.
167  cultured in hypoxia condition, GSCs rapidly exported muscleblind-like-1 (MBNL1) out of the nucleus,
168  Rad23 also accumulated in the nucleus in an export mutant, and bound to higher levels of polyUb prot
169  never remain saturated and must continue to export Na(+) and synaptic Ca(2+) even in bright illumina
170 ptimality-based approach, using net canopy C export (NCE, photosynthesis minus the C cost of leaf gro
171 of inorganic nitrogen and a reduction of DOC export occur following wildfires in streams draining the
172                                              Export occurred throughout the day at equal or higher ra
173 mitochondrial respiration/function, and mRNA export occurs in the absence of Fzo1, which is required
174 ining cellular homeostasis via the regulated export of a range of cargoes, including proteins and sev
175 gA, that are known to selectively assist the export of a subclass of effectors.
176  and N(6)-methyladeonsine (m(6)A) on nuclear export of App mRNA.
177  nascent polypeptide exit tunnel (NPET), and export of assembling subunits to the cytoplasm.
178                                      Nuclear export of both HIV-1 and HERV-K mRNAs is dependent on th
179 onstrate that Fam20C plays a key role in the export of Cab45 clients by fine-tuning Cab45 oligomeriza
180 ogeochemical cycles through the fixation and export of carbon, uptake of nutrients, and production an
181 Ras signaling in EC that is necessary for EC export of collagen IV, thus permitting the development o
182 ortal for efficient finding, exploration and export of data.
183 uring anaerobiosis, enabling the cytoplasmic export of eIF5A/Tsc2 mRNA complexes for translational en
184 l forcing causes changes in sea-ice mediated export of freshwater into areas of active deep convectio
185 nd p24 proteins, which are receptors for the export of GPI-anchored proteins and have been shown to b
186 acteria and are defective for T6SS-dependent export of hemolysin-coregulated protein (Hcp).
187           The genes involved in assembly and export of HPS are largely undefined, and it has been hyp
188 had no significant impact on the basolateral export of HSV-1 from infected to uninfected cells by dir
189      Retromer orchestrates the selection and export of integral membrane proteins from the endosome v
190 hat is specifically required for the nuclear export of intronless and intron-poor mRNAs and lncRNAs.
191 at CLN6 deficiency results in inefficient ER export of lysosomal enzymes and diminished levels of the
192 vesicles, which goes along with an increased export of LyzC, a Cab45 client.
193 receptor CRM1 is responsible for the nuclear export of many tumor-suppressor proteins and viral ribon
194 pe maintenance, and regulation of import and export of materials.
195                 Despite evidence of seasonal export of MeHg from the HCC, annual loads indicate a 42%
196 during the open water season, but subsequent export of MeHg to downstream ecosystems is limited by pa
197                                     Seasonal export of MeHg was evidenced by increases in monthly mea
198                                      Nuclear export of messenger RNAs (mRNAs) is intimately coupled t
199 s downstream of terminators to block nuclear export of messenger RNAs resulting from RNA polymerase r
200                               The concurrent export of microbial assemblages alongside glacial meltwa
201                        XPO5 mediates nuclear export of miRNA precursors in a RanGTP-dependent manner.
202 at TPR is required for the efficient nuclear export of mRNAs and lncRNAs that are generated from shor
203                       The parasite increased export of nitrogen-15 from the connected, unparasitized
204 ch of the deep sea (>200 m water depth), the export of nutrients from the surface ocean provides a cr
205 rbohydrates, increased ATP turnover, and the export of osmolytes.
206 D1 is functionally active and accompanied by export of other antioxidant enzymes such as thioredoxins
207 ism of protection may be related to impaired export of P. falciparum virulence proteins.
208 nd that NCBP3 positively impacts the nuclear export of polyadenylated RNAs and the expression of larg
209 ng effect and assessed the decomposition and export of preexisting organic matter.
210 es the delivery of inputs (e.g., oxygen) and export of products (e.g., signaling molecules) to and fr
211 hanisms, which together ensure high-capacity export of properly folded proteins from the ER.
212         The C-terminal domain facilitates ER export of proSP-B.
213  and is responsible for hormonally regulated export of PUFAs from adult liver, strongly supports incr
214     HIV-1 Rev is able to mediate the nuclear export of RcRE-containing HERV-K mRNAs, which contribute
215 o-metabolism (priming) potentially increases export of refractory organic matter through increased pr
216  the double-membrane vesicle and would allow export of RNA to the cytosol.
217 ssary and sufficient for the efficient Golgi export of Tac chimeras.
218 1 Rev protein is able to mediate the nuclear export of the HERV-K RcRE, contributing to elevated HERV
219       A critical step on this pathway is the export of the lipid-linked cell wall monomer, Lipid II,
220 ted whether Fmr1(KO) associates with nuclear export of the mRNAs for APP protein processing enzymes,
221 licing of BK channels; this requires nuclear export of the splicing factor Nova-2.
222     Recent studies showed that AP-4 mediates export of the transmembrane autophagy protein ATG9A from
223  of HERV-K loci (Type 2 proviruses), nuclear export of the unspliced HERV-K mRNA appears to be mediat
224 rm TPP, and an MmpL transporter promotes the export of TPP or its precursor across the plasma membran
225 K) pathway is functionally linked to nuclear export of viral ribonucleoprotein (vRNP) complexes, sugg
226 l receptors via members of the PfEMP1 family exported onto the erythrocyte surface.
227 aptamers) during the design process, and the export option for oxDNA simulations are outstanding feat
228 r of genes encoding proteins that are either exported or form part of the export machinery.
229 cell-selective deficiency in S1P production, export, or the S1P(1) receptor substantially exacerbates
230 erature dependence of [Formula: see text] in exported organic matter.
231          Although effector architectures and export pathways tend to be clade specific, phylogenetica
232 revealed a quantitative relationship between export patterns and shallow-versus-deep concentration co
233 vertical chemical contrasts regulate nitrate export patterns under different land use conditions.
234 rter family that proteolytically process and export peptides and proteins.
235          These findings indicate that the re-export process occurs in a tRNA family-specific manner.
236 to examine past variations in dust delivery, export productivity, and bottom-water oxygenation, respe
237 es have shown that inhibition of the nuclear export protein exportin 1 (XPO1) causes nuclear accumula
238 ses the excess cysteine and induces AlaE, an export protein that pumps cysteine back out of the cell
239 e associated interspersed proteins (SURFIN), exported protein family 1 (EPF1) and Plasmodium Helical
240 nism must take in nutrients, secrete wastes, export proteins into the host cell, and eventually egres
241 ing proteins, merozoite surface proteins and exported proteins with unknown function.
242  cytoplasm after the dissociation from their exported proteins.
243 assays to assess inhibition of the bile salt export pump (BSEP), mitotoxicity, reactive metabolite (R
244 all heterodimer partner (SHP), and bile salt export pump (BSEP).
245 (P663L) piglets had alterations in bile salt export pump, a transporter that facilitates bile flow, w
246 mponents or entire compound classes, and can export raw data or graphics for off-line use.
247  to hyper-ubiquitylation of the main nuclear export receptor Mex67 and affects its association with T
248 lated to changes caused by depletion of mRNA export receptor NXF1 or the GANP subunit of the TRanscri
249 ometry, indicated that deforested catchments export relatively more aliphatic and heteroatomic DOM so
250 isualize data details, annotate findings and export resultant diagrams in high-quality figures.
251 ranscription regulation, mRNA processing and export, ribosome biogenesis, translation initiation, and
252                          Defects in the mRNA export scaffold protein GANP, encoded by the MCM3AP gene
253 R) and R507Q (RQ) located within the nuclear export sequence (NES) of human RGS14.
254 lls harboring a mutated IkappaBalpha nuclear export sequence abnormally accumulate inactive cRel:Ikap
255 ccus aureus type VII secretion system (T7SS) exports several proteins that are pivotal for bacterial
256   Using an M mutant with a defective nuclear export signal (MNESmut), however, we revealed that the n
257             The consensus pattern of Nuclear Export Signal (NES) is a short sequence motif that is co
258     Glu571 of CRM1 is located in its nuclear export signal (NES)-binding groove, suggesting that bind
259 nd that the RcRE resembles the HIV-1 nuclear export signal, RRE.
260 ation (NLS1 to -3) and two potential nuclear export signals (NES1 and -2) within MSH3.
261 xtracellular datasets; validate, curate, and export sorting outputs; and more.
262                         Mutations in nuclear export stabilized substrates, and caused accumulation in
263  a Wzx/Wzy-type polysaccharide synthesis and export system.
264 ion, chaperone dissociation and unfolding of exported T3SS proteins.
265 t, wig and bed files as well as csv files to export the location of all approximate k-mers for each g
266 or increasing tolerance to aromatic acids by exporting them out of the cell.
267 lian cells, >25% of synthesized proteins are exported through the secretory pathway.
268 ulated the net primary production and carbon export, thus promoting atmospheric CO(2) drawdown during
269 d to predict the response of recalcitrant OC export to changing environmental conditions.
270 o rivers with the particulate organic carbon export to oceans, we demonstrated that a large fraction
271 nstrated that a large fraction of the carbon export to rivers could have been mineralized in inland w
272       By comparing the eroded organic carbon export to rivers with the particulate organic carbon exp
273 gional emphasis on enhancing aquaculture for export to support economic development.
274 nd retention of organic matter, prior to its export to the coastal oceans.
275 ophores and antibiotics, which often require export to the extracellular environment.
276 ated, including ATXN7L3B, which couples mRNA export to transcription activation by association with t
277  Primary Production and soil respiration) is exported to aquatic systems as leached DOC.
278 % of the eroded organic carbon is eventually exported to inland waters, which is equal to 14% of the
279  and how this intervention can be applied or exported to other health care organizations.
280             Data was entered on Epi-Info and exported to SPSS for analysis.
281 ta were entered in to Epi Info version 7 and exported to SPSS version 20 for analysis.
282 irus 1 (HSV-1), hnRNPA2B1 was quantitatively exported to the cytoplasm and at least a fraction of hnR
283  transcribed in the nucleus and subsequently exported to the cytoplasm where they serve as essential
284  the intermediate heat and salt content were exported to the deep layers from 2009 to 2013 thanks to
285 omposition of dissolved organic matter (DOM) exported to the ocean.
286            Fat-filled milk powders (FMP) are exported to tropical developing markets as inexpensive m
287  In the US coastal southeast-where US pellet exports to the EU originate-there were fewer live and gr
288 x RNA helicases involved in messenger (m)RNA export, translation initiation and termination, and stre
289 licases, with critical roles defined in mRNA export, translation initiation, translation termination,
290                        Inhibition of nuclear export triggered the Zalpha-dependent activation of RIPK
291                                              Exported very-low density lipoprotein particles were iso
292  of Sub2 in the absence of Mdm30 alters mRNA export via splicing defects of export factors and/or mit
293 nt amounts of lactate and protons, which are exported via monocarboxylate transporters (MCTs), suppor
294                                      Glucose export was decreased, but cellular glycogen was increase
295 nd pathways for key vitamin biosynthesis and export were identified across MAGs.
296 TG), and glucose and B-hydroxybutyrate (BHB) export were quantified.
297        Replete stores trigger increased H(+) export which stimulates TORC1 and liberates proteasomes,
298  invest strongly in petals to promote pollen export, while lighter flowers tend to be female-biased a
299 d to contribute extensively to virtual water exports, while much of Africa, India, and the Middle Eas
300 ES2 work synergistically to maximize nuclear export, with both being required for IL-6-induced MSH3 e

 
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