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1  y later when their professional careers had unfolded.
2  shifts in the occupied subspace as movement unfolded.
3 serve mental health complaints as the crisis unfolded.
4 d from its Habc domain and its linker region unfolded.
5 2.5 angstrom), but they are far apart in the unfolded 1,4-isomer (H...H distance ~ 7 angstrom).
6 t of exchange behaviors: PhoA((350-471)), an unfolded 122-residue fragment; barstar, a fully folded r
7 eractions are involved in recognition of the unfolded A2 domain.
8                    The bound guanidineHCl-to-unfolded amino acid ratio is 0.79 for the pretransition
9                                         POT1 unfolded and bound to any conformational form of human t
10 actors that cause different substrates to be unfolded and degraded to different extents are still poo
11 structural information of myoglobin, for the unfolded and even for the molten globule states, models
12                                          The unfolded and flattened surface comprised a narrow strip
13 agnetization transfers between water and the unfolded and folded states; cross-correlated relaxation
14 otein activated at the matrix remains mostly unfolded and is transported back to the IMS to integrate
15 aryotic cells in response to accumulation of unfolded and misfolded proteins.
16                     The dynamics of the acid unfolded and molten globule state are similar in the fra
17 tate (TS) located almost halfway between the unfolded and native states.
18  of secondary structure elements in the acid unfolded and presence of alpha-helices in the molten glo
19 arly in a transition path, N(TAIL) typically unfolded and then refolded after additional intermolecul
20 ntrol that regulate turnover of short-lived, unfolded, and misfolded proteins.
21 ntaneous A2 domain state as either folded or unfolded, and were directly taken from coarse-grained MD
22                              Accumulation of unfolded antibody chains in the ER triggers ER stress th
23 dependent pathway involved in degradation of unfolded antibody HC.
24 ads to the generation of higher fractions of unfolded apo subunits and free hemin, which are known to
25 es to produce populations of both folded and unfolded apoprotein.
26 in that harbors the vinculin-binding site is unfolded at ~6 pN; and 3) unfolding of the M1 domain is
27  dimers, tail-folded antiparallel tetramers, unfolded bipolar tetramers, and small filaments.
28 along with the first transmembrane helix, we unfolded bR in the presence of its retinal.
29 r of drkN SH3, for which HyperW enhanced the unfolded but, surprisingly, enhanced even more certain f
30 nd chemical denaturation: whereas TriEst was unfolded by heating ( T(m) ~ 75 degrees C) or denatured
31                           First, Hsp33 binds unfolded chains, which suppresses aggregation between su
32 ucture of mTXNPx in complex with a thermally unfolded client protein, and revealed that the flexible
33 rcharged [M + zH] (z+) ions are formed under unfolded conditions remains unclear.
34  differing in core properties: folded versus unfolded configurations in a protein molecular dynamics
35 s on beta-lactoglobulin melting temperature, unfolded conformation and subsequent intermolecular inte
36 pseudoknot and promotes a dynamic, partially unfolded conformation.
37 iple folding pathways connecting a myriad of unfolded conformations and a well-defined folded state.
38      Our data show that fluctuations between unfolded conformations are slow, which enables the exper
39 bition by interacting not with the monomeric unfolded conformations of the amyloid-beta symbol (Abeta
40     In this case, rapid fluctuations between unfolded conformations result in apparent two-state beha
41 regation appears to originate from partially unfolded conformations that are sampled through stochast
42 characterize certain folded sites over their unfolded counterparts-are considered to account for them
43 me oxidized in vivo through the mechanism of unfolded domain oxidation (UnDOx).
44                            As a consequence, unfolded domains accumulate during synthesis, leading to
45 s nonconstitutive folding and aggregation of unfolded domains.
46 esidues leads to significant collapse of the unfolded ensemble of pertactin, a secreted autotransport
47 ially folded (molten globule) and completely unfolded, following two different unfolding paths: using
48 rposition of >=100-fold enhancements for its unfolded form, coexisting with more modest enhancements
49  drkN SH3, a protein domain whose folded and unfolded forms interchange rapidly and with temperature-
50 R17, a 13.3 kDa system possessing folded and unfolded forms under slow interconversion; and drkN SH3,
51 ging and time-dependent chemical trapping of unfolded G4s in living cells reveal that G4s fluctuate b
52  recognize microRNAs (miRNAs) that populated unfolded hairpins.
53  neoplasm characterized by the production of unfolded immunoglobulins, which cause endoplasmic reticu
54  how the epidemic and public health response unfolded in Australia up to 13 April.
55                            Proteins that are unfolded in solution produce higher charge states during
56                                          The unfolded, inactive peptide is dephosphorylated, shifting
57  monomeric species, formation of a partially unfolded intermediate in the dimer to tetramer size rang
58 ion has been shown to proceed from partially unfolded intermediates in these proteins; their extreme
59 solvents on the equilibrium of folded versus unfolded isomers.
60  absence of ligand the riboswitch is largely unfolded, lacking the PK helix so that translation can b
61 res of heptameric PA channels with partially unfolded LF and EF at 4.6 and 3.1- angstrom resolution,
62       We also evaluated the influence of the unfolded model in the stability calculations using incre
63 eventing hemin disassociation from partially unfolded, molten globular species during early disassemb
64 s a structural transition from predominately unfolded monomer at low concentrations to an alpha-helic
65                It has been thought that only unfolded monomers assemble into bipolar and side-polar (
66 in (TTR) involves self-assembly of partially unfolded monomers.
67                 Upon release from polysomes, unfolded mRNAs outcompete G3BP auto-inhibitory interacti
68                             Importantly, the unfolded MSD can refold with or without applied forces.
69                       Basophil activation by unfolded mutant Ara h 2 was low (median area under the c
70                                          The unfolded mutant lacking both types of epitopes displayed
71                                              Unfolded mutants without conformational epitopes did not
72                  During microbial infection, unfolded nascent proteins may exceed the folding capacit
73            The resulting compaction can bias unfolded nucleic acids towards folding, resulting in fas
74 ry complex as well as its ability to prevent unfolded OMP (uOMP) aggregation.
75           Together, the results suggest that unfolded OMP substrates bind in a cradle formed between
76 ures, has been proposed to cycle between an "unfolded"/"open" state that allows an NTP substrate to e
77 nonically, they act as "holdases" and buffer unfolded or misfolded proteins against aggregation in an
78 ress induced by the abnormal accumulation of unfolded or misfolded proteins at the endoplasmic reticu
79  productivity and often increase the load of unfolded or misfolded proteins in the endoplasmic reticu
80 structural remodeling in peri-infarct cortex unfolded over the first 2 weeks after stroke, characteri
81 near discriminant analysis, and discriminant unfolded partial least-squares.
82  motor of the cpSec1 translocon that inserts unfolded Plsp1 into the thylakoid.
83 providing a unified picture of the nature of unfolded polypeptide chains in the absence of denaturant
84 strated that water can be a good solvent for unfolded polypeptide chains, even those with a hydrophob
85 ng autophagy, leading to the accumulation of unfolded protein aggregates and dysfunctional mitochondr
86 s-including extracellular matrix regulation, unfolded protein binding, mitochondrial function, and in
87 a dual-color imaging strategy to distinguish unfolded protein oligomers from insoluble aggregates in
88 IF2alpha, and HSPB8 define a novel cytosolic unfolded protein response (cUPR) essential for optimal i
89 M1 deficiency strongly induced mitochondrial unfolded protein response (UPR(mt)) and enhanced mitocho
90                            The mitochondrial unfolded protein response (UPR(mt)) is a mitochondrial-t
91 MNRR1 in DW7 cells induces the mitochondrial unfolded protein response (UPR(mt)), autophagy, and mito
92  exposed to IR, to assess epithelial damage, unfolded protein response (UPR) activation, and inflamma
93 action, ERK1/2 and CREB phosphorylation, and unfolded protein response (UPR) activation.
94               Meanwhile, UL148 activates the unfolded protein response (UPR) and causes large-scale r
95          Previous work showed involvement of unfolded protein response (UPR) and endoplasmic reticulu
96 ignancies exhibit dramatic activation of the unfolded protein response (UPR) and ER stress response v
97                               The integrated unfolded protein response (UPR) and ER-associated degrad
98 lding capacity of the ER is regulated by the unfolded protein response (UPR) and ER-associated degrad
99 e folding capacity of the ER, activating the unfolded protein response (UPR) and restoring the ER to
100           These comprise, in particular, the unfolded protein response (UPR) and the DNA damage respo
101                                          The unfolded protein response (UPR) and the heat shock respo
102 ding networks associated with activating the unfolded protein response (UPR) and the proinflammatory
103 gly, we found a decoupling between different unfolded protein response (UPR) branches in stressed sen
104 ence of galactose, lithium ions activate the unfolded protein response (UPR) by inhibiting phosphoglu
105 pha regulatory subunit of PI3K modulates the unfolded protein response (UPR) by interacting with and
106 se RNF5 exhibit attenuated activation of the unfolded protein response (UPR) components, which coinci
107 f endoplasmic reticulum (ER) stress, and the unfolded protein response (UPR) consistent with elevated
108 rmacologic activation of the ATF6 arm of the unfolded protein response (UPR) during reperfusion, a ty
109 sing an engineered sensor that activates the unfolded protein response (UPR) exclusively when normal
110  of primary CD34 cells, quantitative PCR for unfolded protein response (UPR) genes, and single-cell R
111                                          The unfolded protein response (UPR) has been shown to be act
112 ) in the cytosol and nucleus, as well as the unfolded protein response (UPR) in the endoplasmic retic
113 kine-exposed beta-cells revealed an adaptive unfolded protein response (UPR) including a marked immun
114                                          The unfolded protein response (UPR) is a cellular homeostati
115                                          The unfolded protein response (UPR) is a conserved adaptive
116 ns, an adaptive signaling network termed the unfolded protein response (UPR) is activated.
117                                          The unfolded protein response (UPR) is emerging as the possi
118                                              Unfolded protein response (UPR) of the endoplasmic retic
119 cting endoplasmic reticulum (ER) stress, the unfolded protein response (UPR) orchestrates adaptive ce
120 uction of high mannose is dependent upon the unfolded protein response (UPR) pathway, a pathway previ
121  oxidative stress and aberrant activation of unfolded protein response (UPR) pathway, which was parti
122 ers of endoplasmic reticulum (ER) stress and unfolded protein response (UPR) pathways are increased i
123                                          The unfolded protein response (UPR) plays a central role in
124  reticulum (ER) stress and activation of the unfolded protein response (UPR) promote growth and invas
125                          The PERK arm of the unfolded protein response (UPR) regulates cellular prote
126 he induction of apoptosis by an unresolvable unfolded protein response (UPR) represents a potential n
127 ng and molecular dynamics simulations, human unfolded protein response (UPR) RT(2) PCR profiler array
128                                          The unfolded protein response (UPR) senses defects in the en
129 3-19K glycoprotein specifically triggers the unfolded protein response (UPR) sensor IRE1alpha in the
130 nockdown in pancreatic cancer cells enhanced unfolded protein response (UPR) signaling and cell death
131                     Cancer cells exploit the unfolded protein response (UPR) to mitigate endoplasmic
132 creased antibody synthesis by activating the unfolded protein response (UPR) under the control of the
133 hock response - indicating activation of the unfolded protein response (UPR) with downstream inflamma
134 tant is associated with the induction of the unfolded protein response (UPR), a common response to vi
135 tion, known as ER stress, is buffered by the unfolded protein response (UPR), a set of signaling path
136 proteostasis surveillance is mediated by the unfolded protein response (UPR), a signal transduction p
137 ied the improved workflow to proteins of the unfolded protein response (UPR), a signaling pathway of
138 ng protein glycosylation, causes a sustained Unfolded Protein Response (UPR), a significant attenuati
139                                          The unfolded protein response (UPR), an endoplasmic reticulu
140 placenta is susceptible to activation of the unfolded protein response (UPR), and we hypothesized thi
141 ion of misfolded proteins, activation of the unfolded protein response (UPR), decreased protein synth
142                     Master regulators of the unfolded protein response (UPR), IRE1alpha and PERK, pro
143  an ER membrane-associated protein mediating unfolded protein response (UPR), is required for transdu
144 species (mtROS) production and, in turn, the unfolded protein response (UPR), leading to a distinct t
145 s induce chronic activation of ER stress and unfolded protein response (UPR), leading to T cell death
146                    Chronic activation of the unfolded protein response (UPR), notably the branch comp
147         Here, we show that activation of the unfolded protein response (UPR), specifically phosphoryl
148 asmic reticulum stress and activation of the unfolded protein response (UPR), triggering death of neu
149 argets various cell processes, including the unfolded protein response (UPR), which acts to attenuate
150 gnaling processes, collectively known as the unfolded protein response (UPR), which are designed to r
151  the endoplasmic reticulum (ER) activate the unfolded protein response (UPR), which enhances protein
152 the endoplasmic reticulum (ER) activates the unfolded protein response (UPR)-a signaling network that
153 and refolding malformed proteins through the unfolded protein response (UPR).
154  and bZIP60 but not bZIP17 and bZIP28 in the unfolded protein response (UPR).
155 ers a dynamic signaling pathway known as the unfolded protein response (UPR).
156 tivation of a signaling network known as the unfolded protein response (UPR).
157 t as primary sensor in the activation of the unfolded protein response (UPR).
158 n of ER stress coping responses, such as the unfolded protein response (UPR).
159  ER calcium depletion robustly activates the unfolded protein response (UPR).
160 or extrinsic factors, can be resolved by the unfolded protein response (UPR).
161 epression by various stresses, including the unfolded protein response (UPR).
162 butes to the activation of the mitochondrial unfolded protein response (UPR).
163 to cause ER stress, which then activates the unfolded protein response (UPR).
164 d activates a signaling network known as the unfolded protein response (UPR).
165 nstrated that CXL146 treatment activated the unfolded protein response (UPR); as evidenced by the act
166  requires DRH-1 as well as the mitochondrial unfolded protein response (UPRmt).
167  reticulum (ER) stress proteins, and reduced unfolded protein response activation, while DN mutations
168 r mechanisms of tumor regression through the unfolded protein response and apoptosis.
169 B cells of the I-A(12%) mutant mouse express unfolded protein response and are extremely short lived.
170  respond to OGT inhibition by activating the unfolded protein response and by significantly increasin
171  phosphorylation likely leads to unregulated unfolded protein response and cell death.
172 ex, and showed that these are related to the unfolded protein response and changes.
173 on of two PAWHs constitutively activates the unfolded protein response and compromises stress toleran
174 the S.-japonicus-type phospholipids exhibits unfolded protein response and downregulates secretion.
175  of beta-gal, resulting in activation of the unfolded protein response and endoplasmic reticulum stre
176 -box binding protein 1 (XBP-1s), part of the unfolded protein response and expressed in developing ge
177 get engagement and reduced oxidative stress, unfolded protein response and fibrogenic signaling.
178 ga-3 fatty acid (omega-3)-mediated repair of unfolded protein response and here we show much broader
179 activating tumor-promoting ER stress-induced unfolded protein response and inflammation.
180      SINE-deleted cells exhibit an activated unfolded protein response and PKR and markedly increased
181 d over 2,800 genes, including players in the unfolded protein response and proinflammatory pathways a
182 vation can robustly induce the mitochondrial unfolded protein response and thus could be an appealing
183 NMD-regulated link between activation of the unfolded protein response and transcriptional activation
184  contrast, glucose starvation does not cause unfolded protein response and, in normoxic conditions, o
185 ick-borne encephalitis viruses, activate the unfolded protein response before transcription of interf
186 roliferation via both JNK activation and the unfolded protein response caused by ER stress.
187 ion required activation of the mitochondrial unfolded protein response for neuroprotection against ro
188 enhanced expression of canonic mitochondrial unfolded protein response genes.
189      Moreover, both drugs also inhibited the unfolded protein response in cells that expressed a nonp
190 , we show that an AS15 analogue triggers the unfolded protein response in glioblastoma cells.
191      Among the myriad molecules activated by unfolded protein response in I-A(12%) B cells, Xbp1s sin
192 e 1alpha (IRE1alpha), a key component of the unfolded protein response in mammalian cells and a poten
193 derscore the importance of the mitochondrial unfolded protein response in neuroprotection against var
194   In turn, this forestalls activation of the unfolded protein response in order for circadian rhythms
195 te disturbances in proteostasis, such as the unfolded protein response of the endoplasmic reticulum (
196 ting mucin trafficking, thereby inducing the unfolded protein response pathway (UPR) and apoptosis.
197 homeostasis by activating the PERK-dependent unfolded protein response pathway to consequently facili
198 ction between age, APOE genotype, and sex on unfolded protein response pathway.
199 wever, 2-DG exerts these effects by inducing unfolded protein response rather than by inhibiting glyc
200 olding in the heart and thereby activates an unfolded protein response sensor and effector, activated
201 lcium channel auxiliary subunit BARP and the unfolded protein response sensor IRE1alpha, that are req
202 beta4 surface expression while IRE1alpha, an unfolded protein response sensor, enhanced alpha6beta4 r
203                                show that the unfolded protein response sensor, PERK, enhances MDSC-me
204  that HRI contributes to a general cytosolic unfolded protein response that could be leveraged to bol
205 this stress, cells activate a pathway called unfolded protein response that functions to maintain end
206 enz protect cells from a tunicamycin-induced unfolded protein response to a similar degree.
207 cells expressing IRE1beta have an attenuated unfolded protein response to ER stress.
208 gulated inhibitory (HRI) induced a cytosolic unfolded protein response to prevent aggregation of inna
209  we identify the selective activation of the unfolded protein response transducer IRE1alpha under gen
210 tion is required for ER-phagy to repress the unfolded protein response via IRE1alpha.
211 doplasmic reticulum processes, including the unfolded protein response, a cellular stress response of
212  during biosynthesis in the ER activates the unfolded protein response, a multiarmed program that enh
213          The importance of the mitochondrial unfolded protein response, an emerging pathway that alle
214 ing proteins that comprise the mitochondrial unfolded protein response, and noted 4E-BP1 overexpressi
215 ng in endoplasmic reticulum (ER) stress, the unfolded protein response, and ultimately apoptotic cell
216 lational reprogramming, and induction of the unfolded protein response, consistent with loss of prote
217 ochondrial translation and the mitochondrial unfolded protein response, glycolysis, and the mitogen-a
218 pproach revealed that heat shock, unlike the unfolded protein response, leads to reduced spreading of
219 dative phosphorylation and activation of the unfolded protein response, linking the high-fat Western
220 components (the ubiquitin-proteasome system, unfolded protein response, macroautophagy, mitophagy, an
221 6) that otherwise elicited ER stress and the unfolded protein response, thereby critically reducing m
222 te stress response such as the mitochondrial unfolded protein response, UPRMT.
223      We find that P0Q215X does not elicit an unfolded protein response, which is a key mechanism for
224 lls with GRP78 overexpression via activating unfolded protein response-mediated apoptosis.
225 Case activity in these cells and induced the unfolded protein response.
226 induced XBP1 splicing, a key mediator of the unfolded protein response.
227  expected, as evidenced by activation of the unfolded protein response.
228 me 1 (IRE1) is an essential component of the Unfolded Protein Response.
229  TKI resistance via induction of Jun and the unfolded protein response.
230 4E-BP1 activation promoted the mitochondrial unfolded protein response.
231  of eIF2alpha, a major defensive step of the unfolded protein response.
232 ation via mechanisms outside its role in the unfolded protein response.
233 iculum kinase (PERK), a key component of the unfolded protein response.
234 n metabolic and oxidation processes, and the unfolded protein response.
235  most evolutionarily conserved branch of the unfolded protein response.
236 several genetic rescue interventions and the unfolded protein response.
237 transcription factor, a critical part of the unfolded protein response.
238 otif enhances colon epithelial repair via an unfolded protein response.
239 quitylated proteins and the induction of the unfolded protein response.
240 in the ER by initiating the widely conserved unfolded protein response.
241 nstead retained the ER where it activates an unfolded protein response.
242 way, autophagy, proteasome function, and the unfolded protein response.
243 P or deletion of Ryr2 equivalently inhibited unfolded protein response/ER stress, activation of the C
244 ve been implicated in key processes like the unfolded protein response; however, they have not been s
245 ses previously implicated in DILI, including unfolded protein responses and oxidative stress.
246 ignaling pathway regulates lipid metabolism, unfolded protein responses, secretion of extracellular m
247 ocesses such as those required for auxin and unfolded protein responses, signaling, and cell wall bio
248 enhancements were >=300x, as expected for an unfolded protein sequence.
249 ention is required to characterize partially unfolded protein states and to gain more insight into th
250                      The UPR is triggered by unfolded protein stress and leads to up-regulation of ce
251 defect is the uncontrolled initiation of the unfolded protein stress response, with single-cell analy
252  without affecting the endoplasmic reticulum unfolded protein stress-induced ISR, mediated by the rel
253        It is hypothesised that the partially unfolded protein structures have a lower number of hydro
254  Ubl-containing proteins (if present with an unfolded protein) increased proteasomal adenosine 5'-tri
255  tolerance following phagocytosis through an unfolded protein/endoplasmic reticulum stress response p
256  strongly up-regulated genes are involved in unfolded-protein stress response, and cells exposed to m
257 by a feedback inhibition mechanism involving unfolded proteins and folding intermediates when their l
258 ink between stresses such as accumulation of unfolded proteins and modulation of autophagy, which rem
259 a highly active chaperone holdase that binds unfolded proteins and prevents their aggregation.
260    We show how the peak shapes of folded and unfolded proteins are preserved under added salt (0-140
261 a stress response mechanism to clear out the unfolded proteins by either facilitating their re-foldin
262 olding systems, we reveal the segregation of unfolded proteins from folded proteins in the Golgi.
263                              Accumulation of unfolded proteins in the endoplasmic reticulum (ER) caus
264                              Accumulation of unfolded proteins in the endoplasmic reticulum (ER) init
265                                       Excess unfolded proteins in the ER lumen induce dimerization an
266              Upon sensing an accumulation of unfolded proteins in the ER lumen, IRE1 activates its cy
267      Our results imply that supercharging of unfolded proteins is caused by residual sulfolane that s
268  "CEM supercharging model" proposed here for unfolded proteins is distinct from the charge trapping m
269                                              Unfolded proteins likely follow the chain ejection model
270 re committed to lysosomal degradation, while unfolded proteins localize to the endoplasmic reticulum
271           The Sec channel enables passage of unfolded proteins through the bacterial plasma membrane,
272                                 In solution, unfolded proteins typically find this native structure t
273 osylation of S/T-rich protein substrates and unfolded proteins.
274                             We show that the unfolded regions face the air-water interface.
275 nabled monitoring of charge migration to the unfolded regions.
276 ve state, observable intermediate state, and unfolded state for ETR-3 RRM-3, which has canonical RRM
277 rienced by C. elegans, the population of the unfolded state of the TZF domain of MEX-5 varies.
278             The long lifetime, ~10 s, of the unfolded state presents ample opportunities for the poly
279  < 10 pN, titin domains are recruited to the unfolded state, and produce 41.5 zJ mechanical work duri
280 d state and a knowledge-based energy for the unfolded state.
281  substrate segments cross the membrane in an unfolded state.
282 ssitate that water is a poor solvent for its unfolded state.
283  pulled together), a balance that stabilizes unfolded states and facilitates the folding of Twister,
284 y profiles reveal stabilization of partially unfolded states by Mg(2+), as observed in unfolding expe
285 wo minor native-like states, and two locally unfolded states in aqueous solution.
286 ns of the ion with compact intermediates and unfolded states of RNA is challenging to investigate, an
287 imply that water is a "poor" solvent for the unfolded states of these same proteins?
288 pendent NMR signals from both the folded and unfolded states revealed the population of at least one
289 the intrinsic fluctuations of the folded and unfolded states, which was measured by single-molecule (
290 ased energy function for both the folded and unfolded states.
291 reveal that G4s fluctuate between folded and unfolded states.
292                      Moreover, the partially unfolded structure of alpha-lactalbumin in the nanoprobe
293 hosphorylated by various kinases because the unfolded structure of Tau makes them accessible.
294 hypothesised that denatured proteins with an unfolded structure, would have greater interaction with
295                             In addition, the unfolded structures originating from mechanical pulling
296 teracts with the heads (10S) and one with an unfolded tail (6S).
297  of contour length changes as the structures unfolded through intermediate states was compared to the
298 h allow us to visualize how these migrations unfolded through time and space.
299                                          The unfolded ubiquitin molecule binds to Npl4 and projects i
300             Surprisingly, the domain remains unfolded until it is fully synthesized, without collapsi

 
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