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1  random access of data (selective access and erasure).
2 g to chromatin, whereas ACF will not support erasure.
3 y, arise from exactly the opposite model for erasure.
4 nges including DNA demethylation and imprint erasure.
5 d selectively, because dopamine blocks their erasure.
6 ishable solid-state emitters because of path erasure.
7 te to circuit remodeling, memory encoding or erasure.
8 eservoirs by performing perfect non-Landauer erasure.
9  and infralimbic (IL) cortex to prevent fear erasure.
10 hey are downstream consequences of H2AK119Ub erasure.
11  reorganization, X reactivation, and imprint erasure.
12 printed genes remain relatively resistant to erasure.
13 d accounts for the unique process of imprint erasure.
14 ate that 98% of errors can be converted into erasures.
15 s(9) or conversion of errors into detectable erasures(10).
16 gers adaptive chromosome destabilization via erasure a centromeric histone H3, CENP-A; a process that
17       Differentiating between extinction and erasure accounts is extremely difficult and requires man
18 be robust and nonvolatile even after thermal erasure across its ordering temperature.
19  work cost applies for classical and quantum erasure alike.
20 odifications require DNA repair pathways for erasure and by the recent discoveries that oxidative DNA
21 te of the brain, constantly promoting memory erasure and competing with processes that promote memory
22  images implies an active mechanism of image erasure and creation as the basis of normal visual proce
23 reprogram their epigenomes via a genome-wide erasure and de novo rewriting of DNA methylation marks.
24 ood process of germ cell allocation, imprint erasure and gamete formation, with 4-6 weeks being requi
25 m switch of TET1 regulates epigenetic memory erasure and mouse development.
26  through PKMzeta inhibition is due to memory erasure and not to retrieval failure.
27 cribe the health effects of settler colonial erasure and racial capitalist exploitation, also reveali
28                                      Thermal erasure and reentry into the low-temperature ground stat
29 ive zones or disk formatting for information erasure and rewriting.
30                                              Erasure and subsequent reinstatement of DNA methylation
31 esults reveal a molecular mechanism for fear erasure and the relative instability of recent memory.
32 ting time, hours of image persistence, rapid erasure, and large area-a combination of properties that
33 act in 8.5- to 9.5-dpc PGCs and then undergo erasure at approximately 10.5 dpc as the PGCs enter the
34  show no evidence of DNA methylation imprint erasure at the cis-acting PSW imprinting center.
35 three circuit's constituent processes: basal erasure, auto and cross-catalysis, and recruited erasure
36 ctivating a fear memory results in effective erasure by subsequent extinction training.
37 city qubit channels can assist an incomplete erasure channel in sending quantum information.
38 s, quantum-limited amplifiers, dephasing and erasure channels in arbitrary dimension.
39 erest, including dephasing, depolarizing and erasure channels.
40 ectors and has a variety of implications for erasure coding, compressed sensing, and sparse recovery.
41                     Here we demonstrate both erasure conversion and high-fidelity Bell state generati
42 ion of technical improvements, and shows how erasure conversion can be utilized in NISQ devices.
43                             We further apply erasure conversion in a quantum simulation experiment fo
44 d behind competitors(15,16) and this type of erasure conversion is yet to be realized for matter-base
45                                              Erasure conversion should benefit any error correcting c
46 erformed mid-circuit readout and mid-circuit erasure detection through local shelving into motional s
47 challenges in making inferences about memory erasure during extinction.
48 ntext, which protects existing memories from erasure during new motor learning.
49        These results suggest that imprinting erasure during reprogramming depends on the epigenetic l
50             Whole genome profiling showed an erasure effect of IL-1beta and TNF-alpha, resulting in a
51 n two phase 3, double-blind, 52-week trials, ERASURE (Efficacy of Response and Safety of Two Fixed Se
52  with single-atom resolution(7,8), a form of erasure error conversion(9-12).
53 he transmon can be detected and converted to erasure errors in all operations, leaving background Pau
54                      When excising data with erasure errors observed via fast imaging of alkaline-ear
55 ss errors can be detected and converted into erasure errors, which are in general much easier to corr
56 ection of these errors, we convert them into erasure errors; during detection, the induced error prob
57 nism that converts motional excitations into erasures, errors with a known location.
58 s that this should produce persistent memory erasure even after the inhibitory agent is removed.
59              This contrasts with information erasure, first investigated by Landauer, for which a the
60  memories in juvenile rodents are subject to erasure following extinction training, while after closu
61                                  In females, erasure follows loss of X inactivation, causing X dosage
62 havior, which suggests that emotional memory erasure has occurred.
63 y insulated from its environment during fast erasures, i.e., fast protocols are adiabatic as no heat
64 tus of PGCLCs resembles the dynamics of 5meC erasure in embryonic PGCs remains controversial.
65 diated pluripotent reprogramming and imprint erasure in somatic cells.
66   A closer look at H19 ICR revealed complete erasure in SSCiPSC in contrast to fiPSC.
67                                   Imprinting erasure in SSCiPSC was maintained even after in vivo dif
68     Here, we report that ALKBH5-mediated m6A erasure in the nuclei of spermatocytes and round spermat
69 ee text], and that Landauer's bound for fast erasures in underdamped systems becomes the adiabatic bo
70 f PGCLCs in studying the germline epigenetic erasure including imprinted genes, epimutations, and era
71 ior to mitosis, which we refer to as mitotic erasure, inducing periods of inactivity, thus providing
72  the energy dissipation in the memory during erasure is the most essential dissipation process in a d
73 at a central component of extinction-induced erasure is the synaptic removal of calcium-permeable alp
74 y considering the consequence of information erasure, it is argued that biological systems can proces
75         UBP5 promotes H2A monoubiquitination erasure, leading to transcriptional de-repression.
76                        Conversely, in males, erasure leads to permanent X dosage decompensation.
77 lematic because, in the limit of progressive erasure, no record remains.
78        In this setting of shared physiologic erasure, NSEs harbor a malignancy-associated hypermethyl
79                                              Erasure occurred without displacing the transcription fa
80 ly in renal development, followed by imprint erasure, occurs during Wilms' tumourigenesis.
81 ic regulation through its involvement in the erasure of 5-methylcytosine.
82                                   The global erasure of 5mC from the parental genomes during preimpla
83 lecular requirements, rather than simply the erasure of a previously learned process.
84 ns(6,12-14,17,18), preventing corrections or erasure of a shape, or sustained stimulation(5,7-11,25),
85 evelopment and in cloned animals, and in the erasure of acquired epigenetic information.
86 lencing machinery and its DUB partner allows erasure of active PTMs and the de novo transition of a t
87 ternally, both deletions are associated with erasure of all maternal GNAS methylation imprints and au
88 ications include, genome-wide demethylation, erasure of allele-specific methylation associated with i
89 y of PGCs showed nearly complete or complete erasure of allele-specific methylation in both H19 and S
90 patterning that allows repeated creation and erasure of arbitrary shapes of thin-film ferromagnetic s
91 nding of the establishment, maintenance, and erasure of cellular identities in plants remains limited
92 cell mass, whereas others may require active erasure of chromatin marks.
93 tic tissues of the flower, necessitating the erasure of chromatin modifications that have accumulated
94                     This produced persistent erasure of conditioned place avoidance.
95 the disorder may result from the progressive erasure of cortically based memory representations.
96                    Here, we demonstrate that erasure of CpG methylation (5mC) in PGCs occurs via conv
97 fferentiation to memory cells was coupled to erasure of de novo methylation programs and re-expressio
98                                  Genome-wide erasure of DNA cytosine-5 methylation has been reported
99                                              Erasure of DNA methylation and repressive chromatin mark
100  extensively reprogrammed through the global erasure of DNA methylation and the exchange of histones
101 ic reprogramming steps, including the global erasure of DNA methylation at the 5-position of cytosine
102                              Although global erasure of DNA methylation has been observed in zygotes
103  genomic regions are resistant to widespread erasure of DNA methylation in mouse embryonic stem cells
104                      Our results reveal that erasure of DNA methylation in the germ line is a global
105   AID deficiency interferes with genome-wide erasure of DNA methylation patterns, indicating that AID
106                                  Genome-wide erasure of DNA methylation takes place in primordial ger
107                The mechanisms of genome-wide erasure of DNA methylation, which involve modifications
108 network and progressive and conserved global erasure of DNA methylation.
109  Dnmt3b, leading to transient and reversible erasure of DNA methylation.
110 osine, potential intermediates in the active erasure of DNA-methylation marks.
111 n of organotypic vascular niche cues lead to erasure of EC signatures, contributing to the pathogenes
112 gramming involves processes that lead to the erasure of epigenetic information, reverting the chromat
113 ogramming in the germline contributes to the erasure of epigenetic inheritance across generations in
114 2'-deoxycytidine, an intermediate during the erasure of epigenetic marker 5-methyl-2'-deoxycytidine,
115                                              Erasure of epigenetic memory is required to convert soma
116 ng specification of PGCs that results in the erasure of epigenetic memory of EpiSCs following reactiv
117 t stem cells synergistically and enhance the erasure of epigenetic memory.
118 of pluripotency-specific genes and extensive erasure of epigenetic modifications.
119 ypothesis that extinction causes the partial erasure of fear memories remains viable.
120  report that Tet1 has a critical role in the erasure of genomic imprinting.
121 tablishes a critical function of Tet1 in the erasure of genomic imprinting.
122 gratory primordial germ cells coincides with erasure of genomic imprints and reactivation of the inac
123 t control the establishment, maintenance and erasure of germline epigenetic imprints.
124 oietic precursor cell line results in global erasure of H2AK119Ub, striking depletion of H3K27me3, se
125 erve as a stable epigenetic memory, and that erasure of H3K4me2 by LSD/KDM1 in the germline prevents
126                             Signal-dependent erasure of H4K20me3 is required for effective gene activ
127 ependent JMJD6 recruitment on A-PEs mediates erasure of H4R3me(2(s)), which is directly read by 7SK s
128                                The enzymatic erasure of histone modifications is widely assumed to be
129 mmatory responses by altering the reading or erasure of histone modifications required for inflammato
130 f genomic imprinting, cell lineage-dependent erasure of imprinting, an unidentified mechanism of X ch
131 d in early embryos, and is important for the erasure of imprints and epimutations, and the return to
132 s Tet1 and Tet2 participate in the efficient erasure of imprints in this model system.
133  donors, and revealed that demethylation, or erasure of imprints, was already initiated in PGCs at 10
134 h certificates, resulting in the statistical erasure of Indigenous people in routine vital statistics
135 cal stability of DNA challenges the complete erasure of information encoded in DNA sequences.
136 ng slow-wave sleep, leading to the selective erasure of information from hippocampal circuits as memo
137 nucleotides, and enables rapid and permanent erasure of information.
138 t also, more importantly, contributes to the erasure of intersex, transgender, nonbinary, and agender
139 e two key features, together with stochastic erasure of intervening stop codons, resulted in a unique
140 rrier progressively as they proceed with the erasure of key properties of epiblast cells, resulting i
141                 This accompanies substantial erasure of lamina-associated domains, generating spermat
142 ated that deterministic, nonvolatile writing/erasure of large-area patterns of this electromechanical
143   Most generally, TGCTs conserve PGC-lineage erasure of maternal and paternal genomic imprints and DP
144                          In AD, such a rapid erasure of memories soon after they are acquired during
145                            We show here that erasure of methylation marks during male germ-line devel
146   Wild-type PGCs revealed marked genome-wide erasure of methylation to a level below that of methylat
147                                  Conversely, erasure of methylation was observed at the identified CG
148 ure, auto and cross-catalysis, and recruited erasure of modifications.
149             Here, we report the creation and erasure of nanoscale conducting regions at the interface
150 l exposure, may open a window for editing or erasure of neural representations that drive pathologica
151 ntenance of some of these modifications, but erasure of others.
152 elopment has emerged wherein the genome-wide erasure of parental DNA methylation is required for embr
153  regulated and is not an undirected, radical erasure of parental epigenomes.
154 in this context is DNA demethylation and the erasure of parental imprints in mouse primordial germ ce
155 c, most PGCs did not demonstrate significant erasure of paternal allele-specific methylation until 10
156  evidence supporting the role of Tet1 in the erasure of paternal imprints in the female germ line.
157 ing chromatin state was achieved by specific erasure of preexisting chromatin marks in the precursor
158 lectively, these findings suggest that rapid erasure of repressive histone marks by KDM7A and UTX is
159 ear architecture accompanied by an extensive erasure of several histone modifications and exchange of
160 golith layer, as well as the degradation and erasure of small impact craters (less than approximately
161 ion-inhibition networks leads to an adaptive erasure of spurious sequences.
162 n states that effectively amounts to partial erasure of stored information.
163 ore propose that the previously demonstrated erasure of stored spatial memory and the disruption of p
164 upted ATX1 and CLF functions did not lead to erasure of the CLF- and ATX1-generated epigenetic marks,
165 chanism coupling eukaryotic transcription to erasure of the H2A.Z epigenetic signal.
166 rned responses, which is often attributed to erasure of the memory; in the case of Pavlovian learning
167                    Embryonic germ cells show erasure of the methylation markers (imprints) of the Igf
168 s thought to embody new learning rather than erasure of the original fear memory, although it is unkn
169 rrent theories suggest extinction is not the erasure of the original learning but involves new learni
170 mic reorganization demonstrate that complete erasure of the polycomb repressive mark H3K27me3 is not
171    Here, we show that dynamic generation and erasure of the repressive histone modification tri-methy
172 imately 2-3 times this interval, a near full erasure of the synaptic connectivity pattern.
173 ts to a direct link between eviction-coupled erasure of the ubiquitin mark from ubH2B and co-transcri
174 oans, including in Drosophila, for which the erasure of this epigenetic mark has been ascribed to the
175          As a consequence of both incomplete erasure of tissue-specific methylation and aberrant de n
176 potentiation (a cellular substrate of memory erasure) of conditioning-induced potentiation at LA syna
177               m(6)A inhibitor leads to m(6)A erasure on massive retrotransposons.
178 3, one of the m(6)A methylases, led to m(6)A erasure on select target genes, prolonged Nanog expressi
179 on of new memories rather than in the simple erasure or forgetting of memories from acquisition.
180 urons (PV-TrkB hCKO) in IntelliCage and fear erasure paradigms, we show that chronic treatment with f
181  with information theory through information erasure principle.
182                         Using a fast optimal erasure protocol, we also show that these adiabatic proc
183  PGC-like state of genomic-imprint and DPPA3 erasure, recurrent hypermethylation of cancer-associated
184  contribution of these two mechanisms to 5mC erasure remains unclear.
185 including imprinted genes, epimutations, and erasure-resistant loci, which may be involved in transge
186 g no heat are separated from heat-generating erasure steps which are logically irreversible but therm
187 ), we randomly assigned 738 patients (in the ERASURE study) and 1306 patients (in the FIXTURE study)
188 dose than with placebo or etanercept: in the ERASURE study, the rates were 65.3% with 300 mg of secuk
189 dose than with placebo or etanercept: in the ERASURE study, the rates were 81.6% with 300 mg of secuk
190 ile mammals undergo two rounds of global 5mC erasure, teleosts, for example, exhibit localized matern
191 he most direct test of a storage role is the erasure test.
192 ctures, are more stable against thermal self-erasure than conventional memory devices.
193 processes of memory consolidation and memory erasure that occur during sleep.
194 t converts the dominant physical errors into erasures, that is, errors in known locations.
195 otential for TE activation during global 5mC erasure, thereby acting as a failsafe to ensure TE suppr
196 bservation suggests that the track undergoes erasure to approximately half of its amplitude, achieved
197 rsion process provides the necessary quantum erasure to eliminate which-path information in the photo
198  of manipulation progresses - from creation, erasure, to transition - can be accurately implemented o
199 is based on cycles of staining, imaging, and erasure, using photobleaching of fluorescent labels of r
200        Although the beginning of methylation erasure was evident on the H19 paternal allele at 9.5 dp
201 tical analysis of the physics of information erasure, we clarify the link between information and the
202 served global 5-hydroxymethylcytosine (5hmC) erasure within three days of culture initiation.

 
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