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1 state functional magnetic resonance imaging template.
2 linear polymers prepared in the presence of template.
3 lective BRD7/9 inhibitor from a pyridazinone template.
4 he same RNA target strand, serving here as a template.
5 clinician communication using an information template.
6 int mutations without supplying a DNA-repair template.
7 resolve G-quadruplexes on the lagging-strand template.
8 mRNA output is higher when PQS is in the non-template.
9 ch in turn generates G4 structure in the non-template.
10 oparticles in the presence of glucose as the template.
11 the shape and chemical functionality to the template.
12 quinolinones, an underrepresented privileged template.
13 tly confirming the localized presence of the template.
14 the first RNA strand that is later used as a template.
15 n of both precursors (Ni and Ce) on the 3DOM template.
16 ing tetrabutylammonium perchlorate as a soft-template.
17 but not Pol II, could transcribe nucleosomal templates.
18 hout requiring double-strand breaks or donor templates.
19 tin and other bulky adducts in synthetic DNA templates.
20 cleotides does not impede the copying of RNA templates.
21 plication of both undamaged and base-damaged templates.
22 h affinity for supercoiled and catenated DNA templates.
23 s on both short (10-nt) and long (25-nt) RNA templates.
24 ition as the matching of patterns to learned templates.
25 line and some of its methylated analogues as templates.
26 provided different single-stranded donor DNA templates.
27 ein propagates via prion-like conformational templating.
28 der structures was complex and involved self-templating.
29 n of ventricular segment based on population templates, (2) population-based localization within a se
30 superheat of just 2.2 degrees C for the salt templated 3 wt% GNP draped 20 um diameter copper particl
33 nal inferential method using potential donor templates absent from B cell genomes, we obtain estimate
36 yeast mtRNAP that explain promoter melting, template alignment, DNA scrunching, abortive synthesis,
37 ntercellular transmission and the subsequent templated amplification of these misfolded proteins are
40 talytic system leveraging a remote directing template and a transient norbornene mediator to selectiv
41 1 RNA serves two functions, as a translation template and as a viral genome, individual RNA molecules
42 re biasing terms, the addition of homologous template and co-evolutionary restraints to AWSEM-Suite g
43 host genomes by using tags to identify each template and demanding consensus over multiple reads.
45 thesized using three C bases in the DNA as a template and extends RNA without displacement of the pro
47 mplexan cytoskeletons, illuminating how they template and orient critical processes during infection.
49 ing double-cysteine-modified peptides as the templates and adsorbing the templates on a gold surface
51 ions of folding-enhancing mutations into GFP templates and screening for brightness and expression ra
53 The assay was developed with synthetic DNA templates and validated with DNA from two breast cancer
55 ral RdRp elongation traces on kilobases long templates, and this has shown that RdRp nucleotide addit
58 (synthesized for the first time, via a soft-templating approach, with high phase-purity) can be used
59 CR is diminished at higher concentrations of template approaching 100 percent positive partitions, wi
62 ows for accurate modeling of receptors using templates as low as 20% sequence identity, which account
64 en the Bayesian optimal observer weights the template at each pixel location by the estimated reliabi
66 ferentiation of an incoming nucleotide and a template base and the N-terminal domain of DNA ligase I
68 es Prim-PolC to couple primer extension with template base dislocation, ensuring that the unpaired te
69 jacent Val-557 is in direct contact with the template base, and the V557L mutation is implicated in l
74 g this additional information in a so-called template-based method has the potential to significantly
77 With this protein localization atlas and template-based protein structure modeling, we have assem
79 base dislocation, ensuring that the unpaired templating bases in the gap are ushered into the active
81 a model in which the 3' terminus of the vRNA template binds in the mode B site during elongation.
82 y further sequence engineering of the set of template/blocker scaffolds and their coupling to a nicki
88 is a strategy to prepare chiral AgNP arrays templated by two constitutionally isomeric aromatic pept
89 incorporation of chemical lesions into dsDNA templates by sequential PCR and translesion synthesis.
90 hese modifications enable the copying of RNA templates by the multistep ligation of tetranucleotide b
91 placement of the excised region with a donor template carrying the wild-type repeat size to maintain
92 he directed evolution of RT function for any template chemistry called compartmentalized bead labelli
93 The intrinsic collagen-like structure of templated CMP pairs helps to explain the success of stic
94 ncounters with R-loops on the leading-strand template (co-directional) resulted in gaps in the nascen
95 neuronal SNARE assembly through an obligate template complex intermediate containing Munc18-1 and 2
96 utational studies suggest that the MUN-bound template complex is functionally important for SNARE ass
100 allohelices inhibit DNA synthesis on the RNA template containing four repeats of the human telomeric
101 rmed by untemplated polymerization, but that template copying chemistry favored RNA synthesis; multip
103 Finally, facile integration of the bottom-up templated crystallization with emerging top-down techniq
104 tion with DNA substrates containing either a templating cytosine (nonmutagenic) or adenine (mutagenic
105 o-GTP adopts an anti conformation opposite a templating cytosine and a syn conformation opposite aden
106 metric-space nearest neighbor search over a template database of fixed-length amino acid words to de
107 on step of RT-qPCR with a rapid nucleic-acid-template-dependent DNA chemical ligation system, that al
108 ve data provide strong evidence to show that template-dependent inhibition of SARS-CoV-2 RdRp by RDV
109 In doing so, they relied predominantly on a template derived from the expression of REM sleep in the
113 a wide range of transition-metal-catalyzed, template-directed remote C-H activation reactions of alc
115 he link between allosteric cooperativity and template-directed synthesis has been investigated by stu
118 s on template DNA and how RNA polymerase and template DNA determine length of reiterative RNA product
119 ing bidirectional transcription when the non-template DNA strand bonds with the hybrid duplex (collap
120 also performed biochemical assays to monitor template DNA translocation during RNA synthesis from the
121 encoding an intrinsic stall site within the template DNA, our chemical transcription roadblocking ap
122 synthesis requires a considerable amount of template DNA, the preparation of high-quality DNA "parts
129 ntly specified by a homology-directed repair template during editing with Cascade-Cas3, but not Cas9.
130 enhances the physical search for an ectopic template during homology-directed repair (HDR), we teste
132 1,5-naphthalene units, have been obtained by template effect in a thermodynamically controlled synthe
133 prisingly, the chloride anion had a negative template effect in opposition to the results obtained fo
134 ver, the bromide anion had a clear catalytic template effect in the macrocyclization reaction, and su
135 ix is directly correlated to the "reciprocal templating" effect, which modulates the interactions bet
136 tic resonance spectroscopy confirms that the templated electro-synthesis affords structural defects i
137 to a view- and orientation-independent face template encoded in a face-centered reference frame, tha
140 disorder-to-order transition in IDPs termed "templated folding," whereby the binding partner dictates
141 l)methyl benzamide scaffold was studied as a template for (18)F-positron emission tomography ((18)F-P
146 40), and the ligand is an effective Vernier template for directing the synthesis of the 12-porphyrin
147 nto one comparative model, the best possible template for every region of a target can be used expand
152 tral role in viral replication, serving as a template for Gag/Gag-Pol translation and as a genome for
153 We defined the minimal length of the RNA template for in vitro de novo RNA synthesis using the pu
158 ption initiation factor that engages the DNA template for RNA priming and growth and disengages when
159 uman telomerase RNA (hTR), which serves as a template for the addition of telomeric repeats to chromo
160 e tryptophan moiety as a solid pharmacophore template for the design of highly potent modulators of T
161 thin physiological complexes could provide a template for the design of safer and more effective ther
164 model suggests that RDV, when serving as the template for the incoming UTP, is not properly positione
167 hydrogels can be employed as precursors and templates for architecting three-dimensional frameworks
169 eceived high-index Cu foils can serve as the templates for producing high-index single-crystal Cu-bas
170 res that can be used as optical microarrays, templates for soft lithography, and ordering matrices fo
172 alpha-synuclein peptides were synthesized as templates for the molecular imprinting of conductive pol
174 accumulation of ssDNA in the lagging-strand template fosters the formation of a triplex between the
175 phi29 polymerase used in MDA is sensitive to template fragmentation and presence of sites with DNA da
181 ligand, performs conformational sampling and template-guided energy refinement to produce a variety o
184 NNS) RNA viruses possess a ribonucleoprotein template in which the genomic RNA is sequestered within
185 en the recombinogenic filament and the donor template in yeast, limiting strand rejection by the Sgs1
187 ng the endogenous homologous transcript as a template, indicating ATXN3's role in PNKP-mediated error
190 e ends of the homology-directed repair (HDR) template interact with Cas9 ribonucleoproteins (RNPs) to
191 offer catalytic activity and an ultrasmooth templating interface that promotes Frank-van der Merwe r
192 ts and a homologous recombination (HR) donor template into embryos to trigger homology directed repai
193 Pooled knockin of dozens of unique barcoded templates into the T cell receptor (TCR)-locus revealed
198 R) to develop the chimpanzee brain reference template Juna.Chimp for spatial registration and the mac
203 s to predesigned hairpins H(E) and H(F), the templates M'/M and N'/N, the RNAp/NTPs machinery, and th
204 se that was constructed so that the standard template-matching (TM) observer performs equally well wh
205 nalytical difficulties, we developed a novel template-matching-based spike sorting method, which enab
207 lar strands within a discrete layer by anion-template metal-ion coordination opens the way for the sy
209 egies, including biomaterial fabrication and templating, might be used to overcome existing challenge
211 ted nested Laplace approximations (INLA) and Template Model Builder (TMB) for Bayesian and frequentis
214 aFold created high-accuracy structures (with template modelling (TM) scores(6) of 0.7 or higher) for
215 ization with poly-sialic acid (PolySia) as a template molecule and p-aminobenzeneboronic (p-ABA) acid
216 nylenediamine (o-PD) in the presence of PFOS template molecules on a glassy carbon macroelectrode.
219 ion fork DNA helicase, and 2) on the damaged template, nascent leading-strand gaps were generated by
220 to pure tones, similar to cortical "harmonic template neurons" (Feng and Wang, 2017), but to a lesser
221 base-specific interactions with flipped non-template (NT) nucleotides "AAGT" at -4 to -1 positions o
222 antly higher probability that the downstream template nucleotide coded for the incoming nucleotide.
225 fined point following infection to clear the template of ribosomes to allow efficient replication.
227 lating, the complete exchange of metals in a template, of group 11 clusters across the entire coinage
228 peptides as the templates and adsorbing the templates on a gold surface by means of forming self-ass
229 ted in samples with a high load of nontarget template or influenza B virus, demonstrating assay speci
231 ds as diverse as bioinspired mineralization, templating, pharmaceuticals, colloidal crystallization,
233 our results show that memory-guided identity templates proactively impact perception and are associat
235 2Bub1) has central functions in multiple DNA-templated processes, including gene transcription, DNA r
238 ures of the SARS-CoV-2 holo-RdRp with an RNA template product in complex with two molecules of the ns
239 tential model for how these interactions can template protein-protein interactions causative of cellu
241 scent leading strand, whereas lagging-strand template R-loops (head-on) had little impact on replicat
242 The experimental parameters, such as monomer/template ratio, electropolymerization cycle and adsorpti
243 orporation of the complementary UTP opposite template RDV is compromised, providing a second opportun
244 xample of an electrochemical oligonucleotide-templated reaction (EOTR), whereby two PNA probes - func
245 hybridization architecture that enhances the templated reaction and enables the uncaging of a substra
246 tion factors and synthetic DNA transcription templates regulates the synthesis of a fluorescence-acti
247 circuit components beyond naturally-derived templates remains challenging due to poorly understood d
248 en grids, followed by the removal of the ion template, result in a wholly organic molecular material
250 is not known what controls the formation and templated seeding of strain-specific structures associat
251 with AgNCs/PMAA (PMAA = polymethyl acrylate templating several AgNC) are also electroactive for H(2)
252 hese findings suggest that a chromatin donor template should be useful for a wide range of HDR applic
254 n hurdles, including secondary structures in template, slowed helicase, or uncoupled helicase-polymer
257 play a crucial role in RNA priming by aiding template strand alignment in the active site for high-af
261 c IgG antibody to two antigen-conjugated DNA templating strands that triggers a chemical reaction tha
262 ntegrate organic and inorganic structures by templating strategies and electrodeposition to create ma
263 ls for bulk Ag(3) PO(4) , and offers a fresh template strategy for the synthesis of silver NCs with h
265 ion of the strengthening phase theta' onto a template structure in the aluminium-copper alloy system.
267 ot most, of these events are associated with template switching in postreplication gaps as opposed to
270 Here, we report on the metal-free active template synthesis of [2]rotaxanes in one step, up to 95
273 CDN to two hairpins, H(A) and H(B), and two templates T(A) and T(B) and a nicking/replication machin
274 istic dissection of the Coriobacteriia and a template that can be applied to study other genetically
275 lates), which defines a suite of class-based templates that allows users to develop and implement hig
277 sit the strategies - including soft and hard templating - that have been developed for generating nan
278 process requires tetrafluoroborate anions to template the assembly of the interwoven grid by binding
281 eaves 3D-like perovskites which surprisingly templates the growth of layered perovskites, enabled by
282 These aggregates were thought to act by templating the formation of an assembly-competent nuclea
283 g Ni by successive infiltration in the solid template, the CeO(2) crystal size is reduced, Ni dispers
284 enes, we report and rationalize the absolute templating, the complete exchange of metals in a templat
286 rtan-bound human AT1R (PDB:4ZUD) served as a template to create an inactive apo-AT1R via molecular dy
287 sed vector was defined from the pyridazinone template to enable bifunctional molecule synthesis, and
288 as9 ribonucleoproteins (RNPs) to shuttle the template to the nucleus, enhancing HDR efficiency approx
289 n-loop amplification reaction using circular templates to generate intermediate amplicons, and an off
290 ility of combining synthetic gRNAs and dsDNA templates to perform homology directed repair and genome
292 -3 can add long stretches of alternating non-templated uridine (U) and guanosine (G) ribonucleotides
293 ense genomic and negative-sense replicative, template viral RNA; essential viral replication proteins
294 elements with examples that can be used as a template when preparing and submitting ML-based manuscri
295 tive interphase layer will be formed outside templates when the redox potential exceeds the potential
296 ed struct (Statistics in R using Class-based Templates), which defines a suite of class-based templat
298 ine ecological responses as suitable habitat templates with enough usable surface area to support GRD
300 pically transcribed from random-sequence DNA templates, yielding a highly diverse set of RNAs that co