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1 est interactions with uncaging and molecular cleavage).
2 otenoids as substrate or perform double-bond cleavage.
3 ngaged in R-loops and the other by MutLgamma cleavage.
4 ce that exposes an otherwise buried site for cleavage.
5 reased IQGAP1 acetylation and reduced IQGAP1 cleavage.
6 ospholipids (PE, PS, and PC), via ester bond cleavage.
7 from modified SM lipid anions via amide bond cleavage.
8 but also activates it for efficient O-O bond cleavage.
9 via a single Cu atom to accomplish N-O bond cleavage.
10 alytic mechanisms exist for xylan and glucan cleavage.
11 ssembly and dictate the extent of maturation cleavage.
12 al kinase activation and initiator caspase 8 cleavage.
13 dogenous functions, such as stimulating Ctr1 cleavage.
14 precursor, which substantially enhances its cleavage.
15 poor protection capability against enzymatic cleavage.
16 ts own proteolytic activity mediates zymogen cleavage.
17 part, to make their backbones accessible for cleavage.
18 steine protease, Prp, which carries out this cleavage.
19 ns upon derivatization followed by reductive cleavage, a degradative method that cleaves beta-ether b
21 a1 induction of enzymes that cause autocrine cleavage/activation of PAR2, possibly through a biased s
22 tion drastically accelerates the proteolytic cleavage activity, even in the absence of forces or dena
24 mice with this inhibitor reduces tau and APP cleavage, ameliorates synapse loss and augments long-ter
28 ssociated with significant decline in oocyte cleavage and blastocyst development after in-vitro ferti
29 ive of the isotope effects pertinent to bond-cleavage and bond-formation reactions during chloraminat
30 ep is not rate-determining, but the C-H bond cleavage and C-Si bond-forming steps together influence
34 ately characterize intestinal alpha-carotene cleavage and its relative contribution to postprandial v
38 e we have systematically mapped and compared cleavage and polyadenylation sites (PASs) in two yeast s
39 n the pre-mRNA polyadenylation signal by the cleavage and polyadenylation specificity factor (CPSF) c
40 primarily interact with Fip1, a component of cleavage and polyadenylation specificity factor (CPSF).
41 utations decreased the binding of NS1 to the cleavage and polyadenylation specificity factor 30 (CPSF
45 lar potassium significantly reduced IL-1beta cleavage and release in response to T. gondii infection,
47 QCA was likely formed through oxidative ring cleavage and subsequent decarboxylation of acridine, a w
49 beta maturation and secretion, pro-caspase-1 cleavage, and speck formation by apoptosis-associated sp
50 esion by protecting the cohesin complex from cleavage, and this has been shown in yeasts to be mediat
54 pport degradation pathways that include meta-cleavage as well as ortho-cleavage, which has not been p
56 nd XBP1-depleted cells, validation using RNA cleavage assays, and 5' RACE identified the prooncogenic
59 uctural microheterogeneity of signal peptide cleavage at the amino terminus of FGF2, whereas IGF1 dis
60 of both molecular interactions (for example, cleavage, binding, folding and unfolding) and biological
61 h molecules is arbitrated by their regulated cleavage brought about by components of a multiprotein c
62 ed Cdc48 cofactor Ufd1 is required for SREBP cleavage but does not interact with the Cdc48-Rbd2 compl
63 omain (Toc159G) of pea (Pisum sativum) using cleavage by bound preproteins conjugated with the artifi
64 The coronavirus (CoV) S protein requires cleavage by host cell proteases to mediate virus-cell an
65 rategy in which antibody-targeted controlled cleavage by micrococcal nuclease releases specific prote
66 ally using kinetic isotope effects show that cleavage by oxidative addition of an O-H bond in H2O is
67 re ASOs, 3'-SpSpRp, that promotes target RNA cleavage by RNase H1 in vitro and provides a more durabl
71 cts the peptidoglycan of dividing cells from cleavage by the major autolysin LytA and occurs at the s
75 s evidence on compounded deprivation, racial cleavages, civic engagement, institutional cynicism, and
76 served local sequence preferences, occurs in cleavage cluster regions (CCRs), and is enriched in intr
79 ls that target DNA gyrase by stabilizing DNA-cleavage complexes, but their clinical utility has been
80 ntiproliferative effect of Cas9-mediated DNA cleavage confounds such measurement of genetic dependenc
84 c-resistant alpha1C Prevention of C-terminal cleavage did not alter beta-adrenergic stimulation of Ca
85 that miR-449b expression improves the first cleavage division, epigenetic reprogramming and apoptoti
86 ryonic development is characterized by rapid cleavage divisions, which impose significant constraints
87 ransposase binding to the inner 12DRs (where cleavage does not occur), followed by capture of the 12D
88 XRN2, a key coordinator of multiple pre-rRNA cleavages, driving mature rRNA formation and discarded r
89 We therefore conclude that inhibition of C5 cleavage during the bacteremic stage of sepsis could be
90 e identify a strong correlation between Cas9 cleavage efficiency and the stability of the DNA-RNA (R-
92 esins from chromosomes without changing Scc1 cleavage efficiency, promoting dissolution of cohesion.
95 tional characteristic marker ions from alpha-cleavage, enables convenient structure assignment of ca.
96 is protected by Sgo2 from Separase-mediated cleavage ensuring that sister chromatids are kept togeth
97 -carotene oxygenase 2 (BCO2) is a carotenoid cleavage enzyme located in the inner mitochondrial membr
98 which is a product of both alpha- and gamma-cleavage events, could also induce TrkB phosphorylation.
100 s solfataricus TFS1 functions as a bona fide cleavage factor, while the paralogous TFS4 evolved into
103 lowers the activation barrier for C-OH bond cleavage from the metallocarboxylic acid intermediate.
104 (ECM) remodeling is thought to stabilize the cleavage furrow and maintain cell shape during cytokines
105 cence polarization microscopy and found that cleavage furrow ingression initiates by contraction of a
106 unequal cortical expansion, ensuring correct cleavage furrow positioning and the establishment of phy
108 and use the technology to characterize TOP2A cleavage genome-wide in the human K562 leukemia cell lin
109 nyl sulfide also showed competitive C-S bond cleavage giving phenyl sulfinic acid and ionization to d
111 visiae promote site-specific endonucleolytic cleavage in 25S ribosomal RNA (rRNA) adjacent to the c l
112 ein that promotes proofreading by transcript cleavage in elongation complexes backtracked by nucleoti
113 eavage in oxidation by persulfate, C-Cl bond cleavage in Fe(0)-mediated reductive dechlorination and
115 a "bottom-up" fundamental insight, C-H bond cleavage in methane over Ni-based catalysts was investig
116 agreement with expected mechanisms (C-H bond cleavage in oxidation by persulfate, C-Cl bond cleavage
117 Depletion of FXII in AD mice inhibited HK cleavage in plasma and reduced neuroinflammation, fibrin
118 ations as well as a functional role of TOP2A cleavage in regulating transcription elongation and gene
120 rocessing as well as downstream procaspase-3 cleavage in several cell types and under multiple condit
124 active isoforms of PKCs generated by calpain cleavage, in the sensory neuron and L7 are required to m
129 sign to improve the efficiency of target/DNA cleavage is critical to ensure the success of CRISPR scr
132 use the accumulation of S-OPA1 due to L-OPA1 cleavage is observed in mitochondrial fragmentation and
134 s increased in a mouse model of AD, and this cleavage is temporally correlated with the onset of brai
137 at a lincRNA-specific co-transcriptional RNA cleavage mechanism acts to induce premature termination.
138 per understanding of Cas9 activation and its cleavage mechanism can enable further optimization of Ca
143 ng this process in vitro, Hfq guides RNase E cleavage of a representative small-RNA precursor for int
144 aimed at inhibiting this protease-dependent cleavage of Akt may prove beneficial in preventing tau h
145 ons in APP that increase toxic amyloidogenic cleavage of APP and produce amyloid beta (Abeta) at the
146 ulating BACE1 distribution in axons and beta cleavage of APP at synapses remain largely unknown.
147 estriction, Gag promotes secretase-dependent cleavage of APP, resulting in the overproduction of toxi
150 ences in enzyme selectivity for peptide bond cleavage of camel and bovine milk proteins as well as di
151 n induced Beclin-1 cleavage with concomitant cleavage of caspase-3, indicating the onset of apoptosis
154 process is an attractive drug target because cleavage of concatemeric DNA is not required in mammalia
155 Metal homoenolates, produced via C-C bond cleavage of cyclopropanols, have been extensively invest
157 ng these factors revealed that Ire1-mediated cleavage of ER-associated mRNAs results in ribosome stal
158 nt and proinflammatory functions mediated by cleavage of fibrinogen and PAR1, the trypsin-like protea
159 onooxygenases (LPMOs) catalyze the oxidative cleavage of glycosidic bonds in recalcitrant polysacchar
160 show how the rate of reversible heterolytic cleavage of H2 can be controlled, spanning 4 orders of m
161 and P), have been developed for heterolytic cleavage of H2 into a proton and a hydride, akin to frus
165 poptosis through activation of caspase-3 and cleavage of HuR in paclitaxel-resistant oral cancer cell
166 ying biologic process driving production and cleavage of iFGF23, or alternatively the increased level
167 LDL secretion and free fatty acid uptake via cleavage of LFABP, which occurs in response to oleic aci
170 ypass activation of C3 is mediated by direct cleavage of native C3 by mannan-binding lectin-associate
171 olled vascular gateway specifically opens by cleavage of NPY by CD26 signaling via NPY2 and NPY5 rece
172 lete PACE4 knock-out mice suggested that the cleavage of overexpressed proprotein C is predominantly
173 led vessel method is a new approach for fast cleavage of PCB from phycocyanin and gave at 120 degrees
174 GF, that HMW-EGF is active, that proteolytic cleavage of pro-EGF first occurs at the C-terminal argin
178 th excitation of fully cyclized GNRs induces cleavage of sacrificial carbonyl groups, resulting in at
180 didate endonucleases have been implicated in cleavage of stalled replication forks to permit end rese
187 d TBHP as the green oxidant via the C-H bond cleavage of the benzylic carbon under mild reaction cond
188 ura and Buchwald-Hartwig reactions involving cleavage of the C(acyl)-O bond of aryl esters that proce
189 he metal center of Cp*RhCl to accelerate the cleavage of the C-H bond of N-pentafluorophenylbenzamide
190 nd NacNacAl (1) results in the unprecedented cleavage of the C-N multiple bond to give, after rearran
191 c residues facilitate the post-translational cleavage of the CaValpha2delta1 subunit at the predicted
192 omes and lysosomes does not provide complete cleavage of the drug from the nanoparticle, but that onc
193 dephosphorylation by ALP, but CES-catalyzed cleavage of the ester bond on the molecules results in d
194 nt types of indels obtained by Cas9-mediated cleavage of the GFP gene, guided by three independent sg
195 Furthermore, we observed that proteolytic cleavage of the host extracellular matrix protein fibron
196 Here, we provide evidence that proteolytic cleavage of the macrophage efferocytosis receptor c-Mer
197 on the back of the sensor to accelerate the cleavage of the magnetic nanobeads-peptide moieties away
198 he mutant APP, and inhibited gamma-secretase cleavage of the mutant C99 to generate Abeta, leading to
200 ding oxidation of the benzene ring after the cleavage of the piperazine ring (e.g., CIP product with
201 gands activate Notch by inducing proteolytic cleavage of the receptor ectodomain, an event that requi
207 einase) proteases are involved in ectodomain cleavage of transmembrane proteins, and ADAM17 is known
211 ell cycle asynchrony maintains the invariant cleavage pattern driving morphogenesis of the ascidian b
213 s method will aid in developing enzymes with cleavage patterns optimized for producing paCOS with def
214 rement of chromatin accessibility to DNase I cleavage, permitting identification of de novo active ci
215 lymerase II termination via depletion of the cleavage/polyadenylation machinery, circular RNA levels
219 tions in the VWF A2 domain, facilitating the cleavage process, cause a distinct form of von Willebran
222 y and levels of the matrix metalloproteinase cleavage product soluble receptor for advanced glycation
223 ionizing radiation (IR), determined that HuR cleavage product-1 (HuR-CP1) bound and promoted the expr
224 n pathways of complement activation, and its cleavage products C3a and C3b mediate several functions
225 y, WRN also influences the formation of FEN1 cleavage products during strand displacement on a nontel
229 loaded transferrin blocked MT2-mediated Tfr2 cleavage, providing further insights into the mechanism
230 kinetics revealed a 20-fold increase in the cleavage rate for the Gly1629Glu mutant compared with th
233 osidases that exhibit selective carbohydrate cleavage reactivity toward l-fucose over d-glucose.
239 o We found evidence that defined proteolytic cleavage results in various proteoforms of important pod
241 hat the overall rate-limiting step for aldol cleavage shifted from C-C bond scission (or an earlier s
242 tracellular site different from the thrombin-cleavage site and thus initiates biased receptor signali
243 n, which inserts the segment upstream of the cleavage site as an extra beta-strand in a central beta-
244 rate prior to T1 closure such that the U5-A6 cleavage site becomes embraced to achieve its cleavage c
246 an "immature" Chikungunya virus in which the cleavage site has been mutated to inhibit proteolysis.
247 hat cells clear trailing chromatids from the cleavage site in a two-step cell elongation and demonstr
250 the domain immediately downstream of the S2' cleavage site is the FP (amino acids 798-818 SFIEDLLFNKV
251 pro-TGF-beta1 with the proprotein convertase cleavage site mutated to mimic the structure of the TGF-
252 APP mutation, shifted the preferential beta-cleavage site of BACE1 in APP from the Glu(11) site to t
253 pared human FXII variants lacking the Arg353 cleavage site required for conversion to alphaFXIIa (FXI
254 P673 regulates APP processing, and the BACE1 cleavage site selection is critical for amyloidogenesis
255 PP673 regulates APP processing and the BACE1 cleavage site selection is critical for amyloidogenesis
256 by an increased availability of the ADAMTS13 cleavage site through A2-domain-fold thermodynamic desta
257 s residue is just before the gamma-secretase cleavage site, we then investigated whether the p75(alph
263 haFXIIa (FXII-R353A), or lacking the 3 known cleavage sites at Arg334, Arg343, and Arg353 (FXII-T, fo
264 oughput sequencing technology to define TOP2 cleavage sites at single-base precision, and use the tec
266 Site-directed mutagenesis of the phytaspase cleavage sites in prosystemin abrogated not only the phy
271 nds are at or near preferred gamma-secretase cleavage sites, suggesting that the sequence of APP and
274 ples approach to determining the binding and cleavage specificity of novel LHEs that should also be g
276 three individual H3.3 residues in oogenesis, cleavage-stage embryogenesis and early development.
277 mouse cells maintained modest activation of cleavage-stage genes driven by conventional promoters bu
278 isotope effects indicated that the C-H bond cleavage step is not rate-determining, but the C-H bond
280 eplication fork repair by mediating the fork cleavage that permits initiation of HR-mediated repair a
283 res after urine precipitation with conjugate cleavage (UglucP) or dried urine spot workup by conjugat
285 ompanied by increased Caspase-1 and IL-1beta cleavage upon NLRP3, but not AIM2 or NLRC4 inflammasome
286 s9 in two allele-specific systems, comparing cleavage using a SNP-derived PAM to a guide specific app
288 a 2-kDa macrocyclic peptide inhibitor of C5 cleavage, using in vitro whole-blood assays and an in vi
289 positively charged N-terminal anchors, whose cleavage via the prepilin peptidase, essential for pilin
290 tion and mediates post-translational BMPR-II cleavage via the sheddases, ADAM10 and ADAM17 in pulmona
293 nd in CEs when the exergonicity of C-Cl bond cleavage was reduced in an organic solvent (reaction wit
294 14 RNAi phenotypes and its infection-induced cleavage were abolished in a TEP1 loss-of-function backg
295 culature revealed that aggrecan and aggrecan cleavage were more abundant in human arteries than in hu
297 se 3C directly targets GSDMD and induces its cleavage, which is dependent on the protease activity.
298 as IGF1 displayed homogeneous amino-terminal cleavage with complete removal of the bombyxin signal pe
299 time, B. abortus infection induced Beclin-1 cleavage with concomitant cleavage of caspase-3, indicat
300 mmunoproteasome reduced internal destructive cleavages within the ALY epitope compared with the const
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