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2 We here explore the therapeutic potential of naked and adeno-associated virus (AAV)-packaged AONs in
3 d regulated budding yeast DNA replication on naked and chromatinized templates in vitro, providing ke
8 carriers for multiple cargos, including both naked and nanoparticle-encapsulated chemotherapeutics, g
9 nt human cohesin-NIPBL complex compacts both naked and nucleosome-bound DNA by extruding DNA loops.
14 e factors contributing to altered hearing in naked and the related Damaraland mole-rats and to examin
15 utant with reduced binding affinity to both "naked" and phospholipid-coated oil-water interfaces.
17 in a 1:1 molar ratio) gives the first stable naked anionic dithiolene radical 3(*), which, when coupl
18 ed analysis of structural parameters of the "naked" anions of [3]TrTol without interference from meta
22 , and p = 0.001 for sacituzumab govitecan vs naked antibody, and sacituzumab govitecan vs control-ADC
27 Electrical Resistivity (ER) surveys showed a naked burial produced large, low-resistivity anomalies f
33 Our results challenge the old vision of "naked" chromium species (i.e., low coordinated) as the a
35 ration of heme-peroxo-Cu compounds, using a "naked" complex synthon, [(F8)Fe(III)-(O2(2-))-Cu(II)(MeT
36 One of these immediate early genes encodes naked cuticle homolog 1 (NKD1), which is a repressor of
40 e first time, the formation of O(4)-POBdT in naked DNA and in genomic DNA of cultured mammalian cells
42 tive, Hoogsteen (HG) base pairing pattern in naked DNA duplexes, and estimated its relative stability
45 Here, we visualized the binding of PRC2 to naked DNA in liquid at the single-molecule level using a
48 sviruses infecting animals and humans, where naked DNA is packed under very high pressure due to the
49 ndamental question of whether nucleosomal or naked DNA is the preferred substrate of plant and animal
50 dingly, we demonstrate confluent staining of naked DNA molecules presented within microfluidic device
52 s [(6-4)PPs] from UV-irradiated cellular and naked DNA revealed that the effect of transcription fact
54 termediates that occurs during the repair of naked DNA substrates differs significantly from that in
56 relatively little effect on Cas9 cleavage of naked DNA substrates, but strongly inhibit cleavage of n
57 bunit Rpa12.2 showed a lower processivity on naked DNA templates, which was even more reduced in the
58 tion of the DNA template, as it evolved from naked DNA to chromatin, in the biochemical analysis of t
59 was at least sevenfold greater than that of naked DNA, and chromatin gave patterns of transcription
61 e binding orientation of the metallohelix to naked DNA, but does not substantially alter the overall
62 the nucleosomal sites relative to those for naked DNA, demonstrating that the high affinities are ac
65 osomes with similar binding affinities as to naked DNA, trapping a partially unwrapped nucleosome wit
66 As herpesvirus genomes enter the nucleus as naked DNA, we asked whether the HIRA chaperone complex a
67 hexasome H2A-H2B distal side is identical to naked DNA, while the accessibility on the H2A-H2B proxim
70 by using a candidate preventive/therapeutic naked-DNA vaccine that expresses human calreticulin (hCR
71 (ATM) kinase is activated synergistically by naked dsDNA and the Mre11-Rad50-Xrs2(NBS1) complex (MRX)
78 (Zea mays [Zm]) has a single aleurone layer, naked endosperm (nkd) mutants produce multiple outer cel
80 etic parameters are improved compared to the naked enzyme suggesting longer blood circulation after i
82 ny forming unit per 1 mL (CFU mL(-1)) by the naked eye and 10(1) CFU mL(-1) using ImageJ software.
83 ssembled monolayer (SAM) was detected by the naked eye and analysed using an image analysis software
84 netic nanobeads moieties was detected by the naked eye and analysed using ImageJ analysis software fo
85 e liquid mineral phase visible even with the naked eye and its transformation into amorphous nanopart
86 entify significant traces not visible to the naked eye and not detectable by XRF spot measurements or
87 es the detection of a few molecules with the naked eye and quantified by an auto-analysis software.
89 show any obvious signs of iridescence to the naked eye but where a highly ordered chloroplast structu
93 r sensors give a yes or no response with the naked eye down to 10 muM when a preconcentration step wa
96 ion of adenosine as a model analyte with the naked eye in buffer samples and undiluted human serum.
101 les such as cancer-biomarker miRNAs with the naked eye is seemingly impossible in molecular diagnosti
103 uared) lithography-free sensing films with a naked eye limit of detection of ~3 pg/mm(2), lower than
104 by taking advantage of excellent generality, naked eye observation, the 4-plex detection, simplicity,
105 source and a colored plastic gel filter, the naked eye or a camera can easily discriminate between po
106 Results can be visually observed by the naked eye or imaged by a smartphone camera under a porta
107 umor phenotypes that fail to be perceived by naked eye that semantic features do not describe and vic
108 connected to a visual readout, allowing the naked eye to evaluate and quantify direct bacterial elec
109 This quenching could be visualized by the naked eye under a UV (365 nm) lamp and performed almost
111 The SNF markers can be easily identified by naked eye using a novel micro Spin-Tube device "Spin-Tub
112 s enable the detection of hydrazine with the naked eye well below sub-ppm concentrations (ca. 30 ppb)
113 ntrations of rabbit IgG and human PSA by the naked eye were down to 0.1 and 4 ng/mL, respectively.
114 rations through UV-vis absorption and by the naked eye were estimated to be 0.3 and 60nM, respectivel
117 line with probe P2 can be viewed through the naked eye, and the corresponding fluorescence turn-on de
118 ctrode, which is clearly measurable with the naked eye, correlates linearly with an analyte concentra
119 of megafauna and/microbial mats (DM) to the naked eye, covered with bacterial mats (BM), or colonize
120 h deposits or cryptotephra, invisible to the naked eye, discovered within Greenland ice-cores, and ra
121 examining the samples surfaces with both the naked eye, first, and microscopically (10x and 50x), imm
122 6 mM), SM sensing can be visualized with the naked eye, leading to the formation of a fluorescent gre
124 micrometer-sized droplets, invisible to the naked eye, persists on leaves during daytime due to deli
125 he presence of the final DNA amplicon to the naked eye, providing a "sample-to-answer" diagnosis from
126 ary tumors before they become visible to the naked eye, supporting the added value of this technique
129 blue ECL emission, easily observable even by naked eye, with quantum yield higher than the standard 9
164 he developed mini-column at visible light by naked eye; where MG was seen as compact green band at th
165 generation, enabling unprecedented one-pot, naked-eye detection of a catalytic reporter from 1 mum d
166 tional ELISA counterparts for ultrasensitive naked-eye detection of biomolecules and small contaminan
168 and avidin-conjugated GOx for the selective naked-eye detection of rabbit immunoglobulin G (IgG) and
169 a surfactant-induced aggregation, results in naked-eye detection of these common anionic surfactants
170 amplification (LAMP) and provides real-time, naked-eye detection with Hydroxynaphthol blue reagent in
172 most cases, the detection is made by simple naked-eye observation of agglutinates without any access
173 assay has some advantages such as useful for naked-eye observation, disposable, not time-consuming, i
175 e proposed plasmonic immunoassay allowed the naked-eye quantification of 0-10 ng/mL PSA at an interva
176 initially describes the design of low-cost, naked-eye quantitative aptamer-based assays by using mic
179 e observed enhanced "turn-on" emission and a naked-eye sensitive blue-green color in the medium is at
180 nt, the proposed method was further used for naked-eye tracking glycolytic inhibition in living cells
181 s are fused in the form of fluorene, allows "naked-eye" detection of fluoride in subppm levels (<1.0
182 can be simply interpreted through the human naked-eye, it provides a simple method for fast-screenin
183 ir multicolor emission from green to red and naked-eye-sensitive green emission with tunable lifetime
184 spray kit to directly spot the explosives by naked eyes, implying great potential for quick, low-cost
190 he immunologic effectors stimulated by these naked HER2 antibodies provide only modest activity as mo
191 RNAs vectors targeting the IL-8 gene and the naked homologous repair DNA carrying different haplotype
192 tergent, we have been able to interrogate a "naked" HTL complex, with the scattering contribution of
194 mputations support the catalytic activity of naked In(I)(+) ions, with an outer sphere mechanism for
195 t syngeneic CC islets was lower than that of naked islets, we showed that CC (PEG MG) islets from ful
196 , and cancer cell killing effect compared to naked KOX or KOX/PEGbPHF at pH7.4, demonstrating that KO
200 story nicely demonstrates that the future of naked mAbs is to design agents with optimized and tailor
206 K4a/b) is present in both cultured cells and naked mole rat tissues but is absent in human and mouse
211 e mitochondria of various tissues from mice, naked mole rats (NMRs), and bats possess two mechanistic
212 usion is consistent with the hypothesis that naked mole rats are neotenous, with retention of juvenil
214 ochlear innervation in mature and developing naked mole rats compared to mice (Mus musculus), gerbils
216 some studies of social mole rats (including naked mole rats, Heterocephalus glaber, and Damaraland m
219 tly demonstrated by us and Liang et al. that naked mole-rat (NMR) cells are more resistant to SV40LT
221 l role of HA in the cancer resistance of the naked mole-rat (NMR), we undertook to explore the struct
222 adds to a growing list of adaptations in the naked mole-rat and provides a plausible proximate mechan
224 rences from the brain of the closely related naked mole-rat as well as from epigeic mammals (rat), wi
229 as fish and amphibians, suggesting that the naked mole-rat is a powerful model for exploring the mec
231 mouse and human p53, a larger proportion of naked mole-rat p53 protein is constitutively localized i
232 We determined that the long half-life of the naked mole-rat p53 protein reflects protein-extrinsic re
233 d basal nuclear localization of p53 in NEFs, naked mole-rat p53 retains its canonical tumor suppressi
235 Fructose-driven glycolytic respiration in naked mole-rat tissues avoids feedback inhibition of gly
236 mers may reflect a further adaptation of the naked mole-rat to living in an environment with high-car
237 eight African rodent species related to the naked mole-rat with the painful substances capsaicin, ac
240 observed in long-lived species including the naked mole-rat, bats, and the bowhead whale, but these a
242 isms underlying the cancer resistance of the naked mole-rat, we investigated the regulation and funct
244 erformed a Kaplan-Meier survival analysis of naked mole-rats (Heterocephalus glaber) and concluded th
248 with the diminished function of KCC2, adult naked mole-rats demonstrate a reduced efficacy of inhibi
249 sites at which the level of CRF1 binding in naked mole-rats exceeds that in Cape mole-rats include t
250 thout pharmacological intervention, in adult naked mole-rats exposed to a simulated hyperthermic surf
251 2 binding, the sites with a greater level in naked mole-rats include the basolateral amygdaloid nucle
253 ppress neuronal activity, we studied whether naked mole-rats might demonstrate energy savings in GABA
257 into the neurobiology of social hierarchy in naked mole-rats, and add to a growing body of work that
258 d historical lifespan data on more than 3200 naked mole-rats, collected over a total observation peri
260 dy, we performed optic nerve injury in adult naked mole-rats, the longest living rodent, with a maxim
261 hole-colony behavioral monitoring of captive naked mole-rats, we found a durable nest, characterized
263 d of Micro encapsulated (MRT, 8 days) versus naked (MRT, 36 days; P < 0.01) baboon islets transplante
266 over that the molecular mechanism underlying Naked/NKD function relies on its assembly into ultra-sta
271 tumor growth suppression when compared with naked oAd and 9.5 x 10(6)-fold increased tumor-to-liver
272 ted more potent antitumor effect compared to naked oAd/RLX or oAd/RLX-treated hMSC in pancreatic tumo
273 y clinical trials have been done with either naked oncolytic Ad or combination with chemotherapies.
274 nd reproducible gene expression of exogenous naked pDNA in human skin using volumes that are consider
275 Anti-HER2 IgG was induced by Ad/E2TM or naked pE2TM, both encoding HER2 extracellular and transm
276 overwriting the original precursor with the naked peptide m/z and removing all of the glycan-related
278 h HSV or CMV, or transient transfection with naked plasmid DNA, HIRA re-localizes to PML bodies, site
281 onstrate that L alone initiates synthesis on naked RNA and that P serves to enhance the initiation an
282 se of VSV P stimulated RABV RdRP activity on naked RNA but was insufficient to permit initiation on t
291 ernalized, consistent with slow recycling of naked TAS2R14 in the absence of the heterodimeric milieu
292 life extension in NMRI mice from t1/2 12min (naked) to t1/2 45min (single cholesteryl) and t1/2 71min
293 he HIRA chaperone complex represses incoming naked viral DNAs through chromatinization as part of int
297 cell spread within the liver, whereas stable naked virions shed in feces are optimized for environmen
298 as quasi-enveloped particles and apically as naked virions, recapitulating essential steps of the nat
299 7 degrees C identified numerous examples of naked virus capsids located immediately beneath the plas
300 er, we and others have observed that various naked viruses, such as CVB, can trigger the release of i