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1 silk protein fibers that embody strength and beauty.
2 itude increases linearly with the feeling of beauty.
3 and then judged whether they had experienced beauty.
4 evolutionary advantages and often with great beauty.
5 tand a simple cell in all its complexity and beauty.
6 total synthesis of molecules of unimaginable beauty and diversity such as the four discussed in this
7 ever, I question his ensuing arguments about beauty and goodness, and thereby the practical value of
8 bert Burns Woodward's publications exhibit a beauty and majesty infrequently seen in the scientific l
9 ermline transposition frequency for Sleeping Beauty and piggyBac was approximately 10% or about one n
10 ompare them with the preferences of Sleeping Beauty and piggyBac, showing that each superfamily has a
12 ies in providing ecosystem services, natural beauty and pleasure, and sustaining human lives is a mes
13 Physiogenic and pathogenic oscillations: the beauty and the beast, based on presentations at the annu
15 analysis of 23,417 piggyBac, 30,303 Sleeping Beauty, and 27,985 TcBuster integrations in HEK-293 cell
17 wo transposon systems, PiggyBac and Sleeping Beauty, and give guidance on the use of different engine
18 al role in visual art, it is often linked to beauty, and observers can detect it efficiently in the l
19 d by their geometrical perfection, intrinsic beauty, and particular properties of polyhedranes, a ser
20 e attention due to their symmetry, aesthetic beauty, and potential applications in catalysis, plasmon
22 tion by trace element analysis in edible and beauty argan oil is a method that can be generalised.
23 ere assessed by ICP-AES in virgin edible and beauty argan oil samples prepared from four remote locat
24 ons of human ICC, we electroporated Sleeping Beauty-based oncogenic transposon plasmids into the left
26 ransposon biology and indicate that Sleeping Beauty can be readily improved for enhanced genetic rese
28 , practitioners will encounter more and more beauty-conscious teenagers using these products for prev
30 ue that such sites potentially devolve into "beauty contests" where patients in need are evaluated on
31 c toxicity at smelters, mercury in paint and beauty creams, dioxin in waste oil in Missouri, polychlo
33 on sense and philosophy suggest that feeling beauty differs from sensuous pleasures such as eating or
34 ained by non-viral gene transfer of Sleeping Beauty DNA plasmids and selectively expanded ex vivo usi
35 n delivered into the genome via the Sleeping Beauty DNA transposon, suggesting that the observed meth
36 colorectal cancer (CRC) in several Sleeping Beauty DNA transposon-based forward genetic screens in m
37 cer susceptibility gene in multiple Sleeping Beauty DNA transposon-based forward genetic screens in m
44 accelerates tumorigenesis following Sleeping Beauty insertional mutagenesis in a mouse model of melan
53 A forward genetic screen utilizing Sleeping Beauty mutagenesis in mice previously identified potenti
55 An understanding of the complexities and beauty of the biological process of hearing itself is un
58 able position of being able to share the raw beauty of the world around us-and in the case of neurosc
60 e point during his or her education, and the beauty of this process has led many of us to go deeper a
61 n: either consensus judgments about physical beauty (paracingulate cortex) or individualized preferen
68 te-based and stereotype explanations for the beauty premium, have too many confounding effects, and l
71 dividual by highlighting the type of hygiene/beauty products the person uses, diet, medical status, a
78 at only the pleasure associated with feeling beauty requires thought and disprove his claim that sens
79 manuel Kant [1, 2] claimed that experiencing beauty requires thought but that sensuous pleasure can b
80 encing and bioinformatics pipeline, Sleeping Beauty (SB) capture hybridization sequencing (SBCapSeq),
81 es the DNA damage introduced during Sleeping Beauty (SB) element excision and reinsertion in mammalia
82 he chromosomal transposition of the Sleeping Beauty (SB) element in mouse embryonic stem cells, provi
83 mariner family transposable element Sleeping Beauty (SB) for transgenesis and long-term expression st
84 enesis strategy based on a two-step Sleeping Beauty (SB) forward genetic screen to identify and valid
85 conducted a mutagenic screen using Sleeping Beauty (SB) in mice to identify new candidate cancer gen
89 vanced DNA vectors derived from the Sleeping Beauty (SB) system to avoid the expense and manufacturin
90 rmits conditional mobilization of a Sleeping Beauty (SB) transposase allele by Cre recombinase to ind
93 a novel nonviral vector system, the Sleeping Beauty (SB) transposon (Tn) to insert a wild-type beta-g
101 cer (CRC) progression, we performed Sleeping Beauty (SB) transposon mutagenesis screens in mice carry
104 leukemia, we targeted cre-dependent Sleeping Beauty (SB) transposon mutagenesis to the blood-forming
113 sly described an approach using the Sleeping Beauty (SB) transposon system to model hematopoietic mal
114 his study we utilized the non-viral Sleeping Beauty (SB) transposon system using the SB100X hyperacti
117 nt non-viral approach combining the Sleeping Beauty (SB) Transposon System with selective proliferati
122 ment and metastasis, we performed a Sleeping Beauty (SB) transposon-based forward genetic screen in m
123 ecently, two groups have shown that sleeping beauty (SB) transposon-based insertional mutagenesis can
124 s of MPNST development, we used the Sleeping Beauty (SB) transposon-based somatic mutagenesis system
128 were genetically modified using the Sleeping Beauty (SB) transposon/transposase system to express a C
129 ling of the piggyBac (PB), Tol2 and Sleeping Beauty (SB) transposons and the murine leukemia virus (M
130 preferential integration sites for Sleeping Beauty (SB) transposons into a particular 100 bp region
133 However, since the resurrection of Sleeping Beauty (SB), the possibility of performing forward genet
134 ssion, through a human IDO-encoding Sleeping Beauty (SB)-based nonviral gene-integrating approach, ha
137 ficiencies of piggyBac, hyperactive Sleeping Beauty (SB11), Tol2, and Mos1 in four mammalian cell lin
139 cells genetically modified with the Sleeping Beauty system to express D-CAR stably were propagated se
141 ed T cells were generated using the Sleeping Beauty system to stably introduce the CD19-specific CAR
142 ercome this constraint, we used the Sleeping Beauty transposable element to achieve chromosomal integ
143 e transcription unit expressing the Sleeping Beauty transposase (SB) and another expressing human uri
148 in-deleted canine FVIII in cis with Sleeping Beauty transposase in hyaluronan nanocapsules and inject
149 uitously express either piggyBac or Sleeping Beauty transposase were generated by standard zygote inj
151 tructed by ligating the CMV-driven "Sleeping Beauty" transposase gene downstream to the Tc1-like tran
152 sposition but were inactive against Sleeping Beauty transposition and long interspersed nucleotide el
155 -CA) with mice in which a mutagenic Sleeping Beauty transposon (T2/Onc) was mobilized only in B cells
158 l of this approach, we encapsulated Sleeping Beauty transposon expressing the B domain-deleted canine
161 ted this hypothesis by performing a Sleeping Beauty transposon mutagenesis screen in which common ins
165 dentified in previous retroviral or Sleeping Beauty transposon screens, including Spic, which encodes
166 y shows for the first time that the Sleeping Beauty transposon system can be used to identify candida
167 uced pluripotent stem cells using a Sleeping Beauty transposon system carrying the micro-utrophin gen
168 d insertional mutagenesis using the Sleeping Beauty transposon system in mice carrying germline or so
169 tional mutagenesis screen using the Sleeping Beauty transposon system in mice with mammary-specific i
170 sorders have shown efficacy for the Sleeping Beauty transposon system in the treatment of hemophilia,
171 factor in prostate cancer, and the Sleeping Beauty transposon system is a useful tool for identifyin
172 ional mutagenesis indicate that the Sleeping Beauty transposon system may be a safer alternative than
173 in Nature, Sun et al. (2014) used a sleeping beauty transposon system to demonstrate that natural hem
176 Here we report the ability of the Sleeping Beauty transposon to act as a somatic insertional mutage
178 ation of a single-copy inactivating Sleeping Beauty transposon to Pten disruption within the same gen
179 liary tract was accomplished by the Sleeping Beauty transposon transfection system with transduction
181 g the local hopping activity of the Sleeping Beauty transposon, the lacZ reporter gene was dispersed
182 e identified such mutations using a Sleeping Beauty transposon, which caused rapid-onset AML in 80% o
185 a novel tyrosinase minigene-tagged Sleeping Beauty transposon-mediated mutagenesis, which allows for
187 ed human PAX7+ satellite cells with Sleeping Beauty transposon-mediated nonviral gene transfer, highl
191 hMet and mutant-beta-catenin using sleeping beauty transposon/transposase leads to hepatocellular ca
192 , introducing DNA plasmids from the Sleeping Beauty transposon/transposase system to directly express
193 MA148 was genetically modified by "Sleeping Beauty" transposon-mediated delivery of DsRed2 fluoresce
195 ce and forward genetic screens with Sleeping Beauty transposons implicate additional signaling cascad
197 nts, which were further deployed by Sleeping Beauty transposons throughout the genome of human bone e
198 have also been developed to deliver Sleeping Beauty transposons to the lung, liver and tumors for tre
200 These results support the use of Sleeping Beauty vectors in carrying an insulated IHK-beta-globin
201 o construct a synthetic transposon, Sleeping Beauty, which could be identical or equivalent to an anc
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