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1 ding-yeast pathway, we performed an unbiased genetic selection.
2 ne using ribosome binding site libraries and genetic selection.
3 f protein engineering that uses the power of genetic selection.
4 d biosensors and to engineer enzymes through genetic selection.
5 cts positive clones by positive and negative genetic selection.
6 ring infection were recently identified in a genetic selection.
7 00)-Arg(712) by using random mutagenesis and genetic selection.
8 X inactivation but the dominant mechanism is genetic selection.
9 ng a telomeric linear plasmid and a two-step genetic selection.
10 f Na+ tolerance to yeast, can be isolated by genetic selection.
11 herefore subjected to random mutagenesis and genetic selection.
12 ence-activated cell sorter (FACS) to perform genetic selection.
13 dered variants of dihydrofolate reductase by genetic selection.
14 ell-characterized evolutionary mechanism for genetic selection.
15  genes using unbiased genome-wide functional genetic selection.
16 lendar season and the desirable direction of genetic selection.
17 h affinity and specificity by direct in vivo genetic selection.
18 ents between 1N and 3N without involving any genetic selection.
19 ne approaches to search for evidence of such genetic selection.
20 ype levels by random mutagenesis of purF and genetic selection.
21 unction as logic gates were isolated by dual genetic selection.
22 ied site saturation strategy with functional genetic selection.
23 or by using RNAi in phenotype-based, forward genetic selections.
24 lly applicable to the analysis of a range of genetic selections.
25 ty of Red-mediated recombination in targeted genetic selections.
26 dified yeast two-hybrid system which enables genetic selection against a specific protein/protein int
27 erated the normally slow response to relaxed genetic selection against deafness that began in many We
28  is required to be paired, we observe strong genetic selection against viruses that contain a deletio
29 ge libraries, coupled with the benefits of a genetic selection, allowed us to identify rare, uniquely
30        Using this observation as a basis for genetic selection, an extragenic suppressor of Tus-media
31 ion strategies have traditionally focused on genetic selection and cost-effective ration formulation
32 rol initiation, respectively, we developed a genetic selection and identified seqA, datA, dnaN and hd
33                  Here we describe a combined genetic selection and screen that allows the rapid evolu
34                        Previously, extensive genetic selection and screening approaches were employed
35                                              Genetic selection and site-directed mutagenesis experime
36              To uncover the mechanism of the genetic selection and the functional role of this glutam
37 termination, were recovered in a powerful F1 genetic selection and used to investigate how sc was rec
38                   In this study, we employed genetic selections and experimental evolution to identif
39  plant Arabidopsis thaliana were isolated by genetic selections and fluorescence screens.
40 individuals who are interested in population genetics, selection and evolution of polymorphic human g
41 ii) genes within de novo CNVs under negative genetic selection, and (iii) genes identified by clinica
42 uctase (VKORc1) as a reporter, we describe a genetic selection approach allowing the isolation of Esc
43                           We developed a new genetic selection approach to screen for mutations that
44                          Both plasticity and genetic selection are potential drivers that allow for t
45                                              Genetic selections are available for each behavior.
46 l aminoacyl-tRNA synthetase is generated and genetic selections are performed on the library in Sacch
47    Collectively, these results establish our genetic selection as a useful and potentially generaliza
48 unique opportunity to examine the impacts of genetic selection as humans adapted to multiple new envi
49 se explanations is correct, the evidence for genetic selection at the EPAS1 locus from the GWADS stud
50                                            A genetic selection based on a UAS2-dependent ADH2 reporte
51 clease (RNase A) and human angiogenin, and a genetic selection based on the intrinsic cytotoxicity of
52                                    We used a genetic selection based on the yeast two-hybrid assay to
53                  Degenerate (doped) in vitro genetic selection, based on a pool of randomized 39-mers
54 fy rules linked to function, we leverage the genetic selection bias of condensate-promoting oncofusio
55 e- mediated exchange of DNA to systems where genetic selection can be applied.
56          Nearly all positive clones from the genetic selection carried mutations at lysine 155 in tra
57                       Findings argue against genetic selection/concentration as an explanation for ne
58                          By contrast, modest genetic selection/concentration was evident for teen pre
59  of a particular residue as revealed by this genetic selection correlated with its sequence conservat
60                Here, we present results of a genetic selection designed to identify additional compon
61              Here, we present results from a genetic selection designed to identify mutants that miss
62                                         In a genetic selection designed to isolate Escherichia coli m
63                                      Using a genetic selection designed to isolate PtdIns(3)P-binding
64                  We have implemented a yeast genetic selection developed previously by our laboratory
65  breeding values was shown to have a greater genetic selection differential and reduced future diseas
66                                              Genetic selection experiments in a glucokinase-deficient
67                                              Genetic selection experiments suggested that such sequen
68                     We report the results of genetic selection experiments that identify nine genes f
69                            In agreement with genetic selection experiments, the affinity of triclosan
70 ives of bacteriophage P22 that enable direct genetic selection for a specific RNA-protein interaction
71  unbalanced body conformation due to intense genetic selection for additional breast muscle (pectoral
72                               We showed that genetic selection for blunted glucocorticoid responsiven
73       Moreover, the effects were modified by genetic selection for body weight, which altered the qua
74                                         In a genetic selection for budding yeast mutants that were de
75                                    A forward genetic selection for Caulobacter crescentus cell cycle
76 further dissection of phosphate signaling by genetic selection for constitutive phosphate starvation
77 by profiling Drosophila strains subjected to genetic selection for differences in aggressiveness.
78 pproaches, including saturation mutagenesis, genetic selection for DNA-binding mutants, photo cross-l
79 e DNA binding by TBP in vivo, we performed a genetic selection for extragenic suppressors of a yeast
80 rofitability (p<0.01), but an improvement in genetic selection for fertility (p<0.01) and overall cow
81 hically circumscribed population rather than genetic selection for heterosexual transmission.
82  Short Sleep lines of mice were developed by genetic selection for high or low alcohol sensitivity.
83                                      Using a genetic selection for increased frameshifting in a repor
84                    The first tier involves a genetic selection for intracellular protein stability th
85         Here we describe a facile and robust genetic selection for isolating full-length IgG antibodi
86 lating MAL gene expression, we carried out a genetic selection for MAL constitutive mutants.
87                                            A genetic selection for multicopy suppressors of a framesh
88 that are important for ligand specificity, a genetic selection for mutants of the inosine-guanosine-s
89                                            A genetic selection for mutants that activate this pathway
90 ptional regulation of PHO5, we carried out a genetic selection for mutants that express PHO5 constitu
91 ing domain barrier components, we designed a genetic selection for mutants with reduced negative supe
92                                We utilized a genetic selection for mutations that affect the regulati
93 UR1 and BUR2 were previously identified by a genetic selection for mutations that increase transcript
94 w phosphatase, PTP3, have been isolated in a genetic selection for negative regulators of an osmotic
95 ) substitutions were previously isolated via genetic selection for photosynthetic ability at the 35 d
96 To this end, we applied a recently developed genetic selection for protein folding and solubility bas
97                As part of an effort to begin genetic selection for resistance to OsHV-1, 71 families
98 ng sickness (Trypanosoma brucei) have driven genetic selection for resistance.
99                             In this study, a genetic selection for second-site mutations that could p
100                                  A bacterial genetic selection for second-site suppressors using an a
101 lling the postharvest storage atmosphere and genetic selection for slow or late ripening varieties.
102                    Therefore, we developed a genetic selection for splicing-dependent kanamycin resis
103 ifferential behavior provided the basis of a genetic selection for STE5 gain-of-function mutations.
104                                              Genetic selection for suppressors of a polyadenylation d
105                                              Genetic selection for suppressors of pap1-1 yielded two
106 in phospholipid biosynthesis, we performed a genetic selection for suppressors of the inositol auxotr
107                                    Through a genetic selection for T. gondii mutants resistant to the
108                                              Genetic selection for the ability to repress translation
109             However, harnessing the power of genetic selection for the detection of specific, nonendo
110 OL1 variants - which have undergone positive genetic selection for their ability to confer resistance
111                                     Although genetic selection for thermoregulatory adaptation is fre
112                                      Using a genetic selection for tmRNA activity in Escherichia coli
113                              Through forward genetic selection for variants capable of virus spread,
114                                              Genetic selection for whole-plant water use efficiency (
115 esigned to bind heme or CO, nor subjected to genetic selections for heme or CO binding.
116 s, potentially improving both crop yield and genetic selection gains.
117 expression of a reporter gene are useful for genetic selections, high-throughput screening, and multi
118 ific disciplines of environmental design and genetic selection, however understanding the ecological
119 rent issue of the Journal do not support the genetic selection hypothesis.
120                               In this study, genetic selection identified extein sequences with Ser+1
121 onucleotide formyltransferase (PurN) and, by genetic selection, identified PurN heterodimers capable
122 onal randomization of the loop, coupled with genetic selection in a glucokinase-deficient bacterium,
123                                        Thus, genetic selection in cancer cells can be used as a tool
124 igand, suggesting that it is possible to use genetic selection in E. coli to discover synthetic ribos
125 m sequence mutagenesis coupled with positive genetic selection in E. coli yields large numbers of fun
126                                      Using a genetic selection in Escherichia coli, we identified add
127              Here, we used a single round of genetic selection in mouse cells to isolate chemically s
128                                              Genetic selection in Saccharomyces cerevisiae for gain o
129 es in the cell of origin dramatically affect genetic selection in tumors.
130 random saturation mutagenesis coupled with a genetic selection in yeast to determine the relative imp
131       Thus, this approach, which is based on genetic selection in yeast, is safe, economic, and a rel
132 genes that play a role in this process using genetic selections in conventional cell culture systems.
133             Mutational analysis and in vitro genetic selection indicate that U2AF35 has a sequence-sp
134         When carried out in the context of a genetic selection, interacting pairs can be rapidly isol
135 ents and omit potential gains by integrating genetic selection into existing breeding programs.
136 molecular evolution to proteins for which no genetic selection is available.
137 that phenotypic adjustment and/or beneficial genetic selection is possible for some species, indicati
138                 In the practice of microbial genetics, selection is used to detect and enumerate pre-
139                                     Separate genetic selections isolated two AsiA mutants (S22F and Q
140     Since Top7 was created in the absence of genetic selection, it provides a rare opportunity to inv
141                              In this study a genetic selection led to the identification of a bacteri
142                                The fact that genetic selection maintains similar molecular interactio
143                                              Genetic selection maintains the altered phenotypes in su
144 rom the Finnish Twin Registry suggested that genetic selection may account for some of the physical-a
145 oped a rapid and broadly applicable in vitro genetic selection method based on T7 phage display.
146                                         This genetic selection method was shown to generate expressio
147                                            A genetic selection method, the P22 challenge-phage assay,
148       This result supports the hypothesis of genetic selection of an individual's environment, which
149                                              Genetic selection of borrelidin-resistant mutants showed
150                                              Genetic selection of cotransin-resistant cancer cells un
151 bored in recipient pigs and that within-host genetic selection of IAV is more likely to occur in pigs
152   We have therefore developed a strategy for genetic selection of lineage-restricted precursors from
153 n interesting raw material for the design or genetic selection of modifiers of gene expression.
154                                       By the genetic selection of mouse cDNAs encoding secreted prote
155 ned to report mutations without the need for genetic selection of mutant cells.
156       The RNA challenge phage system enables genetic selection of proteins with RNA-binding activity
157 kinase originally identified in yeast by the genetic selection of rapamycin-resistant mutants.
158    Mechanistically, this is not elicited via genetic selection of tumor subclones, but through an epi
159 on of LASV-LCMV domain-swapping experiments, genetic selection of viral variants, and site-directed m
160                                 The powerful genetic selections of the forward and reverse n-hybrid s
161 on theory to assess the non-linear impact of genetic selection on field measures of epidemic risk and
162               Our results show that although genetic selection on susceptibility reduces disease risk
163 based screen performed by imposing different genetic selections on thousands of yeast mutants in para
164 d hydrophobic core sequence, imposed without genetic selection or computer-based design, is sufficien
165 t the processes of zoonotic transmission and genetic selection or modification ensure that plasma-der
166 lting libraries are subjected to large-scale genetic selection or screening to identify those chimera
167 ctional trade-offs may limit the capacity of genetic selection or synthetic biology to simultaneously
168          The technique makes use of a facile genetic selection performed in a strain of Saccharomyces
169 r, suggest that they have been adapted under genetic selection pressure for optimal performance.
170                                   An in vivo genetic selection previously developed to identify DNA b
171 unction of the glycosome, we used a positive genetic selection procedure to isolate the first Leishma
172     We have previously employed an in vitro (genetic) selection procedure to select RNase P ribozyme
173 s purified, we developed a modified in vitro genetic selection protocol.
174                                     Positive genetic selection provides a rapid mechanism to identify
175 aturation mutagenesis technique and positive genetic selection provides a simple and efficient means
176                                              Genetic selection provides the most powerful method to a
177 echanisms behind the rise of innovativeness (genetic selection, rational choice, and phenotypic plast
178                                          The genetic selections recapitulate major features of the co
179 r these phenotypic trends are underpinned by genetic selection responses, and to evaluate the potenti
180 onucleotide-directed mutagenesis followed by genetic selection resulted in mutant GlnRS enzymes that
181                              Engineering and genetic selections revealed the required features of bot
182                             Here we report a genetic selection revealing DinB residues essential to e
183                                            A genetic selection scheme against specific protein/protei
184 process called "pseudotaxis." Therefore, our genetic selection scheme generated suppressors of pseudo
185                      We report here a simple genetic selection scheme through which to search librari
186                                   By a novel genetic selection/screening process, two BstYI variants
187 and scoring for fitness in plants by in vivo genetic selection (SELEX) resulted in winning sequences
188                           Results of in vivo genetic selection (SELEX: systematic evolution of ligand
189                               A quantitative genetic selection showed that +4 to +15 repeat expansion
190                 We have developed a reliable genetic selection strategy for isolating interacting pro
191                          Here, we describe a genetic selection strategy for routine laboratory isolat
192 ec7p and its interacting proteins, we used a genetic selection strategy in which a human HepG2 cDNA l
193                            Here, we report a genetic selection strategy that directly links CycN-inde
194                     We devised a noninvasive genetic selection strategy to identify positive regulato
195                 We have developed and used a genetic selection system in Escherichia coli to study fu
196      This system can be used as an efficient genetic selection system to map protein-protein interact
197 ic LacI protein as an example, we describe a genetic selection system using a bidirectional reporter
198 so demonstrates that the P22 challenge phage genetic selection system, modified for use with a mammal
199  in vitro translate directly into an in vivo genetic selection system.
200 henicol acetyltransferase (split-CAT) -based genetic selection system.
201                         Furthermore, because genetic selection takes place predominantly in the reduc
202                             Although in vivo genetic selection techniques have been used to identify
203 yeast two-hybrid system is the provision for genetic selection techniques that enable the identificat
204                        We have established a genetic-selection technology (intracellular antibody cap
205 is negative regulation, we developed a novel genetic selection that detects altered expression from t
206                           Here we describe a genetic selection that directly links the in vivo stabil
207                               By employing a genetic selection that forces the cell to fold an unstab
208                                      Using a genetic selection that forces the phage to decrease or a
209            In this paper, we have utilized a genetic selection that links protein stability to antibi
210 hia coli that was previously identified by a genetic selection that rescued sensitivity to dithiothre
211 re and function in vivo, we have developed a genetic selection that ties the life of Escherichia coli
212                                 We created a genetic selection that ties the life of Escherichia coli
213 nd expression of these genes, we developed a genetic selection that uses transposon mutagenesis to id
214                           Herein we describe genetic selections that allow single amino acid changes
215 terize the tagging process, we developed two genetic selections that link tmRNA activity to cell deat
216                                              Genetic selections that use proteinaceous transdominant
217 nd culture procedure, which facilitates, via genetic selection, the differentiation of hES cells into
218 d infectivity was combined with quantitative genetics selection theory to assess the non-linear impac
219                                 We have used genetic selection to characterize the terminator of the
220 e of random mutagenesis followed by positive genetic selection to create such a mutant gene.
221  To test this hypothesis, we have designed a genetic selection to detect a leading strand intermolecu
222 oorly in many cell types, can be modified by genetic selection to generate a nonpathogenic variant th
223       This study demonstrates the power of a genetic selection to identify a variant virus that uses
224 ted mutagenesis procedures were coupled with genetic selection to identify an "oxygen-insensitive" mu
225 his type of approach to form the basis for a genetic selection to identify proteins that exert an act
226    We used this observation as the basis for genetic selection to identify two alleles of umuD' and s
227                                   In a novel genetic selection to isolate genes required for DIF sign
228  understand this patterning process, we used genetic selection to isolate mutants in the DIF-1 respon
229 nvolved in nuclear protein import, we used a genetic selection to isolate mutants that mislocalized a
230 dues at multiple positions and carried out a genetic selection to isolate variants that support life
231 RNA interference (RNAi) library in a forward genetic selection to study the mechanism of toxicity of
232         With this approach, we used powerful genetic selections to identify functional circuits and s
233                                  Here, using genetic selections to probe interactions of an exemplar
234                                  Our forward genetic selection unearthed the Krebs cycle enzyme citra
235 te these structures by using high-throughput genetic selections, unigenic evolution, and analyses of
236                               We exploited a genetic selection using a dominant negative variant of t
237                                We designed a genetic selection using cDNA library suppression of 3xAs
238                                              Genetic selections using P22 challenge phages were used
239 th kernel hardness, for which a new, simpler genetic selection was designed.
240                                              Genetic selection was exploited in combination with stru
241 albicans KEX2 homologue in Sap activation, a genetic selection was performed based on KEX2 function.
242                                            A genetic selection was performed for eps (ER-retained pma
243 e domain of DnaC that interacts with DnaB, a genetic selection was used based on the lethal effect of
244 associated with active site substitutions, a genetic selection was used to find second site mutations
245                                              Genetic selection was used to identify 33 amino acid sub
246                                      A novel genetic selection was used to identify genes regulating
247  substitutions in the AUGC repeats, in vitro genetic selection was used to identify RNAs that bound c
248                                    Bacterial genetic selection was used to isolate individual donor-t
249 d in transcription start site utilization, a genetic selection was used to isolate S. cerevisiae TFII
250                                      In vivo genetic selection was used to study the sequences and st
251      The combination of in vitro and in vivo genetic selections was crucial for obtaining RNA aptamer
252                                Using PCR and genetic selection, we found that generalist and host-spe
253                                      Using a genetic selection, we have screened a random peptide lib
254                                      Using a genetic selection, we isolated an infectious retrovirus
255                                    By direct genetic selections, we identified mutations in 16S rRNA
256 tion of complexity, progressive and targeted genetic selections were employed to lessen and finally e
257                                              Genetic selections were used to find peptides that inhib
258                  In the present study, yeast genetic selections were used to optimize the RNA aptamer
259           Inherent factors are determined by genetic selection, which appears to be controlled by ada
260 ecause domestication is a dynamic process of genetic selection, which may not be completely character
261 the ability to isolate intrabodies by direct genetic selection, which obviates the need for in vitro
262                                 Further, the genetic selection yields mutants at only a limited numbe

 
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