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1 (1-30%, depending on genetic background and growth conditions).
2 an depend on both the genetic background and growth condition.
3 in active rRNA synthesis under a rich medium growth condition.
4 nockout cells that are viable under specific growth conditions.
5 nate those two cycles across a wide range of growth conditions.
6 ed decay so far, probably due to unfavorable growth conditions.
7 cross the shell in response to environmental/growth conditions.
8 oxygen vacancies are introduced by adjusting growth conditions.
9 mRNA upregulating its expression in several growth conditions.
10 of NS1 on RAS-mediated signaling in 2D vs 3D growth conditions.
11 nding across the genomic DNA under different growth conditions.
12 3580 and 4/74 grown in 16 infection-relevant growth conditions.
13 , which is essentially studied by changes in growth conditions.
14 kinetics of Escherichia coli under different growth conditions.
15 at GIs can be easily assayed across multiple growth conditions.
16 help regulate DNA replication in response to growth conditions.
17 ay periodicity can be tuned by adjusting the growth conditions.
18 nce between the two proteomes under standard growth conditions.
19 starch granule per chloroplast under normal growth conditions.
20 e differentially expressed, depending on the growth conditions.
21 native transcription initiation under normal growth conditions.
22 anced virus production under carbon-limiting growth conditions.
23 plasmic reticulum (ER) stress in unfavorable growth conditions.
24 icroorganisms are uniquely determined by the growth conditions.
25 ostructures are accessible by modulating the growth conditions.
26 ibutable to stroma, extrinsic signaling, and growth conditions.
27 ssion of several transporters in ambient CO2 growth conditions.
28 e and consistent over a range of tissues and growth conditions.
29 ed if climate change leads to more favorable growth conditions.
30 ain, display various phenotypes depending on growth conditions.
31 ompared with the wild type, in two different growth conditions.
32 elle genomes, and transcriptome from diverse growth conditions.
33 t are not expressed under typical laboratory growth conditions.
34 measured their phenotypic profile across 214 growth conditions.
35 ickly meet demand upon sudden improvement in growth conditions.
36 hat silences the gene cluster under standard growth conditions.
37 utant shows growth retardation under regular growth conditions.
38 pecific interactions can vary with different growth conditions.
39 redict microbial response under non-standard growth conditions.
40 DH mediated stress responses under favorable growth conditions.
41 has not yet been described under controlled growth conditions.
42 tabolic models and across three experimental growth conditions.
43 ised close to a miscibility transition under growth conditions.
44 ReS2 (1.62 eV) by precisely controlling the growth conditions.
45 criptional capacity of RNAPIII under optimal growth conditions.
46 switch between gluconeogenic and glycolytic growth conditions.
47 portantly, fern stomatal responses depend on growth conditions.
48 sition studies of AB under industrially safe growth conditions.
49 fairly synchronous sporulation in submerged growth conditions.
50 in molecular structure that depend on fibril growth conditions.
51 p DeltauvrD cells being inviable under rapid growth conditions.
52 show shorter primary roots under restrictive growth conditions.
53 fect the bulk chromosome segregation in slow growth conditions.
54 d trials that have been biased towards mesic growth conditions.
55 pathway negatively regulates HR under normal growth conditions.
56 cultured rat hepatocytes grown under normal growth conditions.
57 ) and elevated (950 ppm CO(2), 30 degrees C) growth conditions.
58 strain these levels declined under the same growth conditions.
59 t high yield using high-cell-density E. coli growth conditions.
60 utant strains under different substrates and growth conditions.
61 t low levels and is dispensable under normal growth conditions.
62 e genes were highly upregulated under normal growth conditions.
63 ctivated when the bacterium enters anaerobic growth conditions.
64 thesis by Escherichia coli, focusing on slow-growth conditions.
65 switch between phases as a result of varying growth conditions.
66 enesis, and/or allow adaptation to different growth conditions.
67 s were studied phenotypically using standard growth conditions.
68 ases in young cells in the lifespan-altering growth conditions.
69 mutant yeast strains simulated in different growth conditions.
70 sistently upregulated during diverse biofilm growth conditions.
71 ncreased SPI1 gene expression under the same growth conditions.
72 es were translated under standard laboratory growth conditions.
73 s a spectrum of cell states defined by their growth conditions.
74 s that function optimally within a subset of growth conditions.
75 activate expression of nitrogenase under all growth conditions.
76 ch include platelets released during ex vivo growth conditions.
77 enable them to thrive in less than favorable growth conditions.
78 l sorting and plated in endothelial-specific growth conditions.
79 ensory systems necessary to detect favorable growth conditions.
80 d became photobleached under high light (HL) growth conditions.
81 onribosomal production as a function of cell growth conditions.
82 lidate our methods on a phenomics dataset of growth conditions.
83 tosynthetic carbon metabolism under variable growth conditions.
84 ed by the degree of cation site disorder via growth conditions.
85 enesis and biomass synthesis under different growth conditions.
86 nvasions under normal and pathophysiological growth conditions.
87 assimilate acetate under both light and dark growth conditions.
88 eving optimal nucleation kinetics under mild growth conditions.
89 pid droplets in the tgd2 mutant under normal growth conditions.
90 beit unaltered leaf morphology under optimal growth conditions.
91 t of the MCM complex at Ser-205 under normal growth conditions.
92 oteins that aid in survival during stressful growth conditions.
93 ction of more than a E. coli promoters in 12 growth conditions.
94 varied from 290 nm to 355 nm by changing the growth conditions.
95 the increasing cellular energy demand under growth conditions.
96 es rapid acquisition of tolerance to altered growth conditions.
97 activation or repression under steady-state growth conditions.
98 compared with wild-type strains under normal growth conditions.
99 temperature response across plant types and growth conditions.
100 plast development and acclimation to adverse growth conditions.
101 ve in their ability to regrow upon return to growth conditions.
102 it-28B) mutants do not form PBs under normal growth conditions.
103 for the adaptation of bacteria to different growth conditions.
104 n vivo in Salmonella enterica under multiple growth conditions.
105 oordinated, changing together in response to growth conditions.
106 olic redox cellular environment under normal growth conditions.
107 er chloroplast peroxiredoxins under standard growth conditions.
108 too slow and is most significant for typical growth conditions.
109 pression of genomic instability under normal growth conditions.
110 6% during drought, regardless of species and growth conditions.
111 ncer cell-line (MCF7) across three different growth conditions.
112 n single E. coli cells in both slow and fast growth conditions.
113 nd that the domains remain nanoscale for all growth conditions.
114 t rates exceeding 200 um h(-1) using similar growth conditions.
115 levels change significantly in different Pi growth conditions.
116 l as nectar volume and sugar under different growth conditions.
117 CO(2) for one light period, and returned to growth conditions.
118 root hairs four times longer than with other growth conditions.
119 art in both daughter and mother cells across growth conditions.
120 ting ESCRT components at MVEs under multiple growth conditions.
121 pecies by studying many pathogen strains and growth conditions.
122 ranules harbor translated mRNAs under active growth conditions.
123 of the family, are expressed under different growth conditions.
125 (plant) under well watered and water-limited growth conditions, a high-throughput phenotyping facilit
127 for plant and fungal cells during different growth conditions, after treatment with IAA, and in diff
128 I) thin films is achieved at the iodine-rich growth condition, allowing for the record high room-temp
129 he magnitude of TFIID dependence varies with growth conditions, although this variation is similar ge
130 Recent studies have revealed, in normoxic growth conditions, an interface made exclusively by Cox5
131 oth proper stomatal functioning under normal growth conditions and adaptive developmental responses t
133 protein in the cytosol requires both anoxic growth conditions and co-expression of NifH and NifM wit
134 ce of ODX with different bacterial types and growth conditions and compared it with a commercial benc
135 knowledge of gene essentiality under optimal growth conditions and conditions relevant to the natural
137 D shoot architectures, representing multiple growth conditions and developmental time points for two
138 acking studies were carried out under normal growth conditions and during amino acid starvation.
141 astrocyte and neuronal cultures under normal growth conditions and in response to manganese (Mn) trea
142 phenotypic traits under 30 distinct in vitro growth conditions and in two different hosts (insect lar
144 s kept 14 generation periods over a range of growth conditions and kept phase for hundreds of generat
145 demonstrated the robustness of our method to growth conditions and species that have not been trained
146 ssentiality for many bacteria under standard growth conditions and the ability of several eukaryotic
148 this state lends itself to manipulation via growth conditions and the material parameters such as Fe
149 of cellular biomass under nutrient-limiting growth conditions and the rate of increase in investment
150 ratio has been shown to change under various growth conditions and to determine the response of the b
151 blocking BCAA catabolism during both normal growth conditions and under energy-limited conditions.
152 gical nature of these materials changes with growth conditions and, more specifically, chalcogen cont
153 SiGe strips, without the need to modify the growth conditions, and by using low cost, low thermal-bu
154 9 and crRNA expression levels, organisms and growth conditions, and experimental conditions collectiv
155 ased by H2O2, in the diauxic phase of normal growth conditions, and in cells under alphaSyn-mediated
156 , where each section requires its own set of growth conditions, and methods for preparing such wires
157 E. coli than in B. japonicum under identical growth conditions, and Mur responded to iron in a B. jap
158 um are not expressed under normal laboratory growth conditions, and our understanding of how they are
159 aspect ratio is independent of cell size and growth conditions, and predicts cell morphological chang
160 iva) crops will likely experience a range of growth conditions, and root architectural plasticity wil
161 ted within specific zones, as defined by the growth conditions, and show how occlusion can govern cha
162 n of S. oneidensis to changing and stressful growth conditions, and this ability is probably widespre
163 he spatial density functions across species, growth conditions, and time, which suggests functional s
164 ending on cellular physiology and changes in growth conditions, and translation errors are not always
165 scence meristem kinase2, which under optimal growth conditions are absent from plasmodesmata, rapidly
166 x) for varying chalcogen ratios and constant growth conditions as a function of both temperature and
167 To this end, we model a large compendium of growth conditions as a multiplex network consisting of t
168 phagy, and leaf senescence under nonlimiting growth conditions as well as extensive repression of chl
169 lux levels of Escherichia coli under various growth conditions as well as in the catalytic rate const
170 r autotrophic, mixotrophic and heterotrophic growth conditions, as well as knockout conditions that e
172 dispensable for proliferation under optimal growth conditions but is required for starvation and str
174 0 is not expressed under usual (unstressful) growth conditions, but is induced upon starvation or osm
176 omic network approach to infer similarity of growth conditions by integrating layers of the multiplex
177 e complex responds differently to changes in growth conditions by tuning phosphorylation dynamics.
178 toxin YafQ is suppressed under steady state growth conditions by virtue of its interaction with its
179 l types, yet within a specific cell type and growth condition, cell size is narrowly distributed.
180 ecutive generations under tightly controlled growth conditions, cells of interest are isolated and pr
181 kout mutant was viable and, depending on the growth conditions, contained 10% to 20% Asc relative to
183 0-fold higher than that in gDNA under normal growth conditions, corresponding to approximately four 6
184 d situations and under anchorage-independent growth conditions, demonstrating a PRL-2.CNNM3 complex-d
185 equencing analysis suggests that culture and growth conditions do not affect the genomic information
186 y bacterial adaptive responses to changes in growth conditions due to biotic and abiotic factors invo
187 core autophagy component ATG12 under normal growth conditions (e.g., lipids and secondary metabolism
188 nO: Ga was achieved due to using oxygen poor growth conditions enabled by diethylzinc and triethylgal
189 regulate monomer concentration, stabilizing growth conditions even as depletion rates change, and th
190 Here, we demonstrate that under etiolated growth conditions, extensive interdependence/overlap occ
194 nic mutants (i) exhibited a lower fitness in growth conditions found in human tissues, such as hypero
195 vapor growth (SSVG) method, and the optimum growth conditions have been experimentally determined.
197 re expressed under Bvg negative (Bvg-) phase growth conditions; however, these appear to be primarily
198 th phenotype was only evident under specific growth conditions; however, UTEX 2973 accumulated high l
199 y may have different habitat preferences and growth conditions, implying that the two genetically div
200 duct quality of the clones and the effect of growth conditions in a fast and cost-effective manner.
202 studies suggested that H. ducreyi encounters growth conditions in human lesions resembling those foun
203 uble-mutant collection under a wide range of growth conditions in order to search for additional gene
204 es are transcribed maximally under anaerobic growth conditions in the presence of low nitrate concent
206 sm, such as shape, metabolic substrates, and growth conditions) in microbial bioinformatics has been
207 -mismatch-induced strain, and roughness, and growth conditions, in particular, growth time and growth
208 different carbon sources and under different growth conditions, including both aerobic and anaerobic
209 he the energy efficiency of cells under fast growth conditions, indicating a tradeoff between the hig
210 , regardless of the large off-stoichiometric growth conditions (inducing disorder by samarium vacanci
213 al and translational elongation under normal growth conditions is implemented by guanosine tetraphosp
214 species, life history, evolutionary age, and growth conditions is required to gain insight into the e
216 s where it is difficult to quantify specific growth conditions, it becomes critical to develop method
217 transcription centers under the rich medium growth condition; its spatial arrangement at the cellula
218 erpene oils to include completely controlled growth conditions, just-in-time and scalable production,
220 ally driven variations in upper water column growth conditions (light, nutrient, and temperature).
221 cts were also linked to secondary effects on growth, condition, liver size, blood chemistry and compo
222 acteria are silent under standard laboratory growth conditions, making it challenging to uncover any
226 he level of PotA was elevated under in vitro growth conditions mimicking unfed ticks compared to the
228 evisiae, which reveals that under favourable growth conditions mRNAs coding for proteins involved in
231 ns revealed that, under these 'non-standard' growth conditions, numerous uncharacterised regulators a
233 S) media of A. flavus was investigated under growth conditions of 29 degrees C in the dark for a 168
235 dowed with rich polymorph chemistry, but the growth conditions of the various polymorphs are not unde
236 on events and the effects of the alternative growth conditions on lifespan indicates that genomic ins
239 m L.) that were induced under drought-stress growth conditions, one encoded a protein with significan
242 mulate as linear RNAs under either saturated-growth conditions or other stresses that cause prolonged
243 We previously reported that mildly acidic growth conditions (pH 5.8) downregulate expression of ge
245 rylated FDH and, in response to unfavourable growth conditions, reduction in FDH phosphorylation leve
247 his dualism of synergy and competition under growth conditions relevant in contaminated aquifers, we
248 tive phosphatases under 30 distinct in vitro growth conditions, revealing at least one function for 6
250 vity assays demonstrated that under standard growth conditions, sepA is repressed by the global regul
251 spectrometry of P. aeruginosa under standard growth conditions showed that p3MDO is expressed in low
252 Analysis of these mutants under different growth conditions showed that these systems are not redu
254 , results using transformed cells or altered growth conditions suggested that late-stage defects in p
255 ects cellular survival under non-fermentable growth conditions, suggesting an overlapping role for bo
256 equal affinity during aerobic and anaerobic growth conditions, suggesting that the dual-purpose salv
257 ergent regulation of CD2AP in different axon growth conditions suggests that separate mechanisms exis
258 der intrinsically safe, atmospheric pressure growth conditions, suitable for application in roll-to-r
259 ignment of a 3' UTR sRNA from a non-standard growth condition supports the notion that mRNA crossregu
260 cells propagated for a short duration under growth conditions that enable epithelial reprogramming.
261 e is a root vegetable grown under a range of growth conditions that may influence the product quality
262 le cell lines under smooth muscle cell (SMC) growth conditions that retained a patient-specific genom
263 Saccharomyces cerevisiae exposed to several growth conditions that shortened or extended yeast chron
264 We identified second-site mutations and growth conditions that suppress LD lethality in the muta
265 idity of our results showing that under fast growth conditions, the beneficial effect of high CO2 on
268 t metabolism under both normal and stressful growth conditions, the impact of drought and heat stress
270 hese methods typically depend on specialized growth conditions, they have been largely restricted to
271 media) and assessment of microbial bioload (growth conditions, time of growth, specificity of microb
273 n the complement study, we also optimize the growth conditions to speed up the process and yield a 10
274 fining our analysis to relatively unstressed growth conditions, total incident solar radiation and av
276 hlight that growing plants under square wave growth conditions ultimately fails to predict plant perf
279 ion to that of C. reinhardtii at its optimal growth condition, UWO241 grown under its natural conditi
283 diverse metastases, under typical metastasis growth conditions, we find that 10 to 150 cells seeded e
284 and cell-cycle timing in both slow and fast growth conditions, we found that well-studied models of
285 Using pulsed laser deposition at identical growth conditions, we have synthesized epitaxial LAO thi
286 In two greenhouse experiments with different growth conditions, we monitored variation in branch diam
287 able leaf-clip Raman sensor under full-light growth conditions were consistent with those obtained wi
288 ere developed from Tripterygium regelii, and growth conditions were optimized for the abundant produc
289 he overall expression profiles under the two growth conditions were rather similar, distinct differen
290 ) studies conducted in relatively unstressed growth conditions were used to determine the means, grea
291 lS ectopically makes only AdoCbl, even under growth conditions where the synthesis of pseudoCbl is fa
292 growing E. coli, the only known steady-state growth condition wherein E. coli significantly deviates
293 ystalline substrate and precisely controlled growth conditions, which limit the price competitiveness
294 after 5 days of nitrogen-limited and normal growth conditions, which show clear differences and the
295 on is strictly regulated under physiological growth conditions with increased expression during surfa
296 mol(-1)) CO2, and then shifted seedlings to growth conditions with short photoperiod (8/16 h) and lo
297 r in phenotype to the wild type under normal growth conditions, with comparable numbers of starch gra
299 e yeast Saccharomyces cerevisiae across nine growth conditions, with replication, for a total of 44 m
300 lic pathways in Synechocystis in autotrophic growth conditions without prominent effects on photosynt