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1 (1-30%, depending on genetic background and growth conditions).
2 established to directly identify the optimal growth condition.
3 phenotypes of the bacteria under a specific growth condition.
4 utant synthesizes more granules under either growth condition.
5 fer a fitness disadvantage under a specified growth condition.
6 help regulate DNA replication in response to growth conditions.
7 ay periodicity can be tuned by adjusting the growth conditions.
8 native transcription initiation under normal growth conditions.
9 switch between phases as a result of varying growth conditions.
10 plasmic reticulum (ER) stress in unfavorable growth conditions.
11 s were studied phenotypically using standard growth conditions.
12 ases in young cells in the lifespan-altering growth conditions.
13 icroorganisms are uniquely determined by the growth conditions.
14 mutant yeast strains simulated in different growth conditions.
15 sistently upregulated during diverse biofilm growth conditions.
16 ncreased SPI1 gene expression under the same growth conditions.
17 es were translated under standard laboratory growth conditions.
18 ostructures are accessible by modulating the growth conditions.
19 s a spectrum of cell states defined by their growth conditions.
20 s that function optimally within a subset of growth conditions.
21 activate expression of nitrogenase under all growth conditions.
22 ch include platelets released during ex vivo growth conditions.
23 ibutable to stroma, extrinsic signaling, and growth conditions.
24 enable them to thrive in less than favorable growth conditions.
25 l sorting and plated in endothelial-specific growth conditions.
26 ensory systems necessary to detect favorable growth conditions.
27 d became photobleached under high light (HL) growth conditions.
28 onribosomal production as a function of cell growth conditions.
29 lidate our methods on a phenomics dataset of growth conditions.
30 tosynthetic carbon metabolism under variable growth conditions.
31 ed by the degree of cation site disorder via growth conditions.
32 enesis and biomass synthesis under different growth conditions.
33 nvasions under normal and pathophysiological growth conditions.
34 assimilate acetate under both light and dark growth conditions.
35 ssion of several transporters in ambient CO2 growth conditions.
36 eving optimal nucleation kinetics under mild growth conditions.
37 pid droplets in the tgd2 mutant under normal growth conditions.
38 beit unaltered leaf morphology under optimal growth conditions.
39 t of the MCM complex at Ser-205 under normal growth conditions.
40 oteins that aid in survival during stressful growth conditions.
41 S cluster biogenesis varies with fluctuating growth conditions.
42 cross different Escherichia coli strains and growth conditions.
43 in vivo phenotypic traits under 32 distinct growth conditions.
44 autotrophic tissues, at least under standard growth conditions.
45 ning to find suitable nucleation and crystal growth conditions.
46 is bacterium under aerobic and heterotrophic growth conditions.
47 e and consistent over a range of tissues and growth conditions.
48 to a similar target in its mRNA during poor growth conditions.
49 lux according to product demand under normal growth conditions.
50 iverse bacterial species across more than 60 growth conditions.
51 ucleotide excision repair (NER) under normal growth conditions.
52 ressed in vitro under biofilm and planktonic growth conditions.
53 nce between the two proteomes under standard growth conditions.
54 ntrations but dispensable under microaerobic growth conditions.
55 dvantage over control cells under suboptimal growth conditions.
56 onstitute two separate operons under hypoxic growth conditions.
57 he expression levels of all promoters in two growth conditions.
58 h various functions in response to different growth conditions.
59 ain, display various phenotypes depending on growth conditions.
60 bon-limiting, nitrogen-limiting, and optimal growth conditions.
61 o a bleaching phenotype under moderate light growth conditions.
62 dynamics of growth and division in balanced growth conditions.
63 ompared with the wild type, in two different growth conditions.
64 217 ORFs) is extremely stable under the same growth conditions.
65 apacity to maximize survival under differing growth conditions.
66 e likely to be utilized for more-specialized growth conditions.
67 lis cells under a wide range of steady-state growth conditions.
68 elle genomes, and transcriptome from diverse growth conditions.
69 ncrease ADP1 fitness under common laboratory growth conditions.
70 during chromosome segregation under various growth conditions.
71 enzyme de novo synthesis in photoautotrophic growth conditions.
72 Pck anaplerotic function under fermentative growth conditions.
73 g deliberate and specific non-stoichiometric growth conditions.
74 ptional and translational control under both growth conditions.
75 uctuations in growth rate, even under steady growth conditions.
76 enic Spn1 genes were expressed under routine growth conditions.
77 siderably during translation under different growth conditions.
78 ing growth, particularly under nutrient poor growth conditions.
79 efore difficult to perform under exponential growth conditions.
80 to characterize acclimation to light-limited growth conditions.
81 brane repair and signaling under exponential growth conditions.
82 e transport was investigated under different growth conditions.
83 of the lamellar structures under phototropic growth conditions.
84 for regulating DNA replication under adverse growth conditions.
85 , no gene expression was detected under most growth conditions.
86 change as the tumor evolves under different growth conditions.
87 ic and anaerobic, and optimal and suboptimal growth conditions.
88 cultivatable bacterium under a wide range of growth conditions.
89 gregation and did not transpose under normal growth conditions.
90 t are not expressed under typical laboratory growth conditions.
91 ween the wild type and pho2 mutant under two growth conditions.
92 measured their phenotypic profile across 214 growth conditions.
93 ickly meet demand upon sudden improvement in growth conditions.
94 hat silences the gene cluster under standard growth conditions.
95 utant shows growth retardation under regular growth conditions.
96 pecific interactions can vary with different growth conditions.
97 DH mediated stress responses under favorable growth conditions.
98 has not yet been described under controlled growth conditions.
99 tabolic models and across three experimental growth conditions.
100 ised close to a miscibility transition under growth conditions.
101 starch granule per chloroplast under normal growth conditions.
102 ReS2 (1.62 eV) by precisely controlling the growth conditions.
103 criptional capacity of RNAPIII under optimal growth conditions.
104 portantly, fern stomatal responses depend on growth conditions.
105 sition studies of AB under industrially safe growth conditions.
106 fairly synchronous sporulation in submerged growth conditions.
107 in molecular structure that depend on fibril growth conditions.
108 e differentially expressed, depending on the growth conditions.
109 p DeltauvrD cells being inviable under rapid growth conditions.
110 show shorter primary roots under restrictive growth conditions.
111 fect the bulk chromosome segregation in slow growth conditions.
112 d trials that have been biased towards mesic growth conditions.
113 pathway negatively regulates HR under normal growth conditions.
114 cultured rat hepatocytes grown under normal growth conditions.
115 strain these levels declined under the same growth conditions.
116 t high yield using high-cell-density E. coli growth conditions.
117 utant strains under different substrates and growth conditions.
118 e genes were highly upregulated under normal growth conditions.
119 ctivated when the bacterium enters anaerobic growth conditions.
120 thesis by Escherichia coli, focusing on slow-growth conditions.
122 for plant and fungal cells during different growth conditions, after treatment with IAA, and in diff
123 I) thin films is achieved at the iodine-rich growth condition, allowing for the record high room-temp
124 he magnitude of TFIID dependence varies with growth conditions, although this variation is similar ge
125 ith replication, their frequency varies with growth condition and chromosomal coordinate, and they sh
126 oth proper stomatal functioning under normal growth conditions and adaptive developmental responses t
127 the difficulties of both identifying proper growth conditions and characterizing and isolating each
128 protein in the cytosol requires both anoxic growth conditions and co-expression of NifH and NifM wit
129 fatty acid types in leaves were affected by growth conditions and cold acclimatisation, being genera
131 ulon whose expression is enhanced under good growth conditions and down-regulated under starvation co
133 acking studies were carried out under normal growth conditions and during amino acid starvation.
134 tarvation-induced chlorosis during short-day growth conditions and extended darkness, indicating that
135 phosphate-regulated (PHO) genes under normal growth conditions and for full induction of PHO5 and the
136 charomyces cerevisiae proteome under various growth conditions and genetic backgrounds using the GFP
138 astrocyte and neuronal cultures under normal growth conditions and in response to manganese (Mn) trea
139 on yeast growth were examined under regular growth conditions and in the presence of caffeine, a kno
140 phenotypic traits under 30 distinct in vitro growth conditions and in two different hosts (insect lar
142 s kept 14 generation periods over a range of growth conditions and kept phase for hundreds of generat
143 ange between attached and mobile cells under growth conditions and negligible cell detachment under s
144 expression of the EBR1 paralogues depends on growth conditions and on the presence of the single EBR1
145 ture-sensitive growth defect under oxidative growth conditions and produce colonies with dysfunctiona
146 this state lends itself to manipulation via growth conditions and the material parameters such as Fe
147 of cellular biomass under nutrient-limiting growth conditions and the rate of increase in investment
148 ratio has been shown to change under various growth conditions and to determine the response of the b
149 blocking BCAA catabolism during both normal growth conditions and under energy-limited conditions.
150 SiGe strips, without the need to modify the growth conditions, and by using low cost, low thermal-bu
151 9 and crRNA expression levels, organisms and growth conditions, and experimental conditions collectiv
152 ased by H2O2, in the diauxic phase of normal growth conditions, and in cells under alphaSyn-mediated
153 E. coli than in B. japonicum under identical growth conditions, and Mur responded to iron in a B. jap
154 um are not expressed under normal laboratory growth conditions, and our understanding of how they are
155 iva) crops will likely experience a range of growth conditions, and root architectural plasticity wil
156 ted within specific zones, as defined by the growth conditions, and show how occlusion can govern cha
157 n of S. oneidensis to changing and stressful growth conditions, and this ability is probably widespre
158 he spatial density functions across species, growth conditions, and time, which suggests functional s
159 l strains or the same strain under different growth conditions, and to identify the essential archite
160 ending on cellular physiology and changes in growth conditions, and translation errors are not always
162 To this end, we model a large compendium of growth conditions as a multiplex network consisting of t
163 using the combined metabolic traits from all growth conditions as an input indicated that inclusion o
164 r autotrophic, mixotrophic and heterotrophic growth conditions, as well as knockout conditions that e
167 the surface, lag phase adjustment to the new growth conditions (B), the length at birth, LB, and cell
168 iew on seed oil biosynthesis under different growth conditions, bringing together gene expression lev
169 In both 2-dimensional and 3-dimensional growth conditions, BST2-silenced tumor cells displayed a
170 dispensable for proliferation under optimal growth conditions but is required for starvation and str
171 dispensable for proliferation under optimal growth conditions but is required for starvation and str
173 differentiation of hormogonia under standard growth conditions, but, upon addition of a symbiotic par
175 omic network approach to infer similarity of growth conditions by integrating layers of the multiplex
176 e complex responds differently to changes in growth conditions by tuning phosphorylation dynamics.
177 toxin YafQ is suppressed under steady state growth conditions by virtue of its interaction with its
179 enzymes such that, upon entry into favorable growth conditions, cells can quickly alter lipid flux by
181 iana plants grown under the same macroscopic growth conditions contain as much information on the und
183 d situations and under anchorage-independent growth conditions, demonstrating a PRL-2.CNNM3 complex-d
185 competes with biodegradation, (ii) bacterial growth conditions (dissolution flux and resulting chemic
186 y bacterial adaptive responses to changes in growth conditions due to biotic and abiotic factors invo
187 on of expression under at least one of three growth conditions examined, we predicted 14,868 TSS cand
188 Here, we demonstrate that under etiolated growth conditions, extensive interdependence/overlap occ
189 with the main barriers being the effects of growth conditions, fixations and inherent complexities i
190 n cancer cell lines cultured under different growth conditions, followed by subsequent structure-acti
193 d host immune response, which in turn alters growth conditions for microbes in airways, promoting fur
194 the intein for full activity only at optimal growth conditions for the native organism, while sparing
195 nic mutants (i) exhibited a lower fitness in growth conditions found in human tissues, such as hypero
197 vapor growth (SSVG) method, and the optimum growth conditions have been experimentally determined.
199 ed profound effects in anchorage-independent growth conditions, however, including impaired colony fo
201 re expressed under Bvg negative (Bvg-) phase growth conditions; however, these appear to be primarily
203 studies suggested that H. ducreyi encounters growth conditions in human lesions resembling those foun
204 uble-mutant collection under a wide range of growth conditions in order to search for additional gene
206 es are transcribed maximally under anaerobic growth conditions in the presence of low nitrate concent
207 nd less efficient upon partially respiratory growth conditions in which glycerol production is signif
208 sm, such as shape, metabolic substrates, and growth conditions) in microbial bioinformatics has been
209 -mismatch-induced strain, and roughness, and growth conditions, in particular, growth time and growth
210 when Dhc195 was subjected to four suboptimal growth conditions, including decreased temperature (-13.
211 he the energy efficiency of cells under fast growth conditions, indicating a tradeoff between the hig
212 species, life history, evolutionary age, and growth conditions is required to gain insight into the e
213 r-intensive culture process, unphysiological growth conditions, lack of reproducibility and limited t
215 ally driven variations in upper water column growth conditions (light, nutrient, and temperature).
216 cts were also linked to secondary effects on growth, condition, liver size, blood chemistry and compo
218 he level of PotA was elevated under in vitro growth conditions mimicking unfed ticks compared to the
219 evisiae, which reveals that under favourable growth conditions mRNAs coding for proteins involved in
222 ns revealed that, under these 'non-standard' growth conditions, numerous uncharacterised regulators a
224 -to-culture and site-to-site, the effects of growth condition on the isotope fractionation during red
225 on events and the effects of the alternative growth conditions on lifespan indicates that genomic ins
228 m L.) that were induced under drought-stress growth conditions, one encoded a protein with significan
231 oplasmic Gln3 sequestration under repressive growth conditions or relocation to the nucleus following
232 ind that regardless of the miRNA, cell type, growth condition, or translational state, mRNA destabili
233 We previously reported that mildly acidic growth conditions (pH 5.8) downregulate expression of ge
235 t to produce CAI-1 under particular limiting growth conditions presumably through a ribosome slippage
238 ed peak transpiration across plant sizes and growth conditions (R = 0.86, P < 0.001) and was relative
239 ings indicate that, under photoheterotrophic growth conditions, R. palustris can degrade meta-hydroxy
240 rylated FDH and, in response to unfavourable growth conditions, reduction in FDH phosphorylation leve
242 his dualism of synergy and competition under growth conditions relevant in contaminated aquifers, we
243 arly Golgi in Saccharomyces cerevisiae under growth conditions, relocates to a compartment called com
245 Transcriptome analyses under different salt growth conditions revealed, among other things different
247 vity assays demonstrated that under standard growth conditions, sepA is repressed by the global regul
248 spectrometry of P. aeruginosa under standard growth conditions showed that p3MDO is expressed in low
249 Analysis of these mutants under different growth conditions showed that these systems are not redu
250 ice were viable and fertile under laboratory growth conditions showing no obvious phenotypic abnormal
251 or growth in CF sputum compared with defined growth conditions shows that the latter requires several
252 ects cellular survival under non-fermentable growth conditions, suggesting an overlapping role for bo
253 o vacuole-nucleus contact sites depending on growth conditions, suggesting that ERMES function can be
254 ergent regulation of CD2AP in different axon growth conditions suggests that separate mechanisms exis
255 der intrinsically safe, atmospheric pressure growth conditions, suitable for application in roll-to-r
256 as a defect in acclimation to sulfur-limited growth conditions, sulfur acclimation (sac) mutants, whi
257 pear to be functionally redundant under most growth conditions tested, NlpD is specifically required
258 cells propagated for a short duration under growth conditions that enable epithelial reprogramming.
259 e is a root vegetable grown under a range of growth conditions that may influence the product quality
261 ave shown that cell widening is abrogated in growth conditions that promote higher surface area to vo
263 le cell lines under smooth muscle cell (SMC) growth conditions that retained a patient-specific genom
264 Saccharomyces cerevisiae exposed to several growth conditions that shortened or extended yeast chron
265 We identified second-site mutations and growth conditions that suppress LD lethality in the muta
266 idity of our results showing that under fast growth conditions, the beneficial effect of high CO2 on
268 sociated with gluconeogenesis under standard growth conditions, the enzyme can catalyze the reverse r
272 distinct predesigned subunits under similar growth condition, thus facilitating manifold control of
273 d epithelial cells (phmSG) and optimized the growth conditions to achieve the maintenance of phmSG in
275 ssess mechanisms to inhibit eEF2K under good growth conditions, to allow protein synthesis to proceed
276 fining our analysis to relatively unstressed growth conditions, total incident solar radiation and av
278 hlight that growing plants under square wave growth conditions ultimately fails to predict plant perf
279 d metabolite data obtained under contrasting growth conditions using principal component analysis sug
283 derstand how this organism reacts to dynamic growth conditions, we challenged it with a series of dif
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 rowth phenotype in which the only permissive growth conditions were a 6-aminopurine source in the pre
287 NA half-lives for 12 genes under Fe-depleted growth conditions were longer than those in FA1090.
288 ere developed from Tripterygium regelii, and growth conditions were optimized for the abundant produc
289 ) studies conducted in relatively unstressed growth conditions were used to determine the means, grea
290 ters remain 'silent' under common laboratory growth conditions where activation is obtained through g
291 lS ectopically makes only AdoCbl, even under growth conditions where the synthesis of pseudoCbl is fa
292 ial and stationary growth phase under normal growth conditions, whereas the other two are induced upo
293 microbial cultures can vary depending on the growth conditions, which may complicate source tracing d
294 the conventional SecA1 pathway under normal growth conditions while preventing ordinary precursor pr
296 on is strictly regulated under physiological growth conditions with increased expression during surfa
297 mol(-1)) CO2, and then shifted seedlings to growth conditions with short photoperiod (8/16 h) and lo
298 ically monitoring a mutant library under two growth conditions, with and without interferon, by deep
299 r in phenotype to the wild type under normal growth conditions, with comparable numbers of starch gra
300 lic pathways in Synechocystis in autotrophic growth conditions without prominent effects on photosynt
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