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1 otics were abundant in EVs released from the stressed condition.
2 yield reduction was observed compared to non-stressed conditions.
3 cogen synthesis and increased survival under stressed conditions.
4 [eCO(2)] with greater difference under water-stressed conditions.
5 d by Mps1 MAP kinase, particularly under the stressed conditions.
6 and RPL30) in S. cerevisiae under normal and stressed conditions.
7 rowth under nutrient deprivation or nutrient stressed conditions.
8 root development of crops both in normal and stressed conditions.
9 es genes that support metabolic functions in stressed conditions.
10 l microRNAs will vary between unstressed and stressed conditions.
11 and low compensation point in unstressed and stressed conditions.
12 n roots and leaves under unstressed and salt stressed conditions.
13 under both well-watered and moderate drought-stressed conditions.
14  target gene expression under both basal and stressed conditions.
15 ostasis via recycling nutrients under normal/stressed conditions.
16 nous system and right heart under normal and stressed conditions.
17 facilitate DNA replication, especially under stressed conditions.
18 ) regulates expression of hCtr1 under copper-stressed conditions.
19 ted much less scrambling under the same heat-stressed conditions.
20  new functions for autophagy under basal and stressed conditions.
21 e GLS2 expression under both nonstressed and stressed conditions.
22 ctly regulates p21/CIP1 expression under non-stressed conditions.
23 the ER membrane and in the cytosol under non-stressed conditions.
24 r to that of wild-type MCL-1 under basal and stressed conditions.
25 ers of growth arrest and apoptosis under non-stressed conditions.
26 ability are critical for cell survival under stressed conditions.
27 ression is critical for cell viability under stressed conditions.
28 M. truncatula grown under normal and drought-stressed conditions.
29 nd immunostaining under normal and glutamate-stressed conditions.
30 stance because of their critical roles under stressed conditions.
31 n repair (NER), and in DNA replication under stressed conditions.
32 is of the kidney in SCD under unstressed and stressed conditions.
33  bridges under both resting and mechanically stressed conditions.
34 s of ice plant under unstressed and salinity stressed conditions.
35  normal myocardial oxygen consumption during stressed conditions.
36 Allium cepa) under hydrated and mechanically stressed conditions.
37 howed protein binding, under both normal and stressed conditions.
38  kDa (HpuB), and binds hemoglobin under iron-stressed conditions.
39  measured in all subjects under baseline and stressed conditions.
40 637 million people to production under water-stressed conditions.
41 ting intrinsic variation under heat or water stressed conditions.
42  grown under well-watered as well as drought-stressed conditions.
43 wards higher TL in the case of recovery from stressed conditions.
44 of effector functions in addition to typical stressed conditions.
45 rough compartmentalizing DNPS enzymes during stressed conditions.
46 d infestation under well-watered and drought-stressed conditions.
47 ed consistently across both stressed and non-stressed conditions.
48 stoglobules under unstressed and 5-day light-stressed conditions.
49 s to return to normal homeostasis after IFN "stressed" conditions.
50                  Here we show that under non-stressed conditions, activating transcription factor-2 (
51 xpression is upregulated under metabolically stressed conditions and ACSS2 silencing reduced the grow
52 at Gfral knockout mice are hyperphagic under stressed conditions and are resistant to chemotherapy-in
53 n EBLN1 accumulate DNA damage both under non-stressed conditions and following exogenously induced DN
54 nd progenitor cells (HSPCs) under normal and stressed conditions and found that HSPCs lacking Nras ex
55 during the season, in well-watered and water-stressed conditions and in newer and older generation ma
56 lower diversity panel under control and salt-stressed conditions and measured a suite of morphologica
57 th factor responsiveness under metabolically stressed conditions and provide a novel mechanism by whi
58 ity, myocardial performance under normal and stressed conditions, and lifespan are severely reduced.
59  Glutamine induces autophagy under basal and stressed conditions, and prevents apoptosis under heat s
60 ts (EVPOMEs) were fabricated under thermally stressed conditions at 43 degrees C for 24 h to create a
61                            Under normal, non-stressed conditions, both control (HaCaT) and IEX-1-tran
62  protein is found in the cytoplasm under non-stressed conditions but rapidly accumulates in the nucle
63 xperience optimal growth under mildly acidic stressed conditions, but murMN strain displays growth ar
64 ences between samples grown under normal and stressed conditions can be determined.
65  phosphorus by phytoplankton under phosphate-stressed conditions can overcompensate the previously pr
66                  Importantly, under severely stressed conditions, chronic administration of a D1 rece
67 he lamellar phases were prepared under water-stressed conditions, despite the fact that x-ray-induced
68                                      In heat-stressed conditions, differential regulation of HSPA1A a
69 to sensitive japonica M103 under control and stressed conditions during PI stage.
70 nsitive genotypes under control and salinity-stressed conditions during vegetative growth.
71                  Sequestration occurs during stressed conditions, for example heat, which transcripti
72 ve cellular energy state under metabolically stressed conditions in a robust, reductionist in vitro m
73 Popdc2 leads to sinus node dysfunction under stressed conditions in aged mice.
74 area were grown under well-watered and water-stressed conditions in greenhouse mesocosms and in the f
75 CCFN were grown under well-watered and water-stressed conditions in greenhouse mesocosms and in the f
76 eous depression-like behaviors under the non-stressed conditions in mice, while systemic or neuron-sp
77  a defect in biofilm formation under ethanol-stressed conditions in S. mutans.
78 mays) genotypes under well-watered and water-stressed conditions in the field.
79 tative and qualitative characteristics under stressed conditions in young and aged mice is unknown.
80 tructure (HOS) of monoclonal antibodies upon stressed conditions is critical to gaining a better unde
81 tional activity (under both constitutive and stressed conditions) may be partially dependent on the l
82 xpression of the lipE gene was induced under stressed conditions mimicking M. tuberculosis' intracell
83 uadrivalent influenza vaccines (aQIVc) under stressed conditions of heating, oxidation, lowered and e
84 s allow coral to persist under these El Nino-stressed conditions, often recovering from these events
85            Under both well-watered and water-stressed conditions over 4 years, DMNB-T6P stimulated yi
86 ageB2 in cancer cells both under cycling and stressed conditions, presenting a distinct functional fe
87  bile acid (BA) levels under both normal and stressed conditions primarily through up-regulating expr
88 ly produced between well-watered and drought-stressed conditions, representing effective indicators o
89 aximum photosynthetic rates during non-water-stressed conditions, revealing a trade-off between maxim
90                           Furthermore, under stressed conditions, skin wounds, but not mucosal wounds
91                                        Under stressed conditions such as DNA damage, p53 escapes MDM2
92 n a broad range of biological pathways under stressed condition, such as ABC transporters, two-compon
93 growing under what are generally classed as "stressed" conditions, such as low intensity illumination
94 he normal state of these helicases under non-stressed conditions that promote their RNA unwinding and
95               By combining these models with stressed conditions, the authors assessed the contributi
96               The results support the use of stressed conditions to generate low abundance species fo
97 elanoma cells were studied under resting and stressed conditions using tumor necrosis factor-alpha as
98 selective growth advantage under oxidatively stressed conditions via the disregulation of apoptosis,
99 s on pectin methyl esterification under salt stressed conditions was further validated through in vit
100  secretion of EVs from MRSA under antibiotic stressed conditions was increased by 22.4-fold compared
101 host development and when sorghum is drought stressed, conditions when mycobiomes are small.
102                                   During non-stressed conditions, when eIF2 phosphorylation is low, r
103 uite similar to the wild type (WT) under non-stressed conditions yet have many distinct changes in re

 
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