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1 d by Mps1 MAP kinase, particularly under the stressed conditions.
2 l microRNAs will vary between unstressed and stressed conditions.
3 and low compensation point in unstressed and stressed conditions.
4 n roots and leaves under unstressed and salt stressed conditions.
5 and RPL30) in S. cerevisiae under normal and stressed conditions.
6 under both well-watered and moderate drought-stressed conditions.
7 ostasis via recycling nutrients under normal/stressed conditions.
8 nous system and right heart under normal and stressed conditions.
9 facilitate DNA replication, especially under stressed conditions.
10 ) regulates expression of hCtr1 under copper-stressed conditions.
11 ted much less scrambling under the same heat-stressed conditions.
12  new functions for autophagy under basal and stressed conditions.
13 e GLS2 expression under both nonstressed and stressed conditions.
14 ctly regulates p21/CIP1 expression under non-stressed conditions.
15 the ER membrane and in the cytosol under non-stressed conditions.
16 r to that of wild-type MCL-1 under basal and stressed conditions.
17 ers of growth arrest and apoptosis under non-stressed conditions.
18 ability are critical for cell survival under stressed conditions.
19 ression is critical for cell viability under stressed conditions.
20 M. truncatula grown under normal and drought-stressed conditions.
21 nd immunostaining under normal and glutamate-stressed conditions.
22 stance because of their critical roles under stressed conditions.
23 n repair (NER), and in DNA replication under stressed conditions.
24 is of the kidney in SCD under unstressed and stressed conditions.
25  bridges under both resting and mechanically stressed conditions.
26 s of ice plant under unstressed and salinity stressed conditions.
27  normal myocardial oxygen consumption during stressed conditions.
28 rowth under nutrient deprivation or nutrient stressed conditions.
29 Allium cepa) under hydrated and mechanically stressed conditions.
30 howed protein binding, under both normal and stressed conditions.
31  kDa (HpuB), and binds hemoglobin under iron-stressed conditions.
32  measured in all subjects under baseline and stressed conditions.
33 root development of crops both in normal and stressed conditions.
34 es genes that support metabolic functions in stressed conditions.
35 s to return to normal homeostasis after IFN "stressed" conditions.
36                  Here we show that under non-stressed conditions, activating transcription factor-2 (
37 xpression is upregulated under metabolically stressed conditions and ACSS2 silencing reduced the grow
38 at Gfral knockout mice are hyperphagic under stressed conditions and are resistant to chemotherapy-in
39 n EBLN1 accumulate DNA damage both under non-stressed conditions and following exogenously induced DN
40 nd progenitor cells (HSPCs) under normal and stressed conditions and found that HSPCs lacking Nras ex
41 th factor responsiveness under metabolically stressed conditions and provide a novel mechanism by whi
42 ity, myocardial performance under normal and stressed conditions, and lifespan are severely reduced.
43  Glutamine induces autophagy under basal and stressed conditions, and prevents apoptosis under heat s
44 ts (EVPOMEs) were fabricated under thermally stressed conditions at 43 degrees C for 24 h to create a
45                            Under normal, non-stressed conditions, both control (HaCaT) and IEX-1-tran
46  protein is found in the cytoplasm under non-stressed conditions but rapidly accumulates in the nucle
47 ences between samples grown under normal and stressed conditions can be determined.
48 he lamellar phases were prepared under water-stressed conditions, despite the fact that x-ray-induced
49                                      In heat-stressed conditions, differential regulation of HSPA1A a
50 to sensitive japonica M103 under control and stressed conditions during PI stage.
51 nsitive genotypes under control and salinity-stressed conditions during vegetative growth.
52 ve cellular energy state under metabolically stressed conditions in a robust, reductionist in vitro m
53 Popdc2 leads to sinus node dysfunction under stressed conditions in aged mice.
54 area were grown under well-watered and water-stressed conditions in greenhouse mesocosms and in the f
55 CCFN were grown under well-watered and water-stressed conditions in greenhouse mesocosms and in the f
56 tative and qualitative characteristics under stressed conditions in young and aged mice is unknown.
57 tional activity (under both constitutive and stressed conditions) may be partially dependent on the l
58 ageB2 in cancer cells both under cycling and stressed conditions, presenting a distinct functional fe
59  bile acid (BA) levels under both normal and stressed conditions primarily through up-regulating expr
60                           Furthermore, under stressed conditions, skin wounds, but not mucosal wounds
61                                        Under stressed conditions such as DNA damage, p53 escapes MDM2
62 n a broad range of biological pathways under stressed condition, such as ABC transporters, two-compon
63 growing under what are generally classed as "stressed" conditions, such as low intensity illumination
64               The results support the use of stressed conditions to generate low abundance species fo
65 elanoma cells were studied under resting and stressed conditions using tumor necrosis factor-alpha as
66 selective growth advantage under oxidatively stressed conditions via the disregulation of apoptosis,
67 s on pectin methyl esterification under salt stressed conditions was further validated through in vit
68                                   During non-stressed conditions, when eIF2 phosphorylation is low, r

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