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1 t animal and its symbiont use during modeled microgravity.
2 t, has emerged as a possible major impact of microgravity.
3 otein during cardiac adaptation in simulated microgravity.
4 ts were clustered in the subapical region in microgravity.
5 and matrix were measured after activation in microgravity.
6 How cells (might) sense microgravity.
7 orientation of the FN matrix after 27.5 h in microgravity.
8 ease PDGF-BB showed significant responses in microgravity.
9 ctivated osteoblasts even during exposure to microgravity.
10 action data collected from crystals grown in microgravity.
11 n pulmonary function that occur in sustained microgravity.
12 late the host stress responses under modeled microgravity.
13 visual impairments in astronauts exposed to microgravity.
14 c reticulum were differentially modulated in microgravity.
15 e observed in the 3D culture under simulated microgravity.
16 ty, and gene expression was suppressed under microgravity.
17 d with limb muscles, which were unaltered in microgravity.
18 f fluctuations during transient diffusion in microgravity.
19 ts to ameliorate some effects of exposure to microgravity.
20 mals spending nine days (from P15 to P24) in microgravity.
21 N mRNA synthesis is significantly reduced in microgravity (0-G) when compared to ground (GR) osteobla
22 easured by RT-qPCR, was also up-regulated in microgravity (+12.94, +2.98 and +16.85 fold respectively
23 4 +/- 2 mmHg) and ICP (supine, 17 +/- 2 vs. microgravity, 13 +/- 2 mmHg) were reduced in acute zero
24 central venous pressure (supine, 7 +/- 3 vs. microgravity, 4 +/- 2 mmHg) and ICP (supine, 17 +/- 2 vs
26 tions induced by thermophoretic diffusion in microgravity, a regime not accessible to analytical calc
30 esults reported here indicate that simulated microgravity alters the expression of miRNAs and genes i
31 Head down-tilt bed rest (HDBR) serves as a microgravity analog because it mimics the headward fluid
35 closing volume was approximately the same in microgravity and in normal gravity, emphasizing the impo
37 ht, quiescent osteoblasts were launched into microgravity and were then sera activated with and witho
39 eton as an active site of rapid bone loss in microgravity, and indicate that this loss is not limited
40 h in experiments using vibrated grains under microgravity, and we describe novel predicted spatiotemp
43 uous extravehicular activities or to monitor microgravity-associated changes in musculoskeletal anato
45 h suggest that exposure of healthy humans to microgravity augments arterial pressure and sympathetic
46 ouse islets cultured in stationary dishes or microgravity bioreactors were transplanted to streptozot
47 f amyloplasts per cell remained unchanged in microgravity but decreased on the clinostat, and (iii) t
48 at individual amyloplast volume increased in microgravity but remained constant in seedlings grown fo
49 hat pulmonary function is greatly altered in microgravity, but none of the changes observed so far wi
50 d trabecular bone surfaces also increased in microgravity by 170% (p = 0.004), indicating osteoclasti
52 cephalogram (EEG) arousals also decreased in microgravity (by 19%), and this decrease was almost enti
53 e, a combination of 3D culture and simulated microgravity can be used to efficiently generate highly
54 a possible physiological explanation for how microgravity can cause symptoms similar to those seen in
56 These data support our conclusion that in microgravity cardiomyocytes attempt to maintain mitochon
57 Myofibril force measurements revealed that microgravity caused a 3-fold decrease in specific force
59 s was changed significantly in the simulated microgravity condition including miR-150, miR-34a, miR-4
61 ant (P < 0.05) suppression of 85 genes under microgravity conditions compared to normal gravity sampl
62 RNA-Seq analysis of squid exposed to modeled microgravity conditions exhibited extensive differential
63 Human bladder 5637 cells cultivated under microgravity conditions formed organoids that displayed
65 remedy these problems we cultured islets in microgravity conditions to improve their function and to
68 st 24 h of activation using both spaceflight microgravity culture and a ground-based model system tha
69 hibition of T cell proliferative response in microgravity culture is a result of alterations in signa
71 lation of purified T cells with Bead-Leu4 in microgravity culture resulted in the engagement and inte
72 uble anti-CD3 (Leu4) in clinorotation and in microgravity culture shows a dramatic reduction in surfa
73 en T cells were stimulated with Bead-Leu4 in microgravity culture, they were able to partially expres
78 little is known regarding the effects of the microgravity environment of space flight upon the action
79 re, a corresponding 24-hour average TLCPD in microgravity environment was simulated to be 6.7mmHg.
87 ed time under conditions of minimal gravity (microgravity) experience an array of biological alterati
88 ndividing human fibroblast cells in culture, microgravity experienced in space has little effect on g
89 ower in sponges from animals with 10 days of microgravity exposure (P<0.01, ANOVA) and further reduce
90 and results published earlier indicate that microgravity exposure augments sympathetic, and diminish
91 during early microgravity exposure, fell as microgravity exposure continued, and descended to prefli
92 during early microgravity exposure, rose as microgravity exposure continued, and drifted back to pre
93 R intervals) rose significantly during early microgravity exposure, fell as microgravity exposure con
94 preflight levels: pressure fell during early microgravity exposure, rose as microgravity exposure con
96 16-week-old female C57BL/6J mice (n = 8) to microgravity for 15-days on the STS-131 space shuttle mi
97 ture environment has also been used to model microgravity for ground-based studies regarding the impa
99 ased animal models simulating the effects of microgravity have shown that decrements in cerebral perf
101 mune response was suppressed under simulated microgravity; however, there was an acceleration of bact
103 y, we tested the hypothesis that exposure to microgravity impairs autonomic neural control of sympath
104 , and tested the hypothesis that exposure to microgravity impairs sympathetic as well as vagal barore
106 , we found that these macrophages adapted to microgravity in an ultra-fast manner within seconds, aft
107 in spinal cord tissue from animals reared in microgravity in comparison with 1G-reared controls.
108 h either in the rotating condition to model microgravity in space or in the static condition as a co
110 The surprisingly ultra-fast adaptation to microgravity indicates that mammalian macrophages are eq
111 herefore, this study offers new evidence for microgravity-induced osteocytic osteolysis, and CDKN1a/p
113 eviously demonstrated that low-shear modeled microgravity (LSMMG) under optimized rotation suspension
114 transitions from a 1 g linear force field to microgravity (<1 g); however, it appears that the three-
115 logical perturbations in cardiac function in microgravity may be a consequence of alterations in mole
116 rrelationships can occur as a consequence of microgravity-mediated perturbations in cellular architec
119 rica serovar Typhimurium grown under modeled microgravity (MMG) were more virulent and were recovered
120 the analogous immune suppression observed in microgravity, MMG, and aging, further investigation may
124 ve) cells of Zea mays seedlings grown in the microgravity of outer space allocate significantly less
126 tested the hypothesis that adaptation to the microgravity of space impairs sympathetic neural respons
129 otion; therefore, we examined the effects of microgravity on mouse shoulder muscles for the 15-d Spac
130 nature of their pathologies, the effects of microgravity on pathophysiology, and the alterations in
132 ould yield new information on the effects of microgravity on the biological activities of various cla
133 the first to report the effects of simulated microgravity on the expression of miRNA and related gene
134 een conducted in space or by using simulated microgravity on the ground have focused on the growth or
135 In this study, we examine the impact of microgravity on the interactions between the squid Eupry
142 al volume was unexpectedly reduced by 18% in microgravity, possibly because of uniform alveolar expan
147 se interactions occur in a confined space in microgravity, providing ample opportunity for heavy micr
150 trast to prevailing theory, we observed that microgravity reduces central venous and intracranial pre
151 We tested the hypotheses that exposure to microgravity reduces sympathetic neural outflow and impa
152 pace medicine, incorporating past studies of microgravity-related conditions and their terrestrial co
153 host health and examining its resiliency in microgravity represents a new frontier for space biology
154 te that the environment created by simulated microgravity represents a novel environmental regulatory
156 f Escherichia coli under low-shear simulated microgravity (SMG) conditions resulted in enhanced stres
157 stem can be used for a variety of controlled microgravity studies of cartilage and other tissues.
158 cation of cTnI up-regulated during simulated microgravity suggests a potential role of the NH(2)-term
159 erating deltoid muscle was more sensitive to microgravity than the joint-stabilizing rotator cuff mus
160 ugh the fetal otolith organs are unloaded in microgravity, the fetus' semicircular canals receive hig
161 ntermeasures probably reduced the effects of microgravity, the results support the idea that ground-b
162 stigates the health effects of adaptation to microgravity: the nature of their pathologies, the effec
163 n the absence of the symbiont during modeled microgravity there was an enrichment of genes and pathwa
165 m cells and exposed the spheres to simulated microgravity using a random positioning machine for 3 da
166 catory and appendicular muscles responses to microgravity, using mice aboard the space shuttle Space
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