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1                             Of four putative osmoregulatory ABC transporters in DC3000, one, designat
2     Consistent with the previously described osmoregulatory actions of GH and PRL in teleosts, we obs
3 efulness of the CBS domains as predictors of osmoregulatory activity.
4                                              Osmoregulatory adaptation is the most crucial change, ne
5 o-freshwater transition suggests that strong osmoregulatory adaptations may have facilitated their co
6 water is scarce, underpinned by their unique osmoregulatory adaptations.
7                                 The putative osmoregulatory agent, taurine, is lost from the brain du
8 cal resilience of shore crabs in maintaining osmoregulatory and respiratory function after acute expo
9 e NAA intercompartmental cycle appears to be osmoregulatory, and in this role it may be the primary m
10 glia that perform key structural, signaling, osmoregulatory, and mechanosensory functions within the
11 pathologic roles, and has been shown to have osmoregulatory, antioxidative, antiapoptotic, anti-infla
12 hic period during which sea lamprey increase osmoregulatory capacity and acquire seawater (SW) tolera
13 R abundance are associated with increases in osmoregulatory capacity during metamorphosis.
14 t spironolactone treatment in vivo increases osmoregulatory capacity.
15 -smolt or smolt based on body morphology and osmoregulatory capacity.
16 se peptides (AT1aR, SCTR) are coexpressed in osmoregulatory centers, a possible mechanism is formatio
17                                              Osmoregulatory changes, another pregnancy adaptation, ar
18 ents with SIAD could be grouped according to osmoregulatory defect: Ten percent of patients had gross
19           Although the mechanisms underlying osmoregulatory defects in individual patients are presum
20 nd that the endogenous sensory properties of osmoregulatory effector neurons contribute to their home
21                 In conclusion, the renal and osmoregulatory effects of chronic RLX administration to
22 ion factor, body coloration, morphology, and osmoregulatory enzymes during the smoltification period.
23  lend additional theoretical support to the "osmoregulatory flow" hypothesis, which argues that effic
24 nce of these CBS domains was correlated with osmoregulatory function among the putative transporters
25 inner mitochondrial membrane protein with an osmoregulatory function controlling mitochondrial volume
26 ssion of a long C-terminal tail suggested an osmoregulatory function for this tail; this function was
27              Thus, we find no support for an osmoregulatory function of brevetoxins.
28 detected effects of food restriction on hypo-osmoregulatory function of migrants that may influence t
29 ropelling planarian movement, as well as the osmoregulatory function of protonephridia.
30 CNSS-mediated production of CRF peptides has osmoregulatory functions and provide a resource for inve
31 n-releasing factor (CRF) peptides-which have osmoregulatory functions and were highly abundant in the
32 etin (SCT) share overlapping, interdependent osmoregulatory functions in brain, where SCT peptide/rec
33 ivation of TonEBP did not cause induction of osmoregulatory genes.
34 ernate binding pattern, as yet unreported in osmoregulatory genes.
35 etween the mating pheromone response and the osmoregulatory (high-osmolarity glycerol response [HOG])
36 ther, these results demonstrate that S is an osmoregulatory hormone in lamprey and that receptor-medi
37 been shown to stimulate the secretion of the osmoregulatory hormone vasopressin (VP), linking nutriti
38 e been shown to be part of the physiological osmoregulatory mechanism whereby renal tubular cells adj
39 , its formation may require energy-consuming osmoregulatory mechanisms able to draw water and exert m
40            Little is known about cytoplasmic osmoregulatory mechanisms in plants, and even less is un
41                          Understanding brain osmoregulatory mechanisms may provide new insights into
42     Therefore, CLP affects the properties of osmoregulatory neurons in a manner that can affect syste
43   The contractile vacuole (CV) system is the osmoregulatory organelle required for survival for many
44 omplex in Dictyostelium is a tubulovesicular osmoregulatory organelle that exhibits extensive motilit
45 membranes, with prominent localization to an osmoregulatory organelle, the contractile vacuole.
46 acts at the contractile vacuole, an exocytic osmoregulatory organelle.
47  Shark kidney is expressed in multiple shark osmoregulatory organs, including specific tubules of the
48  cerevisiae Hog1p MAP kinase involved in the osmoregulatory pathway.
49                   Here we review some of the osmoregulatory pathways in guard cell metabolism, genes
50 t NMDA receptor activation disrupts neuronal osmoregulatory pathways.
51              The presence of many additional osmoregulatory peptides in Tribolium agrees well with it
52 g of joint cavitation as an energy-requiring osmoregulatory process that accrues a water-based fluid
53 ality on biopolymer processes in general and osmoregulatory processes in particular in the E. coli cy
54 ical glycoside that limits pump activity and osmoregulatory processes, joint cavitation in embryos wa
55 ing phosphotransfer (HPt) protein YPD1 is an osmoregulatory protein in yeast that facilitates phospho
56 diolipin concentrations, cardiolipin and the osmoregulatory protein ProP fail to localize to the pole
57                           Bacteria cells use osmoregulatory proteins as emergency valves to respond t
58  pressure is used as a feedback variable for osmoregulatory pumps instead of being directly responsib
59 hat acute sepsis disrupts centrally mediated osmoregulatory reflexes through differential effects on
60 racterize MeHg-induced changes in astrocytic osmoregulatory release processes.
61  MeHg is associated with specific effects on osmoregulatory release, leading to significant inhibitio
62  impact of morphology on arthropod mobility, osmoregulatory/respiratory systems, and defensive strate
63 otic pressure, which in turn, stimulates the osmoregulatory response from the cells.
64                                           An osmoregulatory response to the increase in brain glutami
65 view that changes in myo-inositol reflect an osmoregulatory response.
66 nd (2) which endocrine systems contribute to osmoregulatory responses in the CNSS.
67 1(-/-) mice suggest that acute and long-term osmoregulatory responses remain largely intact.
68                                              Osmoregulatory roles for the CNSS have been hypothesized
69        In addition to its cytoprotective and osmoregulatory roles, taurine may also serve as an agoni
70 port the hypothesis that K(+) is the central osmoregulatory signal in Enterobacteriaceae.
71  of the extra chromosome 21, where the human osmoregulatory sodium/myo-inositol cotransporter gene is
72    HAI PP2C mutants had enhanced proline and osmoregulatory solute accumulation at low water potentia
73 ce CaCO3 in their intestine as part of their osmoregulatory strategy.
74 ire reversal of osmotic gradients and, thus, osmoregulatory systems.
75 at are activated by hypertonicity, but whose osmoregulatory targets are not yet known.
76  TonEBP expression correlated with canonical osmoregulatory targets TauT/SLC6A6, SMIT/SLC5A3, and AR/
77 fold increases in protein abundance in major osmoregulatory tissues following transfer of fish to sea
78 ressed highly in the brain and moderately in osmoregulatory tissues.
79 and was found to be predictive of functional osmoregulatory transporters in other pseudomonads.