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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                                 The putative osmoregulatory agent, taurine, is lost from the brain du
6 cal resilience of shore crabs in maintaining osmoregulatory and respiratory function after acute expo
7 e NAA intercompartmental cycle appears to be osmoregulatory, and in this role it may be the primary m
8 glia that perform key structural, signaling, osmoregulatory, and mechanosensory functions within the
9 pathologic roles, and has been shown to have osmoregulatory, antioxidative, antiapoptotic, anti-infla
10 se peptides (AT1aR, SCTR) are coexpressed in osmoregulatory centers, a possible mechanism is formatio
11                                              Osmoregulatory changes, another pregnancy adaptation, ar
12 ents with SIAD could be grouped according to osmoregulatory defect: Ten percent of patients had gross
13           Although the mechanisms underlying osmoregulatory defects in individual patients are presum
14                 In conclusion, the renal and osmoregulatory effects of chronic RLX administration to
15 ion factor, body coloration, morphology, and osmoregulatory enzymes during the smoltification period.
16  lend additional theoretical support to the "osmoregulatory flow" hypothesis, which argues that effic
17 nce of these CBS domains was correlated with osmoregulatory function among the putative transporters
18 ssion of a long C-terminal tail suggested an osmoregulatory function for this tail; this function was
19              Thus, we find no support for an osmoregulatory function of brevetoxins.
20 etin (SCT) share overlapping, interdependent osmoregulatory functions in brain, where SCT peptide/rec
21 ivation of TonEBP did not cause induction of osmoregulatory genes.
22 ernate binding pattern, as yet unreported in osmoregulatory genes.
23 etween the mating pheromone response and the osmoregulatory (high-osmolarity glycerol response [HOG])
24 been shown to stimulate the secretion of the osmoregulatory hormone vasopressin (VP), linking nutriti
25 e been shown to be part of the physiological osmoregulatory mechanism whereby renal tubular cells adj
26            Little is known about cytoplasmic osmoregulatory mechanisms in plants, and even less is un
27                          Understanding brain osmoregulatory mechanisms may provide new insights into
28     Therefore, CLP affects the properties of osmoregulatory neurons in a manner that can affect syste
29   The contractile vacuole (CV) system is the osmoregulatory organelle required for survival for many
30 omplex in Dictyostelium is a tubulovesicular osmoregulatory organelle that exhibits extensive motilit
31 membranes, with prominent localization to an osmoregulatory organelle, the contractile vacuole.
32  Shark kidney is expressed in multiple shark osmoregulatory organs, including specific tubules of the
33  cerevisiae Hog1p MAP kinase involved in the osmoregulatory pathway.
34 t NMDA receptor activation disrupts neuronal osmoregulatory pathways.
35              The presence of many additional osmoregulatory peptides in Tribolium agrees well with it
36 ality on biopolymer processes in general and osmoregulatory processes in particular in the E. coli cy
37 ing phosphotransfer (HPt) protein YPD1 is an osmoregulatory protein in yeast that facilitates phospho
38 diolipin concentrations, cardiolipin and the osmoregulatory protein ProP fail to localize to the pole
39                           Bacteria cells use osmoregulatory proteins as emergency valves to respond t
40  pressure is used as a feedback variable for osmoregulatory pumps instead of being directly responsib
41 hat acute sepsis disrupts centrally mediated osmoregulatory reflexes through differential effects on
42 racterize MeHg-induced changes in astrocytic osmoregulatory release processes.
43  MeHg is associated with specific effects on osmoregulatory release, leading to significant inhibitio
44  impact of morphology on arthropod mobility, osmoregulatory/respiratory systems, and defensive strate
45 otic pressure, which in turn, stimulates the osmoregulatory response from the cells.
46                                           An osmoregulatory response to the increase in brain glutami
47 view that changes in myo-inositol reflect an osmoregulatory response.
48 1(-/-) mice suggest that acute and long-term osmoregulatory responses remain largely intact.
49        In addition to its cytoprotective and osmoregulatory roles, taurine may also serve as an agoni
50 port the hypothesis that K(+) is the central osmoregulatory signal in Enterobacteriaceae.
51  of the extra chromosome 21, where the human osmoregulatory sodium/myo-inositol cotransporter gene is
52    HAI PP2C mutants had enhanced proline and osmoregulatory solute accumulation at low water potentia
53 ce CaCO3 in their intestine as part of their osmoregulatory strategy.
54 ire reversal of osmotic gradients and, thus, osmoregulatory systems.
55 at are activated by hypertonicity, but whose osmoregulatory targets are not yet known.
56  TonEBP expression correlated with canonical osmoregulatory targets TauT/SLC6A6, SMIT/SLC5A3, and AR/
57 fold increases in protein abundance in major osmoregulatory tissues following transfer of fish to sea
58 and was found to be predictive of functional osmoregulatory transporters in other pseudomonads.

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