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1 -min hypoxia followed by reoxygenation under isosmotic (293 mOsm) conditions.
2 llecting duct (mIMCD) were exposed to either isosmotic (300 mosmol/kg) or hyperosmotic medium (isosmo
3                                              Isosmotic addition of 50 mM propionate to the standard H
4  cell swelling, which could be blocked by an isosmotic addition of a pore-impermeable solute (sucrose
5 oxicity of reference toxicants was tested in isosmotic and hypoosmotic exposure media in RTgill-W1 ce
6 -19755 (50 microM) completely protected both isosmotic and hyposmotic (233 mOsm) slices against hypox
7 le whole-cell currents were elicited by both isosmotic and hyposmotic cell swelling.
8 rane potential (Em) was -58 and -32 mV under isosmotic and hyposmotic conditions, respectively.
9 ile during I- influx, together with Em under isosmotic and hyposmotic conditions, were used to calcul
10 O3- Ringer's were exposed to I- pulses under isosmotic and, subsequently, hyposmotic conditions.
11 gh water permeabilities, consistent with the isosmotic ASL theory, and the capacity to restore water
12  and CF airway epithelia, consistent with an isosmotic ASL.
13                          For resuspension in isosmotic buffer (osmotic upshift, or Delta, of 0), the
14                                 Importantly, isosmotic cell swelling obtained by parallel activation
15 ity under hyposmotic condition to that under isosmotic condition (termed enhancement ratio or ER) was
16 entration (1.8 to </=1.6 mM) in an otherwise isosmotic condition, real-time AFM imaging revealed a si
17                Jdw was determined in control isosmotic conditions and after either changes in osmolar
18 erved under both hyperosmotic conditions and isosmotic conditions associated with osmotic stress.
19 , ICl,swell was persistently activated under isosmotic conditions in CHF myocytes, and 9AC increased
20 (Cir,swell) was persistently activated under isosmotic conditions in CHF myocytes, and Gd3+ decreased
21                                        Under isosmotic conditions or with activation of the kinases S
22         However, the function of NFAT5 under isosmotic conditions present in vivo remains unknown.
23 ificantly faster under hyposmotic than under isosmotic conditions.
24 posmotic media (170 mosmol kg-1) relative to isosmotic control (300 mosmol kg-1) values, it decreased
25 h after onset of hyperosmolality, but not in isosmotic controls, growth arrest and DNA damage-inducib
26 ring moderate hyperosmotic stress but not in isosmotic controls.
27 greater in the hyperosmotic papilla than the isosmotic cortex but was not affected by the animal's hy
28 ignificantly increased after 6 h exposure to isosmotic EtOH, but not hyperosmotic EtOH.
29                                              Isosmotic exposure of MMDD1 cells to low NaCl (60 mm) ca
30 egulate ASL volume by modulating the flow of isosmotic fluid across the epithelium, whereas an altern
31                   Acute dynamic exercise and isosmotic fluid ingestion each seem to change IOP throug
32 rformed after dehydration and hydration with isosmotic fluid.
33 go reversible volume changes when exposed to isosmotic glucose-fructose exchange.
34 go reversible volume changes when exposed to isosmotic glucose-fructose exchange.
35 s depolarized and excited in proportion with isosmotic increases in [Na(+)].
36 d by a return of extracellular osmolality to isosmotic levels.
37 dehydration, and after hydration with 946 ml isosmotic liquid (345 mOsM).
38 otic (300 mosmol/kg) or hyperosmotic medium (isosmotic medium + 150 mM NaCl) after seeding.
39 zalkonium chloride, compared to exposures in isosmotic medium and showed toxicity levels similar to t
40 ckle cell disease (SCD) lyse in deoxygenated isosmotic non-electrolyte solutions.
41 nsport after brief exposure to hypo-osmotic, isosmotic or hyperosmotic medium (170, 300 and 430 mosmo
42 up to 7%, but 9AC had no effect on volume in isosmotic or hyperosmotic solutions.
43                  Strain on the TM induced by isosmotic PEG solutions of different molecular masses wa
44               In normoxia and in hypoxia, an isosmotic reduction in [Na+]o caused a proportional decr
45                                          The isosmotic replacement of NaCl with choline chloride had
46 ium chloride in the bathing fluid and during isosmotic replacement of sodium chloride with mannitol.
47 uring hyperosmotic stress and dissolves upon isosmotic rescue (over ~100 s) with minimal effect on ce
48 erosmotic samples were shifted compared with isosmotic samples showing a gap of 18 h but had the same
49 llular physiological calcium in an otherwise isosmotic situation.
50  of the antagonist provided no protection to isosmotic slices (51% vs. 57% recovery rate) while affor
51  to hyposmotic conditions as 57% of control (isosmotic) slices showed recovery compared with 51%, 35%
52 l myocytes, osmotic swelling in 0.9x to 0.6x isosmotic solution (296 mOsm/L) was required to elicit a
53            Osmotic shrinkage in 1.1x to 1.5x isosmotic solution inhibited both I(Cir,swell) and Gd3+-
54 9T to 0.6T solution (T, relative osmolarity; isosmotic solution, 296 mOsmol/L) was required to elicit
55 ely 10%, but Gd3+ had no effect on volume in isosmotic solution.
56 y extrapolation of osmolalities of predicted isosmotic state at 8,000-8,500 m may indicate a possible
57 ies from bathyal and abyssal fishes, predict isosmotic state at 8,200 m.
58                                     Although isosmotic substitution of extracellular Na(+) ions block
59 iated inward current, which was sensitive to isosmotic substitution of Na(+) or Cl(-) ion.
60                                      Neither isosmotic substitution of sucrose for NaCl in the medium
61 als showed progressive lysis in deoxygenated isosmotic sucrose solution at pH 7.4 to a level greater