ライフサイエンスコーパス: permeability of @2 to

1 Permeability of TM monolayers to [(14)C]-sucrose was als

2 x day(-1)) for 1 and 7 days led to increased permeability of the BBB to [14C]-sucrose without signifi

3 Bound RNA increases the permeability of liposomes to (22)Na(+).

4 n or pactamycin, respectively, increased the permeability of the RER to 4-MalphaG by 20-30%.

5 sistance of skin, a surrogate measure of the permeability of skin to a variety of compounds, was meas

6 del, Pdgfb(ret/ret), shown to have increased permeability of the BBB to a range of low-molecular mass

7 lizing the plasma membrane and measuring the permeability of the RER to a small molecule, 4-methyl-um

8 lutions increased Lp of microvessels and the permeability of endothelial monolayers to alpha-lactalbu

9 d drug, and daunomycin seems to increase the permeability of parasites to aminoquinolines.

10 The relative permeability of this conductance to anions was P(I)>P(Cl

11 vesicle for several hours, which allowed the permeability of the bilayer to be investigated by monito

12 cose deprivation (OGD), leads to an enhanced permeability of AMPARs to Ca(2+), resulting in delayed c

13 move through Cx26 hemichannels and that the permeability of the hemichannels to Ca(2+) is high, simi

14 ATP-gated current carried by calcium or the permeability of calcium relative to cesium.

15 The permeability of plasma membranes to charged fluorescent

16 produces an energy-dependent increase in the permeability of resistant parasites to chloroquine.

17 was dominant, which in turn caused the water permeability of chlorinated membrane to decrease.

18 of the transmonolayer electrical resistance, permeability of endothelial monolayers to dextran (40 kD

19 treatment with VEGF (20 mug; i.v.) increased permeability of the BBB to Evans blue dye and TTC as det

20 Passive permeability of BBB to FL was estimated by brain uptake

21 At the same time, the permeability of both materials to fluid flow was impaire

22 Due to the high permeability of tumor vessels to fluids and plasma prote

23 Paracellular permeability of cell monolayers to fluorescently labeled

24 The limited permeability of membranes to H(2)O(2) rationalizes the c

25 The relative permeability of the conductances to I(-) and Cl(-) (P(I)

26 hat acute stress by immobilization increased permeability of rat BBB to intravenous 99Technetium gluc

27 the bilayer and, consequently, increases the permeabilities of the membrane to ions, compared to the

28 ouse PrP (moPrP) significantly increases the permeability of living cells to K(+), and forms K(+)- an

29 one can adequately account for the increased permeability of infected RBCs to key solutes.

30 memory" and that Na+(o) regulates the inward permeability of P2X7Rs to large molecules.

31 Although the permeability of the epithelium to macro-molecules is low

32 LFS) has been well documented to enhance the permeability of skin to macromolecular drugs via inducti

33 encing also revealed that Snail enhanced the permeability of endothelial monolayers to macromolecules

34 delivery has many potential advantages, the permeability of skin to macromolecules is extremely low.

35 The high permeability of K+ channels to monovalent thallium (Tl+)

36 NA expression but did not change the partial permeability of the membrane to Na+.

37 this region increased the apparent relative permeability of the channel to NH4+.

38 ontinuous incubation in Na+-free medium, the permeability of the P2X7Rs to NMDG+ gradually increased.

39 AC2 were incorporated into liposomes and the permeability of resulting liposomes to nonelectrolytes o

40 0 s of epithelial exposure to TGF-beta1; the permeability of epithelial monolayers to passage of macr

41 enediaminediacetate, suggesting an increased permeability of the membrane to polar solutes.

42 ly studied is due to a transient increase in permeability of nuclear membrane to proteins and occurs

43 To test these models, we measured the permeability of phospholipid bilayers to protons, potass

44 f Sjogren's syndrome by increasing the water permeability of the gland to restore saliva flow.

45 high-concentration salt solutions, and lower permeability of the capsids to salt ions than to water m

46 l (2-h-old) rats gave rise to an increase in permeability of vessels to serum proteins in the meninge

47 n susceptible strains of mice and alters the permeability of infected brains to small molecules, whic

48 attachment protein] Receptors) increase the permeability of membranes to small molecules and that th

49 n postulated by physiologists to explain the permeability of muscle capillaries to small macromolecul

50 membrane proteins that regulate paracellular permeability of renal epithelia to small ions, solutes,

51 The selective permeability of the membrane to small ions allows effici

52 icroscopy (SECM) to quantitatively study the permeability of the NPCs to small probe ions with a wide

53 The high permeability of nuclei to sucrose was confirmed with Fic

54 Pore radius, estimated by fitting relative permeabilities of organic cations to the Renkin equation

55 plasma membrane correlates with the enhanced permeability of cells to the translation inhibitor hygro

56 eption was that radiation did not affect the permeability of pial vessels to the 150-kDa molecule.

57 s coincided with an increase of paracellular permeability of the BBB to the small tracers sodium fluo

58 nced GFP stops after 2 h, inside the vesicle permeability of the membrane to the feeding solution pro

59 Experiments record a physical anisotropy in permeability of one to two orders of magnitude.

60 l (PESAC), likely accounts for the increased permeability of infected RBCs to various small solutes,

61 Aquaporins, proteins that enhance the permeability of biological membranes to water, are widel

62 The osmotic permeability of cytoplasmic liposomes to water (P(f)), s

63 r VEGF contributes to the high physiological permeability of mammalian glomeruli to water through an

64 relation between the amount of cutin and the permeability of the cuticle to water, but that cutin pla