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1 cal domains necessary for maintaining tissue impermeability.
2  is limited by inefficient delivery and cell impermeability.
3 low survival by partially restoring membrane impermeability.
4  which, paradoxically, contribute to bladder impermeability.
5  which plays a major role in maintaining BBB impermeability.
6 ssage of molecules while preserving membrane impermeability.
7  this ordered monolayer while preserving its impermeability.
8 ell membrane integrity with propidium iodide impermeability and light scatter using the flow cytomete
9                          Underlying this dye impermeability are morphological changes, including an i
10 tion in the ppsC gene which reduced cellular impermeability but did not impact cytotoxicity in macrop
11 rovides both mechanical support and chemical impermeability essential to developing embryos.
12                  Nevertheless, the vesicles' impermeability, even toward ions and other small molecul
13                                          The impermeability for nitrogen in as-prepared state indicat
14 d reduced CFTR function, leading to chloride impermeability in CF epithelia and heterologous systems.
15                  Here we show that seed-coat impermeability in wild soybean is controlled by a single
16                                              Impermeability, in which bacteria have reduced susceptib
17 It has yet to be determined whether membrane impermeability is maintained when MalFGK2 cycles between
18                                         This impermeability is partially imparted by the outer membra
19 layers are ubiquitous in modern cells, their impermeability, lack of dynamic properties, and syntheti
20 ratio, chemical resistance, flexibility, and impermeability make it a promising candidate for inclusi
21                                         When impermeability occurred, MICs of a genotypic group varie
22                            However, the cell impermeability of ATP analogues has largely limited thei
23                                          The impermeability of ferrocyanide molecules in the absence
24 orescein conjugate (SF) was synthesized, and impermeability of plasma membranes to this compound was
25 gthened as the voltage increased, suggesting impermeability of the channel for the ligands.
26                  As a consequence, a loss of impermeability of the inner membranes of spores, accompa
27                                          The impermeability of the P. aeruginosa outer membrane contr
28                                          The impermeability of the plasma membrane towards large, hyd
29                  This is probably due to the impermeability of the testa to the GUS substrate.
30 s in living cells is impeded by the membrane impermeability of these anionic lipids.
31                            If outer membrane impermeability persists, the disruption of mitochondrial
32                  These findings suggest that impermeability resistance occurs in only a fraction of t
33  mechanical strength, relative inertness and impermeability to all standard gases.
34 t of an N-formyl group for channel activity, impermeability to cations with a diameter >4 A, high mon
35 eir susceptibility to cellular nucleases and impermeability to cell membranes.
36 s integrity; this leads to a reversal of its impermeability to exogenous substrates.
37 alability over a wide temperature range, and impermeability to fluids.
38 ncluding low density, high strength, extreme impermeability to gas and liquid and resistance to chemi
39  high electronic and thermal conductivities, impermeability to gases, as well as many other supreme p
40 receptor subunit (GluR2), which confers Ca2+ impermeability to heteromeric channels.
41           Because of the glycosomal membrane impermeability to nucleotides, ATP molecules consumed by
42                          The transition from impermeability to permeability in domesticated soybean w
43 limited by their proteolytic instability and impermeability to the cell membrane.
44 e high affinity of cyclen 1 to pyranine, its impermeability to the lipid bilayer membrane, fast kinet
45                  Transepithelial resistance, impermeability to trypan blue, and confocal microscopy c
46 o the crystal structure, as evidenced by its impermeability to water.
47  manner, thus eliminating the limitations of impermeability, toxicity, and specificity of the fluores
48                            Loss of seed-coat impermeability was essential in the domestication of man
49 experiments, demonstrated a loss of membrane impermeability with similar time and concentration depen

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