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1 ze-dependent leakage of molecules from small unilamellar liposomes.
2 rately or together into membrane bilayers in unilamellar liposomes.
3 ated derivatives hydrated to generate large, unilamellar liposomes.
4 eloped a unique system to observe Z rings in unilamellar liposomes.
5 data indicate that thermodynamically stable, unilamellar liposomes are formed spontaneously by simple
6 t membrane probes, phosphatidylcholine-based unilamellar liposomes are harnessed to investigate membr
7 that TLF efficiently binds and permeabilizes unilamellar liposomes at lysosomal pH, whereas non-lytic
10 e observed when LDL acceptor was replaced by unilamellar liposomes, consistent with desorption from t
11 cterize the transmembrane asymmetry of small unilamellar liposomes consisting of zwitterionic and cha
13 se, we have reconstituted the Ca-ATPase into unilamellar liposomes containing defined amounts of diol
14 to probe interactions between PH domains and unilamellar liposomes containing different phospholipids
19 of large (approximately 100 nm in diameter) unilamellar liposomes in the presence of 100 mM NaCl, pH
22 violet light exposure of two-component large unilamellar liposomes (LUV) composed of a 3:1 molar mixt
23 L) reconstituted on immobilized single small unilamellar liposomes of different diameter and therefor
24 Free radical oxidations of multilamellar and unilamellar liposomes of various mixtures of glycerophos
25 diol accumulation) in Triton X-100 micelles, unilamellar liposomes, or erythrocyte ghost membranes in
29 ridinols were assayed in phosphatidylcholine unilamellar liposomes using a recently developed high-th
30 ggregation state on the membrane fluidity of unilamellar liposomes was assessed by monitoring the ani
33 H17SH]4- ion has been encapsulated in small, unilamellar liposomes, which are capable of delivering t
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