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1

Does the defection kinetics in model biomembranes lead to a certain non-trivial scaling law?

100%
Gadomski A., Kriechbaum M., Laggner P.
Biophysics of Membrane Transport
|
1994
|
tom 12
|
nr 2
2

Exploring the effect of anaesthetic gases on biomembranes

80%
Stimson L. M., Vattulainen I., Rog T., Karttunen M.
Cellular and Molecular Biology Letters
|
2005
|
tom 10
|
nr Suppl.
3

Bilayer lipid membrane based electrochemical sensors

80%
Leitmannova-Ottova A., Ti Tien H.
Polish Journal of Environmental Studies
|
1993
|
tom 02
|
nr 2
4

Exploring the effect of xenon on biomembranes

70%
Stimson L. M., Vattulainen I., Rog T., Karttunen M.
Cellular and Molecular Biology Letters
|
2005
|
tom 10
|
nr 4
5

Monolayers as model biomembranes

61%
Kinnunen P. K. J.
Cellular and Molecular Biology Letters
|
1999
|
tom 04
|
nr 2
6

Bilayer lipid membranes [BLM]: an experimental system for biomolecular electronic devices development

61%
Ottova-Leitmannova A., Tien H. T.
Biophysics of Membrane Transport
|
1992
|
tom 11
|
nr 2
7

NMR studies on single lipid bilayers supported in cylindrical aluminium oxide nanopores - reconstitution of GPCR

61%
Geade H. C., Soubias O., Luckett K. M., Polozov I. V., Wong K. K. Y., Yeliseev A. A., Gawrisch K.
Cellular and Molecular Biology Letters
|
2005
|
tom 10
|
nr Suppl.
8

Membranes at interfaces: structure studies by AFM and time-resolved neutron reflectivity

61%
Klosgen B., Spangenberg T., Niehus H., Gutberlet T., Steitz R., Fragneto G.
Cellular and Molecular Biology Letters
|
2002
|
tom 07
|
nr 2
9

Kinetic models for stochastically modified ionic channels

51%
Wozinski A., Iwaniszewski J.
Cellular and Molecular Biology Letters
|
2008
|
tom 13
|
nr 3
421-429
Ionic channels form pores in biomembranes. These pores are large macromolecular structures. Due to thermal fluctuations of countless degrees-of-freedom of the biomembrane material, the actual form of the pores is permanently subject to modification. Furthermore, the arrival of an ion at the binding site can change this form by repolarizing the surrounding aminoacids. In any case the variations of the pore structure are stochastic. In this paper, we discuss the effect of such modifications on the channel conductivity. Applying a simple kinetic description, we show that stochastic variations in channel properties can significantly alter the ionic current, even leading to its substantial increase or decrease for the specific matching of some time-scales of the system.
10

Calcium uptake by sarcoplasmic reticulum in the presence of methylparathion

51%
Blasiak J.
Biophysics of Membrane Transport
|
1994
|
tom 12
|
nr 2
11

Oxidative status evaluated in rats exposed to 1-butanol and ethanol

41%
Jajte J., Stetkiewicz J., Wronska-Nofer T.
Acta Toxicologica
|
2003
|
tom 11
|
nr 2
12

Effects of methyl parathion on model membrane fluidity: Polarization of diphenylhexatriene and intramolecular excimerization of a pyrene derivative

41%
Blasiak J.
Current Topics in Biophysics
|
1993
|
tom 17
|
nr 1-2
13

Insertion of GPI-anchored alkaline phosphatase into supported membranes: a combined AFM and fluorescence microscopy study

41%
Rieu J. P., Ronzon F., Place C., Dekkiche F., Cross B., Roux B.
Acta Biochimica Polonica
|
2004
|
tom 51
|
nr 1
A new method based on combined atomic force microscopy (AFM) and fluorescence microscopy observations, is proposed to visualize the insertion of glycosylphos- phatidyl inositol (GPI) anchored alkaline phosphatase from buffer solutions into sup­ported phospholipid bilayers. The technique involves the use of 27 nm diameter fluo­rescent latex beads covalently coupled to the amine groups of proteins. Fluorescence microscopy allows the estimation of the relative protein coverage into the membrane and also introduces a height amplification for the detection of protein/bead com­plexes with the AFM. The coupling of the beads with the amine groups is not specific; this new and simple approach opens up new ways to investigate proteins into sup­ported membrane systems.
14

Basic study on functional liposomes and their application

41%
Oku N.
Cellular and Molecular Biology Letters
|
1996
|
tom 01
|
nr 4
Liposomes have been used as models of biomembranes and tools in the field of drug delivery systems. Liposomalization of various drugs has been revealed to enhance their efficacy and to reduce the side effect of the drugs. For site-specific delivery, intracellular targeting, and controlled release of drugs, many functional liposomes have been developed based on their nature as models of biomembranes. In this paper, preparation and characterization of three kinds of functional liposomes are presented, namely, thermosensitive liposomes for delivering macromolecules, pH-sensitive liposomes for cytosolic delivery of the encapsulated materials, and reticuloendothelial system (RES)-avoiding liposomes for passive targeting to tumor tissues. The actual usefulness of RES-avoiding liposomes modified with a uronic acid derivative, palmityl-D-glucuronide, for tumor imaging and therapy was demonstrated. Recently, a method to analyze liposomal trafficking in living animals, which is important in the use of liposomes as drug carriers, was developed by use of positron emission tomography. In this paper, liver accumulation of liposomes having various charges is shown.
15

Microstructure of DNA - liposome aggregates in presence of metal cations

41%
Uhrikova D., Hanulova M., Lengyel A., Funari S. S., Balgavy P.
Cellular and Molecular Biology Letters
|
2005
|
tom 10
|
nr Suppl.
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