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1

Separation of large DNA molecules on agarose gel. I. Classical (stable field) electrophoresis

100%
Wojcierowski J., Wojcierowski P.
Applied Biology Communications. Lublin Scientific Center
|
1991
|
tom 01
|
nr 6
2

DNA condensation characterised by fluorescence correlation spectroscopy [FCS]

88%
Hof M., Kral T., Langner M., Adjimatera N., Blagbrough I. S.
Cellular and Molecular Biology Letters
|
2005
|
tom 10
|
nr Suppl.
3

Liposomes: from the origin of life to nanotherapy

88%
Mozafari M. R.
Cellular and Molecular Biology Letters
|
2005
|
tom 10
|
nr Suppl.
4

Separation of megabased-sized DNA molecules of Aspergillus niger using pulsed field gel electrophoresis

88%
Coral G., Colak O., Unaldi M. N.
Folia Biologica
|
2002
|
tom 50
|
nr 1-2
5

Does the near-infrared radiation (NIR) destabilize the DNA molecule?

75%
Szymborska-Malek K., Komorowska M.
Current Topics in Biophysics. Supplement
|
2011
|
tom 34
|
nr A: Posters
6

The effect of PS content on the ability of natural membranes to fuse with positively charged liposomes and lipoplexes

75%
Stebelska K., Dubielecka P. M., Sikorski A. F.
Cellular and Molecular Biology Letters
|
2005
|
tom 10
|
nr Suppl.
7

In search of ionizing radiation effect on nucleosides: radiolysis of cytidine

63%
Zavyalova O., Janiak A., Misiura K., Truszkowski S., Chostenko A.
Current Topics in Biophysics. Supplement
|
2011
|
tom 34
|
nr A: Posters
8

A restriction polymorphism of mitochondrial gene orf25 in selected species of rye

63%
Skuza L., Rogalska S. M.
Seria Biologiczna. Uniwersytet im. Adama Mickiewicza w Poznaniu
|
2005
|
tom 72
9

Structure and genetic organization of the polyploid macronucleus of ciliates: a comparative review

63%
Raikov I. B.
Acta Protozoologica
|
1995
|
tom 34
|
nr 3
10

Human mitochondria in health, disease, aging and cancer

63%
Bartnik E.
Cellular and Molecular Biology Letters
|
2002
|
tom 07
|
nr Suppl.
11

Synthetic virus-like gene transfer system

63%
Szala S.
Postępy Biochemii
|
1995
|
tom 41
|
nr 5
12

Integration host factor [IHF] applied for partial digestion by restriction endonucleases in large DNA molecules [IARC procedure]

63%
Kur J.
Acta Microbiologica Polonica
|
1993
|
tom 42
|
nr 2
13
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Content available

How to study G-quadruplex structures

51%
Malgowska M., Gudanis D., Teubert A., Dominiak G., Gdaniec Z.
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
|
2012
|
tom 93
|
nr 4
14

Rearrangements between differently replicating DNA strands in asymmetric bacterial genomes

51%
Mackiewicz D., Mackiewicz P., Kowalczuk M., Dudkiewicz M., Dudek M. R., Cebrat S.
Acta Microbiologica Polonica
|
2003
|
tom 52
|
nr 3
15

The intracellular fate of non-viral DNA carriers

51%
Langner M.
Cellular and Molecular Biology Letters
|
2000
|
tom 05
|
nr 3
Rapid progress in molecular biology and genetic engineering techniques has made the induction of cell behavior modifications by altering genetic material possible. This allows us to think about the medical application of gene therapy as an alternative to classical pharmacology and as a means of introducing a new approach to treating hereditary diseases. The major obstacle that prevents the application of this method in clinical practice is the difficulty of delivering genetic material to its destination. The fragile DNA molecule (very unstable in in vivo) requires the assistance of supramolecular structures in order to ensure its extended lifetime in circulation. A number of DNA delivery methods have been considered. One of them, a viral carrier, has been extensively studied as a potential candidate for this purpose. Unfortunately, a number of serious problems exist associated with this approach. The risk of accidental infection has not been eliminated and virus presentation causes the immune system to activate. Transfection efficiency achieved with viral vectors is superior to that of other methods, but safety concerns and financial considerations have stimulated studies aimed at the development of non-viral DNA carriers. At present, the transfection efficiency of such carriers is very low. This paper discusses problems encountered when developing a stable and efficient lipid-DNA aggregate, capable of delivering genetic material into the targeted cell nucleus. Discussion is limited to aggregate interaction with the cellular plasma membrane and its fate in the cytosol.
16

Interaction of oligonucleotides with positively charged liposomes using fluorescence techniques

51%
Jurkiewicz P., Kral T., Okruszek A., Hof M., Langner M.
Cellular and Molecular Biology Letters
|
2002
|
tom 07
|
nr 2
17

Microstructure of DNA - liposome aggregates in presence of metal cations

51%
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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