Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yulia G. Suzdaltseva"'
Autor:
Ekaterina V. Silina, Natalia E. Manturova, Olga S. Ivanova, Alexander E. Baranchikov, Elena B. Artyushkova, Olga A. Medvedeva, Alexey A. Kryukov, Svetlana A. Dodonova, Mikhail P. Gladchenko, Ekaterina S. Vorsina, Maria P. Kruglova, Oleg V. Kalyuzhin, Yulia G. Suzdaltseva, Victor A. Stupin
Publikováno v:
Molecules, Vol 29, Iss 12, p 2853 (2024)
Purpose of the study: the creation of a dextran coating on cerium oxide crystals using different ratios of cerium and dextran to synthesize nanocomposites, and the selection of the best nanocomposite to develop a nanodrug that accelerates quality wou
Externí odkaz:
https://doaj.org/article/91478443e793414d948f6848d0ce0e41
Block Polycationic Oligonucleotide Derivative: Synthesis and Inhibition of Herpes Virus Reproduction
Publikováno v:
Bioconjugate Chemistry. 7:3-6
The block polycationic oligonucleotide (oligo) consisting of a phosphodiester 12-mer linked to the polycation chain at the 3'-end and cholesteryl group at the 5'-end was synthesized. The polycation chain was grown on the solid support using the monom
Publikováno v:
Bioconjugate Chemistry. 6:639-643
Water-soluble, block copolymeric carriers consisting of polyoxyethylene (PEO) and polyspermine (PS) chains have been developed for the delivery of antisense oligonucleotides (oligo) into the target cells. These copolymers spontaneously form complexes
Autor:
G Paradis, Alexander V. Kabanov, E V Bartakova, B. Ochietti, Tatiana K. Bronich, N Guérin, Yulia G. Suzdaltseva, Serguei V. Vinogradov, H. K. Nguyen, Yves St-Pierre, Catherine L. Gebhart, Pierre Lemieux, V Y Alakhov
Publikováno v:
Journal of drug targeting. 8(2)
Self-assembling complexes from nucleic acids and synthetic polymers are evaluated for plasmid and oligonucleotide (oligo) delivery. Polycations having linear, branched, dendritic. block- or graft copolymer architectures are used in these studies. All
Publikováno v:
Biochemical and biophysical research communications. 203(2)
Antisense oligonucleotides were modified by their ends with hydrophobic substituents which permitted enhancing their activity. The effect of hydrophobized oligonucleotides on reproduction of Herpes Simplex Virus type 1 in Vero cells was studied. Two