Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Antisense strategy--new trends]

M Koziołkiewicz1

  • 1Centrum Badań Molekularnych i Makromolekularnych, Zakład Chemii Bioorganicznej, Lódź.

Postepy Biochemii
|October 14, 1998
PubMed
Summary

No abstract available in PubMed .

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Japanese quince (Chaenomeles japonica) leaf phenol extract as modulator of the inflammatory response in lipopolysaccharide-triggered murine macrophage RAW 264.7 cells.

Journal of physiology and pharmacology : an official journal of the Polish Physiological Society·2021
Same author

Aptamer inhibits degradation of platelet proteolytically activatable receptor, PAR-1, by thrombin.

Thrombosis research·2001
Same author

Stereochemistry of cleavage of internucleotide bonds by Serratia marcescens endonuclease.

Bioorganic & medicinal chemistry·2001
Same author

The mononucleotide-dependent, nonantisense mechanism of action of phosphodiester and phosphorothioate oligonucleotides depends upon the activity of an ecto-5'-nucleotidase.

Blood·2001
Same author

Inhibition of plasminogen activator inhibitor release in endothelial cell cultures by antisense oligodeoxyribonucleotides with a 5'-end lipophilic modification.

Acta biochimica Polonica·2000
Same author

Enzymatic assignment of diastereomeric purity of stereodefined phosphorothioate oligonucleotides.

Antisense & nucleic acid drug development·1999