The DOI matches its Crossref record; 241 of the 243 references it cites were found in a registry or an index.
Progress in Antisense Technology
Abstract
Antisense technology exploits oligonucleotide analogs to bind to target RNAs via Watson-Crick hybridization. Once bound, the antisense agent either disables or induces the degradation of the target RNA. Antisense agents can also alter splicing. During the past decade, much has been learned about the basic mechanisms of antisense, the medicinal chemistry, and the pharmacologic, pharmacokinetic, and toxicologic properties of antisense molecules. Antisense technology has proven valuable in gene functionalization and target validation. With one drug marketed, Vitravenetm, and approximately 20 antisense drugs in clinical development, it appears that antisense drugs may prove important in the treatment of a wide range of diseases.
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“Though fat accumulation, and specifically diacylglycerol accumulation, was equal in all groups, the PKCε antisense oligonucleotide improved hepatic insulin sensitivity and insulin signalling.”
From Lipid-induced insulin resistance: unravelling the mechanism (2010) · cites this paper as [107]
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“, proteins and peptides, saccharides, fluorophores and photoprobes, inhibitors, and vitamins) that provide the conjugate with a desired novel property offers a feasible way to address these requirements [1–16].”
BACTERIAL GENE EXPRESSION INHIBITION WITH ANTISENSE PEPTIDE NUCLEIC ACIDS
Dryselius, R. (2005) · Figshare
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“Following hybridization to the mRNA, the ASO inhibits translation and splicing and leads to degradation of the mRNA by ribonuclease (RNase).(3) ASO kinetics are characterized by a large and rapid distribution to the liver following parenteral administration, thus making”
MethodEntry of antisense oligonucleotides into Streptococcus mutans
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BackgroundAmino-Functionalized Oligonucleotides with Peptide Internucleotide Linkages
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“ON analogs are extensively used for manipulation of gene expression via antisense or RNA interference mechanisms [1-8].”
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Metadata
- Authors
- Crooke, S. T.
- Affiliations
- Ionis Pharmaceuticals (United States) (US)
- Corresponding author
- Crooke, Stanley T.
- ORCID
- Crooke, Stanley T.
- Venue
- Annual Review of Medicine
- Publisher
- Annual Reviews
- Published
- 2004-02-01
- Volume
- 55
- Issue
- 1
- Pages
- 61-95
- ISSN
- 0066-4219 (ISSN-L)
- 1545-326X
- OpenAlex
- W2138668121
- Cited by
- 417
- References
- 243
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 5 · 2023: 10 · 2022: 7 · 2021: 8 · 2020: 3 · 2019: 9 · 2018: 5 · 2017: 15 · 2016: 12 · 2015: 14 · 2014: 16 · 2013: 24 · 2012: 32
- FWCI
- 3.07
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- antisense technology, oligonucleotide analogues, RNA hybridization, RNA degradation, RNA splicing, antisense drug development, pharmacokinetics, toxicity, target validation
- MeSH terms
- Animals, Humans, Oligonucleotides, Antisense, Biomedical Technology
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