Antisense technology has been used for several years to "knock down" the expression of specific genes in living tissues to study the functions of their protein products. Specifically designed antisense oligonucleotides (ODNs) are short lengths of man-made genetic material designed to interfere with the production of the protein encoded by the gene. This can shed light on the function of the protein; alternatively, if a disease process results from an excess of a certain protein, the method can in theory correct the problem. Faster than transgenic techniques, but more similarly problematic in practice, antisense has been seen as something of a "black art". There are many technical problems to understand and overcome. This is the first book to provide a critical review of the uses of this technology in the central nervous system. Antisense Technology in the Central Nervous System describes the promises and the pitfalls of this approach, and compares it to other approaches. The practical experience of leading researchers is combined with a thorough description of the theoretical foundation of the technique, making the book ideal for researchers and clinicians alike.
Sprache
Verlagsort
Zielgruppe
Illustrationen
tables, line ill., num. halftones
numerous halftones, line illustrations, tables
Maße
Höhe: 234 mm
Breite: 156 mm
Gewicht
ISBN-13
978-0-19-850316-3 (9780198503163)
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Schweitzer Klassifikation
1. Antisense oligonucleotide regulation of gene expression in the CNS: an overview; 2. Antisense knockdown in the CNS - optimizing the strategy; 3. The design of appropriate control experiments to ensure specificity in antisense oligonucleotide function; 4. Modulation of gene expression in the central nervous system as a tool in behavioral pharmacology; 5. Behavioural and neuroendocrine effects of antisense targeting in the rat; 6. Electrophysiological and behavioural effects of dopamine receptor knockdown in the brain; 7. Antisense mapping: exploring the functioual significance of alternative splicing; 8. Medicinal chemistry of antisense oligonucleotides; 9. Retinal neuronal development in trkB antisense 'knockdowns'; 10. Pluronic gel as a means of antisense delivery; 11. Delivery of antisense by viral vectors for prolonged antisense effects in vivo; 12. Regulation of gene expression in the CNS by natural antisense RNAs; 13. Aptamers: Another use for oligonucleotides; 14. Ribozymes: oligonucleotides with enzymatic activity have potential as regulators of gene expression in the CNS; 15. Antisense approaches to neural signalling in Caenorhabditis elegans