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OverviewIn his research, David Dannheisig investigates the influence of lysine129 acetylation on the biological function of survivin including alteration of nucleocytoplasmic shuttling as well as dimerization behavior. Since survivin participates in two major hallmarks of oncogenesis, namely cell death inhibition and chromosomal segregation during the cell cycle, it reflects a valuable target in cancer therapy and research. The author establishes proximity-dependent, fluorescence-microscopic methods to quantify the interaction of survivin with the export receptor Crm1 as well as the homodimerization itself. In the future, those systems can be usedto examine the feasible effect of chemical modulators which are targeting these interactions in a cellular background. The outcome achieved is an essential step towards the enhancement of potential cancer therapies. Full Product DetailsAuthor: David DannheisigPublisher: Springer Fachmedien Wiesbaden Imprint: Springer Spektrum Edition: 1st ed. 2017 Weight: 1.757kg ISBN: 9783658186227ISBN 10: 3658186224 Pages: 104 Publication Date: 16 June 2017 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: Manufactured on demand ![]() We will order this item for you from a manufactured on demand supplier. Table of ContentsApoptosis – The Programmed Suicide.- Cancer – The Enemy Inside.- Nucleocytoplasmic Transport– Cellular Navigation.- Biological Function of Survivin.- Protein modification – Make-Up for Proteins.- Cell cycle – Virchow’s Heritage.ReviewsAuthor InformationDavid Dannheisig currently is a student of the International Graduate School in Molecular Medicine (IGradU) pursuing his PhD (Dr. rer. nat) degree at the Institute of Biochemistry and Molecular Biology (iBMB) at Ulm University, Germany. Tab Content 6Author Website:Countries AvailableAll regions |