Impact of Survivin Acetylation on its Biological Function

In 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 inhi...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας: Dannheisig, David (Συγγραφέας)
Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: Wiesbaden : Springer Fachmedien Wiesbaden : Imprint: Springer Spektrum, 2017.
Σειρά:BestMasters
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
LEADER 03401nam a22004815i 4500
001 978-3-658-18623-4
003 DE-He213
005 20170623141642.0
007 cr nn 008mamaa
008 170606s2017 gw | s |||| 0|eng d
020 |a 9783658186234  |9 978-3-658-18623-4 
024 7 |a 10.1007/978-3-658-18623-4  |2 doi 
040 |d GrThAP 
050 4 |a RC261-271 
072 7 |a MJCL  |2 bicssc 
072 7 |a MED062000  |2 bisacsh 
082 0 4 |a 614.5999  |2 23 
100 1 |a Dannheisig, David.  |e author. 
245 1 0 |a Impact of Survivin Acetylation on its Biological Function  |h [electronic resource] /  |c by David Dannheisig. 
264 1 |a Wiesbaden :  |b Springer Fachmedien Wiesbaden :  |b Imprint: Springer Spektrum,  |c 2017. 
300 |a XXIII, 104 p. 41 illus., 10 illus. in color.  |b online resource. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
347 |a text file  |b PDF  |2 rda 
490 1 |a BestMasters 
505 0 |a Apoptosis – 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. 
520 |a In 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 used to 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. Contents Apoptosis – 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 Target Groups Lecturers, students and researchers in the biological-medical sector Practitioners in the fields of molecular biology, cell biology, fluorescence microscopy, medical biology, protein interaction studies The Author David 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. 
650 0 |a Medicine. 
650 0 |a Cancer research. 
650 0 |a Biomedical engineering. 
650 0 |a Cell biology. 
650 1 4 |a Biomedicine. 
650 2 4 |a Cancer Research. 
650 2 4 |a Biomedical Engineering/Biotechnology. 
650 2 4 |a Cell Biology. 
710 2 |a SpringerLink (Online service) 
773 0 |t Springer eBooks 
776 0 8 |i Printed edition:  |z 9783658186227 
830 0 |a BestMasters 
856 4 0 |u http://dx.doi.org/10.1007/978-3-658-18623-4  |z Full Text via HEAL-Link 
912 |a ZDB-2-SBL 
950 |a Biomedical and Life Sciences (Springer-11642)