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You searched for subject:(Glioblastom). Showing records 1 – 9 of 9 total matches.

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Ruhr Universität Bochum

1. Wolfkühler, Dörte. Einfluss von Dexamethason auf ein In-vitro-Gliom-Modell.

Degree: 2009, Ruhr Universität Bochum

 Dexamethason ist ein häufig eingesetztes Medikament zur Behandlung zerebraler Ödeme bei Patienten mit Glioblastom. Diese Dissertation untersucht den Einfluss von Dexamethason auf die interzelluläre-Kopplung, die… (more)

Subjects/Keywords: Astrozyt; Connexin; Glioblastom; Mikroglia; Steroide

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wolfkühler, D. (2009). Einfluss von Dexamethason auf ein In-vitro-Gliom-Modell. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-26795

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wolfkühler, Dörte. “Einfluss von Dexamethason auf ein In-vitro-Gliom-Modell.” 2009. Thesis, Ruhr Universität Bochum. Accessed January 24, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-26795.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wolfkühler, Dörte. “Einfluss von Dexamethason auf ein In-vitro-Gliom-Modell.” 2009. Web. 24 Jan 2020.

Vancouver:

Wolfkühler D. Einfluss von Dexamethason auf ein In-vitro-Gliom-Modell. [Internet] [Thesis]. Ruhr Universität Bochum; 2009. [cited 2020 Jan 24]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-26795.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wolfkühler D. Einfluss von Dexamethason auf ein In-vitro-Gliom-Modell. [Thesis]. Ruhr Universität Bochum; 2009. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-26795

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Ruhr Universität Bochum

2. Steenken, Sabine. Nabelschnurblutzellen als therapeutische Vehikel im Ratten-C6-Gliommodell.

Degree: 2011, Ruhr Universität Bochum

 Ein experimenteller Behandlungsansatz zur Therapie von Gliomen könnte in der Nutzbarkeit der Migration von Stammzellen zu diesen Tumoren liegen. In dieser Arbeit wurde die Fähigkeit… (more)

Subjects/Keywords: Migration; Glioblastom; Hämatopoese; Zentralnervensystem; Tiermodell

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APA (6th Edition):

Steenken, S. (2011). Nabelschnurblutzellen als therapeutische Vehikel im Ratten-C6-Gliommodell. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-32154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Steenken, Sabine. “Nabelschnurblutzellen als therapeutische Vehikel im Ratten-C6-Gliommodell.” 2011. Thesis, Ruhr Universität Bochum. Accessed January 24, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-32154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Steenken, Sabine. “Nabelschnurblutzellen als therapeutische Vehikel im Ratten-C6-Gliommodell.” 2011. Web. 24 Jan 2020.

Vancouver:

Steenken S. Nabelschnurblutzellen als therapeutische Vehikel im Ratten-C6-Gliommodell. [Internet] [Thesis]. Ruhr Universität Bochum; 2011. [cited 2020 Jan 24]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-32154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Steenken S. Nabelschnurblutzellen als therapeutische Vehikel im Ratten-C6-Gliommodell. [Thesis]. Ruhr Universität Bochum; 2011. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-32154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Ruhr Universität Bochum

3. Brösicke, Nicole. Tenascin-C-aktivierte Signalwege bei der Migration humaner Gliomazellen unter Berücksichtigung kleiner GTP-bindender Proteine.

Degree: 2010, Ruhr Universität Bochum

 Tumore des Typs Glioblastoma multiforme sind charakterisiert durch infiltratives Wachstum, ausgeprägtes Migrationsverhalten, sowie durch die Expression des extrazellulären Matrix-Proteins Tenascin-C (TN-C). Durch seinen multimodularen Aufbau… (more)

Subjects/Keywords: Krebs (Medizin); Glioblastom; Zellmigration; Glykoproteine; Guanosintriphosphatasen

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APA (6th Edition):

Brösicke, N. (2010). Tenascin-C-aktivierte Signalwege bei der Migration humaner Gliomazellen unter Berücksichtigung kleiner GTP-bindender Proteine. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-28483

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Brösicke, Nicole. “Tenascin-C-aktivierte Signalwege bei der Migration humaner Gliomazellen unter Berücksichtigung kleiner GTP-bindender Proteine.” 2010. Thesis, Ruhr Universität Bochum. Accessed January 24, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-28483.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Brösicke, Nicole. “Tenascin-C-aktivierte Signalwege bei der Migration humaner Gliomazellen unter Berücksichtigung kleiner GTP-bindender Proteine.” 2010. Web. 24 Jan 2020.

Vancouver:

Brösicke N. Tenascin-C-aktivierte Signalwege bei der Migration humaner Gliomazellen unter Berücksichtigung kleiner GTP-bindender Proteine. [Internet] [Thesis]. Ruhr Universität Bochum; 2010. [cited 2020 Jan 24]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-28483.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Brösicke N. Tenascin-C-aktivierte Signalwege bei der Migration humaner Gliomazellen unter Berücksichtigung kleiner GTP-bindender Proteine. [Thesis]. Ruhr Universität Bochum; 2010. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-28483

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Johannes Gutenberg Universität Mainz

4. Stahler, Christina. Wechselwirkungen von Schwerionenstrahlung, Migration und EGFR-Signalwegen in Glioblastomzelllinien.

Degree: 2013, Johannes Gutenberg Universität Mainz

Die Bildung von lokalen Rezidiven wird bei Glioblastomen vor allem durch das stark infiltrierende Wachstum gefördert. Die Rolle der angewendeten Therapieverfahren bei der Induktion der… (more)

Subjects/Keywords: Glioblastom, Zellmigration, Schwerionen, Bestrahlung, EGFR; glioma, migration, carbon ion, irradiation, egfr; Life sciences

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Stahler, C. (2013). Wechselwirkungen von Schwerionenstrahlung, Migration und EGFR-Signalwegen in Glioblastomzelllinien. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3447/

Chicago Manual of Style (16th Edition):

Stahler, Christina. “Wechselwirkungen von Schwerionenstrahlung, Migration und EGFR-Signalwegen in Glioblastomzelllinien.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed January 24, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2013/3447/.

MLA Handbook (7th Edition):

Stahler, Christina. “Wechselwirkungen von Schwerionenstrahlung, Migration und EGFR-Signalwegen in Glioblastomzelllinien.” 2013. Web. 24 Jan 2020.

Vancouver:

Stahler C. Wechselwirkungen von Schwerionenstrahlung, Migration und EGFR-Signalwegen in Glioblastomzelllinien. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2020 Jan 24]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3447/.

Council of Science Editors:

Stahler C. Wechselwirkungen von Schwerionenstrahlung, Migration und EGFR-Signalwegen in Glioblastomzelllinien. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3447/


Johannes Gutenberg Universität Mainz

5. Peters, Tanja. Development and in vitro testing of liposomal gadolinium-formulations for neutron capture therapy of glioblastoma multiforme.

Degree: 2013, Johannes Gutenberg Universität Mainz

For the improvement of current neutron capture therapy, several liposomal formulations of neutron capture agent gadolinium were developed and tested in a glioma cell model.… (more)

Subjects/Keywords: Liposomen; Neutroneneinfangtherapie; Glioblastom; liposomes; neutron capture therapy; glioblastoma; Natural sciences and mathematics

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APA (6th Edition):

Peters, T. (2013). Development and in vitro testing of liposomal gadolinium-formulations for neutron capture therapy of glioblastoma multiforme. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3559/

Chicago Manual of Style (16th Edition):

Peters, Tanja. “Development and in vitro testing of liposomal gadolinium-formulations for neutron capture therapy of glioblastoma multiforme.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed January 24, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2013/3559/.

MLA Handbook (7th Edition):

Peters, Tanja. “Development and in vitro testing of liposomal gadolinium-formulations for neutron capture therapy of glioblastoma multiforme.” 2013. Web. 24 Jan 2020.

Vancouver:

Peters T. Development and in vitro testing of liposomal gadolinium-formulations for neutron capture therapy of glioblastoma multiforme. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2020 Jan 24]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3559/.

Council of Science Editors:

Peters T. Development and in vitro testing of liposomal gadolinium-formulations for neutron capture therapy of glioblastoma multiforme. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3559/

6. Smrdel, Uroš. Imunohisotkemični in geentski označevalci pri glioblastomu multiforme.

Degree: 2016, Univerza v Mariboru

Glioblastom (GBM) je najpogostejši primarni možganski tumor. Njegova incidenca v Sloveniji znaša 2,9 bolnika na 100.000 prebivalcev. Na Onkološkem inštitutu Ljubljana smo v letih od… (more)

Subjects/Keywords: glioblastom; dolgotrajno preživetje; MGMT; IDH1; kortikosteroidi; RPA; glioblastoma; long term survival; MGMT; IDH1; corticosteroids; RPA

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Smrdel, U. (2016). Imunohisotkemični in geentski označevalci pri glioblastomu multiforme. (Doctoral Dissertation). Univerza v Mariboru. Retrieved from https://dk.um.si/IzpisGradiva.php?id=55353 ; https://dk.um.si/Dokument.php?id=88012&dn= ; https://plus.si.cobiss.net/opac7/bib/284783104?lang=sl

Chicago Manual of Style (16th Edition):

Smrdel, Uroš. “Imunohisotkemični in geentski označevalci pri glioblastomu multiforme.” 2016. Doctoral Dissertation, Univerza v Mariboru. Accessed January 24, 2020. https://dk.um.si/IzpisGradiva.php?id=55353 ; https://dk.um.si/Dokument.php?id=88012&dn= ; https://plus.si.cobiss.net/opac7/bib/284783104?lang=sl.

MLA Handbook (7th Edition):

Smrdel, Uroš. “Imunohisotkemični in geentski označevalci pri glioblastomu multiforme.” 2016. Web. 24 Jan 2020.

Vancouver:

Smrdel U. Imunohisotkemični in geentski označevalci pri glioblastomu multiforme. [Internet] [Doctoral dissertation]. Univerza v Mariboru; 2016. [cited 2020 Jan 24]. Available from: https://dk.um.si/IzpisGradiva.php?id=55353 ; https://dk.um.si/Dokument.php?id=88012&dn= ; https://plus.si.cobiss.net/opac7/bib/284783104?lang=sl.

Council of Science Editors:

Smrdel U. Imunohisotkemični in geentski označevalci pri glioblastomu multiforme. [Doctoral Dissertation]. Univerza v Mariboru; 2016. Available from: https://dk.um.si/IzpisGradiva.php?id=55353 ; https://dk.um.si/Dokument.php?id=88012&dn= ; https://plus.si.cobiss.net/opac7/bib/284783104?lang=sl


Johannes Gutenberg Universität Mainz

7. Quiros Barrantes, Steve. Mechanistic study of cell death induction by O 6-methylating agents, focusing on the role of homologous recombination as a molecular target for sensitization of tumor cells to chemotherapeutic alkylating agents.

Degree: 2012, Johannes Gutenberg Universität Mainz

 Chemotherapeutic SN1‑methylating agents are important anticancer drugs. They induce several covalent modifications in the DNA, from which O6‑methylguanine (O6MeG) is the main toxic lesion. In… (more)

Subjects/Keywords: O6‑Methylguanin, Temozolomid, Chemotherapeutika, Glioblastom, Apoptose; O6‑Methylguanine, Temozolomide, Chemotherapeutic, Glioblastoma, Apoptosis; Natural sciences and mathematics

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Quiros Barrantes, S. (2012). Mechanistic study of cell death induction by O 6-methylating agents, focusing on the role of homologous recombination as a molecular target for sensitization of tumor cells to chemotherapeutic alkylating agents. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2012/3165/

Chicago Manual of Style (16th Edition):

Quiros Barrantes, Steve. “Mechanistic study of cell death induction by O 6-methylating agents, focusing on the role of homologous recombination as a molecular target for sensitization of tumor cells to chemotherapeutic alkylating agents.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed January 24, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2012/3165/.

MLA Handbook (7th Edition):

Quiros Barrantes, Steve. “Mechanistic study of cell death induction by O 6-methylating agents, focusing on the role of homologous recombination as a molecular target for sensitization of tumor cells to chemotherapeutic alkylating agents.” 2012. Web. 24 Jan 2020.

Vancouver:

Quiros Barrantes S. Mechanistic study of cell death induction by O 6-methylating agents, focusing on the role of homologous recombination as a molecular target for sensitization of tumor cells to chemotherapeutic alkylating agents. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2020 Jan 24]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3165/.

Council of Science Editors:

Quiros Barrantes S. Mechanistic study of cell death induction by O 6-methylating agents, focusing on the role of homologous recombination as a molecular target for sensitization of tumor cells to chemotherapeutic alkylating agents. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3165/


University of Vienna

8. van Schoonhoven, Sushilla Tamara. Characterization of fibroblast growth factor receptor 4 as contributor to oncogenesis in Glioblastoma multiforme.

Degree: 2018, University of Vienna

Mit 45-55% aller malignen Gliomen ist das Glioblastom (GBM) der häufigste Tumor des zentralen Nervensystems (ZNS) in Erwachsenen. Das GBM ist der aggressivste primäre Gehirntumor… (more)

Subjects/Keywords: 42.13 Molekularbiologie; 42.20 Genetik; Gliomen / Glioblastom / GBM / FGFR4 / Gly388Arg / Klonierung / Migration / 3D-Wachstum / Klonformation; Gliomas / Glioblastoma / GBM / FGFR4 / Gly388Arg / Cloning / Migration / 3D-Growth / Colony formation

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

van Schoonhoven, S. T. (2018). Characterization of fibroblast growth factor receptor 4 as contributor to oncogenesis in Glioblastoma multiforme. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/50626/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

van Schoonhoven, Sushilla Tamara. “Characterization of fibroblast growth factor receptor 4 as contributor to oncogenesis in Glioblastoma multiforme.” 2018. Thesis, University of Vienna. Accessed January 24, 2020. http://othes.univie.ac.at/50626/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

van Schoonhoven, Sushilla Tamara. “Characterization of fibroblast growth factor receptor 4 as contributor to oncogenesis in Glioblastoma multiforme.” 2018. Web. 24 Jan 2020.

Vancouver:

van Schoonhoven ST. Characterization of fibroblast growth factor receptor 4 as contributor to oncogenesis in Glioblastoma multiforme. [Internet] [Thesis]. University of Vienna; 2018. [cited 2020 Jan 24]. Available from: http://othes.univie.ac.at/50626/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

van Schoonhoven ST. Characterization of fibroblast growth factor receptor 4 as contributor to oncogenesis in Glioblastoma multiforme. [Thesis]. University of Vienna; 2018. Available from: http://othes.univie.ac.at/50626/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

9. Podolski-Renić Ana. The establishing of resistant cancer cell lines as a model for testing of new chemotherapeutics: molecular characterization of resistance developed after continuous treatment with paclitaxel.

Degree: PhD, Biology, 2013, University of Belgrade

 Multi-drug resistance (MDR) is a major obstacle to successful cancer treatment. The efficacy of paclitaxel (PTX) is often limited by appearance of drug resistance. The… (more)

Subjects/Keywords: Multi-drug resistance (MDR); paclitaxel (PTX); colon cancer; glioblastoma; P-glycoprotein; anti-cancer agents; Višestruka (engl. „multi-drug“) rezistencija (MDR); paklitaksel (PTX); karcinom debelog creva; glioblastom; P-glikoprotein; anti-kancer agensi

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APA (6th Edition):

Ana, P. (2013). The establishing of resistant cancer cell lines as a model for testing of new chemotherapeutics: molecular characterization of resistance developed after continuous treatment with paclitaxel. (Doctoral Dissertation). University of Belgrade. Retrieved from http://dx.doi.org/10.2298/BG20130704PODOLSKIRENIC ; http://eteze.bg.ac.rs/application/showtheses?thesesId=804 ; https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=1024577970

Chicago Manual of Style (16th Edition):

Ana, Podolski-Renić. “The establishing of resistant cancer cell lines as a model for testing of new chemotherapeutics: molecular characterization of resistance developed after continuous treatment with paclitaxel.” 2013. Doctoral Dissertation, University of Belgrade. Accessed January 24, 2020. http://dx.doi.org/10.2298/BG20130704PODOLSKIRENIC ; http://eteze.bg.ac.rs/application/showtheses?thesesId=804 ; https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=1024577970.

MLA Handbook (7th Edition):

Ana, Podolski-Renić. “The establishing of resistant cancer cell lines as a model for testing of new chemotherapeutics: molecular characterization of resistance developed after continuous treatment with paclitaxel.” 2013. Web. 24 Jan 2020.

Vancouver:

Ana P. The establishing of resistant cancer cell lines as a model for testing of new chemotherapeutics: molecular characterization of resistance developed after continuous treatment with paclitaxel. [Internet] [Doctoral dissertation]. University of Belgrade; 2013. [cited 2020 Jan 24]. Available from: http://dx.doi.org/10.2298/BG20130704PODOLSKIRENIC ; http://eteze.bg.ac.rs/application/showtheses?thesesId=804 ; https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=1024577970.

Council of Science Editors:

Ana P. The establishing of resistant cancer cell lines as a model for testing of new chemotherapeutics: molecular characterization of resistance developed after continuous treatment with paclitaxel. [Doctoral Dissertation]. University of Belgrade; 2013. Available from: http://dx.doi.org/10.2298/BG20130704PODOLSKIRENIC ; http://eteze.bg.ac.rs/application/showtheses?thesesId=804 ; https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=1024577970

.