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You searched for subject:(Anti cancer agents). Showing records 1 – 30 of 49 total matches.

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Baylor University

1. Jones, Lindsay M. Design and synthesis of functionalized small-molecule inhibitors of cathepsins L and K.

Degree: Chemistry and Biochemistry., 2012, Baylor University

 Inhibition of a class of cysteine proteases known as the cathepsins has received increasing attention in recent years, since these enzymes play key roles in… (more)

Subjects/Keywords: Anti-cancer agents.

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APA (6th Edition):

Jones, L. M. (2012). Design and synthesis of functionalized small-molecule inhibitors of cathepsins L and K. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/8438

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):

Jones, Lindsay M. “Design and synthesis of functionalized small-molecule inhibitors of cathepsins L and K. ” 2012. Thesis, Baylor University. Accessed November 20, 2019. http://hdl.handle.net/2104/8438.

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

MLA Handbook (7th Edition):

Jones, Lindsay M. “Design and synthesis of functionalized small-molecule inhibitors of cathepsins L and K. ” 2012. Web. 20 Nov 2019.

Vancouver:

Jones LM. Design and synthesis of functionalized small-molecule inhibitors of cathepsins L and K. [Internet] [Thesis]. Baylor University; 2012. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/2104/8438.

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

Council of Science Editors:

Jones LM. Design and synthesis of functionalized small-molecule inhibitors of cathepsins L and K. [Thesis]. Baylor University; 2012. Available from: http://hdl.handle.net/2104/8438

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


University of New South Wales

2. Wang, Haiqiang. Binding of Pixantrone with DNA Bulge Sequences.

Degree: Physical, Environmental & Mathematical Sciences Canberra, 2011, University of New South Wales

 The binding of the aza-anthracenedione anti-neoplastic drug pixantrone (6,9-bis[92- aminoethyl)amino]benzo[g]isoquinoline-5,10-dione fumarate) to the tridecanucleotide d(CCGAGAATTCCGG)2 that contains a single bulged adenine on each strand and… (more)

Subjects/Keywords: Anti-cancer agents; Pixantrone; Binding sites

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APA (6th Edition):

Wang, H. (2011). Binding of Pixantrone with DNA Bulge Sequences. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52058 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10728/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Wang, Haiqiang. “Binding of Pixantrone with DNA Bulge Sequences.” 2011. Masters Thesis, University of New South Wales. Accessed November 20, 2019. http://handle.unsw.edu.au/1959.4/52058 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10728/SOURCE01?view=true.

MLA Handbook (7th Edition):

Wang, Haiqiang. “Binding of Pixantrone with DNA Bulge Sequences.” 2011. Web. 20 Nov 2019.

Vancouver:

Wang H. Binding of Pixantrone with DNA Bulge Sequences. [Internet] [Masters thesis]. University of New South Wales; 2011. [cited 2019 Nov 20]. Available from: http://handle.unsw.edu.au/1959.4/52058 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10728/SOURCE01?view=true.

Council of Science Editors:

Wang H. Binding of Pixantrone with DNA Bulge Sequences. [Masters Thesis]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/52058 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10728/SOURCE01?view=true


University of Newcastle

3. Hizartzidis, Lacey. The development of flow chemistry methodologies for the synthesis of potential anti-cancer agents.

Degree: PhD, 2015, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

The discovery and development of more specific and targeted small molecule anti-cancer drugs over the last decade, has… (more)

Subjects/Keywords: flow chemistry; chemistry; anti-cancer agents; norcantharidin

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APA (6th Edition):

Hizartzidis, L. (2015). The development of flow chemistry methodologies for the synthesis of potential anti-cancer agents. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1310026

Chicago Manual of Style (16th Edition):

Hizartzidis, Lacey. “The development of flow chemistry methodologies for the synthesis of potential anti-cancer agents.” 2015. Doctoral Dissertation, University of Newcastle. Accessed November 20, 2019. http://hdl.handle.net/1959.13/1310026.

MLA Handbook (7th Edition):

Hizartzidis, Lacey. “The development of flow chemistry methodologies for the synthesis of potential anti-cancer agents.” 2015. Web. 20 Nov 2019.

Vancouver:

Hizartzidis L. The development of flow chemistry methodologies for the synthesis of potential anti-cancer agents. [Internet] [Doctoral dissertation]. University of Newcastle; 2015. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/1959.13/1310026.

Council of Science Editors:

Hizartzidis L. The development of flow chemistry methodologies for the synthesis of potential anti-cancer agents. [Doctoral Dissertation]. University of Newcastle; 2015. Available from: http://hdl.handle.net/1959.13/1310026


University of KwaZulu-Natal

4. Mbatha, Sbongile Happyness. Identification of anti-cancer agents using integrated computational tools.

Degree: 2015, University of KwaZulu-Natal

Cancer is a heterogeneous disease that is responsible for various molecular changes and pathological entities that play vital roles in its response to treatment, survival,… (more)

Subjects/Keywords: Antineoplastic agents - health - computer network - resources.; Anti-cancer agents.; Cancer.; Cathepsin B.; Hsp90.; Cancer drug design.

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APA (6th Edition):

Mbatha, S. H. (2015). Identification of anti-cancer agents using integrated computational tools. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/14911

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):

Mbatha, Sbongile Happyness. “Identification of anti-cancer agents using integrated computational tools.” 2015. Thesis, University of KwaZulu-Natal. Accessed November 20, 2019. http://hdl.handle.net/10413/14911.

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

MLA Handbook (7th Edition):

Mbatha, Sbongile Happyness. “Identification of anti-cancer agents using integrated computational tools.” 2015. Web. 20 Nov 2019.

Vancouver:

Mbatha SH. Identification of anti-cancer agents using integrated computational tools. [Internet] [Thesis]. University of KwaZulu-Natal; 2015. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/10413/14911.

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

Council of Science Editors:

Mbatha SH. Identification of anti-cancer agents using integrated computational tools. [Thesis]. University of KwaZulu-Natal; 2015. Available from: http://hdl.handle.net/10413/14911

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


University of Aberdeen

5. Saunders, Fiona R. An investigation of non-steroidal anti-inflammatory drug mediated modulation of the polyamine pathway in an in vitro model of colorectal cancer.

Degree: 2008, University of Aberdeen

 Our hypothesis is that the polyamine biosynthetic pathway, a pathway essential in many cellular functions, is modulated by NSAIDs and that this is, at least… (more)

Subjects/Keywords: 615.1; Colon (Anatomy) : Anti-Inflammatory Agents, Non-Steroidal : Cancer research

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APA (6th Edition):

Saunders, F. R. (2008). An investigation of non-steroidal anti-inflammatory drug mediated modulation of the polyamine pathway in an in vitro model of colorectal cancer. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=53328 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509123

Chicago Manual of Style (16th Edition):

Saunders, Fiona R. “An investigation of non-steroidal anti-inflammatory drug mediated modulation of the polyamine pathway in an in vitro model of colorectal cancer.” 2008. Doctoral Dissertation, University of Aberdeen. Accessed November 20, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=53328 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509123.

MLA Handbook (7th Edition):

Saunders, Fiona R. “An investigation of non-steroidal anti-inflammatory drug mediated modulation of the polyamine pathway in an in vitro model of colorectal cancer.” 2008. Web. 20 Nov 2019.

Vancouver:

Saunders FR. An investigation of non-steroidal anti-inflammatory drug mediated modulation of the polyamine pathway in an in vitro model of colorectal cancer. [Internet] [Doctoral dissertation]. University of Aberdeen; 2008. [cited 2019 Nov 20]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=53328 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509123.

Council of Science Editors:

Saunders FR. An investigation of non-steroidal anti-inflammatory drug mediated modulation of the polyamine pathway in an in vitro model of colorectal cancer. [Doctoral Dissertation]. University of Aberdeen; 2008. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=53328 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509123


Brunel University

6. Sadiq, Samina. Studies of some fused-ring heterocycles and 2,6-Diarylpyridine derivatives.

Degree: 1999, Brunel University

 This work reported is divided into two parts: the first part deals with quinoxaline derivatives and includes the preparation and characterisation of novel linear tricyclic… (more)

Subjects/Keywords: 547; Quinoxaline; Anti-cancer agents

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APA (6th Edition):

Sadiq, S. (1999). Studies of some fused-ring heterocycles and 2,6-Diarylpyridine derivatives. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/7281 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310079

Chicago Manual of Style (16th Edition):

Sadiq, Samina. “Studies of some fused-ring heterocycles and 2,6-Diarylpyridine derivatives.” 1999. Doctoral Dissertation, Brunel University. Accessed November 20, 2019. http://bura.brunel.ac.uk/handle/2438/7281 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310079.

MLA Handbook (7th Edition):

Sadiq, Samina. “Studies of some fused-ring heterocycles and 2,6-Diarylpyridine derivatives.” 1999. Web. 20 Nov 2019.

Vancouver:

Sadiq S. Studies of some fused-ring heterocycles and 2,6-Diarylpyridine derivatives. [Internet] [Doctoral dissertation]. Brunel University; 1999. [cited 2019 Nov 20]. Available from: http://bura.brunel.ac.uk/handle/2438/7281 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310079.

Council of Science Editors:

Sadiq S. Studies of some fused-ring heterocycles and 2,6-Diarylpyridine derivatives. [Doctoral Dissertation]. Brunel University; 1999. Available from: http://bura.brunel.ac.uk/handle/2438/7281 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310079


Georgia State University

7. Draganov, Alexander B. Novel Rhein Analogues as Potential Anicancer Agents and a Novel Metal Free Synthesis of 6H-ISOINDOLO[2,1-A]INDOL-6-ONE.

Degree: MS, Chemistry, 2011, Georgia State University

  The first section of this work describes the synthesis of a library of novel rhein analogues that are potential anticancer agents. The design of… (more)

Subjects/Keywords: Anti- cancer agents; Rhein; DNA intercalators; Alkylation; IC50; Beckmann rearrangement

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APA (6th Edition):

Draganov, A. B. (2011). Novel Rhein Analogues as Potential Anicancer Agents and a Novel Metal Free Synthesis of 6H-ISOINDOLO[2,1-A]INDOL-6-ONE. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/40

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):

Draganov, Alexander B. “Novel Rhein Analogues as Potential Anicancer Agents and a Novel Metal Free Synthesis of 6H-ISOINDOLO[2,1-A]INDOL-6-ONE.” 2011. Thesis, Georgia State University. Accessed November 20, 2019. https://scholarworks.gsu.edu/chemistry_theses/40.

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

MLA Handbook (7th Edition):

Draganov, Alexander B. “Novel Rhein Analogues as Potential Anicancer Agents and a Novel Metal Free Synthesis of 6H-ISOINDOLO[2,1-A]INDOL-6-ONE.” 2011. Web. 20 Nov 2019.

Vancouver:

Draganov AB. Novel Rhein Analogues as Potential Anicancer Agents and a Novel Metal Free Synthesis of 6H-ISOINDOLO[2,1-A]INDOL-6-ONE. [Internet] [Thesis]. Georgia State University; 2011. [cited 2019 Nov 20]. Available from: https://scholarworks.gsu.edu/chemistry_theses/40.

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

Council of Science Editors:

Draganov AB. Novel Rhein Analogues as Potential Anicancer Agents and a Novel Metal Free Synthesis of 6H-ISOINDOLO[2,1-A]INDOL-6-ONE. [Thesis]. Georgia State University; 2011. Available from: https://scholarworks.gsu.edu/chemistry_theses/40

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


Dublin City University

8. Mooney, Aine. Synthesis, Characterisation and Biological Evaluation of Novel N-Ferrocenyl Naphthoyl Amino Acid and Dipeptide Derivatives as Potential Anti-Cancer Agents.

Degree: School of Chemical Sciences, 2010, Dublin City University

Subjects/Keywords: Ferrocene; dipeptides anti-cancer agents

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APA (6th Edition):

Mooney, A. (2010). Synthesis, Characterisation and Biological Evaluation of Novel N-Ferrocenyl Naphthoyl Amino Acid and Dipeptide Derivatives as Potential Anti-Cancer Agents. (Thesis). Dublin City University. Retrieved from http://doras.dcu.ie/15713/

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):

Mooney, Aine. “Synthesis, Characterisation and Biological Evaluation of Novel N-Ferrocenyl Naphthoyl Amino Acid and Dipeptide Derivatives as Potential Anti-Cancer Agents.” 2010. Thesis, Dublin City University. Accessed November 20, 2019. http://doras.dcu.ie/15713/.

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

MLA Handbook (7th Edition):

Mooney, Aine. “Synthesis, Characterisation and Biological Evaluation of Novel N-Ferrocenyl Naphthoyl Amino Acid and Dipeptide Derivatives as Potential Anti-Cancer Agents.” 2010. Web. 20 Nov 2019.

Vancouver:

Mooney A. Synthesis, Characterisation and Biological Evaluation of Novel N-Ferrocenyl Naphthoyl Amino Acid and Dipeptide Derivatives as Potential Anti-Cancer Agents. [Internet] [Thesis]. Dublin City University; 2010. [cited 2019 Nov 20]. Available from: http://doras.dcu.ie/15713/.

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

Council of Science Editors:

Mooney A. Synthesis, Characterisation and Biological Evaluation of Novel N-Ferrocenyl Naphthoyl Amino Acid and Dipeptide Derivatives as Potential Anti-Cancer Agents. [Thesis]. Dublin City University; 2010. Available from: http://doras.dcu.ie/15713/

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


University of Sydney

9. Koolaji, Nooshin. Development of novel anti-cancer agents derived from omega-3 fatty acid metabolites .

Degree: 2017, University of Sydney

 Experimental and dietary studies have shown that omega-3 polyunsaturated fatty acids (ω-3 PUFAs) such as docosahexaenoic acid (DHA; C22:6 ù-3) and eicosapentaenoic acid (EPA; C20:5… (more)

Subjects/Keywords: Anti-cancer agents; Synthetic epoxy fatty acids; PUFA epoxide; Epoxide isostere

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APA (6th Edition):

Koolaji, N. (2017). Development of novel anti-cancer agents derived from omega-3 fatty acid metabolites . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17615

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):

Koolaji, Nooshin. “Development of novel anti-cancer agents derived from omega-3 fatty acid metabolites .” 2017. Thesis, University of Sydney. Accessed November 20, 2019. http://hdl.handle.net/2123/17615.

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

MLA Handbook (7th Edition):

Koolaji, Nooshin. “Development of novel anti-cancer agents derived from omega-3 fatty acid metabolites .” 2017. Web. 20 Nov 2019.

Vancouver:

Koolaji N. Development of novel anti-cancer agents derived from omega-3 fatty acid metabolites . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/2123/17615.

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

Council of Science Editors:

Koolaji N. Development of novel anti-cancer agents derived from omega-3 fatty acid metabolites . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17615

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


University of Wollongong

10. Zhang, Jichao. Development of novel sialyltransferase transition-state analogue inhibitors as anti-cancer agents.

Degree: MS- Research, 2013, University of Wollongong

Cancer is a leading cause of disease and death around the world, and is thought to be the largest challenge to human beings in… (more)

Subjects/Keywords: sialyltransferase; transition-state analogue; cancer; anti-metastasis agents

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APA (6th Edition):

Zhang, J. (2013). Development of novel sialyltransferase transition-state analogue inhibitors as anti-cancer agents. (Masters Thesis). University of Wollongong. Retrieved from 030499 Medicinal and Biomolecular Chemistry not elsewhere classified ; https://ro.uow.edu.au/theses/3865

Chicago Manual of Style (16th Edition):

Zhang, Jichao. “Development of novel sialyltransferase transition-state analogue inhibitors as anti-cancer agents.” 2013. Masters Thesis, University of Wollongong. Accessed November 20, 2019. 030499 Medicinal and Biomolecular Chemistry not elsewhere classified ; https://ro.uow.edu.au/theses/3865.

MLA Handbook (7th Edition):

Zhang, Jichao. “Development of novel sialyltransferase transition-state analogue inhibitors as anti-cancer agents.” 2013. Web. 20 Nov 2019.

Vancouver:

Zhang J. Development of novel sialyltransferase transition-state analogue inhibitors as anti-cancer agents. [Internet] [Masters thesis]. University of Wollongong; 2013. [cited 2019 Nov 20]. Available from: 030499 Medicinal and Biomolecular Chemistry not elsewhere classified ; https://ro.uow.edu.au/theses/3865.

Council of Science Editors:

Zhang J. Development of novel sialyltransferase transition-state analogue inhibitors as anti-cancer agents. [Masters Thesis]. University of Wollongong; 2013. Available from: 030499 Medicinal and Biomolecular Chemistry not elsewhere classified ; https://ro.uow.edu.au/theses/3865


University of Glasgow

11. Narquizian, Robert. Synthetic studies on the pederin family of antitumour agents : syntheses of pederin, mycalamide B and analogues.

Degree: PhD, 2000, University of Glasgow

 A general modular approach to members of the pederin family of antitumour agents, exemplified by syntheses of pederin (1.1), mycalamide B (1.5) and analogues (17-epi-1.5,… (more)

Subjects/Keywords: 547; Anti-cancer agents

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APA (6th Edition):

Narquizian, R. (2000). Synthetic studies on the pederin family of antitumour agents : syntheses of pederin, mycalamide B and analogues. (Doctoral Dissertation). University of Glasgow. Retrieved from http://theses.gla.ac.uk/71252/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274781

Chicago Manual of Style (16th Edition):

Narquizian, Robert. “Synthetic studies on the pederin family of antitumour agents : syntheses of pederin, mycalamide B and analogues.” 2000. Doctoral Dissertation, University of Glasgow. Accessed November 20, 2019. http://theses.gla.ac.uk/71252/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274781.

MLA Handbook (7th Edition):

Narquizian, Robert. “Synthetic studies on the pederin family of antitumour agents : syntheses of pederin, mycalamide B and analogues.” 2000. Web. 20 Nov 2019.

Vancouver:

Narquizian R. Synthetic studies on the pederin family of antitumour agents : syntheses of pederin, mycalamide B and analogues. [Internet] [Doctoral dissertation]. University of Glasgow; 2000. [cited 2019 Nov 20]. Available from: http://theses.gla.ac.uk/71252/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274781.

Council of Science Editors:

Narquizian R. Synthetic studies on the pederin family of antitumour agents : syntheses of pederin, mycalamide B and analogues. [Doctoral Dissertation]. University of Glasgow; 2000. Available from: http://theses.gla.ac.uk/71252/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274781


University of Bath

12. Qarawi, Mousa Adel. Studies on the feasibility of targeting cytotoxics to melanoma.

Degree: PhD, 1997, University of Bath

Subjects/Keywords: 610; Anti-cancer agents

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APA (6th Edition):

Qarawi, M. A. (1997). Studies on the feasibility of targeting cytotoxics to melanoma. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/studies-on-the-feasibility-of-targeting-cytotoxics-to-melanoma(a11511ca-65c9-48d0-a37e-bded53f95673).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362285

Chicago Manual of Style (16th Edition):

Qarawi, Mousa Adel. “Studies on the feasibility of targeting cytotoxics to melanoma.” 1997. Doctoral Dissertation, University of Bath. Accessed November 20, 2019. https://researchportal.bath.ac.uk/en/studentthesis/studies-on-the-feasibility-of-targeting-cytotoxics-to-melanoma(a11511ca-65c9-48d0-a37e-bded53f95673).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362285.

MLA Handbook (7th Edition):

Qarawi, Mousa Adel. “Studies on the feasibility of targeting cytotoxics to melanoma.” 1997. Web. 20 Nov 2019.

Vancouver:

Qarawi MA. Studies on the feasibility of targeting cytotoxics to melanoma. [Internet] [Doctoral dissertation]. University of Bath; 1997. [cited 2019 Nov 20]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/studies-on-the-feasibility-of-targeting-cytotoxics-to-melanoma(a11511ca-65c9-48d0-a37e-bded53f95673).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362285.

Council of Science Editors:

Qarawi MA. Studies on the feasibility of targeting cytotoxics to melanoma. [Doctoral Dissertation]. University of Bath; 1997. Available from: https://researchportal.bath.ac.uk/en/studentthesis/studies-on-the-feasibility-of-targeting-cytotoxics-to-melanoma(a11511ca-65c9-48d0-a37e-bded53f95673).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362285


University of Southern California

13. Millard, Melissa. Discovery of novel small molecules targeting cancer cell metabolism.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Southern California

 Advanced age is a risk-factor common to most cancers. In coming years, a marked increase in the population aged 65 and over will compound the… (more)

Subjects/Keywords: small molecule anti-cancer agents; pancreatic cancer; breast cancer; mitochondria; cancer cell metabolism; PKM2; pyruvate kinase M2; oncology; cancer therapy

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APA (6th Edition):

Millard, M. (2013). Discovery of novel small molecules targeting cancer cell metabolism. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2027

Chicago Manual of Style (16th Edition):

Millard, Melissa. “Discovery of novel small molecules targeting cancer cell metabolism.” 2013. Doctoral Dissertation, University of Southern California. Accessed November 20, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2027.

MLA Handbook (7th Edition):

Millard, Melissa. “Discovery of novel small molecules targeting cancer cell metabolism.” 2013. Web. 20 Nov 2019.

Vancouver:

Millard M. Discovery of novel small molecules targeting cancer cell metabolism. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Nov 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2027.

Council of Science Editors:

Millard M. Discovery of novel small molecules targeting cancer cell metabolism. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2027


Univerzitet u Beogradu

14. Podolski-Renić, Ana. 1980-. Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu.

Degree: Biološki fakultet, 2014, Univerzitet u Beogradu

Molekularna onkologija - Kancerogeneza / Molecular oncology - Cancerogenesis

Glavni uzrok neuspeha hemioterapije u lečenju kancera je pojava višestruke (engl. „multi-drug“) rezistencije (MDR). Efikasnost paklitaksela… (more)

Subjects/Keywords: Multi-drug resistance (MDR); paclitaxel (PTX); colon cancer; glioblastoma; P-glycoprotein; anti-cancer agents

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APA (6th Edition):

Podolski-Renić, A. 1. (2014). Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get

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):

Podolski-Renić, Ana 1980-. “Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu.” 2014. Thesis, Univerzitet u Beogradu. Accessed November 20, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get.

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

MLA Handbook (7th Edition):

Podolski-Renić, Ana 1980-. “Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu.” 2014. Web. 20 Nov 2019.

Vancouver:

Podolski-Renić A1. Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2019 Nov 20]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get.

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

Council of Science Editors:

Podolski-Renić A1. Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get

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


University of the Western Cape

15. Omoruyi, Sylvester Ifeanyi. Investigating the anti-cancer activity of novel phenothiazines in glioblastoma .

Degree: 2018, University of the Western Cape

 Glioblastoma multiforme (GBM) remains the most malignant of all primary adult brain tumours. It is a highly invasive and vascularized neoplasm with limited treatment options… (more)

Subjects/Keywords: Drug repurposing; Phenothiazines; Chemotherapy; Anti-cancer agents; Cancer; Brain tumours; Glioblastoma; DNA damage; Apoptosis; Autophagy

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APA (6th Edition):

Omoruyi, S. I. (2018). Investigating the anti-cancer activity of novel phenothiazines in glioblastoma . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/6329

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):

Omoruyi, Sylvester Ifeanyi. “Investigating the anti-cancer activity of novel phenothiazines in glioblastoma .” 2018. Thesis, University of the Western Cape. Accessed November 20, 2019. http://hdl.handle.net/11394/6329.

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

MLA Handbook (7th Edition):

Omoruyi, Sylvester Ifeanyi. “Investigating the anti-cancer activity of novel phenothiazines in glioblastoma .” 2018. Web. 20 Nov 2019.

Vancouver:

Omoruyi SI. Investigating the anti-cancer activity of novel phenothiazines in glioblastoma . [Internet] [Thesis]. University of the Western Cape; 2018. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/11394/6329.

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

Council of Science Editors:

Omoruyi SI. Investigating the anti-cancer activity of novel phenothiazines in glioblastoma . [Thesis]. University of the Western Cape; 2018. Available from: http://hdl.handle.net/11394/6329

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


University of Johannesburg

16. Orsmond, Colette. Modulation of heat shock proteins following the synergistic treatment of sodium salicylate and heat shock in oesophageal cancer cells.

Degree: 2012, University of Johannesburg

M.Sc.

Statistics provided by the World Health Organization state that cancer accounted for 7.9 million deaths worldwide in 2007, with numbers expected to increase to… (more)

Subjects/Keywords: Esophagus cancer treatment; Anti-inflammatory agents; Cancer cells; Heat shock proteins; Thermotherapy

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APA (6th Edition):

Orsmond, C. (2012). Modulation of heat shock proteins following the synergistic treatment of sodium salicylate and heat shock in oesophageal cancer cells. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/6282

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):

Orsmond, Colette. “Modulation of heat shock proteins following the synergistic treatment of sodium salicylate and heat shock in oesophageal cancer cells.” 2012. Thesis, University of Johannesburg. Accessed November 20, 2019. http://hdl.handle.net/10210/6282.

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

MLA Handbook (7th Edition):

Orsmond, Colette. “Modulation of heat shock proteins following the synergistic treatment of sodium salicylate and heat shock in oesophageal cancer cells.” 2012. Web. 20 Nov 2019.

Vancouver:

Orsmond C. Modulation of heat shock proteins following the synergistic treatment of sodium salicylate and heat shock in oesophageal cancer cells. [Internet] [Thesis]. University of Johannesburg; 2012. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/10210/6282.

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

Council of Science Editors:

Orsmond C. Modulation of heat shock proteins following the synergistic treatment of sodium salicylate and heat shock in oesophageal cancer cells. [Thesis]. University of Johannesburg; 2012. Available from: http://hdl.handle.net/10210/6282

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


University of Manitoba

17. Ogunsina, Makanjuola Ojo. Structural activity and mechanistic studies on glycosylated antitumor ether lipids (GAELs).

Degree: Chemistry, 2016, University of Manitoba

 A major impediment to successful treatment of cancer is the inability of clinically available drugs to kill cancer stems cells (CSCs), a subset of tumor… (more)

Subjects/Keywords: Cancer stem cells; L-sugar; Glycosylated antitumor ether lipids; cancer; anti-cancer stem cells' agents; glycoside

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APA (6th Edition):

Ogunsina, M. O. (2016). Structural activity and mechanistic studies on glycosylated antitumor ether lipids (GAELs). (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/31925

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):

Ogunsina, Makanjuola Ojo. “Structural activity and mechanistic studies on glycosylated antitumor ether lipids (GAELs).” 2016. Thesis, University of Manitoba. Accessed November 20, 2019. http://hdl.handle.net/1993/31925.

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

MLA Handbook (7th Edition):

Ogunsina, Makanjuola Ojo. “Structural activity and mechanistic studies on glycosylated antitumor ether lipids (GAELs).” 2016. Web. 20 Nov 2019.

Vancouver:

Ogunsina MO. Structural activity and mechanistic studies on glycosylated antitumor ether lipids (GAELs). [Internet] [Thesis]. University of Manitoba; 2016. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/1993/31925.

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

Council of Science Editors:

Ogunsina MO. Structural activity and mechanistic studies on glycosylated antitumor ether lipids (GAELs). [Thesis]. University of Manitoba; 2016. Available from: http://hdl.handle.net/1993/31925

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


Nelson Mandela Metropolitan University

18. Freidberg, Ryno. An investigation into the antimicrobial and anticancer activities of Geranium incanum, Artemisia afra and Artemisia absinthium.

Degree: MTech, Faculty of Health Sciences, 2009, Nelson Mandela Metropolitan University

 It has been estimated that between 3000 and 4000 plant species are used for their medicinal properties throughout South Africa, with approximately 27 million South… (more)

Subjects/Keywords: Medicinal plants  – South Africa; Cancer  – Alternative treatment  – South Africa; Anti-infective agents

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APA (6th Edition):

Freidberg, R. (2009). An investigation into the antimicrobial and anticancer activities of Geranium incanum, Artemisia afra and Artemisia absinthium. (Masters Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/1045

Chicago Manual of Style (16th Edition):

Freidberg, Ryno. “An investigation into the antimicrobial and anticancer activities of Geranium incanum, Artemisia afra and Artemisia absinthium.” 2009. Masters Thesis, Nelson Mandela Metropolitan University. Accessed November 20, 2019. http://hdl.handle.net/10948/1045.

MLA Handbook (7th Edition):

Freidberg, Ryno. “An investigation into the antimicrobial and anticancer activities of Geranium incanum, Artemisia afra and Artemisia absinthium.” 2009. Web. 20 Nov 2019.

Vancouver:

Freidberg R. An investigation into the antimicrobial and anticancer activities of Geranium incanum, Artemisia afra and Artemisia absinthium. [Internet] [Masters thesis]. Nelson Mandela Metropolitan University; 2009. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/10948/1045.

Council of Science Editors:

Freidberg R. An investigation into the antimicrobial and anticancer activities of Geranium incanum, Artemisia afra and Artemisia absinthium. [Masters Thesis]. Nelson Mandela Metropolitan University; 2009. Available from: http://hdl.handle.net/10948/1045


Ohio University

19. Roberts, Dennis A. Design and Synthesis of Stable Glucose Uptake Inhibitors.

Degree: PhD, Chemistry and Biochemistry (Arts and Sciences), 2016, Ohio University

 There are many mechanisms that can be targeted when designing anticancer compounds. Due to the Warburg effect, the different steps of glycolysis have been potential… (more)

Subjects/Keywords: Chemistry; Glucose uptake inhibition; GLUT; Glucose transport proteins; anti-cancer agents; Warburg effect

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APA (6th Edition):

Roberts, D. A. (2016). Design and Synthesis of Stable Glucose Uptake Inhibitors. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou14791141897033

Chicago Manual of Style (16th Edition):

Roberts, Dennis A. “Design and Synthesis of Stable Glucose Uptake Inhibitors.” 2016. Doctoral Dissertation, Ohio University. Accessed November 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou14791141897033.

MLA Handbook (7th Edition):

Roberts, Dennis A. “Design and Synthesis of Stable Glucose Uptake Inhibitors.” 2016. Web. 20 Nov 2019.

Vancouver:

Roberts DA. Design and Synthesis of Stable Glucose Uptake Inhibitors. [Internet] [Doctoral dissertation]. Ohio University; 2016. [cited 2019 Nov 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou14791141897033.

Council of Science Editors:

Roberts DA. Design and Synthesis of Stable Glucose Uptake Inhibitors. [Doctoral Dissertation]. Ohio University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou14791141897033


University of Bradford

20. Elkashef, Sara M. Pharmacological evaluation of novel polysialyltransferase inhibitors as anti-metastatic agents and development of analytical methods for assessment of polysialylation inhibition : in vitro assessment of the effects of novel polysialyltransferase inhibitors on tumour cell function and development of quantitative HPLC-based methods for evaluation of novel polysialyltransferase inhibitors.

Degree: PhD, 2016, University of Bradford

 Polysialic acid (polySia) is a carbohydrate polymer highly expressed during embryonic development but rarely expressed during postnatal development. Two polysialyltransferase (polyST) enzymes are responsible for… (more)

Subjects/Keywords: 616.99; Cancer; Metastasis; Polysialic acid; Polysialyltransferase; Novel polysialyltransferase inhibitors; Anti-metastatic agents; Therapeutics; Migration

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APA (6th Edition):

Elkashef, S. M. (2016). Pharmacological evaluation of novel polysialyltransferase inhibitors as anti-metastatic agents and development of analytical methods for assessment of polysialylation inhibition : in vitro assessment of the effects of novel polysialyltransferase inhibitors on tumour cell function and development of quantitative HPLC-based methods for evaluation of novel polysialyltransferase inhibitors. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/14123

Chicago Manual of Style (16th Edition):

Elkashef, Sara M. “Pharmacological evaluation of novel polysialyltransferase inhibitors as anti-metastatic agents and development of analytical methods for assessment of polysialylation inhibition : in vitro assessment of the effects of novel polysialyltransferase inhibitors on tumour cell function and development of quantitative HPLC-based methods for evaluation of novel polysialyltransferase inhibitors.” 2016. Doctoral Dissertation, University of Bradford. Accessed November 20, 2019. http://hdl.handle.net/10454/14123.

MLA Handbook (7th Edition):

Elkashef, Sara M. “Pharmacological evaluation of novel polysialyltransferase inhibitors as anti-metastatic agents and development of analytical methods for assessment of polysialylation inhibition : in vitro assessment of the effects of novel polysialyltransferase inhibitors on tumour cell function and development of quantitative HPLC-based methods for evaluation of novel polysialyltransferase inhibitors.” 2016. Web. 20 Nov 2019.

Vancouver:

Elkashef SM. Pharmacological evaluation of novel polysialyltransferase inhibitors as anti-metastatic agents and development of analytical methods for assessment of polysialylation inhibition : in vitro assessment of the effects of novel polysialyltransferase inhibitors on tumour cell function and development of quantitative HPLC-based methods for evaluation of novel polysialyltransferase inhibitors. [Internet] [Doctoral dissertation]. University of Bradford; 2016. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/10454/14123.

Council of Science Editors:

Elkashef SM. Pharmacological evaluation of novel polysialyltransferase inhibitors as anti-metastatic agents and development of analytical methods for assessment of polysialylation inhibition : in vitro assessment of the effects of novel polysialyltransferase inhibitors on tumour cell function and development of quantitative HPLC-based methods for evaluation of novel polysialyltransferase inhibitors. [Doctoral Dissertation]. University of Bradford; 2016. Available from: http://hdl.handle.net/10454/14123


Rhodes University

21. Rapulenyane, Nomasonto. Photophysicochemical and photodynamic antimicrobial chemotherapeutic studies of novel phthalocyanines conjugated to silver nanoparticles.

Degree: Faculty of Science, Chemistry, 2013, Rhodes University

 This work reports on the synthesis, characterization and the physicochemical properties of novel unsymmetrically substituted zinc phthalocyanines: namely tris{11,19, 27-(1,2- diethylaminoethylthiol)-2-(captopril) phthalocyanine Zn ((ZnMCapPc (1.5)),… (more)

Subjects/Keywords: Phthalocyanines; Photochemistry; Photochemotherapy; Cancer  – Photochemotherapy; Anti-infective agents; Escherichia coli; Nanoparticles; Silver; Zinc

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APA (6th Edition):

Rapulenyane, N. (2013). Photophysicochemical and photodynamic antimicrobial chemotherapeutic studies of novel phthalocyanines conjugated to silver nanoparticles. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1003912

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):

Rapulenyane, Nomasonto. “Photophysicochemical and photodynamic antimicrobial chemotherapeutic studies of novel phthalocyanines conjugated to silver nanoparticles.” 2013. Thesis, Rhodes University. Accessed November 20, 2019. http://hdl.handle.net/10962/d1003912.

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

MLA Handbook (7th Edition):

Rapulenyane, Nomasonto. “Photophysicochemical and photodynamic antimicrobial chemotherapeutic studies of novel phthalocyanines conjugated to silver nanoparticles.” 2013. Web. 20 Nov 2019.

Vancouver:

Rapulenyane N. Photophysicochemical and photodynamic antimicrobial chemotherapeutic studies of novel phthalocyanines conjugated to silver nanoparticles. [Internet] [Thesis]. Rhodes University; 2013. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/10962/d1003912.

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

Council of Science Editors:

Rapulenyane N. Photophysicochemical and photodynamic antimicrobial chemotherapeutic studies of novel phthalocyanines conjugated to silver nanoparticles. [Thesis]. Rhodes University; 2013. Available from: http://hdl.handle.net/10962/d1003912

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

22. Pinto, Bebiana Maria Sousa. Novos complexos micelares de metais de transição para aplicação na terapia dirigida contra o cancro.

Degree: 2016, Universidade de Évora

 O cancro é a segunda causa de mortalidade a nível mundial. Um dos problemas nos tratamentos atuais de quimioterapia relaciona-se com os efeitos secundários causados… (more)

Subjects/Keywords: Agentes anticancerígenos; Copolímeros; Micelas; Compostos de coordenação; Anti-cancer agents; Copolymers; Micelles; Coordination compounds

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APA (6th Edition):

Pinto, B. M. S. (2016). Novos complexos micelares de metais de transição para aplicação na terapia dirigida contra o cancro. (Thesis). Universidade de Évora. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:dspace.uevora.pt:10174/19425

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):

Pinto, Bebiana Maria Sousa. “Novos complexos micelares de metais de transição para aplicação na terapia dirigida contra o cancro.” 2016. Thesis, Universidade de Évora. Accessed November 20, 2019. https://www.rcaap.pt/detail.jsp?id=oai:dspace.uevora.pt:10174/19425.

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

MLA Handbook (7th Edition):

Pinto, Bebiana Maria Sousa. “Novos complexos micelares de metais de transição para aplicação na terapia dirigida contra o cancro.” 2016. Web. 20 Nov 2019.

Vancouver:

Pinto BMS. Novos complexos micelares de metais de transição para aplicação na terapia dirigida contra o cancro. [Internet] [Thesis]. Universidade de Évora; 2016. [cited 2019 Nov 20]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:dspace.uevora.pt:10174/19425.

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

Council of Science Editors:

Pinto BMS. Novos complexos micelares de metais de transição para aplicação na terapia dirigida contra o cancro. [Thesis]. Universidade de Évora; 2016. Available from: https://www.rcaap.pt/detail.jsp?id=oai:dspace.uevora.pt:10174/19425

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


Brigham Young University

23. Oliveira, Marcelio. Synthesis and Evaluation of N6,5'-Bis-Ureido-5'-Amino-5'-Deoxyadenosine Derivatives: Novel Nucleosides with Antiproliferative and Protein Kinase Binding Activities.

Degree: MS, 2009, Brigham Young University

  A new series of N6,5'-bis-ureido-5'-amino-5'-deoxyadenosine derivatives was prepared and evaluated for anticancer activities using the NCI 60 panel of human cancers. Certain of the… (more)

Subjects/Keywords: Anti-cancer agents; N6; 5'-bis-ureido deoxyadenosine; protein kinases; Biochemistry; Chemistry

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APA (6th Edition):

Oliveira, M. (2009). Synthesis and Evaluation of N6,5'-Bis-Ureido-5'-Amino-5'-Deoxyadenosine Derivatives: Novel Nucleosides with Antiproliferative and Protein Kinase Binding Activities. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=2963&context=etd

Chicago Manual of Style (16th Edition):

Oliveira, Marcelio. “Synthesis and Evaluation of N6,5'-Bis-Ureido-5'-Amino-5'-Deoxyadenosine Derivatives: Novel Nucleosides with Antiproliferative and Protein Kinase Binding Activities.” 2009. Masters Thesis, Brigham Young University. Accessed November 20, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=2963&context=etd.

MLA Handbook (7th Edition):

Oliveira, Marcelio. “Synthesis and Evaluation of N6,5'-Bis-Ureido-5'-Amino-5'-Deoxyadenosine Derivatives: Novel Nucleosides with Antiproliferative and Protein Kinase Binding Activities.” 2009. Web. 20 Nov 2019.

Vancouver:

Oliveira M. Synthesis and Evaluation of N6,5'-Bis-Ureido-5'-Amino-5'-Deoxyadenosine Derivatives: Novel Nucleosides with Antiproliferative and Protein Kinase Binding Activities. [Internet] [Masters thesis]. Brigham Young University; 2009. [cited 2019 Nov 20]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=2963&context=etd.

Council of Science Editors:

Oliveira M. Synthesis and Evaluation of N6,5'-Bis-Ureido-5'-Amino-5'-Deoxyadenosine Derivatives: Novel Nucleosides with Antiproliferative and Protein Kinase Binding Activities. [Masters Thesis]. Brigham Young University; 2009. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=2963&context=etd


University of Glasgow

24. Farid, Yahya Yahya Zeki. The development of HPLC methods for the determination of methotrexate and doxorubicin metabolites and their application to clinical studies.

Degree: PhD, 1983, University of Glasgow

 This thesis describes the development of specific assays for two important anti-cancer agents which have been available for some time, methotrexate (MTX) introduced in 1… (more)

Subjects/Keywords: 615.1; Assays for anti-cancer agents

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APA (6th Edition):

Farid, Y. Y. Z. (1983). The development of HPLC methods for the determination of methotrexate and doxorubicin metabolites and their application to clinical studies. (Doctoral Dissertation). University of Glasgow. Retrieved from http://theses.gla.ac.uk/72335/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383242

Chicago Manual of Style (16th Edition):

Farid, Yahya Yahya Zeki. “The development of HPLC methods for the determination of methotrexate and doxorubicin metabolites and their application to clinical studies.” 1983. Doctoral Dissertation, University of Glasgow. Accessed November 20, 2019. http://theses.gla.ac.uk/72335/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383242.

MLA Handbook (7th Edition):

Farid, Yahya Yahya Zeki. “The development of HPLC methods for the determination of methotrexate and doxorubicin metabolites and their application to clinical studies.” 1983. Web. 20 Nov 2019.

Vancouver:

Farid YYZ. The development of HPLC methods for the determination of methotrexate and doxorubicin metabolites and their application to clinical studies. [Internet] [Doctoral dissertation]. University of Glasgow; 1983. [cited 2019 Nov 20]. Available from: http://theses.gla.ac.uk/72335/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383242.

Council of Science Editors:

Farid YYZ. The development of HPLC methods for the determination of methotrexate and doxorubicin metabolites and their application to clinical studies. [Doctoral Dissertation]. University of Glasgow; 1983. Available from: http://theses.gla.ac.uk/72335/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383242


University of Western Sydney

25. Rajamanickam, Adeline. Biological activity of N4-tetradentate ligands and their copper(II) complexes.

Degree: 2018, University of Western Sydney

Cancer has long been a global health concern and the recent resurgence of resistant microbial infections has led to the prediction that both of these… (more)

Subjects/Keywords: cancer; treatment; ligands (biochemistry); microbial carcinogenesis; anti-infective agents; antineoplastic agents; metal complexes; synthesis; Thesis (M.Res. (Sci.)) – Western Sydney University, 2018

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APA (6th Edition):

Rajamanickam, A. (2018). Biological activity of N4-tetradentate ligands and their copper(II) complexes. (Thesis). University of Western Sydney. Retrieved from http://hdl.handle.net/1959.7/uws:51206

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):

Rajamanickam, Adeline. “Biological activity of N4-tetradentate ligands and their copper(II) complexes.” 2018. Thesis, University of Western Sydney. Accessed November 20, 2019. http://hdl.handle.net/1959.7/uws:51206.

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

MLA Handbook (7th Edition):

Rajamanickam, Adeline. “Biological activity of N4-tetradentate ligands and their copper(II) complexes.” 2018. Web. 20 Nov 2019.

Vancouver:

Rajamanickam A. Biological activity of N4-tetradentate ligands and their copper(II) complexes. [Internet] [Thesis]. University of Western Sydney; 2018. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/1959.7/uws:51206.

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

Council of Science Editors:

Rajamanickam A. Biological activity of N4-tetradentate ligands and their copper(II) complexes. [Thesis]. University of Western Sydney; 2018. Available from: http://hdl.handle.net/1959.7/uws:51206

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


University College Cork

26. Miller, Charlotte M. Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents.

Degree: 2011, University College Cork

 This thesis describes work carried out on the synthesis of novel 5- and 11-substituted ellipticines and derivatives of the ellipticine analogues, isoellipticine and deazaellipticine, followed… (more)

Subjects/Keywords: Ellipticine; Anti-cancer; Topoisomerase inhibitor; Organic synthesis; Antineoplastic agents – Development; Enzyme inhibitors; Drugs – Design; Cancer – Chemotherapy; Organic compounds – Synthesis

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APA (6th Edition):

Miller, C. M. (2011). Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/534

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):

Miller, Charlotte M. “Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents.” 2011. Thesis, University College Cork. Accessed November 20, 2019. http://hdl.handle.net/10468/534.

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

MLA Handbook (7th Edition):

Miller, Charlotte M. “Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents.” 2011. Web. 20 Nov 2019.

Vancouver:

Miller CM. Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents. [Internet] [Thesis]. University College Cork; 2011. [cited 2019 Nov 20]. Available from: http://hdl.handle.net/10468/534.

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

Council of Science Editors:

Miller CM. Design, synthesis and evaluation of novel ellipticine derivatives and analogues as anti-cancer agents. [Thesis]. University College Cork; 2011. Available from: http://hdl.handle.net/10468/534

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


Kent State University

27. YARABARLA, SRIRAMAKRISHNA. Synthesis and Application of Polymer Stabilized, Water Dispersible Copper Based Nanoparticles as Anti-cancer and Diagnostic Agents.

Degree: PhD, College of Arts and Sciences / Department of Chemistry, 2017, Kent State University

 The objectives of this dissertation work are twofold. The first of the two is to evaluate the anti-cancer properties of a series of copper based… (more)

Subjects/Keywords: Chemistry; Nanoscience; Nanoparticles; copper tetrathiomolybdate; copper hydroxyphosphate; Libethenite; Prussian blue analog; anti-cancer; PET; MRI contrast agent; theranostic agents

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APA (6th Edition):

YARABARLA, S. (2017). Synthesis and Application of Polymer Stabilized, Water Dispersible Copper Based Nanoparticles as Anti-cancer and Diagnostic Agents. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1492608832326

Chicago Manual of Style (16th Edition):

YARABARLA, SRIRAMAKRISHNA. “Synthesis and Application of Polymer Stabilized, Water Dispersible Copper Based Nanoparticles as Anti-cancer and Diagnostic Agents.” 2017. Doctoral Dissertation, Kent State University. Accessed November 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=kent1492608832326.

MLA Handbook (7th Edition):

YARABARLA, SRIRAMAKRISHNA. “Synthesis and Application of Polymer Stabilized, Water Dispersible Copper Based Nanoparticles as Anti-cancer and Diagnostic Agents.” 2017. Web. 20 Nov 2019.

Vancouver:

YARABARLA S. Synthesis and Application of Polymer Stabilized, Water Dispersible Copper Based Nanoparticles as Anti-cancer and Diagnostic Agents. [Internet] [Doctoral dissertation]. Kent State University; 2017. [cited 2019 Nov 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1492608832326.

Council of Science Editors:

YARABARLA S. Synthesis and Application of Polymer Stabilized, Water Dispersible Copper Based Nanoparticles as Anti-cancer and Diagnostic Agents. [Doctoral Dissertation]. Kent State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1492608832326


RMIT University

28. Chintakunta, P. Part I Design, synthesis and evaluation of novel peptide based organocatalysts - Part II Studies towards the preparation and biological evaluation of [1,4]-dibenzodiazepinone analogues.

Degree: 2015, RMIT University

 Use of small organic molecules in asymmetric organic transformations has been popularly increasing every year since the turn of this century. The disadvantages associated with… (more)

Subjects/Keywords: Fields of Research; Organocatalysis; Peptide catalysis; Asymmetric Michael addition reaction; Enamine mechanism; Dibenzodiazepinone; Anti-cancer agents; Apoptosis

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APA (6th Edition):

Chintakunta, P. (2015). Part I Design, synthesis and evaluation of novel peptide based organocatalysts - Part II Studies towards the preparation and biological evaluation of [1,4]-dibenzodiazepinone analogues. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:161542

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):

Chintakunta, P. “Part I Design, synthesis and evaluation of novel peptide based organocatalysts - Part II Studies towards the preparation and biological evaluation of [1,4]-dibenzodiazepinone analogues.” 2015. Thesis, RMIT University. Accessed November 20, 2019. http://researchbank.rmit.edu.au/view/rmit:161542.

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

MLA Handbook (7th Edition):

Chintakunta, P. “Part I Design, synthesis and evaluation of novel peptide based organocatalysts - Part II Studies towards the preparation and biological evaluation of [1,4]-dibenzodiazepinone analogues.” 2015. Web. 20 Nov 2019.

Vancouver:

Chintakunta P. Part I Design, synthesis and evaluation of novel peptide based organocatalysts - Part II Studies towards the preparation and biological evaluation of [1,4]-dibenzodiazepinone analogues. [Internet] [Thesis]. RMIT University; 2015. [cited 2019 Nov 20]. Available from: http://researchbank.rmit.edu.au/view/rmit:161542.

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

Council of Science Editors:

Chintakunta P. Part I Design, synthesis and evaluation of novel peptide based organocatalysts - Part II Studies towards the preparation and biological evaluation of [1,4]-dibenzodiazepinone analogues. [Thesis]. RMIT University; 2015. Available from: http://researchbank.rmit.edu.au/view/rmit:161542

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


University of Western Australia

29. Chew, Angela Christine. The anti-proliferative effects of thiazolidinediones and non-steriodal anti-inflammatory drugs on androgen-independent prostate cancer.

Degree: PhD, 2009, University of Western Australia

 [Truncated abstract] In recent years a better understanding of the biology of PPAR , a nuclear transcription factor, has emerged, leading to a resurgence in… (more)

Subjects/Keywords: Prostate; Thiazoles; Nonsteroidal anti-inflammatory agents; Thiazolidinediones; Androgen-independent prostate cancer; Wnt/B-catenin signalling cascade

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APA (6th Edition):

Chew, A. C. (2009). The anti-proliferative effects of thiazolidinediones and non-steriodal anti-inflammatory drugs on androgen-independent prostate cancer. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=4243&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Chew, Angela Christine. “The anti-proliferative effects of thiazolidinediones and non-steriodal anti-inflammatory drugs on androgen-independent prostate cancer.” 2009. Doctoral Dissertation, University of Western Australia. Accessed November 20, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=4243&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Chew, Angela Christine. “The anti-proliferative effects of thiazolidinediones and non-steriodal anti-inflammatory drugs on androgen-independent prostate cancer.” 2009. Web. 20 Nov 2019.

Vancouver:

Chew AC. The anti-proliferative effects of thiazolidinediones and non-steriodal anti-inflammatory drugs on androgen-independent prostate cancer. [Internet] [Doctoral dissertation]. University of Western Australia; 2009. [cited 2019 Nov 20]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=4243&local_base=GEN01-INS01.

Council of Science Editors:

Chew AC. The anti-proliferative effects of thiazolidinediones and non-steriodal anti-inflammatory drugs on androgen-independent prostate cancer. [Doctoral Dissertation]. University of Western Australia; 2009. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=4243&local_base=GEN01-INS01


University of Hong Kong

30. Zhu, Genghui. Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells.

Degree: PhD, 1998, University of Hong Kong

published_or_final_version

Medicine

Doctoral

Doctor of Philosophy

Subjects/Keywords: Stomach - Cancer.; Epithelial cells.; Anti-inflammatory agents.

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APA (6th Edition):

Zhu, G. (1998). Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zhu, G. [朱耿慧]. (1998). Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123984 ; http://dx.doi.org/10.5353/th_b3123984 ; http://hdl.handle.net/10722/35535

Chicago Manual of Style (16th Edition):

Zhu, Genghui. “Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells.” 1998. Doctoral Dissertation, University of Hong Kong. Accessed November 20, 2019. Zhu, G. [朱耿慧]. (1998). Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123984 ; http://dx.doi.org/10.5353/th_b3123984 ; http://hdl.handle.net/10722/35535.

MLA Handbook (7th Edition):

Zhu, Genghui. “Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells.” 1998. Web. 20 Nov 2019.

Vancouver:

Zhu G. Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells. [Internet] [Doctoral dissertation]. University of Hong Kong; 1998. [cited 2019 Nov 20]. Available from: Zhu, G. [朱耿慧]. (1998). Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123984 ; http://dx.doi.org/10.5353/th_b3123984 ; http://hdl.handle.net/10722/35535.

Council of Science Editors:

Zhu G. Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells. [Doctoral Dissertation]. University of Hong Kong; 1998. Available from: Zhu, G. [朱耿慧]. (1998). Nonsteroidal antiinflammatory drugs and apoptosis of human gastric epithelial cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123984 ; http://dx.doi.org/10.5353/th_b3123984 ; http://hdl.handle.net/10722/35535

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