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You searched for subject:(Cisplatin). Showing records 1 – 30 of 285 total matches.

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University of Cape Town

1. Chakara, Zenzo Stanford. The efficacy of strategies used to minimise and prevent cisplatin ototoxicity in patients.

Degree: MSc, Division of Comm. Sciences & Disorders, 2018, University of Cape Town

 This study aimed to evaluate the efficacy of different treatment modifications used to prevent or minimise hearing loss during Cisplatin-based chemotherapy as part of patient… (more)

Subjects/Keywords: audiology; Cisplatin; Cancer

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

APA (6th Edition):

Chakara, Z. S. (2018). The efficacy of strategies used to minimise and prevent cisplatin ototoxicity in patients. (Masters Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/29453

Chicago Manual of Style (16th Edition):

Chakara, Zenzo Stanford. “The efficacy of strategies used to minimise and prevent cisplatin ototoxicity in patients.” 2018. Masters Thesis, University of Cape Town. Accessed April 19, 2019. http://hdl.handle.net/11427/29453.

MLA Handbook (7th Edition):

Chakara, Zenzo Stanford. “The efficacy of strategies used to minimise and prevent cisplatin ototoxicity in patients.” 2018. Web. 19 Apr 2019.

Vancouver:

Chakara ZS. The efficacy of strategies used to minimise and prevent cisplatin ototoxicity in patients. [Internet] [Masters thesis]. University of Cape Town; 2018. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/11427/29453.

Council of Science Editors:

Chakara ZS. The efficacy of strategies used to minimise and prevent cisplatin ototoxicity in patients. [Masters Thesis]. University of Cape Town; 2018. Available from: http://hdl.handle.net/11427/29453


University of Hawaii – Manoa

2. Mitchell, Kathryn Allison. Synthesis, characterization, and reactivity of platinum cysteinato and related thiolato complexes : model studies of the reversal of cisplatin nephrotoxicity.

Degree: PhD, 2009, University of Hawaii – Manoa

Microfiche.

xvii, 123 leaves, bound ill. 29 cm

Reaction of PtCl2(2,2'-bipyridine) (1) with N-acetyl-L-cysteine (L-accysH), mercaptopropanoic acid (mpaH), mercaptoacetic acid (maaH), 2-aminoethanethiol (aetH), L-cysteine (cysH),… (more)

Subjects/Keywords: Cisplatin; Organoplatinum compounds; Toxicological interactions

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APA (6th Edition):

Mitchell, K. A. (2009). Synthesis, characterization, and reactivity of platinum cysteinato and related thiolato complexes : model studies of the reversal of cisplatin nephrotoxicity. (Doctoral Dissertation). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/9526

Chicago Manual of Style (16th Edition):

Mitchell, Kathryn Allison. “Synthesis, characterization, and reactivity of platinum cysteinato and related thiolato complexes : model studies of the reversal of cisplatin nephrotoxicity.” 2009. Doctoral Dissertation, University of Hawaii – Manoa. Accessed April 19, 2019. http://hdl.handle.net/10125/9526.

MLA Handbook (7th Edition):

Mitchell, Kathryn Allison. “Synthesis, characterization, and reactivity of platinum cysteinato and related thiolato complexes : model studies of the reversal of cisplatin nephrotoxicity.” 2009. Web. 19 Apr 2019.

Vancouver:

Mitchell KA. Synthesis, characterization, and reactivity of platinum cysteinato and related thiolato complexes : model studies of the reversal of cisplatin nephrotoxicity. [Internet] [Doctoral dissertation]. University of Hawaii – Manoa; 2009. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10125/9526.

Council of Science Editors:

Mitchell KA. Synthesis, characterization, and reactivity of platinum cysteinato and related thiolato complexes : model studies of the reversal of cisplatin nephrotoxicity. [Doctoral Dissertation]. University of Hawaii – Manoa; 2009. Available from: http://hdl.handle.net/10125/9526


University of Debrecen

3. Cayasso, Mayella Roberta. Chemotherapeutic Treatment of Advanced Cervical Cancer .

Degree: DE – Általános Orvostudományi Kar, 2014, University of Debrecen

 In this day and age, management of advanced, recurrent or persistent cervical cancer includes radiotherapy and chemotherapy. Radiation has been the primary treatment modality for… (more)

Subjects/Keywords: Chemotherapy; Cisplatin; Cervical; Cancer

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APA (6th Edition):

Cayasso, M. R. (2014). Chemotherapeutic Treatment of Advanced Cervical Cancer . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/194764

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):

Cayasso, Mayella Roberta. “Chemotherapeutic Treatment of Advanced Cervical Cancer .” 2014. Thesis, University of Debrecen. Accessed April 19, 2019. http://hdl.handle.net/2437/194764.

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

MLA Handbook (7th Edition):

Cayasso, Mayella Roberta. “Chemotherapeutic Treatment of Advanced Cervical Cancer .” 2014. Web. 19 Apr 2019.

Vancouver:

Cayasso MR. Chemotherapeutic Treatment of Advanced Cervical Cancer . [Internet] [Thesis]. University of Debrecen; 2014. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2437/194764.

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

Council of Science Editors:

Cayasso MR. Chemotherapeutic Treatment of Advanced Cervical Cancer . [Thesis]. University of Debrecen; 2014. Available from: http://hdl.handle.net/2437/194764

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


University of Waterloo

4. Kalantari, Saeed. Time-Resolved Femtosecond Laser Spectroscopic Study of the Reaction.

Degree: 2007, University of Waterloo

 Being currently the second and potentially becoming the first cause of death in North America, cancer has been the focus of researchers from various areas… (more)

Subjects/Keywords: Cisplatin; Chemotherapy

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APA (6th Edition):

Kalantari, S. (2007). Time-Resolved Femtosecond Laser Spectroscopic Study of the Reaction. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/3220

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):

Kalantari, Saeed. “Time-Resolved Femtosecond Laser Spectroscopic Study of the Reaction.” 2007. Thesis, University of Waterloo. Accessed April 19, 2019. http://hdl.handle.net/10012/3220.

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

MLA Handbook (7th Edition):

Kalantari, Saeed. “Time-Resolved Femtosecond Laser Spectroscopic Study of the Reaction.” 2007. Web. 19 Apr 2019.

Vancouver:

Kalantari S. Time-Resolved Femtosecond Laser Spectroscopic Study of the Reaction. [Internet] [Thesis]. University of Waterloo; 2007. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10012/3220.

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

Council of Science Editors:

Kalantari S. Time-Resolved Femtosecond Laser Spectroscopic Study of the Reaction. [Thesis]. University of Waterloo; 2007. Available from: http://hdl.handle.net/10012/3220

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


University of Waterloo

5. Nguyen, Jenny. Study of a Molecular Promoter for Enhancing Cisplatin Cancer Chemotherapy.

Degree: 2010, University of Waterloo

Cisplatin is one of the most widely used chemotherapeutic anti-cancer drugs due to its ability to effectively damage DNA and cause cell death. Despite this,… (more)

Subjects/Keywords: cisplatin; CDDP; chemotherapy; cancer

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APA (6th Edition):

Nguyen, J. (2010). Study of a Molecular Promoter for Enhancing Cisplatin Cancer Chemotherapy. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/5246

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):

Nguyen, Jenny. “Study of a Molecular Promoter for Enhancing Cisplatin Cancer Chemotherapy.” 2010. Thesis, University of Waterloo. Accessed April 19, 2019. http://hdl.handle.net/10012/5246.

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

MLA Handbook (7th Edition):

Nguyen, Jenny. “Study of a Molecular Promoter for Enhancing Cisplatin Cancer Chemotherapy.” 2010. Web. 19 Apr 2019.

Vancouver:

Nguyen J. Study of a Molecular Promoter for Enhancing Cisplatin Cancer Chemotherapy. [Internet] [Thesis]. University of Waterloo; 2010. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10012/5246.

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

Council of Science Editors:

Nguyen J. Study of a Molecular Promoter for Enhancing Cisplatin Cancer Chemotherapy. [Thesis]. University of Waterloo; 2010. Available from: http://hdl.handle.net/10012/5246

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


University of Waterloo

6. Zhang, Qinrong. A Novel Combination Therapy of Cisplatin with a Molecular Promoter for Cancer Treatment.

Degree: 2017, University of Waterloo

Cisplatin is the first and most widely used platinum-based chemotherapy drug and is the cornerstone agent in treating a broad spectrum of cancers, including ovarian… (more)

Subjects/Keywords: Cancer; Combination Therapy; Cisplatin

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APA (6th Edition):

Zhang, Q. (2017). A Novel Combination Therapy of Cisplatin with a Molecular Promoter for Cancer Treatment. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/11272

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):

Zhang, Qinrong. “A Novel Combination Therapy of Cisplatin with a Molecular Promoter for Cancer Treatment.” 2017. Thesis, University of Waterloo. Accessed April 19, 2019. http://hdl.handle.net/10012/11272.

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

MLA Handbook (7th Edition):

Zhang, Qinrong. “A Novel Combination Therapy of Cisplatin with a Molecular Promoter for Cancer Treatment.” 2017. Web. 19 Apr 2019.

Vancouver:

Zhang Q. A Novel Combination Therapy of Cisplatin with a Molecular Promoter for Cancer Treatment. [Internet] [Thesis]. University of Waterloo; 2017. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10012/11272.

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

Council of Science Editors:

Zhang Q. A Novel Combination Therapy of Cisplatin with a Molecular Promoter for Cancer Treatment. [Thesis]. University of Waterloo; 2017. Available from: http://hdl.handle.net/10012/11272

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


University of Oregon

7. Moghaddam, Alan. A STUDY OF THE BEHAVIOR AND LOCALIZATION OF PT(II) AZIDE AND ALKYNE-MODIFIED DERIVATIVES IN CELLS USING BIOORTHOGONAL CHEMISTRY AND FLUORESCENCE MICROSCOPY.

Degree: 2016, University of Oregon

 Despite their ubiquitous use, Pt(II) anti-cancer drugs still suffer from many issues such as off-drug target effects, renal and nephrotoxicity as well as acquired and… (more)

Subjects/Keywords: alkyne; azide; cisplatin; click; platinum

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APA (6th Edition):

Moghaddam, A. (2016). A STUDY OF THE BEHAVIOR AND LOCALIZATION OF PT(II) AZIDE AND ALKYNE-MODIFIED DERIVATIVES IN CELLS USING BIOORTHOGONAL CHEMISTRY AND FLUORESCENCE MICROSCOPY. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/20727

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):

Moghaddam, Alan. “A STUDY OF THE BEHAVIOR AND LOCALIZATION OF PT(II) AZIDE AND ALKYNE-MODIFIED DERIVATIVES IN CELLS USING BIOORTHOGONAL CHEMISTRY AND FLUORESCENCE MICROSCOPY.” 2016. Thesis, University of Oregon. Accessed April 19, 2019. http://hdl.handle.net/1794/20727.

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

MLA Handbook (7th Edition):

Moghaddam, Alan. “A STUDY OF THE BEHAVIOR AND LOCALIZATION OF PT(II) AZIDE AND ALKYNE-MODIFIED DERIVATIVES IN CELLS USING BIOORTHOGONAL CHEMISTRY AND FLUORESCENCE MICROSCOPY.” 2016. Web. 19 Apr 2019.

Vancouver:

Moghaddam A. A STUDY OF THE BEHAVIOR AND LOCALIZATION OF PT(II) AZIDE AND ALKYNE-MODIFIED DERIVATIVES IN CELLS USING BIOORTHOGONAL CHEMISTRY AND FLUORESCENCE MICROSCOPY. [Internet] [Thesis]. University of Oregon; 2016. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1794/20727.

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

Council of Science Editors:

Moghaddam A. A STUDY OF THE BEHAVIOR AND LOCALIZATION OF PT(II) AZIDE AND ALKYNE-MODIFIED DERIVATIVES IN CELLS USING BIOORTHOGONAL CHEMISTRY AND FLUORESCENCE MICROSCOPY. [Thesis]. University of Oregon; 2016. Available from: http://hdl.handle.net/1794/20727

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


University of Oregon

8. Plakos, Kory. Platinum-seq: High-throughput mapping of small-molecule platinum adducts on cellular RNA.

Degree: 2017, University of Oregon

 Methods to map small-molecule interactions with cellular RNAs are important for understanding endogenous activation, such as in riboswitches, as well as the potential for exogenous… (more)

Subjects/Keywords: cisplatin; click; platinum; RNA; sequencing

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APA (6th Edition):

Plakos, K. (2017). Platinum-seq: High-throughput mapping of small-molecule platinum adducts on cellular RNA. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/22269

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):

Plakos, Kory. “Platinum-seq: High-throughput mapping of small-molecule platinum adducts on cellular RNA.” 2017. Thesis, University of Oregon. Accessed April 19, 2019. http://hdl.handle.net/1794/22269.

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

MLA Handbook (7th Edition):

Plakos, Kory. “Platinum-seq: High-throughput mapping of small-molecule platinum adducts on cellular RNA.” 2017. Web. 19 Apr 2019.

Vancouver:

Plakos K. Platinum-seq: High-throughput mapping of small-molecule platinum adducts on cellular RNA. [Internet] [Thesis]. University of Oregon; 2017. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1794/22269.

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

Council of Science Editors:

Plakos K. Platinum-seq: High-throughput mapping of small-molecule platinum adducts on cellular RNA. [Thesis]. University of Oregon; 2017. Available from: http://hdl.handle.net/1794/22269

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


University of Ottawa

9. Baghai, Tabassom. ATF3 as a Key Regulator of Cisplatin Cytotoxicity: Combining ATF3 Inducing Agents Enhances Cisplatin Activity in NSCLC .

Degree: 2018, University of Ottawa

 Lung cancer is the leading cause of cancer and cancer deaths worldwide, with non-small-cell lung carcinomas (NSCLC) representing 85% of all diagnosed lung cancers. Platinum-combination… (more)

Subjects/Keywords: Cancer therapeutics; NSCLC; Cisplatin; ATF3

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APA (6th Edition):

Baghai, T. (2018). ATF3 as a Key Regulator of Cisplatin Cytotoxicity: Combining ATF3 Inducing Agents Enhances Cisplatin Activity in NSCLC . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37963

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):

Baghai, Tabassom. “ATF3 as a Key Regulator of Cisplatin Cytotoxicity: Combining ATF3 Inducing Agents Enhances Cisplatin Activity in NSCLC .” 2018. Thesis, University of Ottawa. Accessed April 19, 2019. http://hdl.handle.net/10393/37963.

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

MLA Handbook (7th Edition):

Baghai, Tabassom. “ATF3 as a Key Regulator of Cisplatin Cytotoxicity: Combining ATF3 Inducing Agents Enhances Cisplatin Activity in NSCLC .” 2018. Web. 19 Apr 2019.

Vancouver:

Baghai T. ATF3 as a Key Regulator of Cisplatin Cytotoxicity: Combining ATF3 Inducing Agents Enhances Cisplatin Activity in NSCLC . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10393/37963.

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

Council of Science Editors:

Baghai T. ATF3 as a Key Regulator of Cisplatin Cytotoxicity: Combining ATF3 Inducing Agents Enhances Cisplatin Activity in NSCLC . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/37963

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


University of New South Wales

10. Nguyen, Hanh Thi Quynh. The Interaction of Cisplatin and Bleomycin with Telomeric DNA Sequences.

Degree: Biotechnology & Biomolecular Sciences, 2012, University of New South Wales

 Telomeres could be one of the main targets of several anti-tumour drugs. However, the interaction of these drugs with telomeric DNA sequences has not previously… (more)

Subjects/Keywords: Telomeric sequences; Cisplatin; Bleomycin

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APA (6th Edition):

Nguyen, H. T. Q. (2012). The Interaction of Cisplatin and Bleomycin with Telomeric DNA Sequences. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52109 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10779/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Nguyen, Hanh Thi Quynh. “The Interaction of Cisplatin and Bleomycin with Telomeric DNA Sequences.” 2012. Masters Thesis, University of New South Wales. Accessed April 19, 2019. http://handle.unsw.edu.au/1959.4/52109 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10779/SOURCE01?view=true.

MLA Handbook (7th Edition):

Nguyen, Hanh Thi Quynh. “The Interaction of Cisplatin and Bleomycin with Telomeric DNA Sequences.” 2012. Web. 19 Apr 2019.

Vancouver:

Nguyen HTQ. The Interaction of Cisplatin and Bleomycin with Telomeric DNA Sequences. [Internet] [Masters thesis]. University of New South Wales; 2012. [cited 2019 Apr 19]. Available from: http://handle.unsw.edu.au/1959.4/52109 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10779/SOURCE01?view=true.

Council of Science Editors:

Nguyen HTQ. The Interaction of Cisplatin and Bleomycin with Telomeric DNA Sequences. [Masters Thesis]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/52109 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10779/SOURCE01?view=true


University of New South Wales

11. Paul, Moumita. The interaction of cisplatin with telomeric DNA sequences.

Degree: Biotechnology & Biomolecular Sciences, 2010, University of New South Wales

 The anti-tumor drug cisplatin (cis-diamminedichloroplatinum(II)) has been in clinical use for nearly forty years and is highly effective in the treatment of a variety of… (more)

Subjects/Keywords: Fragment analysis; Cisplatin; Telomere

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APA (6th Edition):

Paul, M. (2010). The interaction of cisplatin with telomeric DNA sequences. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50380 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9267/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Paul, Moumita. “The interaction of cisplatin with telomeric DNA sequences.” 2010. Masters Thesis, University of New South Wales. Accessed April 19, 2019. http://handle.unsw.edu.au/1959.4/50380 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9267/SOURCE02?view=true.

MLA Handbook (7th Edition):

Paul, Moumita. “The interaction of cisplatin with telomeric DNA sequences.” 2010. Web. 19 Apr 2019.

Vancouver:

Paul M. The interaction of cisplatin with telomeric DNA sequences. [Internet] [Masters thesis]. University of New South Wales; 2010. [cited 2019 Apr 19]. Available from: http://handle.unsw.edu.au/1959.4/50380 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9267/SOURCE02?view=true.

Council of Science Editors:

Paul M. The interaction of cisplatin with telomeric DNA sequences. [Masters Thesis]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/50380 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9267/SOURCE02?view=true


University of Missouri – Columbia

12. Bommarito, David. Tavocept (BNP7787): a novel chemoprotector/sensitizer and radioprotector/sensitizer.

Degree: 2011, University of Missouri – Columbia

 Introduction: Tavocept is a novel chemoprotector/ sensitizer that has been used in combination with cisplatin to treat adenocarcinomas. The objectives of this study were to… (more)

Subjects/Keywords: nasal tumors; adenocarcinoma; cisplatin; mesna

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APA (6th Edition):

Bommarito, D. (2011). Tavocept (BNP7787): a novel chemoprotector/sensitizer and radioprotector/sensitizer. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/14956

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):

Bommarito, David. “Tavocept (BNP7787): a novel chemoprotector/sensitizer and radioprotector/sensitizer.” 2011. Thesis, University of Missouri – Columbia. Accessed April 19, 2019. http://hdl.handle.net/10355/14956.

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

MLA Handbook (7th Edition):

Bommarito, David. “Tavocept (BNP7787): a novel chemoprotector/sensitizer and radioprotector/sensitizer.” 2011. Web. 19 Apr 2019.

Vancouver:

Bommarito D. Tavocept (BNP7787): a novel chemoprotector/sensitizer and radioprotector/sensitizer. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10355/14956.

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

Council of Science Editors:

Bommarito D. Tavocept (BNP7787): a novel chemoprotector/sensitizer and radioprotector/sensitizer. [Thesis]. University of Missouri – Columbia; 2011. Available from: http://hdl.handle.net/10355/14956

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


Australian National University

13. Galgamuwa Arachchige, Ramindhu. An Investigation Into The Prevention Of Cisplatin-Induced Nephrotoxicity By Dichloroacetate .

Degree: 2016, Australian National University

Cisplatin is a highly effective anticancer drug used to treat a range of cancers. However, cisplatin use often leads to nephrotoxicity, which limits its clinical… (more)

Subjects/Keywords: Cisplatin-Induced Nephrotoxicity; Dichloroacetate

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APA (6th Edition):

Galgamuwa Arachchige, R. (2016). An Investigation Into The Prevention Of Cisplatin-Induced Nephrotoxicity By Dichloroacetate . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/114502

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):

Galgamuwa Arachchige, Ramindhu. “An Investigation Into The Prevention Of Cisplatin-Induced Nephrotoxicity By Dichloroacetate .” 2016. Thesis, Australian National University. Accessed April 19, 2019. http://hdl.handle.net/1885/114502.

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

MLA Handbook (7th Edition):

Galgamuwa Arachchige, Ramindhu. “An Investigation Into The Prevention Of Cisplatin-Induced Nephrotoxicity By Dichloroacetate .” 2016. Web. 19 Apr 2019.

Vancouver:

Galgamuwa Arachchige R. An Investigation Into The Prevention Of Cisplatin-Induced Nephrotoxicity By Dichloroacetate . [Internet] [Thesis]. Australian National University; 2016. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1885/114502.

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

Council of Science Editors:

Galgamuwa Arachchige R. An Investigation Into The Prevention Of Cisplatin-Induced Nephrotoxicity By Dichloroacetate . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/114502

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


Michigan State University

14. Rosenberg, Jeffrey Mark. Messenger RNA as a target for the cytotoxic action of the antitumor agent cisplatin : drug induced inhibition of in vitro translation.

Degree: PhD, 1988, Michigan State University

Subjects/Keywords: Cisplatin; RNA

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

APA (6th Edition):

Rosenberg, J. M. (1988). Messenger RNA as a target for the cytotoxic action of the antitumor agent cisplatin : drug induced inhibition of in vitro translation. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:21560

Chicago Manual of Style (16th Edition):

Rosenberg, Jeffrey Mark. “Messenger RNA as a target for the cytotoxic action of the antitumor agent cisplatin : drug induced inhibition of in vitro translation.” 1988. Doctoral Dissertation, Michigan State University. Accessed April 19, 2019. http://etd.lib.msu.edu/islandora/object/etd:21560.

MLA Handbook (7th Edition):

Rosenberg, Jeffrey Mark. “Messenger RNA as a target for the cytotoxic action of the antitumor agent cisplatin : drug induced inhibition of in vitro translation.” 1988. Web. 19 Apr 2019.

Vancouver:

Rosenberg JM. Messenger RNA as a target for the cytotoxic action of the antitumor agent cisplatin : drug induced inhibition of in vitro translation. [Internet] [Doctoral dissertation]. Michigan State University; 1988. [cited 2019 Apr 19]. Available from: http://etd.lib.msu.edu/islandora/object/etd:21560.

Council of Science Editors:

Rosenberg JM. Messenger RNA as a target for the cytotoxic action of the antitumor agent cisplatin : drug induced inhibition of in vitro translation. [Doctoral Dissertation]. Michigan State University; 1988. Available from: http://etd.lib.msu.edu/islandora/object/etd:21560


Western Kentucky University

15. Robey, Stephanie. Reactions of Platinum(II) Compounds with Selenium Containing Amino Acids.

Degree: MS, Department of Chemistry, 2013, Western Kentucky University

  Platinum(II) anticancer medications essentially react with DNA forming kinks in the double helix of DNA and causing apoptosis. It has also been noted that… (more)

Subjects/Keywords: Amino Acids; Platinum; Selenium; Cisplatin; Cisplatin-Chemistry; Cisplatin- Pharmacology; Cancer; Chemistry; Medicinal-Pharmaceutical Chemistry; Organic Chemistry

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APA (6th Edition):

Robey, S. (2013). Reactions of Platinum(II) Compounds with Selenium Containing Amino Acids. (Masters Thesis). Western Kentucky University. Retrieved from https://digitalcommons.wku.edu/theses/1252

Chicago Manual of Style (16th Edition):

Robey, Stephanie. “Reactions of Platinum(II) Compounds with Selenium Containing Amino Acids.” 2013. Masters Thesis, Western Kentucky University. Accessed April 19, 2019. https://digitalcommons.wku.edu/theses/1252.

MLA Handbook (7th Edition):

Robey, Stephanie. “Reactions of Platinum(II) Compounds with Selenium Containing Amino Acids.” 2013. Web. 19 Apr 2019.

Vancouver:

Robey S. Reactions of Platinum(II) Compounds with Selenium Containing Amino Acids. [Internet] [Masters thesis]. Western Kentucky University; 2013. [cited 2019 Apr 19]. Available from: https://digitalcommons.wku.edu/theses/1252.

Council of Science Editors:

Robey S. Reactions of Platinum(II) Compounds with Selenium Containing Amino Acids. [Masters Thesis]. Western Kentucky University; 2013. Available from: https://digitalcommons.wku.edu/theses/1252


University of Akron

16. Medvetz, Douglas Allen. The Synthesis, Characterization, and Antitumor Properties of Ag(I), Cu(II), and Rh(III) Metal Complexes.

Degree: PhD, Chemistry, 2008, University of Akron

 The anticancer drug cisplatin, which has been approved to treat ovarian, testicular, head and neck, certain types of lung, and metastatic breast cancers, has been… (more)

Subjects/Keywords: Chemistry; cisplatin; Cl; COMPLEXES; anticancer; Rh; silver

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APA (6th Edition):

Medvetz, D. A. (2008). The Synthesis, Characterization, and Antitumor Properties of Ag(I), Cu(II), and Rh(III) Metal Complexes. (Doctoral Dissertation). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1216840371

Chicago Manual of Style (16th Edition):

Medvetz, Douglas Allen. “The Synthesis, Characterization, and Antitumor Properties of Ag(I), Cu(II), and Rh(III) Metal Complexes.” 2008. Doctoral Dissertation, University of Akron. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1216840371.

MLA Handbook (7th Edition):

Medvetz, Douglas Allen. “The Synthesis, Characterization, and Antitumor Properties of Ag(I), Cu(II), and Rh(III) Metal Complexes.” 2008. Web. 19 Apr 2019.

Vancouver:

Medvetz DA. The Synthesis, Characterization, and Antitumor Properties of Ag(I), Cu(II), and Rh(III) Metal Complexes. [Internet] [Doctoral dissertation]. University of Akron; 2008. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1216840371.

Council of Science Editors:

Medvetz DA. The Synthesis, Characterization, and Antitumor Properties of Ag(I), Cu(II), and Rh(III) Metal Complexes. [Doctoral Dissertation]. University of Akron; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1216840371


NSYSU

17. Liu, Ye-Chong. Epigallocatechin gallate attenuate Cisplatin induced acute renal failure in rat.

Degree: Master, Biological Sciences, 2010, NSYSU

 Abstract Cisplatin is one of the most effective chemotherapeutic agents used in treatment of a variety of human solid tumors. The most common adverse side… (more)

Subjects/Keywords: acute renal failure; Cisplatin; epigallocatechin gallate

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APA (6th Edition):

Liu, Y. (2010). Epigallocatechin gallate attenuate Cisplatin induced acute renal failure in rat. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0819110-105433

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):

Liu, Ye-Chong. “Epigallocatechin gallate attenuate Cisplatin induced acute renal failure in rat.” 2010. Thesis, NSYSU. Accessed April 19, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0819110-105433.

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

MLA Handbook (7th Edition):

Liu, Ye-Chong. “Epigallocatechin gallate attenuate Cisplatin induced acute renal failure in rat.” 2010. Web. 19 Apr 2019.

Vancouver:

Liu Y. Epigallocatechin gallate attenuate Cisplatin induced acute renal failure in rat. [Internet] [Thesis]. NSYSU; 2010. [cited 2019 Apr 19]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0819110-105433.

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

Council of Science Editors:

Liu Y. Epigallocatechin gallate attenuate Cisplatin induced acute renal failure in rat. [Thesis]. NSYSU; 2010. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0819110-105433

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


Ruhr Universität Bochum

18. Will, Joanna. Massenspektrometrische Ermittlung der Proteintargets von zytotoxischen Metallkomplexen in Blutserum und E. coli-Zellen.

Degree: 2008, Ruhr Universität Bochum

 Mittels kombinierter flüssigchromatographischer und ESI-MS/MS Methoden wurden die folgenden Verbindungen [(η6-p- Cymol)RuCl2(DMSO)], [Pt(dien)(H2O)](NO3)2, Hexacarbonyl[2-propyn-1-yl-acetylsalicylat]dicobalt (Co-ASS) und Cisplatin (cis- [(NH3)2PtCl2]) auf mögliche Bindungsstellen in den Proteinen… (more)

Subjects/Keywords: Tandem-Massenspektrometrie; Cisplatin; Serumproteine; Escherichia coli; Blutserum

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APA (6th Edition):

Will, J. (2008). Massenspektrometrische Ermittlung der Proteintargets von zytotoxischen Metallkomplexen in Blutserum und E. coli-Zellen. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-23342

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):

Will, Joanna. “Massenspektrometrische Ermittlung der Proteintargets von zytotoxischen Metallkomplexen in Blutserum und E. coli-Zellen.” 2008. Thesis, Ruhr Universität Bochum. Accessed April 19, 2019. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-23342.

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

MLA Handbook (7th Edition):

Will, Joanna. “Massenspektrometrische Ermittlung der Proteintargets von zytotoxischen Metallkomplexen in Blutserum und E. coli-Zellen.” 2008. Web. 19 Apr 2019.

Vancouver:

Will J. Massenspektrometrische Ermittlung der Proteintargets von zytotoxischen Metallkomplexen in Blutserum und E. coli-Zellen. [Internet] [Thesis]. Ruhr Universität Bochum; 2008. [cited 2019 Apr 19]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-23342.

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

Council of Science Editors:

Will J. Massenspektrometrische Ermittlung der Proteintargets von zytotoxischen Metallkomplexen in Blutserum und E. coli-Zellen. [Thesis]. Ruhr Universität Bochum; 2008. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-23342

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


Ruhr Universität Bochum

19. Stefanopoulou, Maria. Mass spectrometric analysis of the differential protein expression of living cell systems in the presence of metal-based antitumor compounds.

Degree: 2011, Ruhr Universität Bochum

 Seit der zufälligen Entdeckung der zytostatischen Wirkung von cisplatin in den 60er Jahren bei Rosenberg et al. ist vieles schon über den Wirkungsmechanismus dieses Therapeutikums… (more)

Subjects/Keywords: Massenspektrometrie; Cisplatin; Escherichia coli; Quantifizierung; Proteom

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APA (6th Edition):

Stefanopoulou, M. (2011). Mass spectrometric analysis of the differential protein expression of living cell systems in the presence of metal-based antitumor compounds. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-32753

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):

Stefanopoulou, Maria. “Mass spectrometric analysis of the differential protein expression of living cell systems in the presence of metal-based antitumor compounds.” 2011. Thesis, Ruhr Universität Bochum. Accessed April 19, 2019. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-32753.

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

MLA Handbook (7th Edition):

Stefanopoulou, Maria. “Mass spectrometric analysis of the differential protein expression of living cell systems in the presence of metal-based antitumor compounds.” 2011. Web. 19 Apr 2019.

Vancouver:

Stefanopoulou M. Mass spectrometric analysis of the differential protein expression of living cell systems in the presence of metal-based antitumor compounds. [Internet] [Thesis]. Ruhr Universität Bochum; 2011. [cited 2019 Apr 19]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-32753.

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

Council of Science Editors:

Stefanopoulou M. Mass spectrometric analysis of the differential protein expression of living cell systems in the presence of metal-based antitumor compounds. [Thesis]. Ruhr Universität Bochum; 2011. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-32753

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


University of Western Australia

20. Cregan, Inez Lidia. Biochemical mechanisms involved in cisplatin-induced apoptosis in malignant mesothelioma cells.

Degree: PhD, 2008, University of Western Australia

Malignant mesothelioma (MM) is an aggressive malignancy that originates from mesothelial cells and is highly resistant to conventional forms of anti-cancer therapy. Defects in apoptotic… (more)

Subjects/Keywords: Mesothelioma; Apoptosis; Cisplatin; Malignant mesothelioma; Cancer

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APA (6th Edition):

Cregan, I. L. (2008). Biochemical mechanisms involved in cisplatin-induced apoptosis in malignant mesothelioma cells. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=5870&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Cregan, Inez Lidia. “Biochemical mechanisms involved in cisplatin-induced apoptosis in malignant mesothelioma cells.” 2008. Doctoral Dissertation, University of Western Australia. Accessed April 19, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=5870&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Cregan, Inez Lidia. “Biochemical mechanisms involved in cisplatin-induced apoptosis in malignant mesothelioma cells.” 2008. Web. 19 Apr 2019.

Vancouver:

Cregan IL. Biochemical mechanisms involved in cisplatin-induced apoptosis in malignant mesothelioma cells. [Internet] [Doctoral dissertation]. University of Western Australia; 2008. [cited 2019 Apr 19]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=5870&local_base=GEN01-INS01.

Council of Science Editors:

Cregan IL. Biochemical mechanisms involved in cisplatin-induced apoptosis in malignant mesothelioma cells. [Doctoral Dissertation]. University of Western Australia; 2008. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=5870&local_base=GEN01-INS01


Texas Medical Center

21. Izaguirre, Daisy I. THE ROLE OF GDF15 IN OVARIAN CANCER.

Degree: PhD, 2016, Texas Medical Center

  Growth Differentiation Factor 15 (GDF15) is induced in situations such as stress, inflammation, treatment with non-steroidal anti-inflammatory drugs, as well as other therapeutic agents.… (more)

Subjects/Keywords: ovarian cancer; GDF15; cisplatin; p53; Cancer Biology

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APA (6th Edition):

Izaguirre, D. I. (2016). THE ROLE OF GDF15 IN OVARIAN CANCER. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/678

Chicago Manual of Style (16th Edition):

Izaguirre, Daisy I. “THE ROLE OF GDF15 IN OVARIAN CANCER.” 2016. Doctoral Dissertation, Texas Medical Center. Accessed April 19, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/678.

MLA Handbook (7th Edition):

Izaguirre, Daisy I. “THE ROLE OF GDF15 IN OVARIAN CANCER.” 2016. Web. 19 Apr 2019.

Vancouver:

Izaguirre DI. THE ROLE OF GDF15 IN OVARIAN CANCER. [Internet] [Doctoral dissertation]. Texas Medical Center; 2016. [cited 2019 Apr 19]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/678.

Council of Science Editors:

Izaguirre DI. THE ROLE OF GDF15 IN OVARIAN CANCER. [Doctoral Dissertation]. Texas Medical Center; 2016. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/678

22. Kong, Bao. THE ROLE AND REGULATION of MITOCHONDRIAL DYNAMICS IN CISPLATIN RESISTANCE IN HUMAN GYNECOLOGIC CANCER CELLS .

Degree: 2015, University of Ottawa

 Cervical cancer (CECA) and ovarian cancer (OVCA) rank first and third in the number of new cases diagnosed among gynecologic cancers,and chemoresistance severely limits their… (more)

Subjects/Keywords: Cisplatin; Resistance

…the combination of a platinum compound, such as cisplatin or carboplatin, and a taxane (… …sometimes combined with radiation therapy. Cisplatin, 5-fluorouracil and ifosfamide are the most… …and chemotherapy (Scatchard, Forrest et al. 2012). 9 2. Cisplatin and its… …anticancer actions Cisplatin (CDDP), also called cisplatinum, or cis… …and 10 Gu 2009). 2.2 Treatment of cancer Cisplatin has been used as a… 

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APA (6th Edition):

Kong, B. (2015). THE ROLE AND REGULATION of MITOCHONDRIAL DYNAMICS IN CISPLATIN RESISTANCE IN HUMAN GYNECOLOGIC CANCER CELLS . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32461

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):

Kong, Bao. “THE ROLE AND REGULATION of MITOCHONDRIAL DYNAMICS IN CISPLATIN RESISTANCE IN HUMAN GYNECOLOGIC CANCER CELLS .” 2015. Thesis, University of Ottawa. Accessed April 19, 2019. http://hdl.handle.net/10393/32461.

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

MLA Handbook (7th Edition):

Kong, Bao. “THE ROLE AND REGULATION of MITOCHONDRIAL DYNAMICS IN CISPLATIN RESISTANCE IN HUMAN GYNECOLOGIC CANCER CELLS .” 2015. Web. 19 Apr 2019.

Vancouver:

Kong B. THE ROLE AND REGULATION of MITOCHONDRIAL DYNAMICS IN CISPLATIN RESISTANCE IN HUMAN GYNECOLOGIC CANCER CELLS . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10393/32461.

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

Council of Science Editors:

Kong B. THE ROLE AND REGULATION of MITOCHONDRIAL DYNAMICS IN CISPLATIN RESISTANCE IN HUMAN GYNECOLOGIC CANCER CELLS . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32461

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


Kent State University

23. Calderon-Salgado, Esther Lilia. Effect of progesterone and RU486 on cisplatin resistance in OV2008 and C13 ovarian epithelial cancer cell lines.

Degree: MS, College of Arts and Sciences / Department of Biological Sciences, 2008, Kent State University

  Ovarian cancer is the sixth most common cancer and has the highest mortality rate of any gynecological cancer among women. About 90% of ovarian… (more)

Subjects/Keywords: Biology; Biomedical Research; Ovarian cancer; progesterone; cisplatin

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APA (6th Edition):

Calderon-Salgado, E. L. (2008). Effect of progesterone and RU486 on cisplatin resistance in OV2008 and C13 ovarian epithelial cancer cell lines. (Masters Thesis). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1208532125

Chicago Manual of Style (16th Edition):

Calderon-Salgado, Esther Lilia. “Effect of progesterone and RU486 on cisplatin resistance in OV2008 and C13 ovarian epithelial cancer cell lines.” 2008. Masters Thesis, Kent State University. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=kent1208532125.

MLA Handbook (7th Edition):

Calderon-Salgado, Esther Lilia. “Effect of progesterone and RU486 on cisplatin resistance in OV2008 and C13 ovarian epithelial cancer cell lines.” 2008. Web. 19 Apr 2019.

Vancouver:

Calderon-Salgado EL. Effect of progesterone and RU486 on cisplatin resistance in OV2008 and C13 ovarian epithelial cancer cell lines. [Internet] [Masters thesis]. Kent State University; 2008. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1208532125.

Council of Science Editors:

Calderon-Salgado EL. Effect of progesterone and RU486 on cisplatin resistance in OV2008 and C13 ovarian epithelial cancer cell lines. [Masters Thesis]. Kent State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1208532125

24. 稗田, 敏雄. 腫瘍溶解ウィルスとシスプラチンとの併用効果の検討 : Combination effect of oncolytic adenovirus with cisplatin; 腫瘍溶解ウイルスとシスプラチンとの併用効果.

Degree: 博士(歯学), 2016, Hokkaido University / 北海道大学

【背景】がんに対する治療法には, 一般的に外科手術, 化学療法, 放射線療法がある. その中でも化学療法は, 現在までにがんに対して優れた治療効果をもたらしてきたが, 抵抗性を示す場合も報告されている. また, 高濃度の抗がん剤は, 様々な副作用を引き起こすため, 現状よりも低濃度での使用が望まれている. そのため, 高濃度の抗がん剤と同様の効果を示すには, 他の補助療法が必要とされている. 一方, 腫瘍細胞で選択的に増殖する腫瘍溶解ウイルス(Oncolytic virus)によるがん治療は, 高い治療効果と選択性が期待される.口腔病理病態学教室では, アデノウイルスの複製に最も重要な E1A 遺伝子にAU-rich element(ARE)を組み込んだ腫瘍溶解アデノウイルス(Ad-ARET)を作成した. 本研究では, がん細胞に対する Ad-ARET… (more)

Subjects/Keywords: シスプラチン; Ad-ARET; HuR; ARE-mRNA; cisplatin

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APA (6th Edition):

稗田, . (2016). 腫瘍溶解ウィルスとシスプラチンとの併用効果の検討 : Combination effect of oncolytic adenovirus with cisplatin; 腫瘍溶解ウイルスとシスプラチンとの併用効果. (Thesis). Hokkaido University / 北海道大学. Retrieved from http://hdl.handle.net/2115/62229 ; http://dx.doi.org/10.14943/doctoral.k12169

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):

稗田, 敏雄. “腫瘍溶解ウィルスとシスプラチンとの併用効果の検討 : Combination effect of oncolytic adenovirus with cisplatin; 腫瘍溶解ウイルスとシスプラチンとの併用効果.” 2016. Thesis, Hokkaido University / 北海道大学. Accessed April 19, 2019. http://hdl.handle.net/2115/62229 ; http://dx.doi.org/10.14943/doctoral.k12169.

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

MLA Handbook (7th Edition):

稗田, 敏雄. “腫瘍溶解ウィルスとシスプラチンとの併用効果の検討 : Combination effect of oncolytic adenovirus with cisplatin; 腫瘍溶解ウイルスとシスプラチンとの併用効果.” 2016. Web. 19 Apr 2019.

Vancouver:

稗田 . 腫瘍溶解ウィルスとシスプラチンとの併用効果の検討 : Combination effect of oncolytic adenovirus with cisplatin; 腫瘍溶解ウイルスとシスプラチンとの併用効果. [Internet] [Thesis]. Hokkaido University / 北海道大学; 2016. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2115/62229 ; http://dx.doi.org/10.14943/doctoral.k12169.

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

Council of Science Editors:

稗田 . 腫瘍溶解ウィルスとシスプラチンとの併用効果の検討 : Combination effect of oncolytic adenovirus with cisplatin; 腫瘍溶解ウイルスとシスプラチンとの併用効果. [Thesis]. Hokkaido University / 北海道大学; 2016. Available from: http://hdl.handle.net/2115/62229 ; http://dx.doi.org/10.14943/doctoral.k12169

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


University of Sydney

25. Bulanadi, Jerikho Christian. Prodrug Amphiphile Nanoassemblies for Targeted Treatment of Pancreatic Cancer .

Degree: 2017, University of Sydney

 Cancer is a diverse and complex condition. Tackling cancer effectively requires a multidisciplinary team and close collaboration between clinicians, biologists, chemists and material scientists. The… (more)

Subjects/Keywords: chemotherapy; prodrug; nanoparticle; pancreatic cancer; cisplatin; gemcitabine

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APA (6th Edition):

Bulanadi, J. C. (2017). Prodrug Amphiphile Nanoassemblies for Targeted Treatment of Pancreatic Cancer . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18819

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):

Bulanadi, Jerikho Christian. “Prodrug Amphiphile Nanoassemblies for Targeted Treatment of Pancreatic Cancer .” 2017. Thesis, University of Sydney. Accessed April 19, 2019. http://hdl.handle.net/2123/18819.

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

MLA Handbook (7th Edition):

Bulanadi, Jerikho Christian. “Prodrug Amphiphile Nanoassemblies for Targeted Treatment of Pancreatic Cancer .” 2017. Web. 19 Apr 2019.

Vancouver:

Bulanadi JC. Prodrug Amphiphile Nanoassemblies for Targeted Treatment of Pancreatic Cancer . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2123/18819.

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

Council of Science Editors:

Bulanadi JC. Prodrug Amphiphile Nanoassemblies for Targeted Treatment of Pancreatic Cancer . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/18819

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


Universidade Nova

26. Marques, Mara Lisa Miranda. Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets.

Degree: 2014, Universidade Nova

Review article Martins, P., Marques, M., Coito, L., Pombeiro, A.J.L., Baptista, P.V., Fernandes, A.R. 2014. Organometallic Compounds in Cancer Therapy: Past Lessons and Future Directions. Anti-cancer Agents in Medicinal Chemistry 14. PMID: 25173559 Advisors/Committee Members: Fernandes, Maria Alexandra.

Subjects/Keywords: Cancer; Cisplatin; Citotoxicity; Combined therapeutics; Doxorubicin; Rhenium

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APA (6th Edition):

Marques, M. L. M. (2014). Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13912

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):

Marques, Mara Lisa Miranda. “Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets.” 2014. Thesis, Universidade Nova. Accessed April 19, 2019. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13912.

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

MLA Handbook (7th Edition):

Marques, Mara Lisa Miranda. “Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets.” 2014. Web. 19 Apr 2019.

Vancouver:

Marques MLM. Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets. [Internet] [Thesis]. Universidade Nova; 2014. [cited 2019 Apr 19]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13912.

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

Council of Science Editors:

Marques MLM. Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets. [Thesis]. Universidade Nova; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13912

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


Vanderbilt University

27. Pendleton, Christopher Stephen. Mechanisms of Cisplatin Resistance in Triple Negative Breast Cancer.

Degree: MS, Biochemistry, 2014, Vanderbilt University

 Genomic instability and deregulated proliferation are hallmarks of human tumors. Cytotoxic chemotherapeutics, including cisplatin, have been used for over forty years to combat cancers that… (more)

Subjects/Keywords: triple negative; breast cancer; cancer; chemotherapy; cisplatin

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APA (6th Edition):

Pendleton, C. S. (2014). Mechanisms of Cisplatin Resistance in Triple Negative Breast Cancer. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11242014-103854/ ;

Chicago Manual of Style (16th Edition):

Pendleton, Christopher Stephen. “Mechanisms of Cisplatin Resistance in Triple Negative Breast Cancer.” 2014. Masters Thesis, Vanderbilt University. Accessed April 19, 2019. http://etd.library.vanderbilt.edu/available/etd-11242014-103854/ ;.

MLA Handbook (7th Edition):

Pendleton, Christopher Stephen. “Mechanisms of Cisplatin Resistance in Triple Negative Breast Cancer.” 2014. Web. 19 Apr 2019.

Vancouver:

Pendleton CS. Mechanisms of Cisplatin Resistance in Triple Negative Breast Cancer. [Internet] [Masters thesis]. Vanderbilt University; 2014. [cited 2019 Apr 19]. Available from: http://etd.library.vanderbilt.edu/available/etd-11242014-103854/ ;.

Council of Science Editors:

Pendleton CS. Mechanisms of Cisplatin Resistance in Triple Negative Breast Cancer. [Masters Thesis]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu/available/etd-11242014-103854/ ;

28. Hori, Kiyomi; Ozaki, Noriyuki; Suzuki, Shigeyuki. Upregulations of P2X3 and ASIC3 involve in hyperalgesia induced by cisplatin administration in rats.

Degree: 博士(医学), 2018, Nagoya University / 名古屋大学

The role of ion channels expressed in sensory neurons on mechanical and thermal hyperalgesia was examined in a rat model of cisplatin-induced peripheral neuropathy. The… (more)

Subjects/Keywords: Cisplatin; TRPV1; TRPV2; P2X3; ASIC3; Hyperalgesia

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APA (6th Edition):

Hori, Kiyomi; Ozaki, Noriyuki; Suzuki, S. (2018). Upregulations of P2X3 and ASIC3 involve in hyperalgesia induced by cisplatin administration in rats. (Thesis). Nagoya University / 名古屋大学. Retrieved from http://hdl.handle.net/2237/23011

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):

Hori, Kiyomi; Ozaki, Noriyuki; Suzuki, Shigeyuki. “Upregulations of P2X3 and ASIC3 involve in hyperalgesia induced by cisplatin administration in rats.” 2018. Thesis, Nagoya University / 名古屋大学. Accessed April 19, 2019. http://hdl.handle.net/2237/23011.

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

MLA Handbook (7th Edition):

Hori, Kiyomi; Ozaki, Noriyuki; Suzuki, Shigeyuki. “Upregulations of P2X3 and ASIC3 involve in hyperalgesia induced by cisplatin administration in rats.” 2018. Web. 19 Apr 2019.

Vancouver:

Hori, Kiyomi; Ozaki, Noriyuki; Suzuki S. Upregulations of P2X3 and ASIC3 involve in hyperalgesia induced by cisplatin administration in rats. [Internet] [Thesis]. Nagoya University / 名古屋大学; 2018. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2237/23011.

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

Council of Science Editors:

Hori, Kiyomi; Ozaki, Noriyuki; Suzuki S. Upregulations of P2X3 and ASIC3 involve in hyperalgesia induced by cisplatin administration in rats. [Thesis]. Nagoya University / 名古屋大学; 2018. Available from: http://hdl.handle.net/2237/23011

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


University of Waterloo

29. McMillan, Michael Elliott. Examining the Role of Autophagy in Skeletal Muscle Cell Death and Differentiation.

Degree: 2015, University of Waterloo

 Autophagy is catabolic process which sequesters large portions of cytoplasm as well as selected organelles and proteins for degradation. Recently, autophagy has been a topic… (more)

Subjects/Keywords: Autophagy; Apoptosis; Muscle; Differentiation; Regeneration; Cisplatin

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APA (6th Edition):

McMillan, M. E. (2015). Examining the Role of Autophagy in Skeletal Muscle Cell Death and Differentiation. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/9045

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):

McMillan, Michael Elliott. “Examining the Role of Autophagy in Skeletal Muscle Cell Death and Differentiation.” 2015. Thesis, University of Waterloo. Accessed April 19, 2019. http://hdl.handle.net/10012/9045.

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

MLA Handbook (7th Edition):

McMillan, Michael Elliott. “Examining the Role of Autophagy in Skeletal Muscle Cell Death and Differentiation.” 2015. Web. 19 Apr 2019.

Vancouver:

McMillan ME. Examining the Role of Autophagy in Skeletal Muscle Cell Death and Differentiation. [Internet] [Thesis]. University of Waterloo; 2015. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10012/9045.

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

Council of Science Editors:

McMillan ME. Examining the Role of Autophagy in Skeletal Muscle Cell Death and Differentiation. [Thesis]. University of Waterloo; 2015. Available from: http://hdl.handle.net/10012/9045

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


University of Lethbridge

30. University of Lethbridge. Faculty of Arts and Science. Investigation of checkpoint adaptation in human cancer cells treated with the genotoxic agent cisplatin .

Degree: 2015, University of Lethbridge

 We investigated checkpoint adaptation in HT-29 colorectal adenocarcinoma cells treated with cisplatin. Cells that undergo checkpoint adaptation arrest at and then abrogate the G2/M checkpoint… (more)

Subjects/Keywords: apoptosis; checkpoint adaptation; cisplatin; genotoxic agents; mitosis

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

APA (6th Edition):

Science, U. o. L. F. o. A. a. (2015). Investigation of checkpoint adaptation in human cancer cells treated with the genotoxic agent cisplatin . (Thesis). University of Lethbridge. Retrieved from http://hdl.handle.net/10133/3813

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):

Science, University of Lethbridge. Faculty of Arts and. “Investigation of checkpoint adaptation in human cancer cells treated with the genotoxic agent cisplatin .” 2015. Thesis, University of Lethbridge. Accessed April 19, 2019. http://hdl.handle.net/10133/3813.

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

MLA Handbook (7th Edition):

Science, University of Lethbridge. Faculty of Arts and. “Investigation of checkpoint adaptation in human cancer cells treated with the genotoxic agent cisplatin .” 2015. Web. 19 Apr 2019.

Vancouver:

Science UoLFoAa. Investigation of checkpoint adaptation in human cancer cells treated with the genotoxic agent cisplatin . [Internet] [Thesis]. University of Lethbridge; 2015. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10133/3813.

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

Council of Science Editors:

Science UoLFoAa. Investigation of checkpoint adaptation in human cancer cells treated with the genotoxic agent cisplatin . [Thesis]. University of Lethbridge; 2015. Available from: http://hdl.handle.net/10133/3813

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

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