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You searched for subject:( carcinogenesis). Showing records 1 – 30 of 608 total matches.

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1. Khare, Shikha. Chemopreventive action of purified herbal agents in animal models of carcinogenesis.

Degree: 2005, Jamia Hamdard University

newline Advisors/Committee Members: Athar, Mohammad.

Subjects/Keywords: carcinogenesis

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

APA (6th Edition):

Khare, S. (2005). Chemopreventive action of purified herbal agents in animal models of carcinogenesis. (Thesis). Jamia Hamdard University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/37388

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):

Khare, Shikha. “Chemopreventive action of purified herbal agents in animal models of carcinogenesis.” 2005. Thesis, Jamia Hamdard University. Accessed June 26, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/37388.

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

MLA Handbook (7th Edition):

Khare, Shikha. “Chemopreventive action of purified herbal agents in animal models of carcinogenesis.” 2005. Web. 26 Jun 2019.

Vancouver:

Khare S. Chemopreventive action of purified herbal agents in animal models of carcinogenesis. [Internet] [Thesis]. Jamia Hamdard University; 2005. [cited 2019 Jun 26]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37388.

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

Council of Science Editors:

Khare S. Chemopreventive action of purified herbal agents in animal models of carcinogenesis. [Thesis]. Jamia Hamdard University; 2005. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37388

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


Oregon State University

2. Orner, Gayle A. Dehydroepiandrosterone carcinogenesis and tumor modulating effects in trout.

Degree: PhD, Toxicology, 1995, Oregon State University

Subjects/Keywords: Carcinogenesis

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APA (6th Edition):

Orner, G. A. (1995). Dehydroepiandrosterone carcinogenesis and tumor modulating effects in trout. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/34877

Chicago Manual of Style (16th Edition):

Orner, Gayle A. “Dehydroepiandrosterone carcinogenesis and tumor modulating effects in trout.” 1995. Doctoral Dissertation, Oregon State University. Accessed June 26, 2019. http://hdl.handle.net/1957/34877.

MLA Handbook (7th Edition):

Orner, Gayle A. “Dehydroepiandrosterone carcinogenesis and tumor modulating effects in trout.” 1995. Web. 26 Jun 2019.

Vancouver:

Orner GA. Dehydroepiandrosterone carcinogenesis and tumor modulating effects in trout. [Internet] [Doctoral dissertation]. Oregon State University; 1995. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/1957/34877.

Council of Science Editors:

Orner GA. Dehydroepiandrosterone carcinogenesis and tumor modulating effects in trout. [Doctoral Dissertation]. Oregon State University; 1995. Available from: http://hdl.handle.net/1957/34877


Michigan State University

3. Mugera, G. M. (Gerald Munene). Cycad toxicosis and related carcinogenesis in animals.

Degree: PhD, Department of Pathology, 1965, Michigan State University

Subjects/Keywords: Carcinogenesis

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APA (6th Edition):

Mugera, G. M. (. M. (1965). Cycad toxicosis and related carcinogenesis in animals. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:35146

Chicago Manual of Style (16th Edition):

Mugera, G M (Gerald Munene). “Cycad toxicosis and related carcinogenesis in animals.” 1965. Doctoral Dissertation, Michigan State University. Accessed June 26, 2019. http://etd.lib.msu.edu/islandora/object/etd:35146.

MLA Handbook (7th Edition):

Mugera, G M (Gerald Munene). “Cycad toxicosis and related carcinogenesis in animals.” 1965. Web. 26 Jun 2019.

Vancouver:

Mugera GM(M. Cycad toxicosis and related carcinogenesis in animals. [Internet] [Doctoral dissertation]. Michigan State University; 1965. [cited 2019 Jun 26]. Available from: http://etd.lib.msu.edu/islandora/object/etd:35146.

Council of Science Editors:

Mugera GM(M. Cycad toxicosis and related carcinogenesis in animals. [Doctoral Dissertation]. Michigan State University; 1965. Available from: http://etd.lib.msu.edu/islandora/object/etd:35146


Hong Kong University of Science and Technology

4. Yang, Lei. Understanding the role of RGS20 in tumorigenesis and metastasis.

Degree: 2012, Hong Kong University of Science and Technology

 RGS (regulator of G protein signaling) proteins serve as negative regulators of G protein signaling. Since the discovery of the first RGS protein, more than… (more)

Subjects/Keywords: G proteins; Carcinogenesis

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APA (6th Edition):

Yang, L. (2012). Understanding the role of RGS20 in tumorigenesis and metastasis. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1190240 ; http://repository.ust.hk/ir/bitstream/1783.1-63087/1/th_redirect.html

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):

Yang, Lei. “Understanding the role of RGS20 in tumorigenesis and metastasis.” 2012. Thesis, Hong Kong University of Science and Technology. Accessed June 26, 2019. https://doi.org/10.14711/thesis-b1190240 ; http://repository.ust.hk/ir/bitstream/1783.1-63087/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Yang, Lei. “Understanding the role of RGS20 in tumorigenesis and metastasis.” 2012. Web. 26 Jun 2019.

Vancouver:

Yang L. Understanding the role of RGS20 in tumorigenesis and metastasis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2019 Jun 26]. Available from: https://doi.org/10.14711/thesis-b1190240 ; http://repository.ust.hk/ir/bitstream/1783.1-63087/1/th_redirect.html.

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

Council of Science Editors:

Yang L. Understanding the role of RGS20 in tumorigenesis and metastasis. [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: https://doi.org/10.14711/thesis-b1190240 ; http://repository.ust.hk/ir/bitstream/1783.1-63087/1/th_redirect.html

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


University of Limerick

5. Hayes, Christopher J. The utilisation of microfluidic qPCR technology for the identification of novel cancer biomarkers.

Degree: 2017, University of Limerick

peer-reviewed

Cancer is a major cause of death worldwide causing 1 in 6 deaths globally with approximately 14 million new cases and 8.8 million cancer… (more)

Subjects/Keywords: cancer; Ireland; carcinogenesis; biomarkers; genetic

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APA (6th Edition):

Hayes, C. J. (2017). The utilisation of microfluidic qPCR technology for the identification of novel cancer biomarkers. (Thesis). University of Limerick. Retrieved from http://hdl.handle.net/10344/6556

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):

Hayes, Christopher J. “The utilisation of microfluidic qPCR technology for the identification of novel cancer biomarkers.” 2017. Thesis, University of Limerick. Accessed June 26, 2019. http://hdl.handle.net/10344/6556.

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

MLA Handbook (7th Edition):

Hayes, Christopher J. “The utilisation of microfluidic qPCR technology for the identification of novel cancer biomarkers.” 2017. Web. 26 Jun 2019.

Vancouver:

Hayes CJ. The utilisation of microfluidic qPCR technology for the identification of novel cancer biomarkers. [Internet] [Thesis]. University of Limerick; 2017. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/10344/6556.

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

Council of Science Editors:

Hayes CJ. The utilisation of microfluidic qPCR technology for the identification of novel cancer biomarkers. [Thesis]. University of Limerick; 2017. Available from: http://hdl.handle.net/10344/6556

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

6. Nayeem Bilal. Biochemical studies on the effects of chronic unpredictable stress on nitrosamine induced carcinogenesis; -.

Degree: Biochemistry, 2013, Aligarh Muslim University

None

Bibliography given

Advisors/Committee Members: Naheed Banu.

Subjects/Keywords: biochemistry; Carcinogenesis

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APA (6th Edition):

Bilal, N. (2013). Biochemical studies on the effects of chronic unpredictable stress on nitrosamine induced carcinogenesis; -. (Thesis). Aligarh Muslim University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/12844

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):

Bilal, Nayeem. “Biochemical studies on the effects of chronic unpredictable stress on nitrosamine induced carcinogenesis; -.” 2013. Thesis, Aligarh Muslim University. Accessed June 26, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/12844.

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

MLA Handbook (7th Edition):

Bilal, Nayeem. “Biochemical studies on the effects of chronic unpredictable stress on nitrosamine induced carcinogenesis; -.” 2013. Web. 26 Jun 2019.

Vancouver:

Bilal N. Biochemical studies on the effects of chronic unpredictable stress on nitrosamine induced carcinogenesis; -. [Internet] [Thesis]. Aligarh Muslim University; 2013. [cited 2019 Jun 26]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12844.

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

Council of Science Editors:

Bilal N. Biochemical studies on the effects of chronic unpredictable stress on nitrosamine induced carcinogenesis; -. [Thesis]. Aligarh Muslim University; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12844

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

7. Nida Suhail. Biochemical studies on the effect of stress on DMBA -TPA induced carcinogenesis; -.

Degree: Biochemistry, 2013, Aligarh Muslim University

Cancer is one of the leading causes of death in most well developed countries. It has been established that multiple stepwise alterations of the original… (more)

Subjects/Keywords: biochemistry; Carcinogenesis; Chemoprevention; Stress

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APA (6th Edition):

Suhail, N. (2013). Biochemical studies on the effect of stress on DMBA -TPA induced carcinogenesis; -. (Thesis). Aligarh Muslim University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/12846

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):

Suhail, Nida. “Biochemical studies on the effect of stress on DMBA -TPA induced carcinogenesis; -.” 2013. Thesis, Aligarh Muslim University. Accessed June 26, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/12846.

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

MLA Handbook (7th Edition):

Suhail, Nida. “Biochemical studies on the effect of stress on DMBA -TPA induced carcinogenesis; -.” 2013. Web. 26 Jun 2019.

Vancouver:

Suhail N. Biochemical studies on the effect of stress on DMBA -TPA induced carcinogenesis; -. [Internet] [Thesis]. Aligarh Muslim University; 2013. [cited 2019 Jun 26]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12846.

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

Council of Science Editors:

Suhail N. Biochemical studies on the effect of stress on DMBA -TPA induced carcinogenesis; -. [Thesis]. Aligarh Muslim University; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12846

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


NSYSU

8. Huang, Jian-yuan. Investigation of the Homeobox (HOX) gene expression in human gastric carcinogenesis.

Degree: Master, Institute of Biomedical Sciences, 2009, NSYSU

 In the past study, we used a human gastric stem cell clone, KMU-GI2, isolated from endoscopically biopsied gastric mucosa. As we maintained this KMU-GI2 cell… (more)

Subjects/Keywords: HOX; Homeobox; gastric carcinogenesis

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APA (6th Edition):

Huang, J. (2009). Investigation of the Homeobox (HOX) gene expression in human gastric carcinogenesis. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0623109-181128

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):

Huang, Jian-yuan. “Investigation of the Homeobox (HOX) gene expression in human gastric carcinogenesis.” 2009. Thesis, NSYSU. Accessed June 26, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0623109-181128.

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

MLA Handbook (7th Edition):

Huang, Jian-yuan. “Investigation of the Homeobox (HOX) gene expression in human gastric carcinogenesis.” 2009. Web. 26 Jun 2019.

Vancouver:

Huang J. Investigation of the Homeobox (HOX) gene expression in human gastric carcinogenesis. [Internet] [Thesis]. NSYSU; 2009. [cited 2019 Jun 26]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0623109-181128.

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

Council of Science Editors:

Huang J. Investigation of the Homeobox (HOX) gene expression in human gastric carcinogenesis. [Thesis]. NSYSU; 2009. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0623109-181128

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


Cape Peninsula University of Technology

9. Petrova, Antoinette. Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms .

Degree: 2009, Cape Peninsula University of Technology

 This thesis provides the first scientific evidence of the photoprotective properties of rooibos and honeybush herbal tea extracts and to some extent, two major honeybush… (more)

Subjects/Keywords: rooibos; honeybush; carcinogenesis; mouse model

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APA (6th Edition):

Petrova, A. (2009). Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms . (Thesis). Cape Peninsula University of Technology. Retrieved from http://etd.cput.ac.za/handle/20.500.11838/1487

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):

Petrova, Antoinette. “Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms .” 2009. Thesis, Cape Peninsula University of Technology. Accessed June 26, 2019. http://etd.cput.ac.za/handle/20.500.11838/1487.

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

MLA Handbook (7th Edition):

Petrova, Antoinette. “Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms .” 2009. Web. 26 Jun 2019.

Vancouver:

Petrova A. Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms . [Internet] [Thesis]. Cape Peninsula University of Technology; 2009. [cited 2019 Jun 26]. Available from: http://etd.cput.ac.za/handle/20.500.11838/1487.

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

Council of Science Editors:

Petrova A. Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms . [Thesis]. Cape Peninsula University of Technology; 2009. Available from: http://etd.cput.ac.za/handle/20.500.11838/1487

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


University of Hong Kong

10. 胡晓斌; Hu, Xiaobin. The role of Uhrf1 in development and tumorigenesis.

Degree: PhD, 2014, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Ubiquitin; Carcinogenesis

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APA (6th Edition):

胡晓斌; Hu, X. (2014). The role of Uhrf1 in development and tumorigenesis. (Doctoral Dissertation). University of Hong Kong. Retrieved from Hu, X. [胡晓斌]. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736666 ; http://hdl.handle.net/10722/225205

Chicago Manual of Style (16th Edition):

胡晓斌; Hu, Xiaobin. “The role of Uhrf1 in development and tumorigenesis.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed June 26, 2019. Hu, X. [胡晓斌]. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736666 ; http://hdl.handle.net/10722/225205.

MLA Handbook (7th Edition):

胡晓斌; Hu, Xiaobin. “The role of Uhrf1 in development and tumorigenesis.” 2014. Web. 26 Jun 2019.

Vancouver:

胡晓斌; Hu X. The role of Uhrf1 in development and tumorigenesis. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2019 Jun 26]. Available from: Hu, X. [胡晓斌]. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736666 ; http://hdl.handle.net/10722/225205.

Council of Science Editors:

胡晓斌; Hu X. The role of Uhrf1 in development and tumorigenesis. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Hu, X. [胡晓斌]. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736666 ; http://hdl.handle.net/10722/225205


Hong Kong University of Science and Technology

11. Wang, Yingchun. RGS19 inhibits oncogene-induced neoplastic transformation.

Degree: 2010, Hong Kong University of Science and Technology

 Many growth factors stimulate cell proliferation through mitogenic pathways such as the Ras/Raf/MEK/ERK cascade. Defective Ras signaling has long been associated with cancer progression and… (more)

Subjects/Keywords: G proteins; Cell transformation; Carcinogenesis

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APA (6th Edition):

Wang, Y. (2010). RGS19 inhibits oncogene-induced neoplastic transformation. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1115676 ; http://repository.ust.hk/ir/bitstream/1783.1-7545/1/th_redirect.html

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):

Wang, Yingchun. “RGS19 inhibits oncogene-induced neoplastic transformation.” 2010. Thesis, Hong Kong University of Science and Technology. Accessed June 26, 2019. https://doi.org/10.14711/thesis-b1115676 ; http://repository.ust.hk/ir/bitstream/1783.1-7545/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Wang, Yingchun. “RGS19 inhibits oncogene-induced neoplastic transformation.” 2010. Web. 26 Jun 2019.

Vancouver:

Wang Y. RGS19 inhibits oncogene-induced neoplastic transformation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2010. [cited 2019 Jun 26]. Available from: https://doi.org/10.14711/thesis-b1115676 ; http://repository.ust.hk/ir/bitstream/1783.1-7545/1/th_redirect.html.

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

Council of Science Editors:

Wang Y. RGS19 inhibits oncogene-induced neoplastic transformation. [Thesis]. Hong Kong University of Science and Technology; 2010. Available from: https://doi.org/10.14711/thesis-b1115676 ; http://repository.ust.hk/ir/bitstream/1783.1-7545/1/th_redirect.html

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

12. Papanagnou, Panagiota. Διερεύνηση του μηχανισμού δράσης των ογκοκατασταλτικών πρωτεϊνών p21WAF1/CIP1 και ARF.

Degree: 2014, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

P21WAF1/CIP1 is a universal cyclin-dependent kinase inhibitor and plays a crucial role in the DNA damage response (DDR) pathway. P21WAF1/CIP1 is a multifunctional molecule whose… (more)

Subjects/Keywords: Καρκινογένεση; Carcinogenesis; P21WAF1/Cip1; ARF

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APA (6th Edition):

Papanagnou, P. (2014). Διερεύνηση του μηχανισμού δράσης των ογκοκατασταλτικών πρωτεϊνών p21WAF1/CIP1 και ARF. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/41756

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):

Papanagnou, Panagiota. “Διερεύνηση του μηχανισμού δράσης των ογκοκατασταλτικών πρωτεϊνών p21WAF1/CIP1 και ARF.” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed June 26, 2019. http://hdl.handle.net/10442/hedi/41756.

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

MLA Handbook (7th Edition):

Papanagnou, Panagiota. “Διερεύνηση του μηχανισμού δράσης των ογκοκατασταλτικών πρωτεϊνών p21WAF1/CIP1 και ARF.” 2014. Web. 26 Jun 2019.

Vancouver:

Papanagnou P. Διερεύνηση του μηχανισμού δράσης των ογκοκατασταλτικών πρωτεϊνών p21WAF1/CIP1 και ARF. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/10442/hedi/41756.

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

Council of Science Editors:

Papanagnou P. Διερεύνηση του μηχανισμού δράσης των ογκοκατασταλτικών πρωτεϊνών p21WAF1/CIP1 και ARF. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/41756

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


University of British Columbia

13. Hanham, Ann Frances. The clastogenic activity of phenolic oxidation products .

Degree: 1983, University of British Columbia

 Several epidemiological studies .have demonstrated the importance of diet in the development of gastro-intestinal carcinomas in man. This study examines the role of plant phenolics,… (more)

Subjects/Keywords: Phenols; Carcinogenesis

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APA (6th Edition):

Hanham, A. F. (1983). The clastogenic activity of phenolic oxidation products . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/24298

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):

Hanham, Ann Frances. “The clastogenic activity of phenolic oxidation products .” 1983. Thesis, University of British Columbia. Accessed June 26, 2019. http://hdl.handle.net/2429/24298.

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

MLA Handbook (7th Edition):

Hanham, Ann Frances. “The clastogenic activity of phenolic oxidation products .” 1983. Web. 26 Jun 2019.

Vancouver:

Hanham AF. The clastogenic activity of phenolic oxidation products . [Internet] [Thesis]. University of British Columbia; 1983. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2429/24298.

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

Council of Science Editors:

Hanham AF. The clastogenic activity of phenolic oxidation products . [Thesis]. University of British Columbia; 1983. Available from: http://hdl.handle.net/2429/24298

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


Euskal Herriko Unibertsitatea / Universidad del País Vasco

14. Varela González, Pedro. Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales .

Degree: 2015, Euskal Herriko Unibertsitatea / Universidad del País Vasco

 En el presente trabajo de tesis doctoral se realizó un análisis de 3 enzimas convertidoras de angiotensina (ACE, ACE2 y APA) en diferentes histotipos de… (more)

Subjects/Keywords: carcinogenesis; oncology; carcinogénesis; oncología

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APA (6th Edition):

Varela González, P. (2015). Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales . (Doctoral Dissertation). Euskal Herriko Unibertsitatea / Universidad del País Vasco. Retrieved from http://hdl.handle.net/10810/16778

Chicago Manual of Style (16th Edition):

Varela González, Pedro. “Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales .” 2015. Doctoral Dissertation, Euskal Herriko Unibertsitatea / Universidad del País Vasco. Accessed June 26, 2019. http://hdl.handle.net/10810/16778.

MLA Handbook (7th Edition):

Varela González, Pedro. “Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales .” 2015. Web. 26 Jun 2019.

Vancouver:

Varela González P. Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales . [Internet] [Doctoral dissertation]. Euskal Herriko Unibertsitatea / Universidad del País Vasco; 2015. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/10810/16778.

Council of Science Editors:

Varela González P. Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales . [Doctoral Dissertation]. Euskal Herriko Unibertsitatea / Universidad del País Vasco; 2015. Available from: http://hdl.handle.net/10810/16778


Michigan State University

15. Baranyi, Bonnie Lynn. Factors involved in target specificity of the hepatocarcinogen N-2-acetylaminofluorene with regard to cell type and location within the genome.

Degree: PhD, Department of Pharmacology and Toxicology, 1982, Michigan State University

Subjects/Keywords: Carcinogens; Carcinogenesis

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APA (6th Edition):

Baranyi, B. L. (1982). Factors involved in target specificity of the hepatocarcinogen N-2-acetylaminofluorene with regard to cell type and location within the genome. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:34585

Chicago Manual of Style (16th Edition):

Baranyi, Bonnie Lynn. “Factors involved in target specificity of the hepatocarcinogen N-2-acetylaminofluorene with regard to cell type and location within the genome.” 1982. Doctoral Dissertation, Michigan State University. Accessed June 26, 2019. http://etd.lib.msu.edu/islandora/object/etd:34585.

MLA Handbook (7th Edition):

Baranyi, Bonnie Lynn. “Factors involved in target specificity of the hepatocarcinogen N-2-acetylaminofluorene with regard to cell type and location within the genome.” 1982. Web. 26 Jun 2019.

Vancouver:

Baranyi BL. Factors involved in target specificity of the hepatocarcinogen N-2-acetylaminofluorene with regard to cell type and location within the genome. [Internet] [Doctoral dissertation]. Michigan State University; 1982. [cited 2019 Jun 26]. Available from: http://etd.lib.msu.edu/islandora/object/etd:34585.

Council of Science Editors:

Baranyi BL. Factors involved in target specificity of the hepatocarcinogen N-2-acetylaminofluorene with regard to cell type and location within the genome. [Doctoral Dissertation]. Michigan State University; 1982. Available from: http://etd.lib.msu.edu/islandora/object/etd:34585


Columbia University

16. Henckels, Eric Patrick. Regulation of Matrix Metallopeptidase-1 in Breast Cancer Metastasis.

Degree: 2013, Columbia University

 Matrix Metallopeptidase 1 (MMP-1) expression has repeatedly been correlated to tumorigenesis and metastasis. Yet, MMP-1 regulation in a metastatic context remains largely unknown. Here we… (more)

Subjects/Keywords: Oncology; Metastasis; Carcinogenesis; Breast – Cancer

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APA (6th Edition):

Henckels, E. P. (2013). Regulation of Matrix Metallopeptidase-1 in Breast Cancer Metastasis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8TT4Z9W

Chicago Manual of Style (16th Edition):

Henckels, Eric Patrick. “Regulation of Matrix Metallopeptidase-1 in Breast Cancer Metastasis.” 2013. Doctoral Dissertation, Columbia University. Accessed June 26, 2019. https://doi.org/10.7916/D8TT4Z9W.

MLA Handbook (7th Edition):

Henckels, Eric Patrick. “Regulation of Matrix Metallopeptidase-1 in Breast Cancer Metastasis.” 2013. Web. 26 Jun 2019.

Vancouver:

Henckels EP. Regulation of Matrix Metallopeptidase-1 in Breast Cancer Metastasis. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2019 Jun 26]. Available from: https://doi.org/10.7916/D8TT4Z9W.

Council of Science Editors:

Henckels EP. Regulation of Matrix Metallopeptidase-1 in Breast Cancer Metastasis. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8TT4Z9W


University of Florida

17. Hiller, Joshua P. On Some Variations of the Multistage Model of Carcinogenesis.

Degree: PhD, Mathematics, 2017, University of Florida

 The multistage model of carcinogenesis has been a hallmark of mathematical cancer modeling for over 60 years. In this work we explore several problems related… (more)

Subjects/Keywords: cancer  – carcinogenesis  – incidence  – markov

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APA (6th Edition):

Hiller, J. P. (2017). On Some Variations of the Multistage Model of Carcinogenesis. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0051242

Chicago Manual of Style (16th Edition):

Hiller, Joshua P. “On Some Variations of the Multistage Model of Carcinogenesis.” 2017. Doctoral Dissertation, University of Florida. Accessed June 26, 2019. http://ufdc.ufl.edu/UFE0051242.

MLA Handbook (7th Edition):

Hiller, Joshua P. “On Some Variations of the Multistage Model of Carcinogenesis.” 2017. Web. 26 Jun 2019.

Vancouver:

Hiller JP. On Some Variations of the Multistage Model of Carcinogenesis. [Internet] [Doctoral dissertation]. University of Florida; 2017. [cited 2019 Jun 26]. Available from: http://ufdc.ufl.edu/UFE0051242.

Council of Science Editors:

Hiller JP. On Some Variations of the Multistage Model of Carcinogenesis. [Doctoral Dissertation]. University of Florida; 2017. Available from: http://ufdc.ufl.edu/UFE0051242


University of Southern California

18. Shahin, Sophia Allaf. Ascorbate and dehydroascorbate enhance the cytotoxicity and morphological transformation of C3H/10T½ C1 8 mouse embryo cells induced by soluble chromium (VI) compounds.

Degree: MS, Experimental and Molecular Pathology, 2014, University of Southern California

 Hexavalent chromium [Cr(VI)]‐containing compounds are human carcinogens. They cause cancers in the respiratory system when inhaled, and stomach, kidney/other internal cancers when ingested. Soluble and… (more)

Subjects/Keywords: chemical; chromium; physical carcinogenesis

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APA (6th Edition):

Shahin, S. A. (2014). Ascorbate and dehydroascorbate enhance the cytotoxicity and morphological transformation of C3H/10T½ C1 8 mouse embryo cells induced by soluble chromium (VI) compounds. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385505/rec/923

Chicago Manual of Style (16th Edition):

Shahin, Sophia Allaf. “Ascorbate and dehydroascorbate enhance the cytotoxicity and morphological transformation of C3H/10T½ C1 8 mouse embryo cells induced by soluble chromium (VI) compounds.” 2014. Masters Thesis, University of Southern California. Accessed June 26, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385505/rec/923.

MLA Handbook (7th Edition):

Shahin, Sophia Allaf. “Ascorbate and dehydroascorbate enhance the cytotoxicity and morphological transformation of C3H/10T½ C1 8 mouse embryo cells induced by soluble chromium (VI) compounds.” 2014. Web. 26 Jun 2019.

Vancouver:

Shahin SA. Ascorbate and dehydroascorbate enhance the cytotoxicity and morphological transformation of C3H/10T½ C1 8 mouse embryo cells induced by soluble chromium (VI) compounds. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2019 Jun 26]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385505/rec/923.

Council of Science Editors:

Shahin SA. Ascorbate and dehydroascorbate enhance the cytotoxicity and morphological transformation of C3H/10T½ C1 8 mouse embryo cells induced by soluble chromium (VI) compounds. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385505/rec/923


University of New South Wales

19. Kalyuga , Maria. Exploration of the role of the ETS transcription factor ESE2 in breast cancer.

Degree: Clinical School - St Vincent's Hospital, 2011, University of New South Wales

 Thesis abstract: Breast cancer represents a leading cancer-related diagnosis of Australian women, with treatments ultimately still ineffective for many patients. Investigating the mechanisms behind normal… (more)

Subjects/Keywords: Breast cancer; Human breast carcinogenesis

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APA (6th Edition):

Kalyuga , M. (2011). Exploration of the role of the ETS transcription factor ESE2 in breast cancer. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51251 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9903/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Kalyuga , Maria. “Exploration of the role of the ETS transcription factor ESE2 in breast cancer.” 2011. Doctoral Dissertation, University of New South Wales. Accessed June 26, 2019. http://handle.unsw.edu.au/1959.4/51251 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9903/SOURCE02?view=true.

MLA Handbook (7th Edition):

Kalyuga , Maria. “Exploration of the role of the ETS transcription factor ESE2 in breast cancer.” 2011. Web. 26 Jun 2019.

Vancouver:

Kalyuga M. Exploration of the role of the ETS transcription factor ESE2 in breast cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2019 Jun 26]. Available from: http://handle.unsw.edu.au/1959.4/51251 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9903/SOURCE02?view=true.

Council of Science Editors:

Kalyuga M. Exploration of the role of the ETS transcription factor ESE2 in breast cancer. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51251 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9903/SOURCE02?view=true


University of Texas Southwestern Medical Center

20. Lee, Eunmyong. The Role of Autophagy in Early Development and Tumor Suppression Using a Zebrafish Model System.

Degree: 2013, University of Texas Southwestern Medical Center

 Autophagy is an evolutionarily conserved lysosomal degradation pathway which involves the sequestration of cytoplasmic components into a double membraned structure called the autophagosome. By using… (more)

Subjects/Keywords: Autophagy; Carcinogenesis; Morphogenesis; Zebrafish

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APA (6th Edition):

Lee, E. (2013). The Role of Autophagy in Early Development and Tumor Suppression Using a Zebrafish Model System. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1738

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):

Lee, Eunmyong. “The Role of Autophagy in Early Development and Tumor Suppression Using a Zebrafish Model System.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed June 26, 2019. http://hdl.handle.net/2152.5/1738.

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

MLA Handbook (7th Edition):

Lee, Eunmyong. “The Role of Autophagy in Early Development and Tumor Suppression Using a Zebrafish Model System.” 2013. Web. 26 Jun 2019.

Vancouver:

Lee E. The Role of Autophagy in Early Development and Tumor Suppression Using a Zebrafish Model System. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2152.5/1738.

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

Council of Science Editors:

Lee E. The Role of Autophagy in Early Development and Tumor Suppression Using a Zebrafish Model System. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1738

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


Penn State University

21. Markell, Lauren Mordasky. PHARMACOLOGICAL INHIBITION OF THE TGF-BETA TYPE I RECEPTOR REVEALS A DUAL ROLE OF TGF-BETA IN CARCINOGENESIS.

Degree: PhD, Integrative Biosciences, 2010, Penn State University

 Transforming growth factor-beta 1 (TGF-beta 1) is a member of a large family of regulatory molecules that play both positive and negative roles in epithelial… (more)

Subjects/Keywords: skin; skin carcinogenesis; TGF-beta; chemically-induced carcinogenesis

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APA (6th Edition):

Markell, L. M. (2010). PHARMACOLOGICAL INHIBITION OF THE TGF-BETA TYPE I RECEPTOR REVEALS A DUAL ROLE OF TGF-BETA IN CARCINOGENESIS. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11358

Chicago Manual of Style (16th Edition):

Markell, Lauren Mordasky. “PHARMACOLOGICAL INHIBITION OF THE TGF-BETA TYPE I RECEPTOR REVEALS A DUAL ROLE OF TGF-BETA IN CARCINOGENESIS.” 2010. Doctoral Dissertation, Penn State University. Accessed June 26, 2019. https://etda.libraries.psu.edu/catalog/11358.

MLA Handbook (7th Edition):

Markell, Lauren Mordasky. “PHARMACOLOGICAL INHIBITION OF THE TGF-BETA TYPE I RECEPTOR REVEALS A DUAL ROLE OF TGF-BETA IN CARCINOGENESIS.” 2010. Web. 26 Jun 2019.

Vancouver:

Markell LM. PHARMACOLOGICAL INHIBITION OF THE TGF-BETA TYPE I RECEPTOR REVEALS A DUAL ROLE OF TGF-BETA IN CARCINOGENESIS. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2019 Jun 26]. Available from: https://etda.libraries.psu.edu/catalog/11358.

Council of Science Editors:

Markell LM. PHARMACOLOGICAL INHIBITION OF THE TGF-BETA TYPE I RECEPTOR REVEALS A DUAL ROLE OF TGF-BETA IN CARCINOGENESIS. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11358


University of Arizona

22. JAFFE, DEBORAH RUTH. MOUSE SKIN TUMOR INITIATION BY IONIZING RADIATION AND THE DETECTION OF DOMINANT TRANSFORMING GENE(S).

Degree: 1987, University of Arizona

 The initiating potential of a range of 4 MeV X-rays was studied using the mouse skin two-stage model of carcinogenesis. A single dose of radiation… (more)

Subjects/Keywords: Radiation carcinogenesis.; Ionizing radiation.; Carcinogenesis.

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APA (6th Edition):

JAFFE, D. R. (1987). MOUSE SKIN TUMOR INITIATION BY IONIZING RADIATION AND THE DETECTION OF DOMINANT TRANSFORMING GENE(S). (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/184146

Chicago Manual of Style (16th Edition):

JAFFE, DEBORAH RUTH. “MOUSE SKIN TUMOR INITIATION BY IONIZING RADIATION AND THE DETECTION OF DOMINANT TRANSFORMING GENE(S). ” 1987. Doctoral Dissertation, University of Arizona. Accessed June 26, 2019. http://hdl.handle.net/10150/184146.

MLA Handbook (7th Edition):

JAFFE, DEBORAH RUTH. “MOUSE SKIN TUMOR INITIATION BY IONIZING RADIATION AND THE DETECTION OF DOMINANT TRANSFORMING GENE(S). ” 1987. Web. 26 Jun 2019.

Vancouver:

JAFFE DR. MOUSE SKIN TUMOR INITIATION BY IONIZING RADIATION AND THE DETECTION OF DOMINANT TRANSFORMING GENE(S). [Internet] [Doctoral dissertation]. University of Arizona; 1987. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/10150/184146.

Council of Science Editors:

JAFFE DR. MOUSE SKIN TUMOR INITIATION BY IONIZING RADIATION AND THE DETECTION OF DOMINANT TRANSFORMING GENE(S). [Doctoral Dissertation]. University of Arizona; 1987. Available from: http://hdl.handle.net/10150/184146


Penn State University

23. Bility, Moses Turkle. MODULATION OF SKIN CANCER BY PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA.

Degree: PhD, Integrative Biosciences, 2008, Penn State University

 Pparb/d-null mice exhibit enhanced tumorigenesis in a two-stage carcinogenesis bioassay model when compared to wild-type mice, which is likely due in part to enhanced epidermal… (more)

Subjects/Keywords: PPARb/d; nuclear receptors; v-rasHa-induced skin carcinogenesis; chemically-induced skin carcinogenesis; skin carcinogenesis; PPARs

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APA (6th Edition):

Bility, M. T. (2008). MODULATION OF SKIN CANCER BY PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9430

Chicago Manual of Style (16th Edition):

Bility, Moses Turkle. “MODULATION OF SKIN CANCER BY PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA.” 2008. Doctoral Dissertation, Penn State University. Accessed June 26, 2019. https://etda.libraries.psu.edu/catalog/9430.

MLA Handbook (7th Edition):

Bility, Moses Turkle. “MODULATION OF SKIN CANCER BY PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA.” 2008. Web. 26 Jun 2019.

Vancouver:

Bility MT. MODULATION OF SKIN CANCER BY PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2019 Jun 26]. Available from: https://etda.libraries.psu.edu/catalog/9430.

Council of Science Editors:

Bility MT. MODULATION OF SKIN CANCER BY PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/9430


The Ohio State University

24. Chang, Ming Jen Wu. Molecular basis for the neoplastic transformation of neuroectodermal cells by N-nitrosoureas.

Degree: PhD, Graduate School, 1978, The Ohio State University

Subjects/Keywords: Chemistry; Nitrosoureas; Carcinogenesis

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APA (6th Edition):

Chang, M. J. W. (1978). Molecular basis for the neoplastic transformation of neuroectodermal cells by N-nitrosoureas. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487073463651824

Chicago Manual of Style (16th Edition):

Chang, Ming Jen Wu. “Molecular basis for the neoplastic transformation of neuroectodermal cells by N-nitrosoureas.” 1978. Doctoral Dissertation, The Ohio State University. Accessed June 26, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487073463651824.

MLA Handbook (7th Edition):

Chang, Ming Jen Wu. “Molecular basis for the neoplastic transformation of neuroectodermal cells by N-nitrosoureas.” 1978. Web. 26 Jun 2019.

Vancouver:

Chang MJW. Molecular basis for the neoplastic transformation of neuroectodermal cells by N-nitrosoureas. [Internet] [Doctoral dissertation]. The Ohio State University; 1978. [cited 2019 Jun 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487073463651824.

Council of Science Editors:

Chang MJW. Molecular basis for the neoplastic transformation of neuroectodermal cells by N-nitrosoureas. [Doctoral Dissertation]. The Ohio State University; 1978. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487073463651824

25. Soni, Bihari Lal. Global protein profiling during rat lingual carcinogenesis and validation of differentiator proteins in human tongue; -.

Degree: Life Science, 2015, INFLIBNET

None

Bibliography p.110 - 123 Appendix p.124 - 143 and Publication P.144

Advisors/Committee Members: Vaidya, Milind M.

Subjects/Keywords: Carcinogenesis; Global; Protein

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APA (6th Edition):

Soni, B. L. (2015). Global protein profiling during rat lingual carcinogenesis and validation of differentiator proteins in human tongue; -. (Thesis). INFLIBNET. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/49148

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):

Soni, Bihari Lal. “Global protein profiling during rat lingual carcinogenesis and validation of differentiator proteins in human tongue; -.” 2015. Thesis, INFLIBNET. Accessed June 26, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/49148.

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

MLA Handbook (7th Edition):

Soni, Bihari Lal. “Global protein profiling during rat lingual carcinogenesis and validation of differentiator proteins in human tongue; -.” 2015. Web. 26 Jun 2019.

Vancouver:

Soni BL. Global protein profiling during rat lingual carcinogenesis and validation of differentiator proteins in human tongue; -. [Internet] [Thesis]. INFLIBNET; 2015. [cited 2019 Jun 26]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/49148.

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

Council of Science Editors:

Soni BL. Global protein profiling during rat lingual carcinogenesis and validation of differentiator proteins in human tongue; -. [Thesis]. INFLIBNET; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/49148

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

26. Batazzi, Adriana. Elucidating the role of Keratin 17 in cervical carcinogenesis.

Degree: 2014, Johns Hopkins University

 Cervical malignancies develop when viral genes from high-risk strains of the Human Papilloma Virus (HPV) such as HPV type 16 and 18 are expressed in… (more)

Subjects/Keywords: Cervical Carcinogenesis; Keratin 17; Inflammatory Immune Response

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APA (6th Edition):

Batazzi, A. (2014). Elucidating the role of Keratin 17 in cervical carcinogenesis. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37211

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):

Batazzi, Adriana. “Elucidating the role of Keratin 17 in cervical carcinogenesis.” 2014. Thesis, Johns Hopkins University. Accessed June 26, 2019. http://jhir.library.jhu.edu/handle/1774.2/37211.

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

MLA Handbook (7th Edition):

Batazzi, Adriana. “Elucidating the role of Keratin 17 in cervical carcinogenesis.” 2014. Web. 26 Jun 2019.

Vancouver:

Batazzi A. Elucidating the role of Keratin 17 in cervical carcinogenesis. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2019 Jun 26]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37211.

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

Council of Science Editors:

Batazzi A. Elucidating the role of Keratin 17 in cervical carcinogenesis. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/37211

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


University of Hong Kong

27. Tee, Kah Meng. First detection of a phylogenetically distinct and highly prevalent human polyomavirus 6 in human bile samples.

Degree: M. Phil., 2017, University of Hong Kong

Oncovirus associated malignancies are potentially preventable diseases with major public health significance. Human polyomaviruses (HPyVs) may be associated with oncogenesis or symptomatic illnesses in immunocompromised… (more)

Subjects/Keywords: Pathogenesis - Cancer - Bile ducts; Polyomaviruses; Viral carcinogenesis

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APA (6th Edition):

Tee, K. M. (2017). First detection of a phylogenetically distinct and highly prevalent human polyomavirus 6 in human bile samples. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/244292

Chicago Manual of Style (16th Edition):

Tee, Kah Meng. “First detection of a phylogenetically distinct and highly prevalent human polyomavirus 6 in human bile samples.” 2017. Masters Thesis, University of Hong Kong. Accessed June 26, 2019. http://hdl.handle.net/10722/244292.

MLA Handbook (7th Edition):

Tee, Kah Meng. “First detection of a phylogenetically distinct and highly prevalent human polyomavirus 6 in human bile samples.” 2017. Web. 26 Jun 2019.

Vancouver:

Tee KM. First detection of a phylogenetically distinct and highly prevalent human polyomavirus 6 in human bile samples. [Internet] [Masters thesis]. University of Hong Kong; 2017. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/10722/244292.

Council of Science Editors:

Tee KM. First detection of a phylogenetically distinct and highly prevalent human polyomavirus 6 in human bile samples. [Masters Thesis]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/244292


University of Louisville

28. denDekker, Aaron D. Genetic mapping and mechanism of action of rat mammary carcinoma susceptibility quantitative trait locus Mcs1b.

Degree: PhD, 2013, University of Louisville

 Breast cancer is a complex disease that involves genetic, epigenetic, and environmental components. High and moderate penetrant genes have been identified that affect risk to… (more)

Subjects/Keywords: Breast cancer susceptibility; MIER3; Mammary carcinogenesis; Mcs1b

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APA (6th Edition):

denDekker, A. D. (2013). Genetic mapping and mechanism of action of rat mammary carcinoma susceptibility quantitative trait locus Mcs1b. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/330 ; https://ir.library.louisville.edu/etd/330

Chicago Manual of Style (16th Edition):

denDekker, Aaron D. “Genetic mapping and mechanism of action of rat mammary carcinoma susceptibility quantitative trait locus Mcs1b.” 2013. Doctoral Dissertation, University of Louisville. Accessed June 26, 2019. 10.18297/etd/330 ; https://ir.library.louisville.edu/etd/330.

MLA Handbook (7th Edition):

denDekker, Aaron D. “Genetic mapping and mechanism of action of rat mammary carcinoma susceptibility quantitative trait locus Mcs1b.” 2013. Web. 26 Jun 2019.

Vancouver:

denDekker AD. Genetic mapping and mechanism of action of rat mammary carcinoma susceptibility quantitative trait locus Mcs1b. [Internet] [Doctoral dissertation]. University of Louisville; 2013. [cited 2019 Jun 26]. Available from: 10.18297/etd/330 ; https://ir.library.louisville.edu/etd/330.

Council of Science Editors:

denDekker AD. Genetic mapping and mechanism of action of rat mammary carcinoma susceptibility quantitative trait locus Mcs1b. [Doctoral Dissertation]. University of Louisville; 2013. Available from: 10.18297/etd/330 ; https://ir.library.louisville.edu/etd/330


University of Hong Kong

29. 朱盈盈.; Chu, Ying-ying, Jamie. Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme.

Degree: PhD, 2011, University of Hong Kong

 Glioblastoma multiforme (GBMs) are the most common and severe form of malignant brain tumors. Despite recent advancement in the fields of surgical resection, radiotherapy and… (more)

Subjects/Keywords: Oncogenes.; Glioblastoma multiforme.; Carcinogenesis.; Cell cycle.

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APA (6th Edition):

朱盈盈.; Chu, Ying-ying, J. (2011). Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme. (Doctoral Dissertation). University of Hong Kong. Retrieved from Chu, Y. J. [朱盈盈]. (2011). Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784941 ; http://dx.doi.org/10.5353/th_b4784941 ; http://hdl.handle.net/10722/182308

Chicago Manual of Style (16th Edition):

朱盈盈.; Chu, Ying-ying, Jamie. “Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed June 26, 2019. Chu, Y. J. [朱盈盈]. (2011). Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784941 ; http://dx.doi.org/10.5353/th_b4784941 ; http://hdl.handle.net/10722/182308.

MLA Handbook (7th Edition):

朱盈盈.; Chu, Ying-ying, Jamie. “Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme.” 2011. Web. 26 Jun 2019.

Vancouver:

朱盈盈.; Chu, Ying-ying J. Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2019 Jun 26]. Available from: Chu, Y. J. [朱盈盈]. (2011). Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784941 ; http://dx.doi.org/10.5353/th_b4784941 ; http://hdl.handle.net/10722/182308.

Council of Science Editors:

朱盈盈.; Chu, Ying-ying J. Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: Chu, Y. J. [朱盈盈]. (2011). Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784941 ; http://dx.doi.org/10.5353/th_b4784941 ; http://hdl.handle.net/10722/182308


Penn State University

30. Borland, Michael Gregory. PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA MODULATES ARYL HYDROCARBON RECEPTOR-DEPENDENT SIGNALING AND SKIN CARCINOGENESIS.

Degree: PhD, Biochemistry, Microbiology, and Molecular Biology, 2010, Penn State University

 Since its identification in the early 1990fs, the physiological roles of the nuclear hormone receptor peroxisome proliferator-activated receptor-ƒÀ/ƒÂ (PPARƒÀ/ƒÂ) have become better understood. This ligand-activated… (more)

Subjects/Keywords: PPARBeta/Delta; AHR; PAH; Bioactivation; Skin carcinogenesis

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

APA (6th Edition):

Borland, M. G. (2010). PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA MODULATES ARYL HYDROCARBON RECEPTOR-DEPENDENT SIGNALING AND SKIN CARCINOGENESIS. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11381

Chicago Manual of Style (16th Edition):

Borland, Michael Gregory. “PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA MODULATES ARYL HYDROCARBON RECEPTOR-DEPENDENT SIGNALING AND SKIN CARCINOGENESIS.” 2010. Doctoral Dissertation, Penn State University. Accessed June 26, 2019. https://etda.libraries.psu.edu/catalog/11381.

MLA Handbook (7th Edition):

Borland, Michael Gregory. “PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA MODULATES ARYL HYDROCARBON RECEPTOR-DEPENDENT SIGNALING AND SKIN CARCINOGENESIS.” 2010. Web. 26 Jun 2019.

Vancouver:

Borland MG. PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA MODULATES ARYL HYDROCARBON RECEPTOR-DEPENDENT SIGNALING AND SKIN CARCINOGENESIS. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2019 Jun 26]. Available from: https://etda.libraries.psu.edu/catalog/11381.

Council of Science Editors:

Borland MG. PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA MODULATES ARYL HYDROCARBON RECEPTOR-DEPENDENT SIGNALING AND SKIN CARCINOGENESIS. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11381

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