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You searched for subject:(Carcinogenesis). Showing records 1 – 30 of 486 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Khare S. Chemopreventive action of purified herbal agents in animal models of carcinogenesis. [Internet] [Thesis]. Jamia Hamdard University; 2005. [cited 2017 Oct 24]. 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 October 24, 2017. http://hdl.handle.net/1957/34877.

MLA Handbook (7th Edition):

Orner, Gayle A. “Dehydroepiandrosterone carcinogenesis and tumor modulating effects in trout.” 1995. Web. 24 Oct 2017.

Vancouver:

Orner GA. Dehydroepiandrosterone carcinogenesis and tumor modulating effects in trout. [Internet] [Doctoral dissertation]. Oregon State University; 1995. [cited 2017 Oct 24]. 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


Hong Kong University of Science and Technology

3. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Yang L. Understanding the role of RGS20 in tumorigenesis and metastasis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2017 Oct 24]. 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 British Columbia

4. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Hanham AF. The clastogenic activity of phenolic oxidation products . [Internet] [Thesis]. University of British Columbia; 1983. [cited 2017 Oct 24]. 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

5. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Bilal N. Biochemical studies on the effects of chronic unpredictable stress on nitrosamine induced carcinogenesis; -. [Internet] [Thesis]. Aligarh Muslim University; 2013. [cited 2017 Oct 24]. 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

6. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Suhail N. Biochemical studies on the effect of stress on DMBA -TPA induced carcinogenesis; -. [Internet] [Thesis]. Aligarh Muslim University; 2013. [cited 2017 Oct 24]. 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


University of Southern California

7. 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/921

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 October 24, 2017. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385505/rec/921.

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. 24 Oct 2017.

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 2017 Oct 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385505/rec/921.

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/921


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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Huang J. Investigation of the Homeobox (HOX) gene expression in human gastric carcinogenesis. [Internet] [Thesis]. NSYSU; 2009. [cited 2017 Oct 24]. 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


University of Texas Southwestern Medical Center

9. 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 October 24, 2017. 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. 24 Oct 2017.

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 2017 Oct 24]. 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


Cape Peninsula University of Technology

10. 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 October 24, 2017. 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. 24 Oct 2017.

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 2017 Oct 24]. 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

11. 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: Carcinogenesis; Ubiquitin

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APA (6th Edition):

Hu, X. (2014). The role of Uhrf1 in development and tumorigenesis. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/225205

Chicago Manual of Style (16th Edition):

Hu, Xiaobin. “The role of Uhrf1 in development and tumorigenesis.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed October 24, 2017. http://hdl.handle.net/10722/225205.

MLA Handbook (7th Edition):

Hu, Xiaobin. “The role of Uhrf1 in development and tumorigenesis.” 2014. Web. 24 Oct 2017.

Vancouver:

Hu X. The role of Uhrf1 in development and tumorigenesis. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2017 Oct 24]. Available from: http://hdl.handle.net/10722/225205.

Council of Science Editors:

Hu X. The role of Uhrf1 in development and tumorigenesis. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: http://hdl.handle.net/10722/225205

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

Degree: 2016, 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. (2016). Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales. (Thesis). Universidad del País Vasco. Retrieved from http://hdl.handle.net/10810/16778

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):

Varela González, Pedro. “Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales.” 2016. Thesis, Universidad del País Vasco. Accessed October 24, 2017. http://hdl.handle.net/10810/16778.

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

MLA Handbook (7th Edition):

Varela González, Pedro. “Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales.” 2016. Web. 24 Oct 2017.

Vancouver:

Varela González P. Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales. [Internet] [Thesis]. Universidad del País Vasco; 2016. [cited 2017 Oct 24]. Available from: http://hdl.handle.net/10810/16778.

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

Council of Science Editors:

Varela González P. Actividad y expresión de enzimas convertidoras de angiotensina en neoplasias renales. [Thesis]. Universidad del País Vasco; 2016. Available from: http://hdl.handle.net/10810/16778

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


University of New South Wales

13. 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

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 October 24, 2017. http://handle.unsw.edu.au/1959.4/51251.

MLA Handbook (7th Edition):

Kalyuga , Maria. “Exploration of the role of the ETS transcription factor ESE2 in breast cancer.” 2011. Web. 24 Oct 2017.

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 2017 Oct 24]. Available from: http://handle.unsw.edu.au/1959.4/51251.

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


Hong Kong University of Science and Technology

14. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Wang Y. RGS19 inhibits oncogene-induced neoplastic transformation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2010. [cited 2017 Oct 24]. 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

15. 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 October 24, 2017. 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. 24 Oct 2017.

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 2017 Oct 24]. 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


Penn State University

16. 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 October 24, 2017. 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. 24 Oct 2017.

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 2017 Oct 24]. 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

17. 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 October 24, 2017. 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. 24 Oct 2017.

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 2017 Oct 24]. 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

18. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Bility MT. MODULATION OF SKIN CANCER BY PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR BETA/DELTA. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2017 Oct 24]. 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


West Virginia University

19. Vongsutilers, Vorasit. The effect of C8-arylguanine adducts on B/Z-DNA equilibrium.

Degree: 2009, West Virginia University

 Aryl hydrazines and related compounds have been shown to be carcinogenic but the mechanism is still unclear. C8-Arylguanine adducts, formed from oxidative metabolites of aryl… (more)

Subjects/Keywords: Hydrazines.; Carcinogenesis.; Hydrazines.; Carcinogens.; DNA, Z-Form.

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APA (6th Edition):

Vongsutilers, V. (2009). The effect of C8-arylguanine adducts on B/Z-DNA equilibrium. (Thesis). West Virginia University. Retrieved from http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=22151

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):

Vongsutilers, Vorasit. “The effect of C8-arylguanine adducts on B/Z-DNA equilibrium.” 2009. Thesis, West Virginia University. Accessed October 24, 2017. http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=22151.

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

MLA Handbook (7th Edition):

Vongsutilers, Vorasit. “The effect of C8-arylguanine adducts on B/Z-DNA equilibrium.” 2009. Web. 24 Oct 2017.

Vancouver:

Vongsutilers V. The effect of C8-arylguanine adducts on B/Z-DNA equilibrium. [Internet] [Thesis]. West Virginia University; 2009. [cited 2017 Oct 24]. Available from: http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=22151.

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

Council of Science Editors:

Vongsutilers V. The effect of C8-arylguanine adducts on B/Z-DNA equilibrium. [Thesis]. West Virginia University; 2009. Available from: http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=22151

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


The Ohio State University

20. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Chang MJW. Molecular basis for the neoplastic transformation of neuroectodermal cells by N-nitrosoureas. [Internet] [Doctoral dissertation]. The Ohio State University; 1978. [cited 2017 Oct 24]. 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

21. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Soni BL. Global protein profiling during rat lingual carcinogenesis and validation of differentiator proteins in human tongue; -. [Internet] [Thesis]. INFLIBNET; 2015. [cited 2017 Oct 24]. 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


University of Aberdeen

22. Nadal Catala, Gema. The differential ability of methylated folate and folic acid to maintain DNA stability and normal characteristics in human colon cells in vitro.

Degree: PhD, 2017, University of Aberdeen

 Folates are water-soluble B vitamins, which maintain DNA stability by regulating nucleotide synthesis and DNA methylation. Folates influence CRC risk and their ability to prevent… (more)

Subjects/Keywords: DNA; Methylation; Carcinogenesis; Folic acid; Colon (Anatomy)

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APA (6th Edition):

Nadal Catala, G. (2017). The differential ability of methylated folate and folic acid to maintain DNA stability and normal characteristics in human colon cells in vitro. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=231796 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715469

Chicago Manual of Style (16th Edition):

Nadal Catala, Gema. “The differential ability of methylated folate and folic acid to maintain DNA stability and normal characteristics in human colon cells in vitro.” 2017. Doctoral Dissertation, University of Aberdeen. Accessed October 24, 2017. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=231796 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715469.

MLA Handbook (7th Edition):

Nadal Catala, Gema. “The differential ability of methylated folate and folic acid to maintain DNA stability and normal characteristics in human colon cells in vitro.” 2017. Web. 24 Oct 2017.

Vancouver:

Nadal Catala G. The differential ability of methylated folate and folic acid to maintain DNA stability and normal characteristics in human colon cells in vitro. [Internet] [Doctoral dissertation]. University of Aberdeen; 2017. [cited 2017 Oct 24]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=231796 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715469.

Council of Science Editors:

Nadal Catala G. The differential ability of methylated folate and folic acid to maintain DNA stability and normal characteristics in human colon cells in vitro. [Doctoral Dissertation]. University of Aberdeen; 2017. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=231796 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715469


University of Gothenburg / Göteborgs Universitet

23. Wang, Wanzhong. INFLAMMATION AND PROSTATIC CARCINOGENESIS – A MORPHOLOGICAL STUDY OF THE HUMAN PROSTATE.

Degree: 2008, University of Gothenburg / Göteborgs Universitet

 Chronic inflammation has been suggested to be linked to cancers. Inflammatory infiltrates are often found in and around foci of prostatic atrophy. These foci, called… (more)

Subjects/Keywords: prostate; carcinogenesis; chronic inflammation; atrophy; morphology; immunohistochemistry

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APA (6th Edition):

Wang, W. (2008). INFLAMMATION AND PROSTATIC CARCINOGENESIS – A MORPHOLOGICAL STUDY OF THE HUMAN PROSTATE. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/9634

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, Wanzhong. “INFLAMMATION AND PROSTATIC CARCINOGENESIS – A MORPHOLOGICAL STUDY OF THE HUMAN PROSTATE.” 2008. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 24, 2017. http://hdl.handle.net/2077/9634.

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

MLA Handbook (7th Edition):

Wang, Wanzhong. “INFLAMMATION AND PROSTATIC CARCINOGENESIS – A MORPHOLOGICAL STUDY OF THE HUMAN PROSTATE.” 2008. Web. 24 Oct 2017.

Vancouver:

Wang W. INFLAMMATION AND PROSTATIC CARCINOGENESIS – A MORPHOLOGICAL STUDY OF THE HUMAN PROSTATE. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2008. [cited 2017 Oct 24]. Available from: http://hdl.handle.net/2077/9634.

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

Council of Science Editors:

Wang W. INFLAMMATION AND PROSTATIC CARCINOGENESIS – A MORPHOLOGICAL STUDY OF THE HUMAN PROSTATE. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2008. Available from: http://hdl.handle.net/2077/9634

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


Rutgers University

24. Wilimczyk, Barbara J. Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells.

Degree: MS, Microbiology and Molecular Genetics, 2009, Rutgers University

 Within the United States, skin cancer has become a predominant form of cancer that occurs across all age groups, racial backgrounds, and to both genders… (more)

Subjects/Keywords: Cancer cells – Proliferation; Carcinogenesis; Cancer – Treatment

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APA (6th Edition):

Wilimczyk, B. J. (2009). Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051419

Chicago Manual of Style (16th Edition):

Wilimczyk, Barbara J. “Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells.” 2009. Masters Thesis, Rutgers University. Accessed October 24, 2017. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051419.

MLA Handbook (7th Edition):

Wilimczyk, Barbara J. “Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells.” 2009. Web. 24 Oct 2017.

Vancouver:

Wilimczyk BJ. Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells. [Internet] [Masters thesis]. Rutgers University; 2009. [cited 2017 Oct 24]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051419.

Council of Science Editors:

Wilimczyk BJ. Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells. [Masters Thesis]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051419


Rutgers University

25. Kuo, Yu-Ching, 1980-. Effects of inotilone on inflammation and inflammation-associated tumorigenesis.

Degree: PhD, Food Science, 2010, Rutgers University

Inflammation, a complex process, involving numerous mediators of cellular and plasma origins, is considered to be a critical factor in many human diseases and conditions,… (more)

Subjects/Keywords: Inflammation – Mediators; Anti-inflammatory agents; Carcinogenesis

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APA (6th Edition):

Kuo, Yu-Ching, 1. (2010). Effects of inotilone on inflammation and inflammation-associated tumorigenesis. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056479

Chicago Manual of Style (16th Edition):

Kuo, Yu-Ching, 1980-. “Effects of inotilone on inflammation and inflammation-associated tumorigenesis.” 2010. Doctoral Dissertation, Rutgers University. Accessed October 24, 2017. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056479.

MLA Handbook (7th Edition):

Kuo, Yu-Ching, 1980-. “Effects of inotilone on inflammation and inflammation-associated tumorigenesis.” 2010. Web. 24 Oct 2017.

Vancouver:

Kuo, Yu-Ching 1. Effects of inotilone on inflammation and inflammation-associated tumorigenesis. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2017 Oct 24]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056479.

Council of Science Editors:

Kuo, Yu-Ching 1. Effects of inotilone on inflammation and inflammation-associated tumorigenesis. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056479


Rutgers University

26. Liu, Yingying. The role of Pak4 in tumorigenesis in vivo.

Degree: PhD, Pharmacology, Cellular and Molecular, 2010, Rutgers University

The Pak4 (P21 activated kinase) serine/threonine kinase is an important effector of Rho GTPases and has been implicated in the regulation of cell morphology and… (more)

Subjects/Keywords: Carcinogenesis; Cells – Morphology; Nude mouse – Research

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APA (6th Edition):

Liu, Y. (2010). The role of Pak4 in tumorigenesis in vivo. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056516

Chicago Manual of Style (16th Edition):

Liu, Yingying. “The role of Pak4 in tumorigenesis in vivo.” 2010. Doctoral Dissertation, Rutgers University. Accessed October 24, 2017. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056516.

MLA Handbook (7th Edition):

Liu, Yingying. “The role of Pak4 in tumorigenesis in vivo.” 2010. Web. 24 Oct 2017.

Vancouver:

Liu Y. The role of Pak4 in tumorigenesis in vivo. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2017 Oct 24]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056516.

Council of Science Editors:

Liu Y. The role of Pak4 in tumorigenesis in vivo. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056516


Rutgers University

27. Gomez, Yury Y., 1982-. Synergestic induction of NRF-2 gene by curcumin and sulforaphane and pharmacokinetics/metabolism of 13C/Dim in rats by UPLC/MS.

Degree: MS, Pharmaceutical Science, 2011, Rutgers University

 Curcumin (CUR) and Sulforaphane (SFN) have shown remarkable cancer chemopreventive effects in numerous studies and combinations of low doses of chemopreventive agents can reduce toxicity… (more)

Subjects/Keywords: Cancer – Chemoprevention; Cancer – Treatment; Carcinogenesis; Phytochemicals

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APA (6th Edition):

Gomez, Yury Y., 1. (2011). Synergestic induction of NRF-2 gene by curcumin and sulforaphane and pharmacokinetics/metabolism of 13C/Dim in rats by UPLC/MS. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057585

Chicago Manual of Style (16th Edition):

Gomez, Yury Y., 1982-. “Synergestic induction of NRF-2 gene by curcumin and sulforaphane and pharmacokinetics/metabolism of 13C/Dim in rats by UPLC/MS.” 2011. Masters Thesis, Rutgers University. Accessed October 24, 2017. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057585.

MLA Handbook (7th Edition):

Gomez, Yury Y., 1982-. “Synergestic induction of NRF-2 gene by curcumin and sulforaphane and pharmacokinetics/metabolism of 13C/Dim in rats by UPLC/MS.” 2011. Web. 24 Oct 2017.

Vancouver:

Gomez, Yury Y. 1. Synergestic induction of NRF-2 gene by curcumin and sulforaphane and pharmacokinetics/metabolism of 13C/Dim in rats by UPLC/MS. [Internet] [Masters thesis]. Rutgers University; 2011. [cited 2017 Oct 24]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057585.

Council of Science Editors:

Gomez, Yury Y. 1. Synergestic induction of NRF-2 gene by curcumin and sulforaphane and pharmacokinetics/metabolism of 13C/Dim in rats by UPLC/MS. [Masters Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057585


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 ; http://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 October 24, 2017. 10.18297/etd/330 ; http://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. 24 Oct 2017.

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 2017 Oct 24]. Available from: 10.18297/etd/330 ; http://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 ; http://ir.library.louisville.edu/etd/330

29. 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 October 24, 2017. 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. 24 Oct 2017.

Vancouver:

Batazzi A. Elucidating the role of Keratin 17 in cervical carcinogenesis. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2017 Oct 24]. 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

30. 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: Glioblastoma multiforme.; Carcinogenesis.; Cell cycle.; Oncogenes.

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

APA (6th Edition):

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 http://hdl.handle.net/10722/182308

Chicago Manual of Style (16th Edition):

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 October 24, 2017. http://hdl.handle.net/10722/182308.

MLA Handbook (7th Edition):

Chu, Ying-ying, Jamie. “Molecular characterization of the novel oncogene human cell cycle-related kinase (CCRK) in glioblastoma multiforme.” 2011. Web. 24 Oct 2017.

Vancouver:

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 2017 Oct 24]. Available from: http://hdl.handle.net/10722/182308.

Council of Science Editors:

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: http://hdl.handle.net/10722/182308

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