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You searched for subject:(Metastasis). Showing records 1 – 30 of 1276 total matches.

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Tulane University

1. Cunningham, David. Mouse models of prostate cancer bone metastasis: therapies and mechanisms.

Degree: 2018, Tulane University

1

David M. Cunningham

Advisors/Committee Members: You, Zongbing (Thesis advisor), School of Medicine Biomedical Sciences Graduate Program (Degree granting institution).

Subjects/Keywords: metastasis

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APA (6th Edition):

Cunningham, D. (2018). Mouse models of prostate cancer bone metastasis: therapies and mechanisms. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:78947

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):

Cunningham, David. “Mouse models of prostate cancer bone metastasis: therapies and mechanisms.” 2018. Thesis, Tulane University. Accessed September 30, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:78947.

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

MLA Handbook (7th Edition):

Cunningham, David. “Mouse models of prostate cancer bone metastasis: therapies and mechanisms.” 2018. Web. 30 Sep 2020.

Vancouver:

Cunningham D. Mouse models of prostate cancer bone metastasis: therapies and mechanisms. [Internet] [Thesis]. Tulane University; 2018. [cited 2020 Sep 30]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:78947.

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

Council of Science Editors:

Cunningham D. Mouse models of prostate cancer bone metastasis: therapies and mechanisms. [Thesis]. Tulane University; 2018. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:78947

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


Wake Forest University

2. Doheny, Daniel Lawrence. Targeting tGLI1-positive Breast Cancer with Ketoconazole.

Degree: 2018, Wake Forest University

 Despite improvements in early detection and therapies, breast cancer remains the second leading cause of cancer-related death in women and the second most common cancer… (more)

Subjects/Keywords: brain metastasis

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APA (6th Edition):

Doheny, D. L. (2018). Targeting tGLI1-positive Breast Cancer with Ketoconazole. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/93054

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):

Doheny, Daniel Lawrence. “Targeting tGLI1-positive Breast Cancer with Ketoconazole.” 2018. Thesis, Wake Forest University. Accessed September 30, 2020. http://hdl.handle.net/10339/93054.

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

MLA Handbook (7th Edition):

Doheny, Daniel Lawrence. “Targeting tGLI1-positive Breast Cancer with Ketoconazole.” 2018. Web. 30 Sep 2020.

Vancouver:

Doheny DL. Targeting tGLI1-positive Breast Cancer with Ketoconazole. [Internet] [Thesis]. Wake Forest University; 2018. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/10339/93054.

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

Council of Science Editors:

Doheny DL. Targeting tGLI1-positive Breast Cancer with Ketoconazole. [Thesis]. Wake Forest University; 2018. Available from: http://hdl.handle.net/10339/93054

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


Montana State University

3. Aslakson, Cheryl Juline. Humoral enhancement of metastasis : circulating IgG interactions with tumor-bearing lymphocytes.

Degree: MS, College of Agriculture, 1986, Montana State University

Subjects/Keywords: Lymphatic metastasis.; Metastasis.

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APA (6th Edition):

Aslakson, C. J. (1986). Humoral enhancement of metastasis : circulating IgG interactions with tumor-bearing lymphocytes. (Masters Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/4037

Chicago Manual of Style (16th Edition):

Aslakson, Cheryl Juline. “Humoral enhancement of metastasis : circulating IgG interactions with tumor-bearing lymphocytes.” 1986. Masters Thesis, Montana State University. Accessed September 30, 2020. https://scholarworks.montana.edu/xmlui/handle/1/4037.

MLA Handbook (7th Edition):

Aslakson, Cheryl Juline. “Humoral enhancement of metastasis : circulating IgG interactions with tumor-bearing lymphocytes.” 1986. Web. 30 Sep 2020.

Vancouver:

Aslakson CJ. Humoral enhancement of metastasis : circulating IgG interactions with tumor-bearing lymphocytes. [Internet] [Masters thesis]. Montana State University; 1986. [cited 2020 Sep 30]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/4037.

Council of Science Editors:

Aslakson CJ. Humoral enhancement of metastasis : circulating IgG interactions with tumor-bearing lymphocytes. [Masters Thesis]. Montana State University; 1986. Available from: https://scholarworks.montana.edu/xmlui/handle/1/4037


Cornell University

4. Mitchell, Michael. Mechanotransduction And Therapeutic Targeting Of Cells In The Circulation.

Degree: PhD, Biomedical Engineering, 2014, Cornell University

 The application of fluid shear stress on leukocytes and tumor cells in the circulation plays a critical role in the progression of inflammation and cancer… (more)

Subjects/Keywords: Inflammation; Metastasis; Nanomedicine

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APA (6th Edition):

Mitchell, M. (2014). Mechanotransduction And Therapeutic Targeting Of Cells In The Circulation. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39384

Chicago Manual of Style (16th Edition):

Mitchell, Michael. “Mechanotransduction And Therapeutic Targeting Of Cells In The Circulation.” 2014. Doctoral Dissertation, Cornell University. Accessed September 30, 2020. http://hdl.handle.net/1813/39384.

MLA Handbook (7th Edition):

Mitchell, Michael. “Mechanotransduction And Therapeutic Targeting Of Cells In The Circulation.” 2014. Web. 30 Sep 2020.

Vancouver:

Mitchell M. Mechanotransduction And Therapeutic Targeting Of Cells In The Circulation. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1813/39384.

Council of Science Editors:

Mitchell M. Mechanotransduction And Therapeutic Targeting Of Cells In The Circulation. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/39384


Cornell University

5. Santana, Steven. Microfluidic Analysis Of Metastatic Cancer Biomarkers.

Degree: PhD, Mechanical Engineering, 2014, Cornell University

 Cancer is the second-leading cause of death in the United States. Metastasis is responsible for 90% of cancer-related death and progresses through multifarious, poorly-understood cascades… (more)

Subjects/Keywords: microfluidic; metastasis; biomarker

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APA (6th Edition):

Santana, S. (2014). Microfluidic Analysis Of Metastatic Cancer Biomarkers. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/38925

Chicago Manual of Style (16th Edition):

Santana, Steven. “Microfluidic Analysis Of Metastatic Cancer Biomarkers.” 2014. Doctoral Dissertation, Cornell University. Accessed September 30, 2020. http://hdl.handle.net/1813/38925.

MLA Handbook (7th Edition):

Santana, Steven. “Microfluidic Analysis Of Metastatic Cancer Biomarkers.” 2014. Web. 30 Sep 2020.

Vancouver:

Santana S. Microfluidic Analysis Of Metastatic Cancer Biomarkers. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1813/38925.

Council of Science Editors:

Santana S. Microfluidic Analysis Of Metastatic Cancer Biomarkers. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38925


University of New South Wales

6. Byrne, Frances Louise. Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis.

Degree: Children's Cancer Institute Australia for Medical Research, 2012, University of New South Wales

 Neuroblastoma is a highly metastatic childhood cancer that originates from primitive cells of the neural crest and contributes to 15% of all paediatric cancer deaths.… (more)

Subjects/Keywords: Stathmin; Neuroblastoma; Metastasis

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APA (6th Edition):

Byrne, F. L. (2012). Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51779 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10446/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Byrne, Frances Louise. “Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis.” 2012. Doctoral Dissertation, University of New South Wales. Accessed September 30, 2020. http://handle.unsw.edu.au/1959.4/51779 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10446/SOURCE02?view=true.

MLA Handbook (7th Edition):

Byrne, Frances Louise. “Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis.” 2012. Web. 30 Sep 2020.

Vancouver:

Byrne FL. Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2020 Sep 30]. Available from: http://handle.unsw.edu.au/1959.4/51779 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10446/SOURCE02?view=true.

Council of Science Editors:

Byrne FL. Investigation of stathmin's role in neuroblastoma drug resistance, differentiation and metastasis. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/51779 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10446/SOURCE02?view=true


University of Sydney

7. Menezes, Sharleen Valerie. Understanding the molecular mechanisms that underlie the anti-cancer activity of the metastasis suppressor, NDRG1 in the treatment of cancer.

Degree: 2018, University of Sydney

 Pancreatic cancer is an aggressive disease that continues to be associated with low survival rates, therefore there is a need for more targeted therapies. This… (more)

Subjects/Keywords: Cancer; Metastasis; EGFR

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APA (6th Edition):

Menezes, S. V. (2018). Understanding the molecular mechanisms that underlie the anti-cancer activity of the metastasis suppressor, NDRG1 in the treatment of cancer. (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20193

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):

Menezes, Sharleen Valerie. “Understanding the molecular mechanisms that underlie the anti-cancer activity of the metastasis suppressor, NDRG1 in the treatment of cancer. ” 2018. Thesis, University of Sydney. Accessed September 30, 2020. http://hdl.handle.net/2123/20193.

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

MLA Handbook (7th Edition):

Menezes, Sharleen Valerie. “Understanding the molecular mechanisms that underlie the anti-cancer activity of the metastasis suppressor, NDRG1 in the treatment of cancer. ” 2018. Web. 30 Sep 2020.

Vancouver:

Menezes SV. Understanding the molecular mechanisms that underlie the anti-cancer activity of the metastasis suppressor, NDRG1 in the treatment of cancer. [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/2123/20193.

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

Council of Science Editors:

Menezes SV. Understanding the molecular mechanisms that underlie the anti-cancer activity of the metastasis suppressor, NDRG1 in the treatment of cancer. [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/20193

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


University of Melbourne

8. Yang, Lie. The control of melanoma by the Hippo pathway.

Degree: 2018, University of Melbourne

 Melanoma is an aggressive cancer with extremely unfavourable prognosis. Two main types of melanoma include cutaneous melanoma (CM) accounting for around 95% and uveal melanoma… (more)

Subjects/Keywords: melanoma; YAP; metastasis

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APA (6th Edition):

Yang, L. (2018). The control of melanoma by the Hippo pathway. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/220752

Chicago Manual of Style (16th Edition):

Yang, Lie. “The control of melanoma by the Hippo pathway.” 2018. Masters Thesis, University of Melbourne. Accessed September 30, 2020. http://hdl.handle.net/11343/220752.

MLA Handbook (7th Edition):

Yang, Lie. “The control of melanoma by the Hippo pathway.” 2018. Web. 30 Sep 2020.

Vancouver:

Yang L. The control of melanoma by the Hippo pathway. [Internet] [Masters thesis]. University of Melbourne; 2018. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/11343/220752.

Council of Science Editors:

Yang L. The control of melanoma by the Hippo pathway. [Masters Thesis]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/220752


University of Arizona

9. Kunihiro, Andrew. Bone-Specific Metabolism and Mechanism of Action of Curcuminoids in Blocking Osteolysis in Breast Cancer and Other Resorptive Bone Diseases .

Degree: 2019, University of Arizona

 Osteoclast-mediated bone resorptive disorders, including post-menopausal osteoporosis, age-related bone loss, rheumatoid arthritis, and osteolytic bone metastases, affect over 55 million Americans each year. Breast cancer… (more)

Subjects/Keywords: cancer; curcumin; metastasis

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APA (6th Edition):

Kunihiro, A. (2019). Bone-Specific Metabolism and Mechanism of Action of Curcuminoids in Blocking Osteolysis in Breast Cancer and Other Resorptive Bone Diseases . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/636687

Chicago Manual of Style (16th Edition):

Kunihiro, Andrew. “Bone-Specific Metabolism and Mechanism of Action of Curcuminoids in Blocking Osteolysis in Breast Cancer and Other Resorptive Bone Diseases .” 2019. Doctoral Dissertation, University of Arizona. Accessed September 30, 2020. http://hdl.handle.net/10150/636687.

MLA Handbook (7th Edition):

Kunihiro, Andrew. “Bone-Specific Metabolism and Mechanism of Action of Curcuminoids in Blocking Osteolysis in Breast Cancer and Other Resorptive Bone Diseases .” 2019. Web. 30 Sep 2020.

Vancouver:

Kunihiro A. Bone-Specific Metabolism and Mechanism of Action of Curcuminoids in Blocking Osteolysis in Breast Cancer and Other Resorptive Bone Diseases . [Internet] [Doctoral dissertation]. University of Arizona; 2019. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/10150/636687.

Council of Science Editors:

Kunihiro A. Bone-Specific Metabolism and Mechanism of Action of Curcuminoids in Blocking Osteolysis in Breast Cancer and Other Resorptive Bone Diseases . [Doctoral Dissertation]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/636687


Georgia Tech

10. Oh, Jaeho. Cell adhesion chromatography system for biophysical to biochemical analysis of human colon cancer metastasis through the vasculature.

Degree: MS, Mechanical Engineering, 2014, Georgia Tech

 Circulating cell adhesion amidst the high shear environment of the vasculature is central to several physiological and pathophysiological processes, including leukocyte recruitment to sites of… (more)

Subjects/Keywords: Chromatography; Caner metastasis

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APA (6th Edition):

Oh, J. (2014). Cell adhesion chromatography system for biophysical to biochemical analysis of human colon cancer metastasis through the vasculature. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52307

Chicago Manual of Style (16th Edition):

Oh, Jaeho. “Cell adhesion chromatography system for biophysical to biochemical analysis of human colon cancer metastasis through the vasculature.” 2014. Masters Thesis, Georgia Tech. Accessed September 30, 2020. http://hdl.handle.net/1853/52307.

MLA Handbook (7th Edition):

Oh, Jaeho. “Cell adhesion chromatography system for biophysical to biochemical analysis of human colon cancer metastasis through the vasculature.” 2014. Web. 30 Sep 2020.

Vancouver:

Oh J. Cell adhesion chromatography system for biophysical to biochemical analysis of human colon cancer metastasis through the vasculature. [Internet] [Masters thesis]. Georgia Tech; 2014. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1853/52307.

Council of Science Editors:

Oh J. Cell adhesion chromatography system for biophysical to biochemical analysis of human colon cancer metastasis through the vasculature. [Masters Thesis]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/52307


Universiteit Utrecht

11. Dummer, A. Role of EphB4/ephrinB2 in breast cancer metastasis.

Degree: 2014, Universiteit Utrecht

 Eph receptors and ephrin ligands are the largest family of tyrosine receptor kinases and the receptor and membrane bound ligand can signal to both the… (more)

Subjects/Keywords: EphB4; ephrinB2; breastcancer; metastasis

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APA (6th Edition):

Dummer, A. (2014). Role of EphB4/ephrinB2 in breast cancer metastasis. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/292107

Chicago Manual of Style (16th Edition):

Dummer, A. “Role of EphB4/ephrinB2 in breast cancer metastasis.” 2014. Masters Thesis, Universiteit Utrecht. Accessed September 30, 2020. http://dspace.library.uu.nl:8080/handle/1874/292107.

MLA Handbook (7th Edition):

Dummer, A. “Role of EphB4/ephrinB2 in breast cancer metastasis.” 2014. Web. 30 Sep 2020.

Vancouver:

Dummer A. Role of EphB4/ephrinB2 in breast cancer metastasis. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2020 Sep 30]. Available from: http://dspace.library.uu.nl:8080/handle/1874/292107.

Council of Science Editors:

Dummer A. Role of EphB4/ephrinB2 in breast cancer metastasis. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/292107


University of Michigan

12. Sura, Rishin. Epigenetic Control of PACE4 Gene Expression Associated with Metastasis.

Degree: Master's, College of Arts and Sciences: Biology, 2013, University of Michigan

 The main purpose of the project is to study the epigenetic change in the PACE4 gene as it is related to stressors that induce PC-associated… (more)

Subjects/Keywords: PACE4 gene; metastasis; stressors

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APA (6th Edition):

Sura, R. (2013). Epigenetic Control of PACE4 Gene Expression Associated with Metastasis. (Masters Thesis). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/117929

Chicago Manual of Style (16th Edition):

Sura, Rishin. “Epigenetic Control of PACE4 Gene Expression Associated with Metastasis.” 2013. Masters Thesis, University of Michigan. Accessed September 30, 2020. http://hdl.handle.net/2027.42/117929.

MLA Handbook (7th Edition):

Sura, Rishin. “Epigenetic Control of PACE4 Gene Expression Associated with Metastasis.” 2013. Web. 30 Sep 2020.

Vancouver:

Sura R. Epigenetic Control of PACE4 Gene Expression Associated with Metastasis. [Internet] [Masters thesis]. University of Michigan; 2013. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/2027.42/117929.

Council of Science Editors:

Sura R. Epigenetic Control of PACE4 Gene Expression Associated with Metastasis. [Masters Thesis]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/117929


Georgia Tech

13. Wu, Yue. Studies in using gold nanoparticles in treating cancer and inhibiting metastasis.

Degree: PhD, Chemistry and Biochemistry, 2019, Georgia Tech

 Based on statistics from the World Health Organization, cancer is among the top killers in the world. Metastasis, which is the process of cancer cells… (more)

Subjects/Keywords: Gold nanoparticles; Metastasis; Cancer; Photothermal

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APA (6th Edition):

Wu, Y. (2019). Studies in using gold nanoparticles in treating cancer and inhibiting metastasis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62682

Chicago Manual of Style (16th Edition):

Wu, Yue. “Studies in using gold nanoparticles in treating cancer and inhibiting metastasis.” 2019. Doctoral Dissertation, Georgia Tech. Accessed September 30, 2020. http://hdl.handle.net/1853/62682.

MLA Handbook (7th Edition):

Wu, Yue. “Studies in using gold nanoparticles in treating cancer and inhibiting metastasis.” 2019. Web. 30 Sep 2020.

Vancouver:

Wu Y. Studies in using gold nanoparticles in treating cancer and inhibiting metastasis. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1853/62682.

Council of Science Editors:

Wu Y. Studies in using gold nanoparticles in treating cancer and inhibiting metastasis. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/62682


Cornell University

14. Li, Jiahe. Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics.

Degree: PhD, Biomedical Engineering, 2015, Cornell University

Metastasis is the cause of about 90% of cancer-associated deaths, yet the mechanisms governing this clinically important process remain poorly understood. Distant metastases rely on… (more)

Subjects/Keywords: Circulating tumor cells; Metastasis; Therapy

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APA (6th Edition):

Li, J. (2015). Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/41110

Chicago Manual of Style (16th Edition):

Li, Jiahe. “Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics.” 2015. Doctoral Dissertation, Cornell University. Accessed September 30, 2020. http://hdl.handle.net/1813/41110.

MLA Handbook (7th Edition):

Li, Jiahe. “Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics.” 2015. Web. 30 Sep 2020.

Vancouver:

Li J. Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1813/41110.

Council of Science Editors:

Li J. Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41110


Cornell University

15. Chandrasekaran, Siddarth. Engineering Approaches To Analyze And Target Cancer Invasion And Metastasis.

Degree: PhD, Biomedical Engineering, 2015, Cornell University

Metastasis of primary tumor accounts for 90% of all deaths in cancer patients. Interaction between cells in the primary tumor is known to play an… (more)

Subjects/Keywords: Cancer Metastasis; Drug Delivery; Immunotherapy

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APA (6th Edition):

Chandrasekaran, S. (2015). Engineering Approaches To Analyze And Target Cancer Invasion And Metastasis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/41158

Chicago Manual of Style (16th Edition):

Chandrasekaran, Siddarth. “Engineering Approaches To Analyze And Target Cancer Invasion And Metastasis.” 2015. Doctoral Dissertation, Cornell University. Accessed September 30, 2020. http://hdl.handle.net/1813/41158.

MLA Handbook (7th Edition):

Chandrasekaran, Siddarth. “Engineering Approaches To Analyze And Target Cancer Invasion And Metastasis.” 2015. Web. 30 Sep 2020.

Vancouver:

Chandrasekaran S. Engineering Approaches To Analyze And Target Cancer Invasion And Metastasis. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1813/41158.

Council of Science Editors:

Chandrasekaran S. Engineering Approaches To Analyze And Target Cancer Invasion And Metastasis. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41158


Cornell University

16. Geng, Yue. Differential Metastatic Adhesion Cascade Of Tumor Cells Bearing Selectin-Binding Ligands.

Degree: PhD, Biomedical Engineering, 2013, Cornell University

 A myriad of previous research has suggested that circulating tumor cells (CTCs) can adhere to the blood vessel wall to eventually extravasate and form secondary… (more)

Subjects/Keywords: cancer metastasis; selectin; glycoprotein

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APA (6th Edition):

Geng, Y. (2013). Differential Metastatic Adhesion Cascade Of Tumor Cells Bearing Selectin-Binding Ligands. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34386

Chicago Manual of Style (16th Edition):

Geng, Yue. “Differential Metastatic Adhesion Cascade Of Tumor Cells Bearing Selectin-Binding Ligands.” 2013. Doctoral Dissertation, Cornell University. Accessed September 30, 2020. http://hdl.handle.net/1813/34386.

MLA Handbook (7th Edition):

Geng, Yue. “Differential Metastatic Adhesion Cascade Of Tumor Cells Bearing Selectin-Binding Ligands.” 2013. Web. 30 Sep 2020.

Vancouver:

Geng Y. Differential Metastatic Adhesion Cascade Of Tumor Cells Bearing Selectin-Binding Ligands. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1813/34386.

Council of Science Editors:

Geng Y. Differential Metastatic Adhesion Cascade Of Tumor Cells Bearing Selectin-Binding Ligands. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34386


Vanderbilt University

17. Ruppender, Nazanin Sabine. Matrix Mechanical Properties and the Invasive Potential of Metastatic Cancer.

Degree: PhD, Chemical Engineering, 2011, Vanderbilt University

 Recent studies suggest that cancer cells undergo genotypic and phenotypic changes in response to the rigidity of the extracellular matrix (ECM). These studies have focused… (more)

Subjects/Keywords: bone metastasis; mechanotransduction; cancer; biomaterials

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APA (6th Edition):

Ruppender, N. S. (2011). Matrix Mechanical Properties and the Invasive Potential of Metastatic Cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11514

Chicago Manual of Style (16th Edition):

Ruppender, Nazanin Sabine. “Matrix Mechanical Properties and the Invasive Potential of Metastatic Cancer.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed September 30, 2020. http://hdl.handle.net/1803/11514.

MLA Handbook (7th Edition):

Ruppender, Nazanin Sabine. “Matrix Mechanical Properties and the Invasive Potential of Metastatic Cancer.” 2011. Web. 30 Sep 2020.

Vancouver:

Ruppender NS. Matrix Mechanical Properties and the Invasive Potential of Metastatic Cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1803/11514.

Council of Science Editors:

Ruppender NS. Matrix Mechanical Properties and the Invasive Potential of Metastatic Cancer. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/11514


Vanderbilt University

18. Bates, Andreia LaShonne. Roles of Fibroblast MMP2 in Breast to Lung Metastasis.

Degree: PhD, Cancer Biology, 2015, Vanderbilt University

 CANCER BIOLOGY Roles of Fibroblast MMP2 in Breast to Lung Metastasis Andreia L. Bates Dissertation under the direction of Barbara Fingleton, PhD Breast cancer five-year… (more)

Subjects/Keywords: MMP2; fibroblasts; metastasis; breast cancer

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APA (6th Edition):

Bates, A. L. (2015). Roles of Fibroblast MMP2 in Breast to Lung Metastasis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10839

Chicago Manual of Style (16th Edition):

Bates, Andreia LaShonne. “Roles of Fibroblast MMP2 in Breast to Lung Metastasis.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed September 30, 2020. http://hdl.handle.net/1803/10839.

MLA Handbook (7th Edition):

Bates, Andreia LaShonne. “Roles of Fibroblast MMP2 in Breast to Lung Metastasis.” 2015. Web. 30 Sep 2020.

Vancouver:

Bates AL. Roles of Fibroblast MMP2 in Breast to Lung Metastasis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1803/10839.

Council of Science Editors:

Bates AL. Roles of Fibroblast MMP2 in Breast to Lung Metastasis. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/10839


Vanderbilt University

19. Nandana, Srinivas Rao. Mouse Models of Prostate Cancer Progression and Bone Metastasis.

Degree: PhD, Cancer Biology, 2010, Vanderbilt University

 CANCER BIOLOGY MOUSE MODELS OF PROSTATE CANCER PROGRESSION AND BONE METASTASIS Srinivas Rao Nandana Dissertation under the direction of Robert J. Matusik, PhD Prostate cancer… (more)

Subjects/Keywords: Metastasis; Mouse

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APA (6th Edition):

Nandana, S. R. (2010). Mouse Models of Prostate Cancer Progression and Bone Metastasis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12940

Chicago Manual of Style (16th Edition):

Nandana, Srinivas Rao. “Mouse Models of Prostate Cancer Progression and Bone Metastasis.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed September 30, 2020. http://hdl.handle.net/1803/12940.

MLA Handbook (7th Edition):

Nandana, Srinivas Rao. “Mouse Models of Prostate Cancer Progression and Bone Metastasis.” 2010. Web. 30 Sep 2020.

Vancouver:

Nandana SR. Mouse Models of Prostate Cancer Progression and Bone Metastasis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1803/12940.

Council of Science Editors:

Nandana SR. Mouse Models of Prostate Cancer Progression and Bone Metastasis. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://hdl.handle.net/1803/12940


Vanderbilt University

20. Mendonsa, Alisha Maria. Cellular and Molecular Changes Impacting Cancer Progression in Non-Alcoholic Fatty Liver Disease.

Degree: PhD, Cancer Biology, 2014, Vanderbilt University

 Non alcoholic fatty liver disease (NAFLD), is recognized as the one of the most common causes of liver disease in the United States and worldwide.… (more)

Subjects/Keywords: NAFLD; liver metastasis; MMP13

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APA (6th Edition):

Mendonsa, A. M. (2014). Cellular and Molecular Changes Impacting Cancer Progression in Non-Alcoholic Fatty Liver Disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15352

Chicago Manual of Style (16th Edition):

Mendonsa, Alisha Maria. “Cellular and Molecular Changes Impacting Cancer Progression in Non-Alcoholic Fatty Liver Disease.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed September 30, 2020. http://hdl.handle.net/1803/15352.

MLA Handbook (7th Edition):

Mendonsa, Alisha Maria. “Cellular and Molecular Changes Impacting Cancer Progression in Non-Alcoholic Fatty Liver Disease.” 2014. Web. 30 Sep 2020.

Vancouver:

Mendonsa AM. Cellular and Molecular Changes Impacting Cancer Progression in Non-Alcoholic Fatty Liver Disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1803/15352.

Council of Science Editors:

Mendonsa AM. Cellular and Molecular Changes Impacting Cancer Progression in Non-Alcoholic Fatty Liver Disease. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/15352


Vanderbilt University

21. Palmer, Trenis Duwon. Regulation of Tumor Cell Metastasis by CD151.

Degree: PhD, Pathology, 2013, Vanderbilt University

 Recently our lab has demonstrated that clustering of the tetraspanin CD151 on the surface of tumor cells is capable of inhibiting cell migration and cancer… (more)

Subjects/Keywords: cell migration; metastasis; CD151; ALCAM

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APA (6th Edition):

Palmer, T. D. (2013). Regulation of Tumor Cell Metastasis by CD151. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13261

Chicago Manual of Style (16th Edition):

Palmer, Trenis Duwon. “Regulation of Tumor Cell Metastasis by CD151.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed September 30, 2020. http://hdl.handle.net/1803/13261.

MLA Handbook (7th Edition):

Palmer, Trenis Duwon. “Regulation of Tumor Cell Metastasis by CD151.” 2013. Web. 30 Sep 2020.

Vancouver:

Palmer TD. Regulation of Tumor Cell Metastasis by CD151. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1803/13261.

Council of Science Editors:

Palmer TD. Regulation of Tumor Cell Metastasis by CD151. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/13261


Texas A&M University

22. Xu, Yixiang. Twist1 Silences Foxa1 Expression to Promote Breast Cancer Progression.

Degree: PhD, Medical Sciences, 2016, Texas A&M University

 Twist1 is a basic helix-loop-helix transcription factor family that serves as one of the master regulators promoting epithelial-mesenchymal transition (EMT). Twist1 has been shown in… (more)

Subjects/Keywords: Twist1; Breast cancer metastasis; Foxa1

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APA (6th Edition):

Xu, Y. (2016). Twist1 Silences Foxa1 Expression to Promote Breast Cancer Progression. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158963

Chicago Manual of Style (16th Edition):

Xu, Yixiang. “Twist1 Silences Foxa1 Expression to Promote Breast Cancer Progression.” 2016. Doctoral Dissertation, Texas A&M University. Accessed September 30, 2020. http://hdl.handle.net/1969.1/158963.

MLA Handbook (7th Edition):

Xu, Yixiang. “Twist1 Silences Foxa1 Expression to Promote Breast Cancer Progression.” 2016. Web. 30 Sep 2020.

Vancouver:

Xu Y. Twist1 Silences Foxa1 Expression to Promote Breast Cancer Progression. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1969.1/158963.

Council of Science Editors:

Xu Y. Twist1 Silences Foxa1 Expression to Promote Breast Cancer Progression. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158963


McMaster University

23. Singh, Mohini. Modelling, characterization, and therapeutic targeting of human brain metastasis.

Degree: PhD, 2018, McMaster University

Brain metastases (BM) are the most frequently diagnosed neoplasm to affect the adult central nervous system (CNS), occurring in 20-40% of all cancer patients throughout… (more)

Subjects/Keywords: Brain Metastasis; Patient-Derived Xenograft

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APA (6th Edition):

Singh, M. (2018). Modelling, characterization, and therapeutic targeting of human brain metastasis. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/23039

Chicago Manual of Style (16th Edition):

Singh, Mohini. “Modelling, characterization, and therapeutic targeting of human brain metastasis.” 2018. Doctoral Dissertation, McMaster University. Accessed September 30, 2020. http://hdl.handle.net/11375/23039.

MLA Handbook (7th Edition):

Singh, Mohini. “Modelling, characterization, and therapeutic targeting of human brain metastasis.” 2018. Web. 30 Sep 2020.

Vancouver:

Singh M. Modelling, characterization, and therapeutic targeting of human brain metastasis. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/11375/23039.

Council of Science Editors:

Singh M. Modelling, characterization, and therapeutic targeting of human brain metastasis. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/23039


Queens University

24. Hoskin, Victoria. A Novel Regulatory Role of Ezrin in Promoting Breast Cancer Cell Invasion and Metastasis .

Degree: Pathology and Molecular Medicine, 2015, Queens University

Metastasis is the leading cause of death for breast cancer patients and poses significant clinical challenges in the successful treatment of breast cancer. The cytoskeleton… (more)

Subjects/Keywords: Calpain ; Ezrin ; Metastasis ; Invasion

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APA (6th Edition):

Hoskin, V. (2015). A Novel Regulatory Role of Ezrin in Promoting Breast Cancer Cell Invasion and Metastasis . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12945

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):

Hoskin, Victoria. “A Novel Regulatory Role of Ezrin in Promoting Breast Cancer Cell Invasion and Metastasis .” 2015. Thesis, Queens University. Accessed September 30, 2020. http://hdl.handle.net/1974/12945.

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

MLA Handbook (7th Edition):

Hoskin, Victoria. “A Novel Regulatory Role of Ezrin in Promoting Breast Cancer Cell Invasion and Metastasis .” 2015. Web. 30 Sep 2020.

Vancouver:

Hoskin V. A Novel Regulatory Role of Ezrin in Promoting Breast Cancer Cell Invasion and Metastasis . [Internet] [Thesis]. Queens University; 2015. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1974/12945.

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

Council of Science Editors:

Hoskin V. A Novel Regulatory Role of Ezrin in Promoting Breast Cancer Cell Invasion and Metastasis . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/12945

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


Queens University

25. Carefoot, Esther. The Src/Stat3 axis in Met signaling in human invasive breast cancer: a potential predictive marker .

Degree: Pathology and Molecular Medicine, 2014, Queens University

 Met has been found to be over-expressed in human breast cancer, correlating with disease progression and poor prognosis. Src and Stat3 have also been found… (more)

Subjects/Keywords: Breast cancer ; xenografts ; Therapeutics ; Metastasis

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APA (6th Edition):

Carefoot, E. (2014). The Src/Stat3 axis in Met signaling in human invasive breast cancer: a potential predictive marker . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8582

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):

Carefoot, Esther. “The Src/Stat3 axis in Met signaling in human invasive breast cancer: a potential predictive marker .” 2014. Thesis, Queens University. Accessed September 30, 2020. http://hdl.handle.net/1974/8582.

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

MLA Handbook (7th Edition):

Carefoot, Esther. “The Src/Stat3 axis in Met signaling in human invasive breast cancer: a potential predictive marker .” 2014. Web. 30 Sep 2020.

Vancouver:

Carefoot E. The Src/Stat3 axis in Met signaling in human invasive breast cancer: a potential predictive marker . [Internet] [Thesis]. Queens University; 2014. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1974/8582.

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

Council of Science Editors:

Carefoot E. The Src/Stat3 axis in Met signaling in human invasive breast cancer: a potential predictive marker . [Thesis]. Queens University; 2014. Available from: http://hdl.handle.net/1974/8582

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


University of Nairobi

26. Gatete, Grace N. Correlation of plain radiography and radionuclide scan findings in breast cancer patients with suspected bone metastasis in Kenyatta National Hospital and Agakhan University Hospital .

Degree: 2014, University of Nairobi

 Introduction The presence of bone metastasis in patients with breast cancer impacts on the management options. The diagnosis of metastatic bone disease is important in… (more)

Subjects/Keywords: Breast Cancer; Bone metastasis

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APA (6th Edition):

Gatete, G. N. (2014). Correlation of plain radiography and radionuclide scan findings in breast cancer patients with suspected bone metastasis in Kenyatta National Hospital and Agakhan University Hospital . (Thesis). University of Nairobi. Retrieved from http://hdl.handle.net/11295/76164

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):

Gatete, Grace N. “Correlation of plain radiography and radionuclide scan findings in breast cancer patients with suspected bone metastasis in Kenyatta National Hospital and Agakhan University Hospital .” 2014. Thesis, University of Nairobi. Accessed September 30, 2020. http://hdl.handle.net/11295/76164.

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

MLA Handbook (7th Edition):

Gatete, Grace N. “Correlation of plain radiography and radionuclide scan findings in breast cancer patients with suspected bone metastasis in Kenyatta National Hospital and Agakhan University Hospital .” 2014. Web. 30 Sep 2020.

Vancouver:

Gatete GN. Correlation of plain radiography and radionuclide scan findings in breast cancer patients with suspected bone metastasis in Kenyatta National Hospital and Agakhan University Hospital . [Internet] [Thesis]. University of Nairobi; 2014. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/11295/76164.

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

Council of Science Editors:

Gatete GN. Correlation of plain radiography and radionuclide scan findings in breast cancer patients with suspected bone metastasis in Kenyatta National Hospital and Agakhan University Hospital . [Thesis]. University of Nairobi; 2014. Available from: http://hdl.handle.net/11295/76164

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


University of Toronto

27. ElZeiry, Maha. Septins in Cancer and Metastasis.

Degree: 2018, University of Toronto

Septins are GTP-binding cytoskeletal proteins that play a role in cancer cell migration. Their role in mesenchymal cell migration has been studied but not in… (more)

Subjects/Keywords: Cancer; Metastasis; Septins; 0487

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APA (6th Edition):

ElZeiry, M. (2018). Septins in Cancer and Metastasis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91341

Chicago Manual of Style (16th Edition):

ElZeiry, Maha. “Septins in Cancer and Metastasis.” 2018. Masters Thesis, University of Toronto. Accessed September 30, 2020. http://hdl.handle.net/1807/91341.

MLA Handbook (7th Edition):

ElZeiry, Maha. “Septins in Cancer and Metastasis.” 2018. Web. 30 Sep 2020.

Vancouver:

ElZeiry M. Septins in Cancer and Metastasis. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1807/91341.

Council of Science Editors:

ElZeiry M. Septins in Cancer and Metastasis. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91341

28. Harper, Kelly. The hypoxic tumor microenvironment regulates the LPA signaling axis to promote cancer cell invasion and metastasis.

Degree: 2020, Université de Sherbrooke

 Abstract : Metastasis is the leading cause of cancer patient mortality yet remains a major hurdle for treatment. Hypoxia, a common feature of solid tumors,… (more)

Subjects/Keywords: Autotaxin; LPA; Invadopodia; Hypoxia; Metastasis

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APA (6th Edition):

Harper, K. (2020). The hypoxic tumor microenvironment regulates the LPA signaling axis to promote cancer cell invasion and metastasis. (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/17234

Chicago Manual of Style (16th Edition):

Harper, Kelly. “The hypoxic tumor microenvironment regulates the LPA signaling axis to promote cancer cell invasion and metastasis.” 2020. Doctoral Dissertation, Université de Sherbrooke. Accessed September 30, 2020. http://hdl.handle.net/11143/17234.

MLA Handbook (7th Edition):

Harper, Kelly. “The hypoxic tumor microenvironment regulates the LPA signaling axis to promote cancer cell invasion and metastasis.” 2020. Web. 30 Sep 2020.

Vancouver:

Harper K. The hypoxic tumor microenvironment regulates the LPA signaling axis to promote cancer cell invasion and metastasis. [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2020. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/11143/17234.

Council of Science Editors:

Harper K. The hypoxic tumor microenvironment regulates the LPA signaling axis to promote cancer cell invasion and metastasis. [Doctoral Dissertation]. Université de Sherbrooke; 2020. Available from: http://hdl.handle.net/11143/17234


Universiteit Utrecht

29. Wiebrands, K. A role of epithelial-mesenchymal transitions in carcinogenic progression.

Degree: 2010, Universiteit Utrecht

 The epithelial-mesenchymal transition plays an important role in several developmental processes, tissue repair, but is also associated with fibrosis and cancer. During tumorigenic progression, EMT… (more)

Subjects/Keywords: epithelial-mesenchymal transition; EMT; metastasis

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APA (6th Edition):

Wiebrands, K. (2010). A role of epithelial-mesenchymal transitions in carcinogenic progression. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/190315

Chicago Manual of Style (16th Edition):

Wiebrands, K. “A role of epithelial-mesenchymal transitions in carcinogenic progression.” 2010. Masters Thesis, Universiteit Utrecht. Accessed September 30, 2020. http://dspace.library.uu.nl:8080/handle/1874/190315.

MLA Handbook (7th Edition):

Wiebrands, K. “A role of epithelial-mesenchymal transitions in carcinogenic progression.” 2010. Web. 30 Sep 2020.

Vancouver:

Wiebrands K. A role of epithelial-mesenchymal transitions in carcinogenic progression. [Internet] [Masters thesis]. Universiteit Utrecht; 2010. [cited 2020 Sep 30]. Available from: http://dspace.library.uu.nl:8080/handle/1874/190315.

Council of Science Editors:

Wiebrands K. A role of epithelial-mesenchymal transitions in carcinogenic progression. [Masters Thesis]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/190315


Universiteit Utrecht

30. Brown, M.K. Inception of the metastatic phenotype by macrophage-cancer cell fusion.

Degree: 2011, Universiteit Utrecht

 It is now well-established that patient outcome are good if the primary tumor has not spread; can be surgically removed; treated locally with radiation; or… (more)

Subjects/Keywords: Metastasis; Cancer; Macrophage; Fusion theory

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APA (6th Edition):

Brown, M. K. (2011). Inception of the metastatic phenotype by macrophage-cancer cell fusion. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/204660

Chicago Manual of Style (16th Edition):

Brown, M K. “Inception of the metastatic phenotype by macrophage-cancer cell fusion.” 2011. Masters Thesis, Universiteit Utrecht. Accessed September 30, 2020. http://dspace.library.uu.nl:8080/handle/1874/204660.

MLA Handbook (7th Edition):

Brown, M K. “Inception of the metastatic phenotype by macrophage-cancer cell fusion.” 2011. Web. 30 Sep 2020.

Vancouver:

Brown MK. Inception of the metastatic phenotype by macrophage-cancer cell fusion. [Internet] [Masters thesis]. Universiteit Utrecht; 2011. [cited 2020 Sep 30]. Available from: http://dspace.library.uu.nl:8080/handle/1874/204660.

Council of Science Editors:

Brown MK. Inception of the metastatic phenotype by macrophage-cancer cell fusion. [Masters Thesis]. Universiteit Utrecht; 2011. Available from: http://dspace.library.uu.nl:8080/handle/1874/204660

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