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You searched for +publisher:"University of North Carolina" +contributor:("Rathmell, W. Kimryn"). Showing records 1 – 16 of 16 total matches.

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University of North Carolina

1. Hacker, Kathryn Esther. Investigating the role of SETD2 mutations and H3K36me3 loss in clear cell renal cell carcinoma.

Degree: 2014, University of North Carolina

 Comprehensive sequencing of human cancers has identified frequent mutations in genes encoding chromatin regulatory proteins, highlighting the importance of chromatin maintenance in tumor suppression. Specifically,… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Hacker, K. E. (2014). Investigating the role of SETD2 mutations and H3K36me3 loss in clear cell renal cell carcinoma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:93949b90-2cff-4ce1-a84b-f4c9c8b5939f

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):

Hacker, Kathryn Esther. “Investigating the role of SETD2 mutations and H3K36me3 loss in clear cell renal cell carcinoma.” 2014. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:93949b90-2cff-4ce1-a84b-f4c9c8b5939f.

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

MLA Handbook (7th Edition):

Hacker, Kathryn Esther. “Investigating the role of SETD2 mutations and H3K36me3 loss in clear cell renal cell carcinoma.” 2014. Web. 28 Sep 2020.

Vancouver:

Hacker KE. Investigating the role of SETD2 mutations and H3K36me3 loss in clear cell renal cell carcinoma. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:93949b90-2cff-4ce1-a84b-f4c9c8b5939f.

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

Council of Science Editors:

Hacker KE. Investigating the role of SETD2 mutations and H3K36me3 loss in clear cell renal cell carcinoma. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:93949b90-2cff-4ce1-a84b-f4c9c8b5939f

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


University of North Carolina

2. Rasmussen, Neal R. Elucidating the role of the receptor tyrosine kinase Ror2 within the Wnt pathway and its contributions to renal cell carcinoma tumorigenesis.

Degree: 2013, University of North Carolina

 Ror2, an important mediator of Wnt signaling cascades, has been shown to be aberrantly expressed in RCC promoting cell migration, invasion, and tumor growth. In… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Rasmussen, N. R. (2013). Elucidating the role of the receptor tyrosine kinase Ror2 within the Wnt pathway and its contributions to renal cell carcinoma tumorigenesis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d6fefb43-2020-4789-8dbc-25f3d8fc1237

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):

Rasmussen, Neal R. “Elucidating the role of the receptor tyrosine kinase Ror2 within the Wnt pathway and its contributions to renal cell carcinoma tumorigenesis.” 2013. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:d6fefb43-2020-4789-8dbc-25f3d8fc1237.

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

MLA Handbook (7th Edition):

Rasmussen, Neal R. “Elucidating the role of the receptor tyrosine kinase Ror2 within the Wnt pathway and its contributions to renal cell carcinoma tumorigenesis.” 2013. Web. 28 Sep 2020.

Vancouver:

Rasmussen NR. Elucidating the role of the receptor tyrosine kinase Ror2 within the Wnt pathway and its contributions to renal cell carcinoma tumorigenesis. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:d6fefb43-2020-4789-8dbc-25f3d8fc1237.

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

Council of Science Editors:

Rasmussen NR. Elucidating the role of the receptor tyrosine kinase Ror2 within the Wnt pathway and its contributions to renal cell carcinoma tumorigenesis. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:d6fefb43-2020-4789-8dbc-25f3d8fc1237

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


University of North Carolina

3. Brannon, Angela R. Molecular stratification and characterization of clear cell renal cell carcinoma.

Degree: 2010, University of North Carolina

 It is estimated that there will be 58,240 new diagnoses of kidney cancer in 2010. Most cases will be clear cell renal cell carcinoma (ccRCC)… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Brannon, A. R. (2010). Molecular stratification and characterization of clear cell renal cell carcinoma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:34c77008-05a8-448c-b381-7e75fc7daf41

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):

Brannon, Angela R. “Molecular stratification and characterization of clear cell renal cell carcinoma.” 2010. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:34c77008-05a8-448c-b381-7e75fc7daf41.

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

MLA Handbook (7th Edition):

Brannon, Angela R. “Molecular stratification and characterization of clear cell renal cell carcinoma.” 2010. Web. 28 Sep 2020.

Vancouver:

Brannon AR. Molecular stratification and characterization of clear cell renal cell carcinoma. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:34c77008-05a8-448c-b381-7e75fc7daf41.

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

Council of Science Editors:

Brannon AR. Molecular stratification and characterization of clear cell renal cell carcinoma. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:34c77008-05a8-448c-b381-7e75fc7daf41

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


University of North Carolina

4. Wright, Tricia M. Identification and characterization of Ror2 as a tumor cancer cell specific kinase in renal cell carcinoma.

Degree: 2010, University of North Carolina

 With the recent advent of molecularly targeted therapy, the potential for novel treatment options for carcinomas has been brought to the forefront. However, few tumor… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Wright, T. M. (2010). Identification and characterization of Ror2 as a tumor cancer cell specific kinase in renal cell carcinoma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:1a280881-e6c1-4d7d-bbac-f662f60fea19

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):

Wright, Tricia M. “Identification and characterization of Ror2 as a tumor cancer cell specific kinase in renal cell carcinoma.” 2010. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:1a280881-e6c1-4d7d-bbac-f662f60fea19.

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

MLA Handbook (7th Edition):

Wright, Tricia M. “Identification and characterization of Ror2 as a tumor cancer cell specific kinase in renal cell carcinoma.” 2010. Web. 28 Sep 2020.

Vancouver:

Wright TM. Identification and characterization of Ror2 as a tumor cancer cell specific kinase in renal cell carcinoma. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:1a280881-e6c1-4d7d-bbac-f662f60fea19.

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

Council of Science Editors:

Wright TM. Identification and characterization of Ror2 as a tumor cancer cell specific kinase in renal cell carcinoma. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:1a280881-e6c1-4d7d-bbac-f662f60fea19

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


University of North Carolina

5. Iglesia, Michael. A Genomic Approach to the Identity, Clonal Diversity, and Clinical Import of Tumor-infiltrating Lymphocytes in Human Cancers.

Degree: 2015, University of North Carolina

 Immune infiltration in solid tumors has emerged as an important aspect of cancer biology. In particular, the presence of tumor-infiltrating lymphocytes (TILs) within the tumor… (more)

Subjects/Keywords: Genetics; Bioinformatics; Immunology; School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Iglesia, M. (2015). A Genomic Approach to the Identity, Clonal Diversity, and Clinical Import of Tumor-infiltrating Lymphocytes in Human Cancers. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d2b0b601-a2c2-4857-a11c-7cfe7d05d97f

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):

Iglesia, Michael. “A Genomic Approach to the Identity, Clonal Diversity, and Clinical Import of Tumor-infiltrating Lymphocytes in Human Cancers.” 2015. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:d2b0b601-a2c2-4857-a11c-7cfe7d05d97f.

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

MLA Handbook (7th Edition):

Iglesia, Michael. “A Genomic Approach to the Identity, Clonal Diversity, and Clinical Import of Tumor-infiltrating Lymphocytes in Human Cancers.” 2015. Web. 28 Sep 2020.

Vancouver:

Iglesia M. A Genomic Approach to the Identity, Clonal Diversity, and Clinical Import of Tumor-infiltrating Lymphocytes in Human Cancers. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:d2b0b601-a2c2-4857-a11c-7cfe7d05d97f.

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

Council of Science Editors:

Iglesia M. A Genomic Approach to the Identity, Clonal Diversity, and Clinical Import of Tumor-infiltrating Lymphocytes in Human Cancers. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:d2b0b601-a2c2-4857-a11c-7cfe7d05d97f

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


University of North Carolina

6. Smallwood, Tangi. THE GENETIC ARCHITECTURE OF ATHEROSCLEROSIS AND THE ATHEROSCLEROSIS-ASSOCIATED METABOLITE TRIMETHYLAMINE-N-OXIDE IN THE DIVERSITY OUTBRED MOUSE POPULATION.

Degree: 2015, University of North Carolina

 Inbred mice exhibit strain-specific variation in susceptibility to complex diseases which renders them useful for dissecting the genetic architecture of these traits. Traditional quantitative trait… (more)

Subjects/Keywords: Genetics; Nutrition; Biology; School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Smallwood, T. (2015). THE GENETIC ARCHITECTURE OF ATHEROSCLEROSIS AND THE ATHEROSCLEROSIS-ASSOCIATED METABOLITE TRIMETHYLAMINE-N-OXIDE IN THE DIVERSITY OUTBRED MOUSE POPULATION. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d119b14d-5628-4433-95aa-ecbe84cbb8ce

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):

Smallwood, Tangi. “THE GENETIC ARCHITECTURE OF ATHEROSCLEROSIS AND THE ATHEROSCLEROSIS-ASSOCIATED METABOLITE TRIMETHYLAMINE-N-OXIDE IN THE DIVERSITY OUTBRED MOUSE POPULATION.” 2015. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:d119b14d-5628-4433-95aa-ecbe84cbb8ce.

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

MLA Handbook (7th Edition):

Smallwood, Tangi. “THE GENETIC ARCHITECTURE OF ATHEROSCLEROSIS AND THE ATHEROSCLEROSIS-ASSOCIATED METABOLITE TRIMETHYLAMINE-N-OXIDE IN THE DIVERSITY OUTBRED MOUSE POPULATION.” 2015. Web. 28 Sep 2020.

Vancouver:

Smallwood T. THE GENETIC ARCHITECTURE OF ATHEROSCLEROSIS AND THE ATHEROSCLEROSIS-ASSOCIATED METABOLITE TRIMETHYLAMINE-N-OXIDE IN THE DIVERSITY OUTBRED MOUSE POPULATION. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:d119b14d-5628-4433-95aa-ecbe84cbb8ce.

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

Council of Science Editors:

Smallwood T. THE GENETIC ARCHITECTURE OF ATHEROSCLEROSIS AND THE ATHEROSCLEROSIS-ASSOCIATED METABOLITE TRIMETHYLAMINE-N-OXIDE IN THE DIVERSITY OUTBRED MOUSE POPULATION. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:d119b14d-5628-4433-95aa-ecbe84cbb8ce

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


University of North Carolina

7. Brooks, Samira. The Regulation of Gene Expression Profiles in Clear Cell Renal Cell Carcinoma by Tumor Heterogeneity and Environmental Exposure.

Degree: 2015, University of North Carolina

 Currently, the disease management and therapeutic strategies for renal cell carcinoma (RCC) have arisen from cancer biology discoveries, but have evolved fairly independently of individual… (more)

Subjects/Keywords: Toxicology; Genetics; Molecular biology; School of Medicine; Curriculum in Toxicology

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APA (6th Edition):

Brooks, S. (2015). The Regulation of Gene Expression Profiles in Clear Cell Renal Cell Carcinoma by Tumor Heterogeneity and Environmental Exposure. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4da406f0-3586-4167-a117-decf80049c41

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):

Brooks, Samira. “The Regulation of Gene Expression Profiles in Clear Cell Renal Cell Carcinoma by Tumor Heterogeneity and Environmental Exposure.” 2015. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:4da406f0-3586-4167-a117-decf80049c41.

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

MLA Handbook (7th Edition):

Brooks, Samira. “The Regulation of Gene Expression Profiles in Clear Cell Renal Cell Carcinoma by Tumor Heterogeneity and Environmental Exposure.” 2015. Web. 28 Sep 2020.

Vancouver:

Brooks S. The Regulation of Gene Expression Profiles in Clear Cell Renal Cell Carcinoma by Tumor Heterogeneity and Environmental Exposure. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:4da406f0-3586-4167-a117-decf80049c41.

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

Council of Science Editors:

Brooks S. The Regulation of Gene Expression Profiles in Clear Cell Renal Cell Carcinoma by Tumor Heterogeneity and Environmental Exposure. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:4da406f0-3586-4167-a117-decf80049c41

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


University of North Carolina

8. Coleman, Kate. Coordination of Replication-Coupled Protein Destruction and Origin Licensing Control During Cell Cycle Transitions.

Degree: 2015, University of North Carolina

 Timely ubiquitin-mediated protein degradation is fundamental to cell cycle control, but the precise degradation order at each cell cycle phase transition is still unclear. In… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Genetics; School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Coleman, K. (2015). Coordination of Replication-Coupled Protein Destruction and Origin Licensing Control During Cell Cycle Transitions. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4fc3087d-39d5-44b7-a350-f45d2fa86e81

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):

Coleman, Kate. “Coordination of Replication-Coupled Protein Destruction and Origin Licensing Control During Cell Cycle Transitions.” 2015. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:4fc3087d-39d5-44b7-a350-f45d2fa86e81.

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

MLA Handbook (7th Edition):

Coleman, Kate. “Coordination of Replication-Coupled Protein Destruction and Origin Licensing Control During Cell Cycle Transitions.” 2015. Web. 28 Sep 2020.

Vancouver:

Coleman K. Coordination of Replication-Coupled Protein Destruction and Origin Licensing Control During Cell Cycle Transitions. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:4fc3087d-39d5-44b7-a350-f45d2fa86e81.

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

Council of Science Editors:

Coleman K. Coordination of Replication-Coupled Protein Destruction and Origin Licensing Control During Cell Cycle Transitions. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:4fc3087d-39d5-44b7-a350-f45d2fa86e81

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


University of North Carolina

9. Fahey, Catherine. The Effect of Cancer-Associated SETD2 Mutations on Transcription and Chromatin Organization.

Degree: 2017, University of North Carolina

 Clear cell renal cell carcinoma is characterized by mutations in chromatin modifying enzymes. Among these is SETD2, a non-redundant histone H3 lysine 36 methyltransferase. Mutations… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Fahey, C. (2017). The Effect of Cancer-Associated SETD2 Mutations on Transcription and Chromatin Organization. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:0fa1e41e-c273-499c-8cfd-f30baee6360f

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):

Fahey, Catherine. “The Effect of Cancer-Associated SETD2 Mutations on Transcription and Chromatin Organization.” 2017. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:0fa1e41e-c273-499c-8cfd-f30baee6360f.

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

MLA Handbook (7th Edition):

Fahey, Catherine. “The Effect of Cancer-Associated SETD2 Mutations on Transcription and Chromatin Organization.” 2017. Web. 28 Sep 2020.

Vancouver:

Fahey C. The Effect of Cancer-Associated SETD2 Mutations on Transcription and Chromatin Organization. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:0fa1e41e-c273-499c-8cfd-f30baee6360f.

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

Council of Science Editors:

Fahey C. The Effect of Cancer-Associated SETD2 Mutations on Transcription and Chromatin Organization. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:0fa1e41e-c273-499c-8cfd-f30baee6360f

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


University of North Carolina

10. Yu, Zhixian. Excess Centrosomes in Endothelial Cells: Causes And Effects.

Degree: 2016, University of North Carolina

 Tumor endothelial cells, which line the interior surface of tumor blood vessels, were considered genetically normal until recent findings showed that they can be aneuploid,… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Yu, Z. (2016). Excess Centrosomes in Endothelial Cells: Causes And Effects. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:2a9d88a7-8d43-41b2-bb9f-27235d174d72

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):

Yu, Zhixian. “Excess Centrosomes in Endothelial Cells: Causes And Effects.” 2016. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:2a9d88a7-8d43-41b2-bb9f-27235d174d72.

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

MLA Handbook (7th Edition):

Yu, Zhixian. “Excess Centrosomes in Endothelial Cells: Causes And Effects.” 2016. Web. 28 Sep 2020.

Vancouver:

Yu Z. Excess Centrosomes in Endothelial Cells: Causes And Effects. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:2a9d88a7-8d43-41b2-bb9f-27235d174d72.

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

Council of Science Editors:

Yu Z. Excess Centrosomes in Endothelial Cells: Causes And Effects. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:2a9d88a7-8d43-41b2-bb9f-27235d174d72

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


University of North Carolina

11. Anderson, Marybeth. Hexokinase 2 is important for tumor growth and metastasis in pancreatic ductal adenocarcinoma.

Degree: 2016, University of North Carolina

 Pancreatic ductal adenocarcinoma (PDAC) is the 4th leading cause of cancer deaths in the United States. The majority of PDAC patients are diagnosed with metastatic… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Anderson, M. (2016). Hexokinase 2 is important for tumor growth and metastasis in pancreatic ductal adenocarcinoma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:05a54123-84e3-464f-8ca8-957c4533b0d3

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):

Anderson, Marybeth. “Hexokinase 2 is important for tumor growth and metastasis in pancreatic ductal adenocarcinoma.” 2016. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:05a54123-84e3-464f-8ca8-957c4533b0d3.

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

MLA Handbook (7th Edition):

Anderson, Marybeth. “Hexokinase 2 is important for tumor growth and metastasis in pancreatic ductal adenocarcinoma.” 2016. Web. 28 Sep 2020.

Vancouver:

Anderson M. Hexokinase 2 is important for tumor growth and metastasis in pancreatic ductal adenocarcinoma. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:05a54123-84e3-464f-8ca8-957c4533b0d3.

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

Council of Science Editors:

Anderson M. Hexokinase 2 is important for tumor growth and metastasis in pancreatic ductal adenocarcinoma. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:05a54123-84e3-464f-8ca8-957c4533b0d3

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


University of North Carolina

12. Rojas, Juan. Contrast-Enhanced Ultrasound for the Assessment of Response to Therapy.

Degree: Biomedical Engineering, 2018, University of North Carolina

 Accurate assessment of cancer response to therapy is important for effective treatment outcome and limiting unnecessary therapeutics. The clinical gold standard for evaluating response to… (more)

Subjects/Keywords: School of Medicine; UNC/NCSU Joint Department of Biomedical Engineering

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

APA (6th Edition):

Rojas, J. (2018). Contrast-Enhanced Ultrasound for the Assessment of Response to Therapy. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:5bb09c00-b187-4bf5-8af7-90a5425821c7

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):

Rojas, Juan. “Contrast-Enhanced Ultrasound for the Assessment of Response to Therapy.” 2018. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:5bb09c00-b187-4bf5-8af7-90a5425821c7.

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

MLA Handbook (7th Edition):

Rojas, Juan. “Contrast-Enhanced Ultrasound for the Assessment of Response to Therapy.” 2018. Web. 28 Sep 2020.

Vancouver:

Rojas J. Contrast-Enhanced Ultrasound for the Assessment of Response to Therapy. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:5bb09c00-b187-4bf5-8af7-90a5425821c7.

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

Council of Science Editors:

Rojas J. Contrast-Enhanced Ultrasound for the Assessment of Response to Therapy. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:5bb09c00-b187-4bf5-8af7-90a5425821c7

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


University of North Carolina

13. Arreola, Alexandra. MOLECULAR AND PHYSIOLOGICAL ROLES OF VON HIPPEL-LINDAU MUTATION AND HYPOXIA INDUCIBLE FACTORS: FINE-TUNED EXPRESSION EFFECTS ON ANGIOGENESIS AND METABOLISM.

Degree: 2014, University of North Carolina

 Renal cell carcinoma (RCC) accounts for approximately 58,000 new cases and over 13,000 deaths annually in the United States, afflicting men and women at a… (more)

Subjects/Keywords: Molecular biology; Genetics; Oncology; School of Medicine; Curriculum in Genetics and Molecular Biology

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

APA (6th Edition):

Arreola, A. (2014). MOLECULAR AND PHYSIOLOGICAL ROLES OF VON HIPPEL-LINDAU MUTATION AND HYPOXIA INDUCIBLE FACTORS: FINE-TUNED EXPRESSION EFFECTS ON ANGIOGENESIS AND METABOLISM. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c239e872-faf0-4a1a-8982-bfc90eb6dff4

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):

Arreola, Alexandra. “MOLECULAR AND PHYSIOLOGICAL ROLES OF VON HIPPEL-LINDAU MUTATION AND HYPOXIA INDUCIBLE FACTORS: FINE-TUNED EXPRESSION EFFECTS ON ANGIOGENESIS AND METABOLISM.” 2014. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:c239e872-faf0-4a1a-8982-bfc90eb6dff4.

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

MLA Handbook (7th Edition):

Arreola, Alexandra. “MOLECULAR AND PHYSIOLOGICAL ROLES OF VON HIPPEL-LINDAU MUTATION AND HYPOXIA INDUCIBLE FACTORS: FINE-TUNED EXPRESSION EFFECTS ON ANGIOGENESIS AND METABOLISM.” 2014. Web. 28 Sep 2020.

Vancouver:

Arreola A. MOLECULAR AND PHYSIOLOGICAL ROLES OF VON HIPPEL-LINDAU MUTATION AND HYPOXIA INDUCIBLE FACTORS: FINE-TUNED EXPRESSION EFFECTS ON ANGIOGENESIS AND METABOLISM. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:c239e872-faf0-4a1a-8982-bfc90eb6dff4.

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

Council of Science Editors:

Arreola A. MOLECULAR AND PHYSIOLOGICAL ROLES OF VON HIPPEL-LINDAU MUTATION AND HYPOXIA INDUCIBLE FACTORS: FINE-TUNED EXPRESSION EFFECTS ON ANGIOGENESIS AND METABOLISM. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:c239e872-faf0-4a1a-8982-bfc90eb6dff4

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


University of North Carolina

14. Wei, Darmood. Elucidating SNF5 Regulated Gene Expression in Malignant Rhabdoid Tumor Development.

Degree: 2014, University of North Carolina

 Malignant Rhabdoid Tumors (MRTs), a pediatric renal cancer, lack SNF5, a subunit of the SWI/SNF chromatin remodeling complex which regulates nucleosome positioning and gene expression.… (more)

Subjects/Keywords: Toxicology; School of Medicine; Curriculum in Toxicology

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

APA (6th Edition):

Wei, D. (2014). Elucidating SNF5 Regulated Gene Expression in Malignant Rhabdoid Tumor Development. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:bcca99e3-3b24-4f32-a7b1-38eb1515c585

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):

Wei, Darmood. “Elucidating SNF5 Regulated Gene Expression in Malignant Rhabdoid Tumor Development.” 2014. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:bcca99e3-3b24-4f32-a7b1-38eb1515c585.

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

MLA Handbook (7th Edition):

Wei, Darmood. “Elucidating SNF5 Regulated Gene Expression in Malignant Rhabdoid Tumor Development.” 2014. Web. 28 Sep 2020.

Vancouver:

Wei D. Elucidating SNF5 Regulated Gene Expression in Malignant Rhabdoid Tumor Development. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:bcca99e3-3b24-4f32-a7b1-38eb1515c585.

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

Council of Science Editors:

Wei D. Elucidating SNF5 Regulated Gene Expression in Malignant Rhabdoid Tumor Development. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:bcca99e3-3b24-4f32-a7b1-38eb1515c585

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


University of North Carolina

15. Bailey, Sean. Inhibition of compensatory survival and proliferative pathway activation induced by mTOR inhibition in renal cell carcinoma.

Degree: 2014, University of North Carolina

 The mammalian target of rapamycin (mTOR) is a key regulator of tumor progression in a variety of cancers and has been shown to be dysregulated… (more)

Subjects/Keywords: Molecular biology; Genetics; School of Medicine; Curriculum in Genetics and Molecular Biology

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

APA (6th Edition):

Bailey, S. (2014). Inhibition of compensatory survival and proliferative pathway activation induced by mTOR inhibition in renal cell carcinoma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:3ecdd41c-8862-4504-a14a-8ead22d81d74

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):

Bailey, Sean. “Inhibition of compensatory survival and proliferative pathway activation induced by mTOR inhibition in renal cell carcinoma.” 2014. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:3ecdd41c-8862-4504-a14a-8ead22d81d74.

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

MLA Handbook (7th Edition):

Bailey, Sean. “Inhibition of compensatory survival and proliferative pathway activation induced by mTOR inhibition in renal cell carcinoma.” 2014. Web. 28 Sep 2020.

Vancouver:

Bailey S. Inhibition of compensatory survival and proliferative pathway activation induced by mTOR inhibition in renal cell carcinoma. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:3ecdd41c-8862-4504-a14a-8ead22d81d74.

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

Council of Science Editors:

Bailey S. Inhibition of compensatory survival and proliferative pathway activation induced by mTOR inhibition in renal cell carcinoma. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:3ecdd41c-8862-4504-a14a-8ead22d81d74

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


University of North Carolina

16. Lee, Caroline Martz. Type 2B von Hippel-Lindau disease: molecular biology, tumor growth, and development.

Degree: 2009, University of North Carolina

 Von Hippel-Lindau (VHL) disease is caused by germline mutations in the VHL tumor suppressor gene, with Type 2B missense VHL mutations predisposing to renal cell… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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

APA (6th Edition):

Lee, C. M. (2009). Type 2B von Hippel-Lindau disease: molecular biology, tumor growth, and development. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c6c29414-22c9-4ae9-b86b-6eb43db37d4c

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, Caroline Martz. “Type 2B von Hippel-Lindau disease: molecular biology, tumor growth, and development.” 2009. Thesis, University of North Carolina. Accessed September 28, 2020. https://cdr.lib.unc.edu/record/uuid:c6c29414-22c9-4ae9-b86b-6eb43db37d4c.

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

MLA Handbook (7th Edition):

Lee, Caroline Martz. “Type 2B von Hippel-Lindau disease: molecular biology, tumor growth, and development.” 2009. Web. 28 Sep 2020.

Vancouver:

Lee CM. Type 2B von Hippel-Lindau disease: molecular biology, tumor growth, and development. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Sep 28]. Available from: https://cdr.lib.unc.edu/record/uuid:c6c29414-22c9-4ae9-b86b-6eb43db37d4c.

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

Council of Science Editors:

Lee CM. Type 2B von Hippel-Lindau disease: molecular biology, tumor growth, and development. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:c6c29414-22c9-4ae9-b86b-6eb43db37d4c

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

.