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University: University of North Carolina

You searched for subject:(Molecular Genetics). Showing records 1 – 30 of 185 total matches.

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University of North Carolina

1. 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 July 13, 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. 13 Jul 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 Jul 13]. 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

2. Damrauer, Jeffrey. Discovery and Characterization of Molecular Subtypes in High-grade Urothelial Carcinoma.

Degree: 2014, University of North Carolina

 Bladder Cancer is the 4th most commonly diagnosed cancer in men and the 8th most deadly. While non-muscle invasive bladder cancer has a relatively high… (more)

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

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APA (6th Edition):

Damrauer, J. (2014). Discovery and Characterization of Molecular Subtypes in High-grade Urothelial Carcinoma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:a8ac8be0-5a5a-45f8-b58a-9a13e00cc2dd

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):

Damrauer, Jeffrey. “Discovery and Characterization of Molecular Subtypes in High-grade Urothelial Carcinoma.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:a8ac8be0-5a5a-45f8-b58a-9a13e00cc2dd.

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

MLA Handbook (7th Edition):

Damrauer, Jeffrey. “Discovery and Characterization of Molecular Subtypes in High-grade Urothelial Carcinoma.” 2014. Web. 13 Jul 2020.

Vancouver:

Damrauer J. Discovery and Characterization of Molecular Subtypes in High-grade Urothelial Carcinoma. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:a8ac8be0-5a5a-45f8-b58a-9a13e00cc2dd.

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

Council of Science Editors:

Damrauer J. Discovery and Characterization of Molecular Subtypes in High-grade Urothelial Carcinoma. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:a8ac8be0-5a5a-45f8-b58a-9a13e00cc2dd

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


University of North Carolina

3. Wozniak, Glenn. Investigation of the Role and Regulation of Histone H2B Ubiquitylation in Transcription.

Degree: 2014, University of North Carolina

 In eukaryotes, DNA is packaged by histone proteins to form nucleosomes - the fundamental unit of chromatin. Aside from their structural role in DNA compaction,… (more)

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

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APA (6th Edition):

Wozniak, G. (2014). Investigation of the Role and Regulation of Histone H2B Ubiquitylation in Transcription. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:bc4a5ff2-743a-4c42-92b4-fcc0e2990cb5

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):

Wozniak, Glenn. “Investigation of the Role and Regulation of Histone H2B Ubiquitylation in Transcription.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:bc4a5ff2-743a-4c42-92b4-fcc0e2990cb5.

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

MLA Handbook (7th Edition):

Wozniak, Glenn. “Investigation of the Role and Regulation of Histone H2B Ubiquitylation in Transcription.” 2014. Web. 13 Jul 2020.

Vancouver:

Wozniak G. Investigation of the Role and Regulation of Histone H2B Ubiquitylation in Transcription. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:bc4a5ff2-743a-4c42-92b4-fcc0e2990cb5.

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

Council of Science Editors:

Wozniak G. Investigation of the Role and Regulation of Histone H2B Ubiquitylation in Transcription. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:bc4a5ff2-743a-4c42-92b4-fcc0e2990cb5

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


University of North Carolina

4. 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 (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 July 13, 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. 13 Jul 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 Jul 13]. 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

5. Leopold, Luciana. SURVEILLANCE AND TARGETING OF ABERRANT TRANSCRIPTS IN CAENORHABDITIS ELEGANS.

Degree: 2014, University of North Carolina

 An organism requires mechanisms with which to protect the fidelity and integrity of the genome, transcriptome, and proteome in order not only to remain healthy… (more)

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

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APA (6th Edition):

Leopold, L. (2014). SURVEILLANCE AND TARGETING OF ABERRANT TRANSCRIPTS IN CAENORHABDITIS ELEGANS. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:ada89d4f-4df5-4185-af49-4684fa99b655

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):

Leopold, Luciana. “SURVEILLANCE AND TARGETING OF ABERRANT TRANSCRIPTS IN CAENORHABDITIS ELEGANS.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:ada89d4f-4df5-4185-af49-4684fa99b655.

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

MLA Handbook (7th Edition):

Leopold, Luciana. “SURVEILLANCE AND TARGETING OF ABERRANT TRANSCRIPTS IN CAENORHABDITIS ELEGANS.” 2014. Web. 13 Jul 2020.

Vancouver:

Leopold L. SURVEILLANCE AND TARGETING OF ABERRANT TRANSCRIPTS IN CAENORHABDITIS ELEGANS. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:ada89d4f-4df5-4185-af49-4684fa99b655.

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

Council of Science Editors:

Leopold L. SURVEILLANCE AND TARGETING OF ABERRANT TRANSCRIPTS IN CAENORHABDITIS ELEGANS. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:ada89d4f-4df5-4185-af49-4684fa99b655

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


University of North Carolina

6. He, Yizhou. Identification of Novel Regulatory and Target Proteins in the p53 Pathway: APC2 and PFK2.

Degree: 2014, University of North Carolina

 The Mdm2 proto-oncoprotein is the primary negative regulator for the tumor suppressor p53. While it is believed that Mdm2 degradation is regulated via its own… (more)

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

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APA (6th Edition):

He, Y. (2014). Identification of Novel Regulatory and Target Proteins in the p53 Pathway: APC2 and PFK2. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:aeef9369-e7e6-440c-834d-19401d853820

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):

He, Yizhou. “Identification of Novel Regulatory and Target Proteins in the p53 Pathway: APC2 and PFK2.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:aeef9369-e7e6-440c-834d-19401d853820.

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

MLA Handbook (7th Edition):

He, Yizhou. “Identification of Novel Regulatory and Target Proteins in the p53 Pathway: APC2 and PFK2.” 2014. Web. 13 Jul 2020.

Vancouver:

He Y. Identification of Novel Regulatory and Target Proteins in the p53 Pathway: APC2 and PFK2. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:aeef9369-e7e6-440c-834d-19401d853820.

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

Council of Science Editors:

He Y. Identification of Novel Regulatory and Target Proteins in the p53 Pathway: APC2 and PFK2. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:aeef9369-e7e6-440c-834d-19401d853820

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


University of North Carolina

7. Griffin, Nicole. Genetic Analysis of Complex and Mendelian Diseases.

Degree: 2014, University of North Carolina

 This work describes approaches for discovering genetic variants that contribute to the etiology of human diseases with complex and simple modes of inheritance through the… (more)

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

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APA (6th Edition):

Griffin, N. (2014). Genetic Analysis of Complex and Mendelian Diseases. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:9e81fbe4-dec8-49a7-bce1-2d04e83d534d

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):

Griffin, Nicole. “Genetic Analysis of Complex and Mendelian Diseases.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:9e81fbe4-dec8-49a7-bce1-2d04e83d534d.

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

MLA Handbook (7th Edition):

Griffin, Nicole. “Genetic Analysis of Complex and Mendelian Diseases.” 2014. Web. 13 Jul 2020.

Vancouver:

Griffin N. Genetic Analysis of Complex and Mendelian Diseases. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:9e81fbe4-dec8-49a7-bce1-2d04e83d534d.

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

Council of Science Editors:

Griffin N. Genetic Analysis of Complex and Mendelian Diseases. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:9e81fbe4-dec8-49a7-bce1-2d04e83d534d

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


University of North Carolina

8. 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 (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 July 13, 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. 13 Jul 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 Jul 13]. 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

9. Kulzer, Jennifer. Molecular and Biological Mechanisms of the ARAP1 Type 2 Diabetes Locus.

Degree: 2014, University of North Carolina

 Genome-wide association studies (GWAS) have identified more than 70 loci associated with type 2 diabetes (T2D), but for most, the underlying causal variants, associated genes,… (more)

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

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APA (6th Edition):

Kulzer, J. (2014). Molecular and Biological Mechanisms of the ARAP1 Type 2 Diabetes Locus. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e27fe8b0-da70-4484-9f89-0396d93d85f1

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):

Kulzer, Jennifer. “Molecular and Biological Mechanisms of the ARAP1 Type 2 Diabetes Locus.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:e27fe8b0-da70-4484-9f89-0396d93d85f1.

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

MLA Handbook (7th Edition):

Kulzer, Jennifer. “Molecular and Biological Mechanisms of the ARAP1 Type 2 Diabetes Locus.” 2014. Web. 13 Jul 2020.

Vancouver:

Kulzer J. Molecular and Biological Mechanisms of the ARAP1 Type 2 Diabetes Locus. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:e27fe8b0-da70-4484-9f89-0396d93d85f1.

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

Council of Science Editors:

Kulzer J. Molecular and Biological Mechanisms of the ARAP1 Type 2 Diabetes Locus. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:e27fe8b0-da70-4484-9f89-0396d93d85f1

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


University of North Carolina

10. Xie, Yuying. ROLE OF EPIDERMAL GROWTH FACTOR RECEPTOR ON CARDIAC FUNCTION.

Degree: 2015, University of North Carolina

 The epidermal growth factor receptor (EGFR/ERBB1) was the first discovered member of the ERBB family of tyrosine kinas receptors that includes ERBB2, ERBB3 and ERBB4.… (more)

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

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APA (6th Edition):

Xie, Y. (2015). ROLE OF EPIDERMAL GROWTH FACTOR RECEPTOR ON CARDIAC FUNCTION. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:90236d9f-a0fa-47de-b9c5-08d4a2dfe021

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):

Xie, Yuying. “ROLE OF EPIDERMAL GROWTH FACTOR RECEPTOR ON CARDIAC FUNCTION.” 2015. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:90236d9f-a0fa-47de-b9c5-08d4a2dfe021.

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

MLA Handbook (7th Edition):

Xie, Yuying. “ROLE OF EPIDERMAL GROWTH FACTOR RECEPTOR ON CARDIAC FUNCTION.” 2015. Web. 13 Jul 2020.

Vancouver:

Xie Y. ROLE OF EPIDERMAL GROWTH FACTOR RECEPTOR ON CARDIAC FUNCTION. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:90236d9f-a0fa-47de-b9c5-08d4a2dfe021.

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

Council of Science Editors:

Xie Y. ROLE OF EPIDERMAL GROWTH FACTOR RECEPTOR ON CARDIAC FUNCTION. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:90236d9f-a0fa-47de-b9c5-08d4a2dfe021

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


University of North Carolina

11. Bellendir, Stephanie. Genetic and Biochemical Characterization of Drosophila Gen during DNA Repair and Recombination.

Degree: 2015, University of North Carolina

 Holliday junction (HJ) resolvases maintain genome stability by processing DNA intermediates that arise during DNA repair. While human GEN1 and several orthologs possess HJ resolvase… (more)

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

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APA (6th Edition):

Bellendir, S. (2015). Genetic and Biochemical Characterization of Drosophila Gen during DNA Repair and Recombination. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:5e095fa6-f6ad-456f-9f0e-c57dab39d1a2

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):

Bellendir, Stephanie. “Genetic and Biochemical Characterization of Drosophila Gen during DNA Repair and Recombination.” 2015. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:5e095fa6-f6ad-456f-9f0e-c57dab39d1a2.

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

MLA Handbook (7th Edition):

Bellendir, Stephanie. “Genetic and Biochemical Characterization of Drosophila Gen during DNA Repair and Recombination.” 2015. Web. 13 Jul 2020.

Vancouver:

Bellendir S. Genetic and Biochemical Characterization of Drosophila Gen during DNA Repair and Recombination. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:5e095fa6-f6ad-456f-9f0e-c57dab39d1a2.

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

Council of Science Editors:

Bellendir S. Genetic and Biochemical Characterization of Drosophila Gen during DNA Repair and Recombination. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:5e095fa6-f6ad-456f-9f0e-c57dab39d1a2

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


University of North Carolina

12. Whittlesey, Rebecca. Identification of Potential Biomarkers in PDAC.

Degree: 2014, University of North Carolina

 Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer deaths in both men and women in the United States, with a 5-year survival… (more)

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

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APA (6th Edition):

Whittlesey, R. (2014). Identification of Potential Biomarkers in PDAC. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:badcaa61-f5a3-4aed-b399-4ae2a6b8b589

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):

Whittlesey, Rebecca. “Identification of Potential Biomarkers in PDAC.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:badcaa61-f5a3-4aed-b399-4ae2a6b8b589.

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

MLA Handbook (7th Edition):

Whittlesey, Rebecca. “Identification of Potential Biomarkers in PDAC.” 2014. Web. 13 Jul 2020.

Vancouver:

Whittlesey R. Identification of Potential Biomarkers in PDAC. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:badcaa61-f5a3-4aed-b399-4ae2a6b8b589.

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

Council of Science Editors:

Whittlesey R. Identification of Potential Biomarkers in PDAC. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:badcaa61-f5a3-4aed-b399-4ae2a6b8b589

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


University of North Carolina

13. Simon, Matt. Germ Cell Immortality in C. elegans: Reduced Insulin Signaling Restores Germline Immortality in PIWI Argonaute PRG-1 Mutants.

Degree: 2014, University of North Carolina

 Germ cells can maintain themselves indefinitely over many generations, effectively free of the proliferative damage that affects most somatic tissues. Deficiency for the C. elegans… (more)

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

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APA (6th Edition):

Simon, M. (2014). Germ Cell Immortality in C. elegans: Reduced Insulin Signaling Restores Germline Immortality in PIWI Argonaute PRG-1 Mutants. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:83e1be90-3472-4025-b47e-1d1e4c61e490

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):

Simon, Matt. “Germ Cell Immortality in C. elegans: Reduced Insulin Signaling Restores Germline Immortality in PIWI Argonaute PRG-1 Mutants.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:83e1be90-3472-4025-b47e-1d1e4c61e490.

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

MLA Handbook (7th Edition):

Simon, Matt. “Germ Cell Immortality in C. elegans: Reduced Insulin Signaling Restores Germline Immortality in PIWI Argonaute PRG-1 Mutants.” 2014. Web. 13 Jul 2020.

Vancouver:

Simon M. Germ Cell Immortality in C. elegans: Reduced Insulin Signaling Restores Germline Immortality in PIWI Argonaute PRG-1 Mutants. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:83e1be90-3472-4025-b47e-1d1e4c61e490.

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

Council of Science Editors:

Simon M. Germ Cell Immortality in C. elegans: Reduced Insulin Signaling Restores Germline Immortality in PIWI Argonaute PRG-1 Mutants. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:83e1be90-3472-4025-b47e-1d1e4c61e490

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


University of North Carolina

14. Waters, Crystal. Factors increasing the flexibility of nonhomologous end joining.

Degree: 2015, University of North Carolina

 Broken chromosomes can be catastrophic for an organism if misrepaired or left unrepaired. Mammals rely predominately on non-homologous end joining (NHEJ) to efficiently repair chromosome… (more)

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

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APA (6th Edition):

Waters, C. (2015). Factors increasing the flexibility of nonhomologous end joining. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:dfed623e-e848-481b-b59b-12eaea501fa8

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):

Waters, Crystal. “Factors increasing the flexibility of nonhomologous end joining.” 2015. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:dfed623e-e848-481b-b59b-12eaea501fa8.

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

MLA Handbook (7th Edition):

Waters, Crystal. “Factors increasing the flexibility of nonhomologous end joining.” 2015. Web. 13 Jul 2020.

Vancouver:

Waters C. Factors increasing the flexibility of nonhomologous end joining. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:dfed623e-e848-481b-b59b-12eaea501fa8.

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

Council of Science Editors:

Waters C. Factors increasing the flexibility of nonhomologous end joining. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:dfed623e-e848-481b-b59b-12eaea501fa8

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


University of North Carolina

15. Tollini, Laura. Exploring the In Vivo Role of the Mdm2 Ring Finger Domain in p53 Regulation.

Degree: 2014, University of North Carolina

 Classically characterized as an “overarching” tumor suppressor, p53 is frequently found mutated, deleted, or misregulated in human cancers. Through its role as a transcription factor,… (more)

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

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APA (6th Edition):

Tollini, L. (2014). Exploring the In Vivo Role of the Mdm2 Ring Finger Domain in p53 Regulation. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:088fdc11-df44-4c72-958f-f21e90a102f0

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):

Tollini, Laura. “Exploring the In Vivo Role of the Mdm2 Ring Finger Domain in p53 Regulation.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:088fdc11-df44-4c72-958f-f21e90a102f0.

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

MLA Handbook (7th Edition):

Tollini, Laura. “Exploring the In Vivo Role of the Mdm2 Ring Finger Domain in p53 Regulation.” 2014. Web. 13 Jul 2020.

Vancouver:

Tollini L. Exploring the In Vivo Role of the Mdm2 Ring Finger Domain in p53 Regulation. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:088fdc11-df44-4c72-958f-f21e90a102f0.

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

Council of Science Editors:

Tollini L. Exploring the In Vivo Role of the Mdm2 Ring Finger Domain in p53 Regulation. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:088fdc11-df44-4c72-958f-f21e90a102f0

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


University of North Carolina

16. Dorr, Kerry. Characterization of the Casz1-Dependent Mechanisms Essential for Cardiomyocyte Development.

Degree: 2015, University of North Carolina

 The heart is one of the first structures to form during development and is required for embryonic growth and survival. The four-chambered mammalian heart arises… (more)

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

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APA (6th Edition):

Dorr, K. (2015). Characterization of the Casz1-Dependent Mechanisms Essential for Cardiomyocyte Development. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:723a77a9-9262-44b6-aab8-a8c0063c26c6

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):

Dorr, Kerry. “Characterization of the Casz1-Dependent Mechanisms Essential for Cardiomyocyte Development.” 2015. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:723a77a9-9262-44b6-aab8-a8c0063c26c6.

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

MLA Handbook (7th Edition):

Dorr, Kerry. “Characterization of the Casz1-Dependent Mechanisms Essential for Cardiomyocyte Development.” 2015. Web. 13 Jul 2020.

Vancouver:

Dorr K. Characterization of the Casz1-Dependent Mechanisms Essential for Cardiomyocyte Development. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:723a77a9-9262-44b6-aab8-a8c0063c26c6.

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

Council of Science Editors:

Dorr K. Characterization of the Casz1-Dependent Mechanisms Essential for Cardiomyocyte Development. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:723a77a9-9262-44b6-aab8-a8c0063c26c6

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


University of North Carolina

17. 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 July 13, 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. 13 Jul 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 Jul 13]. 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

18. 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 July 13, 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. 13 Jul 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 Jul 13]. 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

19. Crowl, Tessa. SOX2 is critical for the maintenance of quiescence and homeostasis in nascent Müller glial cells.

Degree: 2014, University of North Carolina

 SOX2 is a HMG-box transcription factor that defines neural stem cell populations from the earliest stages of embryogenesis to adulthood. Previous studies have shown that… (more)

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

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APA (6th Edition):

Crowl, T. (2014). SOX2 is critical for the maintenance of quiescence and homeostasis in nascent Müller glial cells. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:0f125912-36d0-4999-9812-b7b4ab346bca

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):

Crowl, Tessa. “SOX2 is critical for the maintenance of quiescence and homeostasis in nascent Müller glial cells.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:0f125912-36d0-4999-9812-b7b4ab346bca.

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

MLA Handbook (7th Edition):

Crowl, Tessa. “SOX2 is critical for the maintenance of quiescence and homeostasis in nascent Müller glial cells.” 2014. Web. 13 Jul 2020.

Vancouver:

Crowl T. SOX2 is critical for the maintenance of quiescence and homeostasis in nascent Müller glial cells. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:0f125912-36d0-4999-9812-b7b4ab346bca.

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

Council of Science Editors:

Crowl T. SOX2 is critical for the maintenance of quiescence and homeostasis in nascent Müller glial cells. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:0f125912-36d0-4999-9812-b7b4ab346bca

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


University of North Carolina

20. Bower, Brian. An In Vitro Characterization of Functional Interactions Between Purified Telomere Repeat Binding Factors 1 and 2 and Rad51 Recombinase.

Degree: 2014, University of North Carolina

 A growing body of literature suggests that the homologous recombination/repair (HR) pathway cooperates with components of the shelterin complex to promote both telomere maintenance and… (more)

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

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APA (6th Edition):

Bower, B. (2014). An In Vitro Characterization of Functional Interactions Between Purified Telomere Repeat Binding Factors 1 and 2 and Rad51 Recombinase. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:577c29c0-e2e4-4a85-ac73-7ed54cc4323c

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):

Bower, Brian. “An In Vitro Characterization of Functional Interactions Between Purified Telomere Repeat Binding Factors 1 and 2 and Rad51 Recombinase.” 2014. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:577c29c0-e2e4-4a85-ac73-7ed54cc4323c.

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

MLA Handbook (7th Edition):

Bower, Brian. “An In Vitro Characterization of Functional Interactions Between Purified Telomere Repeat Binding Factors 1 and 2 and Rad51 Recombinase.” 2014. Web. 13 Jul 2020.

Vancouver:

Bower B. An In Vitro Characterization of Functional Interactions Between Purified Telomere Repeat Binding Factors 1 and 2 and Rad51 Recombinase. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:577c29c0-e2e4-4a85-ac73-7ed54cc4323c.

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

Council of Science Editors:

Bower B. An In Vitro Characterization of Functional Interactions Between Purified Telomere Repeat Binding Factors 1 and 2 and Rad51 Recombinase. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:577c29c0-e2e4-4a85-ac73-7ed54cc4323c

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


University of North Carolina

21. Thorner, Aaron R. Determining the Roles of MYB Family Transcription Factors in Breast Tumorigenesis.

Degree: 2010, University of North Carolina

 A major advancement in the field of breast cancer research was the discovery of the breast tumor intrinsic subtypes made through the utilization of gene… (more)

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

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APA (6th Edition):

Thorner, A. R. (2010). Determining the Roles of MYB Family Transcription Factors in Breast Tumorigenesis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:62cba637-b15f-421d-951d-1d23751ea54f

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):

Thorner, Aaron R. “Determining the Roles of MYB Family Transcription Factors in Breast Tumorigenesis.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:62cba637-b15f-421d-951d-1d23751ea54f.

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

MLA Handbook (7th Edition):

Thorner, Aaron R. “Determining the Roles of MYB Family Transcription Factors in Breast Tumorigenesis.” 2010. Web. 13 Jul 2020.

Vancouver:

Thorner AR. Determining the Roles of MYB Family Transcription Factors in Breast Tumorigenesis. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:62cba637-b15f-421d-951d-1d23751ea54f.

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

Council of Science Editors:

Thorner AR. Determining the Roles of MYB Family Transcription Factors in Breast Tumorigenesis. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:62cba637-b15f-421d-951d-1d23751ea54f

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


University of North Carolina

22. Deisenroth, Chad R. Regulation and function of mitochondrial Hep27: a novel modulator of the Mdm2-p53 pathway.

Degree: 2010, University of North Carolina

 The ever-expanding role of p53 in cellular metabolism, apoptosis, and cell cycle control has led to increasing interest in defining the stress response pathways that… (more)

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

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APA (6th Edition):

Deisenroth, C. R. (2010). Regulation and function of mitochondrial Hep27: a novel modulator of the Mdm2-p53 pathway. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:3c800f84-1ac9-4e87-941c-c11ba5dfcec8

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):

Deisenroth, Chad R. “Regulation and function of mitochondrial Hep27: a novel modulator of the Mdm2-p53 pathway.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:3c800f84-1ac9-4e87-941c-c11ba5dfcec8.

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

MLA Handbook (7th Edition):

Deisenroth, Chad R. “Regulation and function of mitochondrial Hep27: a novel modulator of the Mdm2-p53 pathway.” 2010. Web. 13 Jul 2020.

Vancouver:

Deisenroth CR. Regulation and function of mitochondrial Hep27: a novel modulator of the Mdm2-p53 pathway. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:3c800f84-1ac9-4e87-941c-c11ba5dfcec8.

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

Council of Science Editors:

Deisenroth CR. Regulation and function of mitochondrial Hep27: a novel modulator of the Mdm2-p53 pathway. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:3c800f84-1ac9-4e87-941c-c11ba5dfcec8

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


University of North Carolina

23. Gaulton, Kyle J. Candidate-Based Approaches to Identify Genetic Variation Influencing Type 2 Diabetes and Quantitative Traits.

Degree: 2010, University of North Carolina

 Type 2 diabetes (T2D) is a metabolic disorder characterized by insulin resistance and impaired insulin secretion that affects more than 20 million Americans, although the… (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):

Gaulton, K. J. (2010). Candidate-Based Approaches to Identify Genetic Variation Influencing Type 2 Diabetes and Quantitative Traits. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:3753a6d8-08b5-474f-9577-49a399ac7ce7

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):

Gaulton, Kyle J. “Candidate-Based Approaches to Identify Genetic Variation Influencing Type 2 Diabetes and Quantitative Traits.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:3753a6d8-08b5-474f-9577-49a399ac7ce7.

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

MLA Handbook (7th Edition):

Gaulton, Kyle J. “Candidate-Based Approaches to Identify Genetic Variation Influencing Type 2 Diabetes and Quantitative Traits.” 2010. Web. 13 Jul 2020.

Vancouver:

Gaulton KJ. Candidate-Based Approaches to Identify Genetic Variation Influencing Type 2 Diabetes and Quantitative Traits. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:3753a6d8-08b5-474f-9577-49a399ac7ce7.

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

Council of Science Editors:

Gaulton KJ. Candidate-Based Approaches to Identify Genetic Variation Influencing Type 2 Diabetes and Quantitative Traits. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:3753a6d8-08b5-474f-9577-49a399ac7ce7

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


University of North Carolina

24. Marvelle, Amanda F. The genetics of obesity-related traits and lipoproteins in Filipino women.

Degree: 2010, University of North Carolina

 The underlying genetic component of risk factors for cardiovascular disease (CVD) is not well understood. Recently, advances in high-throughput genotyping, single nucleotide polymorphism (SNP) discovery,… (more)

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

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APA (6th Edition):

Marvelle, A. F. (2010). The genetics of obesity-related traits and lipoproteins in Filipino women. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:f8d8fb5f-32fd-4bbb-a8f7-cdda342bc1a6

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):

Marvelle, Amanda F. “The genetics of obesity-related traits and lipoproteins in Filipino women.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:f8d8fb5f-32fd-4bbb-a8f7-cdda342bc1a6.

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

MLA Handbook (7th Edition):

Marvelle, Amanda F. “The genetics of obesity-related traits and lipoproteins in Filipino women.” 2010. Web. 13 Jul 2020.

Vancouver:

Marvelle AF. The genetics of obesity-related traits and lipoproteins in Filipino women. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:f8d8fb5f-32fd-4bbb-a8f7-cdda342bc1a6.

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

Council of Science Editors:

Marvelle AF. The genetics of obesity-related traits and lipoproteins in Filipino women. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:f8d8fb5f-32fd-4bbb-a8f7-cdda342bc1a6

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


University of North Carolina

25. Bayer, Matthew Alexander. Factors affecting the formation, stability, and expression of unintegrated lentiviral vector genomes.

Degree: 2010, University of North Carolina

 Lentiviral vectors present an attractive means of delivering therapeutic transgenes, as they deliver a relatively large, stably integrated and expressed genetic payload to both dividing… (more)

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

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APA (6th Edition):

Bayer, M. A. (2010). Factors affecting the formation, stability, and expression of unintegrated lentiviral vector genomes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e4ff4d83-4758-4983-94cf-7337f7056ea9

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):

Bayer, Matthew Alexander. “Factors affecting the formation, stability, and expression of unintegrated lentiviral vector genomes.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:e4ff4d83-4758-4983-94cf-7337f7056ea9.

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

MLA Handbook (7th Edition):

Bayer, Matthew Alexander. “Factors affecting the formation, stability, and expression of unintegrated lentiviral vector genomes.” 2010. Web. 13 Jul 2020.

Vancouver:

Bayer MA. Factors affecting the formation, stability, and expression of unintegrated lentiviral vector genomes. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:e4ff4d83-4758-4983-94cf-7337f7056ea9.

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

Council of Science Editors:

Bayer MA. Factors affecting the formation, stability, and expression of unintegrated lentiviral vector genomes. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:e4ff4d83-4758-4983-94cf-7337f7056ea9

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


University of North Carolina

26. Andersen, Sabrina L. DmBLM’s Functions in DNA Repair and Recombination.

Degree: 2010, University of North Carolina

 Maintaining stable chromosomes requires an array of repair and recombination proteins. These proteins ensure that chromosomes are accurately replicated, repaired, and segregated. One such protein… (more)

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

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APA (6th Edition):

Andersen, S. L. (2010). DmBLM’s Functions in DNA Repair and Recombination. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:35831d26-ada5-491f-91e3-f8daf9fd3152

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):

Andersen, Sabrina L. “DmBLM’s Functions in DNA Repair and Recombination.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:35831d26-ada5-491f-91e3-f8daf9fd3152.

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

MLA Handbook (7th Edition):

Andersen, Sabrina L. “DmBLM’s Functions in DNA Repair and Recombination.” 2010. Web. 13 Jul 2020.

Vancouver:

Andersen SL. DmBLM’s Functions in DNA Repair and Recombination. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:35831d26-ada5-491f-91e3-f8daf9fd3152.

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

Council of Science Editors:

Andersen SL. DmBLM’s Functions in DNA Repair and Recombination. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:35831d26-ada5-491f-91e3-f8daf9fd3152

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


University of North Carolina

27. Merkhofer, Evan Carroll. The role of the NF-κB pathway in Her2-overexpressing breast cancer.

Degree: 2010, University of North Carolina

 Overexpression of the membrane-bound receptor tyrosine kinase Her2 (ErbB-2, EGFR2) occurs in approximately 30% of all breast cancers and typically correlates with poor prognosis. Overexpression… (more)

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

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APA (6th Edition):

Merkhofer, E. C. (2010). The role of the NF-κB pathway in Her2-overexpressing breast cancer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:5ceae1cf-5b44-495b-9d3f-b073044a35aa

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):

Merkhofer, Evan Carroll. “The role of the NF-κB pathway in Her2-overexpressing breast cancer.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:5ceae1cf-5b44-495b-9d3f-b073044a35aa.

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

MLA Handbook (7th Edition):

Merkhofer, Evan Carroll. “The role of the NF-κB pathway in Her2-overexpressing breast cancer.” 2010. Web. 13 Jul 2020.

Vancouver:

Merkhofer EC. The role of the NF-κB pathway in Her2-overexpressing breast cancer. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:5ceae1cf-5b44-495b-9d3f-b073044a35aa.

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

Council of Science Editors:

Merkhofer EC. The role of the NF-κB pathway in Her2-overexpressing breast cancer. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:5ceae1cf-5b44-495b-9d3f-b073044a35aa

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


University of North Carolina

28. Ince, William L. Evolution of the human immunodeficiency virus type 1 envelope glycoprotein during chronic infection.

Degree: 2010, University of North Carolina

 A hallmark of Human Immunodeficiency Virus Type 1 (HIV-1) chronic infection is the rapid and continual evolution and diversification of the viral Envelope glycoprotein (Env),… (more)

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

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APA (6th Edition):

Ince, W. L. (2010). Evolution of the human immunodeficiency virus type 1 envelope glycoprotein during chronic infection. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:105218c0-1923-486e-9b74-0afba818272a

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):

Ince, William L. “Evolution of the human immunodeficiency virus type 1 envelope glycoprotein during chronic infection.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:105218c0-1923-486e-9b74-0afba818272a.

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

MLA Handbook (7th Edition):

Ince, William L. “Evolution of the human immunodeficiency virus type 1 envelope glycoprotein during chronic infection.” 2010. Web. 13 Jul 2020.

Vancouver:

Ince WL. Evolution of the human immunodeficiency virus type 1 envelope glycoprotein during chronic infection. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:105218c0-1923-486e-9b74-0afba818272a.

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

Council of Science Editors:

Ince WL. Evolution of the human immunodeficiency virus type 1 envelope glycoprotein during chronic infection. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:105218c0-1923-486e-9b74-0afba818272a

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


University of North Carolina

29. 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 July 13, 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. 13 Jul 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 Jul 13]. 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

30. Bash, Ryan. Development and Characterization of a Focally Induced Mouse Model of Glioblastoma Multiforme Originating From Terminally Differentiated Astrocytes.

Degree: 2010, University of North Carolina

 Glioblastoma multiforme (GBM) is a devastating tumor of the central nervous system and is the most frequently occurring primary brain tumor in adults. While much… (more)

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

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APA (6th Edition):

Bash, R. (2010). Development and Characterization of a Focally Induced Mouse Model of Glioblastoma Multiforme Originating From Terminally Differentiated Astrocytes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b935a5ec-f280-45cf-a070-04b66836b957

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):

Bash, Ryan. “Development and Characterization of a Focally Induced Mouse Model of Glioblastoma Multiforme Originating From Terminally Differentiated Astrocytes.” 2010. Thesis, University of North Carolina. Accessed July 13, 2020. https://cdr.lib.unc.edu/record/uuid:b935a5ec-f280-45cf-a070-04b66836b957.

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

MLA Handbook (7th Edition):

Bash, Ryan. “Development and Characterization of a Focally Induced Mouse Model of Glioblastoma Multiforme Originating From Terminally Differentiated Astrocytes.” 2010. Web. 13 Jul 2020.

Vancouver:

Bash R. Development and Characterization of a Focally Induced Mouse Model of Glioblastoma Multiforme Originating From Terminally Differentiated Astrocytes. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Jul 13]. Available from: https://cdr.lib.unc.edu/record/uuid:b935a5ec-f280-45cf-a070-04b66836b957.

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

Council of Science Editors:

Bash R. Development and Characterization of a Focally Induced Mouse Model of Glioblastoma Multiforme Originating From Terminally Differentiated Astrocytes. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:b935a5ec-f280-45cf-a070-04b66836b957

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

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