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University: University of North Carolina

You searched for subject:(Molecular Genetics). Showing records 121 – 150 of 185 total matches.

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University of North Carolina

121. Pronobis, Mira. LOOKING INSIDE THE WNT/BETA-CATENIN DESTRUCTION COMPLEX: MECHANISMS AND THE MINIMAL MACHINE.

Degree: 2016, University of North Carolina

 The Wnt/beta-catenin pathway is one of the most studied signaling pathways. It is essential throughout development, and its dysregulation is linked to various diseases including… (more)

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

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APA (6th Edition):

Pronobis, M. (2016). LOOKING INSIDE THE WNT/BETA-CATENIN DESTRUCTION COMPLEX: MECHANISMS AND THE MINIMAL MACHINE. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:842c06ad-efd2-4cbc-8814-703ced0b2693

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):

Pronobis, Mira. “LOOKING INSIDE THE WNT/BETA-CATENIN DESTRUCTION COMPLEX: MECHANISMS AND THE MINIMAL MACHINE.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:842c06ad-efd2-4cbc-8814-703ced0b2693.

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

MLA Handbook (7th Edition):

Pronobis, Mira. “LOOKING INSIDE THE WNT/BETA-CATENIN DESTRUCTION COMPLEX: MECHANISMS AND THE MINIMAL MACHINE.” 2016. Web. 09 Aug 2020.

Vancouver:

Pronobis M. LOOKING INSIDE THE WNT/BETA-CATENIN DESTRUCTION COMPLEX: MECHANISMS AND THE MINIMAL MACHINE. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:842c06ad-efd2-4cbc-8814-703ced0b2693.

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

Council of Science Editors:

Pronobis M. LOOKING INSIDE THE WNT/BETA-CATENIN DESTRUCTION COMPLEX: MECHANISMS AND THE MINIMAL MACHINE. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:842c06ad-efd2-4cbc-8814-703ced0b2693

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


University of North Carolina

122. Borchardt, Erin. MOLECULAR APPROACHES FOR CONTROLLING RNA STABILITY.

Degree: 2016, University of North Carolina

 Nature utilizes a number of methods for regulating gene expression via modulation of RNA stability. Factors involved in these processes include microRNAs, nucleotide modifications, structural… (more)

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

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APA (6th Edition):

Borchardt, E. (2016). MOLECULAR APPROACHES FOR CONTROLLING RNA STABILITY. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c242e978-f49a-4d24-8c5f-25612cc18169

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):

Borchardt, Erin. “MOLECULAR APPROACHES FOR CONTROLLING RNA STABILITY.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:c242e978-f49a-4d24-8c5f-25612cc18169.

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

MLA Handbook (7th Edition):

Borchardt, Erin. “MOLECULAR APPROACHES FOR CONTROLLING RNA STABILITY.” 2016. Web. 09 Aug 2020.

Vancouver:

Borchardt E. MOLECULAR APPROACHES FOR CONTROLLING RNA STABILITY. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:c242e978-f49a-4d24-8c5f-25612cc18169.

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

Council of Science Editors:

Borchardt E. MOLECULAR APPROACHES FOR CONTROLLING RNA STABILITY. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:c242e978-f49a-4d24-8c5f-25612cc18169

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


University of North Carolina

123. Freeman, Leslie. A Role for the NLR Family Members NLRC4 And NLRP3 in Astrocytic Inflammasome Activation and Astrogliosis.

Degree: 2016, University of North Carolina

 The inflammasome is implicated in many inflammatory diseases but has been primarily studied in the macrophage-myeloid lineage. Here we demonstrate a physiologic role for nucleotide-binding… (more)

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

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APA (6th Edition):

Freeman, L. (2016). A Role for the NLR Family Members NLRC4 And NLRP3 in Astrocytic Inflammasome Activation and Astrogliosis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:ec028a13-7c5a-41ed-af8d-3b5a5865278d

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):

Freeman, Leslie. “A Role for the NLR Family Members NLRC4 And NLRP3 in Astrocytic Inflammasome Activation and Astrogliosis.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:ec028a13-7c5a-41ed-af8d-3b5a5865278d.

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

MLA Handbook (7th Edition):

Freeman, Leslie. “A Role for the NLR Family Members NLRC4 And NLRP3 in Astrocytic Inflammasome Activation and Astrogliosis.” 2016. Web. 09 Aug 2020.

Vancouver:

Freeman L. A Role for the NLR Family Members NLRC4 And NLRP3 in Astrocytic Inflammasome Activation and Astrogliosis. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:ec028a13-7c5a-41ed-af8d-3b5a5865278d.

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

Council of Science Editors:

Freeman L. A Role for the NLR Family Members NLRC4 And NLRP3 in Astrocytic Inflammasome Activation and Astrogliosis. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:ec028a13-7c5a-41ed-af8d-3b5a5865278d

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


University of North Carolina

124. Leslie, Patrick. Analysis of the p53 Regulator MDM2 and the Identification of the Novel p53 Target Gene LRP1.

Degree: 2016, University of North Carolina

 The transcription factor p53 responds to many stresses and regulates many different pathways. The earliest characterized functions of p53 include the induction of cell cycle… (more)

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

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APA (6th Edition):

Leslie, P. (2016). Analysis of the p53 Regulator MDM2 and the Identification of the Novel p53 Target Gene LRP1. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:49a0f53d-536d-4d50-a5a2-22210a46f820

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):

Leslie, Patrick. “Analysis of the p53 Regulator MDM2 and the Identification of the Novel p53 Target Gene LRP1.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:49a0f53d-536d-4d50-a5a2-22210a46f820.

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

MLA Handbook (7th Edition):

Leslie, Patrick. “Analysis of the p53 Regulator MDM2 and the Identification of the Novel p53 Target Gene LRP1.” 2016. Web. 09 Aug 2020.

Vancouver:

Leslie P. Analysis of the p53 Regulator MDM2 and the Identification of the Novel p53 Target Gene LRP1. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:49a0f53d-536d-4d50-a5a2-22210a46f820.

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

Council of Science Editors:

Leslie P. Analysis of the p53 Regulator MDM2 and the Identification of the Novel p53 Target Gene LRP1. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:49a0f53d-536d-4d50-a5a2-22210a46f820

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


University of North Carolina

125. Wyatt, David. Essential Roles for Polymerase Theta-Mediated End Joining in Repair of Chromosome Breaks.

Degree: 2017, University of North Carolina

 DNA double strand breaks (DSBs) constitute a rare but lethal class of genomic damage that must be efficiently repaired. Deficiencies in DSB repair pathways manifest themselves… (more)

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

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APA (6th Edition):

Wyatt, D. (2017). Essential Roles for Polymerase Theta-Mediated End Joining in Repair of Chromosome Breaks. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4231dc9a-de73-4655-8b68-d5a4216995f4

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):

Wyatt, David. “Essential Roles for Polymerase Theta-Mediated End Joining in Repair of Chromosome Breaks.” 2017. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:4231dc9a-de73-4655-8b68-d5a4216995f4.

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

MLA Handbook (7th Edition):

Wyatt, David. “Essential Roles for Polymerase Theta-Mediated End Joining in Repair of Chromosome Breaks.” 2017. Web. 09 Aug 2020.

Vancouver:

Wyatt D. Essential Roles for Polymerase Theta-Mediated End Joining in Repair of Chromosome Breaks. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:4231dc9a-de73-4655-8b68-d5a4216995f4.

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

Council of Science Editors:

Wyatt D. Essential Roles for Polymerase Theta-Mediated End Joining in Repair of Chromosome Breaks. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:4231dc9a-de73-4655-8b68-d5a4216995f4

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


University of North Carolina

126. Irvin, David. Astrocytes and Their Response to Pathology.

Degree: 2016, University of North Carolina

 Glioblastoma (GBM), the most common primary malignant brain tumor, remains fatal and lacks effective treatment options. The influence of initiating mutations and cellular origin on… (more)

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

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APA (6th Edition):

Irvin, D. (2016). Astrocytes and Their Response to Pathology. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:6a03331d-12ce-4c8a-a493-c934e6adf122

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):

Irvin, David. “Astrocytes and Their Response to Pathology.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:6a03331d-12ce-4c8a-a493-c934e6adf122.

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

MLA Handbook (7th Edition):

Irvin, David. “Astrocytes and Their Response to Pathology.” 2016. Web. 09 Aug 2020.

Vancouver:

Irvin D. Astrocytes and Their Response to Pathology. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:6a03331d-12ce-4c8a-a493-c934e6adf122.

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

Council of Science Editors:

Irvin D. Astrocytes and Their Response to Pathology. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:6a03331d-12ce-4c8a-a493-c934e6adf122

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


University of North Carolina

127. Miller, Charles. Investigating Pre-mating and Post-mating Reproductive Isolation in Drosophila.

Degree: 2016, University of North Carolina

 Reproductively isolating barriers which inhibit gene flow between species can be broadly classified into pre-mating and post-mating barriers. Pre-mating barriers evolve rapidly and are thought… (more)

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

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APA (6th Edition):

Miller, C. (2016). Investigating Pre-mating and Post-mating Reproductive Isolation in Drosophila. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b836f140-0d92-4aed-be04-48d387e94c6f

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):

Miller, Charles. “Investigating Pre-mating and Post-mating Reproductive Isolation in Drosophila.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:b836f140-0d92-4aed-be04-48d387e94c6f.

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

MLA Handbook (7th Edition):

Miller, Charles. “Investigating Pre-mating and Post-mating Reproductive Isolation in Drosophila.” 2016. Web. 09 Aug 2020.

Vancouver:

Miller C. Investigating Pre-mating and Post-mating Reproductive Isolation in Drosophila. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:b836f140-0d92-4aed-be04-48d387e94c6f.

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

Council of Science Editors:

Miller C. Investigating Pre-mating and Post-mating Reproductive Isolation in Drosophila. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:b836f140-0d92-4aed-be04-48d387e94c6f

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


University of North Carolina

128. Meserve, Joy. Cell Cycle Regulation During Development and Regeneration.

Degree: 2017, University of North Carolina

 During the development of multicellular organisms, proliferating, undifferentiated cells often transition into a differentiated and quiescent state. Programs coordinating cell cycle progression and differentiation are… (more)

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

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APA (6th Edition):

Meserve, J. (2017). Cell Cycle Regulation During Development and Regeneration. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:15c8138f-3f67-464f-8746-15d7151bae54

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):

Meserve, Joy. “Cell Cycle Regulation During Development and Regeneration.” 2017. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:15c8138f-3f67-464f-8746-15d7151bae54.

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

MLA Handbook (7th Edition):

Meserve, Joy. “Cell Cycle Regulation During Development and Regeneration.” 2017. Web. 09 Aug 2020.

Vancouver:

Meserve J. Cell Cycle Regulation During Development and Regeneration. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:15c8138f-3f67-464f-8746-15d7151bae54.

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

Council of Science Editors:

Meserve J. Cell Cycle Regulation During Development and Regeneration. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:15c8138f-3f67-464f-8746-15d7151bae54

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


University of North Carolina

129. Holk, Alicia. Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer.

Degree: 2016, University of North Carolina

 Cells are subjected to a range of DNA damaging agents from intrinsic, environmental, and therapeutic sources. The ability to cope with DNA damage is essential… (more)

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

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APA (6th Edition):

Holk, A. (2016). Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:44421fcc-2ffd-4fa1-8288-80a18d51f659

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):

Holk, Alicia. “Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:44421fcc-2ffd-4fa1-8288-80a18d51f659.

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

MLA Handbook (7th Edition):

Holk, Alicia. “Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer.” 2016. Web. 09 Aug 2020.

Vancouver:

Holk A. Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:44421fcc-2ffd-4fa1-8288-80a18d51f659.

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

Council of Science Editors:

Holk A. Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:44421fcc-2ffd-4fa1-8288-80a18d51f659

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


University of North Carolina

130. Zapotoczny, Grzegorz. Contribution of DNA Helicases to Genome Stability.

Degree: 2016, University of North Carolina

 DNA double-strand breaks (DSBs) are one of the most deleterious lesions to the cell. Even a single unrepaired DSB can lead to apoptosis, recombination, loss… (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):

Zapotoczny, G. (2016). Contribution of DNA Helicases to Genome Stability. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:1f06ffed-f17f-4dff-b4b4-b01beab9c085

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):

Zapotoczny, Grzegorz. “Contribution of DNA Helicases to Genome Stability.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:1f06ffed-f17f-4dff-b4b4-b01beab9c085.

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

MLA Handbook (7th Edition):

Zapotoczny, Grzegorz. “Contribution of DNA Helicases to Genome Stability.” 2016. Web. 09 Aug 2020.

Vancouver:

Zapotoczny G. Contribution of DNA Helicases to Genome Stability. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:1f06ffed-f17f-4dff-b4b4-b01beab9c085.

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

Council of Science Editors:

Zapotoczny G. Contribution of DNA Helicases to Genome Stability. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:1f06ffed-f17f-4dff-b4b4-b01beab9c085

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


University of North Carolina

131. Romero, Noelle-Erin. Biochemical Activities and Genetic Functions of the Drosophila melanogaster FANCM Helicase in DNA Repair.

Degree: 2016, University of North Carolina

 The DNA damage response in eukaryotes involves multiple, complex, and often redundant pathways that respond to various types of DNA damage that affect one or… (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):

Romero, N. (2016). Biochemical Activities and Genetic Functions of the Drosophila melanogaster FANCM Helicase in DNA Repair. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:67fec902-fa62-4b39-bb59-d61616a6b05e

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):

Romero, Noelle-Erin. “Biochemical Activities and Genetic Functions of the Drosophila melanogaster FANCM Helicase in DNA Repair.” 2016. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:67fec902-fa62-4b39-bb59-d61616a6b05e.

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

MLA Handbook (7th Edition):

Romero, Noelle-Erin. “Biochemical Activities and Genetic Functions of the Drosophila melanogaster FANCM Helicase in DNA Repair.” 2016. Web. 09 Aug 2020.

Vancouver:

Romero N. Biochemical Activities and Genetic Functions of the Drosophila melanogaster FANCM Helicase in DNA Repair. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:67fec902-fa62-4b39-bb59-d61616a6b05e.

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

Council of Science Editors:

Romero N. Biochemical Activities and Genetic Functions of the Drosophila melanogaster FANCM Helicase in DNA Repair. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:67fec902-fa62-4b39-bb59-d61616a6b05e

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


University of North Carolina

132. Albright, Blake. DETERMINANTS OF AAV TRANSPORT ACROSS THE BLOOD-BRAIN BARRIER.

Degree: 2018, University of North Carolina

 Adeno-associated virus (AAV) is currently the most widely used gene therapy vector for treating neurological diseases, showing promising results in preclinical and clinical studies. Nonetheless,… (more)

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

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APA (6th Edition):

Albright, B. (2018). DETERMINANTS OF AAV TRANSPORT ACROSS THE BLOOD-BRAIN BARRIER. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:6198a1fa-46a1-40b9-85b5-fa6f3d813464

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):

Albright, Blake. “DETERMINANTS OF AAV TRANSPORT ACROSS THE BLOOD-BRAIN BARRIER.” 2018. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:6198a1fa-46a1-40b9-85b5-fa6f3d813464.

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

MLA Handbook (7th Edition):

Albright, Blake. “DETERMINANTS OF AAV TRANSPORT ACROSS THE BLOOD-BRAIN BARRIER.” 2018. Web. 09 Aug 2020.

Vancouver:

Albright B. DETERMINANTS OF AAV TRANSPORT ACROSS THE BLOOD-BRAIN BARRIER. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:6198a1fa-46a1-40b9-85b5-fa6f3d813464.

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

Council of Science Editors:

Albright B. DETERMINANTS OF AAV TRANSPORT ACROSS THE BLOOD-BRAIN BARRIER. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:6198a1fa-46a1-40b9-85b5-fa6f3d813464

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


University of North Carolina

133. Wright, Catherine. LGN-Dependent Microtubule Regulation Influences Endothelial Cell Migration, Adhesion, and Sprout Integrity.

Degree: 2014, University of North Carolina

 Blood vessels form during organismal development and maintain integrity to provide oxygen and nutrients to the tissues. Vessels are comprised of endothelial cells that coordinate… (more)

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

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APA (6th Edition):

Wright, C. (2014). LGN-Dependent Microtubule Regulation Influences Endothelial Cell Migration, Adhesion, and Sprout Integrity. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d2f0314f-02a1-4b71-bc04-7234179ca432

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, Catherine. “LGN-Dependent Microtubule Regulation Influences Endothelial Cell Migration, Adhesion, and Sprout Integrity.” 2014. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:d2f0314f-02a1-4b71-bc04-7234179ca432.

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

MLA Handbook (7th Edition):

Wright, Catherine. “LGN-Dependent Microtubule Regulation Influences Endothelial Cell Migration, Adhesion, and Sprout Integrity.” 2014. Web. 09 Aug 2020.

Vancouver:

Wright C. LGN-Dependent Microtubule Regulation Influences Endothelial Cell Migration, Adhesion, and Sprout Integrity. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:d2f0314f-02a1-4b71-bc04-7234179ca432.

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

Council of Science Editors:

Wright C. LGN-Dependent Microtubule Regulation Influences Endothelial Cell Migration, Adhesion, and Sprout Integrity. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:d2f0314f-02a1-4b71-bc04-7234179ca432

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


University of North Carolina

134. Watson, Kelly. MOLECULAR MECHANISM OF THE INTERACTION BETWEEN LGL/TOMOSYN HOMOLOG, SRO7, AND THE RAB GTPASE SEC4 IN POLARIZED EXOCYTOSIS.

Degree: Cell Biology and Physiology, 2015, University of North Carolina

 Polarized exocytosis requires the proper localized delivery, docking and fusion of secretory vesicles with sites of active growth on the plasma membrane. Members of the… (more)

Subjects/Keywords: Cytology; Molecular biology; Genetics; School of Medicine; Department of Cell Biology and Physiology

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APA (6th Edition):

Watson, K. (2015). MOLECULAR MECHANISM OF THE INTERACTION BETWEEN LGL/TOMOSYN HOMOLOG, SRO7, AND THE RAB GTPASE SEC4 IN POLARIZED EXOCYTOSIS. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:51c241d9-e4a4-400c-993a-29940ae1d79a

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):

Watson, Kelly. “MOLECULAR MECHANISM OF THE INTERACTION BETWEEN LGL/TOMOSYN HOMOLOG, SRO7, AND THE RAB GTPASE SEC4 IN POLARIZED EXOCYTOSIS.” 2015. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:51c241d9-e4a4-400c-993a-29940ae1d79a.

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

MLA Handbook (7th Edition):

Watson, Kelly. “MOLECULAR MECHANISM OF THE INTERACTION BETWEEN LGL/TOMOSYN HOMOLOG, SRO7, AND THE RAB GTPASE SEC4 IN POLARIZED EXOCYTOSIS.” 2015. Web. 09 Aug 2020.

Vancouver:

Watson K. MOLECULAR MECHANISM OF THE INTERACTION BETWEEN LGL/TOMOSYN HOMOLOG, SRO7, AND THE RAB GTPASE SEC4 IN POLARIZED EXOCYTOSIS. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:51c241d9-e4a4-400c-993a-29940ae1d79a.

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

Council of Science Editors:

Watson K. MOLECULAR MECHANISM OF THE INTERACTION BETWEEN LGL/TOMOSYN HOMOLOG, SRO7, AND THE RAB GTPASE SEC4 IN POLARIZED EXOCYTOSIS. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:51c241d9-e4a4-400c-993a-29940ae1d79a

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


University of North Carolina

135. Jha, Deepak. Role of histone methylation and variants in genome function.

Degree: Biochemistry and Biophysics, 2014, University of North Carolina

 The eukaryotic genome is compacted in the form of chromatin, which is a complex of DNA and histone proteins. Regulation of chromatin structure influences all… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Genetics; School of Medicine; Department of Biochemistry and Biophysics

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APA (6th Edition):

Jha, D. (2014). Role of histone methylation and variants in genome function. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:a6a8dfde-9472-4c57-825c-05725c4cb4f2

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):

Jha, Deepak. “Role of histone methylation and variants in genome function.” 2014. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:a6a8dfde-9472-4c57-825c-05725c4cb4f2.

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

MLA Handbook (7th Edition):

Jha, Deepak. “Role of histone methylation and variants in genome function.” 2014. Web. 09 Aug 2020.

Vancouver:

Jha D. Role of histone methylation and variants in genome function. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:a6a8dfde-9472-4c57-825c-05725c4cb4f2.

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

Council of Science Editors:

Jha D. Role of histone methylation and variants in genome function. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:a6a8dfde-9472-4c57-825c-05725c4cb4f2

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


University of North Carolina

136. Watson, Leah. Endo-Exocytic Trafficking in Regulation of Cdc42 Polarity.

Degree: Cell Biology and Physiology, 2014, University of North Carolina

 The precise subcellular localization of the Rho GTPase Cdc42 is essential for its spatial and temporal control of polarized growth and division. In budding yeast,… (more)

Subjects/Keywords: Cytology; Molecular biology; Genetics; School of Medicine; Department of Cell Biology and Physiology

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APA (6th Edition):

Watson, L. (2014). Endo-Exocytic Trafficking in Regulation of Cdc42 Polarity. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4c013b02-b8cd-42ea-a474-8994b6ddacbc

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):

Watson, Leah. “Endo-Exocytic Trafficking in Regulation of Cdc42 Polarity.” 2014. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:4c013b02-b8cd-42ea-a474-8994b6ddacbc.

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

MLA Handbook (7th Edition):

Watson, Leah. “Endo-Exocytic Trafficking in Regulation of Cdc42 Polarity.” 2014. Web. 09 Aug 2020.

Vancouver:

Watson L. Endo-Exocytic Trafficking in Regulation of Cdc42 Polarity. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:4c013b02-b8cd-42ea-a474-8994b6ddacbc.

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

Council of Science Editors:

Watson L. Endo-Exocytic Trafficking in Regulation of Cdc42 Polarity. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:4c013b02-b8cd-42ea-a474-8994b6ddacbc

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


University of North Carolina

137. Dunworth, William P. Genetic mouse models elucidate the roles of adrenomedullin in cardiovascular development and physiology.

Degree: 2009, University of North Carolina

 Adrenomedullin (AM) is a highly conserved, secreted 52 amino acid peptide that functions in physiological processes within the nervous, reproductive, and cardiovascular systems. AM is… (more)

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

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APA (6th Edition):

Dunworth, W. P. (2009). Genetic mouse models elucidate the roles of adrenomedullin in cardiovascular development and physiology. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:dafc40a6-7876-48f7-8a2a-adc38117d4c9

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):

Dunworth, William P. “Genetic mouse models elucidate the roles of adrenomedullin in cardiovascular development and physiology.” 2009. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:dafc40a6-7876-48f7-8a2a-adc38117d4c9.

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

MLA Handbook (7th Edition):

Dunworth, William P. “Genetic mouse models elucidate the roles of adrenomedullin in cardiovascular development and physiology.” 2009. Web. 09 Aug 2020.

Vancouver:

Dunworth WP. Genetic mouse models elucidate the roles of adrenomedullin in cardiovascular development and physiology. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:dafc40a6-7876-48f7-8a2a-adc38117d4c9.

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

Council of Science Editors:

Dunworth WP. Genetic mouse models elucidate the roles of adrenomedullin in cardiovascular development and physiology. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:dafc40a6-7876-48f7-8a2a-adc38117d4c9

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


University of North Carolina

138. Kallin, Eric Michael. Epigenetic regulation of gene transcription: Jhdm1b characterization and genome-wide localization of H2A ubiquitylation.

Degree: 2009, University of North Carolina

 Histone methylation and ubiquitylation play important roles in regulating gene expression and form part of the epigenetic memory system that regulates cellular fate. Two general… (more)

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

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APA (6th Edition):

Kallin, E. M. (2009). Epigenetic regulation of gene transcription: Jhdm1b characterization and genome-wide localization of H2A ubiquitylation. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:1d542c82-6742-409b-9766-04780ae54835

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):

Kallin, Eric Michael. “Epigenetic regulation of gene transcription: Jhdm1b characterization and genome-wide localization of H2A ubiquitylation.” 2009. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:1d542c82-6742-409b-9766-04780ae54835.

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

MLA Handbook (7th Edition):

Kallin, Eric Michael. “Epigenetic regulation of gene transcription: Jhdm1b characterization and genome-wide localization of H2A ubiquitylation.” 2009. Web. 09 Aug 2020.

Vancouver:

Kallin EM. Epigenetic regulation of gene transcription: Jhdm1b characterization and genome-wide localization of H2A ubiquitylation. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:1d542c82-6742-409b-9766-04780ae54835.

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

Council of Science Editors:

Kallin EM. Epigenetic regulation of gene transcription: Jhdm1b characterization and genome-wide localization of H2A ubiquitylation. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:1d542c82-6742-409b-9766-04780ae54835

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


University of North Carolina

139. 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 (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 August 09, 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. 09 Aug 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 Aug 09]. 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


University of North Carolina

140. Eversley, Chevonne D. Integrative genomic analysis of sporadic colorectal cancer.

Degree: 2009, University of North Carolina

 Inherited genetic mutations cause a small percentage of all cancers in the United States. The combination of risk factors and accumulated low penetrance susceptibility alleles… (more)

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

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APA (6th Edition):

Eversley, C. D. (2009). Integrative genomic analysis of sporadic colorectal cancer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:de94009b-9bee-4c15-a855-b05b9ea91f2e

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):

Eversley, Chevonne D. “Integrative genomic analysis of sporadic colorectal cancer.” 2009. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:de94009b-9bee-4c15-a855-b05b9ea91f2e.

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

MLA Handbook (7th Edition):

Eversley, Chevonne D. “Integrative genomic analysis of sporadic colorectal cancer.” 2009. Web. 09 Aug 2020.

Vancouver:

Eversley CD. Integrative genomic analysis of sporadic colorectal cancer. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:de94009b-9bee-4c15-a855-b05b9ea91f2e.

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

Council of Science Editors:

Eversley CD. Integrative genomic analysis of sporadic colorectal cancer. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:de94009b-9bee-4c15-a855-b05b9ea91f2e

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


University of North Carolina

141. Hanker, Ariella Binah. Ras family GTPases involved in breast cancer.

Degree: 2009, University of North Carolina

 The Ras branch of the Ras superfamily of small GTPases consists of over thirty-six proteins that regulate a wide array of cellular processes. Mutations in… (more)

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

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APA (6th Edition):

Hanker, A. B. (2009). Ras family GTPases involved in breast cancer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:371d70e6-4d53-4143-adc0-ab60d835474a

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):

Hanker, Ariella Binah. “Ras family GTPases involved in breast cancer.” 2009. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:371d70e6-4d53-4143-adc0-ab60d835474a.

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

MLA Handbook (7th Edition):

Hanker, Ariella Binah. “Ras family GTPases involved in breast cancer.” 2009. Web. 09 Aug 2020.

Vancouver:

Hanker AB. Ras family GTPases involved in breast cancer. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:371d70e6-4d53-4143-adc0-ab60d835474a.

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

Council of Science Editors:

Hanker AB. Ras family GTPases involved in breast cancer. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:371d70e6-4d53-4143-adc0-ab60d835474a

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


University of North Carolina

142. Monahan, Kimberly Beth. Characterization of Ras-driven Melanoma: Understanding the Relationship Between Acute Loss of p16Ink4a and Somatic Activation of Ras in Melanomagenesis.

Degree: 2009, University of North Carolina

 Melanoma is a complex and heterogeneous disease. It is the only cancer with an increase in incidence over the last three decades, which is still… (more)

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

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APA (6th Edition):

Monahan, K. B. (2009). Characterization of Ras-driven Melanoma: Understanding the Relationship Between Acute Loss of p16Ink4a and Somatic Activation of Ras in Melanomagenesis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c815abfa-d956-4c35-a676-3930aa0e3989

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):

Monahan, Kimberly Beth. “Characterization of Ras-driven Melanoma: Understanding the Relationship Between Acute Loss of p16Ink4a and Somatic Activation of Ras in Melanomagenesis.” 2009. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:c815abfa-d956-4c35-a676-3930aa0e3989.

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

MLA Handbook (7th Edition):

Monahan, Kimberly Beth. “Characterization of Ras-driven Melanoma: Understanding the Relationship Between Acute Loss of p16Ink4a and Somatic Activation of Ras in Melanomagenesis.” 2009. Web. 09 Aug 2020.

Vancouver:

Monahan KB. Characterization of Ras-driven Melanoma: Understanding the Relationship Between Acute Loss of p16Ink4a and Somatic Activation of Ras in Melanomagenesis. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:c815abfa-d956-4c35-a676-3930aa0e3989.

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

Council of Science Editors:

Monahan KB. Characterization of Ras-driven Melanoma: Understanding the Relationship Between Acute Loss of p16Ink4a and Somatic Activation of Ras in Melanomagenesis. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:c815abfa-d956-4c35-a676-3930aa0e3989

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


University of North Carolina

143. Whittle, Christina Michelle. The genomic distribution and function of NFI and histone variant H2A.Z during C. elegans development.

Degree: 2009, University of North Carolina

 Development relies on precise spatial and temporal access of the transcription regulatory machinery to genomic information. Throughout development, transcription factors bind a discrete set of… (more)

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

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APA (6th Edition):

Whittle, C. M. (2009). The genomic distribution and function of NFI and histone variant H2A.Z during C. elegans development. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:df0149ba-f22c-416a-9799-624cdf16780b

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):

Whittle, Christina Michelle. “The genomic distribution and function of NFI and histone variant H2A.Z during C. elegans development.” 2009. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:df0149ba-f22c-416a-9799-624cdf16780b.

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

MLA Handbook (7th Edition):

Whittle, Christina Michelle. “The genomic distribution and function of NFI and histone variant H2A.Z during C. elegans development.” 2009. Web. 09 Aug 2020.

Vancouver:

Whittle CM. The genomic distribution and function of NFI and histone variant H2A.Z during C. elegans development. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:df0149ba-f22c-416a-9799-624cdf16780b.

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

Council of Science Editors:

Whittle CM. The genomic distribution and function of NFI and histone variant H2A.Z during C. elegans development. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:df0149ba-f22c-416a-9799-624cdf16780b

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


University of North Carolina

144. O'Hara, Andrea Jayne. Characterization of Cellular and Viral MicroRNAs in Kaposi’s Sarcoma-associated Herpesvirus Malignancies.

Degree: 2009, University of North Carolina

 MicroRNAs (miRNAs) are a class of small non-coding functional RNAs that mediate post-transcriptional regulation of target mRNAs in a sequence-specific manner. They affect a wide… (more)

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

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APA (6th Edition):

O'Hara, A. J. (2009). Characterization of Cellular and Viral MicroRNAs in Kaposi’s Sarcoma-associated Herpesvirus Malignancies. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b55c8656-aaba-4e05-b677-89e36ee07b8f

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):

O'Hara, Andrea Jayne. “Characterization of Cellular and Viral MicroRNAs in Kaposi’s Sarcoma-associated Herpesvirus Malignancies.” 2009. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:b55c8656-aaba-4e05-b677-89e36ee07b8f.

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

MLA Handbook (7th Edition):

O'Hara, Andrea Jayne. “Characterization of Cellular and Viral MicroRNAs in Kaposi’s Sarcoma-associated Herpesvirus Malignancies.” 2009. Web. 09 Aug 2020.

Vancouver:

O'Hara AJ. Characterization of Cellular and Viral MicroRNAs in Kaposi’s Sarcoma-associated Herpesvirus Malignancies. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:b55c8656-aaba-4e05-b677-89e36ee07b8f.

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

Council of Science Editors:

O'Hara AJ. Characterization of Cellular and Viral MicroRNAs in Kaposi’s Sarcoma-associated Herpesvirus Malignancies. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:b55c8656-aaba-4e05-b677-89e36ee07b8f

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


University of North Carolina

145. Wilson, Willie. The regulation of constitutive NF-κB activity by glycogen synthase kinase-3 in pancreatic cancer.

Degree: 2009, University of North Carolina

 The development of pancreatic cancer chemotherapy has evolved into targeting the complex signaling pathways associated with disease progression. Recent focus has been made on targeting… (more)

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

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APA (6th Edition):

Wilson, W. (2009). The regulation of constitutive NF-κB activity by glycogen synthase kinase-3 in pancreatic cancer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:73ea7216-e073-4451-931c-cdd3dfdda4d9

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):

Wilson, Willie. “The regulation of constitutive NF-κB activity by glycogen synthase kinase-3 in pancreatic cancer.” 2009. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:73ea7216-e073-4451-931c-cdd3dfdda4d9.

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

MLA Handbook (7th Edition):

Wilson, Willie. “The regulation of constitutive NF-κB activity by glycogen synthase kinase-3 in pancreatic cancer.” 2009. Web. 09 Aug 2020.

Vancouver:

Wilson W. The regulation of constitutive NF-κB activity by glycogen synthase kinase-3 in pancreatic cancer. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:73ea7216-e073-4451-931c-cdd3dfdda4d9.

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

Council of Science Editors:

Wilson W. The regulation of constitutive NF-κB activity by glycogen synthase kinase-3 in pancreatic cancer. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:73ea7216-e073-4451-931c-cdd3dfdda4d9

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


University of North Carolina

146. Hansen, Maureen Elizabeth. Regulation of ethylene biosynthesis via ACC synthase protein stability.

Degree: 2008, University of North Carolina

 The gaseous plant hormone ethylene is involved in many plant processes including germination, leaf and flower abcission, cell elongation and inhibition, plant defense and fruit… (more)

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

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APA (6th Edition):

Hansen, M. E. (2008). Regulation of ethylene biosynthesis via ACC synthase protein stability. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:fa41fb1a-e6da-4f78-8d26-59fb25946ea2

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):

Hansen, Maureen Elizabeth. “Regulation of ethylene biosynthesis via ACC synthase protein stability.” 2008. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:fa41fb1a-e6da-4f78-8d26-59fb25946ea2.

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

MLA Handbook (7th Edition):

Hansen, Maureen Elizabeth. “Regulation of ethylene biosynthesis via ACC synthase protein stability.” 2008. Web. 09 Aug 2020.

Vancouver:

Hansen ME. Regulation of ethylene biosynthesis via ACC synthase protein stability. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:fa41fb1a-e6da-4f78-8d26-59fb25946ea2.

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

Council of Science Editors:

Hansen ME. Regulation of ethylene biosynthesis via ACC synthase protein stability. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:fa41fb1a-e6da-4f78-8d26-59fb25946ea2

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


University of North Carolina

147. Schliekelman, Mark Jason. Characterization of a Murine Hypomorphic Allele of the Spindle Checkpoint Gene Bub1 and its Role in Tumorigenesis.

Degree: 2008, University of North Carolina

 Bub1 is a serine/threonine kinase originally described as a core component of the spindle assembly checkpoint (SAC) mechanism in yeast. We produced mice harboring a… (more)

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

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APA (6th Edition):

Schliekelman, M. J. (2008). Characterization of a Murine Hypomorphic Allele of the Spindle Checkpoint Gene Bub1 and its Role in Tumorigenesis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:fd329357-3ea5-43ec-a91d-cfa8b0cf4a9d

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):

Schliekelman, Mark Jason. “Characterization of a Murine Hypomorphic Allele of the Spindle Checkpoint Gene Bub1 and its Role in Tumorigenesis.” 2008. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:fd329357-3ea5-43ec-a91d-cfa8b0cf4a9d.

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

MLA Handbook (7th Edition):

Schliekelman, Mark Jason. “Characterization of a Murine Hypomorphic Allele of the Spindle Checkpoint Gene Bub1 and its Role in Tumorigenesis.” 2008. Web. 09 Aug 2020.

Vancouver:

Schliekelman MJ. Characterization of a Murine Hypomorphic Allele of the Spindle Checkpoint Gene Bub1 and its Role in Tumorigenesis. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:fd329357-3ea5-43ec-a91d-cfa8b0cf4a9d.

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

Council of Science Editors:

Schliekelman MJ. Characterization of a Murine Hypomorphic Allele of the Spindle Checkpoint Gene Bub1 and its Role in Tumorigenesis. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:fd329357-3ea5-43ec-a91d-cfa8b0cf4a9d

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


University of North Carolina

148. Leopold, Luciana Eleanor. Development of Real-Time PCR Assays for the Quantitative Detection of Herpesviruses.

Degree: 2008, University of North Carolina

 Kaposis's sarcoma-associated Herpesvirus (KSHV) and Human Epstein-Barr virus (EBV) are gamma herpesviruses that can cause serious complications in immunocompromised patients. Quantitative detection is critical not… (more)

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

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APA (6th Edition):

Leopold, L. E. (2008). Development of Real-Time PCR Assays for the Quantitative Detection of Herpesviruses. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d2f37589-babe-418b-9d5d-c5bcf30933df

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 Eleanor. “Development of Real-Time PCR Assays for the Quantitative Detection of Herpesviruses.” 2008. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:d2f37589-babe-418b-9d5d-c5bcf30933df.

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 Eleanor. “Development of Real-Time PCR Assays for the Quantitative Detection of Herpesviruses.” 2008. Web. 09 Aug 2020.

Vancouver:

Leopold LE. Development of Real-Time PCR Assays for the Quantitative Detection of Herpesviruses. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:d2f37589-babe-418b-9d5d-c5bcf30933df.

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

Council of Science Editors:

Leopold LE. Development of Real-Time PCR Assays for the Quantitative Detection of Herpesviruses. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:d2f37589-babe-418b-9d5d-c5bcf30933df

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


University of North Carolina

149. Rinella, Erica Sue. Impact of diet on EGFR-targeted treatment of colorectal cancer.

Degree: 2008, University of North Carolina

 Colorectal cancer (CRC) continues to be one of the most prevalent cancers and leading causes of cancer-related deaths in Western societies. Molecule-targeted therapies are being… (more)

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

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APA (6th Edition):

Rinella, E. S. (2008). Impact of diet on EGFR-targeted treatment of colorectal cancer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:5732f776-b34c-43ad-ae37-581970d87111

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):

Rinella, Erica Sue. “Impact of diet on EGFR-targeted treatment of colorectal cancer.” 2008. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:5732f776-b34c-43ad-ae37-581970d87111.

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

MLA Handbook (7th Edition):

Rinella, Erica Sue. “Impact of diet on EGFR-targeted treatment of colorectal cancer.” 2008. Web. 09 Aug 2020.

Vancouver:

Rinella ES. Impact of diet on EGFR-targeted treatment of colorectal cancer. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:5732f776-b34c-43ad-ae37-581970d87111.

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

Council of Science Editors:

Rinella ES. Impact of diet on EGFR-targeted treatment of colorectal cancer. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:5732f776-b34c-43ad-ae37-581970d87111

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


University of North Carolina

150. Willingham, Stephen B. Microbial pathogen-induced necrosis mediated by NLRP3 and ASC.

Degree: 2008, University of North Carolina

 NLRP3 and ASC are important components of the inflammasome, a multi-protein complex required for caspase-1 activation and IL-1[beta] production. NLRP3 mutations underlie autoinflammation characterized by… (more)

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

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APA (6th Edition):

Willingham, S. B. (2008). Microbial pathogen-induced necrosis mediated by NLRP3 and ASC. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c9a69df9-afe7-412b-ad22-4613e7f01583

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):

Willingham, Stephen B. “Microbial pathogen-induced necrosis mediated by NLRP3 and ASC.” 2008. Thesis, University of North Carolina. Accessed August 09, 2020. https://cdr.lib.unc.edu/record/uuid:c9a69df9-afe7-412b-ad22-4613e7f01583.

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

MLA Handbook (7th Edition):

Willingham, Stephen B. “Microbial pathogen-induced necrosis mediated by NLRP3 and ASC.” 2008. Web. 09 Aug 2020.

Vancouver:

Willingham SB. Microbial pathogen-induced necrosis mediated by NLRP3 and ASC. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Aug 09]. Available from: https://cdr.lib.unc.edu/record/uuid:c9a69df9-afe7-412b-ad22-4613e7f01583.

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

Council of Science Editors:

Willingham SB. Microbial pathogen-induced necrosis mediated by NLRP3 and ASC. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:c9a69df9-afe7-412b-ad22-4613e7f01583

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

[1] [2] [3] [4] [5] [6] [7]

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