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You searched for +publisher:"Vanderbilt University" +contributor:("James G. Patton"). Showing records 1 – 25 of 25 total matches.

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Vanderbilt University

1. Sebastian, Tessy Tereas. Auto-Inhibitory Mechanism for the Regulation of a P4-ATPase.

Degree: PhD, Biological Sciences, 2014, Vanderbilt University

 Vesicular transport of proteins is a process essential for cell health and viability. Integral membrane proteins, called phospholipid flippases, play important roles in the formation… (more)

Subjects/Keywords: Flippase; Drs2p; Vesicular Trafficking; Membrane Curvature; Regulation; ATPase; PI4P; Phosphoinositide; Auto-regulation

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APA (6th Edition):

Sebastian, T. T. (2014). Auto-Inhibitory Mechanism for the Regulation of a P4-ATPase. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10660

Chicago Manual of Style (16th Edition):

Sebastian, Tessy Tereas. “Auto-Inhibitory Mechanism for the Regulation of a P4-ATPase.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/10660.

MLA Handbook (7th Edition):

Sebastian, Tessy Tereas. “Auto-Inhibitory Mechanism for the Regulation of a P4-ATPase.” 2014. Web. 03 Dec 2020.

Vancouver:

Sebastian TT. Auto-Inhibitory Mechanism for the Regulation of a P4-ATPase. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/10660.

Council of Science Editors:

Sebastian TT. Auto-Inhibitory Mechanism for the Regulation of a P4-ATPase. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/10660


Vanderbilt University

2. Olena, Abigail Frances. microRNA Regulation of Zebrafish Retinal Development.

Degree: PhD, Biological Sciences, 2015, Vanderbilt University

 microRNAs (miRNAs) are small noncoding RNAs that bind the 3’ untranslated regions (UTRs) of mRNA targets and, acting with associated proteins, facilitate translation repression and… (more)

Subjects/Keywords: miR-216a; Notch signaling; microRNA; sorting nexin 5; zebrafish; retina

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APA (6th Edition):

Olena, A. F. (2015). microRNA Regulation of Zebrafish Retinal Development. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10500

Chicago Manual of Style (16th Edition):

Olena, Abigail Frances. “microRNA Regulation of Zebrafish Retinal Development.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/10500.

MLA Handbook (7th Edition):

Olena, Abigail Frances. “microRNA Regulation of Zebrafish Retinal Development.” 2015. Web. 03 Dec 2020.

Vancouver:

Olena AF. microRNA Regulation of Zebrafish Retinal Development. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/10500.

Council of Science Editors:

Olena AF. microRNA Regulation of Zebrafish Retinal Development. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/10500


Vanderbilt University

3. Rao, Mahesh Badeti. Inhibition of GABA Initiates Retina Regeneration in the Zebrafish.

Degree: PhD, Biological Sciences, 2016, Vanderbilt University

 Retina damage or disease in humans often leads to reactive gliosis, preventing the formation of new cells and resulting in visual impairment or blindness. Currently,… (more)

Subjects/Keywords: Muller Glia; GABA; Zebrafish; Retina; Regeneration; Muller Glia; GABA; Regeneration; Retina; Zebrafish

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APA (6th Edition):

Rao, M. B. (2016). Inhibition of GABA Initiates Retina Regeneration in the Zebrafish. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13654

Chicago Manual of Style (16th Edition):

Rao, Mahesh Badeti. “Inhibition of GABA Initiates Retina Regeneration in the Zebrafish.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/13654.

MLA Handbook (7th Edition):

Rao, Mahesh Badeti. “Inhibition of GABA Initiates Retina Regeneration in the Zebrafish.” 2016. Web. 03 Dec 2020.

Vancouver:

Rao MB. Inhibition of GABA Initiates Retina Regeneration in the Zebrafish. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/13654.

Council of Science Editors:

Rao MB. Inhibition of GABA Initiates Retina Regeneration in the Zebrafish. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/13654


Vanderbilt University

4. Khuansuwan, Sataree. A transcription factor network dictates neuronal cell fate decisions in the zebrafish dorsal diencephalon.

Degree: PhD, Biological Sciences, 2014, Vanderbilt University

 The zebrafish epithalamus, which includes the dorsal habenular nuclei and pineal complex, displays robust molecular and anatomical asymmetries. The full elaboration of molecular and anatomical… (more)

Subjects/Keywords: parapineal; left-right asymmetry; Danio rerio; zebrafish; Tbx2b; pineal; pineal complex; transcriptome analysis; Flh; Nr2e3; FACS

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APA (6th Edition):

Khuansuwan, S. (2014). A transcription factor network dictates neuronal cell fate decisions in the zebrafish dorsal diencephalon. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14223

Chicago Manual of Style (16th Edition):

Khuansuwan, Sataree. “A transcription factor network dictates neuronal cell fate decisions in the zebrafish dorsal diencephalon.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/14223.

MLA Handbook (7th Edition):

Khuansuwan, Sataree. “A transcription factor network dictates neuronal cell fate decisions in the zebrafish dorsal diencephalon.” 2014. Web. 03 Dec 2020.

Vancouver:

Khuansuwan S. A transcription factor network dictates neuronal cell fate decisions in the zebrafish dorsal diencephalon. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/14223.

Council of Science Editors:

Khuansuwan S. A transcription factor network dictates neuronal cell fate decisions in the zebrafish dorsal diencephalon. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/14223


Vanderbilt University

5. Guler, Gulfem Dilek. Human DNA helicase B in replication fork surveillance and replication stress recovery.

Degree: PhD, Biological Sciences, 2012, Vanderbilt University

 Correct and faithful genome duplication is crucial for preserving genomic integrity. Genome duplication is, therefore, highly regulated through a complex network of proteins that accomplish… (more)

Subjects/Keywords: Replication protein A; RPA; DNA helicase; DNA replication; DNA repair; replication stress; HelB; HDHB

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APA (6th Edition):

Guler, G. D. (2012). Human DNA helicase B in replication fork surveillance and replication stress recovery. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15350

Chicago Manual of Style (16th Edition):

Guler, Gulfem Dilek. “Human DNA helicase B in replication fork surveillance and replication stress recovery.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/15350.

MLA Handbook (7th Edition):

Guler, Gulfem Dilek. “Human DNA helicase B in replication fork surveillance and replication stress recovery.” 2012. Web. 03 Dec 2020.

Vancouver:

Guler GD. Human DNA helicase B in replication fork surveillance and replication stress recovery. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/15350.

Council of Science Editors:

Guler GD. Human DNA helicase B in replication fork surveillance and replication stress recovery. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/15350


Vanderbilt University

6. Cha, Diana Jean. KRAS-dependent Regulation of Extracellular RNAs in Colorectal Cancer.

Degree: PhD, Biological Sciences, 2017, Vanderbilt University

 There is growing evidence for the regulatory roles of extracellular RNAs (exRNAs) in mediating cell-to-cell communication. To test whether exosomal RNA might also contribute to… (more)

Subjects/Keywords: RAS; ceramide; AGO; extracellular vesicles; exRNA

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APA (6th Edition):

Cha, D. J. (2017). KRAS-dependent Regulation of Extracellular RNAs in Colorectal Cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11544

Chicago Manual of Style (16th Edition):

Cha, Diana Jean. “KRAS-dependent Regulation of Extracellular RNAs in Colorectal Cancer.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/11544.

MLA Handbook (7th Edition):

Cha, Diana Jean. “KRAS-dependent Regulation of Extracellular RNAs in Colorectal Cancer.” 2017. Web. 03 Dec 2020.

Vancouver:

Cha DJ. KRAS-dependent Regulation of Extracellular RNAs in Colorectal Cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/11544.

Council of Science Editors:

Cha DJ. KRAS-dependent Regulation of Extracellular RNAs in Colorectal Cancer. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/11544


Vanderbilt University

7. Kara, Nergis. microRNA Function in Zebrafish Development and Regeneration.

Degree: PhD, Biological Sciences, 2018, Vanderbilt University

 microRNAs (miRNAs) are a family of highly conserved small noncoding RNAs that post transcriptionally regulate gene expression and play important roles in many cellular processes… (more)

Subjects/Keywords: zebrafish; microRNA; development; regeneration; retina; Müller glia

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APA (6th Edition):

Kara, N. (2018). microRNA Function in Zebrafish Development and Regeneration. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14353

Chicago Manual of Style (16th Edition):

Kara, Nergis. “microRNA Function in Zebrafish Development and Regeneration.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/14353.

MLA Handbook (7th Edition):

Kara, Nergis. “microRNA Function in Zebrafish Development and Regeneration.” 2018. Web. 03 Dec 2020.

Vancouver:

Kara N. microRNA Function in Zebrafish Development and Regeneration. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/14353.

Council of Science Editors:

Kara N. microRNA Function in Zebrafish Development and Regeneration. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/14353


Vanderbilt University

8. Wei, Chunyao. Roles of miRNAs During Early Zebrafish Development.

Degree: PhD, Biological Sciences, 2013, Vanderbilt University

 microRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level by specific binding to recognition elements in the 3’ untranslated regions… (more)

Subjects/Keywords: zebrafish; miRNA; miR-153; miR-27; deep sequencing; piRNAs; motor neuron; synaptic activities

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APA (6th Edition):

Wei, C. (2013). Roles of miRNAs During Early Zebrafish Development. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12729

Chicago Manual of Style (16th Edition):

Wei, Chunyao. “Roles of miRNAs During Early Zebrafish Development.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/12729.

MLA Handbook (7th Edition):

Wei, Chunyao. “Roles of miRNAs During Early Zebrafish Development.” 2013. Web. 03 Dec 2020.

Vancouver:

Wei C. Roles of miRNAs During Early Zebrafish Development. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/12729.

Council of Science Editors:

Wei C. Roles of miRNAs During Early Zebrafish Development. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/12729


Vanderbilt University

9. Bertram, Clinton Cody. Bid Maintains Cell Viability and Homeostasis by Regulating Mitochondrial Physiology and the DNA Damage Response.

Degree: PhD, Cell and Developmental Biology, 2015, Vanderbilt University

 Proteins of the Bcl-2 family mediate apoptosis by altering mitochondrial structure, function, and integrity. However, in certain contexts, some members of the Bcl-2 family have… (more)

Subjects/Keywords: DNA damage; Bcl-2 family; metabolism; mitochondria; Apoptosis; Cardiolipin

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APA (6th Edition):

Bertram, C. C. (2015). Bid Maintains Cell Viability and Homeostasis by Regulating Mitochondrial Physiology and the DNA Damage Response. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14278

Chicago Manual of Style (16th Edition):

Bertram, Clinton Cody. “Bid Maintains Cell Viability and Homeostasis by Regulating Mitochondrial Physiology and the DNA Damage Response.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/14278.

MLA Handbook (7th Edition):

Bertram, Clinton Cody. “Bid Maintains Cell Viability and Homeostasis by Regulating Mitochondrial Physiology and the DNA Damage Response.” 2015. Web. 03 Dec 2020.

Vancouver:

Bertram CC. Bid Maintains Cell Viability and Homeostasis by Regulating Mitochondrial Physiology and the DNA Damage Response. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/14278.

Council of Science Editors:

Bertram CC. Bid Maintains Cell Viability and Homeostasis by Regulating Mitochondrial Physiology and the DNA Damage Response. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/14278


Vanderbilt University

10. Talley, Jennell Marie. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.

Degree: PhD, Biological Sciences, 2011, Vanderbilt University

 The work presented in this dissertation focuses on a how the telomerase complex assembles both in vivo and in vitro and begins to explore how… (more)

Subjects/Keywords: proteasome; TERT; cell cycle; Telomere

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APA (6th Edition):

Talley, J. M. (2011). Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13166

Chicago Manual of Style (16th Edition):

Talley, Jennell Marie. “Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/13166.

MLA Handbook (7th Edition):

Talley, Jennell Marie. “Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.” 2011. Web. 03 Dec 2020.

Vancouver:

Talley JM. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/13166.

Council of Science Editors:

Talley JM. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/13166


Vanderbilt University

11. Adams, Clare Marie. The contribution of miRNA biogenesis and Myc-regulated miRNA in apoptosis and tumorigenesis.

Degree: PhD, Pathology, 2015, Vanderbilt University

 microRNA (miRNA) are critical mediators of cellular signaling and regulate most biological processes. Thus, it is not surprising that miRNA dysregulation significantly contributes to tumorigenesis.… (more)

Subjects/Keywords: p53; miRNA; Dicer; Myc; HDAC; Bcl-2; Bcl-xL; apoptosis; tumorigenesis

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APA (6th Edition):

Adams, C. M. (2015). The contribution of miRNA biogenesis and Myc-regulated miRNA in apoptosis and tumorigenesis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14501

Chicago Manual of Style (16th Edition):

Adams, Clare Marie. “The contribution of miRNA biogenesis and Myc-regulated miRNA in apoptosis and tumorigenesis.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/14501.

MLA Handbook (7th Edition):

Adams, Clare Marie. “The contribution of miRNA biogenesis and Myc-regulated miRNA in apoptosis and tumorigenesis.” 2015. Web. 03 Dec 2020.

Vancouver:

Adams CM. The contribution of miRNA biogenesis and Myc-regulated miRNA in apoptosis and tumorigenesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/14501.

Council of Science Editors:

Adams CM. The contribution of miRNA biogenesis and Myc-regulated miRNA in apoptosis and tumorigenesis. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/14501


Vanderbilt University

12. Rajaram, Kamya. miRNA function during zebrafish retina regeneration.

Degree: PhD, Biological Sciences, 2014, Vanderbilt University

 Zebrafish spontaneously regenerate their retinas after a variety of retinal insults. Key to regeneration are resident support cells called Müller glia (MG), which respond to… (more)

Subjects/Keywords: Müller glia; retina regeneration; zebrafish; microRNA

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APA (6th Edition):

Rajaram, K. (2014). miRNA function during zebrafish retina regeneration. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12985

Chicago Manual of Style (16th Edition):

Rajaram, Kamya. “miRNA function during zebrafish retina regeneration.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/12985.

MLA Handbook (7th Edition):

Rajaram, Kamya. “miRNA function during zebrafish retina regeneration.” 2014. Web. 03 Dec 2020.

Vancouver:

Rajaram K. miRNA function during zebrafish retina regeneration. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/12985.

Council of Science Editors:

Rajaram K. miRNA function during zebrafish retina regeneration. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/12985


Vanderbilt University

13. Hinger, Scott Andrew. KRAS-dependent Extracellular Vesicles in Colorectal Cancer: Cargo, Biogenesis, and Function.

Degree: PhD, Biological Sciences, 2020, Vanderbilt University

 Colorectal cancer (CRC) cells release protein-laden extracellular vesicles (EVs) that can alter the tumor microenvironment and spread drug resistance. I compared long RNAs of cells… (more)

Subjects/Keywords: colorectal cancer; extracellular RNA; Rab13; extracellular vesicles

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APA (6th Edition):

Hinger, S. A. (2020). KRAS-dependent Extracellular Vesicles in Colorectal Cancer: Cargo, Biogenesis, and Function. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15304

Chicago Manual of Style (16th Edition):

Hinger, Scott Andrew. “KRAS-dependent Extracellular Vesicles in Colorectal Cancer: Cargo, Biogenesis, and Function.” 2020. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/15304.

MLA Handbook (7th Edition):

Hinger, Scott Andrew. “KRAS-dependent Extracellular Vesicles in Colorectal Cancer: Cargo, Biogenesis, and Function.” 2020. Web. 03 Dec 2020.

Vancouver:

Hinger SA. KRAS-dependent Extracellular Vesicles in Colorectal Cancer: Cargo, Biogenesis, and Function. [Internet] [Doctoral dissertation]. Vanderbilt University; 2020. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/15304.

Council of Science Editors:

Hinger SA. KRAS-dependent Extracellular Vesicles in Colorectal Cancer: Cargo, Biogenesis, and Function. [Doctoral Dissertation]. Vanderbilt University; 2020. Available from: http://hdl.handle.net/1803/15304


Vanderbilt University

14. Clanton, Joshua Aaron. Fgf Signaling Governs the Differentiation of Parapineal Neurons in Zebrafish.

Degree: PhD, Biological Sciences, 2013, Vanderbilt University

 Parapineal precursors arise from the medially located pineal complex anlage and migrate to the left side of the brain. Published data implicates Fgf8a in the… (more)

Subjects/Keywords: Left-right asymmetry; neuron; Differentiation

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APA (6th Edition):

Clanton, J. A. (2013). Fgf Signaling Governs the Differentiation of Parapineal Neurons in Zebrafish. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10639

Chicago Manual of Style (16th Edition):

Clanton, Joshua Aaron. “Fgf Signaling Governs the Differentiation of Parapineal Neurons in Zebrafish.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/10639.

MLA Handbook (7th Edition):

Clanton, Joshua Aaron. “Fgf Signaling Governs the Differentiation of Parapineal Neurons in Zebrafish.” 2013. Web. 03 Dec 2020.

Vancouver:

Clanton JA. Fgf Signaling Governs the Differentiation of Parapineal Neurons in Zebrafish. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/10639.

Council of Science Editors:

Clanton JA. Fgf Signaling Governs the Differentiation of Parapineal Neurons in Zebrafish. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/10639


Vanderbilt University

15. Baldridge, Ryan Douglas. Phospholipid selection and transport by P4-ATPases.

Degree: PhD, Biological Sciences, 2013, Vanderbilt University

 The plasma membrane of eukaryotic cells displays a distinctive asymmetry of the component phospholipids. Type-IV P-type ATPases (P4-ATPases) flip specific phospholipids across the membrane bilayer… (more)

Subjects/Keywords: protein trafficking; phosphatidylserine; P-type ATPase; flippase; membrane biology

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APA (6th Edition):

Baldridge, R. D. (2013). Phospholipid selection and transport by P4-ATPases. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10640

Chicago Manual of Style (16th Edition):

Baldridge, Ryan Douglas. “Phospholipid selection and transport by P4-ATPases.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/10640.

MLA Handbook (7th Edition):

Baldridge, Ryan Douglas. “Phospholipid selection and transport by P4-ATPases.” 2013. Web. 03 Dec 2020.

Vancouver:

Baldridge RD. Phospholipid selection and transport by P4-ATPases. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/10640.

Council of Science Editors:

Baldridge RD. Phospholipid selection and transport by P4-ATPases. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/10640


Vanderbilt University

16. Sammons, Morgan Andrew. Analysis of ZNF9 function in cap-independent translation and myotonic dystrophy type 2.

Degree: PhD, Biological Sciences, 2010, Vanderbilt University

 Myotonic dystrophy type 2 (DM2) is an autosomal dominant human disease caused by the expansion of a tetranucleotide repeat in the first intron of the… (more)

Subjects/Keywords: translation; myotonic dystrophy; ZNF9; RNA

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APA (6th Edition):

Sammons, M. A. (2010). Analysis of ZNF9 function in cap-independent translation and myotonic dystrophy type 2. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13875

Chicago Manual of Style (16th Edition):

Sammons, Morgan Andrew. “Analysis of ZNF9 function in cap-independent translation and myotonic dystrophy type 2.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/13875.

MLA Handbook (7th Edition):

Sammons, Morgan Andrew. “Analysis of ZNF9 function in cap-independent translation and myotonic dystrophy type 2.” 2010. Web. 03 Dec 2020.

Vancouver:

Sammons MA. Analysis of ZNF9 function in cap-independent translation and myotonic dystrophy type 2. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/13875.

Council of Science Editors:

Sammons MA. Analysis of ZNF9 function in cap-independent translation and myotonic dystrophy type 2. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://hdl.handle.net/1803/13875


Vanderbilt University

17. Li, Nan. MiRNA function during early vertebrate development.

Degree: PhD, Biological Sciences, 2010, Vanderbilt University

 microRNAs (miRNAs) are short non-coding RNAs that down-regulate gene expression by pairing with sequences in the 3’UTR of target mRNAs. They play critical roles in… (more)

Subjects/Keywords: zebrafish; microRNA

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APA (6th Edition):

Li, N. (2010). MiRNA function during early vertebrate development. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12868

Chicago Manual of Style (16th Edition):

Li, Nan. “MiRNA function during early vertebrate development.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/12868.

MLA Handbook (7th Edition):

Li, Nan. “MiRNA function during early vertebrate development.” 2010. Web. 03 Dec 2020.

Vancouver:

Li N. MiRNA function during early vertebrate development. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/12868.

Council of Science Editors:

Li N. MiRNA function during early vertebrate development. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://hdl.handle.net/1803/12868


Vanderbilt University

18. Rosenberg, Joshua Adam. Assembly and regulation of signaling proteins at fission yeast microtubule organizing centers.

Degree: PhD, Cell and Developmental Biology, 2007, Vanderbilt University

 The spindle pole body, the yeast analog of the centrosome, serves not only to nucleate and organize microtubules but also as a signaling center to… (more)

Subjects/Keywords: Schizosaccharomyces pombe  – Molecular aspects; spindle pole body; fission yeast; mitosis; cytokinesis; microtubule; Cell cycle  – Regulation

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APA (6th Edition):

Rosenberg, J. A. (2007). Assembly and regulation of signaling proteins at fission yeast microtubule organizing centers. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13601

Chicago Manual of Style (16th Edition):

Rosenberg, Joshua Adam. “Assembly and regulation of signaling proteins at fission yeast microtubule organizing centers.” 2007. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/13601.

MLA Handbook (7th Edition):

Rosenberg, Joshua Adam. “Assembly and regulation of signaling proteins at fission yeast microtubule organizing centers.” 2007. Web. 03 Dec 2020.

Vancouver:

Rosenberg JA. Assembly and regulation of signaling proteins at fission yeast microtubule organizing centers. [Internet] [Doctoral dissertation]. Vanderbilt University; 2007. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/13601.

Council of Science Editors:

Rosenberg JA. Assembly and regulation of signaling proteins at fission yeast microtubule organizing centers. [Doctoral Dissertation]. Vanderbilt University; 2007. Available from: http://hdl.handle.net/1803/13601


Vanderbilt University

19. Ji, Hong. Investigating the role of the n-terminus of yeast telomerase reverse transcriptase in telomere maintenance.

Degree: PhD, Biological Sciences, 2007, Vanderbilt University

 In most eukaryotes, telomere length is maintained by telomerase, a ribonucleoprotein that adds TG-rich telomeric repeats de novo to chromosome ends. Telomeric binding proteins (for… (more)

Subjects/Keywords: Sacchromyces cerevisiae; Telomere; Telomerase; Rap1p/Rif1p/Rif2p

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APA (6th Edition):

Ji, H. (2007). Investigating the role of the n-terminus of yeast telomerase reverse transcriptase in telomere maintenance. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15056

Chicago Manual of Style (16th Edition):

Ji, Hong. “Investigating the role of the n-terminus of yeast telomerase reverse transcriptase in telomere maintenance.” 2007. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/15056.

MLA Handbook (7th Edition):

Ji, Hong. “Investigating the role of the n-terminus of yeast telomerase reverse transcriptase in telomere maintenance.” 2007. Web. 03 Dec 2020.

Vancouver:

Ji H. Investigating the role of the n-terminus of yeast telomerase reverse transcriptase in telomere maintenance. [Internet] [Doctoral dissertation]. Vanderbilt University; 2007. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/15056.

Council of Science Editors:

Ji H. Investigating the role of the n-terminus of yeast telomerase reverse transcriptase in telomere maintenance. [Doctoral Dissertation]. Vanderbilt University; 2007. Available from: http://hdl.handle.net/1803/15056


Vanderbilt University

20. Shariat, Nikki. Growth Hormone Splicing and Treatment of Disease Using RNA Interference.

Degree: PhD, Biological Sciences, 2008, Vanderbilt University

 Splicing is the regulated removal of introns and the concurrent ligation of exons to produce mature mRNA transcripts. Variability in this tightly regulated process is… (more)

Subjects/Keywords: Splicing; Exon skipping; Gene therapy  – Methodology; Growth Hormone; RNAi; RNA editing; Somatotropin; Genetic engineering

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APA (6th Edition):

Shariat, N. (2008). Growth Hormone Splicing and Treatment of Disease Using RNA Interference. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10630

Chicago Manual of Style (16th Edition):

Shariat, Nikki. “Growth Hormone Splicing and Treatment of Disease Using RNA Interference.” 2008. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/10630.

MLA Handbook (7th Edition):

Shariat, Nikki. “Growth Hormone Splicing and Treatment of Disease Using RNA Interference.” 2008. Web. 03 Dec 2020.

Vancouver:

Shariat N. Growth Hormone Splicing and Treatment of Disease Using RNA Interference. [Internet] [Doctoral dissertation]. Vanderbilt University; 2008. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/10630.

Council of Science Editors:

Shariat N. Growth Hormone Splicing and Treatment of Disease Using RNA Interference. [Doctoral Dissertation]. Vanderbilt University; 2008. Available from: http://hdl.handle.net/1803/10630


Vanderbilt University

21. Peng, Rui. Characterization of the essential pre-mRNA splicing factor PSF: investigation of RNA binding specificity and splicing-related complex formation.

Degree: PhD, Biological Sciences, 2005, Vanderbilt University

 PSF (PTB-associated splicing factor) has been implicated in both early and late steps of pre-mRNA splicing as well as multiple nuclear events including transcription regulation,… (more)

Subjects/Keywords: U5 snRNA; spliceosome; splicing; PSF

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APA (6th Edition):

Peng, R. (2005). Characterization of the essential pre-mRNA splicing factor PSF: investigation of RNA binding specificity and splicing-related complex formation. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13872

Chicago Manual of Style (16th Edition):

Peng, Rui. “Characterization of the essential pre-mRNA splicing factor PSF: investigation of RNA binding specificity and splicing-related complex formation.” 2005. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/13872.

MLA Handbook (7th Edition):

Peng, Rui. “Characterization of the essential pre-mRNA splicing factor PSF: investigation of RNA binding specificity and splicing-related complex formation.” 2005. Web. 03 Dec 2020.

Vancouver:

Peng R. Characterization of the essential pre-mRNA splicing factor PSF: investigation of RNA binding specificity and splicing-related complex formation. [Internet] [Doctoral dissertation]. Vanderbilt University; 2005. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/13872.

Council of Science Editors:

Peng R. Characterization of the essential pre-mRNA splicing factor PSF: investigation of RNA binding specificity and splicing-related complex formation. [Doctoral Dissertation]. Vanderbilt University; 2005. Available from: http://hdl.handle.net/1803/13872


Vanderbilt University

22. Robertson, Patrick David. Structural biology of the C-terminal domain of eukaryotic replication factor Mcm10.

Degree: PhD, Biological Sciences, 2010, Vanderbilt University

 Eukaryotic DNA replication is tightly regulated during the initiation phase to ensure that the genome is copied only once and at the proper time during… (more)

Subjects/Keywords: DNA Replication; DNA Binding; Zinc Motif; Mcm10; NMR; C-Terminal Domain

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APA (6th Edition):

Robertson, P. D. (2010). Structural biology of the C-terminal domain of eukaryotic replication factor Mcm10. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12458

Chicago Manual of Style (16th Edition):

Robertson, Patrick David. “Structural biology of the C-terminal domain of eukaryotic replication factor Mcm10.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/12458.

MLA Handbook (7th Edition):

Robertson, Patrick David. “Structural biology of the C-terminal domain of eukaryotic replication factor Mcm10.” 2010. Web. 03 Dec 2020.

Vancouver:

Robertson PD. Structural biology of the C-terminal domain of eukaryotic replication factor Mcm10. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/12458.

Council of Science Editors:

Robertson PD. Structural biology of the C-terminal domain of eukaryotic replication factor Mcm10. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://hdl.handle.net/1803/12458


Vanderbilt University

23. Jiang, Xiaohua. Functional Dynamics of Replication Protein A in initiation of SV40 DNA Replication.

Degree: PhD, Biological Sciences, 2008, Vanderbilt University

 Human replication protein A (RPA) is a single-stranded DNA (ssDNA) binding protein involved in DNA metabolism. RPA binds ssDNA transiently during initiation of DNA replication.… (more)

Subjects/Keywords: Replisome; protein-protein interaction; NMR; structure

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APA (6th Edition):

Jiang, X. (2008). Functional Dynamics of Replication Protein A in initiation of SV40 DNA Replication. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11272

Chicago Manual of Style (16th Edition):

Jiang, Xiaohua. “Functional Dynamics of Replication Protein A in initiation of SV40 DNA Replication.” 2008. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/11272.

MLA Handbook (7th Edition):

Jiang, Xiaohua. “Functional Dynamics of Replication Protein A in initiation of SV40 DNA Replication.” 2008. Web. 03 Dec 2020.

Vancouver:

Jiang X. Functional Dynamics of Replication Protein A in initiation of SV40 DNA Replication. [Internet] [Doctoral dissertation]. Vanderbilt University; 2008. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/11272.

Council of Science Editors:

Jiang X. Functional Dynamics of Replication Protein A in initiation of SV40 DNA Replication. [Doctoral Dissertation]. Vanderbilt University; 2008. Available from: http://hdl.handle.net/1803/11272


Vanderbilt University

24. Speirs, Christina Koo Yang. Prostaglandin Gbetagamma signaling stimulates gastrulation movements by limiting cell adhesion through Snail stabilization.

Degree: PhD, Biological Sciences, 2009, Vanderbilt University

 Prostaglandin E2 (PGE2) influences many processes in vertebrates, including development, homeostasis, and disease through its GPCRs EP receptors 1-4. PGE2 regulates gastrulation movements during zebrafish… (more)

Subjects/Keywords: development; cell motility; protrusion formation; E-cadherin

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APA (6th Edition):

Speirs, C. K. Y. (2009). Prostaglandin Gbetagamma signaling stimulates gastrulation movements by limiting cell adhesion through Snail stabilization. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14101

Chicago Manual of Style (16th Edition):

Speirs, Christina Koo Yang. “Prostaglandin Gbetagamma signaling stimulates gastrulation movements by limiting cell adhesion through Snail stabilization.” 2009. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/14101.

MLA Handbook (7th Edition):

Speirs, Christina Koo Yang. “Prostaglandin Gbetagamma signaling stimulates gastrulation movements by limiting cell adhesion through Snail stabilization.” 2009. Web. 03 Dec 2020.

Vancouver:

Speirs CKY. Prostaglandin Gbetagamma signaling stimulates gastrulation movements by limiting cell adhesion through Snail stabilization. [Internet] [Doctoral dissertation]. Vanderbilt University; 2009. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/14101.

Council of Science Editors:

Speirs CKY. Prostaglandin Gbetagamma signaling stimulates gastrulation movements by limiting cell adhesion through Snail stabilization. [Doctoral Dissertation]. Vanderbilt University; 2009. Available from: http://hdl.handle.net/1803/14101


Vanderbilt University

25. Bristow, Jeanne Malloy. The Rho family GEF Asef2 regulates adhesion dynamics and therefore cell migration by modulating Rac and Rho activity.

Degree: PhD, Biological Sciences, 2010, Vanderbilt University

 BIOLOGICAL SCIENCES THE RHO FAMILY GEF ASEF2 REGULATES ADHESION DYNAMICS AND THEREFORE CELL MIGRATION BY MODULATING RAC AND RHO ACTIVITY JEANNE MALLOY BRISTOW Dissertation under… (more)

Subjects/Keywords: Cdc42; Rac; Akt; focal adhesion; lamellipodium; protrusion; PI3K; turnover; cancer; HT-1080

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APA (6th Edition):

Bristow, J. M. (2010). The Rho family GEF Asef2 regulates adhesion dynamics and therefore cell migration by modulating Rac and Rho activity. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15003

Chicago Manual of Style (16th Edition):

Bristow, Jeanne Malloy. “The Rho family GEF Asef2 regulates adhesion dynamics and therefore cell migration by modulating Rac and Rho activity.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed December 03, 2020. http://hdl.handle.net/1803/15003.

MLA Handbook (7th Edition):

Bristow, Jeanne Malloy. “The Rho family GEF Asef2 regulates adhesion dynamics and therefore cell migration by modulating Rac and Rho activity.” 2010. Web. 03 Dec 2020.

Vancouver:

Bristow JM. The Rho family GEF Asef2 regulates adhesion dynamics and therefore cell migration by modulating Rac and Rho activity. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/1803/15003.

Council of Science Editors:

Bristow JM. The Rho family GEF Asef2 regulates adhesion dynamics and therefore cell migration by modulating Rac and Rho activity. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://hdl.handle.net/1803/15003

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