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University: Vanderbilt University

You searched for subject:(phosphorylation). Showing records 1 – 19 of 19 total matches.

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Vanderbilt University

1. Rohweder, Noelle Holmes. Examining the Role of Phosphorylation in Receptor Localization and Chemotaxis in D. discoideum.

Degree: MS, Biological Sciences, 2012, Vanderbilt University

Phosphorylation of the C-terminus of cAR1 is thought to provide a role in the ability of cells to adapt to cAMP and respond to spatial… (more)

Subjects/Keywords: Dictyostelium discoideum; chemotaxis; Phosphorylation

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APA (6th Edition):

Rohweder, N. H. (2012). Examining the Role of Phosphorylation in Receptor Localization and Chemotaxis in D. discoideum. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-11152012-092638/ ;

Chicago Manual of Style (16th Edition):

Rohweder, Noelle Holmes. “Examining the Role of Phosphorylation in Receptor Localization and Chemotaxis in D. discoideum.” 2012. Masters Thesis, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu//available/etd-11152012-092638/ ;.

MLA Handbook (7th Edition):

Rohweder, Noelle Holmes. “Examining the Role of Phosphorylation in Receptor Localization and Chemotaxis in D. discoideum.” 2012. Web. 15 Oct 2019.

Vancouver:

Rohweder NH. Examining the Role of Phosphorylation in Receptor Localization and Chemotaxis in D. discoideum. [Internet] [Masters thesis]. Vanderbilt University; 2012. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu//available/etd-11152012-092638/ ;.

Council of Science Editors:

Rohweder NH. Examining the Role of Phosphorylation in Receptor Localization and Chemotaxis in D. discoideum. [Masters Thesis]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu//available/etd-11152012-092638/ ;


Vanderbilt University

2. Robbins, Carol Bansbach. Identifying and defining the genome maintenance functions of SMARCAL1.

Degree: PhD, Biochemistry, 2012, Vanderbilt University

 In this dissertation I identify and define SWI/SNF, matrix-associated, actin-dependent regulator of chromatin, A-like 1 (SMARCAL1) as a genome maintenance protein. First, I introduce a… (more)

Subjects/Keywords: phosphorylation; DNA damage response; replication stress

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APA (6th Edition):

Robbins, C. B. (2012). Identifying and defining the genome maintenance functions of SMARCAL1. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-05252012-151148/ ;

Chicago Manual of Style (16th Edition):

Robbins, Carol Bansbach. “Identifying and defining the genome maintenance functions of SMARCAL1.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-05252012-151148/ ;.

MLA Handbook (7th Edition):

Robbins, Carol Bansbach. “Identifying and defining the genome maintenance functions of SMARCAL1.” 2012. Web. 15 Oct 2019.

Vancouver:

Robbins CB. Identifying and defining the genome maintenance functions of SMARCAL1. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-05252012-151148/ ;.

Council of Science Editors:

Robbins CB. Identifying and defining the genome maintenance functions of SMARCAL1. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu/available/etd-05252012-151148/ ;


Vanderbilt University

3. Bohnert, Kenneth Adam. Divide and Prosper: Molecular Mechanisms and Consequences of Cytokinetic Ring Regulation.

Degree: PhD, Cell and Developmental Biology, 2013, Vanderbilt University

 In many organisms, a cytokinetic ring directs daughter cell separation following mitosis. While conserved molecular participants in this process have been defined, the signaling events… (more)

Subjects/Keywords: cytokinesis; cell growth; phosphorylation; formin; kinase; morphogenesis

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APA (6th Edition):

Bohnert, K. A. (2013). Divide and Prosper: Molecular Mechanisms and Consequences of Cytokinetic Ring Regulation. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07172013-203322/ ;

Chicago Manual of Style (16th Edition):

Bohnert, Kenneth Adam. “Divide and Prosper: Molecular Mechanisms and Consequences of Cytokinetic Ring Regulation.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-07172013-203322/ ;.

MLA Handbook (7th Edition):

Bohnert, Kenneth Adam. “Divide and Prosper: Molecular Mechanisms and Consequences of Cytokinetic Ring Regulation.” 2013. Web. 15 Oct 2019.

Vancouver:

Bohnert KA. Divide and Prosper: Molecular Mechanisms and Consequences of Cytokinetic Ring Regulation. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-07172013-203322/ ;.

Council of Science Editors:

Bohnert KA. Divide and Prosper: Molecular Mechanisms and Consequences of Cytokinetic Ring Regulation. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu/available/etd-07172013-203322/ ;


Vanderbilt University

4. Donato, Dominique Maria. The focal adhesion localization of p130Cas: dynamics, targeting mechanism, and signaling.

Degree: PhD, Cell and Developmental Biology, 2010, Vanderbilt University

 Focal adhesions (FAs) are sites at the interface between the cell and the ECM, linking integrin receptors and the actin cytoskeleton. In addition to serving… (more)

Subjects/Keywords: cell motility; FAK; tyrosine phosphorylation; paxillin; focal adhesion; p130Cas

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APA (6th Edition):

Donato, D. M. (2010). The focal adhesion localization of p130Cas: dynamics, targeting mechanism, and signaling. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-06302010-180728/ ;

Chicago Manual of Style (16th Edition):

Donato, Dominique Maria. “The focal adhesion localization of p130Cas: dynamics, targeting mechanism, and signaling.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-06302010-180728/ ;.

MLA Handbook (7th Edition):

Donato, Dominique Maria. “The focal adhesion localization of p130Cas: dynamics, targeting mechanism, and signaling.” 2010. Web. 15 Oct 2019.

Vancouver:

Donato DM. The focal adhesion localization of p130Cas: dynamics, targeting mechanism, and signaling. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-06302010-180728/ ;.

Council of Science Editors:

Donato DM. The focal adhesion localization of p130Cas: dynamics, targeting mechanism, and signaling. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu/available/etd-06302010-180728/ ;


Vanderbilt University

5. Atwood, Allison Annette. Regulation of C/EBPbeta1 in transformed mammary epithelial cells and the role of C/EBPbeta1 in oncogene-induced senescence.

Degree: PhD, Cancer Biology, 2010, Vanderbilt University

 Overexpression of activated oncogenes such as Ras(V12) in primary cells induces senescence rather than transformation, thus suppressing tumorigenesis. C/EBPbeta is required for Ras(V12)-induced senescence in… (more)

Subjects/Keywords: Ras; breast cancer; IL6; senescence; C/EBPbeta; sumoylation; degradation; phosphorylation

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APA (6th Edition):

Atwood, A. A. (2010). Regulation of C/EBPbeta1 in transformed mammary epithelial cells and the role of C/EBPbeta1 in oncogene-induced senescence. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-12102010-121704/ ;

Chicago Manual of Style (16th Edition):

Atwood, Allison Annette. “Regulation of C/EBPbeta1 in transformed mammary epithelial cells and the role of C/EBPbeta1 in oncogene-induced senescence.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-12102010-121704/ ;.

MLA Handbook (7th Edition):

Atwood, Allison Annette. “Regulation of C/EBPbeta1 in transformed mammary epithelial cells and the role of C/EBPbeta1 in oncogene-induced senescence.” 2010. Web. 15 Oct 2019.

Vancouver:

Atwood AA. Regulation of C/EBPbeta1 in transformed mammary epithelial cells and the role of C/EBPbeta1 in oncogene-induced senescence. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-12102010-121704/ ;.

Council of Science Editors:

Atwood AA. Regulation of C/EBPbeta1 in transformed mammary epithelial cells and the role of C/EBPbeta1 in oncogene-induced senescence. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu/available/etd-12102010-121704/ ;

6. Hang, Brian I. Kinase Regulation of XIAP in Wnt Signaling.

Degree: PhD, Cell and Developmental Biology, 2016, Vanderbilt University

 The Wnt signaling pathway plays essential roles in a wide variety of biological processes including early animal development, cell fate determination, cell proliferation, organogenesis, and… (more)

Subjects/Keywords: Wnt; XIAP; phosphorylation; ubiquitination

phosphorylation sites on XIAP that are strongly phosphorylated. Mutational analysis of these two sites… …decreased affinity for Gro/TLE. We propose a model in which phosphorylation is required for the… …initiation step” of receptor activation) results in phosphorylation of the intracellular… …sequential manner. Wnt binding induces phosphorylation by GSK3 and studies have also shown that CK1… …primes the S/T clusters, outside of the PPPSPxS motif, for phosphorylation 4 by GSK3 (… 

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APA (6th Edition):

Hang, B. I. (2016). Kinase Regulation of XIAP in Wnt Signaling. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07072016-135625/ ;

Chicago Manual of Style (16th Edition):

Hang, Brian I. “Kinase Regulation of XIAP in Wnt Signaling.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-07072016-135625/ ;.

MLA Handbook (7th Edition):

Hang, Brian I. “Kinase Regulation of XIAP in Wnt Signaling.” 2016. Web. 15 Oct 2019.

Vancouver:

Hang BI. Kinase Regulation of XIAP in Wnt Signaling. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-07072016-135625/ ;.

Council of Science Editors:

Hang BI. Kinase Regulation of XIAP in Wnt Signaling. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu/available/etd-07072016-135625/ ;

7. Qin, Ximing. Cyanobacterial circadian clock in vitro and in vivo.

Degree: PhD, Biological Sciences, 2010, Vanderbilt University

 Circadian rhythms are intrinsic biological rhythms that have a period close to 24 hours. Prokaryotic cyanobacteria are the simplest organisms that show robust circadian rhythms,… (more)

Subjects/Keywords: Cyanobacteria; KaiC; Phosphorylation; Circadian Clock

…circadian rhythms ….......11 1-4. Circadian phosphorylation of KaiC in the in vitro KaiABC… …reaction ... 13 1-5. The sequential phosphorylation model of the in vitro KaiABC oscillator… …abundance and phosphorylation under different illumination conditions 73 x… …3-2. Increasing expression of KaiA suppresses the KaiC phosphorylation rhythm and the gene… …encoded by those genes were discovered to reconstitute a 24 hour rhythm of phosphorylation of… 

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APA (6th Edition):

Qin, X. (2010). Cyanobacterial circadian clock in vitro and in vivo. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-12212010-120143/ ;

Chicago Manual of Style (16th Edition):

Qin, Ximing. “Cyanobacterial circadian clock in vitro and in vivo.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-12212010-120143/ ;.

MLA Handbook (7th Edition):

Qin, Ximing. “Cyanobacterial circadian clock in vitro and in vivo.” 2010. Web. 15 Oct 2019.

Vancouver:

Qin X. Cyanobacterial circadian clock in vitro and in vivo. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-12212010-120143/ ;.

Council of Science Editors:

Qin X. Cyanobacterial circadian clock in vitro and in vivo. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu/available/etd-12212010-120143/ ;


Vanderbilt University

8. Marks, Christian Randal. Role of Ca2+/Calmodulin-Dependent Protein Kinase II in Regulating the Metabotropic Glutamate Receptor 5.

Degree: PhD, Molecular Physiology and Biophysics, 2019, Vanderbilt University

 Multi-protein complexes formed through protein-protein interactions in the dendrites of neurons are highly regulated to facilitate proper synaptic function. The work presented in this dissertation… (more)

Subjects/Keywords: kinase activity; calicum imaging; neuronal activity; camkii; protein interactions; metabotropic glutamate receptor; phosphorylation; protein binding

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APA (6th Edition):

Marks, C. R. (2019). Role of Ca2+/Calmodulin-Dependent Protein Kinase II in Regulating the Metabotropic Glutamate Receptor 5. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-02202019-113322/ ;

Chicago Manual of Style (16th Edition):

Marks, Christian Randal. “Role of Ca2+/Calmodulin-Dependent Protein Kinase II in Regulating the Metabotropic Glutamate Receptor 5.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-02202019-113322/ ;.

MLA Handbook (7th Edition):

Marks, Christian Randal. “Role of Ca2+/Calmodulin-Dependent Protein Kinase II in Regulating the Metabotropic Glutamate Receptor 5.” 2019. Web. 15 Oct 2019.

Vancouver:

Marks CR. Role of Ca2+/Calmodulin-Dependent Protein Kinase II in Regulating the Metabotropic Glutamate Receptor 5. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-02202019-113322/ ;.

Council of Science Editors:

Marks CR. Role of Ca2+/Calmodulin-Dependent Protein Kinase II in Regulating the Metabotropic Glutamate Receptor 5. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://etd.library.vanderbilt.edu/available/etd-02202019-113322/ ;

9. Tang, Xin. Modulation of GABAA receptor function by PKA and PKC protein phosphorylation.

Degree: PhD, Neuroscience, 2010, Vanderbilt University

 We studied the modulation of ¦Ã4¦Ã3¦Ã2L and ¦Ã4¦Ã3¦à GABAA receptor currents by two protein kinases, PKA and PKC. Although modulation of synaptic ¦Ã1¦Ã¦Ã2 GABAA receptor… (more)

Subjects/Keywords: PKC; GABAA receptor; phosphorylation; PKA

…149 Phosphorylation provides heterogeneous regulation of GABAA receptors in the CNS… …149 Modulation of GABAA receptors by direct phosphorylation… …protein phosphorylation… …154 The relationship of modulation by phosphorylation of GABAA receptors with epilepsy… …3 1.2. Phosphorylation sites in GABAA receptor subunits… 

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APA (6th Edition):

Tang, X. (2010). Modulation of GABAA receptor function by PKA and PKC protein phosphorylation. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03312010-103304/ ;

Chicago Manual of Style (16th Edition):

Tang, Xin. “Modulation of GABAA receptor function by PKA and PKC protein phosphorylation.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-03312010-103304/ ;.

MLA Handbook (7th Edition):

Tang, Xin. “Modulation of GABAA receptor function by PKA and PKC protein phosphorylation.” 2010. Web. 15 Oct 2019.

Vancouver:

Tang X. Modulation of GABAA receptor function by PKA and PKC protein phosphorylation. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-03312010-103304/ ;.

Council of Science Editors:

Tang X. Modulation of GABAA receptor function by PKA and PKC protein phosphorylation. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu/available/etd-03312010-103304/ ;

10. Abiria, Sunday. Ca2+/Calmodulin-dependent Protein Kinase II Anchoring to L-type Ca2+ Channels by the Beta Subunits Enhances Regulatory Phosphorylation at Thr498.

Degree: PhD, Neuroscience, 2010, Vanderbilt University

 Calcium/calmodulin-dependent kinase II (CaMKII) facilitates L-type calcium channel (LTCC) activity physiologically, but may exacerbate LTCC-dependent pathophysiology. We previously showed that CaMKII forms stable complexes with… (more)

Subjects/Keywords: Calcium; Channel; Phosphorylation; Beta; CaMKII

…158 Figure A9. Phosphorylation of β2a in binary complexes with CaMKII................ 160… …Figure A10. Endogenous CaMKII binding enhances β2a phosphorylation at Thr498… …161 Figure A11. Effect of CaMKIIδ isoform binding on β2a phosphorylation at Thr498 in Binary… …Effect of CaMKIIδ isoform binding on β2a phosphorylation at Thr498 in Ternary Complexes… …phosphorylation at Thr498........................................................................... 168… 

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APA (6th Edition):

Abiria, S. (2010). Ca2+/Calmodulin-dependent Protein Kinase II Anchoring to L-type Ca2+ Channels by the Beta Subunits Enhances Regulatory Phosphorylation at Thr498. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03112010-001429/ ;

Chicago Manual of Style (16th Edition):

Abiria, Sunday. “Ca2+/Calmodulin-dependent Protein Kinase II Anchoring to L-type Ca2+ Channels by the Beta Subunits Enhances Regulatory Phosphorylation at Thr498.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu//available/etd-03112010-001429/ ;.

MLA Handbook (7th Edition):

Abiria, Sunday. “Ca2+/Calmodulin-dependent Protein Kinase II Anchoring to L-type Ca2+ Channels by the Beta Subunits Enhances Regulatory Phosphorylation at Thr498.” 2010. Web. 15 Oct 2019.

Vancouver:

Abiria S. Ca2+/Calmodulin-dependent Protein Kinase II Anchoring to L-type Ca2+ Channels by the Beta Subunits Enhances Regulatory Phosphorylation at Thr498. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu//available/etd-03112010-001429/ ;.

Council of Science Editors:

Abiria S. Ca2+/Calmodulin-dependent Protein Kinase II Anchoring to L-type Ca2+ Channels by the Beta Subunits Enhances Regulatory Phosphorylation at Thr498. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu//available/etd-03112010-001429/ ;


Vanderbilt University

11. Moser, Leta Ruth. The role of bad phosphorylation status and binding partners in promoting apoptosis.

Degree: MS, Cancer Biology, 2007, Vanderbilt University

 Although the signaling mechanisms of the apoptotic pathway have been extensively studied, there is still much left unknown. A key regulator protein, 14-3-3, is known… (more)

Subjects/Keywords: 14-3-3; p38; phosphorylation; BAD; apoptosis

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APA (6th Edition):

Moser, L. R. (2007). The role of bad phosphorylation status and binding partners in promoting apoptosis. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-04012007-204633/ ;

Chicago Manual of Style (16th Edition):

Moser, Leta Ruth. “The role of bad phosphorylation status and binding partners in promoting apoptosis.” 2007. Masters Thesis, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-04012007-204633/ ;.

MLA Handbook (7th Edition):

Moser, Leta Ruth. “The role of bad phosphorylation status and binding partners in promoting apoptosis.” 2007. Web. 15 Oct 2019.

Vancouver:

Moser LR. The role of bad phosphorylation status and binding partners in promoting apoptosis. [Internet] [Masters thesis]. Vanderbilt University; 2007. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-04012007-204633/ ;.

Council of Science Editors:

Moser LR. The role of bad phosphorylation status and binding partners in promoting apoptosis. [Masters Thesis]. Vanderbilt University; 2007. Available from: http://etd.library.vanderbilt.edu/available/etd-04012007-204633/ ;


Vanderbilt University

12. Broadus, Matthew Ryan. Mechanisms that control localization of the Schizosaccharomyces pombe Clp1/Cdc14 phosphatase.

Degree: PhD, Cell and Developmental Biology, 2013, Vanderbilt University

 The Cdc14 phosphatase family antagonizes Cdk1 phosphorylation and is important for mitotic exit. Dynamic localization is a major means of regulating this phosphatase family, yet… (more)

Subjects/Keywords: oxidative stress; hydrogen peroxide; nucleolus; Clp1; phosphorylation; H2O2; Flp1; phosphatase; Cdc14; cell stress; cell cycle; kinase

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APA (6th Edition):

Broadus, M. R. (2013). Mechanisms that control localization of the Schizosaccharomyces pombe Clp1/Cdc14 phosphatase. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-04012013-103014/ ;

Chicago Manual of Style (16th Edition):

Broadus, Matthew Ryan. “Mechanisms that control localization of the Schizosaccharomyces pombe Clp1/Cdc14 phosphatase.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu//available/etd-04012013-103014/ ;.

MLA Handbook (7th Edition):

Broadus, Matthew Ryan. “Mechanisms that control localization of the Schizosaccharomyces pombe Clp1/Cdc14 phosphatase.” 2013. Web. 15 Oct 2019.

Vancouver:

Broadus MR. Mechanisms that control localization of the Schizosaccharomyces pombe Clp1/Cdc14 phosphatase. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu//available/etd-04012013-103014/ ;.

Council of Science Editors:

Broadus MR. Mechanisms that control localization of the Schizosaccharomyces pombe Clp1/Cdc14 phosphatase. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu//available/etd-04012013-103014/ ;

13. Pretto Garcia, Dalyir Imelda. Domain-based structural studies of Replication Protein A: analysis of an RPA32N phospho-mimic mutant and the role of RPA70N in binding ssDNA.

Degree: PhD, Biochemistry, 2010, Vanderbilt University

 Replication Protein A (RPA) is the primary eukaryotic ssDNA binding protein utilized in preventing secondary structure formation and re-annealing of unwound DNA strands, thereby controlling… (more)

Subjects/Keywords: RPA; RPA phosphorylation; SAXS; RPA ssDNA binding

…heterotrimer, which forms the basis of the studies described in Chapter II. Phosphorylation of RPA… …Phosphorylation is a common mechanism of regulation of protein activity, and often occurs on more than… …phosphorylate which RPA residues, the order of phosphorylation events and their outcomes. Therefore… …unchanged throughout the cell cycle, but a cell cycle dependent phosphorylation of RPA was… …x5D;. It was observed that phosphorylation was limited to the S and G2 phases of the cell… 

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APA (6th Edition):

Pretto Garcia, D. I. (2010). Domain-based structural studies of Replication Protein A: analysis of an RPA32N phospho-mimic mutant and the role of RPA70N in binding ssDNA. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07122010-152656/ ;

Chicago Manual of Style (16th Edition):

Pretto Garcia, Dalyir Imelda. “Domain-based structural studies of Replication Protein A: analysis of an RPA32N phospho-mimic mutant and the role of RPA70N in binding ssDNA.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-07122010-152656/ ;.

MLA Handbook (7th Edition):

Pretto Garcia, Dalyir Imelda. “Domain-based structural studies of Replication Protein A: analysis of an RPA32N phospho-mimic mutant and the role of RPA70N in binding ssDNA.” 2010. Web. 15 Oct 2019.

Vancouver:

Pretto Garcia DI. Domain-based structural studies of Replication Protein A: analysis of an RPA32N phospho-mimic mutant and the role of RPA70N in binding ssDNA. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-07122010-152656/ ;.

Council of Science Editors:

Pretto Garcia DI. Domain-based structural studies of Replication Protein A: analysis of an RPA32N phospho-mimic mutant and the role of RPA70N in binding ssDNA. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu/available/etd-07122010-152656/ ;

14. Banks, Joshua Ian. Development and Characterization of NMR and MRI Methods for Assessment of Tumor Oxygen Consumption.

Degree: MS, Physics, 2012, Vanderbilt University

 A common feature of invasive cancers is that they have an upregulation of glucose metabolism and reduced oxygen utilization. The overall goal of this research… (more)

Subjects/Keywords: Oxygen-17; Oxidative Phosphorylation; MRI; NMR

…of 15 15 O2 gas. When inhaled, O2 can serve as an indicator of oxidative phosphorylation… …directly access oxidative phosphorylation by measuring the rate that “metabolic” water is being… …indicator of diseases status. 4 As described above, oxidative phosphorylation is implicated in… …x29;.This is particularly useful for studies assessing oxidative phosphorylation because… 

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APA (6th Edition):

Banks, J. I. (2012). Development and Characterization of NMR and MRI Methods for Assessment of Tumor Oxygen Consumption. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-10072012-164828/ ;

Chicago Manual of Style (16th Edition):

Banks, Joshua Ian. “Development and Characterization of NMR and MRI Methods for Assessment of Tumor Oxygen Consumption.” 2012. Masters Thesis, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-10072012-164828/ ;.

MLA Handbook (7th Edition):

Banks, Joshua Ian. “Development and Characterization of NMR and MRI Methods for Assessment of Tumor Oxygen Consumption.” 2012. Web. 15 Oct 2019.

Vancouver:

Banks JI. Development and Characterization of NMR and MRI Methods for Assessment of Tumor Oxygen Consumption. [Internet] [Masters thesis]. Vanderbilt University; 2012. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-10072012-164828/ ;.

Council of Science Editors:

Banks JI. Development and Characterization of NMR and MRI Methods for Assessment of Tumor Oxygen Consumption. [Masters Thesis]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu/available/etd-10072012-164828/ ;


Vanderbilt University

15. Baskir, Rubin Sam. Regulation of the Wnt Pathway by TGFbeta and DYRK2: Mechanisms of Disease and Signal Transduction.

Degree: PhD, Biology, 2016, Vanderbilt University

 My thesis is composed of two independent projects related by the Wnt signaling transduction pathway. The first project provides evidence that vascular-associated adult lung mesenchymal… (more)

Subjects/Keywords: Tgfbeta; Xenopus; mesenchymal stem cells; DYRK2; Wnt; axis duplication; phosphorylation; LRP6; GSK3; lung; embryo; bleomycin; kinase

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

APA (6th Edition):

Baskir, R. S. (2016). Regulation of the Wnt Pathway by TGFbeta and DYRK2: Mechanisms of Disease and Signal Transduction. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-07212016-155418/ ;

Chicago Manual of Style (16th Edition):

Baskir, Rubin Sam. “Regulation of the Wnt Pathway by TGFbeta and DYRK2: Mechanisms of Disease and Signal Transduction.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu//available/etd-07212016-155418/ ;.

MLA Handbook (7th Edition):

Baskir, Rubin Sam. “Regulation of the Wnt Pathway by TGFbeta and DYRK2: Mechanisms of Disease and Signal Transduction.” 2016. Web. 15 Oct 2019.

Vancouver:

Baskir RS. Regulation of the Wnt Pathway by TGFbeta and DYRK2: Mechanisms of Disease and Signal Transduction. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu//available/etd-07212016-155418/ ;.

Council of Science Editors:

Baskir RS. Regulation of the Wnt Pathway by TGFbeta and DYRK2: Mechanisms of Disease and Signal Transduction. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu//available/etd-07212016-155418/ ;


Vanderbilt University

16. Mason, Twila Annette. The role of AKAP350 splice variants in cellular stress response.

Degree: PhD, Cell and Developmental Biology, 2013, Vanderbilt University

 Every organism experiences stress, which occurs when there is a perturbation of homeostasis. Individual cells experience stress throughout their physiological processes and have developed many… (more)

Subjects/Keywords: A Kinase Anchoring Protein; phosphorylation; mitochondria; cellular stress; endoplasmic reticulum; knockout mouse; CG-NAP; stress response; stress granules; AKAP; AKAP350; AKAP9; AKAP450; mitochondria morphology; mitochondria dynamics; caprin

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

APA (6th Edition):

Mason, T. A. (2013). The role of AKAP350 splice variants in cellular stress response. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-10252013-114942/ ;

Chicago Manual of Style (16th Edition):

Mason, Twila Annette. “The role of AKAP350 splice variants in cellular stress response.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu//available/etd-10252013-114942/ ;.

MLA Handbook (7th Edition):

Mason, Twila Annette. “The role of AKAP350 splice variants in cellular stress response.” 2013. Web. 15 Oct 2019.

Vancouver:

Mason TA. The role of AKAP350 splice variants in cellular stress response. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu//available/etd-10252013-114942/ ;.

Council of Science Editors:

Mason TA. The role of AKAP350 splice variants in cellular stress response. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu//available/etd-10252013-114942/ ;

17. Coffee, Jr., Ronald Lane. Insights into the Human Fragile X Syndrome Gene Family Using Drosophila melanogaster.

Degree: PhD, Biological Sciences, 2011, Vanderbilt University

 Fragile X syndrome, resulting from the loss of function of the hFMR1 gene, is the most common heritable cause of intellectual disability. The human genome… (more)

Subjects/Keywords: Drosophila; Fragile X; RNA; autism; phosphorylation; conservation; synaptogenesis; neuronal

…elongation factors are regulated by phosphorylation, sequence-specific RNA binding proteins… …by phosphorylation of translation factor eIF4E binding proteins (4EBPs), causing… …result from stimuli that cause eIF2 phosphorylation through kinase activation. Inhibition can… …activation leading to eEF2 phosphorylation (Sutton et al., 2007). In addition to this… …phosphorylation state is a critical determinant of polyribosome association (Ceman et al., 2003… 

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

APA (6th Edition):

Coffee, Jr., R. L. (2011). Insights into the Human Fragile X Syndrome Gene Family Using Drosophila melanogaster. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-11162011-224402/ ;

Chicago Manual of Style (16th Edition):

Coffee, Jr., Ronald Lane. “Insights into the Human Fragile X Syndrome Gene Family Using Drosophila melanogaster.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu//available/etd-11162011-224402/ ;.

MLA Handbook (7th Edition):

Coffee, Jr., Ronald Lane. “Insights into the Human Fragile X Syndrome Gene Family Using Drosophila melanogaster.” 2011. Web. 15 Oct 2019.

Vancouver:

Coffee, Jr. RL. Insights into the Human Fragile X Syndrome Gene Family Using Drosophila melanogaster. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu//available/etd-11162011-224402/ ;.

Council of Science Editors:

Coffee, Jr. RL. Insights into the Human Fragile X Syndrome Gene Family Using Drosophila melanogaster. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu//available/etd-11162011-224402/ ;


Vanderbilt University

18. Schavolt, Kristy Lynn. Identification and regulation of p53 target genes in primary human epidermal keratinocytes.

Degree: PhD, Biochemistry, 2006, Vanderbilt University

 BIOCHEMISTRY IDENTIFICATION AND REGULATION OF P53 TARGET GENES IN PRIMARY HUMAN EPIDERMAL KERATINOCYTES KRISTY L. SCHAVOLT Dissertation under the direction of Professor Jennifer A. Pietenpol… (more)

Subjects/Keywords: repressor; crosslink; Affymetrix; real-time PCR; p21; 14-3-3sigma; p48; p53R2; Noxa; Fas/APO1; serine-15; phosphorylation; MDM2; DNA damage; adriamycin; ultraviolet radiation; adenovirus; PARP; PCR; transcription factor; Keratinocytes; p53 antioncogene; Cellular control mechanisms

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

APA (6th Edition):

Schavolt, K. L. (2006). Identification and regulation of p53 target genes in primary human epidermal keratinocytes. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-12012006-002106/ ;

Chicago Manual of Style (16th Edition):

Schavolt, Kristy Lynn. “Identification and regulation of p53 target genes in primary human epidermal keratinocytes.” 2006. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-12012006-002106/ ;.

MLA Handbook (7th Edition):

Schavolt, Kristy Lynn. “Identification and regulation of p53 target genes in primary human epidermal keratinocytes.” 2006. Web. 15 Oct 2019.

Vancouver:

Schavolt KL. Identification and regulation of p53 target genes in primary human epidermal keratinocytes. [Internet] [Doctoral dissertation]. Vanderbilt University; 2006. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-12012006-002106/ ;.

Council of Science Editors:

Schavolt KL. Identification and regulation of p53 target genes in primary human epidermal keratinocytes. [Doctoral Dissertation]. Vanderbilt University; 2006. Available from: http://etd.library.vanderbilt.edu/available/etd-12012006-002106/ ;

19. Mazalouskas, Matthew David. Composition, Regulation, and Function of Protein Serine/Threonine Phosphataseâ¢Kinase Signaling Modules.

Degree: PhD, Pharmacology, 2014, Vanderbilt University

 The macromolecular assembly of protein serine/threonine phosphataseâ¢kinase complexes mechanistically enhances the speed and fidelity of cell signaling events. These signaling modules allow for acute regulation… (more)

Subjects/Keywords: Raf; Raf1; CaMKIV; phosphatase; PP2A; PP5; Rac; Ras; S100; S100B; S100A1; ERK2; ERK1; ERK; signaling; small G protein; kinase; MAPK; MEK; feedback; phosphorylation; C-Raf; CRaf; ERK1b; ERK1c; cancer; RASopathy; HRas; KRas

…PP2A-dependent regulation of CaMKIV phosphorylation ........................49… …154 PP5•ERK2 complexes regulate Raf1 phosphorylation ............................157… …161 Regulation of PP5•ERK complexes and Raf1 feedback phosphorylation… …FIGURES Page Figure 1. Reversible phosphorylation of proteins… …ionomycin-induced phosphorylation of endogenous CaMKIV… 

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

APA (6th Edition):

Mazalouskas, M. D. (2014). Composition, Regulation, and Function of Protein Serine/Threonine Phosphataseâ¢Kinase Signaling Modules. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03242014-134955/ ;

Chicago Manual of Style (16th Edition):

Mazalouskas, Matthew David. “Composition, Regulation, and Function of Protein Serine/Threonine Phosphataseâ¢Kinase Signaling Modules.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed October 15, 2019. http://etd.library.vanderbilt.edu/available/etd-03242014-134955/ ;.

MLA Handbook (7th Edition):

Mazalouskas, Matthew David. “Composition, Regulation, and Function of Protein Serine/Threonine Phosphataseâ¢Kinase Signaling Modules.” 2014. Web. 15 Oct 2019.

Vancouver:

Mazalouskas MD. Composition, Regulation, and Function of Protein Serine/Threonine Phosphataseâ¢Kinase Signaling Modules. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2019 Oct 15]. Available from: http://etd.library.vanderbilt.edu/available/etd-03242014-134955/ ;.

Council of Science Editors:

Mazalouskas MD. Composition, Regulation, and Function of Protein Serine/Threonine Phosphataseâ¢Kinase Signaling Modules. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu/available/etd-03242014-134955/ ;

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