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You searched for subject:( Phosphorylation). Showing records 1 – 30 of 1356 total matches.

[1] [2] [3] [4] [5] … [46]

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Anna University

1. Meenakshi N. An investigation of extra clausal Processing methods for extraction Of information from the Bio medical literature;.

Degree: An investigation of extra clausal Processing methods for extraction Of information from the Bio medical literature, 2014, Anna University

The volume of biomedical literature is increasing exponentially newlinelargely due to data from high throughput techniques such as micro arrays and newlinegenome sequencing Efficient methods… (more)

Subjects/Keywords: phosphorylation

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APA (6th Edition):

N, M. (2014). An investigation of extra clausal Processing methods for extraction Of information from the Bio medical literature;. (Thesis). Anna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/28069

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):

N, Meenakshi. “An investigation of extra clausal Processing methods for extraction Of information from the Bio medical literature;.” 2014. Thesis, Anna University. Accessed January 26, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/28069.

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

MLA Handbook (7th Edition):

N, Meenakshi. “An investigation of extra clausal Processing methods for extraction Of information from the Bio medical literature;.” 2014. Web. 26 Jan 2020.

Vancouver:

N M. An investigation of extra clausal Processing methods for extraction Of information from the Bio medical literature;. [Internet] [Thesis]. Anna University; 2014. [cited 2020 Jan 26]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/28069.

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

Council of Science Editors:

N M. An investigation of extra clausal Processing methods for extraction Of information from the Bio medical literature;. [Thesis]. Anna University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/28069

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


University of Hawaii – Manoa

2. Caliva, Maisel Jay. Regulation of integrin trafficking by PEA-15.

Degree: 2015, University of Hawaii – Manoa

Ph.D. University of Hawaii at Manoa 2014.

Integrins function as adhesion receptors that mediate signaling between the cytoskeleton and extracellular matrix. Integrin activation initiates signaling… (more)

Subjects/Keywords: phosphorylation

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APA (6th Edition):

Caliva, M. J. (2015). Regulation of integrin trafficking by PEA-15. (Thesis). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/100540

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):

Caliva, Maisel Jay. “Regulation of integrin trafficking by PEA-15.” 2015. Thesis, University of Hawaii – Manoa. Accessed January 26, 2020. http://hdl.handle.net/10125/100540.

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

MLA Handbook (7th Edition):

Caliva, Maisel Jay. “Regulation of integrin trafficking by PEA-15.” 2015. Web. 26 Jan 2020.

Vancouver:

Caliva MJ. Regulation of integrin trafficking by PEA-15. [Internet] [Thesis]. University of Hawaii – Manoa; 2015. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10125/100540.

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

Council of Science Editors:

Caliva MJ. Regulation of integrin trafficking by PEA-15. [Thesis]. University of Hawaii – Manoa; 2015. Available from: http://hdl.handle.net/10125/100540

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

3. Bolduc, David Michael. PHOSPHORYLATION-INDUCED CONFORMATIONAL CHANGES OF PTEN REVEALED BY PROTEIN SEMISYNTHESIS.

Degree: 2013, Johns Hopkins University

 PTEN (phosphatase and tensin homolog deleted on chromosome 10) is a tumor suppressing lipid phosphatase that negatively regulates the PI3K/PTEN/AKT signaling pathway by dephosphorylating the… (more)

Subjects/Keywords: PTEN; Phosphorylation

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APA (6th Edition):

Bolduc, D. M. (2013). PHOSPHORYLATION-INDUCED CONFORMATIONAL CHANGES OF PTEN REVEALED BY PROTEIN SEMISYNTHESIS. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37060

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):

Bolduc, David Michael. “PHOSPHORYLATION-INDUCED CONFORMATIONAL CHANGES OF PTEN REVEALED BY PROTEIN SEMISYNTHESIS.” 2013. Thesis, Johns Hopkins University. Accessed January 26, 2020. http://jhir.library.jhu.edu/handle/1774.2/37060.

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

MLA Handbook (7th Edition):

Bolduc, David Michael. “PHOSPHORYLATION-INDUCED CONFORMATIONAL CHANGES OF PTEN REVEALED BY PROTEIN SEMISYNTHESIS.” 2013. Web. 26 Jan 2020.

Vancouver:

Bolduc DM. PHOSPHORYLATION-INDUCED CONFORMATIONAL CHANGES OF PTEN REVEALED BY PROTEIN SEMISYNTHESIS. [Internet] [Thesis]. Johns Hopkins University; 2013. [cited 2020 Jan 26]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37060.

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

Council of Science Editors:

Bolduc DM. PHOSPHORYLATION-INDUCED CONFORMATIONAL CHANGES OF PTEN REVEALED BY PROTEIN SEMISYNTHESIS. [Thesis]. Johns Hopkins University; 2013. Available from: http://jhir.library.jhu.edu/handle/1774.2/37060

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


Oregon State University

4. Kuo, Huey-ju. Factors affecting the activation of rabbit muscle phosphofructokinase by actin.

Degree: PhD, Biochemistry and Biophysics, 1986, Oregon State University

 The consistent application of phosphatase inhibitors and a novel final purification step using a connected series of DE-51, DE-52, and DE-53 anion exchange chromatography columns… (more)

Subjects/Keywords: Phosphorylation

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APA (6th Edition):

Kuo, H. (1986). Factors affecting the activation of rabbit muscle phosphofructokinase by actin. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/40607

Chicago Manual of Style (16th Edition):

Kuo, Huey-ju. “Factors affecting the activation of rabbit muscle phosphofructokinase by actin.” 1986. Doctoral Dissertation, Oregon State University. Accessed January 26, 2020. http://hdl.handle.net/1957/40607.

MLA Handbook (7th Edition):

Kuo, Huey-ju. “Factors affecting the activation of rabbit muscle phosphofructokinase by actin.” 1986. Web. 26 Jan 2020.

Vancouver:

Kuo H. Factors affecting the activation of rabbit muscle phosphofructokinase by actin. [Internet] [Doctoral dissertation]. Oregon State University; 1986. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1957/40607.

Council of Science Editors:

Kuo H. Factors affecting the activation of rabbit muscle phosphofructokinase by actin. [Doctoral Dissertation]. Oregon State University; 1986. Available from: http://hdl.handle.net/1957/40607


University of Manchester

5. Keenan, Jemma. An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure.

Degree: 2013, University of Manchester

 Fusel alcohols signal nitrogen scarcity to elicit a range of responses in the yeast Saccharomyces cerevisiae. These alcohols activate pseudohyphal growth and cause rapid inhibition… (more)

Subjects/Keywords: Phosphorylation; eIF2B

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APA (6th Edition):

Keenan, J. (2013). An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:205866

Chicago Manual of Style (16th Edition):

Keenan, Jemma. “An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure.” 2013. Doctoral Dissertation, University of Manchester. Accessed January 26, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:205866.

MLA Handbook (7th Edition):

Keenan, Jemma. “An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure.” 2013. Web. 26 Jan 2020.

Vancouver:

Keenan J. An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Jan 26]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:205866.

Council of Science Editors:

Keenan J. An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:205866

6. Maheshwari, Surabhi. Identification of conserved structural motifs associated with phosphorylation sites in kinases.

Degree: MS, Bioinformatics, 2012, University of Georgia

 Background: Protein phosphorylation plays a crucial role in the regulation of several cellular processes. Protein kinases are enzymes that catalyze the event of phosphorylation and… (more)

Subjects/Keywords: phosphorylation

…14 Figure 2.7: Phosphorylation site in Ser/Thr and Tyrosine Kinases… …46 x CHAPTER 1 INTRODUCTION Reversible protein phosphorylation is one of the most… …phosphorylation as a regulatory mechanism was established after the comprehensive study of glycogen… …family of enzymes called protein kinases that catalyze the event of protein phosphorylation… …phosphorylation are serine, threonine and tyrosine. Phosphorylation of these residues brings about… 

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APA (6th Edition):

Maheshwari, S. (2012). Identification of conserved structural motifs associated with phosphorylation sites in kinases. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/maheshwari_surabhi_201208_ms

Chicago Manual of Style (16th Edition):

Maheshwari, Surabhi. “Identification of conserved structural motifs associated with phosphorylation sites in kinases.” 2012. Masters Thesis, University of Georgia. Accessed January 26, 2020. http://purl.galileo.usg.edu/uga_etd/maheshwari_surabhi_201208_ms.

MLA Handbook (7th Edition):

Maheshwari, Surabhi. “Identification of conserved structural motifs associated with phosphorylation sites in kinases.” 2012. Web. 26 Jan 2020.

Vancouver:

Maheshwari S. Identification of conserved structural motifs associated with phosphorylation sites in kinases. [Internet] [Masters thesis]. University of Georgia; 2012. [cited 2020 Jan 26]. Available from: http://purl.galileo.usg.edu/uga_etd/maheshwari_surabhi_201208_ms.

Council of Science Editors:

Maheshwari S. Identification of conserved structural motifs associated with phosphorylation sites in kinases. [Masters Thesis]. University of Georgia; 2012. Available from: http://purl.galileo.usg.edu/uga_etd/maheshwari_surabhi_201208_ms


Oregon State University

7. Zhao, Zhizhuang. Regulation of phosphofructokinase by reversible inactivation.

Degree: PhD, Biochemistry and Biophysics, 1990, Oregon State University

 The interaction of skeletal muscle phosphofructokinase with a variety of acidic proteins including calmodulin and troponin C and with nucleic acids (RNA and DNA) is… (more)

Subjects/Keywords: Phosphorylation

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APA (6th Edition):

Zhao, Z. (1990). Regulation of phosphofructokinase by reversible inactivation. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/40950

Chicago Manual of Style (16th Edition):

Zhao, Zhizhuang. “Regulation of phosphofructokinase by reversible inactivation.” 1990. Doctoral Dissertation, Oregon State University. Accessed January 26, 2020. http://hdl.handle.net/1957/40950.

MLA Handbook (7th Edition):

Zhao, Zhizhuang. “Regulation of phosphofructokinase by reversible inactivation.” 1990. Web. 26 Jan 2020.

Vancouver:

Zhao Z. Regulation of phosphofructokinase by reversible inactivation. [Internet] [Doctoral dissertation]. Oregon State University; 1990. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1957/40950.

Council of Science Editors:

Zhao Z. Regulation of phosphofructokinase by reversible inactivation. [Doctoral Dissertation]. Oregon State University; 1990. Available from: http://hdl.handle.net/1957/40950


Oregon State University

8. Johnson, Morris Alfred. Evidence for a soluble intermediate of oxidative phosphorylation isolated from cabbage mitochondria.

Degree: PhD, Chemistry, 1966, Oregon State University

 An intermediate of oxidative phosphorylation was apparently solubilized from cabbage mitochondria. The method of solubilization used primarily was extraction of a mitochondrial acetone powder with… (more)

Subjects/Keywords: Phosphorylation

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APA (6th Edition):

Johnson, M. A. (1966). Evidence for a soluble intermediate of oxidative phosphorylation isolated from cabbage mitochondria. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/47603

Chicago Manual of Style (16th Edition):

Johnson, Morris Alfred. “Evidence for a soluble intermediate of oxidative phosphorylation isolated from cabbage mitochondria.” 1966. Doctoral Dissertation, Oregon State University. Accessed January 26, 2020. http://hdl.handle.net/1957/47603.

MLA Handbook (7th Edition):

Johnson, Morris Alfred. “Evidence for a soluble intermediate of oxidative phosphorylation isolated from cabbage mitochondria.” 1966. Web. 26 Jan 2020.

Vancouver:

Johnson MA. Evidence for a soluble intermediate of oxidative phosphorylation isolated from cabbage mitochondria. [Internet] [Doctoral dissertation]. Oregon State University; 1966. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1957/47603.

Council of Science Editors:

Johnson MA. Evidence for a soluble intermediate of oxidative phosphorylation isolated from cabbage mitochondria. [Doctoral Dissertation]. Oregon State University; 1966. Available from: http://hdl.handle.net/1957/47603


Oregon State University

9. Steele, Wilbert Francis. Oxidative phosphorylation and related reactions in particulate fractions from insects.

Degree: PhD, Chemistry, 1965, Oregon State University

 Oxidative phosphorylation and related reactions, particularly as affected by 2, 4-dinitrophenol (DNP), were studied with mitochondria and submitochondrial particles isolated from the flight muscle of… (more)

Subjects/Keywords: Phosphorylation

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APA (6th Edition):

Steele, W. F. (1965). Oxidative phosphorylation and related reactions in particulate fractions from insects. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/48629

Chicago Manual of Style (16th Edition):

Steele, Wilbert Francis. “Oxidative phosphorylation and related reactions in particulate fractions from insects.” 1965. Doctoral Dissertation, Oregon State University. Accessed January 26, 2020. http://hdl.handle.net/1957/48629.

MLA Handbook (7th Edition):

Steele, Wilbert Francis. “Oxidative phosphorylation and related reactions in particulate fractions from insects.” 1965. Web. 26 Jan 2020.

Vancouver:

Steele WF. Oxidative phosphorylation and related reactions in particulate fractions from insects. [Internet] [Doctoral dissertation]. Oregon State University; 1965. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1957/48629.

Council of Science Editors:

Steele WF. Oxidative phosphorylation and related reactions in particulate fractions from insects. [Doctoral Dissertation]. Oregon State University; 1965. Available from: http://hdl.handle.net/1957/48629


Queens University

10. Dalziel, Katie. In Vivo Phosphorylation of Bacterial–Type Phosphoenolpyruvate Carboxylase From Developing Castor Oil Seeds at Threonine-4 and Serine-451 .

Degree: Biology, 2011, Queens University

 Phosphoenolpyruvate carboxylase (PEPC) is a tightly controlled anaplerotic enzyme situated at a pivotal branchpoint of plant C-metabolism. Plant genomes encode several closely related plant-type PEPC… (more)

Subjects/Keywords: PEPC; Phosphorylation

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APA (6th Edition):

Dalziel, K. (2011). In Vivo Phosphorylation of Bacterial–Type Phosphoenolpyruvate Carboxylase From Developing Castor Oil Seeds at Threonine-4 and Serine-451 . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6662

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):

Dalziel, Katie. “In Vivo Phosphorylation of Bacterial–Type Phosphoenolpyruvate Carboxylase From Developing Castor Oil Seeds at Threonine-4 and Serine-451 .” 2011. Thesis, Queens University. Accessed January 26, 2020. http://hdl.handle.net/1974/6662.

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

MLA Handbook (7th Edition):

Dalziel, Katie. “In Vivo Phosphorylation of Bacterial–Type Phosphoenolpyruvate Carboxylase From Developing Castor Oil Seeds at Threonine-4 and Serine-451 .” 2011. Web. 26 Jan 2020.

Vancouver:

Dalziel K. In Vivo Phosphorylation of Bacterial–Type Phosphoenolpyruvate Carboxylase From Developing Castor Oil Seeds at Threonine-4 and Serine-451 . [Internet] [Thesis]. Queens University; 2011. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1974/6662.

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

Council of Science Editors:

Dalziel K. In Vivo Phosphorylation of Bacterial–Type Phosphoenolpyruvate Carboxylase From Developing Castor Oil Seeds at Threonine-4 and Serine-451 . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6662

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


University of Rochester

11. Kobielush, Brent R. S395, a Site Important for Regulating Transcriptional Activity of the Aryl Hydrocarbon Receptor (AhR), is Phosphorylated by Protein Kinase A (PKA).

Degree: PhD, 2009, University of Rochester

 The aryl hydrocarbon receptor (AhR) is a member of the basic helix-loop-helix transcription factor family. The AhR interacts with a wide variety of xenobiotic agonists,… (more)

Subjects/Keywords: AhR; Phosphorylation; PKA

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APA (6th Edition):

Kobielush, B. R. (2009). S395, a Site Important for Regulating Transcriptional Activity of the Aryl Hydrocarbon Receptor (AhR), is Phosphorylated by Protein Kinase A (PKA). (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/8476

Chicago Manual of Style (16th Edition):

Kobielush, Brent R. “S395, a Site Important for Regulating Transcriptional Activity of the Aryl Hydrocarbon Receptor (AhR), is Phosphorylated by Protein Kinase A (PKA).” 2009. Doctoral Dissertation, University of Rochester. Accessed January 26, 2020. http://hdl.handle.net/1802/8476.

MLA Handbook (7th Edition):

Kobielush, Brent R. “S395, a Site Important for Regulating Transcriptional Activity of the Aryl Hydrocarbon Receptor (AhR), is Phosphorylated by Protein Kinase A (PKA).” 2009. Web. 26 Jan 2020.

Vancouver:

Kobielush BR. S395, a Site Important for Regulating Transcriptional Activity of the Aryl Hydrocarbon Receptor (AhR), is Phosphorylated by Protein Kinase A (PKA). [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1802/8476.

Council of Science Editors:

Kobielush BR. S395, a Site Important for Regulating Transcriptional Activity of the Aryl Hydrocarbon Receptor (AhR), is Phosphorylated by Protein Kinase A (PKA). [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/8476


University of Notre Dame

12. Colleen Therese Cole. Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>.

Degree: MS, Biological Sciences, 2011, University of Notre Dame

  The motor protein cytoplasmic dynein has been implicated in mitotic functions that require dynein localization to specific cellular locations. Recent studies in our lab… (more)

Subjects/Keywords: mitosis; phosphorylation; dynein

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APA (6th Edition):

Cole, C. T. (2011). Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/0k225b01f90

Chicago Manual of Style (16th Edition):

Cole, Colleen Therese. “Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>.” 2011. Masters Thesis, University of Notre Dame. Accessed January 26, 2020. https://curate.nd.edu/show/0k225b01f90.

MLA Handbook (7th Edition):

Cole, Colleen Therese. “Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>.” 2011. Web. 26 Jan 2020.

Vancouver:

Cole CT. Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2011. [cited 2020 Jan 26]. Available from: https://curate.nd.edu/show/0k225b01f90.

Council of Science Editors:

Cole CT. Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>. [Masters Thesis]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/0k225b01f90


University of Notre Dame

13. Brendan J. Mahoney. Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>.

Degree: PhD, Chemistry and Biochemistry, 2018, University of Notre Dame

  Proper maintenance of the cell cycle relies on regulation via pathways of signaling proteins. The function of these cell signaling proteins is often modulated… (more)

Subjects/Keywords: allostery; Pin1; phosphorylation

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APA (6th Edition):

Mahoney, B. J. (2018). Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/v118rb7241t

Chicago Manual of Style (16th Edition):

Mahoney, Brendan J.. “Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>.” 2018. Doctoral Dissertation, University of Notre Dame. Accessed January 26, 2020. https://curate.nd.edu/show/v118rb7241t.

MLA Handbook (7th Edition):

Mahoney, Brendan J.. “Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>.” 2018. Web. 26 Jan 2020.

Vancouver:

Mahoney BJ. Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2018. [cited 2020 Jan 26]. Available from: https://curate.nd.edu/show/v118rb7241t.

Council of Science Editors:

Mahoney BJ. Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>. [Doctoral Dissertation]. University of Notre Dame; 2018. Available from: https://curate.nd.edu/show/v118rb7241t


University of Manchester

14. Keenan, Jemma. An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure.

Degree: PhD, 2013, University of Manchester

 Fusel alcohols signal nitrogen scarcity to elicit a range of responses in the yeast Saccharomyces cerevisiae. These alcohols activate pseudohyphal growth and cause rapid inhibition… (more)

Subjects/Keywords: 572; Phosphorylation; eIF2B

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APA (6th Edition):

Keenan, J. (2013). An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-into-the-proteins-responsible-for-the-translational-inhibition-seen-in-the-yeast-saccharomyces-cerevisiae-following-fusel-alcohol-exposure(351e6a87-81f8-4724-ac41-a8311ef50f21).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.668535

Chicago Manual of Style (16th Edition):

Keenan, Jemma. “An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure.” 2013. Doctoral Dissertation, University of Manchester. Accessed January 26, 2020. https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-into-the-proteins-responsible-for-the-translational-inhibition-seen-in-the-yeast-saccharomyces-cerevisiae-following-fusel-alcohol-exposure(351e6a87-81f8-4724-ac41-a8311ef50f21).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.668535.

MLA Handbook (7th Edition):

Keenan, Jemma. “An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure.” 2013. Web. 26 Jan 2020.

Vancouver:

Keenan J. An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Jan 26]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-into-the-proteins-responsible-for-the-translational-inhibition-seen-in-the-yeast-saccharomyces-cerevisiae-following-fusel-alcohol-exposure(351e6a87-81f8-4724-ac41-a8311ef50f21).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.668535.

Council of Science Editors:

Keenan J. An investigation into the proteins responsible for the translational inhibition seen in the yeast Saccharomyces cerevisiae following fusel alcohol exposure. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-into-the-proteins-responsible-for-the-translational-inhibition-seen-in-the-yeast-saccharomyces-cerevisiae-following-fusel-alcohol-exposure(351e6a87-81f8-4724-ac41-a8311ef50f21).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.668535


University of Illinois – Chicago

15. He, Ying. Epigenetic and Post-Translational Mechanisms in Pain: MicroRNA and Phosphorylation.

Degree: 2012, University of Illinois – Chicago

 The molecular and neurobiological mechanisms underlying persistent pain are poorly understood. My dissertation research focused on three problems relevant to chronic pain to elucidate epigenetic… (more)

Subjects/Keywords: Pain; microRNA; phosphorylation

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APA (6th Edition):

He, Y. (2012). Epigenetic and Post-Translational Mechanisms in Pain: MicroRNA and Phosphorylation. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9259

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

Chicago Manual of Style (16th Edition):

He, Ying. “Epigenetic and Post-Translational Mechanisms in Pain: MicroRNA and Phosphorylation.” 2012. Thesis, University of Illinois – Chicago. Accessed January 26, 2020. http://hdl.handle.net/10027/9259.

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

MLA Handbook (7th Edition):

He, Ying. “Epigenetic and Post-Translational Mechanisms in Pain: MicroRNA and Phosphorylation.” 2012. Web. 26 Jan 2020.

Vancouver:

He Y. Epigenetic and Post-Translational Mechanisms in Pain: MicroRNA and Phosphorylation. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10027/9259.

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

Council of Science Editors:

He Y. Epigenetic and Post-Translational Mechanisms in Pain: MicroRNA and Phosphorylation. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9259

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


Rutgers University

16. Yildirim, Evrim, 1981-. Studies aimed at understanding how phosphorylation and miRNAs contribute to the circadian clock mechanism in drosophila.

Degree: PhD, Biochemistry, 2014, Rutgers University

Circadian (≈24 hr) rhythms in physiology and behavior are driven by endogenous cellular clocks that can be synchronized (entrained) by environmental cues, most notably the… (more)

Subjects/Keywords: Circadian rhythms; Phosphorylation

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APA (6th Edition):

Yildirim, Evrim, 1. (2014). Studies aimed at understanding how phosphorylation and miRNAs contribute to the circadian clock mechanism in drosophila. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/45581/

Chicago Manual of Style (16th Edition):

Yildirim, Evrim, 1981-. “Studies aimed at understanding how phosphorylation and miRNAs contribute to the circadian clock mechanism in drosophila.” 2014. Doctoral Dissertation, Rutgers University. Accessed January 26, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/45581/.

MLA Handbook (7th Edition):

Yildirim, Evrim, 1981-. “Studies aimed at understanding how phosphorylation and miRNAs contribute to the circadian clock mechanism in drosophila.” 2014. Web. 26 Jan 2020.

Vancouver:

Yildirim, Evrim 1. Studies aimed at understanding how phosphorylation and miRNAs contribute to the circadian clock mechanism in drosophila. [Internet] [Doctoral dissertation]. Rutgers University; 2014. [cited 2020 Jan 26]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45581/.

Council of Science Editors:

Yildirim, Evrim 1. Studies aimed at understanding how phosphorylation and miRNAs contribute to the circadian clock mechanism in drosophila. [Doctoral Dissertation]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45581/


Rutgers University

17. Hennessy, Meagan L., 1980-. Phosphorylation of lipin 1 beta phosphatidate phosphatase by casein kinase II.

Degree: MS, Nutritional Sciences, 2018, Rutgers University

 Lipin is a phosphatidate phosphatase enzyme that catalyzes the penultimate step in triacylglycerol synthesis, the conversion of phosphatidic acid to diacylglycerol. By controlling this step,… (more)

Subjects/Keywords: Bioinformatics; Phosphorylation; Lipin

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APA (6th Edition):

Hennessy, Meagan L., 1. (2018). Phosphorylation of lipin 1 beta phosphatidate phosphatase by casein kinase II. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/59111/

Chicago Manual of Style (16th Edition):

Hennessy, Meagan L., 1980-. “Phosphorylation of lipin 1 beta phosphatidate phosphatase by casein kinase II.” 2018. Masters Thesis, Rutgers University. Accessed January 26, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/59111/.

MLA Handbook (7th Edition):

Hennessy, Meagan L., 1980-. “Phosphorylation of lipin 1 beta phosphatidate phosphatase by casein kinase II.” 2018. Web. 26 Jan 2020.

Vancouver:

Hennessy, Meagan L. 1. Phosphorylation of lipin 1 beta phosphatidate phosphatase by casein kinase II. [Internet] [Masters thesis]. Rutgers University; 2018. [cited 2020 Jan 26]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/59111/.

Council of Science Editors:

Hennessy, Meagan L. 1. Phosphorylation of lipin 1 beta phosphatidate phosphatase by casein kinase II. [Masters Thesis]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/59111/


Dalhousie University

18. Robinson, Carolyn-Ann. The effect of phosphorylation on oxysterol-binding protein (OSBP) sterol binding activity.

Degree: MS, Department of Biochemistry & Molecular Biology, 2012, Dalhousie University

 Oxysterol binding protein (OSBP) binds 25-hydroxycholesterol (25OH) and cholesterol, which regulates PH and FFAT domain interaction with the Golgi apparatus and endoplasmic reticulum, respectively. Adjacent… (more)

Subjects/Keywords: cholesterol; oxysterol; sterol transport; phosphorylation

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

APA (6th Edition):

Robinson, C. (2012). The effect of phosphorylation on oxysterol-binding protein (OSBP) sterol binding activity. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15489

Chicago Manual of Style (16th Edition):

Robinson, Carolyn-Ann. “The effect of phosphorylation on oxysterol-binding protein (OSBP) sterol binding activity.” 2012. Masters Thesis, Dalhousie University. Accessed January 26, 2020. http://hdl.handle.net/10222/15489.

MLA Handbook (7th Edition):

Robinson, Carolyn-Ann. “The effect of phosphorylation on oxysterol-binding protein (OSBP) sterol binding activity.” 2012. Web. 26 Jan 2020.

Vancouver:

Robinson C. The effect of phosphorylation on oxysterol-binding protein (OSBP) sterol binding activity. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10222/15489.

Council of Science Editors:

Robinson C. The effect of phosphorylation on oxysterol-binding protein (OSBP) sterol binding activity. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15489


University of Alberta

19. Yip, Sophia. Characterisation of novel potential phosphorylation sites in the tumour suppressor Merlin in Drosophila.

Degree: MS, Medical Sciences-Medical Genetics, 2014, University of Alberta

 Neurofibromatosis Type II is an inherited cancer that manifests as various tumours in the nervous system. Mutations and deletions in the tumour suppressor Merlin (moesin,… (more)

Subjects/Keywords: NFII; ERMs; Phosphorylation; Drosophila; Merlin

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APA (6th Edition):

Yip, S. (2014). Characterisation of novel potential phosphorylation sites in the tumour suppressor Merlin in Drosophila. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/2v23vx42t

Chicago Manual of Style (16th Edition):

Yip, Sophia. “Characterisation of novel potential phosphorylation sites in the tumour suppressor Merlin in Drosophila.” 2014. Masters Thesis, University of Alberta. Accessed January 26, 2020. https://era.library.ualberta.ca/files/2v23vx42t.

MLA Handbook (7th Edition):

Yip, Sophia. “Characterisation of novel potential phosphorylation sites in the tumour suppressor Merlin in Drosophila.” 2014. Web. 26 Jan 2020.

Vancouver:

Yip S. Characterisation of novel potential phosphorylation sites in the tumour suppressor Merlin in Drosophila. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2020 Jan 26]. Available from: https://era.library.ualberta.ca/files/2v23vx42t.

Council of Science Editors:

Yip S. Characterisation of novel potential phosphorylation sites in the tumour suppressor Merlin in Drosophila. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/2v23vx42t


University of Edinburgh

20. Sen, Onur. Phospho-regulation of the spindle assembly checkpoint.

Degree: PhD, 2016, University of Edinburgh

 Mitosis is a highly regulated process by which a cell duplicates and distributes its chromosomal DNA into two identical daughter cells equally. Equal distribution of… (more)

Subjects/Keywords: 571.8; phosphorylation; mitotic checkpoint; MCC

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APA (6th Edition):

Sen, O. (2016). Phospho-regulation of the spindle assembly checkpoint. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/15873

Chicago Manual of Style (16th Edition):

Sen, Onur. “Phospho-regulation of the spindle assembly checkpoint.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed January 26, 2020. http://hdl.handle.net/1842/15873.

MLA Handbook (7th Edition):

Sen, Onur. “Phospho-regulation of the spindle assembly checkpoint.” 2016. Web. 26 Jan 2020.

Vancouver:

Sen O. Phospho-regulation of the spindle assembly checkpoint. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1842/15873.

Council of Science Editors:

Sen O. Phospho-regulation of the spindle assembly checkpoint. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/15873


Brock University

21. Caterini, Daniel. THE INFLUENCE OF LENGTH CHANGE SPEED AND DIRECTION ON DYNAMIC FUNCTION POTENTIATION IN FAST MOUSE MUSCLE .

Degree: Applied Health Sciences Program, 2011, Brock University

 The purpose of this study was to test the hypothesis that the potentiation of dynamic function was dependent upon both length change speed and direction.… (more)

Subjects/Keywords: myosin; phosphorylation; concentric; eccentric

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APA (6th Edition):

Caterini, D. (2011). THE INFLUENCE OF LENGTH CHANGE SPEED AND DIRECTION ON DYNAMIC FUNCTION POTENTIATION IN FAST MOUSE MUSCLE . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/3398

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):

Caterini, Daniel. “THE INFLUENCE OF LENGTH CHANGE SPEED AND DIRECTION ON DYNAMIC FUNCTION POTENTIATION IN FAST MOUSE MUSCLE .” 2011. Thesis, Brock University. Accessed January 26, 2020. http://hdl.handle.net/10464/3398.

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

MLA Handbook (7th Edition):

Caterini, Daniel. “THE INFLUENCE OF LENGTH CHANGE SPEED AND DIRECTION ON DYNAMIC FUNCTION POTENTIATION IN FAST MOUSE MUSCLE .” 2011. Web. 26 Jan 2020.

Vancouver:

Caterini D. THE INFLUENCE OF LENGTH CHANGE SPEED AND DIRECTION ON DYNAMIC FUNCTION POTENTIATION IN FAST MOUSE MUSCLE . [Internet] [Thesis]. Brock University; 2011. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10464/3398.

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

Council of Science Editors:

Caterini D. THE INFLUENCE OF LENGTH CHANGE SPEED AND DIRECTION ON DYNAMIC FUNCTION POTENTIATION IN FAST MOUSE MUSCLE . [Thesis]. Brock University; 2011. Available from: http://hdl.handle.net/10464/3398

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


Brock University

22. Bosak, Jan. The Molecular Consequences of CK2-mediated Phosphorylation of the TGA2 Transcription Factor within Systemic Acquired Resistance of Arabidopsis thaliana .

Degree: Centre for Biotechnology, 2014, Brock University

 During infection, the model plant Arabidopsis thaliana is capable of activating long lasting defence responses both in tissue directly affected by the pathogen and in… (more)

Subjects/Keywords: TGA2 phosphorylation; protein kinase CK2

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APA (6th Edition):

Bosak, J. (2014). The Molecular Consequences of CK2-mediated Phosphorylation of the TGA2 Transcription Factor within Systemic Acquired Resistance of Arabidopsis thaliana . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/5529

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):

Bosak, Jan. “The Molecular Consequences of CK2-mediated Phosphorylation of the TGA2 Transcription Factor within Systemic Acquired Resistance of Arabidopsis thaliana .” 2014. Thesis, Brock University. Accessed January 26, 2020. http://hdl.handle.net/10464/5529.

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

MLA Handbook (7th Edition):

Bosak, Jan. “The Molecular Consequences of CK2-mediated Phosphorylation of the TGA2 Transcription Factor within Systemic Acquired Resistance of Arabidopsis thaliana .” 2014. Web. 26 Jan 2020.

Vancouver:

Bosak J. The Molecular Consequences of CK2-mediated Phosphorylation of the TGA2 Transcription Factor within Systemic Acquired Resistance of Arabidopsis thaliana . [Internet] [Thesis]. Brock University; 2014. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10464/5529.

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

Council of Science Editors:

Bosak J. The Molecular Consequences of CK2-mediated Phosphorylation of the TGA2 Transcription Factor within Systemic Acquired Resistance of Arabidopsis thaliana . [Thesis]. Brock University; 2014. Available from: http://hdl.handle.net/10464/5529

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


The Ohio State University

23. Kesic, Matthew John. Identification and characterization of the post-translational modifications of the HTLV types 1 and 2 regulatory protein Rex.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2009, The Ohio State University

 Human T-cell Leukemia Virus (HTLV) types 1-4 are classified as complex retroviruses and are members of the genus Deltaretrovirus. HTLV-1 and HTLV-2 are the most… (more)

Subjects/Keywords: Virology; Rex; HTLV; phosphorylation

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APA (6th Edition):

Kesic, M. J. (2009). Identification and characterization of the post-translational modifications of the HTLV types 1 and 2 regulatory protein Rex. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1241104210

Chicago Manual of Style (16th Edition):

Kesic, Matthew John. “Identification and characterization of the post-translational modifications of the HTLV types 1 and 2 regulatory protein Rex.” 2009. Doctoral Dissertation, The Ohio State University. Accessed January 26, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1241104210.

MLA Handbook (7th Edition):

Kesic, Matthew John. “Identification and characterization of the post-translational modifications of the HTLV types 1 and 2 regulatory protein Rex.” 2009. Web. 26 Jan 2020.

Vancouver:

Kesic MJ. Identification and characterization of the post-translational modifications of the HTLV types 1 and 2 regulatory protein Rex. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2020 Jan 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1241104210.

Council of Science Editors:

Kesic MJ. Identification and characterization of the post-translational modifications of the HTLV types 1 and 2 regulatory protein Rex. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1241104210


University of Cincinnati

24. Kaplan, Fred M. Formation and regulation of the Notchic transcription complex.

Degree: PhD, Medicine : Molecular Genetics, Biochemistry, and Microbiology, 2008, University of Cincinnati

 Numerous intricate cellular processes are implemented through direct cell-to-cell interactions. Depending on cell type, the Notch signal transduction pathway initiates a variety of cellular processes… (more)

Subjects/Keywords: Biochemistry; Notch; multimer; phosphorylation

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APA (6th Edition):

Kaplan, F. M. (2008). Formation and regulation of the Notchic transcription complex. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1204685263

Chicago Manual of Style (16th Edition):

Kaplan, Fred M. “Formation and regulation of the Notchic transcription complex.” 2008. Doctoral Dissertation, University of Cincinnati. Accessed January 26, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1204685263.

MLA Handbook (7th Edition):

Kaplan, Fred M. “Formation and regulation of the Notchic transcription complex.” 2008. Web. 26 Jan 2020.

Vancouver:

Kaplan FM. Formation and regulation of the Notchic transcription complex. [Internet] [Doctoral dissertation]. University of Cincinnati; 2008. [cited 2020 Jan 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1204685263.

Council of Science Editors:

Kaplan FM. Formation and regulation of the Notchic transcription complex. [Doctoral Dissertation]. University of Cincinnati; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1204685263


Case Western Reserve University

25. Stanya, Kristopher J. Phosphorylation-Dependent Regulation of the Corepressor SMRT.

Degree: PhD, Biochemistry, 2009, Case Western Reserve University

  SMRT (silencing mediator of retinoic acid and thyroid hormone receptors) and N-CoR (nuclear receptor corepressor) are large corepressor proteins that mediate repression of various… (more)

Subjects/Keywords: Biochemistry; SMRT; corepressors; phosphorylation

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APA (6th Edition):

Stanya, K. J. (2009). Phosphorylation-Dependent Regulation of the Corepressor SMRT. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1220559727

Chicago Manual of Style (16th Edition):

Stanya, Kristopher J. “Phosphorylation-Dependent Regulation of the Corepressor SMRT.” 2009. Doctoral Dissertation, Case Western Reserve University. Accessed January 26, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1220559727.

MLA Handbook (7th Edition):

Stanya, Kristopher J. “Phosphorylation-Dependent Regulation of the Corepressor SMRT.” 2009. Web. 26 Jan 2020.

Vancouver:

Stanya KJ. Phosphorylation-Dependent Regulation of the Corepressor SMRT. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2009. [cited 2020 Jan 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1220559727.

Council of Science Editors:

Stanya KJ. Phosphorylation-Dependent Regulation of the Corepressor SMRT. [Doctoral Dissertation]. Case Western Reserve University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1220559727


University of Manchester

26. Lee, Dave. Informatics tools for the analysis and assignment of phosphorylation status in proteomics.

Degree: PhD, 2015, University of Manchester

 Presently, progress in the field of phosphoproteomics has been accelerated by mass spectrometry. This is not a surprise owing to not only the accuracy, precision… (more)

Subjects/Keywords: 572; Phosphorylation; Mass spectrometry; Functional

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APA (6th Edition):

Lee, D. (2015). Informatics tools for the analysis and assignment of phosphorylation status in proteomics. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/informatics-tools-for-the-analysis-and-assignment-of-phosphorylation-status-in-proteomics(48d2cc82-5bb2-4f07-9cdd-670467db4378).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644464

Chicago Manual of Style (16th Edition):

Lee, Dave. “Informatics tools for the analysis and assignment of phosphorylation status in proteomics.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 26, 2020. https://www.research.manchester.ac.uk/portal/en/theses/informatics-tools-for-the-analysis-and-assignment-of-phosphorylation-status-in-proteomics(48d2cc82-5bb2-4f07-9cdd-670467db4378).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644464.

MLA Handbook (7th Edition):

Lee, Dave. “Informatics tools for the analysis and assignment of phosphorylation status in proteomics.” 2015. Web. 26 Jan 2020.

Vancouver:

Lee D. Informatics tools for the analysis and assignment of phosphorylation status in proteomics. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Jan 26]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/informatics-tools-for-the-analysis-and-assignment-of-phosphorylation-status-in-proteomics(48d2cc82-5bb2-4f07-9cdd-670467db4378).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644464.

Council of Science Editors:

Lee D. Informatics tools for the analysis and assignment of phosphorylation status in proteomics. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/informatics-tools-for-the-analysis-and-assignment-of-phosphorylation-status-in-proteomics(48d2cc82-5bb2-4f07-9cdd-670467db4378).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644464


University of Manchester

27. Lee, Dave. Informatics tools for the analysis and assignment of phosphorylation status in proteomics.

Degree: 2015, University of Manchester

Presently, progress in the field of phosphoproteomics has been accelerated by mass spectrometry. This is not a surprise owing to not only the accuracy, precision… (more)

Subjects/Keywords: Phosphorylation; Mass spectrometry; Functional

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

APA (6th Edition):

Lee, D. (2015). Informatics tools for the analysis and assignment of phosphorylation status in proteomics. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:259036

Chicago Manual of Style (16th Edition):

Lee, Dave. “Informatics tools for the analysis and assignment of phosphorylation status in proteomics.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 26, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:259036.

MLA Handbook (7th Edition):

Lee, Dave. “Informatics tools for the analysis and assignment of phosphorylation status in proteomics.” 2015. Web. 26 Jan 2020.

Vancouver:

Lee D. Informatics tools for the analysis and assignment of phosphorylation status in proteomics. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Jan 26]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:259036.

Council of Science Editors:

Lee D. Informatics tools for the analysis and assignment of phosphorylation status in proteomics. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:259036


McGill University

28. Côté, André. Protein Phosphorylation and Tropomyosin in Chromaffin Cell Functions.

Degree: PhD, Department of Pharmacology and Therapeutics, 1986, McGill University

Protein phosphorylation is a major general mechanism by which intracellular events respond to external physiological stimuli. It has also been postulated that protein phosphorylation may… (more)

Subjects/Keywords: Protein phosphorylation

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APA (6th Edition):

Côté, A. (1986). Protein Phosphorylation and Tropomyosin in Chromaffin Cell Functions. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154184.pdf

Chicago Manual of Style (16th Edition):

Côté, André. “Protein Phosphorylation and Tropomyosin in Chromaffin Cell Functions.” 1986. Doctoral Dissertation, McGill University. Accessed January 26, 2020. http://digitool.library.mcgill.ca/thesisfile154184.pdf.

MLA Handbook (7th Edition):

Côté, André. “Protein Phosphorylation and Tropomyosin in Chromaffin Cell Functions.” 1986. Web. 26 Jan 2020.

Vancouver:

Côté A. Protein Phosphorylation and Tropomyosin in Chromaffin Cell Functions. [Internet] [Doctoral dissertation]. McGill University; 1986. [cited 2020 Jan 26]. Available from: http://digitool.library.mcgill.ca/thesisfile154184.pdf.

Council of Science Editors:

Côté A. Protein Phosphorylation and Tropomyosin in Chromaffin Cell Functions. [Doctoral Dissertation]. McGill University; 1986. Available from: http://digitool.library.mcgill.ca/thesisfile154184.pdf


Université de Sherbrooke

29. Germain, Pascale. Shp2 régule la phosphorylation des tyrosines de l'arrestine .

Degree: 2009, Université de Sherbrooke

 Les arrestines sont connues pour leurs rôles dans la désensibilisation et l'endocytose des récepteurs couplés aux protéines G (RCPGs). Au fil des ans, plusieurs partenaires… (more)

Subjects/Keywords: Tyrosine; Src; Shp2; Phosphorylation; Arrestine

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APA (6th Edition):

Germain, P. (2009). Shp2 régule la phosphorylation des tyrosines de l'arrestine . (Masters Thesis). Université de Sherbrooke. Retrieved from http://savoirs.usherbrooke.ca/handle/11143/3968

Chicago Manual of Style (16th Edition):

Germain, Pascale. “Shp2 régule la phosphorylation des tyrosines de l'arrestine .” 2009. Masters Thesis, Université de Sherbrooke. Accessed January 26, 2020. http://savoirs.usherbrooke.ca/handle/11143/3968.

MLA Handbook (7th Edition):

Germain, Pascale. “Shp2 régule la phosphorylation des tyrosines de l'arrestine .” 2009. Web. 26 Jan 2020.

Vancouver:

Germain P. Shp2 régule la phosphorylation des tyrosines de l'arrestine . [Internet] [Masters thesis]. Université de Sherbrooke; 2009. [cited 2020 Jan 26]. Available from: http://savoirs.usherbrooke.ca/handle/11143/3968.

Council of Science Editors:

Germain P. Shp2 régule la phosphorylation des tyrosines de l'arrestine . [Masters Thesis]. Université de Sherbrooke; 2009. Available from: http://savoirs.usherbrooke.ca/handle/11143/3968

30. Hébert Chatelain, Etienne. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.

Degree: Docteur es, Sciences, technologie, santé. Biologie cellulaire et physiopathologie, 2011, Université de Bordeaux Segalen

La mitochondrie est une organelle très importante vu son implication dans plusieurs processus cellulaires. Elle produit notamment la majeure partie de l'énergie qui est consommée… (more)

Subjects/Keywords: Mitochondrie; Phosphorylation oxydative; Tyrosine; Phosphorylation; Src kinase; PTP1B; Mitochondria; Oxidative phosphorylation; Tyrosine; Phosphorylation; Src kinase; PTP1B

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

APA (6th Edition):

Hébert Chatelain, E. (2011). Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2011BOR21830

Chicago Manual of Style (16th Edition):

Hébert Chatelain, Etienne. “Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.” 2011. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed January 26, 2020. http://www.theses.fr/2011BOR21830.

MLA Handbook (7th Edition):

Hébert Chatelain, Etienne. “Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.” 2011. Web. 26 Jan 2020.

Vancouver:

Hébert Chatelain E. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2011. [cited 2020 Jan 26]. Available from: http://www.theses.fr/2011BOR21830.

Council of Science Editors:

Hébert Chatelain E. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2011. Available from: http://www.theses.fr/2011BOR21830

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