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You searched for subject:(phosphorylation). Showing records 1 – 30 of 1311 total matches.

[1] [2] [3] [4] [5] … [44]

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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 September 21, 2019. 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. 21 Sep 2019.

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 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Caliva MJ. Regulation of integrin trafficking by PEA-15. [Internet] [Thesis]. University of Hawaii – Manoa; 2015. [cited 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Bolduc DM. PHOSPHORYLATION-INDUCED CONFORMATIONAL CHANGES OF PTEN REVEALED BY PROTEIN SEMISYNTHESIS. [Internet] [Thesis]. Johns Hopkins University; 2013. [cited 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Kuo H. Factors affecting the activation of rabbit muscle phosphofructokinase by actin. [Internet] [Doctoral dissertation]. Oregon State University; 1986. [cited 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

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 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Maheshwari S. Identification of conserved structural motifs associated with phosphorylation sites in kinases. [Internet] [Masters thesis]. University of Georgia; 2012. [cited 2019 Sep 21]. 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 September 21, 2019. http://hdl.handle.net/1957/40950.

MLA Handbook (7th Edition):

Zhao, Zhizhuang. “Regulation of phosphofructokinase by reversible inactivation.” 1990. Web. 21 Sep 2019.

Vancouver:

Zhao Z. Regulation of phosphofructokinase by reversible inactivation. [Internet] [Doctoral dissertation]. Oregon State University; 1990. [cited 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Johnson MA. Evidence for a soluble intermediate of oxidative phosphorylation isolated from cabbage mitochondria. [Internet] [Doctoral dissertation]. Oregon State University; 1966. [cited 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Steele WF. Oxidative phosphorylation and related reactions in particulate fractions from insects. [Internet] [Doctoral dissertation]. Oregon State University; 1965. [cited 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

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 2019 Sep 21]. 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


ETH Zürich

11. Mayer, Daniel. Molecular basis for the recognition of the phosphorylation pattern in the C-terminal tail of GPCRs by arrestins.

Degree: 2017, ETH Zürich

 Arrestins are responsible for desensitization and internalization of activated, phosphorylated G protein-coupled receptors (GPCRs). Over the years, it became clear that they have the potential… (more)

Subjects/Keywords: Arrestin; GPCR; phosphorylation barcode; phosphorylation sites

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APA (6th Edition):

Mayer, D. (2017). Molecular basis for the recognition of the phosphorylation pattern in the C-terminal tail of GPCRs by arrestins. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/215427

Chicago Manual of Style (16th Edition):

Mayer, Daniel. “Molecular basis for the recognition of the phosphorylation pattern in the C-terminal tail of GPCRs by arrestins.” 2017. Doctoral Dissertation, ETH Zürich. Accessed September 21, 2019. http://hdl.handle.net/20.500.11850/215427.

MLA Handbook (7th Edition):

Mayer, Daniel. “Molecular basis for the recognition of the phosphorylation pattern in the C-terminal tail of GPCRs by arrestins.” 2017. Web. 21 Sep 2019.

Vancouver:

Mayer D. Molecular basis for the recognition of the phosphorylation pattern in the C-terminal tail of GPCRs by arrestins. [Internet] [Doctoral dissertation]. ETH Zürich; 2017. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/20.500.11850/215427.

Council of Science Editors:

Mayer D. Molecular basis for the recognition of the phosphorylation pattern in the C-terminal tail of GPCRs by arrestins. [Doctoral Dissertation]. ETH Zürich; 2017. Available from: http://hdl.handle.net/20.500.11850/215427


University of Manchester

12. 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 September 21, 2019. 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. 21 Sep 2019.

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 2019 Sep 21]. 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

13. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

He Y. Epigenetic and Post-Translational Mechanisms in Pain: MicroRNA and Phosphorylation. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2019 Sep 21]. 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


University of Vermont

14. Connors, Emilee. Positive Trafficking Pathways of a Voltage Gated Potassium Channel.

Degree: PhD, Pharmacology, 2009, University of Vermont

 ABSTRACT The voltage-gated potassium channel Kv1.2 is a key determinant of cellular excitability in the nervous and cardiovascular systems. In the brain, Kv1.2 is strongly… (more)

Subjects/Keywords: Potassium Channel; Phosphorylation

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APA (6th Edition):

Connors, E. (2009). Positive Trafficking Pathways of a Voltage Gated Potassium Channel. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/52

Chicago Manual of Style (16th Edition):

Connors, Emilee. “Positive Trafficking Pathways of a Voltage Gated Potassium Channel.” 2009. Doctoral Dissertation, University of Vermont. Accessed September 21, 2019. https://scholarworks.uvm.edu/graddis/52.

MLA Handbook (7th Edition):

Connors, Emilee. “Positive Trafficking Pathways of a Voltage Gated Potassium Channel.” 2009. Web. 21 Sep 2019.

Vancouver:

Connors E. Positive Trafficking Pathways of a Voltage Gated Potassium Channel. [Internet] [Doctoral dissertation]. University of Vermont; 2009. [cited 2019 Sep 21]. Available from: https://scholarworks.uvm.edu/graddis/52.

Council of Science Editors:

Connors E. Positive Trafficking Pathways of a Voltage Gated Potassium Channel. [Doctoral Dissertation]. University of Vermont; 2009. Available from: https://scholarworks.uvm.edu/graddis/52


University of Rochester

15. 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 September 21, 2019. 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. 21 Sep 2019.

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 2019 Sep 21]. 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

16. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Cole CT. Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2011. [cited 2019 Sep 21]. 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

17. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Mahoney BJ. Understanding Response Mechanisms of Post-Translational Phosphorylation in Signaling Proteins</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2018. [cited 2019 Sep 21]. 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


Rutgers University

18. 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 September 21, 2019. 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. 21 Sep 2019.

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 2019 Sep 21]. 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

19. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Hennessy, Meagan L. 1. Phosphorylation of lipin 1 beta phosphatidate phosphatase by casein kinase II. [Internet] [Masters thesis]. Rutgers University; 2018. [cited 2019 Sep 21]. 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

20. 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 (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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Robinson C. The effect of phosphorylation on oxysterol-binding protein (OSBP) sterol binding activity. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2019 Sep 21]. 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

21. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Yip S. Characterisation of novel potential phosphorylation sites in the tumour suppressor Merlin in Drosophila. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2019 Sep 21]. 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

22. 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 September 21, 2019. http://hdl.handle.net/1842/15873.

MLA Handbook (7th Edition):

Sen, Onur. “Phospho-regulation of the spindle assembly checkpoint.” 2016. Web. 21 Sep 2019.

Vancouver:

Sen O. Phospho-regulation of the spindle assembly checkpoint. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2019 Sep 21]. 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


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 September 21, 2019. 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. 21 Sep 2019.

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 2019 Sep 21]. 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Kaplan FM. Formation and regulation of the Notchic transcription complex. [Internet] [Doctoral dissertation]. University of Cincinnati; 2008. [cited 2019 Sep 21]. 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


Cornell University

25. Krauchunas, Amber. Nature And Regulation Of Protein Phosphorylation Changes During Egg Activation In Drosophila Melanogaster .

Degree: 2012, Cornell University

 Mature oocytes are held in a developmentally-quiescent, arrested state. For development to occur, these oocytes must transition to a new cellular state that can support… (more)

Subjects/Keywords: Egg activation; Phosphorylation; Proteomics

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APA (6th Edition):

Krauchunas, A. (2012). Nature And Regulation Of Protein Phosphorylation Changes During Egg Activation In Drosophila Melanogaster . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/30979

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):

Krauchunas, Amber. “Nature And Regulation Of Protein Phosphorylation Changes During Egg Activation In Drosophila Melanogaster .” 2012. Thesis, Cornell University. Accessed September 21, 2019. http://hdl.handle.net/1813/30979.

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

MLA Handbook (7th Edition):

Krauchunas, Amber. “Nature And Regulation Of Protein Phosphorylation Changes During Egg Activation In Drosophila Melanogaster .” 2012. Web. 21 Sep 2019.

Vancouver:

Krauchunas A. Nature And Regulation Of Protein Phosphorylation Changes During Egg Activation In Drosophila Melanogaster . [Internet] [Thesis]. Cornell University; 2012. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/1813/30979.

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

Council of Science Editors:

Krauchunas A. Nature And Regulation Of Protein Phosphorylation Changes During Egg Activation In Drosophila Melanogaster . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/30979

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


Hong Kong University of Science and Technology

26. Jiang, Tianwei. Sequence alignment : algorithm development and applications.

Degree: 2009, Hong Kong University of Science and Technology

 Sequence alignment is a critical step towards sequence comparison and it can reveal genetic/functional relationships among evolutionarily related species. The alignment addresses similarities among sequences… (more)

Subjects/Keywords: Sequence alignment (Bioinformatics); Phosphorylation; Algorithms

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APA (6th Edition):

Jiang, T. (2009). Sequence alignment : algorithm development and applications. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1070938 ; http://repository.ust.hk/ir/bitstream/1783.1-6372/1/th_redirect.html

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):

Jiang, Tianwei. “Sequence alignment : algorithm development and applications.” 2009. Thesis, Hong Kong University of Science and Technology. Accessed September 21, 2019. https://doi.org/10.14711/thesis-b1070938 ; http://repository.ust.hk/ir/bitstream/1783.1-6372/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Jiang, Tianwei. “Sequence alignment : algorithm development and applications.” 2009. Web. 21 Sep 2019.

Vancouver:

Jiang T. Sequence alignment : algorithm development and applications. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2009. [cited 2019 Sep 21]. Available from: https://doi.org/10.14711/thesis-b1070938 ; http://repository.ust.hk/ir/bitstream/1783.1-6372/1/th_redirect.html.

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

Council of Science Editors:

Jiang T. Sequence alignment : algorithm development and applications. [Thesis]. Hong Kong University of Science and Technology; 2009. Available from: https://doi.org/10.14711/thesis-b1070938 ; http://repository.ust.hk/ir/bitstream/1783.1-6372/1/th_redirect.html

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


Hong Kong University of Science and Technology

27. Pun, Sing. High resolution mapping of ethylene signal transduction pathways via quantitative phosphoproteomics study of ethylene-insensitive double mutant ein3-1/eil1-1.

Degree: 2013, Hong Kong University of Science and Technology

 Ethylene is a major plant hormone that plays an important role in virtually all physiological events in plant, yet the underlying molecular mechanism is very… (more)

Subjects/Keywords: Ethylene; Phosphorylation; Cellular signal transduction

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APA (6th Edition):

Pun, S. (2013). High resolution mapping of ethylene signal transduction pathways via quantitative phosphoproteomics study of ethylene-insensitive double mutant ein3-1/eil1-1. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1213354 ; http://repository.ust.hk/ir/bitstream/1783.1-7856/1/th_redirect.html

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):

Pun, Sing. “High resolution mapping of ethylene signal transduction pathways via quantitative phosphoproteomics study of ethylene-insensitive double mutant ein3-1/eil1-1.” 2013. Thesis, Hong Kong University of Science and Technology. Accessed September 21, 2019. https://doi.org/10.14711/thesis-b1213354 ; http://repository.ust.hk/ir/bitstream/1783.1-7856/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Pun, Sing. “High resolution mapping of ethylene signal transduction pathways via quantitative phosphoproteomics study of ethylene-insensitive double mutant ein3-1/eil1-1.” 2013. Web. 21 Sep 2019.

Vancouver:

Pun S. High resolution mapping of ethylene signal transduction pathways via quantitative phosphoproteomics study of ethylene-insensitive double mutant ein3-1/eil1-1. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2013. [cited 2019 Sep 21]. Available from: https://doi.org/10.14711/thesis-b1213354 ; http://repository.ust.hk/ir/bitstream/1783.1-7856/1/th_redirect.html.

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

Council of Science Editors:

Pun S. High resolution mapping of ethylene signal transduction pathways via quantitative phosphoproteomics study of ethylene-insensitive double mutant ein3-1/eil1-1. [Thesis]. Hong Kong University of Science and Technology; 2013. Available from: https://doi.org/10.14711/thesis-b1213354 ; http://repository.ust.hk/ir/bitstream/1783.1-7856/1/th_redirect.html

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


Hong Kong University of Science and Technology

28. Zhu, Lin. Functional phosphoproteomics analysis of novel ethylene signaling component ERF110.

Degree: 2012, Hong Kong University of Science and Technology

 As one of the major hormones in plant, ethylene plays an important role in regulating numerous physiological events, including flowering. Although being extensively studied, the… (more)

Subjects/Keywords: Ethylene; Phosphorylation; Cellular signal transduction

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APA (6th Edition):

Zhu, L. (2012). Functional phosphoproteomics analysis of novel ethylene signaling component ERF110. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1180063 ; http://repository.ust.hk/ir/bitstream/1783.1-70596/1/th_redirect.html

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):

Zhu, Lin. “Functional phosphoproteomics analysis of novel ethylene signaling component ERF110.” 2012. Thesis, Hong Kong University of Science and Technology. Accessed September 21, 2019. https://doi.org/10.14711/thesis-b1180063 ; http://repository.ust.hk/ir/bitstream/1783.1-70596/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Zhu, Lin. “Functional phosphoproteomics analysis of novel ethylene signaling component ERF110.” 2012. Web. 21 Sep 2019.

Vancouver:

Zhu L. Functional phosphoproteomics analysis of novel ethylene signaling component ERF110. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2019 Sep 21]. Available from: https://doi.org/10.14711/thesis-b1180063 ; http://repository.ust.hk/ir/bitstream/1783.1-70596/1/th_redirect.html.

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

Council of Science Editors:

Zhu L. Functional phosphoproteomics analysis of novel ethylene signaling component ERF110. [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: https://doi.org/10.14711/thesis-b1180063 ; http://repository.ust.hk/ir/bitstream/1783.1-70596/1/th_redirect.html

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


Case Western Reserve University

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

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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Stanya KJ. Phosphorylation-Dependent Regulation of the Corepressor SMRT. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2009. [cited 2019 Sep 21]. 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

30. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 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 September 21, 2019. 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. 21 Sep 2019.

Vancouver:

Lee D. Informatics tools for the analysis and assignment of phosphorylation status in proteomics. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Sep 21]. 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

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