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You searched for subject:(Protein phosphorylation). Showing records 1 – 30 of 310 total matches.

[1] [2] [3] [4] [5] … [11]

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University of Guelph

1. Zhao, Qianru. Regulation of starch biosynthesis in Arabidopsis thalinan .

Degree: 2015, University of Guelph

 Starch is an important carbohydrate in higher plants and is widely used in food and non-food industries. Starch is synthesized in plastids through the actions… (more)

Subjects/Keywords: starch; protein phosphorylation; protein-protein interaction

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APA (6th Edition):

Zhao, Q. (2015). Regulation of starch biosynthesis in Arabidopsis thalinan . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8787

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):

Zhao, Qianru. “Regulation of starch biosynthesis in Arabidopsis thalinan .” 2015. Thesis, University of Guelph. Accessed November 13, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8787.

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

MLA Handbook (7th Edition):

Zhao, Qianru. “Regulation of starch biosynthesis in Arabidopsis thalinan .” 2015. Web. 13 Nov 2019.

Vancouver:

Zhao Q. Regulation of starch biosynthesis in Arabidopsis thalinan . [Internet] [Thesis]. University of Guelph; 2015. [cited 2019 Nov 13]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8787.

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

Council of Science Editors:

Zhao Q. Regulation of starch biosynthesis in Arabidopsis thalinan . [Thesis]. University of Guelph; 2015. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8787

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


McGill University

2. 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 November 13, 2019. http://digitool.library.mcgill.ca/thesisfile154184.pdf.

MLA Handbook (7th Edition):

Côté, André. “Protein Phosphorylation and Tropomyosin in Chromaffin Cell Functions.” 1986. Web. 13 Nov 2019.

Vancouver:

Côté A. Protein Phosphorylation and Tropomyosin in Chromaffin Cell Functions. [Internet] [Doctoral dissertation]. McGill University; 1986. [cited 2019 Nov 13]. 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


Brock University

3. 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 November 13, 2019. 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. 13 Nov 2019.

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 2019 Nov 13]. 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


Stellenbosch University

4. Van der Westhuyzen, Aletta Elizabeth. Synthesis of novel staurosporine analogues as potential kinase inhibitors.

Degree: MSc, Chemistry and Polymer Science, 2015, Stellenbosch University

ENGLISH ABSTRACT: Protein kinases are enzymes that promote phosphorylation – transferring a phosphate group from ATP to a substrate protein. Due to the central involvement… (more)

Subjects/Keywords: Protein kinases; EGFR; Cancer therapy; UCTD; Phosphorylation

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APA (6th Edition):

Van der Westhuyzen, A. E. (2015). Synthesis of novel staurosporine analogues as potential kinase inhibitors. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/96632

Chicago Manual of Style (16th Edition):

Van der Westhuyzen, Aletta Elizabeth. “Synthesis of novel staurosporine analogues as potential kinase inhibitors.” 2015. Masters Thesis, Stellenbosch University. Accessed November 13, 2019. http://hdl.handle.net/10019.1/96632.

MLA Handbook (7th Edition):

Van der Westhuyzen, Aletta Elizabeth. “Synthesis of novel staurosporine analogues as potential kinase inhibitors.” 2015. Web. 13 Nov 2019.

Vancouver:

Van der Westhuyzen AE. Synthesis of novel staurosporine analogues as potential kinase inhibitors. [Internet] [Masters thesis]. Stellenbosch University; 2015. [cited 2019 Nov 13]. Available from: http://hdl.handle.net/10019.1/96632.

Council of Science Editors:

Van der Westhuyzen AE. Synthesis of novel staurosporine analogues as potential kinase inhibitors. [Masters Thesis]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/96632


University of Hawaii – Manoa

5. Sasaki, Carl Y. The role of protein tyrosine phosphorylation in the resistance mechanism against tumor necrosis factor-mediated lysis.

Degree: PhD, 2009, University of Hawaii – Manoa

Microfiche.

ix, 129 leaves, bound ill. 29 cm

Presently, cancer is a major cause of death of individuals in most developed countries. Despite an international… (more)

Subjects/Keywords: Protein-tyrosine kinase; Phosphorylation; Tumor necrosis factor

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APA (6th Edition):

Sasaki, C. Y. (2009). The role of protein tyrosine phosphorylation in the resistance mechanism against tumor necrosis factor-mediated lysis. (Doctoral Dissertation). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/9995

Chicago Manual of Style (16th Edition):

Sasaki, Carl Y. “The role of protein tyrosine phosphorylation in the resistance mechanism against tumor necrosis factor-mediated lysis.” 2009. Doctoral Dissertation, University of Hawaii – Manoa. Accessed November 13, 2019. http://hdl.handle.net/10125/9995.

MLA Handbook (7th Edition):

Sasaki, Carl Y. “The role of protein tyrosine phosphorylation in the resistance mechanism against tumor necrosis factor-mediated lysis.” 2009. Web. 13 Nov 2019.

Vancouver:

Sasaki CY. The role of protein tyrosine phosphorylation in the resistance mechanism against tumor necrosis factor-mediated lysis. [Internet] [Doctoral dissertation]. University of Hawaii – Manoa; 2009. [cited 2019 Nov 13]. Available from: http://hdl.handle.net/10125/9995.

Council of Science Editors:

Sasaki CY. The role of protein tyrosine phosphorylation in the resistance mechanism against tumor necrosis factor-mediated lysis. [Doctoral Dissertation]. University of Hawaii – Manoa; 2009. Available from: http://hdl.handle.net/10125/9995


University of Hong Kong

6. 郭樱樱; Guo, Yingying. A study of protein phosphorylation and ubiquitination in DNA double strand break responses.

Degree: PhD, 2016, University of Hong Kong

Through altering the properties of DNA damage response (DDR) proteins, posttranslational modifications (PTMs) play pivotal roles in orchestrating timely and accurate cellular responses to DNA… (more)

Subjects/Keywords: DNA damage; Protein kinases; Ubiquitin; Phosphorylation

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APA (6th Edition):

郭樱樱; Guo, Y. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Doctoral Dissertation). University of Hong Kong. Retrieved from Guo, Y. [郭樱樱]. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816256. ; http://dx.doi.org/10.5353/th_b5816256 ; http://hdl.handle.net/10722/237863

Chicago Manual of Style (16th Edition):

郭樱樱; Guo, Yingying. “A study of protein phosphorylation and ubiquitination in DNA double strand break responses.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed November 13, 2019. Guo, Y. [郭樱樱]. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816256. ; http://dx.doi.org/10.5353/th_b5816256 ; http://hdl.handle.net/10722/237863.

MLA Handbook (7th Edition):

郭樱樱; Guo, Yingying. “A study of protein phosphorylation and ubiquitination in DNA double strand break responses.” 2016. Web. 13 Nov 2019.

Vancouver:

郭樱樱; Guo Y. A study of protein phosphorylation and ubiquitination in DNA double strand break responses. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2019 Nov 13]. Available from: Guo, Y. [郭樱樱]. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816256. ; http://dx.doi.org/10.5353/th_b5816256 ; http://hdl.handle.net/10722/237863.

Council of Science Editors:

郭樱樱; Guo Y. A study of protein phosphorylation and ubiquitination in DNA double strand break responses. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: Guo, Y. [郭樱樱]. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816256. ; http://dx.doi.org/10.5353/th_b5816256 ; http://hdl.handle.net/10722/237863


Penn State University

7. Ludgate, Laurie. Regulation of hepadnavirus core protein function by phosphorylation.

Degree: PhD, Microbiology and Immunology, 2011, Penn State University

 Hepatitis B virus (HBV) remains a major global health problem with more than 350 million chronic carriers worldwide. Chronic HBV infection can lead to advanced… (more)

Subjects/Keywords: HBV; DHBV; core protein; phosphorylation; kinase

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APA (6th Edition):

Ludgate, L. (2011). Regulation of hepadnavirus core protein function by phosphorylation. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/12242

Chicago Manual of Style (16th Edition):

Ludgate, Laurie. “Regulation of hepadnavirus core protein function by phosphorylation.” 2011. Doctoral Dissertation, Penn State University. Accessed November 13, 2019. https://etda.libraries.psu.edu/catalog/12242.

MLA Handbook (7th Edition):

Ludgate, Laurie. “Regulation of hepadnavirus core protein function by phosphorylation.” 2011. Web. 13 Nov 2019.

Vancouver:

Ludgate L. Regulation of hepadnavirus core protein function by phosphorylation. [Internet] [Doctoral dissertation]. Penn State University; 2011. [cited 2019 Nov 13]. Available from: https://etda.libraries.psu.edu/catalog/12242.

Council of Science Editors:

Ludgate L. Regulation of hepadnavirus core protein function by phosphorylation. [Doctoral Dissertation]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/12242


University of California – Santa Cruz

8. Burke, Jason R. Structural Studies of Retinoblastoma Protein Phosphorylation.

Degree: Chemistry, 2012, University of California – Santa Cruz

 The Retinoblastoma Protein (Rb) is a sentinel of the cell division process. When phosphorylated, Rb is inactivated and physically releases its protein-binding partner, E2F; a… (more)

Subjects/Keywords: Chemistry; E2F; Phosphorylation; Protein; Rb; Retinoblastoma; Structure

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APA (6th Edition):

Burke, J. R. (2012). Structural Studies of Retinoblastoma Protein Phosphorylation. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/58r8s5d4

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):

Burke, Jason R. “Structural Studies of Retinoblastoma Protein Phosphorylation.” 2012. Thesis, University of California – Santa Cruz. Accessed November 13, 2019. http://www.escholarship.org/uc/item/58r8s5d4.

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

MLA Handbook (7th Edition):

Burke, Jason R. “Structural Studies of Retinoblastoma Protein Phosphorylation.” 2012. Web. 13 Nov 2019.

Vancouver:

Burke JR. Structural Studies of Retinoblastoma Protein Phosphorylation. [Internet] [Thesis]. University of California – Santa Cruz; 2012. [cited 2019 Nov 13]. Available from: http://www.escholarship.org/uc/item/58r8s5d4.

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

Council of Science Editors:

Burke JR. Structural Studies of Retinoblastoma Protein Phosphorylation. [Thesis]. University of California – Santa Cruz; 2012. Available from: http://www.escholarship.org/uc/item/58r8s5d4

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


Virginia Tech

9. Shen, Ying. Direct conversion of chemical energy to mechanical work using a phosphate charged protein.

Degree: MS, Biological Systems Engineering, 2010, Virginia Tech

 Nature is able to convert chemical energy into mechanical work under modest conditions, i.e., physiological pH and ambient temperature and pressure. One of the most… (more)

Subjects/Keywords: re-phosphorylation; dephosphorylation; energy; protein gel; casein

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APA (6th Edition):

Shen, Y. (2010). Direct conversion of chemical energy to mechanical work using a phosphate charged protein. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/31829

Chicago Manual of Style (16th Edition):

Shen, Ying. “Direct conversion of chemical energy to mechanical work using a phosphate charged protein.” 2010. Masters Thesis, Virginia Tech. Accessed November 13, 2019. http://hdl.handle.net/10919/31829.

MLA Handbook (7th Edition):

Shen, Ying. “Direct conversion of chemical energy to mechanical work using a phosphate charged protein.” 2010. Web. 13 Nov 2019.

Vancouver:

Shen Y. Direct conversion of chemical energy to mechanical work using a phosphate charged protein. [Internet] [Masters thesis]. Virginia Tech; 2010. [cited 2019 Nov 13]. Available from: http://hdl.handle.net/10919/31829.

Council of Science Editors:

Shen Y. Direct conversion of chemical energy to mechanical work using a phosphate charged protein. [Masters Thesis]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/31829


Virginia Tech

10. Redbird, Ruth Ann. Identification of a protein kinase substrate in Sulfolobus solfataricus P2.

Degree: PhD, Biochemistry, 2010, Virginia Tech

 Living organisms rely on many different mechanisms to adapt to changes within their environment. Protein phosphorylation and dephosphorylation events are one such way cells can… (more)

Subjects/Keywords: Archaea; ATP Synthase; phosphorylation; protein kinase

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APA (6th Edition):

Redbird, R. A. (2010). Identification of a protein kinase substrate in Sulfolobus solfataricus P2. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/26884

Chicago Manual of Style (16th Edition):

Redbird, Ruth Ann. “Identification of a protein kinase substrate in Sulfolobus solfataricus P2.” 2010. Doctoral Dissertation, Virginia Tech. Accessed November 13, 2019. http://hdl.handle.net/10919/26884.

MLA Handbook (7th Edition):

Redbird, Ruth Ann. “Identification of a protein kinase substrate in Sulfolobus solfataricus P2.” 2010. Web. 13 Nov 2019.

Vancouver:

Redbird RA. Identification of a protein kinase substrate in Sulfolobus solfataricus P2. [Internet] [Doctoral dissertation]. Virginia Tech; 2010. [cited 2019 Nov 13]. Available from: http://hdl.handle.net/10919/26884.

Council of Science Editors:

Redbird RA. Identification of a protein kinase substrate in Sulfolobus solfataricus P2. [Doctoral Dissertation]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/26884


East Carolina University

11. Williams, Brett. CaMKII Protein Expression and Phosphorylation in Mouse Skeletal Muscle Following Atrophy and Hypertrophy.

Degree: 2012, East Carolina University

 The maintenance of skeletal muscle mass is vital for life and elucidation of the molecular mechanisms that control this process is a critical first step… (more)

Subjects/Keywords: Protein kinases; Phosphorylation; Muscular atrophy; Muscles – Hypertrophy

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APA (6th Edition):

Williams, B. (2012). CaMKII Protein Expression and Phosphorylation in Mouse Skeletal Muscle Following Atrophy and Hypertrophy. (Masters Thesis). East Carolina University. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13856

Chicago Manual of Style (16th Edition):

Williams, Brett. “CaMKII Protein Expression and Phosphorylation in Mouse Skeletal Muscle Following Atrophy and Hypertrophy.” 2012. Masters Thesis, East Carolina University. Accessed November 13, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13856.

MLA Handbook (7th Edition):

Williams, Brett. “CaMKII Protein Expression and Phosphorylation in Mouse Skeletal Muscle Following Atrophy and Hypertrophy.” 2012. Web. 13 Nov 2019.

Vancouver:

Williams B. CaMKII Protein Expression and Phosphorylation in Mouse Skeletal Muscle Following Atrophy and Hypertrophy. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2019 Nov 13]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13856.

Council of Science Editors:

Williams B. CaMKII Protein Expression and Phosphorylation in Mouse Skeletal Muscle Following Atrophy and Hypertrophy. [Masters Thesis]. East Carolina University; 2012. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13856


University of Vermont

12. Todero, Jenna E. Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A.

Degree: Biology, 2016, University of Vermont

  Abstract: Protein kinase A (PKA) is a cyclic-AMP (cAMP) dependent kinase and is known to regulate many processes, specifically proliferation and migration. PKA activity… (more)

Subjects/Keywords: Protein Kinase A; PKA; src; phosphorylation

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APA (6th Edition):

Todero, J. E. (2016). Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/hcoltheses/210

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):

Todero, Jenna E. “Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A.” 2016. Thesis, University of Vermont. Accessed November 13, 2019. https://scholarworks.uvm.edu/hcoltheses/210.

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

MLA Handbook (7th Edition):

Todero, Jenna E. “Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A.” 2016. Web. 13 Nov 2019.

Vancouver:

Todero JE. Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A. [Internet] [Thesis]. University of Vermont; 2016. [cited 2019 Nov 13]. Available from: https://scholarworks.uvm.edu/hcoltheses/210.

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

Council of Science Editors:

Todero JE. Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A. [Thesis]. University of Vermont; 2016. Available from: https://scholarworks.uvm.edu/hcoltheses/210

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


Tartu University

13. Venta, Rainis. Studies on signal processing by multisite phosphorylation pathways of the S. cerevisiae cyclin-dependent kinase inhibitor Sic1 .

Degree: 2018, Tartu University

 Rakkude jagunemine käivitatakse DNA-sünteesi algatamisega. See toimub aga alles siis, kui rakud on valmis kogu järgneva raku jagunemise tsükli peatumata läbi tegema. Rakkude jagunemise käivitavad… (more)

Subjects/Keywords: cell division; protein kinases; CDK; phosphorylation; inhibition

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APA (6th Edition):

Venta, R. (2018). Studies on signal processing by multisite phosphorylation pathways of the S. cerevisiae cyclin-dependent kinase inhibitor Sic1 . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/61710

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):

Venta, Rainis. “Studies on signal processing by multisite phosphorylation pathways of the S. cerevisiae cyclin-dependent kinase inhibitor Sic1 .” 2018. Thesis, Tartu University. Accessed November 13, 2019. http://hdl.handle.net/10062/61710.

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

MLA Handbook (7th Edition):

Venta, Rainis. “Studies on signal processing by multisite phosphorylation pathways of the S. cerevisiae cyclin-dependent kinase inhibitor Sic1 .” 2018. Web. 13 Nov 2019.

Vancouver:

Venta R. Studies on signal processing by multisite phosphorylation pathways of the S. cerevisiae cyclin-dependent kinase inhibitor Sic1 . [Internet] [Thesis]. Tartu University; 2018. [cited 2019 Nov 13]. Available from: http://hdl.handle.net/10062/61710.

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

Council of Science Editors:

Venta R. Studies on signal processing by multisite phosphorylation pathways of the S. cerevisiae cyclin-dependent kinase inhibitor Sic1 . [Thesis]. Tartu University; 2018. Available from: http://hdl.handle.net/10062/61710

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


Michigan State University

14. Vacratsis, Panayiotis Orestes. Molecular mechanisms regulating the mixed lineage kinase MLK3.

Degree: PhD, Department of Biochemistry and Molecular Biology, 2001, Michigan State University

Subjects/Keywords: Protein kinases; Phosphorylation

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APA (6th Edition):

Vacratsis, P. O. (2001). Molecular mechanisms regulating the mixed lineage kinase MLK3. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:31083

Chicago Manual of Style (16th Edition):

Vacratsis, Panayiotis Orestes. “Molecular mechanisms regulating the mixed lineage kinase MLK3.” 2001. Doctoral Dissertation, Michigan State University. Accessed November 13, 2019. http://etd.lib.msu.edu/islandora/object/etd:31083.

MLA Handbook (7th Edition):

Vacratsis, Panayiotis Orestes. “Molecular mechanisms regulating the mixed lineage kinase MLK3.” 2001. Web. 13 Nov 2019.

Vancouver:

Vacratsis PO. Molecular mechanisms regulating the mixed lineage kinase MLK3. [Internet] [Doctoral dissertation]. Michigan State University; 2001. [cited 2019 Nov 13]. Available from: http://etd.lib.msu.edu/islandora/object/etd:31083.

Council of Science Editors:

Vacratsis PO. Molecular mechanisms regulating the mixed lineage kinase MLK3. [Doctoral Dissertation]. Michigan State University; 2001. Available from: http://etd.lib.msu.edu/islandora/object/etd:31083


University of Dundee

15. Fulcher, Luke James. Identification and characterisation of FAM83 proteins as key regulators of CK1 protein kinases in cells : FAM83D recruits CK1α to the mitotic spindle for proper spindle positioning.

Degree: PhD, 2019, University of Dundee

 The FAM83 family of proteins are classified based on the presence of a conserved domain of unknown function 1669 (DUF1669) within their N-termini. Although structural… (more)

Subjects/Keywords: cell division; mitosis; protein phosphorylation; cell biology

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APA (6th Edition):

Fulcher, L. J. (2019). Identification and characterisation of FAM83 proteins as key regulators of CK1 protein kinases in cells : FAM83D recruits CK1α to the mitotic spindle for proper spindle positioning. (Doctoral Dissertation). University of Dundee. Retrieved from https://discovery.dundee.ac.uk/en/studentTheses/f2f8ff45-46a0-4cab-987b-d3c8f73de78d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.788031

Chicago Manual of Style (16th Edition):

Fulcher, Luke James. “Identification and characterisation of FAM83 proteins as key regulators of CK1 protein kinases in cells : FAM83D recruits CK1α to the mitotic spindle for proper spindle positioning.” 2019. Doctoral Dissertation, University of Dundee. Accessed November 13, 2019. https://discovery.dundee.ac.uk/en/studentTheses/f2f8ff45-46a0-4cab-987b-d3c8f73de78d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.788031.

MLA Handbook (7th Edition):

Fulcher, Luke James. “Identification and characterisation of FAM83 proteins as key regulators of CK1 protein kinases in cells : FAM83D recruits CK1α to the mitotic spindle for proper spindle positioning.” 2019. Web. 13 Nov 2019.

Vancouver:

Fulcher LJ. Identification and characterisation of FAM83 proteins as key regulators of CK1 protein kinases in cells : FAM83D recruits CK1α to the mitotic spindle for proper spindle positioning. [Internet] [Doctoral dissertation]. University of Dundee; 2019. [cited 2019 Nov 13]. Available from: https://discovery.dundee.ac.uk/en/studentTheses/f2f8ff45-46a0-4cab-987b-d3c8f73de78d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.788031.

Council of Science Editors:

Fulcher LJ. Identification and characterisation of FAM83 proteins as key regulators of CK1 protein kinases in cells : FAM83D recruits CK1α to the mitotic spindle for proper spindle positioning. [Doctoral Dissertation]. University of Dundee; 2019. Available from: https://discovery.dundee.ac.uk/en/studentTheses/f2f8ff45-46a0-4cab-987b-d3c8f73de78d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.788031


Temple University

16. Gone, Swapna. Functional analysis of Ribonuclease III regulation by a viral protein kinase.

Degree: PhD, 2011, Temple University

Chemistry

The bacteriophage T7 protein kinase enhances T7 growth under suboptimal growth conditions, including elevated temperature or limiting carbon source. T7PK phosphorylates numerous E. coli… (more)

Subjects/Keywords: Biochemistry; Molecular Biology; Protein Phosphorylation; Ribonuclease III; T 7 Protein Kinase

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APA (6th Edition):

Gone, S. (2011). Functional analysis of Ribonuclease III regulation by a viral protein kinase. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,159409

Chicago Manual of Style (16th Edition):

Gone, Swapna. “Functional analysis of Ribonuclease III regulation by a viral protein kinase.” 2011. Doctoral Dissertation, Temple University. Accessed November 13, 2019. http://digital.library.temple.edu/u?/p245801coll10,159409.

MLA Handbook (7th Edition):

Gone, Swapna. “Functional analysis of Ribonuclease III regulation by a viral protein kinase.” 2011. Web. 13 Nov 2019.

Vancouver:

Gone S. Functional analysis of Ribonuclease III regulation by a viral protein kinase. [Internet] [Doctoral dissertation]. Temple University; 2011. [cited 2019 Nov 13]. Available from: http://digital.library.temple.edu/u?/p245801coll10,159409.

Council of Science Editors:

Gone S. Functional analysis of Ribonuclease III regulation by a viral protein kinase. [Doctoral Dissertation]. Temple University; 2011. Available from: http://digital.library.temple.edu/u?/p245801coll10,159409


Penn State University

17. Fuentes, Sandra M. FUNCTIONS OF THE RESPIRATORY SYNCYTIAL VIRUS SH AND P PROTEINS.

Degree: PhD, Pathobiology, 2010, Penn State University

 Respiratory syncytial virus (RSV) is the leading cause of pediatric hospitalizations due to lower respiratory tract infections. Immunocompromised and elderly patients can also develop severe… (more)

Subjects/Keywords: apoptosis; small hydrophobic protein; RSV; AKT; P protein phosphorylation

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APA (6th Edition):

Fuentes, S. M. (2010). FUNCTIONS OF THE RESPIRATORY SYNCYTIAL VIRUS SH AND P PROTEINS. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11130

Chicago Manual of Style (16th Edition):

Fuentes, Sandra M. “FUNCTIONS OF THE RESPIRATORY SYNCYTIAL VIRUS SH AND P PROTEINS.” 2010. Doctoral Dissertation, Penn State University. Accessed November 13, 2019. https://etda.libraries.psu.edu/catalog/11130.

MLA Handbook (7th Edition):

Fuentes, Sandra M. “FUNCTIONS OF THE RESPIRATORY SYNCYTIAL VIRUS SH AND P PROTEINS.” 2010. Web. 13 Nov 2019.

Vancouver:

Fuentes SM. FUNCTIONS OF THE RESPIRATORY SYNCYTIAL VIRUS SH AND P PROTEINS. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2019 Nov 13]. Available from: https://etda.libraries.psu.edu/catalog/11130.

Council of Science Editors:

Fuentes SM. FUNCTIONS OF THE RESPIRATORY SYNCYTIAL VIRUS SH AND P PROTEINS. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11130


Macquarie University

18. Semaan, Crystal. Proteomic study of beta-catenin protein interactions in colon cancer.

Degree: 2016, Macquarie University

Empirical thesis.

Running title: Proteomic study of β-catenin protein interactions in colon cancer.

Bibliography: pages 210-242.

1. Introduction  – 2. Methods and materials  – 3.… (more)

Subjects/Keywords: Catenins; Protein-protein interactions; Proteomics; Colon (Anatomy)  – Cancer; Phosphorylation

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APA (6th Edition):

Semaan, C. (2016). Proteomic study of beta-catenin protein interactions in colon cancer. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/1247882

Chicago Manual of Style (16th Edition):

Semaan, Crystal. “Proteomic study of beta-catenin protein interactions in colon cancer.” 2016. Doctoral Dissertation, Macquarie University. Accessed November 13, 2019. http://hdl.handle.net/1959.14/1247882.

MLA Handbook (7th Edition):

Semaan, Crystal. “Proteomic study of beta-catenin protein interactions in colon cancer.” 2016. Web. 13 Nov 2019.

Vancouver:

Semaan C. Proteomic study of beta-catenin protein interactions in colon cancer. [Internet] [Doctoral dissertation]. Macquarie University; 2016. [cited 2019 Nov 13]. Available from: http://hdl.handle.net/1959.14/1247882.

Council of Science Editors:

Semaan C. Proteomic study of beta-catenin protein interactions in colon cancer. [Doctoral Dissertation]. Macquarie University; 2016. Available from: http://hdl.handle.net/1959.14/1247882


University of Western Australia

19. Zu, Xin Lin. Methods for the detection, purification and characterisation of histone H4 histidine kinase and the analysis of protein histidine phosphorylation.

Degree: PhD, 2007, University of Western Australia

[Truncated abstract] Protein phosphorylation, one of the most important forms of post-translational modification, has been demonstrated to play crucial roles in regulation of cell function.… (more)

Subjects/Keywords: Protein kinases; Histones; Phosphorylation; Phosphoprotein phosphatases; Histone H4 histidine kinase; Histidine phosphorylation; Mass spectrometry

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APA (6th Edition):

Zu, X. L. (2007). Methods for the detection, purification and characterisation of histone H4 histidine kinase and the analysis of protein histidine phosphorylation. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au/R/-?func=dbin-jump-full&local_base=GEN01-INS01&object_id=8823 ; http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34933&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Zu, Xin Lin. “Methods for the detection, purification and characterisation of histone H4 histidine kinase and the analysis of protein histidine phosphorylation.” 2007. Doctoral Dissertation, University of Western Australia. Accessed November 13, 2019. http://repository.uwa.edu.au/R/-?func=dbin-jump-full&local_base=GEN01-INS01&object_id=8823 ; http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34933&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Zu, Xin Lin. “Methods for the detection, purification and characterisation of histone H4 histidine kinase and the analysis of protein histidine phosphorylation.” 2007. Web. 13 Nov 2019.

Vancouver:

Zu XL. Methods for the detection, purification and characterisation of histone H4 histidine kinase and the analysis of protein histidine phosphorylation. [Internet] [Doctoral dissertation]. University of Western Australia; 2007. [cited 2019 Nov 13]. Available from: http://repository.uwa.edu.au/R/-?func=dbin-jump-full&local_base=GEN01-INS01&object_id=8823 ; http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34933&local_base=GEN01-INS01.

Council of Science Editors:

Zu XL. Methods for the detection, purification and characterisation of histone H4 histidine kinase and the analysis of protein histidine phosphorylation. [Doctoral Dissertation]. University of Western Australia; 2007. Available from: http://repository.uwa.edu.au/R/-?func=dbin-jump-full&local_base=GEN01-INS01&object_id=8823 ; http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34933&local_base=GEN01-INS01


University of Missouri – Columbia

20. Sun, Yaning, 1978-. Proteomic identification of the differentially expressed and phosphorylated proteins in 20-hydroxyecdysone (20E) signal transduction pathway in salivary gland of Drosophila melanogaster.

Degree: 2010, University of Missouri – Columbia

Protein kinase C (PKC) plays important role in 20-hydroxyecdysone (20E) signal transduction, however, little is known about the exact role of PKC in this process.… (more)

Subjects/Keywords: Ecdysteroid; Phosphorylation; Drosophila; Proteomics; Molting; Signal transduction; Protein kinase C; Phosphorylation; Ecdysone; Apoptosis

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APA (6th Edition):

Sun, Yaning, 1. (2010). Proteomic identification of the differentially expressed and phosphorylated proteins in 20-hydroxyecdysone (20E) signal transduction pathway in salivary gland of Drosophila melanogaster. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/41913

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):

Sun, Yaning, 1978-. “Proteomic identification of the differentially expressed and phosphorylated proteins in 20-hydroxyecdysone (20E) signal transduction pathway in salivary gland of Drosophila melanogaster.” 2010. Thesis, University of Missouri – Columbia. Accessed November 13, 2019. http://hdl.handle.net/10355/41913.

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

MLA Handbook (7th Edition):

Sun, Yaning, 1978-. “Proteomic identification of the differentially expressed and phosphorylated proteins in 20-hydroxyecdysone (20E) signal transduction pathway in salivary gland of Drosophila melanogaster.” 2010. Web. 13 Nov 2019.

Vancouver:

Sun, Yaning 1. Proteomic identification of the differentially expressed and phosphorylated proteins in 20-hydroxyecdysone (20E) signal transduction pathway in salivary gland of Drosophila melanogaster. [Internet] [Thesis]. University of Missouri – Columbia; 2010. [cited 2019 Nov 13]. Available from: http://hdl.handle.net/10355/41913.

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

Council of Science Editors:

Sun, Yaning 1. Proteomic identification of the differentially expressed and phosphorylated proteins in 20-hydroxyecdysone (20E) signal transduction pathway in salivary gland of Drosophila melanogaster. [Thesis]. University of Missouri – Columbia; 2010. Available from: http://hdl.handle.net/10355/41913

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


University of Guelph

21. Subasinghe, Renuka. Role and Regulation of Starch Phosphorylase and Starch Synthase IV in Starch Biosynthesis in Maize Endosperm Amyloplasts .

Degree: 2013, University of Guelph

 Storage starch is synthesized in sub-cellular organelles called amyloplasts in higher plants. The synthesis of the starch granule is a result of the coordinated activity… (more)

Subjects/Keywords: Starch biosynthesis; starch phosphorylase; starch synthase IV; protein phosphorylation; protein-protein interactions

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APA (6th Edition):

Subasinghe, R. (2013). Role and Regulation of Starch Phosphorylase and Starch Synthase IV in Starch Biosynthesis in Maize Endosperm Amyloplasts . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5329

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):

Subasinghe, Renuka. “Role and Regulation of Starch Phosphorylase and Starch Synthase IV in Starch Biosynthesis in Maize Endosperm Amyloplasts .” 2013. Thesis, University of Guelph. Accessed November 13, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5329.

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

MLA Handbook (7th Edition):

Subasinghe, Renuka. “Role and Regulation of Starch Phosphorylase and Starch Synthase IV in Starch Biosynthesis in Maize Endosperm Amyloplasts .” 2013. Web. 13 Nov 2019.

Vancouver:

Subasinghe R. Role and Regulation of Starch Phosphorylase and Starch Synthase IV in Starch Biosynthesis in Maize Endosperm Amyloplasts . [Internet] [Thesis]. University of Guelph; 2013. [cited 2019 Nov 13]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5329.

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

Council of Science Editors:

Subasinghe R. Role and Regulation of Starch Phosphorylase and Starch Synthase IV in Starch Biosynthesis in Maize Endosperm Amyloplasts . [Thesis]. University of Guelph; 2013. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5329

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


University of Toledo Health Science Campus

22. Kaliyaperumal, Saravanan. hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?.

Degree: PhD, College of Medicine, 2009, University of Toledo Health Science Campus

 The Mismatch repair (MMR) system maintains genomic stability byrepairing DNA mismatches and insertion-deletion loops (IDLs) resulting from replicationand recombination errors. Defective MMR can lead to… (more)

Subjects/Keywords: Biology; DNA Repair; Protein Phosphorylation; mismatch repair; alkylation damage response; MSH6 Protein Phosphorylation; MNNG damage signaling

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APA (6th Edition):

Kaliyaperumal, S. (2009). hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1242933021

Chicago Manual of Style (16th Edition):

Kaliyaperumal, Saravanan. “hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?.” 2009. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed November 13, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=mco1242933021.

MLA Handbook (7th Edition):

Kaliyaperumal, Saravanan. “hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?.” 2009. Web. 13 Nov 2019.

Vancouver:

Kaliyaperumal S. hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2009. [cited 2019 Nov 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1242933021.

Council of Science Editors:

Kaliyaperumal S. hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1242933021


IUPUI

23. Baird, Thomas. Novel targets of eiF2 kinases determine cell fate during the integrated stress response.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Eukaryotic cells rapidly modulate protein synthesis in response to environmental cues through the reversible phosphorylation of eukaryotic initiation factor 2… (more)

Subjects/Keywords: eIF2 phosphorylation; PERK; Unfolded Protein Response; Integrated Stress Response; IBTK; Proteins  – Synthesis; Phosphorylation; Enzymatic analysis; Protein kinases; Proteins  – Denaturation; G proteins

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APA (6th Edition):

Baird, T. (2014). Novel targets of eiF2 kinases determine cell fate during the integrated stress response. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/6183

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):

Baird, Thomas. “Novel targets of eiF2 kinases determine cell fate during the integrated stress response.” 2014. Thesis, IUPUI. Accessed November 13, 2019. http://hdl.handle.net/1805/6183.

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

MLA Handbook (7th Edition):

Baird, Thomas. “Novel targets of eiF2 kinases determine cell fate during the integrated stress response.” 2014. Web. 13 Nov 2019.

Vancouver:

Baird T. Novel targets of eiF2 kinases determine cell fate during the integrated stress response. [Internet] [Thesis]. IUPUI; 2014. [cited 2019 Nov 13]. Available from: http://hdl.handle.net/1805/6183.

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

Council of Science Editors:

Baird T. Novel targets of eiF2 kinases determine cell fate during the integrated stress response. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/6183

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


University of North Texas

24. Taylor, Allison Antoinette. Regulation of an S6/H4 Kinase in Crude Lymphosarcoma P1798 Preparations.

Degree: 1998, University of North Texas

 Purified S6/H4 kinase (Mr 60,000) requires autophosphorylation for activation. A rabbit anti-S6/H4 kinase peptide (SVIDPVPAPVGDSHVDGAAK) antibody recognized both the S6/H4 kinase holoenzyme and catalytic domain.… (more)

Subjects/Keywords: protein kinases; phosphorylation; lymphomas; Protein kinases.; Phosphorylation.; Lymphomas.

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APA (6th Edition):

Taylor, A. A. (1998). Regulation of an S6/H4 Kinase in Crude Lymphosarcoma P1798 Preparations. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc501281/

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):

Taylor, Allison Antoinette. “Regulation of an S6/H4 Kinase in Crude Lymphosarcoma P1798 Preparations.” 1998. Thesis, University of North Texas. Accessed November 13, 2019. https://digital.library.unt.edu/ark:/67531/metadc501281/.

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

MLA Handbook (7th Edition):

Taylor, Allison Antoinette. “Regulation of an S6/H4 Kinase in Crude Lymphosarcoma P1798 Preparations.” 1998. Web. 13 Nov 2019.

Vancouver:

Taylor AA. Regulation of an S6/H4 Kinase in Crude Lymphosarcoma P1798 Preparations. [Internet] [Thesis]. University of North Texas; 1998. [cited 2019 Nov 13]. Available from: https://digital.library.unt.edu/ark:/67531/metadc501281/.

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

Council of Science Editors:

Taylor AA. Regulation of an S6/H4 Kinase in Crude Lymphosarcoma P1798 Preparations. [Thesis]. University of North Texas; 1998. Available from: https://digital.library.unt.edu/ark:/67531/metadc501281/

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


University of Alberta

25. Wang, Yang. Analysis of Regulatory Mechanisms on RNA Interference by Molecular Chaperone Hsp90 and Protein Phosphorylation in Yeast.

Degree: PhD, Department of Cell Biology, 2016, University of Alberta

 RNA interference (RNAi) is a conserved mechanism that eukaryotes employ small RNAs to regulate gene expression at transcriptional and post-trnascriptiona levels in a sequence-specific manner.… (more)

Subjects/Keywords: RNA interference; Hsp90; Protein phosphorylation; S. cerevisiae; S. pombe

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APA (6th Edition):

Wang, Y. (2016). Analysis of Regulatory Mechanisms on RNA Interference by Molecular Chaperone Hsp90 and Protein Phosphorylation in Yeast. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/c7m01bk91v

Chicago Manual of Style (16th Edition):

Wang, Yang. “Analysis of Regulatory Mechanisms on RNA Interference by Molecular Chaperone Hsp90 and Protein Phosphorylation in Yeast.” 2016. Doctoral Dissertation, University of Alberta. Accessed November 13, 2019. https://era.library.ualberta.ca/files/c7m01bk91v.

MLA Handbook (7th Edition):

Wang, Yang. “Analysis of Regulatory Mechanisms on RNA Interference by Molecular Chaperone Hsp90 and Protein Phosphorylation in Yeast.” 2016. Web. 13 Nov 2019.

Vancouver:

Wang Y. Analysis of Regulatory Mechanisms on RNA Interference by Molecular Chaperone Hsp90 and Protein Phosphorylation in Yeast. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2019 Nov 13]. Available from: https://era.library.ualberta.ca/files/c7m01bk91v.

Council of Science Editors:

Wang Y. Analysis of Regulatory Mechanisms on RNA Interference by Molecular Chaperone Hsp90 and Protein Phosphorylation in Yeast. [Doctoral Dissertation]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/c7m01bk91v


University of Alberta

26. Ceholski, Delaine K. Molecular insights into the disease-causing mechanisms of human phospholamban mutations.

Degree: PhD, Department of Biochemistry, 2012, University of Alberta

 The movement of calcium across sarcoplasmic reticulum (SR) membranes is essential in the contraction-relaxation cycle of muscle. An influx of calcium into the muscle cell… (more)

Subjects/Keywords: phosphorylation by protein kinase A; hereditary mutations in phospholamban; SERCA dysregulation

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APA (6th Edition):

Ceholski, D. K. (2012). Molecular insights into the disease-causing mechanisms of human phospholamban mutations. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/fn1070088

Chicago Manual of Style (16th Edition):

Ceholski, Delaine K. “Molecular insights into the disease-causing mechanisms of human phospholamban mutations.” 2012. Doctoral Dissertation, University of Alberta. Accessed November 13, 2019. https://era.library.ualberta.ca/files/fn1070088.

MLA Handbook (7th Edition):

Ceholski, Delaine K. “Molecular insights into the disease-causing mechanisms of human phospholamban mutations.” 2012. Web. 13 Nov 2019.

Vancouver:

Ceholski DK. Molecular insights into the disease-causing mechanisms of human phospholamban mutations. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2019 Nov 13]. Available from: https://era.library.ualberta.ca/files/fn1070088.

Council of Science Editors:

Ceholski DK. Molecular insights into the disease-causing mechanisms of human phospholamban mutations. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/fn1070088


University of Cincinnati

27. Qian, Jiang. The Role of Small Heat Shock Protein 20 and Its Phosphorylation in the Regulation of Cardiac Function and Ischemia/Reperfusion Injury.

Degree: PhD, Medicine : Molecular, Cellular and Biochemical Pharmacology, 2010, University of Cincinnati

  The small heat shock protein (sHsp) with apparent molecular mass of 20 kD (Hsp20) is one of 10 members of the sHsp family. Interestingly,… (more)

Subjects/Keywords: Pharmacology; heat shock protein; phosphorylation; cardiac; contractility; ischemia/reperfusion injury

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APA (6th Edition):

Qian, J. (2010). The Role of Small Heat Shock Protein 20 and Its Phosphorylation in the Regulation of Cardiac Function and Ischemia/Reperfusion Injury. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1273168811

Chicago Manual of Style (16th Edition):

Qian, Jiang. “The Role of Small Heat Shock Protein 20 and Its Phosphorylation in the Regulation of Cardiac Function and Ischemia/Reperfusion Injury.” 2010. Doctoral Dissertation, University of Cincinnati. Accessed November 13, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1273168811.

MLA Handbook (7th Edition):

Qian, Jiang. “The Role of Small Heat Shock Protein 20 and Its Phosphorylation in the Regulation of Cardiac Function and Ischemia/Reperfusion Injury.” 2010. Web. 13 Nov 2019.

Vancouver:

Qian J. The Role of Small Heat Shock Protein 20 and Its Phosphorylation in the Regulation of Cardiac Function and Ischemia/Reperfusion Injury. [Internet] [Doctoral dissertation]. University of Cincinnati; 2010. [cited 2019 Nov 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1273168811.

Council of Science Editors:

Qian J. The Role of Small Heat Shock Protein 20 and Its Phosphorylation in the Regulation of Cardiac Function and Ischemia/Reperfusion Injury. [Doctoral Dissertation]. University of Cincinnati; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1273168811


University of Cincinnati

28. Swaminathan, Karthikeyan. Enhanced prediction of Phosphorylation and Disorder in Proteins.

Degree: PhD, Engineering : Biomedical Engineering, 2009, University of Cincinnati

 Over the years, many predictors of structural and functional properties of proteins have beendeveloped on the basis that this information is encoded in the protein(more)

Subjects/Keywords: Biomedical Research; phosphorylation; protein disorder; b-factors; solvent accessibility; prediction

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APA (6th Edition):

Swaminathan, K. (2009). Enhanced prediction of Phosphorylation and Disorder in Proteins. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1259080387

Chicago Manual of Style (16th Edition):

Swaminathan, Karthikeyan. “Enhanced prediction of Phosphorylation and Disorder in Proteins.” 2009. Doctoral Dissertation, University of Cincinnati. Accessed November 13, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1259080387.

MLA Handbook (7th Edition):

Swaminathan, Karthikeyan. “Enhanced prediction of Phosphorylation and Disorder in Proteins.” 2009. Web. 13 Nov 2019.

Vancouver:

Swaminathan K. Enhanced prediction of Phosphorylation and Disorder in Proteins. [Internet] [Doctoral dissertation]. University of Cincinnati; 2009. [cited 2019 Nov 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1259080387.

Council of Science Editors:

Swaminathan K. Enhanced prediction of Phosphorylation and Disorder in Proteins. [Doctoral Dissertation]. University of Cincinnati; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1259080387


NSYSU

29. Yen, Yi-Chen. Molecular Interaction of Tau and Microtubule.

Degree: Master, Institute of Biomedical Sciences, 2002, NSYSU

 Tau protein is one of the microtubule-associated proteins (MAPs) and mainly expressed in neuronal cells. It hasbeen demonstrated that Tau may play an important role… (more)

Subjects/Keywords: phosphorylation; tau protein; microtubule

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

APA (6th Edition):

Yen, Y. (2002). Molecular Interaction of Tau and Microtubule. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0821102-151102

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):

Yen, Yi-Chen. “Molecular Interaction of Tau and Microtubule.” 2002. Thesis, NSYSU. Accessed November 13, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0821102-151102.

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

MLA Handbook (7th Edition):

Yen, Yi-Chen. “Molecular Interaction of Tau and Microtubule.” 2002. Web. 13 Nov 2019.

Vancouver:

Yen Y. Molecular Interaction of Tau and Microtubule. [Internet] [Thesis]. NSYSU; 2002. [cited 2019 Nov 13]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0821102-151102.

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

Council of Science Editors:

Yen Y. Molecular Interaction of Tau and Microtubule. [Thesis]. NSYSU; 2002. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0821102-151102

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


University of Hong Kong

30. Zhu, Kaiyuan. Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell.

Degree: M. Phil., 2014, University of Hong Kong

published_or_final_version

Physiology

Master

Master of Philosophy

Subjects/Keywords: Phosphorylation; Mitosis; Protein kinase

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

APA (6th Edition):

Zhu, K. (2014). Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell. (Masters Thesis). University of Hong Kong. Retrieved from Zhu, K. [祝开元]. (2014). Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5351051 ; http://dx.doi.org/10.5353/th_b5351051 ; http://hdl.handle.net/10722/208019

Chicago Manual of Style (16th Edition):

Zhu, Kaiyuan. “Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell.” 2014. Masters Thesis, University of Hong Kong. Accessed November 13, 2019. Zhu, K. [祝开元]. (2014). Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5351051 ; http://dx.doi.org/10.5353/th_b5351051 ; http://hdl.handle.net/10722/208019.

MLA Handbook (7th Edition):

Zhu, Kaiyuan. “Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell.” 2014. Web. 13 Nov 2019.

Vancouver:

Zhu K. Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2019 Nov 13]. Available from: Zhu, K. [祝开元]. (2014). Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5351051 ; http://dx.doi.org/10.5353/th_b5351051 ; http://hdl.handle.net/10722/208019.

Council of Science Editors:

Zhu K. Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell. [Masters Thesis]. University of Hong Kong; 2014. Available from: Zhu, K. [祝开元]. (2014). Polo-like kinase 1 (Plk1) phosphorylates VCP T76 during mitosis for the fragmentation of Golgi in mammalian cell. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5351051 ; http://dx.doi.org/10.5353/th_b5351051 ; http://hdl.handle.net/10722/208019

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