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You searched for subject:(Phosphoprotein phosphatases). Showing records 1 – 30 of 31 total matches.

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Hong Kong University of Science and Technology

1. Huang, Huiqian LIFS. Role of liprinα1 in activity-dependent synapse development.

Degree: 2016, Hong Kong University of Science and Technology

 Neuronal activity plays an essential role in guiding synapse development, which underlies the experience-dependent shaping of brain circuitry. Synapse development requires the concerted regulation of… (more)

Subjects/Keywords: Synapses ; Growth ; Nerve growth factor ; Phosphoprotein phosphatases

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APA (6th Edition):

Huang, H. L. (2016). Role of liprinα1 in activity-dependent synapse development. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-97101 ; https://doi.org/10.14711/thesis-b1585226 ; http://repository.ust.hk/ir/bitstream/1783.1-97101/1/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):

Huang, Huiqian LIFS. “Role of liprinα1 in activity-dependent synapse development.” 2016. Thesis, Hong Kong University of Science and Technology. Accessed April 15, 2021. http://repository.ust.hk/ir/Record/1783.1-97101 ; https://doi.org/10.14711/thesis-b1585226 ; http://repository.ust.hk/ir/bitstream/1783.1-97101/1/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):

Huang, Huiqian LIFS. “Role of liprinα1 in activity-dependent synapse development.” 2016. Web. 15 Apr 2021.

Vancouver:

Huang HL. Role of liprinα1 in activity-dependent synapse development. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2016. [cited 2021 Apr 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-97101 ; https://doi.org/10.14711/thesis-b1585226 ; http://repository.ust.hk/ir/bitstream/1783.1-97101/1/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:

Huang HL. Role of liprinα1 in activity-dependent synapse development. [Thesis]. Hong Kong University of Science and Technology; 2016. Available from: http://repository.ust.hk/ir/Record/1783.1-97101 ; https://doi.org/10.14711/thesis-b1585226 ; http://repository.ust.hk/ir/bitstream/1783.1-97101/1/th_redirect.html

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


University of Texas Southwestern Medical Center

2. Clark, Catherine Renee. Regulation of Hepatic Glycogen Metabolism by Glycogen Targeting Subunits of Protein Phosphatase 1.

Degree: 2007, University of Texas Southwestern Medical Center

 Glycogen targeting subunits of protein phosphatase 1 play a critical role in fuel homeostasis through the regulation of glycogen metabolism. Adenovirus-mediated overexpression of the liver… (more)

Subjects/Keywords: Glucose; Liver Glycogen; Phosphoprotein Phosphatases

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APA (6th Edition):

Clark, C. R. (2007). Regulation of Hepatic Glycogen Metabolism by Glycogen Targeting Subunits of Protein Phosphatase 1. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/829

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):

Clark, Catherine Renee. “Regulation of Hepatic Glycogen Metabolism by Glycogen Targeting Subunits of Protein Phosphatase 1.” 2007. Thesis, University of Texas Southwestern Medical Center. Accessed April 15, 2021. http://hdl.handle.net/2152.5/829.

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

MLA Handbook (7th Edition):

Clark, Catherine Renee. “Regulation of Hepatic Glycogen Metabolism by Glycogen Targeting Subunits of Protein Phosphatase 1.” 2007. Web. 15 Apr 2021.

Vancouver:

Clark CR. Regulation of Hepatic Glycogen Metabolism by Glycogen Targeting Subunits of Protein Phosphatase 1. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2007. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2152.5/829.

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

Council of Science Editors:

Clark CR. Regulation of Hepatic Glycogen Metabolism by Glycogen Targeting Subunits of Protein Phosphatase 1. [Thesis]. University of Texas Southwestern Medical Center; 2007. Available from: http://hdl.handle.net/2152.5/829

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


University of Texas Southwestern Medical Center

3. Bembenek, Joshua Nathaniel. CDC14 Coordinates Cyclin Destruction with the Onset of Cytokinesis.

Degree: 2004, University of Texas Southwestern Medical Center

 The Cdc14 family of protein phosphatases operate during the final stages of mitosis in various organisms. The Cdc14 phosphatases are downstream components of two homologous… (more)

Subjects/Keywords: Phosphoprotein Phosphatases; Cytokinesis; Signal Transduction

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APA (6th Edition):

Bembenek, J. N. (2004). CDC14 Coordinates Cyclin Destruction with the Onset of Cytokinesis. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/556

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):

Bembenek, Joshua Nathaniel. “CDC14 Coordinates Cyclin Destruction with the Onset of Cytokinesis.” 2004. Thesis, University of Texas Southwestern Medical Center. Accessed April 15, 2021. http://hdl.handle.net/2152.5/556.

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

MLA Handbook (7th Edition):

Bembenek, Joshua Nathaniel. “CDC14 Coordinates Cyclin Destruction with the Onset of Cytokinesis.” 2004. Web. 15 Apr 2021.

Vancouver:

Bembenek JN. CDC14 Coordinates Cyclin Destruction with the Onset of Cytokinesis. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2004. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2152.5/556.

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

Council of Science Editors:

Bembenek JN. CDC14 Coordinates Cyclin Destruction with the Onset of Cytokinesis. [Thesis]. University of Texas Southwestern Medical Center; 2004. Available from: http://hdl.handle.net/2152.5/556

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

4. Chan, Shing Fai. Association of the serine/threonine protein phosphatase 2A with the N-methyl-D-aspartate receptor subunit NR3A.

Degree: 1999, Hong Kong University of Science and Technology

 The N-methyl-D-aspartic acid (NMDA) subclass of excitatory ionotropic glutamate receptors plays critical roles in neuronal development, plasticity and cell death. The NMDA receptors are thought… (more)

Subjects/Keywords: Methyl aspartate  – Receptors ; Phosphoprotein phosphatases

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APA (6th Edition):

Chan, S. F. (1999). Association of the serine/threonine protein phosphatase 2A with the N-methyl-D-aspartate receptor subunit NR3A. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-3858 ; https://doi.org/10.14711/thesis-b647129 ; http://repository.ust.hk/ir/bitstream/1783.1-3858/1/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):

Chan, Shing Fai. “Association of the serine/threonine protein phosphatase 2A with the N-methyl-D-aspartate receptor subunit NR3A.” 1999. Thesis, Hong Kong University of Science and Technology. Accessed April 15, 2021. http://repository.ust.hk/ir/Record/1783.1-3858 ; https://doi.org/10.14711/thesis-b647129 ; http://repository.ust.hk/ir/bitstream/1783.1-3858/1/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):

Chan, Shing Fai. “Association of the serine/threonine protein phosphatase 2A with the N-methyl-D-aspartate receptor subunit NR3A.” 1999. Web. 15 Apr 2021.

Vancouver:

Chan SF. Association of the serine/threonine protein phosphatase 2A with the N-methyl-D-aspartate receptor subunit NR3A. [Internet] [Thesis]. Hong Kong University of Science and Technology; 1999. [cited 2021 Apr 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-3858 ; https://doi.org/10.14711/thesis-b647129 ; http://repository.ust.hk/ir/bitstream/1783.1-3858/1/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:

Chan SF. Association of the serine/threonine protein phosphatase 2A with the N-methyl-D-aspartate receptor subunit NR3A. [Thesis]. Hong Kong University of Science and Technology; 1999. Available from: http://repository.ust.hk/ir/Record/1783.1-3858 ; https://doi.org/10.14711/thesis-b647129 ; http://repository.ust.hk/ir/bitstream/1783.1-3858/1/th_redirect.html

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

5. Pan, Ming-gui. Protein-tyrosine phosphatases : regulation of cell growth and differentiation.

Degree: PhD, 1993, Oregon Health Sciences University

Subjects/Keywords: Protein-Tyrosine-Phosphatases; Phosphoprotein Phosphatases; Cell Division; Cell Differentiation

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APA (6th Edition):

Pan, M. (1993). Protein-tyrosine phosphatases : regulation of cell growth and differentiation. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4P55KQ3 ; http://digitalcommons.ohsu.edu/etd/2843

Chicago Manual of Style (16th Edition):

Pan, Ming-gui. “Protein-tyrosine phosphatases : regulation of cell growth and differentiation.” 1993. Doctoral Dissertation, Oregon Health Sciences University. Accessed April 15, 2021. doi:10.6083/M4P55KQ3 ; http://digitalcommons.ohsu.edu/etd/2843.

MLA Handbook (7th Edition):

Pan, Ming-gui. “Protein-tyrosine phosphatases : regulation of cell growth and differentiation.” 1993. Web. 15 Apr 2021.

Vancouver:

Pan M. Protein-tyrosine phosphatases : regulation of cell growth and differentiation. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1993. [cited 2021 Apr 15]. Available from: doi:10.6083/M4P55KQ3 ; http://digitalcommons.ohsu.edu/etd/2843.

Council of Science Editors:

Pan M. Protein-tyrosine phosphatases : regulation of cell growth and differentiation. [Doctoral Dissertation]. Oregon Health Sciences University; 1993. Available from: doi:10.6083/M4P55KQ3 ; http://digitalcommons.ohsu.edu/etd/2843


Hong Kong University of Science and Technology

6. Shu, Yiwei. Phosphorylated ERF110 regulates arabidopsis inflorescence number and etiolated hypocotyl length.

Degree: 2010, Hong Kong University of Science and Technology

 Protein phosphorylation plays an essential role in nearly all aspects of life cycle. Ethylene linear signal pathway has been established through molecular genetic studies on… (more)

Subjects/Keywords: Phosphoprotein phosphatases ; Ethylene ; Synthesis ; Peptides ; Analysis

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APA (6th Edition):

Shu, Y. (2010). Phosphorylated ERF110 regulates arabidopsis inflorescence number and etiolated hypocotyl length. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-8056 ; https://doi.org/10.14711/thesis-b1115579 ; http://repository.ust.hk/ir/bitstream/1783.1-8056/1/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):

Shu, Yiwei. “Phosphorylated ERF110 regulates arabidopsis inflorescence number and etiolated hypocotyl length.” 2010. Thesis, Hong Kong University of Science and Technology. Accessed April 15, 2021. http://repository.ust.hk/ir/Record/1783.1-8056 ; https://doi.org/10.14711/thesis-b1115579 ; http://repository.ust.hk/ir/bitstream/1783.1-8056/1/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):

Shu, Yiwei. “Phosphorylated ERF110 regulates arabidopsis inflorescence number and etiolated hypocotyl length.” 2010. Web. 15 Apr 2021.

Vancouver:

Shu Y. Phosphorylated ERF110 regulates arabidopsis inflorescence number and etiolated hypocotyl length. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2010. [cited 2021 Apr 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-8056 ; https://doi.org/10.14711/thesis-b1115579 ; http://repository.ust.hk/ir/bitstream/1783.1-8056/1/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:

Shu Y. Phosphorylated ERF110 regulates arabidopsis inflorescence number and etiolated hypocotyl length. [Thesis]. Hong Kong University of Science and Technology; 2010. Available from: http://repository.ust.hk/ir/Record/1783.1-8056 ; https://doi.org/10.14711/thesis-b1115579 ; http://repository.ust.hk/ir/bitstream/1783.1-8056/1/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

7. Zhao, Xiaotao. The role of protein phosphatase signaling in the formation of the neuromuscular junction.

Degree: 2004, Hong Kong University of Science and Technology

 The neuromuscular junction (NMJ) is the synapse formed between a motor nerve and a muscle cell. A hallmark step in NMJ development is the postsynaptic… (more)

Subjects/Keywords: Myoneural junction ; Neuromuscular transmission ; Phosphoprotein phosphatases

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APA (6th Edition):

Zhao, X. (2004). The role of protein phosphatase signaling in the formation of the neuromuscular junction. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-2221 ; https://doi.org/10.14711/thesis-b843346 ; http://repository.ust.hk/ir/bitstream/1783.1-2221/1/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):

Zhao, Xiaotao. “The role of protein phosphatase signaling in the formation of the neuromuscular junction.” 2004. Thesis, Hong Kong University of Science and Technology. Accessed April 15, 2021. http://repository.ust.hk/ir/Record/1783.1-2221 ; https://doi.org/10.14711/thesis-b843346 ; http://repository.ust.hk/ir/bitstream/1783.1-2221/1/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):

Zhao, Xiaotao. “The role of protein phosphatase signaling in the formation of the neuromuscular junction.” 2004. Web. 15 Apr 2021.

Vancouver:

Zhao X. The role of protein phosphatase signaling in the formation of the neuromuscular junction. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2004. [cited 2021 Apr 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-2221 ; https://doi.org/10.14711/thesis-b843346 ; http://repository.ust.hk/ir/bitstream/1783.1-2221/1/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:

Zhao X. The role of protein phosphatase signaling in the formation of the neuromuscular junction. [Thesis]. Hong Kong University of Science and Technology; 2004. Available from: http://repository.ust.hk/ir/Record/1783.1-2221 ; https://doi.org/10.14711/thesis-b843346 ; http://repository.ust.hk/ir/bitstream/1783.1-2221/1/th_redirect.html

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


Michigan State University

8. Lindesmith, Lisa Chon. YopH is degraded into fragments that retain protein tyrosine phosphatase activity in Yersinia pestis.

Degree: MS, Department of Microbiology, 1993, Michigan State University

Subjects/Keywords: Yersinia pestis; Bacterial proteins; Phosphoprotein phosphatases

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APA (6th Edition):

Lindesmith, L. C. (1993). YopH is degraded into fragments that retain protein tyrosine phosphatase activity in Yersinia pestis. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:23272

Chicago Manual of Style (16th Edition):

Lindesmith, Lisa Chon. “YopH is degraded into fragments that retain protein tyrosine phosphatase activity in Yersinia pestis.” 1993. Masters Thesis, Michigan State University. Accessed April 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:23272.

MLA Handbook (7th Edition):

Lindesmith, Lisa Chon. “YopH is degraded into fragments that retain protein tyrosine phosphatase activity in Yersinia pestis.” 1993. Web. 15 Apr 2021.

Vancouver:

Lindesmith LC. YopH is degraded into fragments that retain protein tyrosine phosphatase activity in Yersinia pestis. [Internet] [Masters thesis]. Michigan State University; 1993. [cited 2021 Apr 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:23272.

Council of Science Editors:

Lindesmith LC. YopH is degraded into fragments that retain protein tyrosine phosphatase activity in Yersinia pestis. [Masters Thesis]. Michigan State University; 1993. Available from: http://etd.lib.msu.edu/islandora/object/etd:23272


University of Texas Southwestern Medical Center

9. Esplin, Edward D. Characterization of the Role of the PP2A-AB Gene, a Putative Tumor Suppressor, in Cell Growth and Tumorigenesis.

Degree: 2005, University of Texas Southwestern Medical Center

 The PP2A-Aβ gene (PPP2R1B) encodes the β isoform of the A subunit of serine/threonine protein phosphatase 2A. Mutations in PP2A-Aβ have been identified in a… (more)

Subjects/Keywords: Tumorigenesis; Cell Transformation, Neoplastic; Phosphoprotein Phosphatases; Breast Neoplasms

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APA (6th Edition):

Esplin, E. D. (2005). Characterization of the Role of the PP2A-AB Gene, a Putative Tumor Suppressor, in Cell Growth and Tumorigenesis. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/418

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):

Esplin, Edward D. “Characterization of the Role of the PP2A-AB Gene, a Putative Tumor Suppressor, in Cell Growth and Tumorigenesis.” 2005. Thesis, University of Texas Southwestern Medical Center. Accessed April 15, 2021. http://hdl.handle.net/2152.5/418.

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

MLA Handbook (7th Edition):

Esplin, Edward D. “Characterization of the Role of the PP2A-AB Gene, a Putative Tumor Suppressor, in Cell Growth and Tumorigenesis.” 2005. Web. 15 Apr 2021.

Vancouver:

Esplin ED. Characterization of the Role of the PP2A-AB Gene, a Putative Tumor Suppressor, in Cell Growth and Tumorigenesis. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2005. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2152.5/418.

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

Council of Science Editors:

Esplin ED. Characterization of the Role of the PP2A-AB Gene, a Putative Tumor Suppressor, in Cell Growth and Tumorigenesis. [Thesis]. University of Texas Southwestern Medical Center; 2005. Available from: http://hdl.handle.net/2152.5/418

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


University of Texas Southwestern Medical Center

10. McNamara, Ryan Philip. Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes.

Degree: 2015, University of Texas Southwestern Medical Center

 Gene expression of the human immunodeficiency virus (HIV) and cellular primary responsive genes (PRG’s) is regulated at the step of transcription elongation. Shortly after transcription… (more)

Subjects/Keywords: Phosphoprotein Phosphatases; Positive Transcriptional Elongation Factor B; Promoter Regions, Genetic; Ribonucleoproteins, Small Nuclear; Transcription Elongation, Genetic

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APA (6th Edition):

McNamara, R. P. (2015). Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/2724

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):

McNamara, Ryan Philip. “Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed April 15, 2021. http://hdl.handle.net/2152.5/2724.

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

MLA Handbook (7th Edition):

McNamara, Ryan Philip. “Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes.” 2015. Web. 15 Apr 2021.

Vancouver:

McNamara RP. Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2152.5/2724.

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

Council of Science Editors:

McNamara RP. Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/2724

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

11. Zhou, Jie. Functions of tyrosine kinases and phosphatases in presynaptic development during neuromuscular junction formation.

Degree: 2007, Hong Kong University of Science and Technology

 The neuromuscular junction (NMJ), a chemical synapse formed between a motoneuron and a muscle fiber, has been widely and successfully utilized in studying chemical synapses.… (more)

Subjects/Keywords: Myoneural junction ; Protein-tyrosine kinase ; Phosphoprotein phosphatases ; Presynaptic receptors

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APA (6th Edition):

Zhou, J. (2007). Functions of tyrosine kinases and phosphatases in presynaptic development during neuromuscular junction formation. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-2874 ; https://doi.org/10.14711/thesis-b943606 ; http://repository.ust.hk/ir/bitstream/1783.1-2874/1/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):

Zhou, Jie. “Functions of tyrosine kinases and phosphatases in presynaptic development during neuromuscular junction formation.” 2007. Thesis, Hong Kong University of Science and Technology. Accessed April 15, 2021. http://repository.ust.hk/ir/Record/1783.1-2874 ; https://doi.org/10.14711/thesis-b943606 ; http://repository.ust.hk/ir/bitstream/1783.1-2874/1/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):

Zhou, Jie. “Functions of tyrosine kinases and phosphatases in presynaptic development during neuromuscular junction formation.” 2007. Web. 15 Apr 2021.

Vancouver:

Zhou J. Functions of tyrosine kinases and phosphatases in presynaptic development during neuromuscular junction formation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2007. [cited 2021 Apr 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-2874 ; https://doi.org/10.14711/thesis-b943606 ; http://repository.ust.hk/ir/bitstream/1783.1-2874/1/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:

Zhou J. Functions of tyrosine kinases and phosphatases in presynaptic development during neuromuscular junction formation. [Thesis]. Hong Kong University of Science and Technology; 2007. Available from: http://repository.ust.hk/ir/Record/1783.1-2874 ; https://doi.org/10.14711/thesis-b943606 ; http://repository.ust.hk/ir/bitstream/1783.1-2874/1/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

12. Ng, Wai Sun. Multi-functions of the PP2A domain of axin.

Degree: 2004, Hong Kong University of Science and Technology

 Axin serves as a scaffold protein in Wnt signaling pathway to negatively regulate the stability of β-catenin, and it also facilitates the c-Jun N-terminal/stress-activated protein… (more)

Subjects/Keywords: Protein-protein interactions ; Protein binding ; Phosphoprotein phosphatases

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APA (6th Edition):

Ng, W. S. (2004). Multi-functions of the PP2A domain of axin. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-3764 ; https://doi.org/10.14711/thesis-b839570 ; http://repository.ust.hk/ir/bitstream/1783.1-3764/1/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):

Ng, Wai Sun. “Multi-functions of the PP2A domain of axin.” 2004. Thesis, Hong Kong University of Science and Technology. Accessed April 15, 2021. http://repository.ust.hk/ir/Record/1783.1-3764 ; https://doi.org/10.14711/thesis-b839570 ; http://repository.ust.hk/ir/bitstream/1783.1-3764/1/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):

Ng, Wai Sun. “Multi-functions of the PP2A domain of axin.” 2004. Web. 15 Apr 2021.

Vancouver:

Ng WS. Multi-functions of the PP2A domain of axin. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2004. [cited 2021 Apr 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-3764 ; https://doi.org/10.14711/thesis-b839570 ; http://repository.ust.hk/ir/bitstream/1783.1-3764/1/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:

Ng WS. Multi-functions of the PP2A domain of axin. [Thesis]. Hong Kong University of Science and Technology; 2004. Available from: http://repository.ust.hk/ir/Record/1783.1-3764 ; https://doi.org/10.14711/thesis-b839570 ; http://repository.ust.hk/ir/bitstream/1783.1-3764/1/th_redirect.html

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


Florida Atlantic University

13. Lee, LaTasha Hoskins. Characterization of receptor protein tyrosine phosphatase PTP69D in the giant fiber circuit.

Degree: 2014, Florida Atlantic University

Summary: PTP69D is a receptor protein tyrosine phosphatase (RPTP) with two intracellular catalytic domains (Cat1 and Cat2), which has been shown to play a role… (more)

Subjects/Keywords: Drosophila melanogaster.; Protein-tyrosine phosphatase – Metabolism.; Protein-tyrosine kinase.; Protein kinases – Inhibitors.; Phosphoprotein phosphatases.; Transcription factors.; Cell receptors.; Cellular signal transduction.

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APA (6th Edition):

Lee, L. H. (2014). Characterization of receptor protein tyrosine phosphatase PTP69D in the giant fiber circuit. (Thesis). Florida Atlantic University. Retrieved from http://purl.flvc.org/fau/fd/FA00004301 ; (URL) http://purl.flvc.org/fau/fd/FA00004301

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):

Lee, LaTasha Hoskins. “Characterization of receptor protein tyrosine phosphatase PTP69D in the giant fiber circuit.” 2014. Thesis, Florida Atlantic University. Accessed April 15, 2021. http://purl.flvc.org/fau/fd/FA00004301 ; (URL) http://purl.flvc.org/fau/fd/FA00004301.

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

MLA Handbook (7th Edition):

Lee, LaTasha Hoskins. “Characterization of receptor protein tyrosine phosphatase PTP69D in the giant fiber circuit.” 2014. Web. 15 Apr 2021.

Vancouver:

Lee LH. Characterization of receptor protein tyrosine phosphatase PTP69D in the giant fiber circuit. [Internet] [Thesis]. Florida Atlantic University; 2014. [cited 2021 Apr 15]. Available from: http://purl.flvc.org/fau/fd/FA00004301 ; (URL) http://purl.flvc.org/fau/fd/FA00004301.

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

Council of Science Editors:

Lee LH. Characterization of receptor protein tyrosine phosphatase PTP69D in the giant fiber circuit. [Thesis]. Florida Atlantic University; 2014. Available from: http://purl.flvc.org/fau/fd/FA00004301 ; (URL) http://purl.flvc.org/fau/fd/FA00004301

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


Michigan State University

14. Zhai, Yifan. Characterization of protein tyrosine phosphatases in human breast epithelial cells neoplastically transformed by the NEU oncogene : the potential role as a tumor suppressor.

Degree: PhD, Department of Pharmacology and Toxicology, 1993, Michigan State University

Subjects/Keywords: Phosphoprotein phosphatases; Oncogenes; Breast – Cancer; Tyrosine – Physiological effect

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APA (6th Edition):

Zhai, Y. (1993). Characterization of protein tyrosine phosphatases in human breast epithelial cells neoplastically transformed by the NEU oncogene : the potential role as a tumor suppressor. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:22489

Chicago Manual of Style (16th Edition):

Zhai, Yifan. “Characterization of protein tyrosine phosphatases in human breast epithelial cells neoplastically transformed by the NEU oncogene : the potential role as a tumor suppressor.” 1993. Doctoral Dissertation, Michigan State University. Accessed April 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:22489.

MLA Handbook (7th Edition):

Zhai, Yifan. “Characterization of protein tyrosine phosphatases in human breast epithelial cells neoplastically transformed by the NEU oncogene : the potential role as a tumor suppressor.” 1993. Web. 15 Apr 2021.

Vancouver:

Zhai Y. Characterization of protein tyrosine phosphatases in human breast epithelial cells neoplastically transformed by the NEU oncogene : the potential role as a tumor suppressor. [Internet] [Doctoral dissertation]. Michigan State University; 1993. [cited 2021 Apr 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:22489.

Council of Science Editors:

Zhai Y. Characterization of protein tyrosine phosphatases in human breast epithelial cells neoplastically transformed by the NEU oncogene : the potential role as a tumor suppressor. [Doctoral Dissertation]. Michigan State University; 1993. Available from: http://etd.lib.msu.edu/islandora/object/etd:22489


University of Lethbridge

15. Lanser, Brittany. Characterization of checkpoint adaptation in human fibroblastic glioma cells and an analysis of protein phosphatase inhibitors .

Degree: 2012, University of Lethbridge

 This thesis reports that checkpoint adaptation occurs in human brain cancer cells. M059K cells, after treatment with camptothecin (CPT), recruited γ-histone H2AX, phosphorylated Chk1 and… (more)

Subjects/Keywords: Gliomas; Cancer cells  – Adaptation; Brain  – Tumors; Cellular control mechanisms; Cell cycle  – Regulation; Phosphoprotein phosphatases; Dissertations, Academic

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APA (6th Edition):

Lanser, B. (2012). Characterization of checkpoint adaptation in human fibroblastic glioma cells and an analysis of protein phosphatase inhibitors . (Thesis). University of Lethbridge. Retrieved from http://hdl.handle.net/10133/3390

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):

Lanser, Brittany. “Characterization of checkpoint adaptation in human fibroblastic glioma cells and an analysis of protein phosphatase inhibitors .” 2012. Thesis, University of Lethbridge. Accessed April 15, 2021. http://hdl.handle.net/10133/3390.

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

MLA Handbook (7th Edition):

Lanser, Brittany. “Characterization of checkpoint adaptation in human fibroblastic glioma cells and an analysis of protein phosphatase inhibitors .” 2012. Web. 15 Apr 2021.

Vancouver:

Lanser B. Characterization of checkpoint adaptation in human fibroblastic glioma cells and an analysis of protein phosphatase inhibitors . [Internet] [Thesis]. University of Lethbridge; 2012. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10133/3390.

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

Council of Science Editors:

Lanser B. Characterization of checkpoint adaptation in human fibroblastic glioma cells and an analysis of protein phosphatase inhibitors . [Thesis]. University of Lethbridge; 2012. Available from: http://hdl.handle.net/10133/3390

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


University of New South Wales

16. Holst, Jeffrey Alexander. Regulation of mast cell secretion by protein phosphatase 1 and 2A.

Degree: Medicine. Clinical School - St Vincent's Hospital, 2003, University of New South Wales

Subjects/Keywords: Phosphoprotein phosphatases; Mast cells; Thesis Digitisation Program

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APA (6th Edition):

Holst, J. A. (2003). Regulation of mast cell secretion by protein phosphatase 1 and 2A. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/69362 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:70741/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Holst, Jeffrey Alexander. “Regulation of mast cell secretion by protein phosphatase 1 and 2A.” 2003. Doctoral Dissertation, University of New South Wales. Accessed April 15, 2021. http://handle.unsw.edu.au/1959.4/69362 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:70741/SOURCE01?view=true.

MLA Handbook (7th Edition):

Holst, Jeffrey Alexander. “Regulation of mast cell secretion by protein phosphatase 1 and 2A.” 2003. Web. 15 Apr 2021.

Vancouver:

Holst JA. Regulation of mast cell secretion by protein phosphatase 1 and 2A. [Internet] [Doctoral dissertation]. University of New South Wales; 2003. [cited 2021 Apr 15]. Available from: http://handle.unsw.edu.au/1959.4/69362 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:70741/SOURCE01?view=true.

Council of Science Editors:

Holst JA. Regulation of mast cell secretion by protein phosphatase 1 and 2A. [Doctoral Dissertation]. University of New South Wales; 2003. Available from: http://handle.unsw.edu.au/1959.4/69362 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:70741/SOURCE01?view=true


East Carolina University

17. DeVaul, Nicole. PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics.

Degree: PhD, Anatomy and Cell Biology, 2014, East Carolina University

 The centrosome is a dynamic structure that undergoes structural and functional transitions, which are coordinated with the cell cycle. It functions as the microtubule organizing… (more)

Subjects/Keywords: Cellular biology; Aurora A; Centrosome; Cilia; Nek2; PP1; PPP1R42; Neoplasms; Phosphoprotein Phosphatases – physiology; Protein-Serine-Threonine Kinases – physiology; Centrosome – physiology

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APA (6th Edition):

DeVaul, N. (2014). PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics. (Doctoral Dissertation). East Carolina University. Retrieved from http://hdl.handle.net/10342/4670

Chicago Manual of Style (16th Edition):

DeVaul, Nicole. “PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics.” 2014. Doctoral Dissertation, East Carolina University. Accessed April 15, 2021. http://hdl.handle.net/10342/4670.

MLA Handbook (7th Edition):

DeVaul, Nicole. “PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics.” 2014. Web. 15 Apr 2021.

Vancouver:

DeVaul N. PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics. [Internet] [Doctoral dissertation]. East Carolina University; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10342/4670.

Council of Science Editors:

DeVaul N. PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics. [Doctoral Dissertation]. East Carolina University; 2014. Available from: http://hdl.handle.net/10342/4670

18. Fjeld, Clark Charles. The catalytic mechanism of human serine.

Degree: MS, 1999, Oregon Health Sciences University

Subjects/Keywords: Phosphoprotein Phosphatases; Phosphorylation; Catalysis; Serine  – chemistry; Threonine  – chemistry; Metalloproteins  – chemistry

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APA (6th Edition):

Fjeld, C. C. (1999). The catalytic mechanism of human serine. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M42N50KH ; http://digitalcommons.ohsu.edu/etd/3375

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):

Fjeld, Clark Charles. “The catalytic mechanism of human serine.” 1999. Thesis, Oregon Health Sciences University. Accessed April 15, 2021. doi:10.6083/M42N50KH ; http://digitalcommons.ohsu.edu/etd/3375.

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

MLA Handbook (7th Edition):

Fjeld, Clark Charles. “The catalytic mechanism of human serine.” 1999. Web. 15 Apr 2021.

Vancouver:

Fjeld CC. The catalytic mechanism of human serine. [Internet] [Thesis]. Oregon Health Sciences University; 1999. [cited 2021 Apr 15]. Available from: doi:10.6083/M42N50KH ; http://digitalcommons.ohsu.edu/etd/3375.

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

Council of Science Editors:

Fjeld CC. The catalytic mechanism of human serine. [Thesis]. Oregon Health Sciences University; 1999. Available from: doi:10.6083/M42N50KH ; http://digitalcommons.ohsu.edu/etd/3375

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

19. Chen, Mei-Shya. The role of phosphoprotein phosphatase 5 in glucocorticoid signaling.

Degree: PhD, 1998, Oregon Health Sciences University

Subjects/Keywords: Phosphoprotein Phosphatases  – physiology; Glucocorticoids  – physiology; Signal Transduction; Receptors, Steroid  – physiology

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APA (6th Edition):

Chen, M. (1998). The role of phosphoprotein phosphatase 5 in glucocorticoid signaling. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4C53J2M ; http://digitalcommons.ohsu.edu/etd/2590

Chicago Manual of Style (16th Edition):

Chen, Mei-Shya. “The role of phosphoprotein phosphatase 5 in glucocorticoid signaling.” 1998. Doctoral Dissertation, Oregon Health Sciences University. Accessed April 15, 2021. doi:10.6083/M4C53J2M ; http://digitalcommons.ohsu.edu/etd/2590.

MLA Handbook (7th Edition):

Chen, Mei-Shya. “The role of phosphoprotein phosphatase 5 in glucocorticoid signaling.” 1998. Web. 15 Apr 2021.

Vancouver:

Chen M. The role of phosphoprotein phosphatase 5 in glucocorticoid signaling. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1998. [cited 2021 Apr 15]. Available from: doi:10.6083/M4C53J2M ; http://digitalcommons.ohsu.edu/etd/2590.

Council of Science Editors:

Chen M. The role of phosphoprotein phosphatase 5 in glucocorticoid signaling. [Doctoral Dissertation]. Oregon Health Sciences University; 1998. Available from: doi:10.6083/M4C53J2M ; http://digitalcommons.ohsu.edu/etd/2590

20. Satish Kumar. Transcriptional regulation in Drosophila by intracellular calcium;.

Degree: 2013, University of Mysore

newline

Advisors/Committee Members: Gaiti Hasan.

Subjects/Keywords: Biochemistry; Brain – Growth; Drosophila melanogaster – Development; Phosphoprotein phosphatases; Phosphorylation; RNA; RNA – Analysis

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APA (6th Edition):

Kumar, S. (2013). Transcriptional regulation in Drosophila by intracellular calcium;. (Thesis). University of Mysore. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/37080

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):

Kumar, Satish. “Transcriptional regulation in Drosophila by intracellular calcium;.” 2013. Thesis, University of Mysore. Accessed April 15, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/37080.

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

MLA Handbook (7th Edition):

Kumar, Satish. “Transcriptional regulation in Drosophila by intracellular calcium;.” 2013. Web. 15 Apr 2021.

Vancouver:

Kumar S. Transcriptional regulation in Drosophila by intracellular calcium;. [Internet] [Thesis]. University of Mysore; 2013. [cited 2021 Apr 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37080.

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

Council of Science Editors:

Kumar S. Transcriptional regulation in Drosophila by intracellular calcium;. [Thesis]. University of Mysore; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37080

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

21. Ma, On Ki. Association of the N-methyl-D-aspartate receptor subunit NR3A with protein phosphatase 2A : structural analysis by site-directed mutagenesis.

Degree: 2003, Hong Kong University of Science and Technology

 N-methyl-D-aspartate receptors (NMDARs) belong to a subclass of excitatory ionotropic glutamate receptors that play important roles in neuronal differentiation, synaptic transmission, synaptic integration and plasticity.… (more)

Subjects/Keywords: Neural receptors ; Methyl asparate  – Receptors ; Site-specific mutagenesis ; Phosphoprotein phosphatases

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APA (6th Edition):

Ma, O. K. (2003). Association of the N-methyl-D-aspartate receptor subunit NR3A with protein phosphatase 2A : structural analysis by site-directed mutagenesis. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-3900 ; https://doi.org/10.14711/thesis-b802030 ; http://repository.ust.hk/ir/bitstream/1783.1-3900/1/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):

Ma, On Ki. “Association of the N-methyl-D-aspartate receptor subunit NR3A with protein phosphatase 2A : structural analysis by site-directed mutagenesis.” 2003. Thesis, Hong Kong University of Science and Technology. Accessed April 15, 2021. http://repository.ust.hk/ir/Record/1783.1-3900 ; https://doi.org/10.14711/thesis-b802030 ; http://repository.ust.hk/ir/bitstream/1783.1-3900/1/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):

Ma, On Ki. “Association of the N-methyl-D-aspartate receptor subunit NR3A with protein phosphatase 2A : structural analysis by site-directed mutagenesis.” 2003. Web. 15 Apr 2021.

Vancouver:

Ma OK. Association of the N-methyl-D-aspartate receptor subunit NR3A with protein phosphatase 2A : structural analysis by site-directed mutagenesis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2003. [cited 2021 Apr 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-3900 ; https://doi.org/10.14711/thesis-b802030 ; http://repository.ust.hk/ir/bitstream/1783.1-3900/1/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:

Ma OK. Association of the N-methyl-D-aspartate receptor subunit NR3A with protein phosphatase 2A : structural analysis by site-directed mutagenesis. [Thesis]. Hong Kong University of Science and Technology; 2003. Available from: http://repository.ust.hk/ir/Record/1783.1-3900 ; https://doi.org/10.14711/thesis-b802030 ; http://repository.ust.hk/ir/bitstream/1783.1-3900/1/th_redirect.html

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


Michigan State University

22. Dunn, Jamie D. Polymer-modified plates for enrichment of phosphopeptides prior to analysis by matrix-assisted laser desorption/ionization mass spectrometry.

Degree: PhD, Department of Chemistry, 2007, Michigan State University

Subjects/Keywords: Phosphorylation; Phosphoprotein phosphatases; Cellular control mechanisms; Chromatographic analysis; Mass spectrometry

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APA (6th Edition):

Dunn, J. D. (2007). Polymer-modified plates for enrichment of phosphopeptides prior to analysis by matrix-assisted laser desorption/ionization mass spectrometry. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:39070

Chicago Manual of Style (16th Edition):

Dunn, Jamie D. “Polymer-modified plates for enrichment of phosphopeptides prior to analysis by matrix-assisted laser desorption/ionization mass spectrometry.” 2007. Doctoral Dissertation, Michigan State University. Accessed April 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:39070.

MLA Handbook (7th Edition):

Dunn, Jamie D. “Polymer-modified plates for enrichment of phosphopeptides prior to analysis by matrix-assisted laser desorption/ionization mass spectrometry.” 2007. Web. 15 Apr 2021.

Vancouver:

Dunn JD. Polymer-modified plates for enrichment of phosphopeptides prior to analysis by matrix-assisted laser desorption/ionization mass spectrometry. [Internet] [Doctoral dissertation]. Michigan State University; 2007. [cited 2021 Apr 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:39070.

Council of Science Editors:

Dunn JD. Polymer-modified plates for enrichment of phosphopeptides prior to analysis by matrix-assisted laser desorption/ionization mass spectrometry. [Doctoral Dissertation]. Michigan State University; 2007. Available from: http://etd.lib.msu.edu/islandora/object/etd:39070

23. Sheppard, Vonda Chantal. Identification and characterization of diatom kinases catalyzing the phosphorylation of biomineral forming proteins.

Degree: PhD, Chemistry and Biochemistry, 2010, Georgia Tech

 Diatoms are unicellular photosynthetic algae that display intricately patterned cell walls made of amorphous silicon dioxide (silica). Long-chain polyamines and highly phosphorylated proteins, silaffins and… (more)

Subjects/Keywords: Membrane isolation; Protein phosphorylation; Biomineralization; Silica; Phosphoprotein phosphatases; Phosphoproteins

…proteins29. Instead, dentin sialoprotein (DSP) and dentin phosphoprotein (also known… …residues), phosphophoryn (PP) is a highly acidic phosphoprotein with a strong… …phosphoprotein calcification-associated peptide-1 (CAP-1) from the cuticle ( term for… …Kinases and Phosphatases The prevalence of phosphoproteins in biomineralizing organisms from… …protein can be regulated by phosphatases, which are enzymes that remove phosphate groups in a… 

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APA (6th Edition):

Sheppard, V. C. (2010). Identification and characterization of diatom kinases catalyzing the phosphorylation of biomineral forming proteins. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37227

Chicago Manual of Style (16th Edition):

Sheppard, Vonda Chantal. “Identification and characterization of diatom kinases catalyzing the phosphorylation of biomineral forming proteins.” 2010. Doctoral Dissertation, Georgia Tech. Accessed April 15, 2021. http://hdl.handle.net/1853/37227.

MLA Handbook (7th Edition):

Sheppard, Vonda Chantal. “Identification and characterization of diatom kinases catalyzing the phosphorylation of biomineral forming proteins.” 2010. Web. 15 Apr 2021.

Vancouver:

Sheppard VC. Identification and characterization of diatom kinases catalyzing the phosphorylation of biomineral forming proteins. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1853/37227.

Council of Science Editors:

Sheppard VC. Identification and characterization of diatom kinases catalyzing the phosphorylation of biomineral forming proteins. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/37227


Michigan State University

24. Zhang, Yanfeng. Structural and functional studies of proteins involved in mitochondrial function and structure.

Degree: PhD, Genetics, 2009, Michigan State University

Subjects/Keywords: Mitochondria; Electron transport; Phosphoprotein phosphatases; Protein kinases; Renin-angiotensin system

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APA (6th Edition):

Zhang, Y. (2009). Structural and functional studies of proteins involved in mitochondrial function and structure. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:17199

Chicago Manual of Style (16th Edition):

Zhang, Yanfeng. “Structural and functional studies of proteins involved in mitochondrial function and structure.” 2009. Doctoral Dissertation, Michigan State University. Accessed April 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:17199.

MLA Handbook (7th Edition):

Zhang, Yanfeng. “Structural and functional studies of proteins involved in mitochondrial function and structure.” 2009. Web. 15 Apr 2021.

Vancouver:

Zhang Y. Structural and functional studies of proteins involved in mitochondrial function and structure. [Internet] [Doctoral dissertation]. Michigan State University; 2009. [cited 2021 Apr 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:17199.

Council of Science Editors:

Zhang Y. Structural and functional studies of proteins involved in mitochondrial function and structure. [Doctoral Dissertation]. Michigan State University; 2009. Available from: http://etd.lib.msu.edu/islandora/object/etd:17199


Michigan State University

25. Martin, Katie Renee. An integrative approach to understanding PI(3)P signaling and autophagy.

Degree: 2011, Michigan State University

Thesis Ph. D. Michigan State University. Cell and Molecular Biology 2011.

To investigate this hypothesis, we performed a cell-based RNA interference screen to identify phosphatases(more)

Subjects/Keywords: Lipid membranes; Lipids; Lipoproteins; Phosphoprotein phosphatases; Cellular signal transduction; Cytology – Research; Cellular biology

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APA (6th Edition):

Martin, K. R. (2011). An integrative approach to understanding PI(3)P signaling and autophagy. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:649

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):

Martin, Katie Renee. “An integrative approach to understanding PI(3)P signaling and autophagy.” 2011. Thesis, Michigan State University. Accessed April 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:649.

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

MLA Handbook (7th Edition):

Martin, Katie Renee. “An integrative approach to understanding PI(3)P signaling and autophagy.” 2011. Web. 15 Apr 2021.

Vancouver:

Martin KR. An integrative approach to understanding PI(3)P signaling and autophagy. [Internet] [Thesis]. Michigan State University; 2011. [cited 2021 Apr 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:649.

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

Council of Science Editors:

Martin KR. An integrative approach to understanding PI(3)P signaling and autophagy. [Thesis]. Michigan State University; 2011. Available from: http://etd.lib.msu.edu/islandora/object/etd:649

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


University of Missouri – Columbia

26. Ding, Zhaofeng, 1978-. Kinase-interacting FHA domain of kinase associated protein phosphatase : phosphopeptide interactions and NMR-detected dynamics.

Degree: PhD, 2007, University of Missouri – Columbia

 FHA domains are phosphoThr recognition modules found in diverse signaling proteins. Kinase-associated protein phosphatase (KAPP) from Arabidopsis employs its FHA domain in its negative regulation… (more)

Subjects/Keywords: Forkhead-associated domain.; Forkhead-associated domain; Plants  – Development; Phosphoprotein phosphatases; Protein kinases; Nuclear magnetic resonance; Cellular signal transduction; Mutagenesis

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APA (6th Edition):

Ding, Zhaofeng, 1. (2007). Kinase-interacting FHA domain of kinase associated protein phosphatase : phosphopeptide interactions and NMR-detected dynamics. (Doctoral Dissertation). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/4729

Chicago Manual of Style (16th Edition):

Ding, Zhaofeng, 1978-. “Kinase-interacting FHA domain of kinase associated protein phosphatase : phosphopeptide interactions and NMR-detected dynamics.” 2007. Doctoral Dissertation, University of Missouri – Columbia. Accessed April 15, 2021. http://hdl.handle.net/10355/4729.

MLA Handbook (7th Edition):

Ding, Zhaofeng, 1978-. “Kinase-interacting FHA domain of kinase associated protein phosphatase : phosphopeptide interactions and NMR-detected dynamics.” 2007. Web. 15 Apr 2021.

Vancouver:

Ding, Zhaofeng 1. Kinase-interacting FHA domain of kinase associated protein phosphatase : phosphopeptide interactions and NMR-detected dynamics. [Internet] [Doctoral dissertation]. University of Missouri – Columbia; 2007. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10355/4729.

Council of Science Editors:

Ding, Zhaofeng 1. Kinase-interacting FHA domain of kinase associated protein phosphatase : phosphopeptide interactions and NMR-detected dynamics. [Doctoral Dissertation]. University of Missouri – Columbia; 2007. Available from: http://hdl.handle.net/10355/4729


University of Missouri – Columbia

27. Ghosh, Anuprita, 1978-. Role of Sds22 in the regulation of protein phosphatase-1 in Saccharomyces cerevisiae.

Degree: 2009, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT REQUEST OF AUTHOR.] GLC7 encodes the catalytic subunit of protein phosphatase 1 (PP1) in the budding yeast… (more)

Subjects/Keywords: Saccharomyces cerevisiae Proteins  – metabolism; Protein Phosphotase 1  – metabolism; Phosphoprotein Phosphatases  – metabolism; Saccharomyces cerevisiae Proteins  – genetics; Saccharomyces cervisiae  – enzymology

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

APA (6th Edition):

Ghosh, Anuprita, 1. (2009). Role of Sds22 in the regulation of protein phosphatase-1 in Saccharomyces cerevisiae. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/8793

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):

Ghosh, Anuprita, 1978-. “Role of Sds22 in the regulation of protein phosphatase-1 in Saccharomyces cerevisiae.” 2009. Thesis, University of Missouri – Columbia. Accessed April 15, 2021. http://hdl.handle.net/10355/8793.

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

MLA Handbook (7th Edition):

Ghosh, Anuprita, 1978-. “Role of Sds22 in the regulation of protein phosphatase-1 in Saccharomyces cerevisiae.” 2009. Web. 15 Apr 2021.

Vancouver:

Ghosh, Anuprita 1. Role of Sds22 in the regulation of protein phosphatase-1 in Saccharomyces cerevisiae. [Internet] [Thesis]. University of Missouri – Columbia; 2009. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10355/8793.

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

Council of Science Editors:

Ghosh, Anuprita 1. Role of Sds22 in the regulation of protein phosphatase-1 in Saccharomyces cerevisiae. [Thesis]. University of Missouri – Columbia; 2009. Available from: http://hdl.handle.net/10355/8793

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


IUPUI

28. Widau, Ryan Cole. Protein phosphatase 2A (PP2A) holoenzymes regulate death associated protein kinase (DAPK) in ceramide-induced anoikis.

Degree: 2010, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Modulation of sphingolipid-induced apoptosis is a potential mechanism to enhance the effectiveness of chemotherapeutic drugs. Ceramide is a pleiotropic, sphingolipid… (more)

Subjects/Keywords: SPHINGOLIPID; ADHESION; CERAMIDE; APOPTOSIS; ANOIKIS; PP2A; PROTEIN PHOSPHATASE 2A; DAPK; DEATH ASSOCIATED PROTEIN KINASE; Apoptosis; Ceramides; Sphingolipids; Phosphoprotein phosphatases; Protein kinases; Chemotherapy  – Effectiveness

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APA (6th Edition):

Widau, R. C. (2010). Protein phosphatase 2A (PP2A) holoenzymes regulate death associated protein kinase (DAPK) in ceramide-induced anoikis. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2131

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):

Widau, Ryan Cole. “Protein phosphatase 2A (PP2A) holoenzymes regulate death associated protein kinase (DAPK) in ceramide-induced anoikis.” 2010. Thesis, IUPUI. Accessed April 15, 2021. http://hdl.handle.net/1805/2131.

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

MLA Handbook (7th Edition):

Widau, Ryan Cole. “Protein phosphatase 2A (PP2A) holoenzymes regulate death associated protein kinase (DAPK) in ceramide-induced anoikis.” 2010. Web. 15 Apr 2021.

Vancouver:

Widau RC. Protein phosphatase 2A (PP2A) holoenzymes regulate death associated protein kinase (DAPK) in ceramide-induced anoikis. [Internet] [Thesis]. IUPUI; 2010. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1805/2131.

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

Council of Science Editors:

Widau RC. Protein phosphatase 2A (PP2A) holoenzymes regulate death associated protein kinase (DAPK) in ceramide-induced anoikis. [Thesis]. IUPUI; 2010. Available from: http://hdl.handle.net/1805/2131

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


University of Missouri – Columbia

29. Aikins, Anthea Anita, 1982-. Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae.

Degree: 2010, University of Missouri – Columbia

 GLC7 is an essential gene in Saccharomyces cerevisiae that encodes the catalytic subunit of protein phosphatase-1. Glc7 is conditionally activated by phospho-Glc8, which is phosphorylated… (more)

Subjects/Keywords: Saccharomyces cerevisiae  – Genetics; Saccharomyces cerevisiae  – Metabolism; Phosphoprotein phosphatases  – Metabolism  – Genetic aspects; Cyclins  – Metabolism  – Genetic aspects; DNA damage; DNA repair; Saccharomyces cerevisiae  – metabolism; Saccharomyces cerevisiae  – enzymology; Protein Phosphatase 1  – metabolism; Protein Phosphatase 1  – genetics; Saccharomyces cerevisiae Proteins  – metabolism; Saccharomyces cerevisiae Proteins  – genetics; Cyclins  – metabolism; Cyclins  – genetics; DNA damage; DNA repair

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

APA (6th Edition):

Aikins, Anthea Anita, 1. (2010). Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/10291

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):

Aikins, Anthea Anita, 1982-. “Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae.” 2010. Thesis, University of Missouri – Columbia. Accessed April 15, 2021. https://doi.org/10.32469/10355/10291.

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

MLA Handbook (7th Edition):

Aikins, Anthea Anita, 1982-. “Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae.” 2010. Web. 15 Apr 2021.

Vancouver:

Aikins, Anthea Anita 1. Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae. [Internet] [Thesis]. University of Missouri – Columbia; 2010. [cited 2021 Apr 15]. Available from: https://doi.org/10.32469/10355/10291.

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

Council of Science Editors:

Aikins, Anthea Anita 1. Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae. [Thesis]. University of Missouri – Columbia; 2010. Available from: https://doi.org/10.32469/10355/10291

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


University of Missouri – Columbia

30. Aikins, Anthea Anita, 1982-. Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae.

Degree: 2010, University of Missouri – Columbia

 GLC7 is an essential gene in Saccharomyces cerevisiae that encodes the catalytic subunit of protein phosphatase-1. Glc7 is conditionally activated by phospho-Glc8, which is phosphorylated… (more)

Subjects/Keywords: Saccharomyces cerevisiae  – Genetics; Saccharomyces cerevisiae  – Metabolism; Phosphoprotein phosphatases  – Metabolism  – Genetic aspects; Cyclins  – Metabolism  – Genetic aspects; DNA damage; DNA repair; Saccharomyces cerevisiae  – metabolism; Saccharomyces cerevisiae  – enzymology; Protein Phosphatase 1  – metabolism; Protein Phosphatase 1  – genetics; Saccharomyces cerevisiae Proteins  – metabolism; Saccharomyces cerevisiae Proteins  – genetics; Cyclins  – metabolism; Cyclins  – genetics; DNA damage; DNA repair

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Aikins, Anthea Anita, 1. (2010). Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/10291

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):

Aikins, Anthea Anita, 1982-. “Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae.” 2010. Thesis, University of Missouri – Columbia. Accessed April 15, 2021. http://hdl.handle.net/10355/10291.

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

MLA Handbook (7th Edition):

Aikins, Anthea Anita, 1982-. “Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae.” 2010. Web. 15 Apr 2021.

Vancouver:

Aikins, Anthea Anita 1. Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae. [Internet] [Thesis]. University of Missouri – Columbia; 2010. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10355/10291.

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

Council of Science Editors:

Aikins, Anthea Anita 1. Regulation of Pcl6 and Pcl7 in a Glc7 pathway in Saccharomyces cerevisiae. [Thesis]. University of Missouri – Columbia; 2010. Available from: http://hdl.handle.net/10355/10291

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

[1] [2]

.