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You searched for subject:(Posttranslational modification). Showing records 1 – 20 of 20 total matches.

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University of Sydney

1. Liddy, Kiersten Alexandra. A Post-Translational Investigation into the Molecular Basis for Preconditioning in the Rat Myocardium .

Degree: 2016, University of Sydney

 Cardiovascular disease is the leading cause of morbidity and mortality worldwide. Cell death associated with myocardial infarction can be significantly decreased using a number of… (more)

Subjects/Keywords: Ischaemia/Reperfusion; cardioprotection; phosphoprotemics; posttranslational modification

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APA (6th Edition):

Liddy, K. A. (2016). A Post-Translational Investigation into the Molecular Basis for Preconditioning in the Rat Myocardium . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16189

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):

Liddy, Kiersten Alexandra. “A Post-Translational Investigation into the Molecular Basis for Preconditioning in the Rat Myocardium .” 2016. Thesis, University of Sydney. Accessed December 10, 2019. http://hdl.handle.net/2123/16189.

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

MLA Handbook (7th Edition):

Liddy, Kiersten Alexandra. “A Post-Translational Investigation into the Molecular Basis for Preconditioning in the Rat Myocardium .” 2016. Web. 10 Dec 2019.

Vancouver:

Liddy KA. A Post-Translational Investigation into the Molecular Basis for Preconditioning in the Rat Myocardium . [Internet] [Thesis]. University of Sydney; 2016. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/2123/16189.

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

Council of Science Editors:

Liddy KA. A Post-Translational Investigation into the Molecular Basis for Preconditioning in the Rat Myocardium . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/16189

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


Michigan Technological University

2. Yang, Mu. THE EFFECT OF POSTTRANSLATIONAL MODIFICATIONS ON PROTEIN AGGREGATION, MORPHOLOGY, AND TOXICITY.

Degree: PhD, Department of Chemistry, 2016, Michigan Technological University

  Proteins are one of the most versatile macromolecules in the biological system. The function or activity of a protein highly depends on its 3D… (more)

Subjects/Keywords: Protein aggregation; posttranslational modification; disulfide; acetylation; Biochemistry; Molecular Biology

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APA (6th Edition):

Yang, M. (2016). THE EFFECT OF POSTTRANSLATIONAL MODIFICATIONS ON PROTEIN AGGREGATION, MORPHOLOGY, AND TOXICITY. (Doctoral Dissertation). Michigan Technological University. Retrieved from http://digitalcommons.mtu.edu/etdr/116

Chicago Manual of Style (16th Edition):

Yang, Mu. “THE EFFECT OF POSTTRANSLATIONAL MODIFICATIONS ON PROTEIN AGGREGATION, MORPHOLOGY, AND TOXICITY.” 2016. Doctoral Dissertation, Michigan Technological University. Accessed December 10, 2019. http://digitalcommons.mtu.edu/etdr/116.

MLA Handbook (7th Edition):

Yang, Mu. “THE EFFECT OF POSTTRANSLATIONAL MODIFICATIONS ON PROTEIN AGGREGATION, MORPHOLOGY, AND TOXICITY.” 2016. Web. 10 Dec 2019.

Vancouver:

Yang M. THE EFFECT OF POSTTRANSLATIONAL MODIFICATIONS ON PROTEIN AGGREGATION, MORPHOLOGY, AND TOXICITY. [Internet] [Doctoral dissertation]. Michigan Technological University; 2016. [cited 2019 Dec 10]. Available from: http://digitalcommons.mtu.edu/etdr/116.

Council of Science Editors:

Yang M. THE EFFECT OF POSTTRANSLATIONAL MODIFICATIONS ON PROTEIN AGGREGATION, MORPHOLOGY, AND TOXICITY. [Doctoral Dissertation]. Michigan Technological University; 2016. Available from: http://digitalcommons.mtu.edu/etdr/116

3. Yates, Lisa Marie. INVESTIGATING PROTEIN PYROPHOSPHORYLATION WITH CHEMICALLY SYNTHESIZED PYROPHOSPHOPEPTIDES .

Degree: PhD, 2016, Princeton University

 Protein pyrophosphorylation is a minimally characterized post-translational modification that has been implicated in several diseases, including diabetes, obesity, and cancer. To date, only in vitro… (more)

Subjects/Keywords: inositol pyrophosphate; mass spectrometry; phosphatase; posttranslational modification; pyrophosphorylation; stability

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APA (6th Edition):

Yates, L. M. (2016). INVESTIGATING PROTEIN PYROPHOSPHORYLATION WITH CHEMICALLY SYNTHESIZED PYROPHOSPHOPEPTIDES . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01kd17cw26b

Chicago Manual of Style (16th Edition):

Yates, Lisa Marie. “INVESTIGATING PROTEIN PYROPHOSPHORYLATION WITH CHEMICALLY SYNTHESIZED PYROPHOSPHOPEPTIDES .” 2016. Doctoral Dissertation, Princeton University. Accessed December 10, 2019. http://arks.princeton.edu/ark:/88435/dsp01kd17cw26b.

MLA Handbook (7th Edition):

Yates, Lisa Marie. “INVESTIGATING PROTEIN PYROPHOSPHORYLATION WITH CHEMICALLY SYNTHESIZED PYROPHOSPHOPEPTIDES .” 2016. Web. 10 Dec 2019.

Vancouver:

Yates LM. INVESTIGATING PROTEIN PYROPHOSPHORYLATION WITH CHEMICALLY SYNTHESIZED PYROPHOSPHOPEPTIDES . [Internet] [Doctoral dissertation]. Princeton University; 2016. [cited 2019 Dec 10]. Available from: http://arks.princeton.edu/ark:/88435/dsp01kd17cw26b.

Council of Science Editors:

Yates LM. INVESTIGATING PROTEIN PYROPHOSPHORYLATION WITH CHEMICALLY SYNTHESIZED PYROPHOSPHOPEPTIDES . [Doctoral Dissertation]. Princeton University; 2016. Available from: http://arks.princeton.edu/ark:/88435/dsp01kd17cw26b


Princeton University

4. Marmelstein, Alan Michael. Synthetic Peptide and Protein Pyrophosphorylation: Development of New Chemical Tools to Study the Signaling Function of the Inositol Pyropphosphates .

Degree: PhD, 2017, Princeton University

 The inositol pyrophosphates (PP-InsPs) are a class of highly phosphorylated small molecule second messengers which help regulate diverse processes in eukaryotes, including telomere elongation, vacuole… (more)

Subjects/Keywords: bioconjugation; inositol pyrophosphate; phosphorimidazolide; posttranslational modification; protein phosphorylation; pyrophosphorylation

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APA (6th Edition):

Marmelstein, A. M. (2017). Synthetic Peptide and Protein Pyrophosphorylation: Development of New Chemical Tools to Study the Signaling Function of the Inositol Pyropphosphates . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01h702q902w

Chicago Manual of Style (16th Edition):

Marmelstein, Alan Michael. “Synthetic Peptide and Protein Pyrophosphorylation: Development of New Chemical Tools to Study the Signaling Function of the Inositol Pyropphosphates .” 2017. Doctoral Dissertation, Princeton University. Accessed December 10, 2019. http://arks.princeton.edu/ark:/88435/dsp01h702q902w.

MLA Handbook (7th Edition):

Marmelstein, Alan Michael. “Synthetic Peptide and Protein Pyrophosphorylation: Development of New Chemical Tools to Study the Signaling Function of the Inositol Pyropphosphates .” 2017. Web. 10 Dec 2019.

Vancouver:

Marmelstein AM. Synthetic Peptide and Protein Pyrophosphorylation: Development of New Chemical Tools to Study the Signaling Function of the Inositol Pyropphosphates . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2019 Dec 10]. Available from: http://arks.princeton.edu/ark:/88435/dsp01h702q902w.

Council of Science Editors:

Marmelstein AM. Synthetic Peptide and Protein Pyrophosphorylation: Development of New Chemical Tools to Study the Signaling Function of the Inositol Pyropphosphates . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp01h702q902w


Duke University

5. Hsueh, Ming-Feng. Elucidating the Molecular Architecture of Cartilage by Proteomics .

Degree: 2015, Duke University

  Articular cartilage is a highly specialized avascular tissue and consists of chondrocytes and two major components, a collagen-rich framework and highly abundant proteoglycans. The… (more)

Subjects/Keywords: Pathology; Cartilage; Deamidation; Extracellular matrix; Posttranslational modification; Proteomics

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APA (6th Edition):

Hsueh, M. (2015). Elucidating the Molecular Architecture of Cartilage by Proteomics . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9938

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):

Hsueh, Ming-Feng. “Elucidating the Molecular Architecture of Cartilage by Proteomics .” 2015. Thesis, Duke University. Accessed December 10, 2019. http://hdl.handle.net/10161/9938.

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

MLA Handbook (7th Edition):

Hsueh, Ming-Feng. “Elucidating the Molecular Architecture of Cartilage by Proteomics .” 2015. Web. 10 Dec 2019.

Vancouver:

Hsueh M. Elucidating the Molecular Architecture of Cartilage by Proteomics . [Internet] [Thesis]. Duke University; 2015. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10161/9938.

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

Council of Science Editors:

Hsueh M. Elucidating the Molecular Architecture of Cartilage by Proteomics . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/9938

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


Victoria University of Wellington

6. Matthewson, Benjamin. Lessons from Biomineralisation: the Role of Post-translational Modification.

Degree: 2009, Victoria University of Wellington

 In this thesis we present our findings following analysis of the acidic organic matrix (SMP) occluded in the calcite spines of the New Zealand sea… (more)

Subjects/Keywords: Sea urchins; Posttranslational modification; Biomineralization; Biomineralisation

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APA (6th Edition):

Matthewson, B. (2009). Lessons from Biomineralisation: the Role of Post-translational Modification. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1218

Chicago Manual of Style (16th Edition):

Matthewson, Benjamin. “Lessons from Biomineralisation: the Role of Post-translational Modification.” 2009. Doctoral Dissertation, Victoria University of Wellington. Accessed December 10, 2019. http://hdl.handle.net/10063/1218.

MLA Handbook (7th Edition):

Matthewson, Benjamin. “Lessons from Biomineralisation: the Role of Post-translational Modification.” 2009. Web. 10 Dec 2019.

Vancouver:

Matthewson B. Lessons from Biomineralisation: the Role of Post-translational Modification. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2009. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10063/1218.

Council of Science Editors:

Matthewson B. Lessons from Biomineralisation: the Role of Post-translational Modification. [Doctoral Dissertation]. Victoria University of Wellington; 2009. Available from: http://hdl.handle.net/10063/1218


Université Montpellier II

7. Courtellemont, Thibault. Septin regulation by the Protein Kinase C in the budding yeast, Saccharomyces cerevisiae : Régulation des septines par la Protéine Kinase C dans la levure bourgeonnante.

Degree: Docteur es, Biologie Santé, 2014, Université Montpellier II

 La cytokinèse est un processus fondamental prenant place à la fin de la mitose et permettant la séparation des deux cellules filles. Un défaut de… (more)

Subjects/Keywords: Septine; Cytokinèse; Levure bourgeonnante; Pkc1; Phosphorylation; Modification post-Traductionnelle; Septin; Cytokinesis; Budding Yeast; Pkc1; Phosphorylation; Posttranslational modification

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APA (6th Edition):

Courtellemont, T. (2014). Septin regulation by the Protein Kinase C in the budding yeast, Saccharomyces cerevisiae : Régulation des septines par la Protéine Kinase C dans la levure bourgeonnante. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2014MON20007

Chicago Manual of Style (16th Edition):

Courtellemont, Thibault. “Septin regulation by the Protein Kinase C in the budding yeast, Saccharomyces cerevisiae : Régulation des septines par la Protéine Kinase C dans la levure bourgeonnante.” 2014. Doctoral Dissertation, Université Montpellier II. Accessed December 10, 2019. http://www.theses.fr/2014MON20007.

MLA Handbook (7th Edition):

Courtellemont, Thibault. “Septin regulation by the Protein Kinase C in the budding yeast, Saccharomyces cerevisiae : Régulation des septines par la Protéine Kinase C dans la levure bourgeonnante.” 2014. Web. 10 Dec 2019.

Vancouver:

Courtellemont T. Septin regulation by the Protein Kinase C in the budding yeast, Saccharomyces cerevisiae : Régulation des septines par la Protéine Kinase C dans la levure bourgeonnante. [Internet] [Doctoral dissertation]. Université Montpellier II; 2014. [cited 2019 Dec 10]. Available from: http://www.theses.fr/2014MON20007.

Council of Science Editors:

Courtellemont T. Septin regulation by the Protein Kinase C in the budding yeast, Saccharomyces cerevisiae : Régulation des septines par la Protéine Kinase C dans la levure bourgeonnante. [Doctoral Dissertation]. Université Montpellier II; 2014. Available from: http://www.theses.fr/2014MON20007


University of Kentucky

8. Zhang, Zhaoshu. INCREASE OF BASAL OXIDATIVE STRESS LEVELS AND IMPAIRMENT OF HEME OXYGENASE-1/BILIVERDIN REDUCTASE POST-TRANSLATIONAL MODIFICATION BY THE DEFECT OF PARKINSON-RELATED GENE OF PINK1.

Degree: 2014, University of Kentucky

 Parkinson disease (PD) is the most common movement disorder and the second most common neurodegenerative disease. PINK1, PTEN-induced kinase 1, functions as a serine/threonine kinase… (more)

Subjects/Keywords: Parkinson disease (PD); PTEN-induced putative kinase 1 (PINK1); Biliverdin reductase (BVR); Oxidative stress; Posttranslational modification; Biochemistry

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APA (6th Edition):

Zhang, Z. (2014). INCREASE OF BASAL OXIDATIVE STRESS LEVELS AND IMPAIRMENT OF HEME OXYGENASE-1/BILIVERDIN REDUCTASE POST-TRANSLATIONAL MODIFICATION BY THE DEFECT OF PARKINSON-RELATED GENE OF PINK1. (Masters Thesis). University of Kentucky. Retrieved from http://uknowledge.uky.edu/chemistry_etds/40

Chicago Manual of Style (16th Edition):

Zhang, Zhaoshu. “INCREASE OF BASAL OXIDATIVE STRESS LEVELS AND IMPAIRMENT OF HEME OXYGENASE-1/BILIVERDIN REDUCTASE POST-TRANSLATIONAL MODIFICATION BY THE DEFECT OF PARKINSON-RELATED GENE OF PINK1.” 2014. Masters Thesis, University of Kentucky. Accessed December 10, 2019. http://uknowledge.uky.edu/chemistry_etds/40.

MLA Handbook (7th Edition):

Zhang, Zhaoshu. “INCREASE OF BASAL OXIDATIVE STRESS LEVELS AND IMPAIRMENT OF HEME OXYGENASE-1/BILIVERDIN REDUCTASE POST-TRANSLATIONAL MODIFICATION BY THE DEFECT OF PARKINSON-RELATED GENE OF PINK1.” 2014. Web. 10 Dec 2019.

Vancouver:

Zhang Z. INCREASE OF BASAL OXIDATIVE STRESS LEVELS AND IMPAIRMENT OF HEME OXYGENASE-1/BILIVERDIN REDUCTASE POST-TRANSLATIONAL MODIFICATION BY THE DEFECT OF PARKINSON-RELATED GENE OF PINK1. [Internet] [Masters thesis]. University of Kentucky; 2014. [cited 2019 Dec 10]. Available from: http://uknowledge.uky.edu/chemistry_etds/40.

Council of Science Editors:

Zhang Z. INCREASE OF BASAL OXIDATIVE STRESS LEVELS AND IMPAIRMENT OF HEME OXYGENASE-1/BILIVERDIN REDUCTASE POST-TRANSLATIONAL MODIFICATION BY THE DEFECT OF PARKINSON-RELATED GENE OF PINK1. [Masters Thesis]. University of Kentucky; 2014. Available from: http://uknowledge.uky.edu/chemistry_etds/40


University of Illinois – Chicago

9. Orozco-Nunnelly, Danielle A. Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana.

Degree: 2015, University of Illinois – Chicago

 As photoautotrophic and sessile organisms, plants are both reliant upon, and vulnerable to abiotic signals. Different wavelengths of light provide information for plant development, but… (more)

Subjects/Keywords: Arabidopsis; G protein pathway; Light signaling; Photomorphogenesis; Pirin; Plant transgenes; Posttranslational modification; Quercetin; Regulation of transcript and protein; Seedling development

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APA (6th Edition):

Orozco-Nunnelly, D. A. (2015). Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19577

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):

Orozco-Nunnelly, Danielle A. “Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana.” 2015. Thesis, University of Illinois – Chicago. Accessed December 10, 2019. http://hdl.handle.net/10027/19577.

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

MLA Handbook (7th Edition):

Orozco-Nunnelly, Danielle A. “Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana.” 2015. Web. 10 Dec 2019.

Vancouver:

Orozco-Nunnelly DA. Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10027/19577.

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

Council of Science Editors:

Orozco-Nunnelly DA. Determining the Role of Pirin1 in Light-Regulated Growth and Cellular Responses in Arabidopsis thaliana. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19577

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

10. Chen, Xueping. Posttranslational oxidative modification of SOD1 in neurodegeneration.

Degree: Human Anatomy and Cell Science, 2012, University of Manitoba

 Converging evidence indicates that SOD1 aggregation is a common feature of mutant SOD1 (mSOD1)-linked FALS, and seems to be directly related to the gain-of-function toxic… (more)

Subjects/Keywords: Oxidative stress; Posttranslational modification; SOD1; PDI

…is particularly susceptible to oxidative posttranslational modification [30]… …36 1.2.11 Oxidative modification of Cys111 in SOD1 aggregates… …37 1.2.12 Oxidative modification of wild-type SOD1 in aggregates formation............. 39… …58 Chapter 3. Oxidative modification of cysteine 111 promotes disulfide bond-independent… …modification accompanied with appearance of an additional upper band under increased oxidative stress… 

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APA (6th Edition):

Chen, X. (2012). Posttranslational oxidative modification of SOD1 in neurodegeneration. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/8359

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):

Chen, Xueping. “Posttranslational oxidative modification of SOD1 in neurodegeneration.” 2012. Thesis, University of Manitoba. Accessed December 10, 2019. http://hdl.handle.net/1993/8359.

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

MLA Handbook (7th Edition):

Chen, Xueping. “Posttranslational oxidative modification of SOD1 in neurodegeneration.” 2012. Web. 10 Dec 2019.

Vancouver:

Chen X. Posttranslational oxidative modification of SOD1 in neurodegeneration. [Internet] [Thesis]. University of Manitoba; 2012. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/1993/8359.

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

Council of Science Editors:

Chen X. Posttranslational oxidative modification of SOD1 in neurodegeneration. [Thesis]. University of Manitoba; 2012. Available from: http://hdl.handle.net/1993/8359

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


Northeastern University

11. Zang, Tianzhu. Analysis of protein modifications: protein N-homocysteinylation and covalent inhibition of the LuxS enzyme by brominated furanones.

Degree: PhD, Department of Chemistry and Chemical Biology, 2012, Northeastern University

 Two projects are described in this thesis. The first project was to develop chemical methods for the analysis of protein N-homocysteinylation and the second project… (more)

Subjects/Keywords: brominated furanone; Chemical derivatization; LuxS enzyme; Protein N-homocysteinylation; Protein posttranslational modification; quorum sensing; Analytical Chemistry; Chemistry

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APA (6th Edition):

Zang, T. (2012). Analysis of protein modifications: protein N-homocysteinylation and covalent inhibition of the LuxS enzyme by brominated furanones. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002940

Chicago Manual of Style (16th Edition):

Zang, Tianzhu. “Analysis of protein modifications: protein N-homocysteinylation and covalent inhibition of the LuxS enzyme by brominated furanones.” 2012. Doctoral Dissertation, Northeastern University. Accessed December 10, 2019. http://hdl.handle.net/2047/d20002940.

MLA Handbook (7th Edition):

Zang, Tianzhu. “Analysis of protein modifications: protein N-homocysteinylation and covalent inhibition of the LuxS enzyme by brominated furanones.” 2012. Web. 10 Dec 2019.

Vancouver:

Zang T. Analysis of protein modifications: protein N-homocysteinylation and covalent inhibition of the LuxS enzyme by brominated furanones. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/2047/d20002940.

Council of Science Editors:

Zang T. Analysis of protein modifications: protein N-homocysteinylation and covalent inhibition of the LuxS enzyme by brominated furanones. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002940


University of Oxford

12. Lercher, Lukas A. Chemical tools for the study of epigenetic mechanisms.

Degree: PhD, 2014, University of Oxford

 The overall goal of my work was to develop and apply new chemical methods for the study of epigenetic DNA and protein modifications. In Chapter… (more)

Subjects/Keywords: 572.8; Chemical biology; Protein chemistry; Organic chemistry; NMR spectroscopy; Molecular biophysics (biochemistry); Epigenetic regulation; posttranslational modifications; DNA modification; protein NMR

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APA (6th Edition):

Lercher, L. A. (2014). Chemical tools for the study of epigenetic mechanisms. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8fec2af6-573b-464a-865e-a70d31fa1c41 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629538

Chicago Manual of Style (16th Edition):

Lercher, Lukas A. “Chemical tools for the study of epigenetic mechanisms.” 2014. Doctoral Dissertation, University of Oxford. Accessed December 10, 2019. http://ora.ox.ac.uk/objects/uuid:8fec2af6-573b-464a-865e-a70d31fa1c41 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629538.

MLA Handbook (7th Edition):

Lercher, Lukas A. “Chemical tools for the study of epigenetic mechanisms.” 2014. Web. 10 Dec 2019.

Vancouver:

Lercher LA. Chemical tools for the study of epigenetic mechanisms. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Dec 10]. Available from: http://ora.ox.ac.uk/objects/uuid:8fec2af6-573b-464a-865e-a70d31fa1c41 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629538.

Council of Science Editors:

Lercher LA. Chemical tools for the study of epigenetic mechanisms. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:8fec2af6-573b-464a-865e-a70d31fa1c41 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629538


University of Georgia

13. Swamy, Prashant Shidram. Transgenic manipulation of tubulins in Populus alters cell wall properties and drought response characteristics.

Degree: PhD, Forest Resources, 2013, University of Georgia

 Microtubules (MTs) are dynamic cytoskeletal polymers of alpha-(TUA) and beta-(TUB) tubulins. Various processes including the deposition of cellulose microfibrils in the developing cell wall are… (more)

Subjects/Keywords: Populus; tubulin; microtubules; posttranslational modification; cell wall property; microfibril angle; wood density; acute drought; chronic drought; photosynthesis; stomatal conductance; transpiration rate; plant cell expansion

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APA (6th Edition):

Swamy, P. S. (2013). Transgenic manipulation of tubulins in Populus alters cell wall properties and drought response characteristics. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/swamy_prashant_s_201308_phd

Chicago Manual of Style (16th Edition):

Swamy, Prashant Shidram. “Transgenic manipulation of tubulins in Populus alters cell wall properties and drought response characteristics.” 2013. Doctoral Dissertation, University of Georgia. Accessed December 10, 2019. http://purl.galileo.usg.edu/uga_etd/swamy_prashant_s_201308_phd.

MLA Handbook (7th Edition):

Swamy, Prashant Shidram. “Transgenic manipulation of tubulins in Populus alters cell wall properties and drought response characteristics.” 2013. Web. 10 Dec 2019.

Vancouver:

Swamy PS. Transgenic manipulation of tubulins in Populus alters cell wall properties and drought response characteristics. [Internet] [Doctoral dissertation]. University of Georgia; 2013. [cited 2019 Dec 10]. Available from: http://purl.galileo.usg.edu/uga_etd/swamy_prashant_s_201308_phd.

Council of Science Editors:

Swamy PS. Transgenic manipulation of tubulins in Populus alters cell wall properties and drought response characteristics. [Doctoral Dissertation]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/swamy_prashant_s_201308_phd


Johannes Gutenberg Universität Mainz

14. Keller, Patrick. Einfluss der Phosphorylierung durch die Casein Kinase II auf den HSP90-Chaperone-Zyklus in humanen Zellen.

Degree: 2012, Johannes Gutenberg Universität Mainz

In der vorliegenden Arbeit wurde eine Analysenmethode auf Basis der Massenbestimmung über Elektrospray-Ionisation qualifiziert, mit der es möglich ist, den Gehalt beider in humanen Zellen… (more)

Subjects/Keywords: HSP90alpha, HSP90beta, Charged Linker, p23, Phosphorylierung, Casein Kinase II, 17AAG, ESI, MALDI, Posttranslationale Modifikationen; HSP90alpha, HSP90beta, charged linker, p23, phosphorylation, Casein Kinase II, 17AAG, ESI, MALDI, posttranslational modification; Life sciences

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APA (6th Edition):

Keller, P. (2012). Einfluss der Phosphorylierung durch die Casein Kinase II auf den HSP90-Chaperone-Zyklus in humanen Zellen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2012/3081/

Chicago Manual of Style (16th Edition):

Keller, Patrick. “Einfluss der Phosphorylierung durch die Casein Kinase II auf den HSP90-Chaperone-Zyklus in humanen Zellen.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed December 10, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2012/3081/.

MLA Handbook (7th Edition):

Keller, Patrick. “Einfluss der Phosphorylierung durch die Casein Kinase II auf den HSP90-Chaperone-Zyklus in humanen Zellen.” 2012. Web. 10 Dec 2019.

Vancouver:

Keller P. Einfluss der Phosphorylierung durch die Casein Kinase II auf den HSP90-Chaperone-Zyklus in humanen Zellen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2019 Dec 10]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3081/.

Council of Science Editors:

Keller P. Einfluss der Phosphorylierung durch die Casein Kinase II auf den HSP90-Chaperone-Zyklus in humanen Zellen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3081/


University of Central Florida

15. Safavi-Khasraghi, Mitra. Expression And Characterization Of Mycobacterium Paratuberculosis 19kda With Posttranslational Modification.

Degree: 2006, University of Central Florida

 Despite the fact that E. coli supports limited posttranslational modification, this bacterium has been universally used as the expression system of choice. Expression of modified… (more)

Subjects/Keywords: Mycobacterium paratuberculosis; Mycobacterium smegmatis; posttranslational modification; Crohn s disease; Microbiology; Molecular Biology

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APA (6th Edition):

Safavi-Khasraghi, M. (2006). Expression And Characterization Of Mycobacterium Paratuberculosis 19kda With Posttranslational Modification. (Masters Thesis). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/964

Chicago Manual of Style (16th Edition):

Safavi-Khasraghi, Mitra. “Expression And Characterization Of Mycobacterium Paratuberculosis 19kda With Posttranslational Modification.” 2006. Masters Thesis, University of Central Florida. Accessed December 10, 2019. https://stars.library.ucf.edu/etd/964.

MLA Handbook (7th Edition):

Safavi-Khasraghi, Mitra. “Expression And Characterization Of Mycobacterium Paratuberculosis 19kda With Posttranslational Modification.” 2006. Web. 10 Dec 2019.

Vancouver:

Safavi-Khasraghi M. Expression And Characterization Of Mycobacterium Paratuberculosis 19kda With Posttranslational Modification. [Internet] [Masters thesis]. University of Central Florida; 2006. [cited 2019 Dec 10]. Available from: https://stars.library.ucf.edu/etd/964.

Council of Science Editors:

Safavi-Khasraghi M. Expression And Characterization Of Mycobacterium Paratuberculosis 19kda With Posttranslational Modification. [Masters Thesis]. University of Central Florida; 2006. Available from: https://stars.library.ucf.edu/etd/964

16. LIU KAI. Developing Chemical Proteomic Tools Connecting Proteins and Small Molecules.

Degree: 2011, National University of Singapore

Subjects/Keywords: activity based protein profiling; bioorthogonal reaction; posttranslational modification; target identification; enzyme function; inhibitor discovery

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APA (6th Edition):

KAI, L. (2011). Developing Chemical Proteomic Tools Connecting Proteins and Small Molecules. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/25837

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):

KAI, LIU. “Developing Chemical Proteomic Tools Connecting Proteins and Small Molecules.” 2011. Thesis, National University of Singapore. Accessed December 10, 2019. http://scholarbank.nus.edu.sg/handle/10635/25837.

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

MLA Handbook (7th Edition):

KAI, LIU. “Developing Chemical Proteomic Tools Connecting Proteins and Small Molecules.” 2011. Web. 10 Dec 2019.

Vancouver:

KAI L. Developing Chemical Proteomic Tools Connecting Proteins and Small Molecules. [Internet] [Thesis]. National University of Singapore; 2011. [cited 2019 Dec 10]. Available from: http://scholarbank.nus.edu.sg/handle/10635/25837.

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

Council of Science Editors:

KAI L. Developing Chemical Proteomic Tools Connecting Proteins and Small Molecules. [Thesis]. National University of Singapore; 2011. Available from: http://scholarbank.nus.edu.sg/handle/10635/25837

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

17. He, Lin. Algorithms for Characterizing Peptides and Glycopeptides with Mass Spectrometry.

Degree: 2013, University of Waterloo

 The emergence of tandem mass spectrometry (MS/MS) technology has significantly accelerated protein identification and quantification in proteomics. It enables high-throughput analysis of proteins and their… (more)

Subjects/Keywords: Bioinformatics; Computational biology; Mass spectrometry; Protein/peptide identification; Protein quantification; Posttranslational modification; Glycosylation

…of posttranslational modifications (PTMs) on proteins is of critical importance… 

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

APA (6th Edition):

He, L. (2013). Algorithms for Characterizing Peptides and Glycopeptides with Mass Spectrometry. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/7920

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

Chicago Manual of Style (16th Edition):

He, Lin. “Algorithms for Characterizing Peptides and Glycopeptides with Mass Spectrometry.” 2013. Thesis, University of Waterloo. Accessed December 10, 2019. http://hdl.handle.net/10012/7920.

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

MLA Handbook (7th Edition):

He, Lin. “Algorithms for Characterizing Peptides and Glycopeptides with Mass Spectrometry.” 2013. Web. 10 Dec 2019.

Vancouver:

He L. Algorithms for Characterizing Peptides and Glycopeptides with Mass Spectrometry. [Internet] [Thesis]. University of Waterloo; 2013. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10012/7920.

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

Council of Science Editors:

He L. Algorithms for Characterizing Peptides and Glycopeptides with Mass Spectrometry. [Thesis]. University of Waterloo; 2013. Available from: http://hdl.handle.net/10012/7920

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


University of Illinois – Urbana-Champaign

18. Bindman, Noah. New chemical and biosynthetic methodologies for the study of lanthipeptides.

Degree: PhD, 0335, 2014, University of Illinois – Urbana-Champaign

 Recent genome sequencing efforts have revealed that a common biosynthetic route to peptide natural products involves ribosomally synthesized and posttranslationally modified peptides (RiPPs). One of… (more)

Subjects/Keywords: peptide natural product; ribosomally synthesized and posttranslationally modified peptide; Lanthionine; Lanthipeptide; methyllanthionine; bioengineering; posttranslational modification; photochemical linker; lacticin 481; nukacin ISK-1; haloduracin; prochlorosin; nisin; hydroxy acid; pyrrolysyl tRNA; α-ketoamide; fluorescently modified lantibiotic

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

APA (6th Edition):

Bindman, N. (2014). New chemical and biosynthetic methodologies for the study of lanthipeptides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49785

Chicago Manual of Style (16th Edition):

Bindman, Noah. “New chemical and biosynthetic methodologies for the study of lanthipeptides.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 10, 2019. http://hdl.handle.net/2142/49785.

MLA Handbook (7th Edition):

Bindman, Noah. “New chemical and biosynthetic methodologies for the study of lanthipeptides.” 2014. Web. 10 Dec 2019.

Vancouver:

Bindman N. New chemical and biosynthetic methodologies for the study of lanthipeptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/2142/49785.

Council of Science Editors:

Bindman N. New chemical and biosynthetic methodologies for the study of lanthipeptides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49785


University of Florida

19. Humbard, Matthew. Post-translational Modification and the 20S Proteasome System of the Haloarchaeon Haloferax volcanii.

Degree: PhD, Microbiology and Cell Science, 2009, University of Florida

 While much of the study of proteasome systems in all organisms, eukaryotes and prokaryotes, focuses on substrate recognition, ubiquitin-like modifiers, or protein targeting, the 20S… (more)

Subjects/Keywords: Acetylation; Amino acids; Archaea; Enzymes; Haloferax volcanii; Ions; Mass spectroscopy; Phosphorylation; Proteins; Yeasts; acetylation, acetyltransferase, activating, archaea, atpase, dimensional, electrophoresis, haloarchaea, haloferax, knock, mass, methylation, modification, ms, nucleotidase, out, pan, phosphorylation, posttranslational, protease, proteasome, proteome, samp, spectrometry, two, ubiquitin, volcanii

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

APA (6th Edition):

Humbard, M. (2009). Post-translational Modification and the 20S Proteasome System of the Haloarchaeon Haloferax volcanii. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0024797

Chicago Manual of Style (16th Edition):

Humbard, Matthew. “Post-translational Modification and the 20S Proteasome System of the Haloarchaeon Haloferax volcanii.” 2009. Doctoral Dissertation, University of Florida. Accessed December 10, 2019. http://ufdc.ufl.edu/UFE0024797.

MLA Handbook (7th Edition):

Humbard, Matthew. “Post-translational Modification and the 20S Proteasome System of the Haloarchaeon Haloferax volcanii.” 2009. Web. 10 Dec 2019.

Vancouver:

Humbard M. Post-translational Modification and the 20S Proteasome System of the Haloarchaeon Haloferax volcanii. [Internet] [Doctoral dissertation]. University of Florida; 2009. [cited 2019 Dec 10]. Available from: http://ufdc.ufl.edu/UFE0024797.

Council of Science Editors:

Humbard M. Post-translational Modification and the 20S Proteasome System of the Haloarchaeon Haloferax volcanii. [Doctoral Dissertation]. University of Florida; 2009. Available from: http://ufdc.ufl.edu/UFE0024797


Northeastern University

20. Liu, Min. Development of methods for the analysis of protein post-translational modifications: isoaspartic acid and protein crosslinking.

Degree: PhD, Department of Chemistry and Chemical Biology, 2014, Northeastern University

 Analysis of protein posttranslational modifications (PTMs) plays pivotal roles for the understanding of their biological importance. Isoaspartic acid (isoAsp) as the smallest PTM is observed… (more)

Subjects/Keywords: 18O-labeling; IgG; degradants; characterization; Isoaspartic acid (isoAsp); protein crosslinks; mass spectrometry; MS; method development for analysis and structure elucidation; protein posttranslational modifications; PTMs; Biochemistry; Biology; Chemistry; Post-translational modification; Isoaspartic acid; Analysis; Proteins; Crosslinking; Analysis; Methylation; Peptides

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

APA (6th Edition):

Liu, M. (2014). Development of methods for the analysis of protein post-translational modifications: isoaspartic acid and protein crosslinking. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20128343

Chicago Manual of Style (16th Edition):

Liu, Min. “Development of methods for the analysis of protein post-translational modifications: isoaspartic acid and protein crosslinking.” 2014. Doctoral Dissertation, Northeastern University. Accessed December 10, 2019. http://hdl.handle.net/2047/d20128343.

MLA Handbook (7th Edition):

Liu, Min. “Development of methods for the analysis of protein post-translational modifications: isoaspartic acid and protein crosslinking.” 2014. Web. 10 Dec 2019.

Vancouver:

Liu M. Development of methods for the analysis of protein post-translational modifications: isoaspartic acid and protein crosslinking. [Internet] [Doctoral dissertation]. Northeastern University; 2014. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/2047/d20128343.

Council of Science Editors:

Liu M. Development of methods for the analysis of protein post-translational modifications: isoaspartic acid and protein crosslinking. [Doctoral Dissertation]. Northeastern University; 2014. Available from: http://hdl.handle.net/2047/d20128343

.