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You searched for subject:(Metal Controlled Protein Dimerization). Showing records 1 – 30 of 31644 total matches.

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University of California – San Diego

1. Maniaci, Brian M. Design of Metal-Controlled Protein-Protein Interactions.

Degree: Chemistry and Biochemistry, 2019, University of California – San Diego

 The field of protein design strives to engineer new molecules that interact in a specific, controlled manner to form novel functional complexes. Engineered proteins that… (more)

Subjects/Keywords: Chemistry; Biochemistry; Biomaterials; Metal-Controlled Protein Dimerization; Protein Design; Protein Engineering

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

APA (6th Edition):

Maniaci, B. M. (2019). Design of Metal-Controlled Protein-Protein Interactions. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0fc2n3qm

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):

Maniaci, Brian M. “Design of Metal-Controlled Protein-Protein Interactions.” 2019. Thesis, University of California – San Diego. Accessed July 07, 2020. http://www.escholarship.org/uc/item/0fc2n3qm.

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

MLA Handbook (7th Edition):

Maniaci, Brian M. “Design of Metal-Controlled Protein-Protein Interactions.” 2019. Web. 07 Jul 2020.

Vancouver:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/0fc2n3qm.

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

Council of Science Editors:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/0fc2n3qm

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


UCLA

2. Decker, Caitlin Gayle. Modulating Protein Activity through Polymer Conjugation.

Degree: Chemistry, 2015, UCLA

Protein therapeutics have become essential to the healthcare and pharmaceutical industries since the first recombinant proteins entered the clinic in the 1980s. Modification of proteins… (more)

Subjects/Keywords: Chemistry; Polymer chemistry; Biochemistry; bioconjugate chemistry; controlled radical polymerization; protein dimerization; superagonist

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APA (6th Edition):

Decker, C. G. (2015). Modulating Protein Activity through Polymer Conjugation. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/3m53s0dd

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):

Decker, Caitlin Gayle. “Modulating Protein Activity through Polymer Conjugation.” 2015. Thesis, UCLA. Accessed July 07, 2020. http://www.escholarship.org/uc/item/3m53s0dd.

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

MLA Handbook (7th Edition):

Decker, Caitlin Gayle. “Modulating Protein Activity through Polymer Conjugation.” 2015. Web. 07 Jul 2020.

Vancouver:

Decker CG. Modulating Protein Activity through Polymer Conjugation. [Internet] [Thesis]. UCLA; 2015. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/3m53s0dd.

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

Council of Science Editors:

Decker CG. Modulating Protein Activity through Polymer Conjugation. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/3m53s0dd

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


Boston College

3. Pace, Christopher John. Towards the Chemical Control of Membrane Protein Function.

Degree: PhD, Chemistry, 2013, Boston College

 The oligomerization of membrane proteins has been shown to play a critical role in a myriad of cellular processes, some of which include signal propagation,… (more)

Subjects/Keywords: Aromatic; Dimerization; Fluorination; Membrane; Noncovalent; Protein

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APA (6th Edition):

Pace, C. J. (2013). Towards the Chemical Control of Membrane Protein Function. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101311

Chicago Manual of Style (16th Edition):

Pace, Christopher John. “Towards the Chemical Control of Membrane Protein Function.” 2013. Doctoral Dissertation, Boston College. Accessed July 07, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101311.

MLA Handbook (7th Edition):

Pace, Christopher John. “Towards the Chemical Control of Membrane Protein Function.” 2013. Web. 07 Jul 2020.

Vancouver:

Pace CJ. Towards the Chemical Control of Membrane Protein Function. [Internet] [Doctoral dissertation]. Boston College; 2013. [cited 2020 Jul 07]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101311.

Council of Science Editors:

Pace CJ. Towards the Chemical Control of Membrane Protein Function. [Doctoral Dissertation]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101311


University of Illinois – Chicago

4. Chavan, Tanmay S. Intra and Intermolecular Interactions of K-Ras4B: From Structure to Function.

Degree: 2015, University of Illinois – Chicago

 Ras proteins are small GTPases that act as signal transducers between cell surface receptors and intracellular signaling cascades. According to the existing paradigm, Ras proteins… (more)

Subjects/Keywords: Ras; K-Ras4B; hypervariable region; protein-protein interactions; dimerization

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APA (6th Edition):

Chavan, T. S. (2015). Intra and Intermolecular Interactions of K-Ras4B: From Structure to Function. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19405

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):

Chavan, Tanmay S. “Intra and Intermolecular Interactions of K-Ras4B: From Structure to Function.” 2015. Thesis, University of Illinois – Chicago. Accessed July 07, 2020. http://hdl.handle.net/10027/19405.

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

MLA Handbook (7th Edition):

Chavan, Tanmay S. “Intra and Intermolecular Interactions of K-Ras4B: From Structure to Function.” 2015. Web. 07 Jul 2020.

Vancouver:

Chavan TS. Intra and Intermolecular Interactions of K-Ras4B: From Structure to Function. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10027/19405.

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

Council of Science Editors:

Chavan TS. Intra and Intermolecular Interactions of K-Ras4B: From Structure to Function. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19405

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


Dalhousie University

5. Charette, Nicholle Jeanine. INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS.

Degree: MS, Department of Pharmacology, 2011, Dalhousie University

 Little is known about the outward trafficking of receptor dimers from the endoplasmic reticulum to the plasma membrane, or the role that trafficking plays in… (more)

Subjects/Keywords: G protein coupled receptor; CXCR4; CCR5; Rab GTPase; Trafficking; Dimerization

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APA (6th Edition):

Charette, N. J. (2011). INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/14023

Chicago Manual of Style (16th Edition):

Charette, Nicholle Jeanine. “INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS.” 2011. Masters Thesis, Dalhousie University. Accessed July 07, 2020. http://hdl.handle.net/10222/14023.

MLA Handbook (7th Edition):

Charette, Nicholle Jeanine. “INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS.” 2011. Web. 07 Jul 2020.

Vancouver:

Charette NJ. INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS. [Internet] [Masters thesis]. Dalhousie University; 2011. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10222/14023.

Council of Science Editors:

Charette NJ. INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS. [Masters Thesis]. Dalhousie University; 2011. Available from: http://hdl.handle.net/10222/14023

6. Ballering, J. Molecular insights into the mechanism of sensing and signal transduction of the thermosensor DesK.

Degree: 2016, Universiteit Utrecht

 The ability to sense and respond to environmental signals is essential for cell survival. Unraveling the molecular mechanisms underlying signaling processes remains a challenge, however.… (more)

Subjects/Keywords: Thermosensing; two-component system; lipid-protein interaction; transmembrane helix dimerization

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APA (6th Edition):

Ballering, J. (2016). Molecular insights into the mechanism of sensing and signal transduction of the thermosensor DesK. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/330663

Chicago Manual of Style (16th Edition):

Ballering, J. “Molecular insights into the mechanism of sensing and signal transduction of the thermosensor DesK.” 2016. Doctoral Dissertation, Universiteit Utrecht. Accessed July 07, 2020. http://dspace.library.uu.nl:8080/handle/1874/330663.

MLA Handbook (7th Edition):

Ballering, J. “Molecular insights into the mechanism of sensing and signal transduction of the thermosensor DesK.” 2016. Web. 07 Jul 2020.

Vancouver:

Ballering J. Molecular insights into the mechanism of sensing and signal transduction of the thermosensor DesK. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2016. [cited 2020 Jul 07]. Available from: http://dspace.library.uu.nl:8080/handle/1874/330663.

Council of Science Editors:

Ballering J. Molecular insights into the mechanism of sensing and signal transduction of the thermosensor DesK. [Doctoral Dissertation]. Universiteit Utrecht; 2016. Available from: http://dspace.library.uu.nl:8080/handle/1874/330663


North Carolina State University

7. MacKenzie, Sarah Helen. The importance of the dimer interface in the folding and assembly of procaspase-3.

Degree: PhD, Biochemistry, 2009, North Carolina State University

 Caspases are a family of cysteine proteases that are intimately involved in apoptosis and exist in the cell as inactive zymogens prior to activation. Initiator… (more)

Subjects/Keywords: dimerization; hysteresis; kinetic folding; caspase; apoptosis; equilibrium folding; protein folding

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APA (6th Edition):

MacKenzie, S. H. (2009). The importance of the dimer interface in the folding and assembly of procaspase-3. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/3688

Chicago Manual of Style (16th Edition):

MacKenzie, Sarah Helen. “The importance of the dimer interface in the folding and assembly of procaspase-3.” 2009. Doctoral Dissertation, North Carolina State University. Accessed July 07, 2020. http://www.lib.ncsu.edu/resolver/1840.16/3688.

MLA Handbook (7th Edition):

MacKenzie, Sarah Helen. “The importance of the dimer interface in the folding and assembly of procaspase-3.” 2009. Web. 07 Jul 2020.

Vancouver:

MacKenzie SH. The importance of the dimer interface in the folding and assembly of procaspase-3. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2020 Jul 07]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3688.

Council of Science Editors:

MacKenzie SH. The importance of the dimer interface in the folding and assembly of procaspase-3. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3688


University of Georgia

8. Hanold, Laura Elizabeth. Cyclization strategies to stabilize epidermal growth factor receptor dimerization arm mimics.

Degree: PhD, Pharmacy, 2016, University of Georgia

Protein-protein interactions (PPIs) have critical roles in the regulation of signal transduction in the cell, and the dysregulation of these signaling pathways contributes to various… (more)

Subjects/Keywords: Epidermal growth factor receptor; Dimerization; Triazole; Selenylsulfide; Peptide; Macrocyclization; Protein-protein interaction

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APA (6th Edition):

Hanold, L. E. (2016). Cyclization strategies to stabilize epidermal growth factor receptor dimerization arm mimics. (Doctoral Dissertation). University of Georgia. Retrieved from http://hdl.handle.net/10724/38319

Chicago Manual of Style (16th Edition):

Hanold, Laura Elizabeth. “Cyclization strategies to stabilize epidermal growth factor receptor dimerization arm mimics.” 2016. Doctoral Dissertation, University of Georgia. Accessed July 07, 2020. http://hdl.handle.net/10724/38319.

MLA Handbook (7th Edition):

Hanold, Laura Elizabeth. “Cyclization strategies to stabilize epidermal growth factor receptor dimerization arm mimics.” 2016. Web. 07 Jul 2020.

Vancouver:

Hanold LE. Cyclization strategies to stabilize epidermal growth factor receptor dimerization arm mimics. [Internet] [Doctoral dissertation]. University of Georgia; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10724/38319.

Council of Science Editors:

Hanold LE. Cyclization strategies to stabilize epidermal growth factor receptor dimerization arm mimics. [Doctoral Dissertation]. University of Georgia; 2016. Available from: http://hdl.handle.net/10724/38319


University of Arizona

9. Shen, Shengyi. Development of Split-protein Systems for Interrogating Biomacromolecules .

Degree: 2013, University of Arizona

 The specific interactions of macromolecules along with the activity of enzymes are central to all aspects of biology. It is well recognized that when the… (more)

Subjects/Keywords: Poly (ADP-ribose); protein kinase; Quantum Dot; split-protein; Chemistry; chemically induced dimerization

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APA (6th Edition):

Shen, S. (2013). Development of Split-protein Systems for Interrogating Biomacromolecules . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/308885

Chicago Manual of Style (16th Edition):

Shen, Shengyi. “Development of Split-protein Systems for Interrogating Biomacromolecules .” 2013. Doctoral Dissertation, University of Arizona. Accessed July 07, 2020. http://hdl.handle.net/10150/308885.

MLA Handbook (7th Edition):

Shen, Shengyi. “Development of Split-protein Systems for Interrogating Biomacromolecules .” 2013. Web. 07 Jul 2020.

Vancouver:

Shen S. Development of Split-protein Systems for Interrogating Biomacromolecules . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10150/308885.

Council of Science Editors:

Shen S. Development of Split-protein Systems for Interrogating Biomacromolecules . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/308885


Penn State University

10. Kenney, Scott Patrick. INSIGHTS INTO RETROVIRAL ASSEMBLY FROM MUTATION OF THE ROUS SARCOMA VIRUS p10 NUCLEAR EXPORT SEQUENCE.

Degree: PhD, Microbiology and Immunology, 2008, Penn State University

 Assembly of retroviruses is mediated by a polyprotein termed Gag, which is both necessary and sufficient to drive particle assembly. Gag functional domains are conserved… (more)

Subjects/Keywords: Retrovirus; retroviral assembly; Gag; p10; nuclear export; protein dimerization; FRET; FLIP; CRM1

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APA (6th Edition):

Kenney, S. P. (2008). INSIGHTS INTO RETROVIRAL ASSEMBLY FROM MUTATION OF THE ROUS SARCOMA VIRUS p10 NUCLEAR EXPORT SEQUENCE. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9234

Chicago Manual of Style (16th Edition):

Kenney, Scott Patrick. “INSIGHTS INTO RETROVIRAL ASSEMBLY FROM MUTATION OF THE ROUS SARCOMA VIRUS p10 NUCLEAR EXPORT SEQUENCE.” 2008. Doctoral Dissertation, Penn State University. Accessed July 07, 2020. https://etda.libraries.psu.edu/catalog/9234.

MLA Handbook (7th Edition):

Kenney, Scott Patrick. “INSIGHTS INTO RETROVIRAL ASSEMBLY FROM MUTATION OF THE ROUS SARCOMA VIRUS p10 NUCLEAR EXPORT SEQUENCE.” 2008. Web. 07 Jul 2020.

Vancouver:

Kenney SP. INSIGHTS INTO RETROVIRAL ASSEMBLY FROM MUTATION OF THE ROUS SARCOMA VIRUS p10 NUCLEAR EXPORT SEQUENCE. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2020 Jul 07]. Available from: https://etda.libraries.psu.edu/catalog/9234.

Council of Science Editors:

Kenney SP. INSIGHTS INTO RETROVIRAL ASSEMBLY FROM MUTATION OF THE ROUS SARCOMA VIRUS p10 NUCLEAR EXPORT SEQUENCE. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/9234


University of Arizona

11. Castillo-Montoya, Javier. Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction .

Degree: 2016, University of Arizona

 The function of most proteins is regulated by post-translational modifications, of which phosphorylation in particular has been shown to be ubiquitous and of paramount importance… (more)

Subjects/Keywords: Kinases; Ligand-Gated Phosphorylation; Protein Engineering; Split-Kinase; Split-Phosphatase; Chemical Inducer of Dimerization

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APA (6th Edition):

Castillo-Montoya, J. (2016). Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/623179

Chicago Manual of Style (16th Edition):

Castillo-Montoya, Javier. “Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction .” 2016. Doctoral Dissertation, University of Arizona. Accessed July 07, 2020. http://hdl.handle.net/10150/623179.

MLA Handbook (7th Edition):

Castillo-Montoya, Javier. “Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction .” 2016. Web. 07 Jul 2020.

Vancouver:

Castillo-Montoya J. Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10150/623179.

Council of Science Editors:

Castillo-Montoya J. Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/623179


Queens University

12. Lai, Yueyang. The interaction between the Sco protein from Bacillus subtilis and copper .

Degree: Biochemistry, 2010, Queens University

 Members of the Sco protein family have been proposed to function in the assembly of cytochrome c oxidase in the respiratory chain of all aerobic… (more)

Subjects/Keywords: Protein folding; Metal stabilization

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APA (6th Edition):

Lai, Y. (2010). The interaction between the Sco protein from Bacillus subtilis and copper . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6245

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):

Lai, Yueyang. “The interaction between the Sco protein from Bacillus subtilis and copper .” 2010. Thesis, Queens University. Accessed July 07, 2020. http://hdl.handle.net/1974/6245.

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

MLA Handbook (7th Edition):

Lai, Yueyang. “The interaction between the Sco protein from Bacillus subtilis and copper .” 2010. Web. 07 Jul 2020.

Vancouver:

Lai Y. The interaction between the Sco protein from Bacillus subtilis and copper . [Internet] [Thesis]. Queens University; 2010. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1974/6245.

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

Council of Science Editors:

Lai Y. The interaction between the Sco protein from Bacillus subtilis and copper . [Thesis]. Queens University; 2010. Available from: http://hdl.handle.net/1974/6245

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


Johannes Gutenberg Universität Mainz

13. Isbert, Simone. Cellular localization and mechanism of amyloid precursor protein (APP) homodimer formation in an oxidizing environment.

Degree: 2012, Johannes Gutenberg Universität Mainz

 The amyloid precursor protein (APP) is a type I transmembrane glycoprotein, which resembles a cell surface receptor, comprising a large ectodomain, a single spanning transmembrane… (more)

Subjects/Keywords: Amyloid Vorläufer Protein (APP); Dimerisierung; Endoplasmatisches Retikulum; Disulfidbrücken; Amyloid Precursor Protein (APP); Dimerization; Endoplasmic Reticulum; Disulfidebonds; Medical sciences Medicine

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APA (6th Edition):

Isbert, S. (2012). Cellular localization and mechanism of amyloid precursor protein (APP) homodimer formation in an oxidizing environment. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2012/3047/

Chicago Manual of Style (16th Edition):

Isbert, Simone. “Cellular localization and mechanism of amyloid precursor protein (APP) homodimer formation in an oxidizing environment.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed July 07, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2012/3047/.

MLA Handbook (7th Edition):

Isbert, Simone. “Cellular localization and mechanism of amyloid precursor protein (APP) homodimer formation in an oxidizing environment.” 2012. Web. 07 Jul 2020.

Vancouver:

Isbert S. Cellular localization and mechanism of amyloid precursor protein (APP) homodimer formation in an oxidizing environment. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2020 Jul 07]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3047/.

Council of Science Editors:

Isbert S. Cellular localization and mechanism of amyloid precursor protein (APP) homodimer formation in an oxidizing environment. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3047/


Freie Universität Berlin

14. Bethge, Tobias. Oligomerization, metal-binding properties, and function of the beta-secretase BACE1.

Degree: 2010, Freie Universität Berlin

 The “β-site APP-cleaving enzyme 1” (BACE1) is an aspartic acid protease with its catalytic activity in the ectodomain, a single transmembrane helix, and a short… (more)

Subjects/Keywords: Alzheimer; Alzheimer's disease; beta-secretase; BACE1; copper; metal-binding properties; dimerization; 500 Naturwissenschaften und Mathematik::540 Chemie

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APA (6th Edition):

Bethge, T. (2010). Oligomerization, metal-binding properties, and function of the beta-secretase BACE1. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-11067

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):

Bethge, Tobias. “Oligomerization, metal-binding properties, and function of the beta-secretase BACE1.” 2010. Thesis, Freie Universität Berlin. Accessed July 07, 2020. http://dx.doi.org/10.17169/refubium-11067.

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

MLA Handbook (7th Edition):

Bethge, Tobias. “Oligomerization, metal-binding properties, and function of the beta-secretase BACE1.” 2010. Web. 07 Jul 2020.

Vancouver:

Bethge T. Oligomerization, metal-binding properties, and function of the beta-secretase BACE1. [Internet] [Thesis]. Freie Universität Berlin; 2010. [cited 2020 Jul 07]. Available from: http://dx.doi.org/10.17169/refubium-11067.

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

Council of Science Editors:

Bethge T. Oligomerization, metal-binding properties, and function of the beta-secretase BACE1. [Thesis]. Freie Universität Berlin; 2010. Available from: http://dx.doi.org/10.17169/refubium-11067

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


University of Pennsylvania

15. Aonbangkhen, Chanat. Optochemical Tools For Protein Dimerization In Living Cells.

Degree: 2017, University of Pennsylvania

 Fundamental biological processes including cell division, migration, and death, are driven by protein interactions. Regulation of protein localization is one of the mechanisms cells utilize… (more)

Subjects/Keywords: Cell signaling; Chemical dimerizers; Optogenetics; Photocaged dimerizers; Photocleavable dimerizers; Protein dimerization; Cell Biology; Chemistry; Organic Chemistry

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APA (6th Edition):

Aonbangkhen, C. (2017). Optochemical Tools For Protein Dimerization In Living Cells. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2738

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):

Aonbangkhen, Chanat. “Optochemical Tools For Protein Dimerization In Living Cells.” 2017. Thesis, University of Pennsylvania. Accessed July 07, 2020. https://repository.upenn.edu/edissertations/2738.

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

MLA Handbook (7th Edition):

Aonbangkhen, Chanat. “Optochemical Tools For Protein Dimerization In Living Cells.” 2017. Web. 07 Jul 2020.

Vancouver:

Aonbangkhen C. Optochemical Tools For Protein Dimerization In Living Cells. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2020 Jul 07]. Available from: https://repository.upenn.edu/edissertations/2738.

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

Council of Science Editors:

Aonbangkhen C. Optochemical Tools For Protein Dimerization In Living Cells. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2738

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

16. Wassim, Ekram. Mécanismes moléculaires gouvernant la sélection et l'encapsidation de l'ARN génomique du VIH-1 : l’encapsidation sélective de l’ARN génomique du VIH-1 : Molecular mechanisms governing the selective encapsidation of HIV-1 genomic RNA.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2012, Université de Strasbourg

La sélection de l’ARNg des rétrovirus repose sur des interactions entre le domaine nucléocapside (NC) du précurseur Gag et des régions de l’ARN viral appelées… (more)

Subjects/Keywords: VIH-1; Pr55Gag; ARN génomique; ARN épissé; Packaging; Dimérisation; Dimerization; Packaging; HIV-1; Genomic RNA; Spliced RNA; Gag protein; 572.8; 579.2

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APA (6th Edition):

Wassim, E. (2012). Mécanismes moléculaires gouvernant la sélection et l'encapsidation de l'ARN génomique du VIH-1 : l’encapsidation sélective de l’ARN génomique du VIH-1 : Molecular mechanisms governing the selective encapsidation of HIV-1 genomic RNA. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAJ027

Chicago Manual of Style (16th Edition):

Wassim, Ekram. “Mécanismes moléculaires gouvernant la sélection et l'encapsidation de l'ARN génomique du VIH-1 : l’encapsidation sélective de l’ARN génomique du VIH-1 : Molecular mechanisms governing the selective encapsidation of HIV-1 genomic RNA.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed July 07, 2020. http://www.theses.fr/2012STRAJ027.

MLA Handbook (7th Edition):

Wassim, Ekram. “Mécanismes moléculaires gouvernant la sélection et l'encapsidation de l'ARN génomique du VIH-1 : l’encapsidation sélective de l’ARN génomique du VIH-1 : Molecular mechanisms governing the selective encapsidation of HIV-1 genomic RNA.” 2012. Web. 07 Jul 2020.

Vancouver:

Wassim E. Mécanismes moléculaires gouvernant la sélection et l'encapsidation de l'ARN génomique du VIH-1 : l’encapsidation sélective de l’ARN génomique du VIH-1 : Molecular mechanisms governing the selective encapsidation of HIV-1 genomic RNA. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2020 Jul 07]. Available from: http://www.theses.fr/2012STRAJ027.

Council of Science Editors:

Wassim E. Mécanismes moléculaires gouvernant la sélection et l'encapsidation de l'ARN génomique du VIH-1 : l’encapsidation sélective de l’ARN génomique du VIH-1 : Molecular mechanisms governing the selective encapsidation of HIV-1 genomic RNA. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAJ027


Freie Universität Berlin

17. Rutz, Natalja. Functional characterization and cellular interactions of KCTD5, the putative substrate adaptor for Cullin3-E3 ubiquitin ligase.

Degree: 2015, Freie Universität Berlin

 KCTD5 (potassium channel tetramerization domain containing protein 5) has been identified as interaction partner of the large regulatory Rep78/Rep68 proteins of adeno-associated virus (AAV-2). It… (more)

Subjects/Keywords: KCTD5; Cullin3 ligase; ubiquitin; protein modification; dimerization; MCM7; FAM193B; ZNF711; AAV; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Rutz, N. (2015). Functional characterization and cellular interactions of KCTD5, the putative substrate adaptor for Cullin3-E3 ubiquitin ligase. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-8493

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):

Rutz, Natalja. “Functional characterization and cellular interactions of KCTD5, the putative substrate adaptor for Cullin3-E3 ubiquitin ligase.” 2015. Thesis, Freie Universität Berlin. Accessed July 07, 2020. http://dx.doi.org/10.17169/refubium-8493.

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

MLA Handbook (7th Edition):

Rutz, Natalja. “Functional characterization and cellular interactions of KCTD5, the putative substrate adaptor for Cullin3-E3 ubiquitin ligase.” 2015. Web. 07 Jul 2020.

Vancouver:

Rutz N. Functional characterization and cellular interactions of KCTD5, the putative substrate adaptor for Cullin3-E3 ubiquitin ligase. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2020 Jul 07]. Available from: http://dx.doi.org/10.17169/refubium-8493.

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

Council of Science Editors:

Rutz N. Functional characterization and cellular interactions of KCTD5, the putative substrate adaptor for Cullin3-E3 ubiquitin ligase. [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-8493

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


McGill University

18. Soo Lum, Bernadette. The Chemistry of Cis and Trans-(C5H5)W(COh(PPh3)SR: Dimerization and Insertion Reactions of CS2 and SO2 into the W-SR Bond.

Degree: PhD, Department of Chemistry, 1990, McGill University

Note:

Treatment of CpW(CO)2(PPh3)H, (Cp = 115-cyclopentadienyl) with methyllithium and subsequently with RS-phth (R = CHMe2, CH2Ph, 4-C6H4Me, Ph and phth; phth = phthalimido), gave… (more)

Subjects/Keywords: Dimerization

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APA (6th Edition):

Soo Lum, B. (1990). The Chemistry of Cis and Trans-(C5H5)W(COh(PPh3)SR: Dimerization and Insertion Reactions of CS2 and SO2 into the W-SR Bond. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile161976.pdf

Chicago Manual of Style (16th Edition):

Soo Lum, Bernadette. “The Chemistry of Cis and Trans-(C5H5)W(COh(PPh3)SR: Dimerization and Insertion Reactions of CS2 and SO2 into the W-SR Bond.” 1990. Doctoral Dissertation, McGill University. Accessed July 07, 2020. http://digitool.library.mcgill.ca/thesisfile161976.pdf.

MLA Handbook (7th Edition):

Soo Lum, Bernadette. “The Chemistry of Cis and Trans-(C5H5)W(COh(PPh3)SR: Dimerization and Insertion Reactions of CS2 and SO2 into the W-SR Bond.” 1990. Web. 07 Jul 2020.

Vancouver:

Soo Lum B. The Chemistry of Cis and Trans-(C5H5)W(COh(PPh3)SR: Dimerization and Insertion Reactions of CS2 and SO2 into the W-SR Bond. [Internet] [Doctoral dissertation]. McGill University; 1990. [cited 2020 Jul 07]. Available from: http://digitool.library.mcgill.ca/thesisfile161976.pdf.

Council of Science Editors:

Soo Lum B. The Chemistry of Cis and Trans-(C5H5)W(COh(PPh3)SR: Dimerization and Insertion Reactions of CS2 and SO2 into the W-SR Bond. [Doctoral Dissertation]. McGill University; 1990. Available from: http://digitool.library.mcgill.ca/thesisfile161976.pdf


Hong Kong University of Science and Technology

19. Liu, Rui. CMOS class-C VCO and QVCO for WLAN applications.

Degree: 2013, Hong Kong University of Science and Technology

 WLAN (Wireless Local Area Network) applications based on 802.11 protocol family have enjoyed a tremendous growth in both home and enterprise market since it was… (more)

Subjects/Keywords: Voltage-controlled oscillators ; Wireless LANs ; Metal oxide semiconductors, Complementary

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APA (6th Edition):

Liu, R. (2013). CMOS class-C VCO and QVCO for WLAN applications. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-62320 ; https://doi.org/10.14711/thesis-b1255633 ; http://repository.ust.hk/ir/bitstream/1783.1-62320/1/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):

Liu, Rui. “CMOS class-C VCO and QVCO for WLAN applications.” 2013. Thesis, Hong Kong University of Science and Technology. Accessed July 07, 2020. http://repository.ust.hk/ir/Record/1783.1-62320 ; https://doi.org/10.14711/thesis-b1255633 ; http://repository.ust.hk/ir/bitstream/1783.1-62320/1/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):

Liu, Rui. “CMOS class-C VCO and QVCO for WLAN applications.” 2013. Web. 07 Jul 2020.

Vancouver:

Liu R. CMOS class-C VCO and QVCO for WLAN applications. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2013. [cited 2020 Jul 07]. Available from: http://repository.ust.hk/ir/Record/1783.1-62320 ; https://doi.org/10.14711/thesis-b1255633 ; http://repository.ust.hk/ir/bitstream/1783.1-62320/1/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:

Liu R. CMOS class-C VCO and QVCO for WLAN applications. [Thesis]. Hong Kong University of Science and Technology; 2013. Available from: http://repository.ust.hk/ir/Record/1783.1-62320 ; https://doi.org/10.14711/thesis-b1255633 ; http://repository.ust.hk/ir/bitstream/1783.1-62320/1/th_redirect.html

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


Miami University

20. Zheng, Liqiang. Protein Adsorption on Metal Oxides.

Degree: MS, Paper Science and Engineering, 2008, Miami University

 This paper presents an investigation on the adsorption of different proteins on ZnO and TiO2 particles surface. Isotherms were prepared to study the adsorbent surface… (more)

Subjects/Keywords: Chemical Engineering; protein adsorption; metal oxides

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APA (6th Edition):

Zheng, L. (2008). Protein Adsorption on Metal Oxides. (Masters Thesis). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1226889330

Chicago Manual of Style (16th Edition):

Zheng, Liqiang. “Protein Adsorption on Metal Oxides.” 2008. Masters Thesis, Miami University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=miami1226889330.

MLA Handbook (7th Edition):

Zheng, Liqiang. “Protein Adsorption on Metal Oxides.” 2008. Web. 07 Jul 2020.

Vancouver:

Zheng L. Protein Adsorption on Metal Oxides. [Internet] [Masters thesis]. Miami University; 2008. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1226889330.

Council of Science Editors:

Zheng L. Protein Adsorption on Metal Oxides. [Masters Thesis]. Miami University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1226889330


University of New South Wales

21. Man, Bradley Yat Wah. Transition metal and lanthanide complexes for catalysis and protein structure determination.

Degree: Chemistry, 2010, University of New South Wales

 This PhD thesis is divided into two sections, where the emphasis of the first section details the synthesis and development of small organic molecules as… (more)

Subjects/Keywords: Catalysis; Transition Metal; Lanthanide; Protein Steuctures

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APA (6th Edition):

Man, B. Y. W. (2010). Transition metal and lanthanide complexes for catalysis and protein structure determination. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/45063 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8358/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Man, Bradley Yat Wah. “Transition metal and lanthanide complexes for catalysis and protein structure determination.” 2010. Doctoral Dissertation, University of New South Wales. Accessed July 07, 2020. http://handle.unsw.edu.au/1959.4/45063 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8358/SOURCE02?view=true.

MLA Handbook (7th Edition):

Man, Bradley Yat Wah. “Transition metal and lanthanide complexes for catalysis and protein structure determination.” 2010. Web. 07 Jul 2020.

Vancouver:

Man BYW. Transition metal and lanthanide complexes for catalysis and protein structure determination. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2020 Jul 07]. Available from: http://handle.unsw.edu.au/1959.4/45063 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8358/SOURCE02?view=true.

Council of Science Editors:

Man BYW. Transition metal and lanthanide complexes for catalysis and protein structure determination. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/45063 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8358/SOURCE02?view=true


University of Alberta

22. Wang, Ruoxi. Barley protein based microcapsules for nutraceutical delivery.

Degree: MS, Department of Agricultural, Food and Nutritional Science, 2011, University of Alberta

 Barley protein based microcapsules (1-5µm) incorporating fish oil/β-carotene were successfully prepared. Well suspended solid microcapsules, rather than emulsions, were able to form after high pressure… (more)

Subjects/Keywords: β-carotene; oxidative stability; fish oil; barley protein; microencapsulation; controlled release

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APA (6th Edition):

Wang, R. (2011). Barley protein based microcapsules for nutraceutical delivery. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/ng451j804

Chicago Manual of Style (16th Edition):

Wang, Ruoxi. “Barley protein based microcapsules for nutraceutical delivery.” 2011. Masters Thesis, University of Alberta. Accessed July 07, 2020. https://era.library.ualberta.ca/files/ng451j804.

MLA Handbook (7th Edition):

Wang, Ruoxi. “Barley protein based microcapsules for nutraceutical delivery.” 2011. Web. 07 Jul 2020.

Vancouver:

Wang R. Barley protein based microcapsules for nutraceutical delivery. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2020 Jul 07]. Available from: https://era.library.ualberta.ca/files/ng451j804.

Council of Science Editors:

Wang R. Barley protein based microcapsules for nutraceutical delivery. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/ng451j804


Anna University

23. Rajesh, S. Identification cloning and characterisation of Translationally Controlled Tumor Protein TCTP from Indian Shrimp Penaeus Indicus;.

Degree: 2013, Anna University

White spot syndrome virus is a highly pathogenic virus causing white spot syndrome that result in severe economic burden in loss of millions of dollars… (more)

Subjects/Keywords: Translationally controlled tumer protein; Indian Shrimp; Penaeus Indicus

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APA (6th Edition):

Rajesh, S. (2013). Identification cloning and characterisation of Translationally Controlled Tumor Protein TCTP from Indian Shrimp Penaeus Indicus;. (Thesis). Anna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/10592

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):

Rajesh, S. “Identification cloning and characterisation of Translationally Controlled Tumor Protein TCTP from Indian Shrimp Penaeus Indicus;.” 2013. Thesis, Anna University. Accessed July 07, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/10592.

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

MLA Handbook (7th Edition):

Rajesh, S. “Identification cloning and characterisation of Translationally Controlled Tumor Protein TCTP from Indian Shrimp Penaeus Indicus;.” 2013. Web. 07 Jul 2020.

Vancouver:

Rajesh S. Identification cloning and characterisation of Translationally Controlled Tumor Protein TCTP from Indian Shrimp Penaeus Indicus;. [Internet] [Thesis]. Anna University; 2013. [cited 2020 Jul 07]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/10592.

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

Council of Science Editors:

Rajesh S. Identification cloning and characterisation of Translationally Controlled Tumor Protein TCTP from Indian Shrimp Penaeus Indicus;. [Thesis]. Anna University; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/10592

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


Virginia Tech

24. Kim, Kevin Dae Keon. The Translationally Controlled Tumor Protein (TCTP) associates to and destabilizes the Circadian Factor Period 2 (Per2).

Degree: MS, Biology, 2010, Virginia Tech

 Period 2 (Per2) is a core circadian factor responsible for its own negative regulation. It operates in the circadian clock, which affects multiple biological functions… (more)

Subjects/Keywords: circadian clock; proteolysis; Period2; Translationally controlled tumor protein

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APA (6th Edition):

Kim, K. D. K. (2010). The Translationally Controlled Tumor Protein (TCTP) associates to and destabilizes the Circadian Factor Period 2 (Per2). (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/76848

Chicago Manual of Style (16th Edition):

Kim, Kevin Dae Keon. “The Translationally Controlled Tumor Protein (TCTP) associates to and destabilizes the Circadian Factor Period 2 (Per2).” 2010. Masters Thesis, Virginia Tech. Accessed July 07, 2020. http://hdl.handle.net/10919/76848.

MLA Handbook (7th Edition):

Kim, Kevin Dae Keon. “The Translationally Controlled Tumor Protein (TCTP) associates to and destabilizes the Circadian Factor Period 2 (Per2).” 2010. Web. 07 Jul 2020.

Vancouver:

Kim KDK. The Translationally Controlled Tumor Protein (TCTP) associates to and destabilizes the Circadian Factor Period 2 (Per2). [Internet] [Masters thesis]. Virginia Tech; 2010. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10919/76848.

Council of Science Editors:

Kim KDK. The Translationally Controlled Tumor Protein (TCTP) associates to and destabilizes the Circadian Factor Period 2 (Per2). [Masters Thesis]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/76848


University of Michigan

25. Pisupati, Karthik. Stability and Structural Analysis of hGH and Infliximab for Controlled Release Depots and Biosimilars.

Degree: PhD, Pharmaceutical Sciences, 2016, University of Michigan

 Therapeutic proteins have revolutionized modern medicine and are a rapidly growing drug class. However, these complex entities suffer from high cost, instability, and the necessity… (more)

Subjects/Keywords: controlled release; biosimilar; protein therapeutics; Pharmacy and Pharmacology; Health Sciences

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APA (6th Edition):

Pisupati, K. (2016). Stability and Structural Analysis of hGH and Infliximab for Controlled Release Depots and Biosimilars. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120777

Chicago Manual of Style (16th Edition):

Pisupati, Karthik. “Stability and Structural Analysis of hGH and Infliximab for Controlled Release Depots and Biosimilars.” 2016. Doctoral Dissertation, University of Michigan. Accessed July 07, 2020. http://hdl.handle.net/2027.42/120777.

MLA Handbook (7th Edition):

Pisupati, Karthik. “Stability and Structural Analysis of hGH and Infliximab for Controlled Release Depots and Biosimilars.” 2016. Web. 07 Jul 2020.

Vancouver:

Pisupati K. Stability and Structural Analysis of hGH and Infliximab for Controlled Release Depots and Biosimilars. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/2027.42/120777.

Council of Science Editors:

Pisupati K. Stability and Structural Analysis of hGH and Infliximab for Controlled Release Depots and Biosimilars. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120777

26. SALVI, Claire. Effect of pH on polyelectrolyte multilayer formation and growth factor release.

Degree: MS, 2015, Worcester Polytechnic Institute

  Because of its high specific strength, durability, and biocompatibility, titanium is a widely used material for orthopedic implants. However, its insufficient binding with the… (more)

Subjects/Keywords: titanium implants; bone morphogenetic protein 2; pH; polyelectrolytes; controlled release

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APA (6th Edition):

SALVI, C. (2015). Effect of pH on polyelectrolyte multilayer formation and growth factor release. (Thesis). Worcester Polytechnic Institute. Retrieved from etd-042215-224151 ; https://digitalcommons.wpi.edu/etd-theses/238

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):

SALVI, Claire. “Effect of pH on polyelectrolyte multilayer formation and growth factor release.” 2015. Thesis, Worcester Polytechnic Institute. Accessed July 07, 2020. etd-042215-224151 ; https://digitalcommons.wpi.edu/etd-theses/238.

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

MLA Handbook (7th Edition):

SALVI, Claire. “Effect of pH on polyelectrolyte multilayer formation and growth factor release.” 2015. Web. 07 Jul 2020.

Vancouver:

SALVI C. Effect of pH on polyelectrolyte multilayer formation and growth factor release. [Internet] [Thesis]. Worcester Polytechnic Institute; 2015. [cited 2020 Jul 07]. Available from: etd-042215-224151 ; https://digitalcommons.wpi.edu/etd-theses/238.

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

Council of Science Editors:

SALVI C. Effect of pH on polyelectrolyte multilayer formation and growth factor release. [Thesis]. Worcester Polytechnic Institute; 2015. Available from: etd-042215-224151 ; https://digitalcommons.wpi.edu/etd-theses/238

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


Rochester Institute of Technology

27. Kovuri, Venkata Aditya. A Metallomics Study on Protein function assignment Using ProMOL.

Degree: MS, 2016, Rochester Institute of Technology

Metal ions are an integral part in both the structural and functional stability of enzymes. The function of an enzyme is exhibited through its… (more)

Subjects/Keywords: Metal databases for proteins; Metal ions in proteins; Predicting protein function; Protein function assignation

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APA (6th Edition):

Kovuri, V. A. (2016). A Metallomics Study on Protein function assignment Using ProMOL. (Masters Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/8978

Chicago Manual of Style (16th Edition):

Kovuri, Venkata Aditya. “A Metallomics Study on Protein function assignment Using ProMOL.” 2016. Masters Thesis, Rochester Institute of Technology. Accessed July 07, 2020. https://scholarworks.rit.edu/theses/8978.

MLA Handbook (7th Edition):

Kovuri, Venkata Aditya. “A Metallomics Study on Protein function assignment Using ProMOL.” 2016. Web. 07 Jul 2020.

Vancouver:

Kovuri VA. A Metallomics Study on Protein function assignment Using ProMOL. [Internet] [Masters thesis]. Rochester Institute of Technology; 2016. [cited 2020 Jul 07]. Available from: https://scholarworks.rit.edu/theses/8978.

Council of Science Editors:

Kovuri VA. A Metallomics Study on Protein function assignment Using ProMOL. [Masters Thesis]. Rochester Institute of Technology; 2016. Available from: https://scholarworks.rit.edu/theses/8978


Penn State University

28. Ross, Daniel Edward. KINETIC AND BIOCHEMCIAL ANALYSIS OF ELECTRON TRANSFER IN DISSIMILATORY METAL REDUCTION BY SHEWANELLA ONEIDENSIS MR-1.

Degree: PhD, Biochemistry and Molecular Biology, 2009, Penn State University

 ABSTRACT Biochemical studies were used to further elucidate the pathway of electron transfer across the outer membrane (OM) of Shewanella oneidensis MR-1 and scaling kinetics… (more)

Subjects/Keywords: dissimilatory metal reduction; scaling kinetics; protein-protein interactions

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APA (6th Edition):

Ross, D. E. (2009). KINETIC AND BIOCHEMCIAL ANALYSIS OF ELECTRON TRANSFER IN DISSIMILATORY METAL REDUCTION BY SHEWANELLA ONEIDENSIS MR-1. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9997

Chicago Manual of Style (16th Edition):

Ross, Daniel Edward. “KINETIC AND BIOCHEMCIAL ANALYSIS OF ELECTRON TRANSFER IN DISSIMILATORY METAL REDUCTION BY SHEWANELLA ONEIDENSIS MR-1.” 2009. Doctoral Dissertation, Penn State University. Accessed July 07, 2020. https://etda.libraries.psu.edu/catalog/9997.

MLA Handbook (7th Edition):

Ross, Daniel Edward. “KINETIC AND BIOCHEMCIAL ANALYSIS OF ELECTRON TRANSFER IN DISSIMILATORY METAL REDUCTION BY SHEWANELLA ONEIDENSIS MR-1.” 2009. Web. 07 Jul 2020.

Vancouver:

Ross DE. KINETIC AND BIOCHEMCIAL ANALYSIS OF ELECTRON TRANSFER IN DISSIMILATORY METAL REDUCTION BY SHEWANELLA ONEIDENSIS MR-1. [Internet] [Doctoral dissertation]. Penn State University; 2009. [cited 2020 Jul 07]. Available from: https://etda.libraries.psu.edu/catalog/9997.

Council of Science Editors:

Ross DE. KINETIC AND BIOCHEMCIAL ANALYSIS OF ELECTRON TRANSFER IN DISSIMILATORY METAL REDUCTION BY SHEWANELLA ONEIDENSIS MR-1. [Doctoral Dissertation]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/9997


University of Oregon

29. Wheeler, Lucas. The Evolution of Metal and Peptide Binding in the S100 Protein Family.

Degree: PhD, Department of Chemistry and Biochemistry, 2018, University of Oregon

 Proteins perform an incredible array of functions facilitated by a diverse set of biochemical properties. Changing these properties is an essential molecular mechanism of evolutionary… (more)

Subjects/Keywords: Metal binding; Phage display; Protein biochemistry; Protein evolution; S100 proteins; Specificity

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

APA (6th Edition):

Wheeler, L. (2018). The Evolution of Metal and Peptide Binding in the S100 Protein Family. (Doctoral Dissertation). University of Oregon. Retrieved from http://hdl.handle.net/1794/23178

Chicago Manual of Style (16th Edition):

Wheeler, Lucas. “The Evolution of Metal and Peptide Binding in the S100 Protein Family.” 2018. Doctoral Dissertation, University of Oregon. Accessed July 07, 2020. http://hdl.handle.net/1794/23178.

MLA Handbook (7th Edition):

Wheeler, Lucas. “The Evolution of Metal and Peptide Binding in the S100 Protein Family.” 2018. Web. 07 Jul 2020.

Vancouver:

Wheeler L. The Evolution of Metal and Peptide Binding in the S100 Protein Family. [Internet] [Doctoral dissertation]. University of Oregon; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1794/23178.

Council of Science Editors:

Wheeler L. The Evolution of Metal and Peptide Binding in the S100 Protein Family. [Doctoral Dissertation]. University of Oregon; 2018. Available from: http://hdl.handle.net/1794/23178

30. Patounas, Odysseas. Investigations on protein arginine methyltransferases in differentiation and cancer.

Degree: 2017, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

 Methylation of arginine residues by the family of Protein Arginine Methyltransferase (PRMT) enzymes is an important modulator of protein function that is involved in epigenetic… (more)

Subjects/Keywords: Μεθυλίωση αργινίνης; Καρκίνος; Νευρική διαφοροποίηση; Μεθυλοτρανσφεράσες της αργινίνης; Επιγενετική; Ολιγομερισμός της PRMT1; Διμερισμός της PRMT1; Βραχίονας διμερισμού της PRMT1; Arginine methylation; Cancer; Neuronal differentiation; Protein arginine methyltransferases; Epigenetics; PRMT1; PRMT8; LUHMES; PRMT1Δarm; PRMT1 oligomerization; PRMT1 dimerization; Dimerization arm of PRMT1

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APA (6th Edition):

Patounas, O. (2017). Investigations on protein arginine methyltransferases in differentiation and cancer. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/44707

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):

Patounas, Odysseas. “Investigations on protein arginine methyltransferases in differentiation and cancer.” 2017. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed July 07, 2020. http://hdl.handle.net/10442/hedi/44707.

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

MLA Handbook (7th Edition):

Patounas, Odysseas. “Investigations on protein arginine methyltransferases in differentiation and cancer.” 2017. Web. 07 Jul 2020.

Vancouver:

Patounas O. Investigations on protein arginine methyltransferases in differentiation and cancer. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2017. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10442/hedi/44707.

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

Council of Science Editors:

Patounas O. Investigations on protein arginine methyltransferases in differentiation and cancer. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2017. Available from: http://hdl.handle.net/10442/hedi/44707

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

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