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You searched for subject:(dimerization). Showing records 1 – 30 of 165 total matches.

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McGill University

1. 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 November 17, 2019. 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. 17 Nov 2019.

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 2019 Nov 17]. 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


University of Alberta

2. Skeik, Reem M. Dimerization of the DEAD-Box Cyanobacterial RNA Helicase Redox, CrhR.

Degree: MS, Department of Biological Sciences, 2012, University of Alberta

 The DEAD-box cyanobacterial RNA helicase redox, or CrhR, in Synechocystis sp. PCC 6803 is capable of unwinding dsRNA and in annealing ssRNA in a bidirectional… (more)

Subjects/Keywords: Dimerization; Helicase; DEAD-box

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APA (6th Edition):

Skeik, R. M. (2012). Dimerization of the DEAD-Box Cyanobacterial RNA Helicase Redox, CrhR. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/2227mr311

Chicago Manual of Style (16th Edition):

Skeik, Reem M. “Dimerization of the DEAD-Box Cyanobacterial RNA Helicase Redox, CrhR.” 2012. Masters Thesis, University of Alberta. Accessed November 17, 2019. https://era.library.ualberta.ca/files/2227mr311.

MLA Handbook (7th Edition):

Skeik, Reem M. “Dimerization of the DEAD-Box Cyanobacterial RNA Helicase Redox, CrhR.” 2012. Web. 17 Nov 2019.

Vancouver:

Skeik RM. Dimerization of the DEAD-Box Cyanobacterial RNA Helicase Redox, CrhR. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2019 Nov 17]. Available from: https://era.library.ualberta.ca/files/2227mr311.

Council of Science Editors:

Skeik RM. Dimerization of the DEAD-Box Cyanobacterial RNA Helicase Redox, CrhR. [Masters Thesis]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/2227mr311


Université Catholique de Louvain

3. Defour, Jean-Philippe. Thrombopoietin receptor : regulation, dimerization, oncogenic activation and bimodal signaling.

Degree: 2016, Université Catholique de Louvain

Philadelphia negative myeloproliferative neoplasms include polycythemia vera, essential thrombocythemia and primary myelofibrosis. Those MPNs are clonal diseases for which the phenotype is almost always driven… (more)

Subjects/Keywords: TpoR; Mpl; Thrombopoietin; Dimerization; Cytokines

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APA (6th Edition):

Defour, J. (2016). Thrombopoietin receptor : regulation, dimerization, oncogenic activation and bimodal signaling. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/171096

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):

Defour, Jean-Philippe. “Thrombopoietin receptor : regulation, dimerization, oncogenic activation and bimodal signaling.” 2016. Thesis, Université Catholique de Louvain. Accessed November 17, 2019. http://hdl.handle.net/2078.1/171096.

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

MLA Handbook (7th Edition):

Defour, Jean-Philippe. “Thrombopoietin receptor : regulation, dimerization, oncogenic activation and bimodal signaling.” 2016. Web. 17 Nov 2019.

Vancouver:

Defour J. Thrombopoietin receptor : regulation, dimerization, oncogenic activation and bimodal signaling. [Internet] [Thesis]. Université Catholique de Louvain; 2016. [cited 2019 Nov 17]. Available from: http://hdl.handle.net/2078.1/171096.

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

Council of Science Editors:

Defour J. Thrombopoietin receptor : regulation, dimerization, oncogenic activation and bimodal signaling. [Thesis]. Université Catholique de Louvain; 2016. Available from: http://hdl.handle.net/2078.1/171096

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


Duquesne University

4. Collins, Tyler. Zinc-Mediated Dimerization of Proteins through a -CxCxxxxCxC- Sequence.

Degree: PhD, Chemistry and Biochemistry, 2009, Duquesne University

Dimerization of cellular proteins has become an intense field of study due to its importance in signal transduction and gene expression, amongst many other functions.… (more)

Subjects/Keywords: CopY; Dimerization; ITC; Zinc

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APA (6th Edition):

Collins, T. (2009). Zinc-Mediated Dimerization of Proteins through a -CxCxxxxCxC- Sequence. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/424

Chicago Manual of Style (16th Edition):

Collins, Tyler. “Zinc-Mediated Dimerization of Proteins through a -CxCxxxxCxC- Sequence.” 2009. Doctoral Dissertation, Duquesne University. Accessed November 17, 2019. https://dsc.duq.edu/etd/424.

MLA Handbook (7th Edition):

Collins, Tyler. “Zinc-Mediated Dimerization of Proteins through a -CxCxxxxCxC- Sequence.” 2009. Web. 17 Nov 2019.

Vancouver:

Collins T. Zinc-Mediated Dimerization of Proteins through a -CxCxxxxCxC- Sequence. [Internet] [Doctoral dissertation]. Duquesne University; 2009. [cited 2019 Nov 17]. Available from: https://dsc.duq.edu/etd/424.

Council of Science Editors:

Collins T. Zinc-Mediated Dimerization of Proteins through a -CxCxxxxCxC- Sequence. [Doctoral Dissertation]. Duquesne University; 2009. Available from: https://dsc.duq.edu/etd/424


Dalhousie University

5. Holland, Patrick. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

 GPCRs are known to form dimeric structures, and this affects their pharmacological properties. The ?2AR and AT1aR are GPCRs that are involved the regulation of… (more)

Subjects/Keywords: GPCRs; Signalling; Polymorphism; Dimerization; Receptor Pharmacology

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APA (6th Edition):

Holland, P. (2012). DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15245

Chicago Manual of Style (16th Edition):

Holland, Patrick. “DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.” 2012. Masters Thesis, Dalhousie University. Accessed November 17, 2019. http://hdl.handle.net/10222/15245.

MLA Handbook (7th Edition):

Holland, Patrick. “DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.” 2012. Web. 17 Nov 2019.

Vancouver:

Holland P. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2019 Nov 17]. Available from: http://hdl.handle.net/10222/15245.

Council of Science Editors:

Holland P. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15245


University of New Mexico

6. Wright, Catherine. ENGINEERING SMALL MOLECULE BASED DIMERIZATION TO INDUCE TRANSLATION AND PROVIDE OPTOGENETIC CONTROL.

Degree: Department of Chemistry and Chemical Biology, 2016, University of New Mexico

  We wanted to develop a system that combines the spatial control of photoactivation and control of translation to build a tool to spatially control… (more)

Subjects/Keywords: translation; dimerization; photocleavage; photodimerization; Biochemistry; Chemistry

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APA (6th Edition):

Wright, C. (2016). ENGINEERING SMALL MOLECULE BASED DIMERIZATION TO INDUCE TRANSLATION AND PROVIDE OPTOGENETIC CONTROL. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/59

Chicago Manual of Style (16th Edition):

Wright, Catherine. “ENGINEERING SMALL MOLECULE BASED DIMERIZATION TO INDUCE TRANSLATION AND PROVIDE OPTOGENETIC CONTROL.” 2016. Doctoral Dissertation, University of New Mexico. Accessed November 17, 2019. https://digitalrepository.unm.edu/chem_etds/59.

MLA Handbook (7th Edition):

Wright, Catherine. “ENGINEERING SMALL MOLECULE BASED DIMERIZATION TO INDUCE TRANSLATION AND PROVIDE OPTOGENETIC CONTROL.” 2016. Web. 17 Nov 2019.

Vancouver:

Wright C. ENGINEERING SMALL MOLECULE BASED DIMERIZATION TO INDUCE TRANSLATION AND PROVIDE OPTOGENETIC CONTROL. [Internet] [Doctoral dissertation]. University of New Mexico; 2016. [cited 2019 Nov 17]. Available from: https://digitalrepository.unm.edu/chem_etds/59.

Council of Science Editors:

Wright C. ENGINEERING SMALL MOLECULE BASED DIMERIZATION TO INDUCE TRANSLATION AND PROVIDE OPTOGENETIC CONTROL. [Doctoral Dissertation]. University of New Mexico; 2016. Available from: https://digitalrepository.unm.edu/chem_etds/59


Boston College

7. 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 November 17, 2019. 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. 17 Nov 2019.

Vancouver:

Pace CJ. Towards the Chemical Control of Membrane Protein Function. [Internet] [Doctoral dissertation]. Boston College; 2013. [cited 2019 Nov 17]. 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 Toronto

8. Cai, Fang. The Role of Dimerization by Escherichia coli HypB in Hydrogenase Biosynthesis.

Degree: 2010, University of Toronto

Nickel insertion into the [NiFe]-hydrogenase requires the accessory protein HypB, which is a GTPase. The GTPase domain of Escherichia coli (E. coli) HypB undergoes dimerization(more)

Subjects/Keywords: Escherichia coli; HypB; Dimerization; Hydrogenase; 0487

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APA (6th Edition):

Cai, F. (2010). The Role of Dimerization by Escherichia coli HypB in Hydrogenase Biosynthesis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25441

Chicago Manual of Style (16th Edition):

Cai, Fang. “The Role of Dimerization by Escherichia coli HypB in Hydrogenase Biosynthesis.” 2010. Masters Thesis, University of Toronto. Accessed November 17, 2019. http://hdl.handle.net/1807/25441.

MLA Handbook (7th Edition):

Cai, Fang. “The Role of Dimerization by Escherichia coli HypB in Hydrogenase Biosynthesis.” 2010. Web. 17 Nov 2019.

Vancouver:

Cai F. The Role of Dimerization by Escherichia coli HypB in Hydrogenase Biosynthesis. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Nov 17]. Available from: http://hdl.handle.net/1807/25441.

Council of Science Editors:

Cai F. The Role of Dimerization by Escherichia coli HypB in Hydrogenase Biosynthesis. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25441


Ohio University

9. Tang, Tang. Monitoring Estrogen Receptor Dimerization via Bipartite Tetracysteine Display.

Degree: MS, Chemistry and Biochemistry (Arts and Sciences), 2019, Ohio University

 The human estrogen receptor (hER) is a ligand-mediated transcription factor that plays a critical role in cell growth, differentiation and development. In the classical model… (more)

Subjects/Keywords: Biochemistry; Biarsenicals; estrogen receptor dimerization; estradiol

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APA (6th Edition):

Tang, T. (2019). Monitoring Estrogen Receptor Dimerization via Bipartite Tetracysteine Display. (Masters Thesis). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1562622108928366

Chicago Manual of Style (16th Edition):

Tang, Tang. “Monitoring Estrogen Receptor Dimerization via Bipartite Tetracysteine Display.” 2019. Masters Thesis, Ohio University. Accessed November 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1562622108928366.

MLA Handbook (7th Edition):

Tang, Tang. “Monitoring Estrogen Receptor Dimerization via Bipartite Tetracysteine Display.” 2019. Web. 17 Nov 2019.

Vancouver:

Tang T. Monitoring Estrogen Receptor Dimerization via Bipartite Tetracysteine Display. [Internet] [Masters thesis]. Ohio University; 2019. [cited 2019 Nov 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1562622108928366.

Council of Science Editors:

Tang T. Monitoring Estrogen Receptor Dimerization via Bipartite Tetracysteine Display. [Masters Thesis]. Ohio University; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1562622108928366


Dalhousie University

10. 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 November 17, 2019. 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. 17 Nov 2019.

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 2019 Nov 17]. 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


Université de Montréal

11. Bourgeois-Daigneault, Marie-Claude. Structure-fonction de MARCH1, une E3 ubiquitine ligase régulant la présentation antigénique par le CMH II .

Degree: 2012, Université de Montréal

 Les molécules classiques du CMH de classe II sont responsables de la présentation de peptides exogènes par les cellules présentatrices d’antigène aux lymphocytes T CD4+.… (more)

Subjects/Keywords: MARCH1; ubiquitination; autorégulation; dimérisation; localisation; autoregulation; dimerization; localization

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APA (6th Edition):

Bourgeois-Daigneault, M. (2012). Structure-fonction de MARCH1, une E3 ubiquitine ligase régulant la présentation antigénique par le CMH II . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/8808

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):

Bourgeois-Daigneault, Marie-Claude. “Structure-fonction de MARCH1, une E3 ubiquitine ligase régulant la présentation antigénique par le CMH II .” 2012. Thesis, Université de Montréal. Accessed November 17, 2019. http://hdl.handle.net/1866/8808.

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

MLA Handbook (7th Edition):

Bourgeois-Daigneault, Marie-Claude. “Structure-fonction de MARCH1, une E3 ubiquitine ligase régulant la présentation antigénique par le CMH II .” 2012. Web. 17 Nov 2019.

Vancouver:

Bourgeois-Daigneault M. Structure-fonction de MARCH1, une E3 ubiquitine ligase régulant la présentation antigénique par le CMH II . [Internet] [Thesis]. Université de Montréal; 2012. [cited 2019 Nov 17]. Available from: http://hdl.handle.net/1866/8808.

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

Council of Science Editors:

Bourgeois-Daigneault M. Structure-fonction de MARCH1, une E3 ubiquitine ligase régulant la présentation antigénique par le CMH II . [Thesis]. Université de Montréal; 2012. Available from: http://hdl.handle.net/1866/8808

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


NSYSU

12. Hong, Kun-jing. Study of the molecular mechanism by which RECK suppresses drug resistance and cancer stemness by regulating Her2/Neu and Notch oncogenic pathways.

Degree: PhD, Institute of Biomedical Sciences, 2016, NSYSU

 Reversion-inducing cysteine rich protein with Kazal motifs (RECK) is an endogenous metastatic suppressor gene, which can inhibit matrix metalloproteinase MMP-2, MMP-9 and MT1-MMP to reduce… (more)

Subjects/Keywords: RECK; glycoprotein; matrix metalloproteinase; metastasis; cancer stem cell; dimerization; autophosphorylation

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APA (6th Edition):

Hong, K. (2016). Study of the molecular mechanism by which RECK suppresses drug resistance and cancer stemness by regulating Her2/Neu and Notch oncogenic pathways. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0028116-155048

Chicago Manual of Style (16th Edition):

Hong, Kun-jing. “Study of the molecular mechanism by which RECK suppresses drug resistance and cancer stemness by regulating Her2/Neu and Notch oncogenic pathways.” 2016. Doctoral Dissertation, NSYSU. Accessed November 17, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0028116-155048.

MLA Handbook (7th Edition):

Hong, Kun-jing. “Study of the molecular mechanism by which RECK suppresses drug resistance and cancer stemness by regulating Her2/Neu and Notch oncogenic pathways.” 2016. Web. 17 Nov 2019.

Vancouver:

Hong K. Study of the molecular mechanism by which RECK suppresses drug resistance and cancer stemness by regulating Her2/Neu and Notch oncogenic pathways. [Internet] [Doctoral dissertation]. NSYSU; 2016. [cited 2019 Nov 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0028116-155048.

Council of Science Editors:

Hong K. Study of the molecular mechanism by which RECK suppresses drug resistance and cancer stemness by regulating Her2/Neu and Notch oncogenic pathways. [Doctoral Dissertation]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0028116-155048

13. 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 November 17, 2019. 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. 17 Nov 2019.

Vancouver:

Ballering J. Molecular insights into the mechanism of sensing and signal transduction of the thermosensor DesK. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2016. [cited 2019 Nov 17]. 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


Lehigh University

14. Su, Pin-Chuan. Understanding the Structural Basis for Transmembrane Signaling in the CLR-RAMP1 Heterodimer.

Degree: PhD, Chemical Engineering, 2014, Lehigh University

 Membrane proteins comprise of 50% of all pharmaceutical targets in the human genome. These proteins reside in equilibrium between resting and active states that are… (more)

Subjects/Keywords: AraTM; CLR; Dimerization; DN-AraTM; OmpF; RAMP1; Chemical Engineering; Engineering

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

APA (6th Edition):

Su, P. (2014). Understanding the Structural Basis for Transmembrane Signaling in the CLR-RAMP1 Heterodimer. (Doctoral Dissertation). Lehigh University. Retrieved from https://preserve.lehigh.edu/etd/1640

Chicago Manual of Style (16th Edition):

Su, Pin-Chuan. “Understanding the Structural Basis for Transmembrane Signaling in the CLR-RAMP1 Heterodimer.” 2014. Doctoral Dissertation, Lehigh University. Accessed November 17, 2019. https://preserve.lehigh.edu/etd/1640.

MLA Handbook (7th Edition):

Su, Pin-Chuan. “Understanding the Structural Basis for Transmembrane Signaling in the CLR-RAMP1 Heterodimer.” 2014. Web. 17 Nov 2019.

Vancouver:

Su P. Understanding the Structural Basis for Transmembrane Signaling in the CLR-RAMP1 Heterodimer. [Internet] [Doctoral dissertation]. Lehigh University; 2014. [cited 2019 Nov 17]. Available from: https://preserve.lehigh.edu/etd/1640.

Council of Science Editors:

Su P. Understanding the Structural Basis for Transmembrane Signaling in the CLR-RAMP1 Heterodimer. [Doctoral Dissertation]. Lehigh University; 2014. Available from: https://preserve.lehigh.edu/etd/1640


University of Illinois – Chicago

15. Zatolochnaya, Olga V. Development of Pd-Catalyzed Alkyne Dimerization and Enyne Benzannulation Methodologies.

Degree: 2015, University of Illinois – Chicago

Dimerization of alkynes represents a fundamental reaction for a straightforward construction of carbon–carbon bonds in atom-economical manner. A general highly regio- and stereoselective palladium-catalyzed head-to-head… (more)

Subjects/Keywords: Aromatic Fluorides; Benzannulation; Dimerization of Alkynes; Enynes; Diynes; Palladium Catalysis

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APA (6th Edition):

Zatolochnaya, O. V. (2015). Development of Pd-Catalyzed Alkyne Dimerization and Enyne Benzannulation Methodologies. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19594

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):

Zatolochnaya, Olga V. “Development of Pd-Catalyzed Alkyne Dimerization and Enyne Benzannulation Methodologies.” 2015. Thesis, University of Illinois – Chicago. Accessed November 17, 2019. http://hdl.handle.net/10027/19594.

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

MLA Handbook (7th Edition):

Zatolochnaya, Olga V. “Development of Pd-Catalyzed Alkyne Dimerization and Enyne Benzannulation Methodologies.” 2015. Web. 17 Nov 2019.

Vancouver:

Zatolochnaya OV. Development of Pd-Catalyzed Alkyne Dimerization and Enyne Benzannulation Methodologies. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Nov 17]. Available from: http://hdl.handle.net/10027/19594.

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

Council of Science Editors:

Zatolochnaya OV. Development of Pd-Catalyzed Alkyne Dimerization and Enyne Benzannulation Methodologies. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19594

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


University of California – Berkeley

16. Huang, Yongjian. Molecular basis for multimerization in the activation of the epidermal growth factor receptor.

Degree: Biophysics, 2016, University of California – Berkeley

 AbstractMolecular basis for multimerization in the activation of the epidermal growth factor receptorbyYongjian HuangDoctor of Philosophy in BiophysicsUniversity of California, BerkeleyProfessor John Kuriyan, ChairThe epidermal… (more)

Subjects/Keywords: Biophysics; Biochemistry; dimerization; EGFR; multimerization; stepwise photobleaching; stoichiometry

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APA (6th Edition):

Huang, Y. (2016). Molecular basis for multimerization in the activation of the epidermal growth factor receptor. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/80q6j5fj

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

Chicago Manual of Style (16th Edition):

Huang, Yongjian. “Molecular basis for multimerization in the activation of the epidermal growth factor receptor.” 2016. Thesis, University of California – Berkeley. Accessed November 17, 2019. http://www.escholarship.org/uc/item/80q6j5fj.

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

MLA Handbook (7th Edition):

Huang, Yongjian. “Molecular basis for multimerization in the activation of the epidermal growth factor receptor.” 2016. Web. 17 Nov 2019.

Vancouver:

Huang Y. Molecular basis for multimerization in the activation of the epidermal growth factor receptor. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Nov 17]. Available from: http://www.escholarship.org/uc/item/80q6j5fj.

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

Council of Science Editors:

Huang Y. Molecular basis for multimerization in the activation of the epidermal growth factor receptor. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/80q6j5fj

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


University of California – Berkeley

17. Engel, Katherine Anne. Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor.

Degree: Molecular & Cell Biology, 2013, University of California – Berkeley

 Ligand binding to the extracellular domain of the epidermal growth factor receptor (EGFR) results in receptor dimerization and allosteric activation of the kinase domain through… (more)

Subjects/Keywords: Biochemistry; Molecular biology; activation; allostery; dimerization; Epidermal Growth Factor Receptor; kinase

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APA (6th Edition):

Engel, K. A. (2013). Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6g31k0nr

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):

Engel, Katherine Anne. “Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor.” 2013. Thesis, University of California – Berkeley. Accessed November 17, 2019. http://www.escholarship.org/uc/item/6g31k0nr.

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

MLA Handbook (7th Edition):

Engel, Katherine Anne. “Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor.” 2013. Web. 17 Nov 2019.

Vancouver:

Engel KA. Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Nov 17]. Available from: http://www.escholarship.org/uc/item/6g31k0nr.

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

Council of Science Editors:

Engel KA. Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/6g31k0nr

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


University of California – San Diego

18. Smith, Thomas Horace. Characterization of protease-activated receptor-4 trafficking and heterodimerization in modulating receptor signaling.

Degree: Biomedical Sciences, 2016, University of California – San Diego

 G protein-coupled receptors (GPCRs) are transmembrane proteins that allow cells to respond to extracellular stimuli. GPCR activation occurs when a ligand binds to the extracellular… (more)

Subjects/Keywords: Pharmacology; Molecular biology; Cellular biology; dimerization; endocytosis; GPCR; thrombin

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APA (6th Edition):

Smith, T. H. (2016). Characterization of protease-activated receptor-4 trafficking and heterodimerization in modulating receptor signaling. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/93g0t82v

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):

Smith, Thomas Horace. “Characterization of protease-activated receptor-4 trafficking and heterodimerization in modulating receptor signaling.” 2016. Thesis, University of California – San Diego. Accessed November 17, 2019. http://www.escholarship.org/uc/item/93g0t82v.

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

MLA Handbook (7th Edition):

Smith, Thomas Horace. “Characterization of protease-activated receptor-4 trafficking and heterodimerization in modulating receptor signaling.” 2016. Web. 17 Nov 2019.

Vancouver:

Smith TH. Characterization of protease-activated receptor-4 trafficking and heterodimerization in modulating receptor signaling. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2019 Nov 17]. Available from: http://www.escholarship.org/uc/item/93g0t82v.

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

Council of Science Editors:

Smith TH. Characterization of protease-activated receptor-4 trafficking and heterodimerization in modulating receptor signaling. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/93g0t82v

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


University of Illinois – Chicago

19. 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 November 17, 2019. 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. 17 Nov 2019.

Vancouver:

Chavan TS. Intra and Intermolecular Interactions of K-Ras4B: From Structure to Function. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Nov 17]. 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


University of Cincinnati

20. Shelton, Catherine L. Conserved Variation in Tandem Repeat Sequences Tunes the Self-Assembly and Stability Characteristics of the Staphylococcus epidermidis Biofilm Protein Aap.

Degree: PhD, Medicine: Molecular Genetics, Biochemistry, & Microbiology, 2016, University of Cincinnati

 <i>Staphylcoccus epidermidis</i> is a ubiquitous commensal of the human skin with few virulence factors; however once inside the body it can form robust biofilms, that… (more)

Subjects/Keywords: Biochemistry; biofilm; intercellular adhesion; Aap; stability; dimerization; Staphylococcus

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APA (6th Edition):

Shelton, C. L. (2016). Conserved Variation in Tandem Repeat Sequences Tunes the Self-Assembly and Stability Characteristics of the Staphylococcus epidermidis Biofilm Protein Aap. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470741409

Chicago Manual of Style (16th Edition):

Shelton, Catherine L. “Conserved Variation in Tandem Repeat Sequences Tunes the Self-Assembly and Stability Characteristics of the Staphylococcus epidermidis Biofilm Protein Aap.” 2016. Doctoral Dissertation, University of Cincinnati. Accessed November 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470741409.

MLA Handbook (7th Edition):

Shelton, Catherine L. “Conserved Variation in Tandem Repeat Sequences Tunes the Self-Assembly and Stability Characteristics of the Staphylococcus epidermidis Biofilm Protein Aap.” 2016. Web. 17 Nov 2019.

Vancouver:

Shelton CL. Conserved Variation in Tandem Repeat Sequences Tunes the Self-Assembly and Stability Characteristics of the Staphylococcus epidermidis Biofilm Protein Aap. [Internet] [Doctoral dissertation]. University of Cincinnati; 2016. [cited 2019 Nov 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470741409.

Council of Science Editors:

Shelton CL. Conserved Variation in Tandem Repeat Sequences Tunes the Self-Assembly and Stability Characteristics of the Staphylococcus epidermidis Biofilm Protein Aap. [Doctoral Dissertation]. University of Cincinnati; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470741409


Indiana University of Pennsylvania

21. Aljagthmi, Wafaa A. Determining the Effect of the R1 Peptide on lhx1a Dimerization.

Degree: MS, Biology, 2018, Indiana University of Pennsylvania

  Kidney disease is a major health problem and current treatments for kidney failure are expensive and have severe limitations. Therefore, an alternative therapy such… (more)

Subjects/Keywords: dimerization; kidney disease; lhx1a; peptide; peptide effect; regenerative therapies; Molecular Biology

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

APA (6th Edition):

Aljagthmi, W. A. (2018). Determining the Effect of the R1 Peptide on lhx1a Dimerization. (Thesis). Indiana University of Pennsylvania. Retrieved from https://knowledge.library.iup.edu/etd/1605

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):

Aljagthmi, Wafaa A. “Determining the Effect of the R1 Peptide on lhx1a Dimerization.” 2018. Thesis, Indiana University of Pennsylvania. Accessed November 17, 2019. https://knowledge.library.iup.edu/etd/1605.

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

MLA Handbook (7th Edition):

Aljagthmi, Wafaa A. “Determining the Effect of the R1 Peptide on lhx1a Dimerization.” 2018. Web. 17 Nov 2019.

Vancouver:

Aljagthmi WA. Determining the Effect of the R1 Peptide on lhx1a Dimerization. [Internet] [Thesis]. Indiana University of Pennsylvania; 2018. [cited 2019 Nov 17]. Available from: https://knowledge.library.iup.edu/etd/1605.

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

Council of Science Editors:

Aljagthmi WA. Determining the Effect of the R1 Peptide on lhx1a Dimerization. [Thesis]. Indiana University of Pennsylvania; 2018. Available from: https://knowledge.library.iup.edu/etd/1605

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


University of California – San Diego

22. 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 November 17, 2019. 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. 17 Nov 2019.

Vancouver:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2019 Nov 17]. 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


University of Minnesota

23. White, Brian Richard. Toward therapeutic nanoassemblies: the design and modeling of protein-protein interactions.

Degree: PhD, Medicinal Chemistry, 2009, University of Minnesota

 Unraveling the nanoscale processes of biological pathways via the testing, replication, and visualization of the underlying mechanisms remains a persistent challenge in the study of… (more)

Subjects/Keywords: Chemically Induced Dimerization; Computational Chemistry; DHFR; Dimerizer; Nanorings; Nanotechnology; Medicinal Chemistry

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

APA (6th Edition):

White, B. R. (2009). Toward therapeutic nanoassemblies: the design and modeling of protein-protein interactions. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/90847

Chicago Manual of Style (16th Edition):

White, Brian Richard. “Toward therapeutic nanoassemblies: the design and modeling of protein-protein interactions.” 2009. Doctoral Dissertation, University of Minnesota. Accessed November 17, 2019. http://purl.umn.edu/90847.

MLA Handbook (7th Edition):

White, Brian Richard. “Toward therapeutic nanoassemblies: the design and modeling of protein-protein interactions.” 2009. Web. 17 Nov 2019.

Vancouver:

White BR. Toward therapeutic nanoassemblies: the design and modeling of protein-protein interactions. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2019 Nov 17]. Available from: http://purl.umn.edu/90847.

Council of Science Editors:

White BR. Toward therapeutic nanoassemblies: the design and modeling of protein-protein interactions. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/90847


Duquesne University

24. Shetty, Sumangala. Essential RNA-RNA Interactions within the Hepatitis C Virus Genome as Potential Targets for Peptide Nucleic Acid Based Therapeutic Strategy.

Degree: PhD, Chemistry and Biochemistry, 2011, Duquesne University

 Hepatitis C, a life threatening disease, caused by the hepatitis C virus (HCV) currently affects over 170-200 million people worldwide (~3% of global human population),… (more)

Subjects/Keywords: Genomic dimerization; Hepatitis C virus; Kissing complex; PNA; RNA; Therapeutic

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

APA (6th Edition):

Shetty, S. (2011). Essential RNA-RNA Interactions within the Hepatitis C Virus Genome as Potential Targets for Peptide Nucleic Acid Based Therapeutic Strategy. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1185

Chicago Manual of Style (16th Edition):

Shetty, Sumangala. “Essential RNA-RNA Interactions within the Hepatitis C Virus Genome as Potential Targets for Peptide Nucleic Acid Based Therapeutic Strategy.” 2011. Doctoral Dissertation, Duquesne University. Accessed November 17, 2019. https://dsc.duq.edu/etd/1185.

MLA Handbook (7th Edition):

Shetty, Sumangala. “Essential RNA-RNA Interactions within the Hepatitis C Virus Genome as Potential Targets for Peptide Nucleic Acid Based Therapeutic Strategy.” 2011. Web. 17 Nov 2019.

Vancouver:

Shetty S. Essential RNA-RNA Interactions within the Hepatitis C Virus Genome as Potential Targets for Peptide Nucleic Acid Based Therapeutic Strategy. [Internet] [Doctoral dissertation]. Duquesne University; 2011. [cited 2019 Nov 17]. Available from: https://dsc.duq.edu/etd/1185.

Council of Science Editors:

Shetty S. Essential RNA-RNA Interactions within the Hepatitis C Virus Genome as Potential Targets for Peptide Nucleic Acid Based Therapeutic Strategy. [Doctoral Dissertation]. Duquesne University; 2011. Available from: https://dsc.duq.edu/etd/1185


University of Pennsylvania

25. Frey, Alexander Jack. Characterization and Targeting of Thromboxane Receptor Dimerization: A Gateway to Novel Therapeutic Developments.

Degree: 2013, University of Pennsylvania

 Thromboxane A2 (TXA2) contributes to cardiovascular disease (CVD) by activating platelets and vascular smooth muscle cell constriction and proliferation. Despite their preclinical efficacy, pharmacological antagonists… (more)

Subjects/Keywords: dimerization; GGL motif; GPCR; thromboxane; thromboxane receptor; Pharmacology

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APA (6th Edition):

Frey, A. J. (2013). Characterization and Targeting of Thromboxane Receptor Dimerization: A Gateway to Novel Therapeutic Developments. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/861

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):

Frey, Alexander Jack. “Characterization and Targeting of Thromboxane Receptor Dimerization: A Gateway to Novel Therapeutic Developments.” 2013. Thesis, University of Pennsylvania. Accessed November 17, 2019. https://repository.upenn.edu/edissertations/861.

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

MLA Handbook (7th Edition):

Frey, Alexander Jack. “Characterization and Targeting of Thromboxane Receptor Dimerization: A Gateway to Novel Therapeutic Developments.” 2013. Web. 17 Nov 2019.

Vancouver:

Frey AJ. Characterization and Targeting of Thromboxane Receptor Dimerization: A Gateway to Novel Therapeutic Developments. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2019 Nov 17]. Available from: https://repository.upenn.edu/edissertations/861.

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

Council of Science Editors:

Frey AJ. Characterization and Targeting of Thromboxane Receptor Dimerization: A Gateway to Novel Therapeutic Developments. [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/861

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


North Carolina State University

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

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 November 17, 2019. 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. 17 Nov 2019.

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 2019 Nov 17]. 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 Rochester

27. Shen, Wen (1984 - ). Factors that Promote Strand Transfer Recombination during HIV-1 Reverse Transcription.

Degree: PhD, 2012, University of Rochester

 Recombination between the two copackaged RNA genomes of HIV-1 creates viral diversity. During reverse transcription, recombination occurs by a strand transfer mechanism that involves a… (more)

Subjects/Keywords: G-Quartet; HIV-1; Recombination; HIV-1 Genome Dimerization

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APA (6th Edition):

Shen, W. (. -. ). (2012). Factors that Promote Strand Transfer Recombination during HIV-1 Reverse Transcription. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/25529

Chicago Manual of Style (16th Edition):

Shen, Wen (1984 - ). “Factors that Promote Strand Transfer Recombination during HIV-1 Reverse Transcription.” 2012. Doctoral Dissertation, University of Rochester. Accessed November 17, 2019. http://hdl.handle.net/1802/25529.

MLA Handbook (7th Edition):

Shen, Wen (1984 - ). “Factors that Promote Strand Transfer Recombination during HIV-1 Reverse Transcription.” 2012. Web. 17 Nov 2019.

Vancouver:

Shen W(-). Factors that Promote Strand Transfer Recombination during HIV-1 Reverse Transcription. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2019 Nov 17]. Available from: http://hdl.handle.net/1802/25529.

Council of Science Editors:

Shen W(-). Factors that Promote Strand Transfer Recombination during HIV-1 Reverse Transcription. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/25529


University of California – San Francisco

28. Matsuguchi, Tetsuya. Dimerization of Telomerase RNA During Telomerase Biogenesis Regulates Telomerase Activity.

Degree: Biochemistry and Molecular Biology, 2011, University of California – San Francisco

 Telomerase is a ribonucleoprotein complex minimally composed of telomerase reverse transcriptase and telomerase RNA, which contains the template region encoding the telomeric repeat sequence. This… (more)

Subjects/Keywords: Biochemistry; Molecular Biology; Genetics; Biogenesis; Dimerization; Telomerase; Telomerase RNA; TLC1

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

APA (6th Edition):

Matsuguchi, T. (2011). Dimerization of Telomerase RNA During Telomerase Biogenesis Regulates Telomerase Activity. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7fc9g5p8

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):

Matsuguchi, Tetsuya. “Dimerization of Telomerase RNA During Telomerase Biogenesis Regulates Telomerase Activity.” 2011. Thesis, University of California – San Francisco. Accessed November 17, 2019. http://www.escholarship.org/uc/item/7fc9g5p8.

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

MLA Handbook (7th Edition):

Matsuguchi, Tetsuya. “Dimerization of Telomerase RNA During Telomerase Biogenesis Regulates Telomerase Activity.” 2011. Web. 17 Nov 2019.

Vancouver:

Matsuguchi T. Dimerization of Telomerase RNA During Telomerase Biogenesis Regulates Telomerase Activity. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Nov 17]. Available from: http://www.escholarship.org/uc/item/7fc9g5p8.

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

Council of Science Editors:

Matsuguchi T. Dimerization of Telomerase RNA During Telomerase Biogenesis Regulates Telomerase Activity. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/7fc9g5p8

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


University of California – San Francisco

29. Tien, Jason. Studies of TMEM16A Calcium Activated Chloride Channel Structure and Function.

Degree: Neuroscience, 2014, University of California – San Francisco

 TMEM16A is a novel calcium-activated chloride channel first cloned in 2008. It is responsible for regulating secretions from the epithelium, excitability of smooth muscle, membrane… (more)

Subjects/Keywords: Biology; Biophysics; Neurosciences; Calcium; Dimerization; Oligomerization; TMEM16A; TMEM16B; TMEM16F

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

APA (6th Edition):

Tien, J. (2014). Studies of TMEM16A Calcium Activated Chloride Channel Structure and Function. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/26s2m1z3

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):

Tien, Jason. “Studies of TMEM16A Calcium Activated Chloride Channel Structure and Function.” 2014. Thesis, University of California – San Francisco. Accessed November 17, 2019. http://www.escholarship.org/uc/item/26s2m1z3.

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

MLA Handbook (7th Edition):

Tien, Jason. “Studies of TMEM16A Calcium Activated Chloride Channel Structure and Function.” 2014. Web. 17 Nov 2019.

Vancouver:

Tien J. Studies of TMEM16A Calcium Activated Chloride Channel Structure and Function. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2019 Nov 17]. Available from: http://www.escholarship.org/uc/item/26s2m1z3.

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

Council of Science Editors:

Tien J. Studies of TMEM16A Calcium Activated Chloride Channel Structure and Function. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/26s2m1z3

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


University of California – San Francisco

30. Loshbaugh, Amanda Lynne. Development and benchmarking of methods for computational design, and experimental characterization, of proteins that bind small-molecule ligands.

Degree: Biophysics, 2019, University of California – San Francisco

 I present computational and experimental methods relating to the design of binding interactions involving proteins, including interactions of protein/small molecule, dimeric protein/protein, and tertiary protein/small… (more)

Subjects/Keywords: Biophysics; Bioinformatics; Biochemistry; binding; biosensor; design; dimerization; protein; Rosetta

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

APA (6th Edition):

Loshbaugh, A. L. (2019). Development and benchmarking of methods for computational design, and experimental characterization, of proteins that bind small-molecule ligands. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2tr9t7vd

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):

Loshbaugh, Amanda Lynne. “Development and benchmarking of methods for computational design, and experimental characterization, of proteins that bind small-molecule ligands.” 2019. Thesis, University of California – San Francisco. Accessed November 17, 2019. http://www.escholarship.org/uc/item/2tr9t7vd.

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

MLA Handbook (7th Edition):

Loshbaugh, Amanda Lynne. “Development and benchmarking of methods for computational design, and experimental characterization, of proteins that bind small-molecule ligands.” 2019. Web. 17 Nov 2019.

Vancouver:

Loshbaugh AL. Development and benchmarking of methods for computational design, and experimental characterization, of proteins that bind small-molecule ligands. [Internet] [Thesis]. University of California – San Francisco; 2019. [cited 2019 Nov 17]. Available from: http://www.escholarship.org/uc/item/2tr9t7vd.

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

Council of Science Editors:

Loshbaugh AL. Development and benchmarking of methods for computational design, and experimental characterization, of proteins that bind small-molecule ligands. [Thesis]. University of California – San Francisco; 2019. Available from: http://www.escholarship.org/uc/item/2tr9t7vd

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

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