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You searched for subject:(Dimerization). Showing records 1 – 30 of 193 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

Le traitement du complexe CpW(CO)2(PPh3)H, (Cp = 115-cyclopentadienyl) avec le methyllithium et ensuite avec le RS-phth (R = CHMe2, CH2Ph, 4-C6H4Me, Ph and phth; phth… (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 https://escholarship.mcgill.ca/downloads/9c67wq05v.pdf ; https://escholarship.mcgill.ca/concern/theses/bv73c293h

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 April 23, 2021. https://escholarship.mcgill.ca/downloads/9c67wq05v.pdf ; https://escholarship.mcgill.ca/concern/theses/bv73c293h.

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. 23 Apr 2021.

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 2021 Apr 23]. Available from: https://escholarship.mcgill.ca/downloads/9c67wq05v.pdf ; https://escholarship.mcgill.ca/concern/theses/bv73c293h.

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: https://escholarship.mcgill.ca/downloads/9c67wq05v.pdf ; https://escholarship.mcgill.ca/concern/theses/bv73c293h


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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Skeik RM. Dimerization of the DEAD-Box Cyanobacterial RNA Helicase Redox, CrhR. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2021 Apr 23]. 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


Harvard University

3. Severson, Eric A. Genome-Wide Identification and Characterization of Notch Transcriptional Complex-Binding Sequence Paired Sites in Leukemia Cells.

Degree: Master of Medical Sciences, 2016, Harvard University

Notch transcription complexes (NTCs) drive target gene expression by binding two distinct types of genomic response elements, NTC monomer sites and sequence-paired sites (SPSs) that… (more)

Subjects/Keywords: Notch1; SPS; dimerization; leukemia

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APA (6th Edition):

Severson, E. A. (2016). Genome-Wide Identification and Characterization of Notch Transcriptional Complex-Binding Sequence Paired Sites in Leukemia Cells. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061442

Chicago Manual of Style (16th Edition):

Severson, Eric A. “Genome-Wide Identification and Characterization of Notch Transcriptional Complex-Binding Sequence Paired Sites in Leukemia Cells.” 2016. Masters Thesis, Harvard University. Accessed April 23, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061442.

MLA Handbook (7th Edition):

Severson, Eric A. “Genome-Wide Identification and Characterization of Notch Transcriptional Complex-Binding Sequence Paired Sites in Leukemia Cells.” 2016. Web. 23 Apr 2021.

Vancouver:

Severson EA. Genome-Wide Identification and Characterization of Notch Transcriptional Complex-Binding Sequence Paired Sites in Leukemia Cells. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2021 Apr 23]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061442.

Council of Science Editors:

Severson EA. Genome-Wide Identification and Characterization of Notch Transcriptional Complex-Binding Sequence Paired Sites in Leukemia Cells. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061442


Université Catholique de Louvain

4. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Defour J. Thrombopoietin receptor : regulation, dimerization, oncogenic activation and bimodal signaling. [Internet] [Thesis]. Université Catholique de Louvain; 2016. [cited 2021 Apr 23]. 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


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 April 23, 2021. 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. 23 Apr 2021.

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 2021 Apr 23]. 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 Toronto

6. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Cai F. The Role of Dimerization by Escherichia coli HypB in Hydrogenase Biosynthesis. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2021 Apr 23]. 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


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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Pace CJ. Towards the Chemical Control of Membrane Protein Function. [Internet] [Doctoral dissertation]. Boston College; 2013. [cited 2021 Apr 23]. 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. Gajadhar, Aaron. In situ Proximity Ligation-­based Analysis Reveals Aberrant Dimerization and Activation of Epidermal Growth Factor Receptors Prevalent in Glioblastoma Multiforme.

Degree: 2011, University of Toronto

Aberrations in Epidermal Growth Factor Receptor (EGFR/ErbB1) signalling are the most common oncogenic stimuli in human glioblastoma multiforme (GBM). Interactions between mutant and wildtype ErbB… (more)

Subjects/Keywords: EGFR; Glioblastoma multiforme; dimerization; activation; 0760

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APA (6th Edition):

Gajadhar, A. (2011). In situ Proximity Ligation-­based Analysis Reveals Aberrant Dimerization and Activation of Epidermal Growth Factor Receptors Prevalent in Glioblastoma Multiforme. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/31755

Chicago Manual of Style (16th Edition):

Gajadhar, Aaron. “In situ Proximity Ligation-­based Analysis Reveals Aberrant Dimerization and Activation of Epidermal Growth Factor Receptors Prevalent in Glioblastoma Multiforme.” 2011. Doctoral Dissertation, University of Toronto. Accessed April 23, 2021. http://hdl.handle.net/1807/31755.

MLA Handbook (7th Edition):

Gajadhar, Aaron. “In situ Proximity Ligation-­based Analysis Reveals Aberrant Dimerization and Activation of Epidermal Growth Factor Receptors Prevalent in Glioblastoma Multiforme.” 2011. Web. 23 Apr 2021.

Vancouver:

Gajadhar A. In situ Proximity Ligation-­based Analysis Reveals Aberrant Dimerization and Activation of Epidermal Growth Factor Receptors Prevalent in Glioblastoma Multiforme. [Internet] [Doctoral dissertation]. University of Toronto; 2011. [cited 2021 Apr 23]. Available from: http://hdl.handle.net/1807/31755.

Council of Science Editors:

Gajadhar A. In situ Proximity Ligation-­based Analysis Reveals Aberrant Dimerization and Activation of Epidermal Growth Factor Receptors Prevalent in Glioblastoma Multiforme. [Doctoral Dissertation]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31755


University of New Mexico

9. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Wright C. ENGINEERING SMALL MOLECULE BASED DIMERIZATION TO INDUCE TRANSLATION AND PROVIDE OPTOGENETIC CONTROL. [Internet] [Doctoral dissertation]. University of New Mexico; 2016. [cited 2021 Apr 23]. 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


NSYSU

10. 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 April 23, 2021. 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. 23 Apr 2021.

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 2021 Apr 23]. 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


Dalhousie University

11. 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 April 23, 2021. 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. 23 Apr 2021.

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 2021 Apr 23]. 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


University of California – Berkeley

12. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Huang Y. Molecular basis for multimerization in the activation of the epidermal growth factor receptor. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2021 Apr 23]. 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

13. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Engel KA. Studies of the Allosteric Activation of the Epidermal Growth Factor Receptor. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2021 Apr 23]. 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

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

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 April 23, 2021. 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. 23 Apr 2021.

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 2021 Apr 23]. 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 Rochester

15. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Shen W(-). Factors that Promote Strand Transfer Recombination during HIV-1 Reverse Transcription. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2021 Apr 23]. 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

16. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Ballering J. Molecular insights into the mechanism of sensing and signal transduction of the thermosensor DesK. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2016. [cited 2021 Apr 23]. 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

17. 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 April 23, 2021. 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. 23 Apr 2021.

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 2021 Apr 23]. 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 California – San Diego

18. 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 (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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2021 Apr 23]. 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 Guelph

19. Jack, Kelsey. Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes.

Degree: MS, Department of Chemistry, 2012, University of Guelph

 Oxabicyclic alkenes have been the focus of many synthetic studies as they are versatile compounds which act as synthetic intermediates to produce a variety of… (more)

Subjects/Keywords: Cycloaddition; Oxabicyclic Alkenes; Dimerization; Cycloaddition; Ring Opening; Ruthenium

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APA (6th Edition):

Jack, K. (2012). Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4738

Chicago Manual of Style (16th Edition):

Jack, Kelsey. “Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes.” 2012. Masters Thesis, University of Guelph. Accessed April 23, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4738.

MLA Handbook (7th Edition):

Jack, Kelsey. “Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes.” 2012. Web. 23 Apr 2021.

Vancouver:

Jack K. Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes. [Internet] [Masters thesis]. University of Guelph; 2012. [cited 2021 Apr 23]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4738.

Council of Science Editors:

Jack K. Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes. [Masters Thesis]. University of Guelph; 2012. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4738


University of Illinois – Chicago

20. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Chavan TS. Intra and Intermolecular Interactions of K-Ras4B: From Structure to Function. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2021 Apr 23]. 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 Illinois – Chicago

21. 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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Zatolochnaya OV. Development of Pd-Catalyzed Alkyne Dimerization and Enyne Benzannulation Methodologies. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2021 Apr 23]. 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

22. Vogel, Holger. Controlling Ras activity by manipulating its localization.

Degree: 2018, Technische Universität Dortmund

 Proteins of the Ras family of small GTPases play a major role in the transduction of extracellular signals, especially growth factor signals, into the cell.… (more)

Subjects/Keywords: Ras; Chemically induced dimerization; Cell biology; 570; 540; Zellbiologie

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

APA (6th Edition):

Vogel, H. (2018). Controlling Ras activity by manipulating its localization. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-19874

Chicago Manual of Style (16th Edition):

Vogel, Holger. “Controlling Ras activity by manipulating its localization.” 2018. Doctoral Dissertation, Technische Universität Dortmund. Accessed April 23, 2021. http://dx.doi.org/10.17877/DE290R-19874.

MLA Handbook (7th Edition):

Vogel, Holger. “Controlling Ras activity by manipulating its localization.” 2018. Web. 23 Apr 2021.

Vancouver:

Vogel H. Controlling Ras activity by manipulating its localization. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2018. [cited 2021 Apr 23]. Available from: http://dx.doi.org/10.17877/DE290R-19874.

Council of Science Editors:

Vogel H. Controlling Ras activity by manipulating its localization. [Doctoral Dissertation]. Technische Universität Dortmund; 2018. Available from: http://dx.doi.org/10.17877/DE290R-19874


Boston University

23. Tucker Zhou, Tracey Beth. The human Klotho VS variant: focus on the processing and function of the V, S and VS isoforms.

Degree: PhD, Pharmacology & Experimental Therapeutics, 2014, Boston University

 Klotho (KL), an anti-aging protein, attracted interest in the aging field because of the dramatic phenotype of KL deficient mice and its connection to signaling… (more)

Subjects/Keywords: Molecular biology; Aging; Dimerization; Enzymatic activity; FGFR signaling; Genetic polymorphisms

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

APA (6th Edition):

Tucker Zhou, T. B. (2014). The human Klotho VS variant: focus on the processing and function of the V, S and VS isoforms. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/13168

Chicago Manual of Style (16th Edition):

Tucker Zhou, Tracey Beth. “The human Klotho VS variant: focus on the processing and function of the V, S and VS isoforms.” 2014. Doctoral Dissertation, Boston University. Accessed April 23, 2021. http://hdl.handle.net/2144/13168.

MLA Handbook (7th Edition):

Tucker Zhou, Tracey Beth. “The human Klotho VS variant: focus on the processing and function of the V, S and VS isoforms.” 2014. Web. 23 Apr 2021.

Vancouver:

Tucker Zhou TB. The human Klotho VS variant: focus on the processing and function of the V, S and VS isoforms. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2021 Apr 23]. Available from: http://hdl.handle.net/2144/13168.

Council of Science Editors:

Tucker Zhou TB. The human Klotho VS variant: focus on the processing and function of the V, S and VS isoforms. [Doctoral Dissertation]. Boston University; 2014. Available from: http://hdl.handle.net/2144/13168


University of Washington

24. Radmall, Kyler. Chemically Inducible Dimerization and Chemically Disruptable Systems for Spatial and Temporal Control of Cellular Processes.

Degree: 2020, University of Washington

 Spatial proximity–defined as the physical distance between two biomolecules–plays an important role in controlling and regulating many cellular functions. Engineered cellular systems have been developed… (more)

Subjects/Keywords: chemical disruption; chemically inducible dimerization; Biochemistry; Cellular biology; Chemistry

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APA (6th Edition):

Radmall, K. (2020). Chemically Inducible Dimerization and Chemically Disruptable Systems for Spatial and Temporal Control of Cellular Processes. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/45889

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):

Radmall, Kyler. “Chemically Inducible Dimerization and Chemically Disruptable Systems for Spatial and Temporal Control of Cellular Processes.” 2020. Thesis, University of Washington. Accessed April 23, 2021. http://hdl.handle.net/1773/45889.

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

MLA Handbook (7th Edition):

Radmall, Kyler. “Chemically Inducible Dimerization and Chemically Disruptable Systems for Spatial and Temporal Control of Cellular Processes.” 2020. Web. 23 Apr 2021.

Vancouver:

Radmall K. Chemically Inducible Dimerization and Chemically Disruptable Systems for Spatial and Temporal Control of Cellular Processes. [Internet] [Thesis]. University of Washington; 2020. [cited 2021 Apr 23]. Available from: http://hdl.handle.net/1773/45889.

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

Council of Science Editors:

Radmall K. Chemically Inducible Dimerization and Chemically Disruptable Systems for Spatial and Temporal Control of Cellular Processes. [Thesis]. University of Washington; 2020. Available from: http://hdl.handle.net/1773/45889

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


University of California – San Francisco

25. 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 (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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Matsuguchi T. Dimerization of Telomerase RNA During Telomerase Biogenesis Regulates Telomerase Activity. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2021 Apr 23]. 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

26. 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 (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 April 23, 2021. 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. 23 Apr 2021.

Vancouver:

Tien J. Studies of TMEM16A Calcium Activated Chloride Channel Structure and Function. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2021 Apr 23]. 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 Minnesota

27. Kreitlow, Benjamin. Exploring the Dimerization of BACE2-CFP Fusion Protein in HEK293 Cells through Fluorescence Microscopy Techniques.

Degree: MS, Integrated Biosciences, 2018, University of Minnesota

 Alzheimer’s disease (AD) is a neurodegenerative disorder frequently characterized by the presence of senile amyloid plaques. These plaques are formed through the aggregation of the… (more)

Subjects/Keywords: 2P-FLIM; Alzheimer's Disease; BACE2; BACE2-CFP; Dimerization; HEK293

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APA (6th Edition):

Kreitlow, B. (2018). Exploring the Dimerization of BACE2-CFP Fusion Protein in HEK293 Cells through Fluorescence Microscopy Techniques. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/216760

Chicago Manual of Style (16th Edition):

Kreitlow, Benjamin. “Exploring the Dimerization of BACE2-CFP Fusion Protein in HEK293 Cells through Fluorescence Microscopy Techniques.” 2018. Masters Thesis, University of Minnesota. Accessed April 23, 2021. http://hdl.handle.net/11299/216760.

MLA Handbook (7th Edition):

Kreitlow, Benjamin. “Exploring the Dimerization of BACE2-CFP Fusion Protein in HEK293 Cells through Fluorescence Microscopy Techniques.” 2018. Web. 23 Apr 2021.

Vancouver:

Kreitlow B. Exploring the Dimerization of BACE2-CFP Fusion Protein in HEK293 Cells through Fluorescence Microscopy Techniques. [Internet] [Masters thesis]. University of Minnesota; 2018. [cited 2021 Apr 23]. Available from: http://hdl.handle.net/11299/216760.

Council of Science Editors:

Kreitlow B. Exploring the Dimerization of BACE2-CFP Fusion Protein in HEK293 Cells through Fluorescence Microscopy Techniques. [Masters Thesis]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/216760


Université Catholique de Louvain

28. Perrin, Florian. Molecular determinants regulating dimerization, processing and signaling of the amyloid precursor protein.

Degree: 2019, Université Catholique de Louvain

Alzheimer’s disease (AD) is characterized by cognitive impairments such as apraxia, aphasia and memory decline. The two majors hallmarks of AD are neurofibrillary tangles and… (more)

Subjects/Keywords: Alzheimer's disease; Amyloid Precursor Protein; Dimerization; Oligomerization; Orientation; Processing

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

APA (6th Edition):

Perrin, F. (2019). Molecular determinants regulating dimerization, processing and signaling of the amyloid precursor protein. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/219632

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):

Perrin, Florian. “Molecular determinants regulating dimerization, processing and signaling of the amyloid precursor protein.” 2019. Thesis, Université Catholique de Louvain. Accessed April 23, 2021. http://hdl.handle.net/2078.1/219632.

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

MLA Handbook (7th Edition):

Perrin, Florian. “Molecular determinants regulating dimerization, processing and signaling of the amyloid precursor protein.” 2019. Web. 23 Apr 2021.

Vancouver:

Perrin F. Molecular determinants regulating dimerization, processing and signaling of the amyloid precursor protein. [Internet] [Thesis]. Université Catholique de Louvain; 2019. [cited 2021 Apr 23]. Available from: http://hdl.handle.net/2078.1/219632.

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

Council of Science Editors:

Perrin F. Molecular determinants regulating dimerization, processing and signaling of the amyloid precursor protein. [Thesis]. Université Catholique de Louvain; 2019. Available from: http://hdl.handle.net/2078.1/219632

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


Duquesne University

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

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 April 23, 2021. https://dsc.duq.edu/etd/424.

MLA Handbook (7th Edition):

Collins, Tyler. “Zinc-Mediated Dimerization of Proteins through a -CxCxxxxCxC- Sequence.” 2009. Web. 23 Apr 2021.

Vancouver:

Collins T. Zinc-Mediated Dimerization of Proteins through a -CxCxxxxCxC- Sequence. [Internet] [Doctoral dissertation]. Duquesne University; 2009. [cited 2021 Apr 23]. 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


Duquesne University

30. 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 April 23, 2021. 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. 23 Apr 2021.

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 2021 Apr 23]. 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

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