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You searched for subject:(protein fluorescence). Showing records 1 – 30 of 275 total matches.

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Texas A&M University

1. Jongsma, Candice Gene. Investigating cotranslational integration of a multi-spanning membrane protein into the endoplasmic reticulum membrane.

Degree: 2009, Texas A&M University

 Most membrane proteins in eukaryotic cells are co-translationally integrated into the endoplasmic reticulum (ER) membrane at aqueous pores termed translocons. During multi-spanning membrane protein (MSMP)… (more)

Subjects/Keywords: MEMBRANE; PROTEIN; FLUORESCENCE

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APA (6th Edition):

Jongsma, C. G. (2009). Investigating cotranslational integration of a multi-spanning membrane protein into the endoplasmic reticulum membrane. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2894

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):

Jongsma, Candice Gene. “Investigating cotranslational integration of a multi-spanning membrane protein into the endoplasmic reticulum membrane.” 2009. Thesis, Texas A&M University. Accessed June 06, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2894.

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

MLA Handbook (7th Edition):

Jongsma, Candice Gene. “Investigating cotranslational integration of a multi-spanning membrane protein into the endoplasmic reticulum membrane.” 2009. Web. 06 Jun 2020.

Vancouver:

Jongsma CG. Investigating cotranslational integration of a multi-spanning membrane protein into the endoplasmic reticulum membrane. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2894.

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

Council of Science Editors:

Jongsma CG. Investigating cotranslational integration of a multi-spanning membrane protein into the endoplasmic reticulum membrane. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2894

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


Texas A&M University

2. Jing, Nan. NANOFLUIDIC SINGLE MOLECULE DETECTION (SMD) FOR PROTEIN DETECTION AND INTERACTION DYNAMICS STUDY.

Degree: 2010, Texas A&M University

 The objective of this work is to develop a micro/nanofluidic-based single molecule detection (SMD) scheme, which would allow us to inspect individual protein or protein(more)

Subjects/Keywords: Single molecule detection; Nanofluidic; Fluorescence; Protein interaction

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APA (6th Edition):

Jing, N. (2010). NANOFLUIDIC SINGLE MOLECULE DETECTION (SMD) FOR PROTEIN DETECTION AND INTERACTION DYNAMICS STUDY. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-377

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):

Jing, Nan. “NANOFLUIDIC SINGLE MOLECULE DETECTION (SMD) FOR PROTEIN DETECTION AND INTERACTION DYNAMICS STUDY.” 2010. Thesis, Texas A&M University. Accessed June 06, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-377.

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

MLA Handbook (7th Edition):

Jing, Nan. “NANOFLUIDIC SINGLE MOLECULE DETECTION (SMD) FOR PROTEIN DETECTION AND INTERACTION DYNAMICS STUDY.” 2010. Web. 06 Jun 2020.

Vancouver:

Jing N. NANOFLUIDIC SINGLE MOLECULE DETECTION (SMD) FOR PROTEIN DETECTION AND INTERACTION DYNAMICS STUDY. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-377.

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

Council of Science Editors:

Jing N. NANOFLUIDIC SINGLE MOLECULE DETECTION (SMD) FOR PROTEIN DETECTION AND INTERACTION DYNAMICS STUDY. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-377

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


The Ohio State University

3. Qiu, Weihong. Ultrafast Protein Hydration Dynamics Investigated by Femtosecond Fluorescence Spectroscopy.

Degree: PhD, Biophysics, 2008, The Ohio State University

Protein hydration dynamics is essential for many biological functions. However, understanding protein hydration dynamics has been technically challenged by the time and spatial resolution. This… (more)

Subjects/Keywords: Biophysics; Protein hydration; femtosecond spectroscopy; fluorescence; quenching

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APA (6th Edition):

Qiu, W. (2008). Ultrafast Protein Hydration Dynamics Investigated by Femtosecond Fluorescence Spectroscopy. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1222202233

Chicago Manual of Style (16th Edition):

Qiu, Weihong. “Ultrafast Protein Hydration Dynamics Investigated by Femtosecond Fluorescence Spectroscopy.” 2008. Doctoral Dissertation, The Ohio State University. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1222202233.

MLA Handbook (7th Edition):

Qiu, Weihong. “Ultrafast Protein Hydration Dynamics Investigated by Femtosecond Fluorescence Spectroscopy.” 2008. Web. 06 Jun 2020.

Vancouver:

Qiu W. Ultrafast Protein Hydration Dynamics Investigated by Femtosecond Fluorescence Spectroscopy. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1222202233.

Council of Science Editors:

Qiu W. Ultrafast Protein Hydration Dynamics Investigated by Femtosecond Fluorescence Spectroscopy. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1222202233


NSYSU

4. Chen, Kuan-Lin. Design and Synthesis of Dihydroquinolin-4-imine and its Application in Protein Fluorescent Labeling.

Degree: Master, Chemistry, 2016, NSYSU

 In this research we have developed Cu (â ) catalysis synthesis of dihydroquinolin-4-imines via ketenimine intermediates. These dihydroquinolin-4-imine molecules have fluorescence properties and show very good… (more)

Subjects/Keywords: Proximity effects; Protein-labeling; Ketenimine; Fluorescence; Dihydroquinoline

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APA (6th Edition):

Chen, K. (2016). Design and Synthesis of Dihydroquinolin-4-imine and its Application in Protein Fluorescent Labeling. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622116-131822

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

Chicago Manual of Style (16th Edition):

Chen, Kuan-Lin. “Design and Synthesis of Dihydroquinolin-4-imine and its Application in Protein Fluorescent Labeling.” 2016. Thesis, NSYSU. Accessed June 06, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622116-131822.

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

MLA Handbook (7th Edition):

Chen, Kuan-Lin. “Design and Synthesis of Dihydroquinolin-4-imine and its Application in Protein Fluorescent Labeling.” 2016. Web. 06 Jun 2020.

Vancouver:

Chen K. Design and Synthesis of Dihydroquinolin-4-imine and its Application in Protein Fluorescent Labeling. [Internet] [Thesis]. NSYSU; 2016. [cited 2020 Jun 06]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622116-131822.

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

Council of Science Editors:

Chen K. Design and Synthesis of Dihydroquinolin-4-imine and its Application in Protein Fluorescent Labeling. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622116-131822

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


University of Ottawa

5. Strmiskova, Miroslava. Development of a Dimaleimide-Based Protein Labelling Technique for Fluorogenic, X-Ray Crystallography and NMR Applications .

Degree: 2016, University of Ottawa

 Fluorescent protein labelling is a powerful tool for the sensitive visualization of proteins in living cells, allowing the elucidation of their localization, trafficking and ultimately… (more)

Subjects/Keywords: fluorogenic labelling; protein; dimaleimide; fluorescence; rational design

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APA (6th Edition):

Strmiskova, M. (2016). Development of a Dimaleimide-Based Protein Labelling Technique for Fluorogenic, X-Ray Crystallography and NMR Applications . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/34175

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):

Strmiskova, Miroslava. “Development of a Dimaleimide-Based Protein Labelling Technique for Fluorogenic, X-Ray Crystallography and NMR Applications .” 2016. Thesis, University of Ottawa. Accessed June 06, 2020. http://hdl.handle.net/10393/34175.

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

MLA Handbook (7th Edition):

Strmiskova, Miroslava. “Development of a Dimaleimide-Based Protein Labelling Technique for Fluorogenic, X-Ray Crystallography and NMR Applications .” 2016. Web. 06 Jun 2020.

Vancouver:

Strmiskova M. Development of a Dimaleimide-Based Protein Labelling Technique for Fluorogenic, X-Ray Crystallography and NMR Applications . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10393/34175.

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

Council of Science Editors:

Strmiskova M. Development of a Dimaleimide-Based Protein Labelling Technique for Fluorogenic, X-Ray Crystallography and NMR Applications . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/34175

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


NSYSU

6. Chiu, Hung-Chi. Synthesis of Lysozyme-Stabilized Gold Nanoclusters for Fluorescent and Naked-Eye Detection of Cyanide.

Degree: Master, Chemistry, 2018, NSYSU

 This study developed a simple strategy to prepare lysozyme nanoparticle-encapsulated gold nanoclusters (LysNP-AuNCs) as a dual emission probe for ratiometric sensing of cyanide in tap… (more)

Subjects/Keywords: ratiometric sensor; protein nanoparticles; gold nanoclusters; fluorescence

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APA (6th Edition):

Chiu, H. (2018). Synthesis of Lysozyme-Stabilized Gold Nanoclusters for Fluorescent and Naked-Eye Detection of Cyanide. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622118-131108

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):

Chiu, Hung-Chi. “Synthesis of Lysozyme-Stabilized Gold Nanoclusters for Fluorescent and Naked-Eye Detection of Cyanide.” 2018. Thesis, NSYSU. Accessed June 06, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622118-131108.

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

MLA Handbook (7th Edition):

Chiu, Hung-Chi. “Synthesis of Lysozyme-Stabilized Gold Nanoclusters for Fluorescent and Naked-Eye Detection of Cyanide.” 2018. Web. 06 Jun 2020.

Vancouver:

Chiu H. Synthesis of Lysozyme-Stabilized Gold Nanoclusters for Fluorescent and Naked-Eye Detection of Cyanide. [Internet] [Thesis]. NSYSU; 2018. [cited 2020 Jun 06]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622118-131108.

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

Council of Science Editors:

Chiu H. Synthesis of Lysozyme-Stabilized Gold Nanoclusters for Fluorescent and Naked-Eye Detection of Cyanide. [Thesis]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622118-131108

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


National University of Ireland – Galway

7. Groza, Radu Constantin. Anisotropy resolved multi-dimensional emission spectroscopy (ARMES): a new tool for the quantitative and structural analysis of proteins .

Degree: 2016, National University of Ireland – Galway

 The quantitative and structural analysis of proteins is of great importance in numerous fields (from industrial to academic research). Requirements like ease of analysis, sample… (more)

Subjects/Keywords: Spectroscopy; Chemometrics; Protein analysis; Fluorescence; Anisotropy; Chemistry

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APA (6th Edition):

Groza, R. C. (2016). Anisotropy resolved multi-dimensional emission spectroscopy (ARMES): a new tool for the quantitative and structural analysis of proteins . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/5645

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):

Groza, Radu Constantin. “Anisotropy resolved multi-dimensional emission spectroscopy (ARMES): a new tool for the quantitative and structural analysis of proteins .” 2016. Thesis, National University of Ireland – Galway. Accessed June 06, 2020. http://hdl.handle.net/10379/5645.

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

MLA Handbook (7th Edition):

Groza, Radu Constantin. “Anisotropy resolved multi-dimensional emission spectroscopy (ARMES): a new tool for the quantitative and structural analysis of proteins .” 2016. Web. 06 Jun 2020.

Vancouver:

Groza RC. Anisotropy resolved multi-dimensional emission spectroscopy (ARMES): a new tool for the quantitative and structural analysis of proteins . [Internet] [Thesis]. National University of Ireland – Galway; 2016. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10379/5645.

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

Council of Science Editors:

Groza RC. Anisotropy resolved multi-dimensional emission spectroscopy (ARMES): a new tool for the quantitative and structural analysis of proteins . [Thesis]. National University of Ireland – Galway; 2016. Available from: http://hdl.handle.net/10379/5645

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


University of Illinois – Urbana-Champaign

8. Jain, Ankur. Probing cellular protein complexes using single-molecule pull-down.

Degree: PhD, 0319, 2014, University of Illinois – Urbana-Champaign

 Cellular processes result from dynamic interactions between biomolecules. The gold standard method for investigating interaction between biomolecules is the pull-down assay. We have extended the… (more)

Subjects/Keywords: single-molecule; fluorescence microscopy; protein interactions

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APA (6th Edition):

Jain, A. (2014). Probing cellular protein complexes using single-molecule pull-down. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46887

Chicago Manual of Style (16th Edition):

Jain, Ankur. “Probing cellular protein complexes using single-molecule pull-down.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed June 06, 2020. http://hdl.handle.net/2142/46887.

MLA Handbook (7th Edition):

Jain, Ankur. “Probing cellular protein complexes using single-molecule pull-down.” 2014. Web. 06 Jun 2020.

Vancouver:

Jain A. Probing cellular protein complexes using single-molecule pull-down. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2142/46887.

Council of Science Editors:

Jain A. Probing cellular protein complexes using single-molecule pull-down. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46887


University of Minnesota

9. Hur, Kwang Ho. Advancing Fluorescence Fluctuation Microscopy in Living Cells: From Non-stationary Signals to Ternary Protein Interactions.

Degree: PhD, Physics, 2015, University of Minnesota

Fluorescence fluctuation spectroscopy (FFS) is a powerful method for quantifying protein interactions. By exploiting the brightness of fluorescence intensity fluctuations we are able to measure… (more)

Subjects/Keywords: brightness analysis; fluorescence fluctuation; protein interaction

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APA (6th Edition):

Hur, K. H. (2015). Advancing Fluorescence Fluctuation Microscopy in Living Cells: From Non-stationary Signals to Ternary Protein Interactions. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/177159

Chicago Manual of Style (16th Edition):

Hur, Kwang Ho. “Advancing Fluorescence Fluctuation Microscopy in Living Cells: From Non-stationary Signals to Ternary Protein Interactions.” 2015. Doctoral Dissertation, University of Minnesota. Accessed June 06, 2020. http://hdl.handle.net/11299/177159.

MLA Handbook (7th Edition):

Hur, Kwang Ho. “Advancing Fluorescence Fluctuation Microscopy in Living Cells: From Non-stationary Signals to Ternary Protein Interactions.” 2015. Web. 06 Jun 2020.

Vancouver:

Hur KH. Advancing Fluorescence Fluctuation Microscopy in Living Cells: From Non-stationary Signals to Ternary Protein Interactions. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/11299/177159.

Council of Science Editors:

Hur KH. Advancing Fluorescence Fluctuation Microscopy in Living Cells: From Non-stationary Signals to Ternary Protein Interactions. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/177159


University of Toronto

10. Li, Yuchong. Insane in the Membrane: The Functional Assembly of a G Protein Coupled Receptor at the Single-Molecule Level.

Degree: PhD, 2018, University of Toronto

 Many aspects of cellular signaling pathways regulated by G protein coupled receptors (GPCRs) are not completely understood. In particular, two questions have been the focus… (more)

Subjects/Keywords: fluorescence microscopy; fluorescence spectroscopy; GPCR; G protein; oligomerization; 0786

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APA (6th Edition):

Li, Y. (2018). Insane in the Membrane: The Functional Assembly of a G Protein Coupled Receptor at the Single-Molecule Level. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/82949

Chicago Manual of Style (16th Edition):

Li, Yuchong. “Insane in the Membrane: The Functional Assembly of a G Protein Coupled Receptor at the Single-Molecule Level.” 2018. Doctoral Dissertation, University of Toronto. Accessed June 06, 2020. http://hdl.handle.net/1807/82949.

MLA Handbook (7th Edition):

Li, Yuchong. “Insane in the Membrane: The Functional Assembly of a G Protein Coupled Receptor at the Single-Molecule Level.” 2018. Web. 06 Jun 2020.

Vancouver:

Li Y. Insane in the Membrane: The Functional Assembly of a G Protein Coupled Receptor at the Single-Molecule Level. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1807/82949.

Council of Science Editors:

Li Y. Insane in the Membrane: The Functional Assembly of a G Protein Coupled Receptor at the Single-Molecule Level. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/82949


University of Minnesota

11. Smith, Elizabeth. Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins.

Degree: PhD, Physics, 2015, University of Minnesota

 The interactions of peripheral membrane proteins with both membrane lipids and proteins are vital for many cellular processes including membrane trafficking, cellular signaling, and cell… (more)

Subjects/Keywords: brightness; fluorescence; peripheral membrane protein; protein-lipid interactions; protein-protein interactions; z-scan

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APA (6th Edition):

Smith, E. (2015). Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/174893

Chicago Manual of Style (16th Edition):

Smith, Elizabeth. “Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins.” 2015. Doctoral Dissertation, University of Minnesota. Accessed June 06, 2020. http://hdl.handle.net/11299/174893.

MLA Handbook (7th Edition):

Smith, Elizabeth. “Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins.” 2015. Web. 06 Jun 2020.

Vancouver:

Smith E. Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/11299/174893.

Council of Science Editors:

Smith E. Quantitative Fluorescence Studies in Living Cells: Extending Fluorescence Fluctuation Spectroscopy to Peripheral Membrane Proteins. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/174893


University of Rochester

12. Dean, Kimberly Marie. Selection, Identification, and Characterization of Codon Pairs that Inhibit Translation and the Development of the RNA-ID Method to Measure the Effects of Cis-Regulatory Elements.

Degree: PhD, 2013, University of Rochester

 It has been known for over 30 years that synonymous codon choice regulates translation, but the characteristics of codons that inhibit translation, and the factors… (more)

Subjects/Keywords: Yeast; Genetic Code; Fluorescence, Green Fluorescent Protein; Red Fluorescent Protein

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APA (6th Edition):

Dean, K. M. (2013). Selection, Identification, and Characterization of Codon Pairs that Inhibit Translation and the Development of the RNA-ID Method to Measure the Effects of Cis-Regulatory Elements. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27301

Chicago Manual of Style (16th Edition):

Dean, Kimberly Marie. “Selection, Identification, and Characterization of Codon Pairs that Inhibit Translation and the Development of the RNA-ID Method to Measure the Effects of Cis-Regulatory Elements.” 2013. Doctoral Dissertation, University of Rochester. Accessed June 06, 2020. http://hdl.handle.net/1802/27301.

MLA Handbook (7th Edition):

Dean, Kimberly Marie. “Selection, Identification, and Characterization of Codon Pairs that Inhibit Translation and the Development of the RNA-ID Method to Measure the Effects of Cis-Regulatory Elements.” 2013. Web. 06 Jun 2020.

Vancouver:

Dean KM. Selection, Identification, and Characterization of Codon Pairs that Inhibit Translation and the Development of the RNA-ID Method to Measure the Effects of Cis-Regulatory Elements. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1802/27301.

Council of Science Editors:

Dean KM. Selection, Identification, and Characterization of Codon Pairs that Inhibit Translation and the Development of the RNA-ID Method to Measure the Effects of Cis-Regulatory Elements. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27301


Columbia University

13. Xu, Fang. Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation.

Degree: 2018, Columbia University

 This thesis focuses on an important aspect of protein functionality – protein-protein interactions (PPI). Three physical chemistry techniques for or derived from protein-protein interaction investigation… (more)

Subjects/Keywords: Chemistry, Physical and theoretical; Protein-protein interactions; Fluorescence; Energy transfer; Biochemistry

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APA (6th Edition):

Xu, F. (2018). Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8PP0HKZ

Chicago Manual of Style (16th Edition):

Xu, Fang. “Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation.” 2018. Doctoral Dissertation, Columbia University. Accessed June 06, 2020. https://doi.org/10.7916/D8PP0HKZ.

MLA Handbook (7th Edition):

Xu, Fang. “Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation.” 2018. Web. 06 Jun 2020.

Vancouver:

Xu F. Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2020 Jun 06]. Available from: https://doi.org/10.7916/D8PP0HKZ.

Council of Science Editors:

Xu F. Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8PP0HKZ


University of Waterloo

14. Farhangi, Shiva. Long Range Polymer Chain Dynamics Probed with Pyrene Excimer Fluorescence.

Degree: 2016, University of Waterloo

 A series of fluorescently labeled vinyl polymers bearing a C1-C18 side-chain (namely poly(methyl methacrylate), poly(butyl methacrylate), poly(octyl methacrylate), poly(lauryl methacrylate), and poly(stearyl methacrylate) were synthesized… (more)

Subjects/Keywords: Peptide; Protein; Protein Folding; Dynamics; Chemistry; Fluorescence; Pyrene; Polymers

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

APA (6th Edition):

Farhangi, S. (2016). Long Range Polymer Chain Dynamics Probed with Pyrene Excimer Fluorescence. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/10915

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):

Farhangi, Shiva. “Long Range Polymer Chain Dynamics Probed with Pyrene Excimer Fluorescence.” 2016. Thesis, University of Waterloo. Accessed June 06, 2020. http://hdl.handle.net/10012/10915.

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

MLA Handbook (7th Edition):

Farhangi, Shiva. “Long Range Polymer Chain Dynamics Probed with Pyrene Excimer Fluorescence.” 2016. Web. 06 Jun 2020.

Vancouver:

Farhangi S. Long Range Polymer Chain Dynamics Probed with Pyrene Excimer Fluorescence. [Internet] [Thesis]. University of Waterloo; 2016. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10012/10915.

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

Council of Science Editors:

Farhangi S. Long Range Polymer Chain Dynamics Probed with Pyrene Excimer Fluorescence. [Thesis]. University of Waterloo; 2016. Available from: http://hdl.handle.net/10012/10915

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


Georgia State University

15. Zhuo, You. Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins.

Degree: PhD, Chemistry, 2013, Georgia State University

  Transient change of cytosolic calcium level leads to physiological actions, which are modulated by the intracellular calcium stores, and gated by membrane calcium channels/pumps.… (more)

Subjects/Keywords: Protein design; Calcium binding; Kinetics; Fluorescence; NMR spectroscopy; Ligand-protein interaction

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APA (6th Edition):

Zhuo, Y. (2013). Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/84

Chicago Manual of Style (16th Edition):

Zhuo, You. “Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins.” 2013. Doctoral Dissertation, Georgia State University. Accessed June 06, 2020. https://scholarworks.gsu.edu/chemistry_diss/84.

MLA Handbook (7th Edition):

Zhuo, You. “Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins.” 2013. Web. 06 Jun 2020.

Vancouver:

Zhuo Y. Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins. [Internet] [Doctoral dissertation]. Georgia State University; 2013. [cited 2020 Jun 06]. Available from: https://scholarworks.gsu.edu/chemistry_diss/84.

Council of Science Editors:

Zhuo Y. Modulating Calcium Signaling by Protein Design and Analysis of Calcium Binding Proteins. [Doctoral Dissertation]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/chemistry_diss/84


University of South Florida

16. Nacheva, Katya Pavlova. Development of a Bio-Molecular Fluorescent Probe Used in Kinetic Target-Guided Synthesis for the Identification of Inhibitors of Enzymatic and Protein-Protein Interaction Targets.

Degree: 2012, University of South Florida

 Abstract Fluorescent molecules used as detection probes and sensors provide vital information about the chemical events in living cells. Despite the large variety of available… (more)

Subjects/Keywords: Fluorescence; Fragment-based lead discovery; Protein-protein interactions; Organic Chemistry

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APA (6th Edition):

Nacheva, K. P. (2012). Development of a Bio-Molecular Fluorescent Probe Used in Kinetic Target-Guided Synthesis for the Identification of Inhibitors of Enzymatic and Protein-Protein Interaction Targets. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4376

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):

Nacheva, Katya Pavlova. “Development of a Bio-Molecular Fluorescent Probe Used in Kinetic Target-Guided Synthesis for the Identification of Inhibitors of Enzymatic and Protein-Protein Interaction Targets.” 2012. Thesis, University of South Florida. Accessed June 06, 2020. https://scholarcommons.usf.edu/etd/4376.

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

MLA Handbook (7th Edition):

Nacheva, Katya Pavlova. “Development of a Bio-Molecular Fluorescent Probe Used in Kinetic Target-Guided Synthesis for the Identification of Inhibitors of Enzymatic and Protein-Protein Interaction Targets.” 2012. Web. 06 Jun 2020.

Vancouver:

Nacheva KP. Development of a Bio-Molecular Fluorescent Probe Used in Kinetic Target-Guided Synthesis for the Identification of Inhibitors of Enzymatic and Protein-Protein Interaction Targets. [Internet] [Thesis]. University of South Florida; 2012. [cited 2020 Jun 06]. Available from: https://scholarcommons.usf.edu/etd/4376.

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

Council of Science Editors:

Nacheva KP. Development of a Bio-Molecular Fluorescent Probe Used in Kinetic Target-Guided Synthesis for the Identification of Inhibitors of Enzymatic and Protein-Protein Interaction Targets. [Thesis]. University of South Florida; 2012. Available from: https://scholarcommons.usf.edu/etd/4376

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


University of Western Australia

17. Xu, Lin. Uncovering the evolutionary history of dual-targeted proteins in land plants.

Degree: PhD, 2013, University of Western Australia

Over 107 proteins have been found to be dual-targeted to either mitochondria and plastids, or mitochondria/plastids and peroxisomes. To investigate whether the orthologs of dual-targeted… (more)

Subjects/Keywords: Mitochondria; Protein targeting; Dual targeting; Fluorescence protein; Peroxisomes; Plastids; Plant evolution; Organellar protein

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APA (6th Edition):

Xu, L. (2013). Uncovering the evolutionary history of dual-targeted proteins in land plants. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=35134&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Xu, Lin. “Uncovering the evolutionary history of dual-targeted proteins in land plants.” 2013. Doctoral Dissertation, University of Western Australia. Accessed June 06, 2020. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=35134&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Xu, Lin. “Uncovering the evolutionary history of dual-targeted proteins in land plants.” 2013. Web. 06 Jun 2020.

Vancouver:

Xu L. Uncovering the evolutionary history of dual-targeted proteins in land plants. [Internet] [Doctoral dissertation]. University of Western Australia; 2013. [cited 2020 Jun 06]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=35134&local_base=GEN01-INS01.

Council of Science Editors:

Xu L. Uncovering the evolutionary history of dual-targeted proteins in land plants. [Doctoral Dissertation]. University of Western Australia; 2013. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=35134&local_base=GEN01-INS01


University of Edinburgh

18. Chen, Kai. Use of green fluorescent protein for the analysis of protein-protein and protein-DNA interactions.

Degree: PhD, 2011, University of Edinburgh

 Restriction modification (RM) systems play a crucial role in preventing the entry of foreign DNA into the bacterial cell. The best studied Type I RM… (more)

Subjects/Keywords: 572.8; GFP; green fluorescent protein; protein-protein; DNA restriction/modification; Time-resolved fluorescence

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APA (6th Edition):

Chen, K. (2011). Use of green fluorescent protein for the analysis of protein-protein and protein-DNA interactions. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4886

Chicago Manual of Style (16th Edition):

Chen, Kai. “Use of green fluorescent protein for the analysis of protein-protein and protein-DNA interactions.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed June 06, 2020. http://hdl.handle.net/1842/4886.

MLA Handbook (7th Edition):

Chen, Kai. “Use of green fluorescent protein for the analysis of protein-protein and protein-DNA interactions.” 2011. Web. 06 Jun 2020.

Vancouver:

Chen K. Use of green fluorescent protein for the analysis of protein-protein and protein-DNA interactions. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1842/4886.

Council of Science Editors:

Chen K. Use of green fluorescent protein for the analysis of protein-protein and protein-DNA interactions. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/4886

19. Vaissiere, Anaïs. Etude de l’interaction de protéines nucléaire : RevErb alpha / NCor par des techniques de fluorescence (Anisotropie et Microscopie) : Study of interaction between the nuclear proteins : RevErb alpha / N-Cor by fluorescence anisotropy and N&B techniques.

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

 Les récepteurs nucléaires sont membres d'une famille de protéines activées par des ligands et qui régulent la transcription de nombreux gènes. Le récepteur nucléaire RevErbα… (more)

Subjects/Keywords: Interactions protéine-Protéine; Microscopie de fluctuation de fluorescence; Anisotropie de fluorescence; Récepteurs nucléaires; Protein-Protein interaction; Fluorescence fluctuation microscopy; Fluorescence anisotropy; Nuclear receptors; 616

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APA (6th Edition):

Vaissiere, A. (2014). Etude de l’interaction de protéines nucléaire : RevErb alpha / NCor par des techniques de fluorescence (Anisotropie et Microscopie) : Study of interaction between the nuclear proteins : RevErb alpha / N-Cor by fluorescence anisotropy and N&B techniques. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2014MON13510

Chicago Manual of Style (16th Edition):

Vaissiere, Anaïs. “Etude de l’interaction de protéines nucléaire : RevErb alpha / NCor par des techniques de fluorescence (Anisotropie et Microscopie) : Study of interaction between the nuclear proteins : RevErb alpha / N-Cor by fluorescence anisotropy and N&B techniques.” 2014. Doctoral Dissertation, Université Montpellier I. Accessed June 06, 2020. http://www.theses.fr/2014MON13510.

MLA Handbook (7th Edition):

Vaissiere, Anaïs. “Etude de l’interaction de protéines nucléaire : RevErb alpha / NCor par des techniques de fluorescence (Anisotropie et Microscopie) : Study of interaction between the nuclear proteins : RevErb alpha / N-Cor by fluorescence anisotropy and N&B techniques.” 2014. Web. 06 Jun 2020.

Vancouver:

Vaissiere A. Etude de l’interaction de protéines nucléaire : RevErb alpha / NCor par des techniques de fluorescence (Anisotropie et Microscopie) : Study of interaction between the nuclear proteins : RevErb alpha / N-Cor by fluorescence anisotropy and N&B techniques. [Internet] [Doctoral dissertation]. Université Montpellier I; 2014. [cited 2020 Jun 06]. Available from: http://www.theses.fr/2014MON13510.

Council of Science Editors:

Vaissiere A. Etude de l’interaction de protéines nucléaire : RevErb alpha / NCor par des techniques de fluorescence (Anisotropie et Microscopie) : Study of interaction between the nuclear proteins : RevErb alpha / N-Cor by fluorescence anisotropy and N&B techniques. [Doctoral Dissertation]. Université Montpellier I; 2014. Available from: http://www.theses.fr/2014MON13510

20. Li, Chenge. Development of bioorthogonal fluorogenic reporters for biological imaging : Développement de marqueurs fluorogéniques bioorthogonaux pour l'imagerie biologique.

Degree: Docteur es, Chimie physique, 2017, Paris Sciences et Lettres

L'étude de la dynamique des protéines est essentielle pour comprendre les processus biologiques. Notre laboratoire a développé une nouvelle classe de protéines fluorescentes semi-synthétiques, appelée… (more)

Subjects/Keywords: Marqueur fluorogénique,; Fluorescence; Marquage protéique; Imagerie biologique; Fluorogenic probes; Fluorescence; Protein labeling; Biological imaging; 541.3

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APA (6th Edition):

Li, C. (2017). Development of bioorthogonal fluorogenic reporters for biological imaging : Développement de marqueurs fluorogéniques bioorthogonaux pour l'imagerie biologique. (Doctoral Dissertation). Paris Sciences et Lettres. Retrieved from http://www.theses.fr/2017PSLEE044

Chicago Manual of Style (16th Edition):

Li, Chenge. “Development of bioorthogonal fluorogenic reporters for biological imaging : Développement de marqueurs fluorogéniques bioorthogonaux pour l'imagerie biologique.” 2017. Doctoral Dissertation, Paris Sciences et Lettres. Accessed June 06, 2020. http://www.theses.fr/2017PSLEE044.

MLA Handbook (7th Edition):

Li, Chenge. “Development of bioorthogonal fluorogenic reporters for biological imaging : Développement de marqueurs fluorogéniques bioorthogonaux pour l'imagerie biologique.” 2017. Web. 06 Jun 2020.

Vancouver:

Li C. Development of bioorthogonal fluorogenic reporters for biological imaging : Développement de marqueurs fluorogéniques bioorthogonaux pour l'imagerie biologique. [Internet] [Doctoral dissertation]. Paris Sciences et Lettres; 2017. [cited 2020 Jun 06]. Available from: http://www.theses.fr/2017PSLEE044.

Council of Science Editors:

Li C. Development of bioorthogonal fluorogenic reporters for biological imaging : Développement de marqueurs fluorogéniques bioorthogonaux pour l'imagerie biologique. [Doctoral Dissertation]. Paris Sciences et Lettres; 2017. Available from: http://www.theses.fr/2017PSLEE044


Vanderbilt University

21. Yirdaw, Robel Birru. Conformational dynamics of proteins by fluorescence fluctuation spectroscopy.

Degree: PhD, Physics, 2012, Vanderbilt University

 Proteins, as intrinsically flexible molecules, exhibit internal motions at equilibrium. In general, the internal motions consist of changes in the three dimensional coordinates of the… (more)

Subjects/Keywords: Single Molecule Fluorescence Spectroscopy; T4 Lysozyme; Fluorescence Fluctuation Spectroscopy; Conformational Dynamics; Protein; Fluorescence Correlation Spectroscopy; Brightness Analysis; Cumulant Analysis

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APA (6th Edition):

Yirdaw, R. B. (2012). Conformational dynamics of proteins by fluorescence fluctuation spectroscopy. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07062012-163740/ ;

Chicago Manual of Style (16th Edition):

Yirdaw, Robel Birru. “Conformational dynamics of proteins by fluorescence fluctuation spectroscopy.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed June 06, 2020. http://etd.library.vanderbilt.edu/available/etd-07062012-163740/ ;.

MLA Handbook (7th Edition):

Yirdaw, Robel Birru. “Conformational dynamics of proteins by fluorescence fluctuation spectroscopy.” 2012. Web. 06 Jun 2020.

Vancouver:

Yirdaw RB. Conformational dynamics of proteins by fluorescence fluctuation spectroscopy. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Jun 06]. Available from: http://etd.library.vanderbilt.edu/available/etd-07062012-163740/ ;.

Council of Science Editors:

Yirdaw RB. Conformational dynamics of proteins by fluorescence fluctuation spectroscopy. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu/available/etd-07062012-163740/ ;


University of Akron

22. Klufas, Megan J. Resolving Membrane Receptor Multimerization in Live Cells using Time Resolved Fluorescence Methods.

Degree: PhD, Chemistry, 2017, University of Akron

 The cell membrane is a complex environment made up of thousands of molecular components. The dynamic assembly of these components regulates a myriad of cellular… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry; fluorescence correlation spectroscopy; fluorescence cross-correlation spectroscopy; pulsed interleaved excitation; homodimerization; homo-oligomerization; membrane organization; protein-protein interactions

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APA (6th Edition):

Klufas, M. J. (2017). Resolving Membrane Receptor Multimerization in Live Cells using Time Resolved Fluorescence Methods. (Doctoral Dissertation). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron151017994353956

Chicago Manual of Style (16th Edition):

Klufas, Megan J. “Resolving Membrane Receptor Multimerization in Live Cells using Time Resolved Fluorescence Methods.” 2017. Doctoral Dissertation, University of Akron. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron151017994353956.

MLA Handbook (7th Edition):

Klufas, Megan J. “Resolving Membrane Receptor Multimerization in Live Cells using Time Resolved Fluorescence Methods.” 2017. Web. 06 Jun 2020.

Vancouver:

Klufas MJ. Resolving Membrane Receptor Multimerization in Live Cells using Time Resolved Fluorescence Methods. [Internet] [Doctoral dissertation]. University of Akron; 2017. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron151017994353956.

Council of Science Editors:

Klufas MJ. Resolving Membrane Receptor Multimerization in Live Cells using Time Resolved Fluorescence Methods. [Doctoral Dissertation]. University of Akron; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron151017994353956


University of Illinois – Urbana-Champaign

23. Guzman Sanchez, Irisbel. Kinetics and thermodynamics of protein-RNA interactions and protein folding in vitro and in cells.

Degree: PhD, Biochemistry, 2015, University of Illinois – Urbana-Champaign

Protein-RNA interactions and protein folding are critical subjects in biochemistry, because of their significance during the formation of active complexes and signaling pathways. Regardless of… (more)

Subjects/Keywords: Protein-RNA interactions; protein folding; fluorescence; fluorescence resonance energy transfer (FRET); fast relaxation imagining (FREI); temperature jump

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APA (6th Edition):

Guzman Sanchez, I. (2015). Kinetics and thermodynamics of protein-RNA interactions and protein folding in vitro and in cells. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78610

Chicago Manual of Style (16th Edition):

Guzman Sanchez, Irisbel. “Kinetics and thermodynamics of protein-RNA interactions and protein folding in vitro and in cells.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed June 06, 2020. http://hdl.handle.net/2142/78610.

MLA Handbook (7th Edition):

Guzman Sanchez, Irisbel. “Kinetics and thermodynamics of protein-RNA interactions and protein folding in vitro and in cells.” 2015. Web. 06 Jun 2020.

Vancouver:

Guzman Sanchez I. Kinetics and thermodynamics of protein-RNA interactions and protein folding in vitro and in cells. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2142/78610.

Council of Science Editors:

Guzman Sanchez I. Kinetics and thermodynamics of protein-RNA interactions and protein folding in vitro and in cells. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78610


Texas A&M University

24. Whitaker, Neal William 1982-. Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties.

Degree: 2012, Texas A&M University

 The Escherichia coli twin-arginine translocation (Tat) system transports fully folded and assembled proteins across the inner membrane into the periplasmic space. The E. coli Tat… (more)

Subjects/Keywords: Protein Translocation; Protein Targeting; Protein Secretion; Protein Export; Membrane Proteins; Intracellular Trafficking; Fluorescence Resonance Energy Transfer (FRET); Escherichia coli

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APA (6th Edition):

Whitaker, N. W. 1. (2012). Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148188

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):

Whitaker, Neal William 1982-. “Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties.” 2012. Thesis, Texas A&M University. Accessed June 06, 2020. http://hdl.handle.net/1969.1/148188.

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

MLA Handbook (7th Edition):

Whitaker, Neal William 1982-. “Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties.” 2012. Web. 06 Jun 2020.

Vancouver:

Whitaker NW1. Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1969.1/148188.

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

Council of Science Editors:

Whitaker NW1. Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148188

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

25. Wilson, Flore Adjélé. Étude du mécanisme de photoprotection lié à l’Orange Carotenoid Protein et ses homologues chez les cyanobactéries : Photoprotective mechanism related to the Orange Carotenoid Protein and paralogs in cyanobacteria.

Degree: Docteur es, Biologie, 2016, Université Paris-Saclay (ComUE)

La lumière est essentielle pour les organismes photosynthétiques qui convertissent l'énergie solaire en énergie chimique. Cependant, la lumière devient dangereuse lorsque l'énergie qui arrive aux… (more)

Subjects/Keywords: Orange Carotenoid Protein; Cyanobacterie; Photoprotection; Photosynthèse; Quenching non photochimique; Fluorescence Recovery Protein; Phycobilisome; Synechocystis; Orange Carotenoid Protein; Cyanobacteria; Photoprotective; Photosynthesis; Non photochemical quenhing; Fluorescence Recovery Protein; Phycobilisome; Synechocystis

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APA (6th Edition):

Wilson, F. A. (2016). Étude du mécanisme de photoprotection lié à l’Orange Carotenoid Protein et ses homologues chez les cyanobactéries : Photoprotective mechanism related to the Orange Carotenoid Protein and paralogs in cyanobacteria. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLS503

Chicago Manual of Style (16th Edition):

Wilson, Flore Adjélé. “Étude du mécanisme de photoprotection lié à l’Orange Carotenoid Protein et ses homologues chez les cyanobactéries : Photoprotective mechanism related to the Orange Carotenoid Protein and paralogs in cyanobacteria.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed June 06, 2020. http://www.theses.fr/2016SACLS503.

MLA Handbook (7th Edition):

Wilson, Flore Adjélé. “Étude du mécanisme de photoprotection lié à l’Orange Carotenoid Protein et ses homologues chez les cyanobactéries : Photoprotective mechanism related to the Orange Carotenoid Protein and paralogs in cyanobacteria.” 2016. Web. 06 Jun 2020.

Vancouver:

Wilson FA. Étude du mécanisme de photoprotection lié à l’Orange Carotenoid Protein et ses homologues chez les cyanobactéries : Photoprotective mechanism related to the Orange Carotenoid Protein and paralogs in cyanobacteria. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2020 Jun 06]. Available from: http://www.theses.fr/2016SACLS503.

Council of Science Editors:

Wilson FA. Étude du mécanisme de photoprotection lié à l’Orange Carotenoid Protein et ses homologues chez les cyanobactéries : Photoprotective mechanism related to the Orange Carotenoid Protein and paralogs in cyanobacteria. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLS503


University of Edinburgh

26. Adie, Jillian E. Structure-based drug design of 11β-hydroxysteroid dehydrogenase type 1 inhibitors.

Degree: 2010, University of Edinburgh

 The enzyme 11β-Hydroxysteroid Dehydrogenase 1 (11β-HSD1) catalyses the intracellular biosynthesis of the active glucocorticoid cortisol. Tissue specific dysregulation of the enzyme has been implicated in… (more)

Subjects/Keywords: 615; drug design; 11ß-HSD1; protein; protein expression; SPA; cortisol; fluorescence assay

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APA (6th Edition):

Adie, J. E. (2010). Structure-based drug design of 11β-hydroxysteroid dehydrogenase type 1 inhibitors. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4673

Chicago Manual of Style (16th Edition):

Adie, Jillian E. “Structure-based drug design of 11β-hydroxysteroid dehydrogenase type 1 inhibitors.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed June 06, 2020. http://hdl.handle.net/1842/4673.

MLA Handbook (7th Edition):

Adie, Jillian E. “Structure-based drug design of 11β-hydroxysteroid dehydrogenase type 1 inhibitors.” 2010. Web. 06 Jun 2020.

Vancouver:

Adie JE. Structure-based drug design of 11β-hydroxysteroid dehydrogenase type 1 inhibitors. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1842/4673.

Council of Science Editors:

Adie JE. Structure-based drug design of 11β-hydroxysteroid dehydrogenase type 1 inhibitors. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4673


University of South Africa

27. Kgokolo, Samuel Maphalle. Optimization of purification and characterisation of over-expressed rotavirus capsid protein VP6.

Degree: 2017, University of South Africa

 Rotavirus is responsible for the death of many children annually, and current vaccines have lower efficiency in developing countries. A reverse translated consensus gene sequence… (more)

Subjects/Keywords: Chromatography; Circular dichroism; Escherichia coli; Fluorescence; Plasmid; Protein conformation; Protein expression; Purification; Rotavirus; VP6

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APA (6th Edition):

Kgokolo, S. M. (2017). Optimization of purification and characterisation of over-expressed rotavirus capsid protein VP6. (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/23726

Chicago Manual of Style (16th Edition):

Kgokolo, Samuel Maphalle. “Optimization of purification and characterisation of over-expressed rotavirus capsid protein VP6.” 2017. Masters Thesis, University of South Africa. Accessed June 06, 2020. http://hdl.handle.net/10500/23726.

MLA Handbook (7th Edition):

Kgokolo, Samuel Maphalle. “Optimization of purification and characterisation of over-expressed rotavirus capsid protein VP6.” 2017. Web. 06 Jun 2020.

Vancouver:

Kgokolo SM. Optimization of purification and characterisation of over-expressed rotavirus capsid protein VP6. [Internet] [Masters thesis]. University of South Africa; 2017. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10500/23726.

Council of Science Editors:

Kgokolo SM. Optimization of purification and characterisation of over-expressed rotavirus capsid protein VP6. [Masters Thesis]. University of South Africa; 2017. Available from: http://hdl.handle.net/10500/23726


University of California – San Francisco

28. Feng, Siyu. Split Fluorescent Protein Engineering and Applications.

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

 Self-associating split fluorescent proteins (SAsFPs) have been widely used for labeling proteins, visualization of subcellular protein localization, scaffolding protein assembly and detecting cell-cell contacts. This… (more)

Subjects/Keywords: Bioengineering; Biology; Biochemistry; directed evolution; fluorescence microscopy; fluorescent protein; genome engineering; protein engineering; split proteins

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

APA (6th Edition):

Feng, S. (2019). Split Fluorescent Protein Engineering and Applications. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9j05p99h

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):

Feng, Siyu. “Split Fluorescent Protein Engineering and Applications.” 2019. Thesis, University of California – San Francisco. Accessed June 06, 2020. http://www.escholarship.org/uc/item/9j05p99h.

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

MLA Handbook (7th Edition):

Feng, Siyu. “Split Fluorescent Protein Engineering and Applications.” 2019. Web. 06 Jun 2020.

Vancouver:

Feng S. Split Fluorescent Protein Engineering and Applications. [Internet] [Thesis]. University of California – San Francisco; 2019. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/9j05p99h.

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

Council of Science Editors:

Feng S. Split Fluorescent Protein Engineering and Applications. [Thesis]. University of California – San Francisco; 2019. Available from: http://www.escholarship.org/uc/item/9j05p99h

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


Georgia State University

29. Reddish, Florence. Design Of Genetically-Encoded Ca2+ Probes With Rapid Kinetics For Subcellular Application.

Degree: PhD, Chemistry, 2017, Georgia State University

  The spatio-temporal attributes of intracellular calcium (Ca2+) transients activate various biological functions. These Ca2+ signaling events are triggered extracellularly through different stimuli and controlled… (more)

Subjects/Keywords: Genetically-Encoded Calcium Indicator; Calcium; Green Fluorescence Protein; Calcium Signaling; Protein Crystallization; JP45

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

APA (6th Edition):

Reddish, F. (2017). Design Of Genetically-Encoded Ca2+ Probes With Rapid Kinetics For Subcellular Application. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/125

Chicago Manual of Style (16th Edition):

Reddish, Florence. “Design Of Genetically-Encoded Ca2+ Probes With Rapid Kinetics For Subcellular Application.” 2017. Doctoral Dissertation, Georgia State University. Accessed June 06, 2020. https://scholarworks.gsu.edu/chemistry_diss/125.

MLA Handbook (7th Edition):

Reddish, Florence. “Design Of Genetically-Encoded Ca2+ Probes With Rapid Kinetics For Subcellular Application.” 2017. Web. 06 Jun 2020.

Vancouver:

Reddish F. Design Of Genetically-Encoded Ca2+ Probes With Rapid Kinetics For Subcellular Application. [Internet] [Doctoral dissertation]. Georgia State University; 2017. [cited 2020 Jun 06]. Available from: https://scholarworks.gsu.edu/chemistry_diss/125.

Council of Science Editors:

Reddish F. Design Of Genetically-Encoded Ca2+ Probes With Rapid Kinetics For Subcellular Application. [Doctoral Dissertation]. Georgia State University; 2017. Available from: https://scholarworks.gsu.edu/chemistry_diss/125


University of Guelph

30. Keeling, Thomas. Characterization of the Interactions Mediated by the Key Structural Protein CcmL: Cornerpiece of the Beta-Carboxysome .

Degree: 2013, University of Guelph

 While much is known about the structure and interactions of the β-carboxysomal proteins, interactions of the proposed vertex protein CcmL with the other components have… (more)

Subjects/Keywords: carboxysome; protein; cyanobacteria; fluorescence; electron microscopy; FRET; x-ray crystallography; protein interaction; tryptophan fluorescence; bacterial microcompartment; dynamic light scattering; Thermosynechococcus elongatus; Nostoc sp. PCC7120; fluorescence resonance energy transfer

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

APA (6th Edition):

Keeling, T. (2013). Characterization of the Interactions Mediated by the Key Structural Protein CcmL: Cornerpiece of the Beta-Carboxysome . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5326

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):

Keeling, Thomas. “Characterization of the Interactions Mediated by the Key Structural Protein CcmL: Cornerpiece of the Beta-Carboxysome .” 2013. Thesis, University of Guelph. Accessed June 06, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5326.

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

MLA Handbook (7th Edition):

Keeling, Thomas. “Characterization of the Interactions Mediated by the Key Structural Protein CcmL: Cornerpiece of the Beta-Carboxysome .” 2013. Web. 06 Jun 2020.

Vancouver:

Keeling T. Characterization of the Interactions Mediated by the Key Structural Protein CcmL: Cornerpiece of the Beta-Carboxysome . [Internet] [Thesis]. University of Guelph; 2013. [cited 2020 Jun 06]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5326.

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

Council of Science Editors:

Keeling T. Characterization of the Interactions Mediated by the Key Structural Protein CcmL: Cornerpiece of the Beta-Carboxysome . [Thesis]. University of Guelph; 2013. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5326

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

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