Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Protein oligomerization). Showing records 1 – 30 of 43 total matches.

[1] [2]

Search Limiters

Last 2 Years | English Only

Country

▼ Search Limiters


University of Stirling

1. Kelly, Sharon Mary. Studies on the unfolding and refolding of oligomeric proteins.

Degree: PhD, 1994, University of Stirling

 The unfolding and refolding of a number of oligomeric enzymes have been studied. These were: fumarase from pig heart, the NAD+ -dependent isocitrate dehydrogenase from… (more)

Subjects/Keywords: Protein folding; Oligomerization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kelly, S. M. (1994). Studies on the unfolding and refolding of oligomeric proteins. (Doctoral Dissertation). University of Stirling. Retrieved from http://hdl.handle.net/1893/21548

Chicago Manual of Style (16th Edition):

Kelly, Sharon Mary. “Studies on the unfolding and refolding of oligomeric proteins.” 1994. Doctoral Dissertation, University of Stirling. Accessed July 24, 2019. http://hdl.handle.net/1893/21548.

MLA Handbook (7th Edition):

Kelly, Sharon Mary. “Studies on the unfolding and refolding of oligomeric proteins.” 1994. Web. 24 Jul 2019.

Vancouver:

Kelly SM. Studies on the unfolding and refolding of oligomeric proteins. [Internet] [Doctoral dissertation]. University of Stirling; 1994. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/1893/21548.

Council of Science Editors:

Kelly SM. Studies on the unfolding and refolding of oligomeric proteins. [Doctoral Dissertation]. University of Stirling; 1994. Available from: http://hdl.handle.net/1893/21548


Washington University in St. Louis

2. Wang, Hanliu. Mass Spectrometry and Protein Analysis: Structure, Oligomerization and Interaction.

Degree: PhD, Chemistry, 2016, Washington University in St. Louis

Protein aggregation is common in biological processes including neurodegenerative diseases, as well as artificial development in biopharmaceutical production and protein storage. Therefore, understanding proteins involved… (more)

Subjects/Keywords: Higher-order structure; Protein Interaction; Protein Mass Spectrometry; Protein Oligomerization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, H. (2016). Mass Spectrometry and Protein Analysis: Structure, Oligomerization and Interaction. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/1008

Chicago Manual of Style (16th Edition):

Wang, Hanliu. “Mass Spectrometry and Protein Analysis: Structure, Oligomerization and Interaction.” 2016. Doctoral Dissertation, Washington University in St. Louis. Accessed July 24, 2019. https://openscholarship.wustl.edu/art_sci_etds/1008.

MLA Handbook (7th Edition):

Wang, Hanliu. “Mass Spectrometry and Protein Analysis: Structure, Oligomerization and Interaction.” 2016. Web. 24 Jul 2019.

Vancouver:

Wang H. Mass Spectrometry and Protein Analysis: Structure, Oligomerization and Interaction. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2016. [cited 2019 Jul 24]. Available from: https://openscholarship.wustl.edu/art_sci_etds/1008.

Council of Science Editors:

Wang H. Mass Spectrometry and Protein Analysis: Structure, Oligomerization and Interaction. [Doctoral Dissertation]. Washington University in St. Louis; 2016. Available from: https://openscholarship.wustl.edu/art_sci_etds/1008


University of Notre Dame

3. Kaveesha J. Wijesinghe. Exploring Structural and Functional Properties of Marburg Virus Matrix Protein-VP40</h1>.

Degree: PhD, Chemistry and Biochemistry, 2018, University of Notre Dame

  Marburg virus causes deadly hemorrhagic fever in humans and non-human primates and is a close relative of Ebola virus. To date, there are no… (more)

Subjects/Keywords: Oligomerization; HDX-MS; Marburg virus matrix protein-VP40; Lipid protein interaction

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wijesinghe, K. J. (2018). Exploring Structural and Functional Properties of Marburg Virus Matrix Protein-VP40</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/wd375t3814f

Chicago Manual of Style (16th Edition):

Wijesinghe, Kaveesha J.. “Exploring Structural and Functional Properties of Marburg Virus Matrix Protein-VP40</h1>.” 2018. Doctoral Dissertation, University of Notre Dame. Accessed July 24, 2019. https://curate.nd.edu/show/wd375t3814f.

MLA Handbook (7th Edition):

Wijesinghe, Kaveesha J.. “Exploring Structural and Functional Properties of Marburg Virus Matrix Protein-VP40</h1>.” 2018. Web. 24 Jul 2019.

Vancouver:

Wijesinghe KJ. Exploring Structural and Functional Properties of Marburg Virus Matrix Protein-VP40</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2018. [cited 2019 Jul 24]. Available from: https://curate.nd.edu/show/wd375t3814f.

Council of Science Editors:

Wijesinghe KJ. Exploring Structural and Functional Properties of Marburg Virus Matrix Protein-VP40</h1>. [Doctoral Dissertation]. University of Notre Dame; 2018. Available from: https://curate.nd.edu/show/wd375t3814f


University of Texas – Austin

4. -1082-7768. Characterization of the Vibrio cholerae ferrous iron transport system, feo.

Degree: Biochemistry, 2015, University of Texas – Austin

 Feo is the major ferrous iron transport system in prokaryotes and has only been partially characterized, as its assembly and mechanism of transport have not… (more)

Subjects/Keywords: Iron; Vibrio cholerae; Transport metal; Protein cross-linking; Protein complex; Oligomerization; Membrane protein; GTPase; Mutagenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

-1082-7768. (2015). Characterization of the Vibrio cholerae ferrous iron transport system, feo. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63894

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

Chicago Manual of Style (16th Edition):

-1082-7768. “Characterization of the Vibrio cholerae ferrous iron transport system, feo.” 2015. Thesis, University of Texas – Austin. Accessed July 24, 2019. http://hdl.handle.net/2152/63894.

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

MLA Handbook (7th Edition):

-1082-7768. “Characterization of the Vibrio cholerae ferrous iron transport system, feo.” 2015. Web. 24 Jul 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-1082-7768. Characterization of the Vibrio cholerae ferrous iron transport system, feo. [Internet] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/2152/63894.

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

Council of Science Editors:

-1082-7768. Characterization of the Vibrio cholerae ferrous iron transport system, feo. [Thesis]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/63894

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


Queens University

5. Adetola, Gbolagade. CHARACTERIZATION OF THE BACULOVIRUS LATE EXPRESSION FACTOR-3 OLIGOMERIZATION INTERACTION DOMAINS USING PROTEIN COMPLEMENTATION ASSAY .

Degree: Microbiology and Immunology, 2011, Queens University

 Late expression factor 3 is one of the six AcMNPV genes essential for DNA replication identified through transient replication assays. LEF-3 is a single stranded… (more)

Subjects/Keywords: Baculovirus; DNA replication; Protein complementation assay; Oligomerization domains

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Adetola, G. (2011). CHARACTERIZATION OF THE BACULOVIRUS LATE EXPRESSION FACTOR-3 OLIGOMERIZATION INTERACTION DOMAINS USING PROTEIN COMPLEMENTATION ASSAY . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6531

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):

Adetola, Gbolagade. “CHARACTERIZATION OF THE BACULOVIRUS LATE EXPRESSION FACTOR-3 OLIGOMERIZATION INTERACTION DOMAINS USING PROTEIN COMPLEMENTATION ASSAY .” 2011. Thesis, Queens University. Accessed July 24, 2019. http://hdl.handle.net/1974/6531.

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

MLA Handbook (7th Edition):

Adetola, Gbolagade. “CHARACTERIZATION OF THE BACULOVIRUS LATE EXPRESSION FACTOR-3 OLIGOMERIZATION INTERACTION DOMAINS USING PROTEIN COMPLEMENTATION ASSAY .” 2011. Web. 24 Jul 2019.

Vancouver:

Adetola G. CHARACTERIZATION OF THE BACULOVIRUS LATE EXPRESSION FACTOR-3 OLIGOMERIZATION INTERACTION DOMAINS USING PROTEIN COMPLEMENTATION ASSAY . [Internet] [Thesis]. Queens University; 2011. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/1974/6531.

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

Council of Science Editors:

Adetola G. CHARACTERIZATION OF THE BACULOVIRUS LATE EXPRESSION FACTOR-3 OLIGOMERIZATION INTERACTION DOMAINS USING PROTEIN COMPLEMENTATION ASSAY . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6531

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


Wesleyan University

6. Blum, Amy Elana. Assessment of the Functionality of the Back-to-back Conformation of the SecYEG.

Degree: Molecular Biology and Biochemistry, 2015, Wesleyan University

  Approximately 30% of proteins produced in E. coli are translocated through the universally conserved SecYEG channel, either for co-translational insertion into the cytoplasmic membrane,… (more)

Subjects/Keywords: SecYEG; Protein Translocation; SecA; Oligomerization; Dimer; E. coli

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Blum, A. E. (2015). Assessment of the Functionality of the Back-to-back Conformation of the SecYEG. (Masters Thesis). Wesleyan University. Retrieved from https://wesscholar.wesleyan.edu/etd_mas_theses/105

Chicago Manual of Style (16th Edition):

Blum, Amy Elana. “Assessment of the Functionality of the Back-to-back Conformation of the SecYEG.” 2015. Masters Thesis, Wesleyan University. Accessed July 24, 2019. https://wesscholar.wesleyan.edu/etd_mas_theses/105.

MLA Handbook (7th Edition):

Blum, Amy Elana. “Assessment of the Functionality of the Back-to-back Conformation of the SecYEG.” 2015. Web. 24 Jul 2019.

Vancouver:

Blum AE. Assessment of the Functionality of the Back-to-back Conformation of the SecYEG. [Internet] [Masters thesis]. Wesleyan University; 2015. [cited 2019 Jul 24]. Available from: https://wesscholar.wesleyan.edu/etd_mas_theses/105.

Council of Science Editors:

Blum AE. Assessment of the Functionality of the Back-to-back Conformation of the SecYEG. [Masters Thesis]. Wesleyan University; 2015. Available from: https://wesscholar.wesleyan.edu/etd_mas_theses/105


Arizona State University

7. Chakraborty, Manas. Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy.

Degree: PhD, Chemistry, 2014, Arizona State University

 Ribulose-1, 5-bisphosphate carboxylase oxygenase, commonly known as RuBisCO, is an enzyme involved in carbon fixation in photosynthetic organisms. The enzyme is subject to a mechanism-based… (more)

Subjects/Keywords: Chemistry; Biophysics; FCS; PCH; Protein oligomerization; Rubisco Activase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chakraborty, M. (2014). Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/25170

Chicago Manual of Style (16th Edition):

Chakraborty, Manas. “Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy.” 2014. Doctoral Dissertation, Arizona State University. Accessed July 24, 2019. http://repository.asu.edu/items/25170.

MLA Handbook (7th Edition):

Chakraborty, Manas. “Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy.” 2014. Web. 24 Jul 2019.

Vancouver:

Chakraborty M. Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy. [Internet] [Doctoral dissertation]. Arizona State University; 2014. [cited 2019 Jul 24]. Available from: http://repository.asu.edu/items/25170.

Council of Science Editors:

Chakraborty M. Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy. [Doctoral Dissertation]. Arizona State University; 2014. Available from: http://repository.asu.edu/items/25170


The Ohio State University

8. Nair, Manoj Sadasivan. Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes.

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

  The most controversial step in the study of the mechanism of action of insecticidal crystal toxins is that of insertion of the toxin into… (more)

Subjects/Keywords: Biochemistry; Biophysics; Entomology; Microbiology; Molecular Biology; Toxicology; Biophysics; Protein-protein interactions; Protein-lipid interactions; Protein oligomerization; Membrane insertion; Toxin- membrane interactions

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nair, M. S. (2008). Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1218558470

Chicago Manual of Style (16th Edition):

Nair, Manoj Sadasivan. “Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes.” 2008. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1218558470.

MLA Handbook (7th Edition):

Nair, Manoj Sadasivan. “Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes.” 2008. Web. 24 Jul 2019.

Vancouver:

Nair MS. Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218558470.

Council of Science Editors:

Nair MS. Mechanism of Action of Insecticidal Crystal Toxins from <i>Bacillus thuringiensis:</i> Biophysical and Biochemical Analyses of the Insertion of Cry1A Toxins into Insect Midgut Membranes. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218558470


University of Guelph

9. Fayaz, Ehsan. The 18.5-kDa Myelin Basic Protein has Loose Tertiary Contacts Regulated by Zinc and Post-Translational Modification .

Degree: 2011, University of Guelph

 Myelin basic protein (MBP) has fascinated researchers and clinicians alike due to its major structural role in myelin and the central nervous system, and its… (more)

Subjects/Keywords: Myelin; MBP; Protein; unstructured; fluorescence; saxs; oligomerization; demyelination; multiple sclerosis; disordered; zinc; divalent cations; structure

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fayaz, E. (2011). The 18.5-kDa Myelin Basic Protein has Loose Tertiary Contacts Regulated by Zinc and Post-Translational Modification . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3202

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):

Fayaz, Ehsan. “The 18.5-kDa Myelin Basic Protein has Loose Tertiary Contacts Regulated by Zinc and Post-Translational Modification .” 2011. Thesis, University of Guelph. Accessed July 24, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3202.

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

MLA Handbook (7th Edition):

Fayaz, Ehsan. “The 18.5-kDa Myelin Basic Protein has Loose Tertiary Contacts Regulated by Zinc and Post-Translational Modification .” 2011. Web. 24 Jul 2019.

Vancouver:

Fayaz E. The 18.5-kDa Myelin Basic Protein has Loose Tertiary Contacts Regulated by Zinc and Post-Translational Modification . [Internet] [Thesis]. University of Guelph; 2011. [cited 2019 Jul 24]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3202.

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

Council of Science Editors:

Fayaz E. The 18.5-kDa Myelin Basic Protein has Loose Tertiary Contacts Regulated by Zinc and Post-Translational Modification . [Thesis]. University of Guelph; 2011. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3202

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


University of Cincinnati

10. Gaddie, Keith J. Structural Elements that Regulate Interactions between the Extracellular and Transmembrane Domains of Human Nucleoside Triphosphate Diphosphohydrolase 3.

Degree: PhD, Medicine : Molecular, Cellular and Biochemical Pharmacology, 2009, University of Cincinnati

  The nucleoside triphosphate diphosphohydrolases (NTPDases) are a family of constitutively expressed, endogenous nucleotidases, some of which regulate purinergic signaling by divalent cation-dependent hydrolysis of… (more)

Subjects/Keywords: Biochemistry; NTPDase3; conserved proline residues; conserved polar residues; oligomerization; transmembrane domain; intra-protein signal transduction

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gaddie, K. J. (2009). Structural Elements that Regulate Interactions between the Extracellular and Transmembrane Domains of Human Nucleoside Triphosphate Diphosphohydrolase 3. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1259077311

Chicago Manual of Style (16th Edition):

Gaddie, Keith J. “Structural Elements that Regulate Interactions between the Extracellular and Transmembrane Domains of Human Nucleoside Triphosphate Diphosphohydrolase 3.” 2009. Doctoral Dissertation, University of Cincinnati. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1259077311.

MLA Handbook (7th Edition):

Gaddie, Keith J. “Structural Elements that Regulate Interactions between the Extracellular and Transmembrane Domains of Human Nucleoside Triphosphate Diphosphohydrolase 3.” 2009. Web. 24 Jul 2019.

Vancouver:

Gaddie KJ. Structural Elements that Regulate Interactions between the Extracellular and Transmembrane Domains of Human Nucleoside Triphosphate Diphosphohydrolase 3. [Internet] [Doctoral dissertation]. University of Cincinnati; 2009. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1259077311.

Council of Science Editors:

Gaddie KJ. Structural Elements that Regulate Interactions between the Extracellular and Transmembrane Domains of Human Nucleoside Triphosphate Diphosphohydrolase 3. [Doctoral Dissertation]. University of Cincinnati; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1259077311


Johannes Gutenberg Universität Mainz

11. Klein, Noreen. Protein-Protein- und Protein-Lipid-Wechselwirkungen beeinflussen die Oligomerisierung und Funktion des E. coli Aquaglyceroporins GlpF.

Degree: 2015, Johannes Gutenberg Universität Mainz

Aquaporine sind hochselektive Transmembrankanäle, die in allen Lebensformen den Fluss von Wasser und kleinen, polaren Molekülen wie Glycerol über Lipidmembranen ermöglichen. Obwohl die Kanalpore für… (more)

Subjects/Keywords: Aquaporine; Lipide; Membranprotein; Oligomerisierung; Aktivität; aquaporin; lipids; membrane protein; oligomerization; activity; Natural sciences and mathematics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Klein, N. (2015). Protein-Protein- und Protein-Lipid-Wechselwirkungen beeinflussen die Oligomerisierung und Funktion des E. coli Aquaglyceroporins GlpF. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2015/4052/

Chicago Manual of Style (16th Edition):

Klein, Noreen. “Protein-Protein- und Protein-Lipid-Wechselwirkungen beeinflussen die Oligomerisierung und Funktion des E. coli Aquaglyceroporins GlpF.” 2015. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed July 24, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2015/4052/.

MLA Handbook (7th Edition):

Klein, Noreen. “Protein-Protein- und Protein-Lipid-Wechselwirkungen beeinflussen die Oligomerisierung und Funktion des E. coli Aquaglyceroporins GlpF.” 2015. Web. 24 Jul 2019.

Vancouver:

Klein N. Protein-Protein- und Protein-Lipid-Wechselwirkungen beeinflussen die Oligomerisierung und Funktion des E. coli Aquaglyceroporins GlpF. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2015. [cited 2019 Jul 24]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4052/.

Council of Science Editors:

Klein N. Protein-Protein- und Protein-Lipid-Wechselwirkungen beeinflussen die Oligomerisierung und Funktion des E. coli Aquaglyceroporins GlpF. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2015. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4052/


University of Saskatchewan

12. Hedlin, Cherise Elizabeth. The essentiality of DivIVAEf oligomerization for proper cell division in enterococcus faecalis and interaction with a novel cell division protein.

Degree: 2009, University of Saskatchewan

 DivIVA is a Gram-positive cell division protein involved in chromosome segregation, midcell placement of the cell division machinery, complete septum closure, and polar growth and… (more)

Subjects/Keywords: Enterococcus faecalis; protein interactions; cell division; DivIVA; oligomerization; immunofluorescence microscopy; Bacterial two-hybrid

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hedlin, C. E. (2009). The essentiality of DivIVAEf oligomerization for proper cell division in enterococcus faecalis and interaction with a novel cell division protein. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-04152009-115838

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):

Hedlin, Cherise Elizabeth. “The essentiality of DivIVAEf oligomerization for proper cell division in enterococcus faecalis and interaction with a novel cell division protein.” 2009. Thesis, University of Saskatchewan. Accessed July 24, 2019. http://hdl.handle.net/10388/etd-04152009-115838.

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

MLA Handbook (7th Edition):

Hedlin, Cherise Elizabeth. “The essentiality of DivIVAEf oligomerization for proper cell division in enterococcus faecalis and interaction with a novel cell division protein.” 2009. Web. 24 Jul 2019.

Vancouver:

Hedlin CE. The essentiality of DivIVAEf oligomerization for proper cell division in enterococcus faecalis and interaction with a novel cell division protein. [Internet] [Thesis]. University of Saskatchewan; 2009. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/10388/etd-04152009-115838.

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

Council of Science Editors:

Hedlin CE. The essentiality of DivIVAEf oligomerization for proper cell division in enterococcus faecalis and interaction with a novel cell division protein. [Thesis]. University of Saskatchewan; 2009. Available from: http://hdl.handle.net/10388/etd-04152009-115838

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


University of Western Sydney

13. El-Kamand, Serene. Defining the molecular details of hSSB1 oligomerisation in response to oxidative DNA damage.

Degree: 2018, University of Western Sydney

 Cells are constantly exposed to sources of oxidative stress. If left unrepaired, the oxidative modification of DNA can result in a loss of genome integrity… (more)

Subjects/Keywords: DNA damage; oxidative stress; oligomerization; DNA-protein interactions; Thesis (M.Phil.) – Western Sydney University, 2018.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

El-Kamand, S. (2018). Defining the molecular details of hSSB1 oligomerisation in response to oxidative DNA damage. (Thesis). University of Western Sydney. Retrieved from http://hdl.handle.net/1959.7/uws:51871

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):

El-Kamand, Serene. “Defining the molecular details of hSSB1 oligomerisation in response to oxidative DNA damage.” 2018. Thesis, University of Western Sydney. Accessed July 24, 2019. http://hdl.handle.net/1959.7/uws:51871.

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

MLA Handbook (7th Edition):

El-Kamand, Serene. “Defining the molecular details of hSSB1 oligomerisation in response to oxidative DNA damage.” 2018. Web. 24 Jul 2019.

Vancouver:

El-Kamand S. Defining the molecular details of hSSB1 oligomerisation in response to oxidative DNA damage. [Internet] [Thesis]. University of Western Sydney; 2018. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/1959.7/uws:51871.

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

Council of Science Editors:

El-Kamand S. Defining the molecular details of hSSB1 oligomerisation in response to oxidative DNA damage. [Thesis]. University of Western Sydney; 2018. Available from: http://hdl.handle.net/1959.7/uws:51871

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


University of Southern California

14. Xu, Meng. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2012, University of Southern California

 The hetero-hexamer of the eukaryotic minichromosome maintenance (MCM) proteins plays an essential role in replication of genomic DNA. The ring-shaped Mcm2-7 hexamers comprising one of… (more)

Subjects/Keywords: helicase; cell cycle proteins; DNA-binding proteins; recombinant proteins; protein binding; protein oligomerization; schizosaccharomyces pombe; Escherichiai coli; simian virus 40

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Xu, M. (2012). Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106

Chicago Manual of Style (16th Edition):

Xu, Meng. “Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.” 2012. Doctoral Dissertation, University of Southern California. Accessed July 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106.

MLA Handbook (7th Edition):

Xu, Meng. “Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.” 2012. Web. 24 Jul 2019.

Vancouver:

Xu M. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jul 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106.

Council of Science Editors:

Xu M. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106

15. Lundberg, Alexander. Studying the Oligomerization of the Kinase Domain of Ephrin type-B Receptor 2 Using Analytical Ultracentrifugation and Development of a Program for Analysis of Acquired Data.

Degree: The Institute of Technology, 2014, Linköping UniversityLinköping University

  Ephrin type-B receptor 2 (EphB2) is a receptor tyrosine kinase which phosphorylates proteins and thereby regulates cell migration, vascular development, axon guidance synaptic plasticity,… (more)

Subjects/Keywords: Ephrin type-B receptor 2; EphB2; Analytical Ultracentrifugation; Oligomerization; Kinase Domain; Protein Expression; Protein Purification; Programming; Analysis of Data

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lundberg, A. (2014). Studying the Oligomerization of the Kinase Domain of Ephrin type-B Receptor 2 Using Analytical Ultracentrifugation and Development of a Program for Analysis of Acquired Data. (Thesis). Linköping UniversityLinköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-110376

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):

Lundberg, Alexander. “Studying the Oligomerization of the Kinase Domain of Ephrin type-B Receptor 2 Using Analytical Ultracentrifugation and Development of a Program for Analysis of Acquired Data.” 2014. Thesis, Linköping UniversityLinköping University. Accessed July 24, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-110376.

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

MLA Handbook (7th Edition):

Lundberg, Alexander. “Studying the Oligomerization of the Kinase Domain of Ephrin type-B Receptor 2 Using Analytical Ultracentrifugation and Development of a Program for Analysis of Acquired Data.” 2014. Web. 24 Jul 2019.

Vancouver:

Lundberg A. Studying the Oligomerization of the Kinase Domain of Ephrin type-B Receptor 2 Using Analytical Ultracentrifugation and Development of a Program for Analysis of Acquired Data. [Internet] [Thesis]. Linköping UniversityLinköping University; 2014. [cited 2019 Jul 24]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-110376.

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

Council of Science Editors:

Lundberg A. Studying the Oligomerization of the Kinase Domain of Ephrin type-B Receptor 2 Using Analytical Ultracentrifugation and Development of a Program for Analysis of Acquired Data. [Thesis]. Linköping UniversityLinköping University; 2014. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-110376

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


Dalhousie University

16. Hammad, Maha. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.

Degree: MS, Department of Pharmacology, 2010, Dalhousie University

 Current drugs used to treat Congestive Heart Failure target the renin-angiotensin and adrenergic systems. Studies showed increased mortality rates in patients treated with a combination… (more)

Subjects/Keywords: G Protein Coupled Receptors; Congestive Heart Failure; Adrenergic Receptors; Angiotensin Receptors; Rab GTPases; Molecular Chaperones; Bimolecular Fluorescence Complementation; GPCRs Oligomerization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hammad, M. (2010). CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/13068

Chicago Manual of Style (16th Edition):

Hammad, Maha. “CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.” 2010. Masters Thesis, Dalhousie University. Accessed July 24, 2019. http://hdl.handle.net/10222/13068.

MLA Handbook (7th Edition):

Hammad, Maha. “CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.” 2010. Web. 24 Jul 2019.

Vancouver:

Hammad M. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. [Internet] [Masters thesis]. Dalhousie University; 2010. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/10222/13068.

Council of Science Editors:

Hammad M. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. [Masters Thesis]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/13068


University of Colorado

17. Takeshita, Ryan Akira. An Analysis of Latent Membrane Protein-1 Signaling Complexes and Their Contribution to Epstein-Barr Virus Infection.

Degree: PhD, 2011, University of Colorado

  In immunocompromised individuals, B cells infected with Epstein-Barr virus often display tumorigenic growth. One of the viral oncoproteins that contributes to this transformation is… (more)

Subjects/Keywords: Epstein-Barr virus; homo-oligomerization; latent membrane protein-1; lipid rafts; subcellular Localization; Cell Biology; Molecular Biology; Virology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Takeshita, R. A. (2011). An Analysis of Latent Membrane Protein-1 Signaling Complexes and Their Contribution to Epstein-Barr Virus Infection. (Doctoral Dissertation). University of Colorado. Retrieved from http://scholar.colorado.edu/mcdb_gradetds/47

Chicago Manual of Style (16th Edition):

Takeshita, Ryan Akira. “An Analysis of Latent Membrane Protein-1 Signaling Complexes and Their Contribution to Epstein-Barr Virus Infection.” 2011. Doctoral Dissertation, University of Colorado. Accessed July 24, 2019. http://scholar.colorado.edu/mcdb_gradetds/47.

MLA Handbook (7th Edition):

Takeshita, Ryan Akira. “An Analysis of Latent Membrane Protein-1 Signaling Complexes and Their Contribution to Epstein-Barr Virus Infection.” 2011. Web. 24 Jul 2019.

Vancouver:

Takeshita RA. An Analysis of Latent Membrane Protein-1 Signaling Complexes and Their Contribution to Epstein-Barr Virus Infection. [Internet] [Doctoral dissertation]. University of Colorado; 2011. [cited 2019 Jul 24]. Available from: http://scholar.colorado.edu/mcdb_gradetds/47.

Council of Science Editors:

Takeshita RA. An Analysis of Latent Membrane Protein-1 Signaling Complexes and Their Contribution to Epstein-Barr Virus Infection. [Doctoral Dissertation]. University of Colorado; 2011. Available from: http://scholar.colorado.edu/mcdb_gradetds/47


Université de Grenoble

18. Nguyen, Hien-Anh. Découverte d'une nouvelle famille de protéine kinases bactériennes : mécanismes de fonctionnement et rôle cellulaire de YdiB, un archétype chez Baccillus subtilis : Discovery of a new bacterial protein kinase family : functioning mechanism and cellular role of YdiB, an archetype from Bacillus subtilis.

Degree: Docteur es, Sciences de la vie, 2012, Université de Grenoble

Les données de séquençage des génomes ont révélé une nouvelle famille de protéines UPF0079, comprenant des protéines de fonction inconnue qui sont exclusivement et largement… (more)

Subjects/Keywords: Protéine kinase; Phosphorylation bactérienne; Oligomérisation; Ribosome; Stress oxydatif; Protein kinase; Bacterial phosphorylation; Oligomerization; Ribosome; Oxidative stress

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nguyen, H. (2012). Découverte d'une nouvelle famille de protéine kinases bactériennes : mécanismes de fonctionnement et rôle cellulaire de YdiB, un archétype chez Baccillus subtilis : Discovery of a new bacterial protein kinase family : functioning mechanism and cellular role of YdiB, an archetype from Bacillus subtilis. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2012GRENV017

Chicago Manual of Style (16th Edition):

Nguyen, Hien-Anh. “Découverte d'une nouvelle famille de protéine kinases bactériennes : mécanismes de fonctionnement et rôle cellulaire de YdiB, un archétype chez Baccillus subtilis : Discovery of a new bacterial protein kinase family : functioning mechanism and cellular role of YdiB, an archetype from Bacillus subtilis.” 2012. Doctoral Dissertation, Université de Grenoble. Accessed July 24, 2019. http://www.theses.fr/2012GRENV017.

MLA Handbook (7th Edition):

Nguyen, Hien-Anh. “Découverte d'une nouvelle famille de protéine kinases bactériennes : mécanismes de fonctionnement et rôle cellulaire de YdiB, un archétype chez Baccillus subtilis : Discovery of a new bacterial protein kinase family : functioning mechanism and cellular role of YdiB, an archetype from Bacillus subtilis.” 2012. Web. 24 Jul 2019.

Vancouver:

Nguyen H. Découverte d'une nouvelle famille de protéine kinases bactériennes : mécanismes de fonctionnement et rôle cellulaire de YdiB, un archétype chez Baccillus subtilis : Discovery of a new bacterial protein kinase family : functioning mechanism and cellular role of YdiB, an archetype from Bacillus subtilis. [Internet] [Doctoral dissertation]. Université de Grenoble; 2012. [cited 2019 Jul 24]. Available from: http://www.theses.fr/2012GRENV017.

Council of Science Editors:

Nguyen H. Découverte d'une nouvelle famille de protéine kinases bactériennes : mécanismes de fonctionnement et rôle cellulaire de YdiB, un archétype chez Baccillus subtilis : Discovery of a new bacterial protein kinase family : functioning mechanism and cellular role of YdiB, an archetype from Bacillus subtilis. [Doctoral Dissertation]. Université de Grenoble; 2012. Available from: http://www.theses.fr/2012GRENV017


Université Montpellier II

19. Comps-Agrar, Laëtitia. Aspects moléculaires et dynamiques du fonctionnement des oligomères de récepteurs couplés aux protéines G : cas du récepteur GABAB : Molecular and dynamic aspects of G-protein coupled receptor oligomers functioning : case of GABAB receptor.

Degree: Docteur es, Pharmacologie moléculaire. Neurosciences, 2010, Université Montpellier II

Les récepteurs couplés aux protéines G (RCPG) constituent la plus grande famille de récepteurs transmembranaires. Ils sont impliqués dans une large variété de processus physiologiques… (more)

Subjects/Keywords: Récepteurs Couplés aux Protéines G; Oligomerisation; Gabab; Fret; Snap-tag; Signalisation; G-protein coupled receptors; Oligomerization; Gabab; Fret; Snap-tag; Signaling

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Comps-Agrar, L. (2010). Aspects moléculaires et dynamiques du fonctionnement des oligomères de récepteurs couplés aux protéines G : cas du récepteur GABAB : Molecular and dynamic aspects of G-protein coupled receptor oligomers functioning : case of GABAB receptor. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2010MON20211

Chicago Manual of Style (16th Edition):

Comps-Agrar, Laëtitia. “Aspects moléculaires et dynamiques du fonctionnement des oligomères de récepteurs couplés aux protéines G : cas du récepteur GABAB : Molecular and dynamic aspects of G-protein coupled receptor oligomers functioning : case of GABAB receptor.” 2010. Doctoral Dissertation, Université Montpellier II. Accessed July 24, 2019. http://www.theses.fr/2010MON20211.

MLA Handbook (7th Edition):

Comps-Agrar, Laëtitia. “Aspects moléculaires et dynamiques du fonctionnement des oligomères de récepteurs couplés aux protéines G : cas du récepteur GABAB : Molecular and dynamic aspects of G-protein coupled receptor oligomers functioning : case of GABAB receptor.” 2010. Web. 24 Jul 2019.

Vancouver:

Comps-Agrar L. Aspects moléculaires et dynamiques du fonctionnement des oligomères de récepteurs couplés aux protéines G : cas du récepteur GABAB : Molecular and dynamic aspects of G-protein coupled receptor oligomers functioning : case of GABAB receptor. [Internet] [Doctoral dissertation]. Université Montpellier II; 2010. [cited 2019 Jul 24]. Available from: http://www.theses.fr/2010MON20211.

Council of Science Editors:

Comps-Agrar L. Aspects moléculaires et dynamiques du fonctionnement des oligomères de récepteurs couplés aux protéines G : cas du récepteur GABAB : Molecular and dynamic aspects of G-protein coupled receptor oligomers functioning : case of GABAB receptor. [Doctoral Dissertation]. Université Montpellier II; 2010. Available from: http://www.theses.fr/2010MON20211

20. Modi, Chintan Kishore. Evolution of structure-function relationships in the GFP-family of proteins.

Degree: Cellular and Molecular Biology, 2014, University of Texas – Austin

 One of the most intriguing questions in evolutionary biology is how biochemical and structural complexity arise through small and incremental changes; however answering this question… (more)

Subjects/Keywords: Molecular evolution; Biochemical complexity; GFP; Protein oligomerization

…the green fluorescent protein (GFP) protein family using an ancestral… …an ancestral green chromophore by perturbing the ancestral protein stability at multiple… …levels of protein structure. Moreover, only three historical mutations are sufficient to… …interactions at tertiary and quaternary protein structure levels. In the fourth chapter, I… …function and homo-oligomerization, and the desirable photophysical characteristics would make… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Modi, C. K. (2014). Evolution of structure-function relationships in the GFP-family of proteins. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/25915

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):

Modi, Chintan Kishore. “Evolution of structure-function relationships in the GFP-family of proteins.” 2014. Thesis, University of Texas – Austin. Accessed July 24, 2019. http://hdl.handle.net/2152/25915.

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

MLA Handbook (7th Edition):

Modi, Chintan Kishore. “Evolution of structure-function relationships in the GFP-family of proteins.” 2014. Web. 24 Jul 2019.

Vancouver:

Modi CK. Evolution of structure-function relationships in the GFP-family of proteins. [Internet] [Thesis]. University of Texas – Austin; 2014. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/2152/25915.

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

Council of Science Editors:

Modi CK. Evolution of structure-function relationships in the GFP-family of proteins. [Thesis]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/25915

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

21. NEELAMEGAM SIVAKUMAR. Structural basis of protein stability at poly-extreme: Crystal structure of AmyA at 1.6 A resolution.

Degree: 2006, National University of Singapore

Subjects/Keywords: Poly-extreme/ thermophilic/ halophilic/ Oligomerization/ Amylase/ Protein stability

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

SIVAKUMAR, N. (2006). Structural basis of protein stability at poly-extreme: Crystal structure of AmyA at 1.6 A resolution. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/15244

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):

SIVAKUMAR, NEELAMEGAM. “Structural basis of protein stability at poly-extreme: Crystal structure of AmyA at 1.6 A resolution.” 2006. Thesis, National University of Singapore. Accessed July 24, 2019. http://scholarbank.nus.edu.sg/handle/10635/15244.

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

MLA Handbook (7th Edition):

SIVAKUMAR, NEELAMEGAM. “Structural basis of protein stability at poly-extreme: Crystal structure of AmyA at 1.6 A resolution.” 2006. Web. 24 Jul 2019.

Vancouver:

SIVAKUMAR N. Structural basis of protein stability at poly-extreme: Crystal structure of AmyA at 1.6 A resolution. [Internet] [Thesis]. National University of Singapore; 2006. [cited 2019 Jul 24]. Available from: http://scholarbank.nus.edu.sg/handle/10635/15244.

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

Council of Science Editors:

SIVAKUMAR N. Structural basis of protein stability at poly-extreme: Crystal structure of AmyA at 1.6 A resolution. [Thesis]. National University of Singapore; 2006. Available from: http://scholarbank.nus.edu.sg/handle/10635/15244

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


University of Western Ontario

22. Mian, Safee. Structure and Function of Stomatin-like Protein 2.

Degree: 2019, University of Western Ontario

 Stomatin-like protein 2 (SLP-2), a member of the SPFH superfamily, is a mitochondrial inner membrane protein required for optimal mitochondrial respiration. SLP-2 binds to the… (more)

Subjects/Keywords: Stomatin-like protein 2; SPFH; mitochondria; oligomerization; variable speed sedimentation velocity; right-handed coiled-coil; Biochemistry; Structural Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mian, S. (2019). Structure and Function of Stomatin-like Protein 2. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6105

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):

Mian, Safee. “Structure and Function of Stomatin-like Protein 2.” 2019. Thesis, University of Western Ontario. Accessed July 24, 2019. https://ir.lib.uwo.ca/etd/6105.

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

MLA Handbook (7th Edition):

Mian, Safee. “Structure and Function of Stomatin-like Protein 2.” 2019. Web. 24 Jul 2019.

Vancouver:

Mian S. Structure and Function of Stomatin-like Protein 2. [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2019 Jul 24]. Available from: https://ir.lib.uwo.ca/etd/6105.

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

Council of Science Editors:

Mian S. Structure and Function of Stomatin-like Protein 2. [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6105

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

23. Muniz, Amanda Bernardes. Estudos estruturais e funcionais dos receptores ativadores da proliferação de peroxissomos.

Degree: PhD, Física Aplicada, 2013, University of São Paulo

Os receptores ativadores da proliferação de peroxissomos (PPARs) pertencem à superfamília de receptores nucleares que funcionam como fatores transcricionais. Eles exercem um papel fundamental em… (more)

Subjects/Keywords: Cristalografia de proteínas; Interação proteína: ligante; Nuclear receptor; Oligomerização de proteínas; Peroxisome proliferator-activated receptor; Protein crystallography; Protein oligomerization; Protein:ligand interaction; Receptor ativador da proliferação de peroxissomos; Receptor nuclear

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Muniz, A. B. (2013). Estudos estruturais e funcionais dos receptores ativadores da proliferação de peroxissomos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/76/76132/tde-31072013-141118/ ;

Chicago Manual of Style (16th Edition):

Muniz, Amanda Bernardes. “Estudos estruturais e funcionais dos receptores ativadores da proliferação de peroxissomos.” 2013. Doctoral Dissertation, University of São Paulo. Accessed July 24, 2019. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-31072013-141118/ ;.

MLA Handbook (7th Edition):

Muniz, Amanda Bernardes. “Estudos estruturais e funcionais dos receptores ativadores da proliferação de peroxissomos.” 2013. Web. 24 Jul 2019.

Vancouver:

Muniz AB. Estudos estruturais e funcionais dos receptores ativadores da proliferação de peroxissomos. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2019 Jul 24]. Available from: http://www.teses.usp.br/teses/disponiveis/76/76132/tde-31072013-141118/ ;.

Council of Science Editors:

Muniz AB. Estudos estruturais e funcionais dos receptores ativadores da proliferação de peroxissomos. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/76/76132/tde-31072013-141118/ ;


Indian Institute of Science

24. Yamuna Kalyani, M. Structural Studies on the Role of Hinge involved in Domain Swapping in Salmonella Typhimurium Stationary Phase Survival Protein (SurE) and Sesbania Mosaic Virus Coat Protein.

Degree: 2014, Indian Institute of Science

 A unique mechanism of protein oligomerization is domain swapping. It is a feature found in some proteins wherein a dimer or a higher oligomer is… (more)

Subjects/Keywords: Salmonella Typhirium Stationary Phase Survival Protein (StSurE); Sesbania Mosaic Virus Coat Protein (SeMV); Protein Oligomerization; Domain Swapping; Salmonella Typhirium SurE (StSurE) Hinge Mutants; C-Terminal Helix Swapping; Protein X-ray Crystallography; Bacterial Protein Structure; Molecular Dynamics Simulations; Bacterial Proteins; H234A; Sesbania Mosaic Virus Coat Protein; Molecular Biophysics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yamuna Kalyani, M. (2014). Structural Studies on the Role of Hinge involved in Domain Swapping in Salmonella Typhimurium Stationary Phase Survival Protein (SurE) and Sesbania Mosaic Virus Coat Protein. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3500 ; http://etd.iisc.ernet.in/abstracts/4367/G26630-Abs.pdf

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):

Yamuna Kalyani, M. “Structural Studies on the Role of Hinge involved in Domain Swapping in Salmonella Typhimurium Stationary Phase Survival Protein (SurE) and Sesbania Mosaic Virus Coat Protein.” 2014. Thesis, Indian Institute of Science. Accessed July 24, 2019. http://etd.iisc.ernet.in/2005/3500 ; http://etd.iisc.ernet.in/abstracts/4367/G26630-Abs.pdf.

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

MLA Handbook (7th Edition):

Yamuna Kalyani, M. “Structural Studies on the Role of Hinge involved in Domain Swapping in Salmonella Typhimurium Stationary Phase Survival Protein (SurE) and Sesbania Mosaic Virus Coat Protein.” 2014. Web. 24 Jul 2019.

Vancouver:

Yamuna Kalyani M. Structural Studies on the Role of Hinge involved in Domain Swapping in Salmonella Typhimurium Stationary Phase Survival Protein (SurE) and Sesbania Mosaic Virus Coat Protein. [Internet] [Thesis]. Indian Institute of Science; 2014. [cited 2019 Jul 24]. Available from: http://etd.iisc.ernet.in/2005/3500 ; http://etd.iisc.ernet.in/abstracts/4367/G26630-Abs.pdf.

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

Council of Science Editors:

Yamuna Kalyani M. Structural Studies on the Role of Hinge involved in Domain Swapping in Salmonella Typhimurium Stationary Phase Survival Protein (SurE) and Sesbania Mosaic Virus Coat Protein. [Thesis]. Indian Institute of Science; 2014. Available from: http://etd.iisc.ernet.in/2005/3500 ; http://etd.iisc.ernet.in/abstracts/4367/G26630-Abs.pdf

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


Indian Institute of Science

25. Williams, Sunanda Margrett. The Dynamics of Iron in Miniferritins : A Structure-Function Connection.

Degree: 2014, Indian Institute of Science

 The DNA binding proteins under starvation (Dps) from M. smegmatis are cage-like structures which internalize iron and bind DNA. They provide resistance to the cells… (more)

Subjects/Keywords: Ferritins; Mycobacterium DNA Binding Protein; Miniferritins; Oligomerization; Mycobacterial DNA Binding Proteins; Ferritin Proteins; Iron Homeostasis; Minniferritins; Mycobacterium Smegmatis DNA Binding Protein; Mycobacterium Smegmatis Dps Iron Co-crystallization; Bacterial Proteins; MsDps1; MsDps2; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Williams, S. M. (2014). The Dynamics of Iron in Miniferritins : A Structure-Function Connection. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2788

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):

Williams, Sunanda Margrett. “The Dynamics of Iron in Miniferritins : A Structure-Function Connection.” 2014. Thesis, Indian Institute of Science. Accessed July 24, 2019. http://hdl.handle.net/2005/2788.

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

MLA Handbook (7th Edition):

Williams, Sunanda Margrett. “The Dynamics of Iron in Miniferritins : A Structure-Function Connection.” 2014. Web. 24 Jul 2019.

Vancouver:

Williams SM. The Dynamics of Iron in Miniferritins : A Structure-Function Connection. [Internet] [Thesis]. Indian Institute of Science; 2014. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/2005/2788.

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

Council of Science Editors:

Williams SM. The Dynamics of Iron in Miniferritins : A Structure-Function Connection. [Thesis]. Indian Institute of Science; 2014. Available from: http://hdl.handle.net/2005/2788

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


Indian Institute of Science

26. Williams, Sunanda Margrett. The Dynamics of Iron in Miniferritins : A Structure-Function Connection.

Degree: 2014, Indian Institute of Science

 The DNA binding proteins under starvation (Dps) from M. smegmatis are cage-like structures which internalize iron and bind DNA. They provide resistance to the cells… (more)

Subjects/Keywords: Ferritins; Mycobacterium DNA Binding Protein; Miniferritins; Oligomerization; Mycobacterial DNA Binding Proteins; Ferritin Proteins; Iron Homeostasis; Minniferritins; Mycobacterium Smegmatis DNA Binding Protein; Mycobacterium Smegmatis Dps Iron Co-crystallization; Bacterial Proteins; MsDps1; MsDps2; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Williams, S. M. (2014). The Dynamics of Iron in Miniferritins : A Structure-Function Connection. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/2788 ; http://etd.ncsi.iisc.ernet.in/abstracts/3655/G26624-Abs.pdf

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):

Williams, Sunanda Margrett. “The Dynamics of Iron in Miniferritins : A Structure-Function Connection.” 2014. Thesis, Indian Institute of Science. Accessed July 24, 2019. http://etd.iisc.ernet.in/handle/2005/2788 ; http://etd.ncsi.iisc.ernet.in/abstracts/3655/G26624-Abs.pdf.

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

MLA Handbook (7th Edition):

Williams, Sunanda Margrett. “The Dynamics of Iron in Miniferritins : A Structure-Function Connection.” 2014. Web. 24 Jul 2019.

Vancouver:

Williams SM. The Dynamics of Iron in Miniferritins : A Structure-Function Connection. [Internet] [Thesis]. Indian Institute of Science; 2014. [cited 2019 Jul 24]. Available from: http://etd.iisc.ernet.in/handle/2005/2788 ; http://etd.ncsi.iisc.ernet.in/abstracts/3655/G26624-Abs.pdf.

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

Council of Science Editors:

Williams SM. The Dynamics of Iron in Miniferritins : A Structure-Function Connection. [Thesis]. Indian Institute of Science; 2014. Available from: http://etd.iisc.ernet.in/handle/2005/2788 ; http://etd.ncsi.iisc.ernet.in/abstracts/3655/G26624-Abs.pdf

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

27. Katebi, Ataur Rahim. Building and simulating protein machines.

Degree: 2013, Iowa State University

 Glycolysis is a central metabolic pathway, present in almost all organisms, that produces energy. The pathway has been extensively investigated by biochemists. There is a… (more)

Subjects/Keywords: dihydroxy acetone phosphate; fructose bisphospahte aldolase; glycolysis; oligomerization; protein dynamics; protein-protein interaction; Atomic, Molecular and Optical Physics; Bioinformatics; Biophysics

oligomerization affect the functional dynamics of this protein and its stability? To answer that 11… …TIM upon oligomerization across different species. We also investigate how the motions of… …effects of the oligomerization of these two enzymes on their functional dynamics and the… …x28;2) the mechanistic synchrony of these two protein machines that may enable them to… …biological functions in an organism. A protein-protein interaction network consists of thousands of… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Katebi, A. R. (2013). Building and simulating protein machines. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/13195

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):

Katebi, Ataur Rahim. “Building and simulating protein machines.” 2013. Thesis, Iowa State University. Accessed July 24, 2019. https://lib.dr.iastate.edu/etd/13195.

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

MLA Handbook (7th Edition):

Katebi, Ataur Rahim. “Building and simulating protein machines.” 2013. Web. 24 Jul 2019.

Vancouver:

Katebi AR. Building and simulating protein machines. [Internet] [Thesis]. Iowa State University; 2013. [cited 2019 Jul 24]. Available from: https://lib.dr.iastate.edu/etd/13195.

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

Council of Science Editors:

Katebi AR. Building and simulating protein machines. [Thesis]. Iowa State University; 2013. Available from: https://lib.dr.iastate.edu/etd/13195

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


Indian Institute of Science

28. Chowdhury, Rakhi Pait. Newer Insights On Structure, Function And Regulation Of Dps Protein From Mycobacterium smegmatis.

Degree: 2009, Indian Institute of Science

 The first chapter will provide an introduction to the physiology, pathogenesis and biology of mycobacteria. Host-pathogen interactions, different modes of resistance of the bacteria, adaptations… (more)

Subjects/Keywords: Dps Proteins; Mycobacterium smegmatis; Bacterial DNA; Mycobacteria - Gene Expression; Mycobacteria - Gene Regulation; DPs Proteins - Oligomerization; Mycobacteria - Transcriptome Analysis; Mycobacterium-Host Interactions; DNA Binding; msdps Promoter; Mycobacterial MsDps2 Protein; Interface Cluster; M. smegmatis; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chowdhury, R. P. (2009). Newer Insights On Structure, Function And Regulation Of Dps Protein From Mycobacterium smegmatis. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/970

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):

Chowdhury, Rakhi Pait. “Newer Insights On Structure, Function And Regulation Of Dps Protein From Mycobacterium smegmatis.” 2009. Thesis, Indian Institute of Science. Accessed July 24, 2019. http://hdl.handle.net/2005/970.

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

MLA Handbook (7th Edition):

Chowdhury, Rakhi Pait. “Newer Insights On Structure, Function And Regulation Of Dps Protein From Mycobacterium smegmatis.” 2009. Web. 24 Jul 2019.

Vancouver:

Chowdhury RP. Newer Insights On Structure, Function And Regulation Of Dps Protein From Mycobacterium smegmatis. [Internet] [Thesis]. Indian Institute of Science; 2009. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/2005/970.

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

Council of Science Editors:

Chowdhury RP. Newer Insights On Structure, Function And Regulation Of Dps Protein From Mycobacterium smegmatis. [Thesis]. Indian Institute of Science; 2009. Available from: http://hdl.handle.net/2005/970

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


Georgia Tech

29. Watt, Terry J. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.

Degree: PhD, Chemistry and Biochemistry, 2007, Georgia Tech

 The human retinoid X receptor alpha (hRXRalpha) is a member of the nuclear receptor super-family of ligand-activated transcription factors. The Doyle laboratory has previously engineered… (more)

Subjects/Keywords: Ligand binding; Protein engineering; Oligomerization; Thermal denaturation; Retinoid X receptor; Retinoids; Nuclear receptors (Biochemistry); Ligand binding (Biochemistry); DNA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Watt, T. J. (2007). Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26647

Chicago Manual of Style (16th Edition):

Watt, Terry J. “Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.” 2007. Doctoral Dissertation, Georgia Tech. Accessed July 24, 2019. http://hdl.handle.net/1853/26647.

MLA Handbook (7th Edition):

Watt, Terry J. “Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.” 2007. Web. 24 Jul 2019.

Vancouver:

Watt TJ. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/1853/26647.

Council of Science Editors:

Watt TJ. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/26647


The Ohio State University

30. Xu, Binjie. Investigating AmrZ-mediated activation of <i>Pseudomonas aeruginosa</i> twitching motility and alginate production.

Degree: PhD, Microbiology, 2015, The Ohio State University

 The Gram negative bacterium <i>Pseudomonas aeruginosa</i> is ubiquitous in the natural environment and responsible for various human infections. Successful <i>P. aeruginosa</i> infections require many virulence… (more)

Subjects/Keywords: Biology; Biomedical Research; Microbiology; Molecular Biology; Pseudomonas aeruginosa; bacterial pathogen; pathogenesis; cystic fibrosis; AmrZ; twitching motility; type IV pilus; alginate; protein oligomerization; gene regulation; transcription; transcription regulation; transcriptome profiling; C-terminal domain

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Xu, B. (2015). Investigating AmrZ-mediated activation of <i>Pseudomonas aeruginosa</i> twitching motility and alginate production. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1447348689

Chicago Manual of Style (16th Edition):

Xu, Binjie. “Investigating AmrZ-mediated activation of <i>Pseudomonas aeruginosa</i> twitching motility and alginate production.” 2015. Doctoral Dissertation, The Ohio State University. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1447348689.

MLA Handbook (7th Edition):

Xu, Binjie. “Investigating AmrZ-mediated activation of <i>Pseudomonas aeruginosa</i> twitching motility and alginate production.” 2015. Web. 24 Jul 2019.

Vancouver:

Xu B. Investigating AmrZ-mediated activation of <i>Pseudomonas aeruginosa</i> twitching motility and alginate production. [Internet] [Doctoral dissertation]. The Ohio State University; 2015. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1447348689.

Council of Science Editors:

Xu B. Investigating AmrZ-mediated activation of <i>Pseudomonas aeruginosa</i> twitching motility and alginate production. [Doctoral Dissertation]. The Ohio State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1447348689

[1] [2]

.