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 +publisher:"University of Colorado" +contributor:("Amy Palmer"). Showing records 1 – 30 of 32 total matches.

[1] [2]

Search Limiters

Last 2 Years | English Only

▼ Search Limiters


University of Colorado

1. Han, Yu. Remodeling of Zinc Homeostasis in Differentiated Mammary Epithelial Cells.

Degree: PhD, 2018, University of Colorado

 Zinc is the second most abundant transition metal in mammals and an essential nutrient required for growth. Coupled with the biological significance of zinc, zinc… (more)

Subjects/Keywords: zinc homeostasis; mammary epithelial cells; biological functions; milk protein; remodeling; Biochemistry; Physiology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Han, Y. (2018). Remodeling of Zinc Homeostasis in Differentiated Mammary Epithelial Cells. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/287

Chicago Manual of Style (16th Edition):

Han, Yu. “Remodeling of Zinc Homeostasis in Differentiated Mammary Epithelial Cells.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/287.

MLA Handbook (7th Edition):

Han, Yu. “Remodeling of Zinc Homeostasis in Differentiated Mammary Epithelial Cells.” 2018. Web. 11 Apr 2021.

Vancouver:

Han Y. Remodeling of Zinc Homeostasis in Differentiated Mammary Epithelial Cells. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/287.

Council of Science Editors:

Han Y. Remodeling of Zinc Homeostasis in Differentiated Mammary Epithelial Cells. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/287


University of Colorado

2. Gao, Yuefeng. Biochemical Characterization of the Human Mediator Complex.

Degree: MS, Chemistry & Biochemistry, 2010, University of Colorado

  RNA polymerase II coordinates with a wide range of factors and catalyzes DNA transcription to synthesize mRNA. One critical step of transcription initiation is… (more)

Subjects/Keywords: Mediator complexes; DNA transcription; RNA polymerase II; Biochemistry; Genetics and Genomics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gao, Y. (2010). Biochemical Characterization of the Human Mediator Complex. (Masters Thesis). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/16

Chicago Manual of Style (16th Edition):

Gao, Yuefeng. “Biochemical Characterization of the Human Mediator Complex.” 2010. Masters Thesis, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/16.

MLA Handbook (7th Edition):

Gao, Yuefeng. “Biochemical Characterization of the Human Mediator Complex.” 2010. Web. 11 Apr 2021.

Vancouver:

Gao Y. Biochemical Characterization of the Human Mediator Complex. [Internet] [Masters thesis]. University of Colorado; 2010. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/16.

Council of Science Editors:

Gao Y. Biochemical Characterization of the Human Mediator Complex. [Masters Thesis]. University of Colorado; 2010. Available from: https://scholar.colorado.edu/chem_gradetds/16


University of Colorado

3. Vonderfecht, Tyson. The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies.

Degree: PhD, Chemistry & Biochemistry, 2012, University of Colorado

  The basal body is a microtubule-organizing center responsible for nucleating the cilium, a cellular structure important for a wide variety of cellular functions such… (more)

Subjects/Keywords: basal body; centrin; cilia; Tetrahymena; Cell Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Vonderfecht, T. (2012). The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/54

Chicago Manual of Style (16th Edition):

Vonderfecht, Tyson. “The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies.” 2012. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/54.

MLA Handbook (7th Edition):

Vonderfecht, Tyson. “The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies.” 2012. Web. 11 Apr 2021.

Vancouver:

Vonderfecht T. The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/54.

Council of Science Editors:

Vonderfecht T. The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/chem_gradetds/54


University of Colorado

4. Garst, Andrew D. Mechanistic Insights into Molecular Recognition and the Regulatory Landscape of the lysine Riboswitch.

Degree: PhD, Chemistry & Biochemistry, 2012, University of Colorado

  RNA plays a central role in gene regulation and information processing in all kingdoms of life. Found in 5' leader sequence of many bacterial… (more)

Subjects/Keywords: lysine biosynthesis; non-coding RNA; regulation; riboswitches; transcription attenuation; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Garst, A. D. (2012). Mechanistic Insights into Molecular Recognition and the Regulatory Landscape of the lysine Riboswitch. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/57

Chicago Manual of Style (16th Edition):

Garst, Andrew D. “Mechanistic Insights into Molecular Recognition and the Regulatory Landscape of the lysine Riboswitch.” 2012. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/57.

MLA Handbook (7th Edition):

Garst, Andrew D. “Mechanistic Insights into Molecular Recognition and the Regulatory Landscape of the lysine Riboswitch.” 2012. Web. 11 Apr 2021.

Vancouver:

Garst AD. Mechanistic Insights into Molecular Recognition and the Regulatory Landscape of the lysine Riboswitch. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/57.

Council of Science Editors:

Garst AD. Mechanistic Insights into Molecular Recognition and the Regulatory Landscape of the lysine Riboswitch. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/chem_gradetds/57


University of Colorado

5. LeBlanc, Marc-Andre. High Precision AFM-Based SMFS of Mechanically Labile Type III Secretion System Effectors.

Degree: PhD, 2018, University of Colorado

  Pathogenic bacteria have developed a wide range of tools for circumventing or overcoming the host’s defenses. Over time, these tools have become increasingly complex,… (more)

Subjects/Keywords: afm; protein unfolding; single-molecule force spectroscopy; specific attachment; type iii secretion system; Biochemistry; Biophysics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

LeBlanc, M. (2018). High Precision AFM-Based SMFS of Mechanically Labile Type III Secretion System Effectors. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/244

Chicago Manual of Style (16th Edition):

LeBlanc, Marc-Andre. “High Precision AFM-Based SMFS of Mechanically Labile Type III Secretion System Effectors.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/244.

MLA Handbook (7th Edition):

LeBlanc, Marc-Andre. “High Precision AFM-Based SMFS of Mechanically Labile Type III Secretion System Effectors.” 2018. Web. 11 Apr 2021.

Vancouver:

LeBlanc M. High Precision AFM-Based SMFS of Mechanically Labile Type III Secretion System Effectors. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/244.

Council of Science Editors:

LeBlanc M. High Precision AFM-Based SMFS of Mechanically Labile Type III Secretion System Effectors. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/244


University of Colorado

6. Perkins, Russell James. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.

Degree: PhD, 2018, University of Colorado

  Many important chemical reactions from all branches of chemistry occur with water as a solvent. Furthermore, in environmental chemistry, biochemistry, and synthetic chemistry, key… (more)

Subjects/Keywords: aqueous interfaces; aromatic aggregation; mechanistic organic chemistry; membrane biophysics; preboitic chemistry; surfactants; Organic Chemistry; Physical Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Perkins, R. J. (2018). Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/273

Chicago Manual of Style (16th Edition):

Perkins, Russell James. “Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/273.

MLA Handbook (7th Edition):

Perkins, Russell James. “Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.” 2018. Web. 11 Apr 2021.

Vancouver:

Perkins RJ. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/273.

Council of Science Editors:

Perkins RJ. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/273


University of Colorado

7. Barsic, Anthony J. Localization of Dense Clusters of Nanoscale Emitters for Super-resolution Microscopy.

Degree: PhD, Electrical, Computer & Energy Engineering, 2014, University of Colorado

  Single-Molecule Localization Microscopy is an optical imaging paradigm which provides computational reconstructions of microscopic objects much smaller than the imaging wavelength. Information regarding physical… (more)

Subjects/Keywords: Fluorescence microscopy; Image processing; Imaging systems; Super-resolution; Three-dimensional image processing; Three-dimensional microscopy; Electromagnetics and Photonics; Optics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Barsic, A. J. (2014). Localization of Dense Clusters of Nanoscale Emitters for Super-resolution Microscopy. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/ecen_gradetds/99

Chicago Manual of Style (16th Edition):

Barsic, Anthony J. “Localization of Dense Clusters of Nanoscale Emitters for Super-resolution Microscopy.” 2014. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/ecen_gradetds/99.

MLA Handbook (7th Edition):

Barsic, Anthony J. “Localization of Dense Clusters of Nanoscale Emitters for Super-resolution Microscopy.” 2014. Web. 11 Apr 2021.

Vancouver:

Barsic AJ. Localization of Dense Clusters of Nanoscale Emitters for Super-resolution Microscopy. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/ecen_gradetds/99.

Council of Science Editors:

Barsic AJ. Localization of Dense Clusters of Nanoscale Emitters for Super-resolution Microscopy. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/ecen_gradetds/99


University of Colorado

8. Hoyer, Melissa J. Novel Factors at Endoplasmic Reticulum-Endosome Contact Sites.

Degree: PhD, 2018, University of Colorado

 The endoplasmic reticulum is the cell’s platform for protein and lipid synthesis. Not only does the ER perform these functions, but it also regulates other… (more)

Subjects/Keywords: endoplasmic reticulum; endosome; fission; membrane contact sites; membrane trafficking; signaling receptor; Cell Biology; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hoyer, M. J. (2018). Novel Factors at Endoplasmic Reticulum-Endosome Contact Sites. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/95

Chicago Manual of Style (16th Edition):

Hoyer, Melissa J. “Novel Factors at Endoplasmic Reticulum-Endosome Contact Sites.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/mcdb_gradetds/95.

MLA Handbook (7th Edition):

Hoyer, Melissa J. “Novel Factors at Endoplasmic Reticulum-Endosome Contact Sites.” 2018. Web. 11 Apr 2021.

Vancouver:

Hoyer MJ. Novel Factors at Endoplasmic Reticulum-Endosome Contact Sites. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/mcdb_gradetds/95.

Council of Science Editors:

Hoyer MJ. Novel Factors at Endoplasmic Reticulum-Endosome Contact Sites. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/mcdb_gradetds/95


University of Colorado

9. Plaks, Joseph Gabriel. Computational Protein Design for Peptide-Directed Bioconjugation.

Degree: PhD, 2019, University of Colorado

  Proteins enable living organisms to perform many of their critical functions, having been applied over evolutionary time to solve problems of overwhelming diversity and… (more)

Subjects/Keywords: bioconjugation; click chemistry; lipoic acid ligase; protein engineering; quorum sensing; rosetta; Biochemistry; Biomedical Engineering and Bioengineering; Materials Science and Engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Plaks, J. G. (2019). Computational Protein Design for Peptide-Directed Bioconjugation. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/140

Chicago Manual of Style (16th Edition):

Plaks, Joseph Gabriel. “Computational Protein Design for Peptide-Directed Bioconjugation.” 2019. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chbe_gradetds/140.

MLA Handbook (7th Edition):

Plaks, Joseph Gabriel. “Computational Protein Design for Peptide-Directed Bioconjugation.” 2019. Web. 11 Apr 2021.

Vancouver:

Plaks JG. Computational Protein Design for Peptide-Directed Bioconjugation. [Internet] [Doctoral dissertation]. University of Colorado; 2019. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chbe_gradetds/140.

Council of Science Editors:

Plaks JG. Computational Protein Design for Peptide-Directed Bioconjugation. [Doctoral Dissertation]. University of Colorado; 2019. Available from: https://scholar.colorado.edu/chbe_gradetds/140


University of Colorado

10. Fiedler, Brett. Time-Resolved Fluorescence Techniques for the Development and Characterization of Genetically-Encoded Biosensors.

Degree: PhD, Chemistry & Biochemistry, 2017, University of Colorado

  Fluorescent biosensors are important measurement tools for in vivo quantification of pH, concentrations of metal ions and other analytes, and physical parameters such as… (more)

Subjects/Keywords: fluorescence; fret; fluorescent protein; biosensor; microfluidic; cell sorting; Analytical Chemistry; Biophysics; Physical Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fiedler, B. (2017). Time-Resolved Fluorescence Techniques for the Development and Characterization of Genetically-Encoded Biosensors. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/jila_gradetds/2

Chicago Manual of Style (16th Edition):

Fiedler, Brett. “Time-Resolved Fluorescence Techniques for the Development and Characterization of Genetically-Encoded Biosensors.” 2017. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/jila_gradetds/2.

MLA Handbook (7th Edition):

Fiedler, Brett. “Time-Resolved Fluorescence Techniques for the Development and Characterization of Genetically-Encoded Biosensors.” 2017. Web. 11 Apr 2021.

Vancouver:

Fiedler B. Time-Resolved Fluorescence Techniques for the Development and Characterization of Genetically-Encoded Biosensors. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/jila_gradetds/2.

Council of Science Editors:

Fiedler B. Time-Resolved Fluorescence Techniques for the Development and Characterization of Genetically-Encoded Biosensors. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/jila_gradetds/2


University of Colorado

11. Farnsworth, Nikki Lynn. The Role of Chondrocyte Age in Cellular Response to External Cues and their Implications in Tissue Engineering.

Degree: PhD, Chemical & Biochemical Engineering, 2012, University of Colorado

  Osteoarthritis is a degenerative joint disease for which there is no cure, but therapies such as tissue engineering offer hope. One of the challenges… (more)

Subjects/Keywords: Age; Chondrocyte; Loading; Osmolarity; Poly(ethylene glycol); Biomechanical Engineering; Cell Biology; Chemical Engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Farnsworth, N. L. (2012). The Role of Chondrocyte Age in Cellular Response to External Cues and their Implications in Tissue Engineering. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/25

Chicago Manual of Style (16th Edition):

Farnsworth, Nikki Lynn. “The Role of Chondrocyte Age in Cellular Response to External Cues and their Implications in Tissue Engineering.” 2012. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chbe_gradetds/25.

MLA Handbook (7th Edition):

Farnsworth, Nikki Lynn. “The Role of Chondrocyte Age in Cellular Response to External Cues and their Implications in Tissue Engineering.” 2012. Web. 11 Apr 2021.

Vancouver:

Farnsworth NL. The Role of Chondrocyte Age in Cellular Response to External Cues and their Implications in Tissue Engineering. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chbe_gradetds/25.

Council of Science Editors:

Farnsworth NL. The Role of Chondrocyte Age in Cellular Response to External Cues and their Implications in Tissue Engineering. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/chbe_gradetds/25


University of Colorado

12. Bresee, James. Combinatorial Display of Small Molecule Ligands on Gold Nanoparticles for Antimicrobial Properties.

Degree: PhD, Chemistry & Biochemistry, 2012, University of Colorado

  The continual emergence of multidrug resistance in bacteria calls for the development of novel antibiotics in order to treat resistant infections. Traditionally, small molecule… (more)

Subjects/Keywords: antibiotics; gold nanoparticles; Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bresee, J. (2012). Combinatorial Display of Small Molecule Ligands on Gold Nanoparticles for Antimicrobial Properties. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/65

Chicago Manual of Style (16th Edition):

Bresee, James. “Combinatorial Display of Small Molecule Ligands on Gold Nanoparticles for Antimicrobial Properties.” 2012. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/65.

MLA Handbook (7th Edition):

Bresee, James. “Combinatorial Display of Small Molecule Ligands on Gold Nanoparticles for Antimicrobial Properties.” 2012. Web. 11 Apr 2021.

Vancouver:

Bresee J. Combinatorial Display of Small Molecule Ligands on Gold Nanoparticles for Antimicrobial Properties. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/65.

Council of Science Editors:

Bresee J. Combinatorial Display of Small Molecule Ligands on Gold Nanoparticles for Antimicrobial Properties. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/chem_gradetds/65


University of Colorado

13. Chapnick, Douglas Andrew. Characterization of the Role of MEK1 Kinase Activity in TGF-Beta Induced Collective Cell Migration.

Degree: PhD, Chemistry & Biochemistry, 2012, University of Colorado

  The migration of individual cells and collective groups of cells has been repeatedly shown to be an important cellular behavior throughout normal biology and… (more)

Subjects/Keywords: Collective Migration; MEK1; Migration; TGF-Beta; Biochemistry; Cell Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chapnick, D. A. (2012). Characterization of the Role of MEK1 Kinase Activity in TGF-Beta Induced Collective Cell Migration. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/68

Chicago Manual of Style (16th Edition):

Chapnick, Douglas Andrew. “Characterization of the Role of MEK1 Kinase Activity in TGF-Beta Induced Collective Cell Migration.” 2012. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/68.

MLA Handbook (7th Edition):

Chapnick, Douglas Andrew. “Characterization of the Role of MEK1 Kinase Activity in TGF-Beta Induced Collective Cell Migration.” 2012. Web. 11 Apr 2021.

Vancouver:

Chapnick DA. Characterization of the Role of MEK1 Kinase Activity in TGF-Beta Induced Collective Cell Migration. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/68.

Council of Science Editors:

Chapnick DA. Characterization of the Role of MEK1 Kinase Activity in TGF-Beta Induced Collective Cell Migration. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/chem_gradetds/68


University of Colorado

14. English, Amber. Rab10 GTPase regulates ER dynamics and morphology.

Degree: PhD, 2012, University of Colorado

  I have identified Rab10 as an ER specific Rab GTPase that regulates ER structure and dynamics. I show that Rab10 localizes to the ER… (more)

Subjects/Keywords: Endoplasmic Reticulum; Fusion; Organelle Biogenesis; Rab10; Rab GTPase; Cell Biology; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

English, A. (2012). Rab10 GTPase regulates ER dynamics and morphology. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/15

Chicago Manual of Style (16th Edition):

English, Amber. “Rab10 GTPase regulates ER dynamics and morphology.” 2012. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/mcdb_gradetds/15.

MLA Handbook (7th Edition):

English, Amber. “Rab10 GTPase regulates ER dynamics and morphology.” 2012. Web. 11 Apr 2021.

Vancouver:

English A. Rab10 GTPase regulates ER dynamics and morphology. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/mcdb_gradetds/15.

Council of Science Editors:

English A. Rab10 GTPase regulates ER dynamics and morphology. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/mcdb_gradetds/15


University of Colorado

15. Lund, Travis John. Asymmetric Recognition of Nucleobase Features by DNA Polymerases.

Degree: PhD, Chemistry & Biochemistry, 2013, University of Colorado

  This work describes an investigation into the recognition of nucleobase features by several DNA polymerases. I used of a series of pyrimidine analogues modified… (more)

Subjects/Keywords: analogue; DNA; fidelity; kinetics; nucleotide; Polymerase; Biochemistry; Organic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lund, T. J. (2013). Asymmetric Recognition of Nucleobase Features by DNA Polymerases. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/75

Chicago Manual of Style (16th Edition):

Lund, Travis John. “Asymmetric Recognition of Nucleobase Features by DNA Polymerases.” 2013. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/75.

MLA Handbook (7th Edition):

Lund, Travis John. “Asymmetric Recognition of Nucleobase Features by DNA Polymerases.” 2013. Web. 11 Apr 2021.

Vancouver:

Lund TJ. Asymmetric Recognition of Nucleobase Features by DNA Polymerases. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/75.

Council of Science Editors:

Lund TJ. Asymmetric Recognition of Nucleobase Features by DNA Polymerases. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/chem_gradetds/75


University of Colorado

16. Morton, Leslie Anne. Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components.

Degree: PhD, Chemistry & Biochemistry, 2013, University of Colorado

  Membrane curvature is a vital function in several significant biological processes. Indeed, this behavior is critical for activating certain signaling processes, membrane budding for… (more)

Subjects/Keywords: lipids; membranes; peptides; proteins; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Morton, L. A. (2013). Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/97

Chicago Manual of Style (16th Edition):

Morton, Leslie Anne. “Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components.” 2013. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/97.

MLA Handbook (7th Edition):

Morton, Leslie Anne. “Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components.” 2013. Web. 11 Apr 2021.

Vancouver:

Morton LA. Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/97.

Council of Science Editors:

Morton LA. Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/chem_gradetds/97


University of Colorado

17. Blair, Rebecca. Using Single Molecule FRET to Study the Mechanisms of DNA Bending by TBP and HMGB1.

Degree: PhD, Chemistry & Biochemistry, 2013, University of Colorado

  Defining mechanisms of transcriptional regulation is important for understanding how gene expression is controlled, which is essential to cellular viability. Outlined in this thesis… (more)

Subjects/Keywords: DNA bending; HMGB1; single molecule FRET; TBP; TIRF; Biochemistry; Molecular Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Blair, R. (2013). Using Single Molecule FRET to Study the Mechanisms of DNA Bending by TBP and HMGB1. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/106

Chicago Manual of Style (16th Edition):

Blair, Rebecca. “Using Single Molecule FRET to Study the Mechanisms of DNA Bending by TBP and HMGB1.” 2013. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/106.

MLA Handbook (7th Edition):

Blair, Rebecca. “Using Single Molecule FRET to Study the Mechanisms of DNA Bending by TBP and HMGB1.” 2013. Web. 11 Apr 2021.

Vancouver:

Blair R. Using Single Molecule FRET to Study the Mechanisms of DNA Bending by TBP and HMGB1. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/106.

Council of Science Editors:

Blair R. Using Single Molecule FRET to Study the Mechanisms of DNA Bending by TBP and HMGB1. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/chem_gradetds/106


University of Colorado

18. Xu, Yemin. Mechanisms of Protein Stability in Lyophilized Samples.

Degree: PhD, Chemistry & Biochemistry, 2014, University of Colorado

  Lyophilization is often the choice for therapeutic proteins when an aqueous formulation is not sufficiently stable to achieve the desired shelf life. Lyophilization incorporates… (more)

Subjects/Keywords: Interface; Lyophilization; Mobility; Protein formulation; Stability; Structure; Medicinal and Pharmaceutical Chemistry; Pharmaceutics and Drug Design

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Xu, Y. (2014). Mechanisms of Protein Stability in Lyophilized Samples. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/110

Chicago Manual of Style (16th Edition):

Xu, Yemin. “Mechanisms of Protein Stability in Lyophilized Samples.” 2014. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/110.

MLA Handbook (7th Edition):

Xu, Yemin. “Mechanisms of Protein Stability in Lyophilized Samples.” 2014. Web. 11 Apr 2021.

Vancouver:

Xu Y. Mechanisms of Protein Stability in Lyophilized Samples. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/110.

Council of Science Editors:

Xu Y. Mechanisms of Protein Stability in Lyophilized Samples. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/chem_gradetds/110


University of Colorado

19. Rowland, Ashley Ann. A New Role for the Endoplasmic Reticulum at Endosome Contact Sites.

Degree: PhD, 2015, University of Colorado

  The Endoplasmic Reticulum (ER) forms a dynamic network that spans throughout the cell. In addition to the well characterized roles in lipid synthesis, protein… (more)

Subjects/Keywords: confocal microscopy; endocytic pathway; endoplasmic reticulum; endosome fission; organelle biogenesis; Cell Biology; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rowland, A. A. (2015). A New Role for the Endoplasmic Reticulum at Endosome Contact Sites. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/49

Chicago Manual of Style (16th Edition):

Rowland, Ashley Ann. “A New Role for the Endoplasmic Reticulum at Endosome Contact Sites.” 2015. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/mcdb_gradetds/49.

MLA Handbook (7th Edition):

Rowland, Ashley Ann. “A New Role for the Endoplasmic Reticulum at Endosome Contact Sites.” 2015. Web. 11 Apr 2021.

Vancouver:

Rowland AA. A New Role for the Endoplasmic Reticulum at Endosome Contact Sites. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/mcdb_gradetds/49.

Council of Science Editors:

Rowland AA. A New Role for the Endoplasmic Reticulum at Endosome Contact Sites. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/mcdb_gradetds/49


University of Colorado

20. 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 https://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 April 11, 2021. https://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. 11 Apr 2021.

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 2021 Apr 11]. Available from: https://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: https://scholar.colorado.edu/mcdb_gradetds/47


University of Colorado

21. Amer, Luke Daniel. Enzymatically Degradable Poly(ethylene glycol) Hydrogels for Diverse Tissue Engineering Applications and for the Study of the Foreign Body Response.

Degree: PhD, Chemical & Biochemical Engineering, 2016, University of Colorado

 The field of tissue engineering aims to create replacements for diseased or damaged tissues which restore function and integrate with the host. Poly(ethylene glycol) (PEG)… (more)

Subjects/Keywords: Foreign Body Response; Photopolymerization; Synthetic Hydrogel; Tissue Engineering; Biological Phenomena, Cell Phenomena, and Immunity; Biomedical Engineering and Bioengineering; Chemical Engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Amer, L. D. (2016). Enzymatically Degradable Poly(ethylene glycol) Hydrogels for Diverse Tissue Engineering Applications and for the Study of the Foreign Body Response. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chen_gradetds/6

Chicago Manual of Style (16th Edition):

Amer, Luke Daniel. “Enzymatically Degradable Poly(ethylene glycol) Hydrogels for Diverse Tissue Engineering Applications and for the Study of the Foreign Body Response.” 2016. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chen_gradetds/6.

MLA Handbook (7th Edition):

Amer, Luke Daniel. “Enzymatically Degradable Poly(ethylene glycol) Hydrogels for Diverse Tissue Engineering Applications and for the Study of the Foreign Body Response.” 2016. Web. 11 Apr 2021.

Vancouver:

Amer LD. Enzymatically Degradable Poly(ethylene glycol) Hydrogels for Diverse Tissue Engineering Applications and for the Study of the Foreign Body Response. [Internet] [Doctoral dissertation]. University of Colorado; 2016. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chen_gradetds/6.

Council of Science Editors:

Amer LD. Enzymatically Degradable Poly(ethylene glycol) Hydrogels for Diverse Tissue Engineering Applications and for the Study of the Foreign Body Response. [Doctoral Dissertation]. University of Colorado; 2016. Available from: https://scholar.colorado.edu/chen_gradetds/6


University of Colorado

22. Bunker, Eric Newman. Novel Insights into Tace Regulation of Autocrine and Paracrine Signaling in Epithelial Cells.

Degree: PhD, 2017, University of Colorado

  A multitude of cellular functions are controlled by the activity of the membrane-bound protease TACE, including immune response and development. Through cleavage of its… (more)

Subjects/Keywords: Adam17; alpha catenin; ERK pulses; kerotinocytes; TACE; Biochemistry; Cell Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bunker, E. N. (2017). Novel Insights into Tace Regulation of Autocrine and Paracrine Signaling in Epithelial Cells. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/216

Chicago Manual of Style (16th Edition):

Bunker, Eric Newman. “Novel Insights into Tace Regulation of Autocrine and Paracrine Signaling in Epithelial Cells.” 2017. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/216.

MLA Handbook (7th Edition):

Bunker, Eric Newman. “Novel Insights into Tace Regulation of Autocrine and Paracrine Signaling in Epithelial Cells.” 2017. Web. 11 Apr 2021.

Vancouver:

Bunker EN. Novel Insights into Tace Regulation of Autocrine and Paracrine Signaling in Epithelial Cells. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/216.

Council of Science Editors:

Bunker EN. Novel Insights into Tace Regulation of Autocrine and Paracrine Signaling in Epithelial Cells. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/216


University of Colorado

23. Perkins, Russell James. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.

Degree: PhD, 2017, University of Colorado

  Many important chemical reactions from all branches of chemistry occur with water as a solvent. Furthermore, in environmental chemistry, biochemistry, and synthetic chemistry, key… (more)

Subjects/Keywords: aqueous interfaces; aromatic aggregation; mechanistic organic chemistry; membrane biophysics; preboitic chemistry; surfactants; Physical Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Perkins, R. J. (2017). Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/219

Chicago Manual of Style (16th Edition):

Perkins, Russell James. “Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.” 2017. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/219.

MLA Handbook (7th Edition):

Perkins, Russell James. “Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions.” 2017. Web. 11 Apr 2021.

Vancouver:

Perkins RJ. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/219.

Council of Science Editors:

Perkins RJ. Beyond Hydrophobicity: Aqueous Interfaces, Interactions and Reactions. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/219


University of Colorado

24. Hopkins, Alex Hunt. Toward a Mechanistic Understanding of Outer Membrane Protein Biogenesis.

Degree: PhD, Chemistry & Biochemistry, 2017, University of Colorado

 The outer membranes of Gram-negative bacteria are essential to their survival and have a unique asymmetric structure that features an outer leaflet of lipopolysaccharide. Bacterial… (more)

Subjects/Keywords: outer membrane lipopolysaccharide; inner membrane; protein; biogenesis; outer membrane protein; crosslinking; Biochemistry; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hopkins, A. H. (2017). Toward a Mechanistic Understanding of Outer Membrane Protein Biogenesis. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/220

Chicago Manual of Style (16th Edition):

Hopkins, Alex Hunt. “Toward a Mechanistic Understanding of Outer Membrane Protein Biogenesis.” 2017. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/220.

MLA Handbook (7th Edition):

Hopkins, Alex Hunt. “Toward a Mechanistic Understanding of Outer Membrane Protein Biogenesis.” 2017. Web. 11 Apr 2021.

Vancouver:

Hopkins AH. Toward a Mechanistic Understanding of Outer Membrane Protein Biogenesis. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/220.

Council of Science Editors:

Hopkins AH. Toward a Mechanistic Understanding of Outer Membrane Protein Biogenesis. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/220


University of Colorado

25. Li, Hanzeng. C. elegans as a Genetics Model to Study Paternal Mitochondria Elimination and Apoptosis Kinetics Regulation.

Degree: PhD, 2016, University of Colorado

  The round worm, Caenorhabditis elegans, provides a simple system to study complex questions. The philosophy behind it is that a single cell contains almost… (more)

Subjects/Keywords: apoptosis; autophagy; mitochondria; Biochemistry; Developmental Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Li, H. (2016). C. elegans as a Genetics Model to Study Paternal Mitochondria Elimination and Apoptosis Kinetics Regulation. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/229

Chicago Manual of Style (16th Edition):

Li, Hanzeng. “C. elegans as a Genetics Model to Study Paternal Mitochondria Elimination and Apoptosis Kinetics Regulation.” 2016. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/229.

MLA Handbook (7th Edition):

Li, Hanzeng. “C. elegans as a Genetics Model to Study Paternal Mitochondria Elimination and Apoptosis Kinetics Regulation.” 2016. Web. 11 Apr 2021.

Vancouver:

Li H. C. elegans as a Genetics Model to Study Paternal Mitochondria Elimination and Apoptosis Kinetics Regulation. [Internet] [Doctoral dissertation]. University of Colorado; 2016. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/229.

Council of Science Editors:

Li H. C. elegans as a Genetics Model to Study Paternal Mitochondria Elimination and Apoptosis Kinetics Regulation. [Doctoral Dissertation]. University of Colorado; 2016. Available from: https://scholar.colorado.edu/chem_gradetds/229


University of Colorado

26. Protter, David Stephen Warren. Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules.

Degree: PhD, Chemistry & Biochemistry, 2017, University of Colorado

  Cells assemble large, non-membrane bound granules of protein and RNA, termed Ri- bonucleoprotein granules (RNP granules), often in response to a wide variety of… (more)

Subjects/Keywords: intrinsically disordered region; phase separation; RNP granule; stress granule; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Protter, D. S. W. (2017). Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/242

Chicago Manual of Style (16th Edition):

Protter, David Stephen Warren. “Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules.” 2017. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/242.

MLA Handbook (7th Edition):

Protter, David Stephen Warren. “Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules.” 2017. Web. 11 Apr 2021.

Vancouver:

Protter DSW. Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/242.

Council of Science Editors:

Protter DSW. Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/242


University of Colorado

27. Sandoval, Cristina Marie. Structural and Biochemical Characterization of Proteins Involved in the Biogenesis of Outer Membrane Proteins.

Degree: PhD, Chemistry & Biochemistry, 2014, University of Colorado

  The cellular envelope of bacterial cells protects it from the extracellular environment it experiences. A key component of this envelope is the outer membrane… (more)

Subjects/Keywords: BamD; Skp; SurA; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sandoval, C. M. (2014). Structural and Biochemical Characterization of Proteins Involved in the Biogenesis of Outer Membrane Proteins. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/120

Chicago Manual of Style (16th Edition):

Sandoval, Cristina Marie. “Structural and Biochemical Characterization of Proteins Involved in the Biogenesis of Outer Membrane Proteins.” 2014. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/120.

MLA Handbook (7th Edition):

Sandoval, Cristina Marie. “Structural and Biochemical Characterization of Proteins Involved in the Biogenesis of Outer Membrane Proteins.” 2014. Web. 11 Apr 2021.

Vancouver:

Sandoval CM. Structural and Biochemical Characterization of Proteins Involved in the Biogenesis of Outer Membrane Proteins. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/120.

Council of Science Editors:

Sandoval CM. Structural and Biochemical Characterization of Proteins Involved in the Biogenesis of Outer Membrane Proteins. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/chem_gradetds/120


University of Colorado

28. Johnson, Laura. Probing the Dynamics of Red Fluorescent Protein Variants using NMR Spectroscopy: How Directed Development Affected Protein Dynamics.

Degree: PhD, Chemistry & Biochemistry, 2013, University of Colorado

  Fluorescent proteins are commonly used genetically encodable tools for probing intracellular events in real time. Red fluorescent proteins (RFPs) are particularly useful because scattering… (more)

Subjects/Keywords: Development; Dynamics; NMR Spectroscopy; Quantum Yield; Red Fluorescent Protein; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Johnson, L. (2013). Probing the Dynamics of Red Fluorescent Protein Variants using NMR Spectroscopy: How Directed Development Affected Protein Dynamics. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/135

Chicago Manual of Style (16th Edition):

Johnson, Laura. “Probing the Dynamics of Red Fluorescent Protein Variants using NMR Spectroscopy: How Directed Development Affected Protein Dynamics.” 2013. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/135.

MLA Handbook (7th Edition):

Johnson, Laura. “Probing the Dynamics of Red Fluorescent Protein Variants using NMR Spectroscopy: How Directed Development Affected Protein Dynamics.” 2013. Web. 11 Apr 2021.

Vancouver:

Johnson L. Probing the Dynamics of Red Fluorescent Protein Variants using NMR Spectroscopy: How Directed Development Affected Protein Dynamics. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/135.

Council of Science Editors:

Johnson L. Probing the Dynamics of Red Fluorescent Protein Variants using NMR Spectroscopy: How Directed Development Affected Protein Dynamics. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/chem_gradetds/135


University of Colorado

29. Gifford, Jennifer Chappell. Interactions of Nanomaterials with Biological Systems: A Study of Bio-Mineralized Nanoparticles and Nanoparticle Antibiotics.

Degree: PhD, Chemistry & Biochemistry, 2015, University of Colorado

  Nature is continually able to out-perform laboratory syntheses of nanomaterials with control of specific properties under ambient temperatures, pressures and pH. The investigation of… (more)

Subjects/Keywords: nanoparticle synthesis; mediation; genetically encodable tags; bacterial interaction; mammalian cell toxicity; on-particle ligand quantitation; Biochemistry; Cell Biology; Nanoscience and Nanotechnology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gifford, J. C. (2015). Interactions of Nanomaterials with Biological Systems: A Study of Bio-Mineralized Nanoparticles and Nanoparticle Antibiotics. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/155

Chicago Manual of Style (16th Edition):

Gifford, Jennifer Chappell. “Interactions of Nanomaterials with Biological Systems: A Study of Bio-Mineralized Nanoparticles and Nanoparticle Antibiotics.” 2015. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chem_gradetds/155.

MLA Handbook (7th Edition):

Gifford, Jennifer Chappell. “Interactions of Nanomaterials with Biological Systems: A Study of Bio-Mineralized Nanoparticles and Nanoparticle Antibiotics.” 2015. Web. 11 Apr 2021.

Vancouver:

Gifford JC. Interactions of Nanomaterials with Biological Systems: A Study of Bio-Mineralized Nanoparticles and Nanoparticle Antibiotics. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chem_gradetds/155.

Council of Science Editors:

Gifford JC. Interactions of Nanomaterials with Biological Systems: A Study of Bio-Mineralized Nanoparticles and Nanoparticle Antibiotics. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/chem_gradetds/155


University of Colorado

30. Godfroy, James Isaac, III. Probing the Role of Transmembrane Domain Interactions in Toll-like Receptor Signaling.

Degree: PhD, Chemical & Biochemical Engineering, 2015, University of Colorado

  Membrane proteins account for approximately 30% of the human proteome, are the therapeutic target of nearly 60% of current pharmacological agents, yet account for… (more)

Subjects/Keywords: FRET; transmembrane peptides as regulators; Biochemistry; Biophysics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Godfroy, James Isaac, I. (2015). Probing the Role of Transmembrane Domain Interactions in Toll-like Receptor Signaling. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/93

Chicago Manual of Style (16th Edition):

Godfroy, James Isaac, III. “Probing the Role of Transmembrane Domain Interactions in Toll-like Receptor Signaling.” 2015. Doctoral Dissertation, University of Colorado. Accessed April 11, 2021. https://scholar.colorado.edu/chbe_gradetds/93.

MLA Handbook (7th Edition):

Godfroy, James Isaac, III. “Probing the Role of Transmembrane Domain Interactions in Toll-like Receptor Signaling.” 2015. Web. 11 Apr 2021.

Vancouver:

Godfroy, James Isaac I. Probing the Role of Transmembrane Domain Interactions in Toll-like Receptor Signaling. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2021 Apr 11]. Available from: https://scholar.colorado.edu/chbe_gradetds/93.

Council of Science Editors:

Godfroy, James Isaac I. Probing the Role of Transmembrane Domain Interactions in Toll-like Receptor Signaling. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/chbe_gradetds/93

[1] [2]

.