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

University: University of California – San Francisco

You searched for subject:(Protein chemistry). Showing records 1 – 18 of 18 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


University of California – San Francisco

1. Cruz, Leslie Ann. Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors.

Degree: Chemistry and Chemical Biology, 2011, University of California – San Francisco

 Numerous small molecules serve to coordinate many biological activities within cells of multicelluar organisms. These ligand-receptor interactions are vital to the control of cellular processes… (more)

Subjects/Keywords: Chemistry; Biophysics; Biochemistry; chemical biology; protein engineering; protein-ligand interactions

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cruz, L. A. (2011). Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/267353tc

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):

Cruz, Leslie Ann. “Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors.” 2011. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/267353tc.

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

MLA Handbook (7th Edition):

Cruz, Leslie Ann. “Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors.” 2011. Web. 16 Jun 2019.

Vancouver:

Cruz LA. Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/267353tc.

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

Council of Science Editors:

Cruz LA. Studies in Structure, Chemistry & Biology Of Receptor-Ligand Interactions for the AMPA & Androgen Receptors. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/267353tc

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


University of California – San Francisco

2. Freilich, Rebecca. Protein-protein interactions of Hsp27.

Degree: Chemistry and Chemical Biology, 2018, University of California – San Francisco

 Small Heat Shock Proteins (sHSPs), including Hsp27, are a non-enzymaticclass of molecular chaperones that bind improperly folded proteins and maintain theirsolubility, acting as a first… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry; Chaperones; Chemical Biology; Hsp27; Protein-Protein Interactions; Small heat shock proteins

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Freilich, R. (2018). Protein-protein interactions of Hsp27. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0g95m86d

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):

Freilich, Rebecca. “Protein-protein interactions of Hsp27.” 2018. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/0g95m86d.

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

MLA Handbook (7th Edition):

Freilich, Rebecca. “Protein-protein interactions of Hsp27.” 2018. Web. 16 Jun 2019.

Vancouver:

Freilich R. Protein-protein interactions of Hsp27. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/0g95m86d.

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

Council of Science Editors:

Freilich R. Protein-protein interactions of Hsp27. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/0g95m86d

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


University of California – San Francisco

3. Miller, Rand Micah. Electrophilic Fragment-Based Design of Reversible Covalent Kinase Inhibitors.

Degree: Chemistry and Chemical Biology, 2014, University of California – San Francisco

Protein kinases are an important class of enzymes that are ubiquitously involved in cellular signal transduction. The misregulation of protein kinases is implicated in many… (more)

Subjects/Keywords: Chemistry; Biochemistry; cyanoacrylamide; inhibitor; MSK1; protein kinase; reversible covalent; small molecule

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Miller, R. M. (2014). Electrophilic Fragment-Based Design of Reversible Covalent Kinase Inhibitors. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/75p4s454

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):

Miller, Rand Micah. “Electrophilic Fragment-Based Design of Reversible Covalent Kinase Inhibitors.” 2014. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/75p4s454.

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

MLA Handbook (7th Edition):

Miller, Rand Micah. “Electrophilic Fragment-Based Design of Reversible Covalent Kinase Inhibitors.” 2014. Web. 16 Jun 2019.

Vancouver:

Miller RM. Electrophilic Fragment-Based Design of Reversible Covalent Kinase Inhibitors. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/75p4s454.

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

Council of Science Editors:

Miller RM. Electrophilic Fragment-Based Design of Reversible Covalent Kinase Inhibitors. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/75p4s454

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


University of California – San Francisco

4. Thomaston, Jessica Leigh. X-ray crystal structures of the influenza A M2 proton channel.

Degree: Chemistry and Chemical Biology, 2018, University of California – San Francisco

 The M2 proton channel is a drug target of the influenza A virus. It is also a model system for the study of the selective,… (more)

Subjects/Keywords: Chemistry; influenza; M2; membrane protein; proton channel; X-ray crystallography

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thomaston, J. L. (2018). X-ray crystal structures of the influenza A M2 proton channel. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7jn6q27x

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):

Thomaston, Jessica Leigh. “X-ray crystal structures of the influenza A M2 proton channel.” 2018. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/7jn6q27x.

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

MLA Handbook (7th Edition):

Thomaston, Jessica Leigh. “X-ray crystal structures of the influenza A M2 proton channel.” 2018. Web. 16 Jun 2019.

Vancouver:

Thomaston JL. X-ray crystal structures of the influenza A M2 proton channel. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/7jn6q27x.

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

Council of Science Editors:

Thomaston JL. X-ray crystal structures of the influenza A M2 proton channel. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/7jn6q27x

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


University of California – San Francisco

5. Barkovich, Krister Jernstedt. Development of chemical tools targeting DEAD-box proteins.

Degree: Chemistry and Chemical Biology, 2018, University of California – San Francisco

 The complexity of the three-dimensional structures formed by RNA is essential for its function and as a result, a large number of protein co-factors are… (more)

Subjects/Keywords: Biochemistry; Chemistry; chemical biology; DEAD-box protein; enzyme inhibitor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Barkovich, K. J. (2018). Development of chemical tools targeting DEAD-box proteins. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/1bq6m023

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):

Barkovich, Krister Jernstedt. “Development of chemical tools targeting DEAD-box proteins.” 2018. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/1bq6m023.

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

MLA Handbook (7th Edition):

Barkovich, Krister Jernstedt. “Development of chemical tools targeting DEAD-box proteins.” 2018. Web. 16 Jun 2019.

Vancouver:

Barkovich KJ. Development of chemical tools targeting DEAD-box proteins. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/1bq6m023.

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

Council of Science Editors:

Barkovich KJ. Development of chemical tools targeting DEAD-box proteins. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/1bq6m023

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


University of California – San Francisco

6. Rubio, Claudia Ani Dabanian. Activating Events of the Unfolded Protein Response in Saccharomyces cerevisiae.

Degree: Biochemistry and Molecular Biology, 2010, University of California – San Francisco

 AbstractIn eukaryotic cells, the untoward accumulation of misfolded proteins inside the endoplasmic reticulum (ER) triggers a transcriptional program that restores cellular homeostasis. This program, called… (more)

Subjects/Keywords: Chemistry, Biochemistry; Biology, Cell; Biology, Molecular; endoplasmic reticulum; Ire1; unfolded protein response; yeast

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rubio, C. A. D. (2010). Activating Events of the Unfolded Protein Response in Saccharomyces cerevisiae. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/41d0j3x6

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):

Rubio, Claudia Ani Dabanian. “Activating Events of the Unfolded Protein Response in Saccharomyces cerevisiae.” 2010. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/41d0j3x6.

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

MLA Handbook (7th Edition):

Rubio, Claudia Ani Dabanian. “Activating Events of the Unfolded Protein Response in Saccharomyces cerevisiae.” 2010. Web. 16 Jun 2019.

Vancouver:

Rubio CAD. Activating Events of the Unfolded Protein Response in Saccharomyces cerevisiae. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/41d0j3x6.

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

Council of Science Editors:

Rubio CAD. Activating Events of the Unfolded Protein Response in Saccharomyces cerevisiae. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/41d0j3x6

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


University of California – San Francisco

7. Erciyas Bailey, Fazila Pinar. Structural Determinants of Protein Dynamics, Cooperativity and Kinetic Stability in Alpha-lytic Protease.

Degree: Biophysics, 2010, University of California – San Francisco

 Structural information on nonnative states of proteins, including folding intermediates and folding and unfolding transition states is crucial for understanding folding and unfolding mechanisms. Kinetically… (more)

Subjects/Keywords: Biophysics, General; Chemistry, Biochemistry; cooperativity; pH; protein folding; salt bridge; transition state; unfolding kinetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Erciyas Bailey, F. P. (2010). Structural Determinants of Protein Dynamics, Cooperativity and Kinetic Stability in Alpha-lytic Protease. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7v04b977

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):

Erciyas Bailey, Fazila Pinar. “Structural Determinants of Protein Dynamics, Cooperativity and Kinetic Stability in Alpha-lytic Protease.” 2010. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/7v04b977.

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

MLA Handbook (7th Edition):

Erciyas Bailey, Fazila Pinar. “Structural Determinants of Protein Dynamics, Cooperativity and Kinetic Stability in Alpha-lytic Protease.” 2010. Web. 16 Jun 2019.

Vancouver:

Erciyas Bailey FP. Structural Determinants of Protein Dynamics, Cooperativity and Kinetic Stability in Alpha-lytic Protease. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/7v04b977.

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

Council of Science Editors:

Erciyas Bailey FP. Structural Determinants of Protein Dynamics, Cooperativity and Kinetic Stability in Alpha-lytic Protease. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/7v04b977

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


University of California – San Francisco

8. Charles, Georgette Mona. Regulation of the SWI/SNF Chromatin Remodeling Complexes by the Non-Catalytic Subunits.

Degree: Biochemistry and Molecular Biology, 2010, University of California – San Francisco

 The primary unit of eukaryotic DNA packaging is a nucleosome, which contains ~150 bp of DNA wrapped around an octamer of histone proteins. This packaging… (more)

Subjects/Keywords: Chemistry, Biochemistry; Biology, Genetics; Biology, Molecular; Chromatin; Enzymology; Protein Biochemistry; Yeast Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Charles, G. M. (2010). Regulation of the SWI/SNF Chromatin Remodeling Complexes by the Non-Catalytic Subunits. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7310t7m3

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):

Charles, Georgette Mona. “Regulation of the SWI/SNF Chromatin Remodeling Complexes by the Non-Catalytic Subunits.” 2010. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/7310t7m3.

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

MLA Handbook (7th Edition):

Charles, Georgette Mona. “Regulation of the SWI/SNF Chromatin Remodeling Complexes by the Non-Catalytic Subunits.” 2010. Web. 16 Jun 2019.

Vancouver:

Charles GM. Regulation of the SWI/SNF Chromatin Remodeling Complexes by the Non-Catalytic Subunits. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/7310t7m3.

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

Council of Science Editors:

Charles GM. Regulation of the SWI/SNF Chromatin Remodeling Complexes by the Non-Catalytic Subunits. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/7310t7m3

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


University of California – San Francisco

9. Tia, Samuel. Microfluidic Frameworks for Immunoanalysis of Multiple Proteins.

Degree: Bioengineering, 2012, University of California – San Francisco

 Immunoassays are workhorse laboratory tools for detecting protein targets based on highly specific antibody-antigen binding interactions. Greater confidence can be ascribed to an immunoassay when… (more)

Subjects/Keywords: Biomedical engineering; Analytical chemistry; immunoassay; isoelectric focusing; microfluidic; multi-protein; post-translational modification; western blot

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tia, S. (2012). Microfluidic Frameworks for Immunoanalysis of Multiple Proteins. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7s62b771

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):

Tia, Samuel. “Microfluidic Frameworks for Immunoanalysis of Multiple Proteins.” 2012. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/7s62b771.

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

MLA Handbook (7th Edition):

Tia, Samuel. “Microfluidic Frameworks for Immunoanalysis of Multiple Proteins.” 2012. Web. 16 Jun 2019.

Vancouver:

Tia S. Microfluidic Frameworks for Immunoanalysis of Multiple Proteins. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/7s62b771.

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

Council of Science Editors:

Tia S. Microfluidic Frameworks for Immunoanalysis of Multiple Proteins. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/7s62b771

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


University of California – San Francisco

10. MacKinnon, Andrew L. Molecular mechanism of cotransin action.

Degree: Chemistry and Chemical Biology, 2011, University of California – San Francisco

 Cotransins are a class of cyclic-heptadepsi-peptides that potently inhibits translocation of a subset of proteins across the membrane of the endoplasmic reticulum (ER). Sensitivity or… (more)

Subjects/Keywords: Biochemistry; Chemistry; Cellular biology; cotransin; cotranslational translocation; mechanism of action; membrane protein biogenesis; photoaffinity labeling; Sec61

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

MacKinnon, A. L. (2011). Molecular mechanism of cotransin action. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/4bt2x57f

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):

MacKinnon, Andrew L. “Molecular mechanism of cotransin action.” 2011. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/4bt2x57f.

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

MLA Handbook (7th Edition):

MacKinnon, Andrew L. “Molecular mechanism of cotransin action.” 2011. Web. 16 Jun 2019.

Vancouver:

MacKinnon AL. Molecular mechanism of cotransin action. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/4bt2x57f.

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

Council of Science Editors:

MacKinnon AL. Molecular mechanism of cotransin action. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/4bt2x57f

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


University of California – San Francisco

11. Apsel, Beth. Dual-Specificity Inhibitors of Lipid and Protein Kinases.

Degree: Chemistry and Chemical Biology, 2008, University of California – San Francisco

 Cancer cells survive by co-opting intracellular growth pathways regulated through kinase signaling. Many kinases in these pathways are validated drug targets and kinase inhibitors are… (more)

Subjects/Keywords: Chemistry, Biochemistry; Phosphoinositide-3-kinase; Protein tyrosine kinases; kinase inhibitors

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Apsel, B. (2008). Dual-Specificity Inhibitors of Lipid and Protein Kinases. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7372d6r8

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):

Apsel, Beth. “Dual-Specificity Inhibitors of Lipid and Protein Kinases.” 2008. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/7372d6r8.

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

MLA Handbook (7th Edition):

Apsel, Beth. “Dual-Specificity Inhibitors of Lipid and Protein Kinases.” 2008. Web. 16 Jun 2019.

Vancouver:

Apsel B. Dual-Specificity Inhibitors of Lipid and Protein Kinases. [Internet] [Thesis]. University of California – San Francisco; 2008. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/7372d6r8.

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

Council of Science Editors:

Apsel B. Dual-Specificity Inhibitors of Lipid and Protein Kinases. [Thesis]. University of California – San Francisco; 2008. Available from: http://www.escholarship.org/uc/item/7372d6r8

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


University of California – San Francisco

12. Kelch, Brian A. Identifying the Structural Determinants of Extreme Folding and Unfolding Barriers.

Degree: Biochemistry and Molecular Biology, 2007, University of California – San Francisco

 Detailed knowledge of folding intermediate and transition state (TS) structures is critical for understanding protein folding mechanisms. For kinetically-stable proteins such as α-lytic protease (αLP)… (more)

Subjects/Keywords: Biophysics, General; Biology, Molecular; Chemistry, Biochemistry; alpha-Lytic Protease; kinetic stability; acid stability; sidechain distortion; thermophile; protein folding

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kelch, B. A. (2007). Identifying the Structural Determinants of Extreme Folding and Unfolding Barriers. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9r9735mm

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):

Kelch, Brian A. “Identifying the Structural Determinants of Extreme Folding and Unfolding Barriers.” 2007. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/9r9735mm.

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

MLA Handbook (7th Edition):

Kelch, Brian A. “Identifying the Structural Determinants of Extreme Folding and Unfolding Barriers.” 2007. Web. 16 Jun 2019.

Vancouver:

Kelch BA. Identifying the Structural Determinants of Extreme Folding and Unfolding Barriers. [Internet] [Thesis]. University of California – San Francisco; 2007. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/9r9735mm.

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

Council of Science Editors:

Kelch BA. Identifying the Structural Determinants of Extreme Folding and Unfolding Barriers. [Thesis]. University of California – San Francisco; 2007. Available from: http://www.escholarship.org/uc/item/9r9735mm

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


University of California – San Francisco

13. Garrison, Jennifer Lynn. Small molecule modulation of protein secretion.

Degree: Chemistry and Chemical Biology, 2007, University of California – San Francisco

 Specific small molecule inhibitors can be used as molecular tools to dissect complex cellular processes and illuminate basic biological questions, such as protein secretion. A… (more)

Subjects/Keywords: Chemistry, Biochemistry; Biology, Cell; cotransin; protein translocation; signal sequence; HUN-7293; small molecule inhibitor; Sec61

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Garrison, J. L. (2007). Small molecule modulation of protein secretion. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/51v3n32d

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):

Garrison, Jennifer Lynn. “Small molecule modulation of protein secretion.” 2007. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/51v3n32d.

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

MLA Handbook (7th Edition):

Garrison, Jennifer Lynn. “Small molecule modulation of protein secretion.” 2007. Web. 16 Jun 2019.

Vancouver:

Garrison JL. Small molecule modulation of protein secretion. [Internet] [Thesis]. University of California – San Francisco; 2007. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/51v3n32d.

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

Council of Science Editors:

Garrison JL. Small molecule modulation of protein secretion. [Thesis]. University of California – San Francisco; 2007. Available from: http://www.escholarship.org/uc/item/51v3n32d

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


University of California – San Francisco

14. Fawzi, Nicolas Lux. Contrasting disease and non-disease protein aggregation by molecular simulations.

Degree: Bioengineering, 2008, University of California – San Francisco

 This work describes the development and application of computational models for the investigation of disease and non-disease protein aggregation. We demonstrate how the aggregate equilibrium,… (more)

Subjects/Keywords: Engineering, Biomedical; Biophysics, General; Chemistry, Physical; Alzheimer's Disease; amyloid; aggregation; protein; molecular dynamics; NMR

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fawzi, N. L. (2008). Contrasting disease and non-disease protein aggregation by molecular simulations. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7v14w7sc

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):

Fawzi, Nicolas Lux. “Contrasting disease and non-disease protein aggregation by molecular simulations.” 2008. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/7v14w7sc.

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

MLA Handbook (7th Edition):

Fawzi, Nicolas Lux. “Contrasting disease and non-disease protein aggregation by molecular simulations.” 2008. Web. 16 Jun 2019.

Vancouver:

Fawzi NL. Contrasting disease and non-disease protein aggregation by molecular simulations. [Internet] [Thesis]. University of California – San Francisco; 2008. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/7v14w7sc.

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

Council of Science Editors:

Fawzi NL. Contrasting disease and non-disease protein aggregation by molecular simulations. [Thesis]. University of California – San Francisco; 2008. Available from: http://www.escholarship.org/uc/item/7v14w7sc

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


University of California – San Francisco

15. Wilbur, Jeremy D. Conformational Switches Regulate Clathrin Mediated Endocytosis.

Degree: Biophysics, 2008, University of California – San Francisco

 Clathrin mediated endocytosis is a fundamental cellular process used to regulate the response of cells to their environment. It has been usurped as a means… (more)

Subjects/Keywords: Biophysics, General; Chemistry, Biochemistry; Biology, Cell; clathrin; X-ray crystallography; huntingtin interacting protein; actin; conformational change

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wilbur, J. D. (2008). Conformational Switches Regulate Clathrin Mediated Endocytosis. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0fd1v310

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):

Wilbur, Jeremy D. “Conformational Switches Regulate Clathrin Mediated Endocytosis.” 2008. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/0fd1v310.

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

MLA Handbook (7th Edition):

Wilbur, Jeremy D. “Conformational Switches Regulate Clathrin Mediated Endocytosis.” 2008. Web. 16 Jun 2019.

Vancouver:

Wilbur JD. Conformational Switches Regulate Clathrin Mediated Endocytosis. [Internet] [Thesis]. University of California – San Francisco; 2008. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/0fd1v310.

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

Council of Science Editors:

Wilbur JD. Conformational Switches Regulate Clathrin Mediated Endocytosis. [Thesis]. University of California – San Francisco; 2008. Available from: http://www.escholarship.org/uc/item/0fd1v310

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


University of California – San Francisco

16. Thomas, Veena Lily. The Structural Bases of Stability-Function Tradeoffs in Antibiotic Resistance Enzymes.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2009, University of California – San Francisco

 Antibiotic use has led to the evolution of antibiotic resistance enzymes able to hydrolyze newer antibiotics, leaving them useless against killing bacteria. Are there biophysical… (more)

Subjects/Keywords: Biophysics, General; Chemistry, Biochemistry; action-at-a-distance; antibiotic resistance; beta-lactamase; evolution; protein stability

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thomas, V. L. (2009). The Structural Bases of Stability-Function Tradeoffs in Antibiotic Resistance Enzymes. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/1817j439

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):

Thomas, Veena Lily. “The Structural Bases of Stability-Function Tradeoffs in Antibiotic Resistance Enzymes.” 2009. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/1817j439.

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

MLA Handbook (7th Edition):

Thomas, Veena Lily. “The Structural Bases of Stability-Function Tradeoffs in Antibiotic Resistance Enzymes.” 2009. Web. 16 Jun 2019.

Vancouver:

Thomas VL. The Structural Bases of Stability-Function Tradeoffs in Antibiotic Resistance Enzymes. [Internet] [Thesis]. University of California – San Francisco; 2009. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/1817j439.

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

Council of Science Editors:

Thomas VL. The Structural Bases of Stability-Function Tradeoffs in Antibiotic Resistance Enzymes. [Thesis]. University of California – San Francisco; 2009. Available from: http://www.escholarship.org/uc/item/1817j439

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


University of California – San Francisco

17. Ianculescu, Alexandra Georgiana. Investigations of 3-iodothyronamine as a novel regulator of thyroid endocrinology.

Degree: Biochemistry and Molecular Biology, 2009, University of California – San Francisco

 3-iodothyronamine (T1AM) is an endogenous thyroid hormone metabolite with distinct, acute biological effects that are largely opposite those of thyroid hormone. Administration of T1AM to… (more)

Subjects/Keywords: Biology, Molecular; Chemistry, Biochemistry; Health Sciences, Pharmacology; membrane transporter; serum binding protein; thyroid hormone; thyroid hormone derivatives; thyronamine; trace amines

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ianculescu, A. G. (2009). Investigations of 3-iodothyronamine as a novel regulator of thyroid endocrinology. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2k21w7bm

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):

Ianculescu, Alexandra Georgiana. “Investigations of 3-iodothyronamine as a novel regulator of thyroid endocrinology.” 2009. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/2k21w7bm.

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

MLA Handbook (7th Edition):

Ianculescu, Alexandra Georgiana. “Investigations of 3-iodothyronamine as a novel regulator of thyroid endocrinology.” 2009. Web. 16 Jun 2019.

Vancouver:

Ianculescu AG. Investigations of 3-iodothyronamine as a novel regulator of thyroid endocrinology. [Internet] [Thesis]. University of California – San Francisco; 2009. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/2k21w7bm.

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

Council of Science Editors:

Ianculescu AG. Investigations of 3-iodothyronamine as a novel regulator of thyroid endocrinology. [Thesis]. University of California – San Francisco; 2009. Available from: http://www.escholarship.org/uc/item/2k21w7bm

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


University of California – San Francisco

18. Atkinson, Holly Jean. The structural and functional landscape of protein superfamilies: From the thioredoxin fold to parasite peptidases.

Degree: Biological and Medical Informatics, 2009, University of California – San Francisco

 All enzymes can be classified into superfamilies that share common mechanistic attributes of catalysis. These catalytic attributes are delivered via variants of a common structural… (more)

Subjects/Keywords: Chemistry, Biochemistry; Biology, Bioinformatics; function annotation; glutathione transferase; peptidase; protein structure; similarity network; thioredoxin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Atkinson, H. J. (2009). The structural and functional landscape of protein superfamilies: From the thioredoxin fold to parasite peptidases. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/6394z0xw

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):

Atkinson, Holly Jean. “The structural and functional landscape of protein superfamilies: From the thioredoxin fold to parasite peptidases.” 2009. Thesis, University of California – San Francisco. Accessed June 16, 2019. http://www.escholarship.org/uc/item/6394z0xw.

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

MLA Handbook (7th Edition):

Atkinson, Holly Jean. “The structural and functional landscape of protein superfamilies: From the thioredoxin fold to parasite peptidases.” 2009. Web. 16 Jun 2019.

Vancouver:

Atkinson HJ. The structural and functional landscape of protein superfamilies: From the thioredoxin fold to parasite peptidases. [Internet] [Thesis]. University of California – San Francisco; 2009. [cited 2019 Jun 16]. Available from: http://www.escholarship.org/uc/item/6394z0xw.

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

Council of Science Editors:

Atkinson HJ. The structural and functional landscape of protein superfamilies: From the thioredoxin fold to parasite peptidases. [Thesis]. University of California – San Francisco; 2009. Available from: http://www.escholarship.org/uc/item/6394z0xw

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

.